Review on the Treatment of Pancreatitis with Traditional Chinese Medicine Targeting the Nrf2 Pathway

In: Current Traditional Medicine · 2024 · vol. 11(6) · doi:10.2174/0122150838299447240621100613 · W4400590297
article OA: closed CC0
Full text JSON View on OpenAlex View at publisher

Abstract

Acute Pancreatitis (AP) is a ubiquitous inflammatory digestive system disease with a high prevalence worldwide. Once it progresses to Severe Acute Pancreatitis (SAP), its mortality can significantly increase. However, until now, there has been no clinical cure for AP, and the treatment of patients has mostly been based on surgery and supportive care. This has become a major medical problem. As for the pharmacological treatment of AP, various Chinese medicine tonics and formulations have shown a surprising appeal in both clinical and scientific research. Studies on AP pathogenesis have shown that physiological processes, such as oxidative stress and inflammatory responses, play important roles in AP. The Nuclear factor E2-related factor 2 (Nrf2) signalling pathway is closely related to the antioxidant and anti-inflammatory properties of the body and may be a promising therapeutic target for the treatment of AP. Therefore, this review focuses on Chinese patent medicine that uses the Nrf2 pathway as a therapeutic target. We list the current research and clinical treatment strategies for AP with the help of Chinese medicine as a cornerstone for future studies. Some of our reflections and conclusions are presented in this review, especially with a focus on the mechanism of action of therapeutic strategies.
Full text 66,287 characters · extracted from oa-doi-fallback · 2 sections · click to expand

Abstract

Acute Pancreatitis (AP) is a ubiquitous inflammatory digestive system disease with a high prevalence worldwide. Once it progresses to Severe Acute Pancreatitis (SAP), its mortality can significantly increase. However, until now, there has been no clinical cure for AP, and the treatment of patients has mostly been based on surgery and supportive care. This has become a major medical problem. As for the pharmacological treatment of AP, various Chinese medicine tonics and formulations have shown a surprising appeal in both clinical and scientific research. Studies on AP pathogenesis have shown that physiological processes, such as oxidative stress and inflammatory responses, play important roles in AP. The Nuclear factor E2-related factor 2 (Nrf2) signalling pathway is closely related to the antioxidant and anti-inflammatory properties of the body and may be a promising therapeutic target for the treatment of AP. Therefore, this review focuses on Chinese patent medicine that uses the Nrf2 pathway as a therapeutic target. We list the current research and clinical treatment strategies for AP with the help of Chinese medicine as a cornerstone for future studies. Some of our reflections and conclusions are presented in this review, especially with a focus on the mechanism of action of therapeutic strategies.

Keywords

Nrf2 signal pathway, oxidative stress, Chinese herbal medicine, SAP, tissue oedema, DAP. [1] Hu, J.X.; Zhao, C.F.; Chen, W.B. Pancreatic cancer: A review of epidemiology, trend, and risk factors. World J. Gastroenterol., 2021, 27(27), 4298-4321. [http://dx.doi.org/10.3748/wjg.v27.i27.4298] [PMID: 34366606] [http://dx.doi.org/10.3748/wjg.v27.i27.4298] [PMID: 34366606] [2] Habtezion, A.; Gukovskaya, A.S.; Pandol, S.J. Acute pancreatitis: A multifaceted set of organelle and cellular interactions. Gastroenterology, 2019, 156(7), 1941-1950. [http://dx.doi.org/10.1053/j.gastro.2018.11.082] [PMID: 30660726] [http://dx.doi.org/10.1053/j.gastro.2018.11.082] [PMID: 30660726] [3] Petrov, M.S.; Yadav, D. Global epidemiology and holistic prevention of pancreatitis. Nat. Rev. Gastroenterol. Hepatol., 2019, 16(3), 175-184. [http://dx.doi.org/10.1038/s41575-018-0087-5] [PMID: 30482911] [http://dx.doi.org/10.1038/s41575-018-0087-5] [PMID: 30482911] [4] Liu, Y.; Liu, H.; Rong, Y. Alterations of oral microbiota are associated with the development and severity of acute pancreatitis. J. Oral Microbiol., 2023, 15(1), 2264619. [http://dx.doi.org/10.1080/20002297.2023.2264619] [PMID: 37808891] [http://dx.doi.org/10.1080/20002297.2023.2264619] [PMID: 37808891] [5] Szatmary, P.; Grammatikopoulos, T.; Cai, W. Acute pancreatitis: Diagnosis and treatment. Drugs, 2022, 82(12), 1251-1276. [http://dx.doi.org/10.1007/s40265-022-01766-4] [PMID: 36074322] [http://dx.doi.org/10.1007/s40265-022-01766-4] [PMID: 36074322] [6] Hines, O.J.; Pandol, S.J. Management of severe acute pancreatitis. BMJ, 2019, 367, l6227. [http://dx.doi.org/10.1136/bmj.l6227] [PMID: 31791953] [http://dx.doi.org/10.1136/bmj.l6227] [PMID: 31791953] [7] Garg, P.K.; Singh, V.P. Organ failure due to systemic injury in acute pancreatitis. Gastroenterology, 2019, 156(7), 2008-2023. [http://dx.doi.org/10.1053/j.gastro.2018.12.041] [PMID: 30768987] [http://dx.doi.org/10.1053/j.gastro.2018.12.041] [PMID: 30768987] [8] Trikudanathan, G.; Wolbrink, D.R.J.; van Santvoort, H.C.; Mallery, S.; Freeman, M.; Besselink, M.G. Current concepts in severe acute and necrotizing pancreatitis: An evidence-based approach. Gastroenterology, 2019, 156(7), 1994-2007.e3. [http://dx.doi.org/10.1053/j.gastro.2019.01.269] [PMID: 30776347] [http://dx.doi.org/10.1053/j.gastro.2019.01.269] [PMID: 30776347] [9] Chadalavada, P.; Simons-Linares, C.R.; Chahal, P. Drug-induced acute pancreatitis: Prevalence, causative agents, and outcomes. Pancreatology, 2020, 20(7), 1281-1286. [http://dx.doi.org/10.1016/j.pan.2020.07.401] [PMID: 32878711] [http://dx.doi.org/10.1016/j.pan.2020.07.401] [PMID: 32878711] [10] Sánchez-Aldehuelo, R.; García García de Paredes, A.; Rojo Lázaro, D. Outcomes of drug-induced acute pancreatitis: A ten-year experience of an academic center. Rev. Esp. Enferm. Dig., 2021, 113(4), 276-279. [PMID: 33256421] [PMID: 33256421] [11] Xiong, G.F.; Li, D.W.; Zheng, M.B.; Liu, S.C. The effects of lycium barbarum polysaccharide (LBP) in a mouse model of cerulein-induced acute pancreatitis. Med. Sci. Monit., 2019, 25, 3880-3886. [http://dx.doi.org/10.12659/MSM.913820] [PMID: 31127077] [http://dx.doi.org/10.12659/MSM.913820] [PMID: 31127077] [12] Barreto, S.G.; Habtezion, A.; Gukovskaya, A. Critical thresholds: Key to unlocking the door to the prevention and specific treatments for acute pancreatitis. Gut, 2021, 70(1), 194-203. [http://dx.doi.org/10.1136/gutjnl-2020-322163] [PMID: 32973069] [http://dx.doi.org/10.1136/gutjnl-2020-322163] [PMID: 32973069] [13] Lee, P.J.; Papachristou, G.I. New insights into acute pancreatitis. Nat. Rev. Gastroenterol. Hepatol., 2019, 16(8), 479-496. [http://dx.doi.org/10.1038/s41575-019-0158-2] [PMID: 31138897] [http://dx.doi.org/10.1038/s41575-019-0158-2] [PMID: 31138897] [14] Zhang, Q.; Li, S.; Yu, Y.; Zhu, Y.; Tong, R. A mini-review of diagnostic and therapeutic nano-tools for pancreatitis. Int. J. Nanomedicine, 2022, 17, 4367-4381. [http://dx.doi.org/10.2147/IJN.S385590] [PMID: 36160469] [http://dx.doi.org/10.2147/IJN.S385590] [PMID: 36160469] [15] Song, Y.D.; Liu, Y.Y.; Li, D.J. Galangin ameliorates severe acute pancreatitis in mice by activating the nuclear factor E2-related factor 2/heme oxygenase 1 pathway. Biomed. Pharmacother., 2021, 144, 112293. [http://dx.doi.org/10.1016/j.biopha.2021.112293] [PMID: 34634559] [http://dx.doi.org/10.1016/j.biopha.2021.112293] [PMID: 34634559] [16] Luo, Y.; Li, Z.; Ge, P. Comprehensive mechanism, novel markers and multidisciplinary treatment of severe acute pancreatitis-associated cardiac injury – A narrative review. J. Inflamm. Res., 2021, 14, 3145-3169. [http://dx.doi.org/10.2147/JIR.S310990] [PMID: 34285540] [http://dx.doi.org/10.2147/JIR.S310990] [PMID: 34285540] [17] Swentek, L.; Chung, D.; Ichii, H. Antioxidant therapy in pancreatitis. Antioxidants, 2021, 10(5), 657. [http://dx.doi.org/10.3390/antiox10050657] [PMID: 33922756] [http://dx.doi.org/10.3390/antiox10050657] [PMID: 33922756] [18] Zhao, J.; Guo, F.; Hou, L.; Zhao, Y.; Sun, P. Electron transfer-based antioxidant nanozymes: Emerging therapeutics for inflammatory diseases. J. Control. Release, 2023, 355, 273-291. [http://dx.doi.org/10.1016/j.jconrel.2023.01.068] [PMID: 36731800] [http://dx.doi.org/10.1016/j.jconrel.2023.01.068] [PMID: 36731800] [19] Tusa, N.V.; Abuelo, A.; Levy, N.A.; Gandy, J.C.; Langlois, D.K.; Cridge, H. Peripheral biomarkers of oxidative stress in dogs with acute pancreatitis. J. Vet. Intern. Med., 2022, 36(6), 1958-1965. [http://dx.doi.org/10.1111/jvim.16535] [PMID: 36086902] [http://dx.doi.org/10.1111/jvim.16535] [PMID: 36086902] [20] Gao, L.; Chong, E.; Pendharkar, S. The effects of NLRP3 inflammasome inhibition in experimental acute pancreatitis. Pancreas, 2022, 51(1), 13-24. [http://dx.doi.org/10.1097/MPA.0000000000001971] [PMID: 35195590] [http://dx.doi.org/10.1097/MPA.0000000000001971] [PMID: 35195590] [21] Zhu, TianHong; Chen, TianQi; Zhao, Wei; Bao, QinHai Effects of Yinchenhao Decoction on Severe Acute Pancreatitis-related Acute Liver injury and p62-keap1-Nrf2 signaling Pathway in Rats J Emerg Tradit, 2019, 28(07), 1167-1170. [22] Machicado, J.D.; Papachristou, G.I. Pharmacologic management and prevention of acute pancreatitis. Curr. Opin. Gastroenterol., 2019, 35(5), 460-467. [http://dx.doi.org/10.1097/MOG.0000000000000563] [PMID: 31205053] [http://dx.doi.org/10.1097/MOG.0000000000000563] [PMID: 31205053] [23] Gubensek, J. The role of apheresis and insulin therapy in hypertriglyceridemic acute pancreatitis—a concise review. BMC Gastroenterol., 2023, 23(1), 341. [http://dx.doi.org/10.1186/s12876-023-02957-3] [PMID: 37789261] [http://dx.doi.org/10.1186/s12876-023-02957-3] [PMID: 37789261] [24] Chen, W.; Yuan, C.; Lu, Y.; Zhu, Q.; Ma, X.; Xiao, W. Tanshinone IIA protects against acute pancreatitis in mice by inhibiting oxidative stress via the Nrf2/ROS pathway. Oxid. Med. Cell. Longev., 2020, 2020, 5390482. [25] Chen, J.; Su, Y.; Lin, F. Effect of paraquat on cytotoxicity involved in oxidative stress and inflammatory reaction: A review of mechanisms and ecological implications. Ecotoxicol. Environ. Saf., 2021, 224, 112711. [http://dx.doi.org/10.1016/j.ecoenv.2021.112711] [PMID: 34455184] [http://dx.doi.org/10.1016/j.ecoenv.2021.112711] [PMID: 34455184] [26] Wang, Y.; Li, A.; Mehmood, K. Long-term exposure to the fluoride blocks the development of chondrocytes in the ducks: The molecular mechanism of fluoride regulating autophagy and apoptosis. Ecotoxicol. Environ. Saf., 2021, 217, 112225. [http://dx.doi.org/10.1016/j.ecoenv.2021.112225] [PMID: 33864983] [http://dx.doi.org/10.1016/j.ecoenv.2021.112225] [PMID: 33864983] [27] Toyokuni, S.; Kong, Y.; Cheng, Z. Carcinogenesis as side effects of iron and oxygen utilization: From the unveiled truth toward ultimate bioengineering. Cancers, 2020, 12(11), 3320. [http://dx.doi.org/10.3390/cancers12113320] [PMID: 33182727] [http://dx.doi.org/10.3390/cancers12113320] [PMID: 33182727] [28] den Toom, W.T.F.; van Soest, D.M.K.; Polderman, P.E. Oxygen-consumption based quantification of chemogenetic H2O2 production in live human cells. Free Radic. Biol. Med., 2023, 206, 134-142. [http://dx.doi.org/10.1016/j.freeradbiomed.2023.06.030] [PMID: 37392950] [http://dx.doi.org/10.1016/j.freeradbiomed.2023.06.030] [PMID: 37392950] [29] Chang, J.; Wang, Y.; Wei, H.; Kong, X.; Dong, B.; Yue, T. Development of a “double reaction” type-based fluorescent probe for the imaging of superoxide anion in living cells. Spectrochim. Acta A Mol. Biomol. Spectrosc., 2023, 302, 123080. [30] Borgonovi, S.M.; Iametti, S.; Di Nunzio, M. Docosahexaenoic acid as master regulator of cellular antioxidant defenses: A systematic review. Antioxidants, 2023, 12(6), 1283. [http://dx.doi.org/10.3390/antiox12061283] [PMID: 37372014] [http://dx.doi.org/10.3390/antiox12061283] [PMID: 37372014] [31] Ahn, Y.J.; Lim, J.W.; Kim, H. Docosahexaenoic acid induces expression of nad(p)h: quinone oxidoreductase and heme oxygenase-1 through activation of Nrf2 in cerulein-stimulated pancreatic acinar cells. Antioxidants, 2020, 9(11), 1084. [http://dx.doi.org/10.3390/antiox9111084] [PMID: 33158207] [http://dx.doi.org/10.3390/antiox9111084] [PMID: 33158207] [32] Tsai, T.H.; Su, Y.F.; Tsai, C.Y.; Wu, C.H.; Lee, K.T.; Hsu, Y.C. RTA dh404 induces cell cycle arrest, apoptosis, and autophagy in glioblastoma cells. Int. J. Mol. Sci., 2023, 24(4), 4006. [http://dx.doi.org/10.3390/ijms24044006] [PMID: 36835414] [http://dx.doi.org/10.3390/ijms24044006] [PMID: 36835414] [33] Xu, L.L.; Zhao, B.; Sun, S.L. High-dose vitamin C alleviates pancreatic injury via the NRF2/NQO1/HO-1 pathway in a rat model of severe acute pancreatitis. Ann. Transl. Med., 2020, 8(14), 852. [http://dx.doi.org/10.21037/atm-19-4552] [PMID: 32793696] [http://dx.doi.org/10.21037/atm-19-4552] [PMID: 32793696] [34] Kong, L.; Deng, J.; Zhou, X. Sitagliptin activates the p62–Keap1–Nrf2 signalling pathway to alleviate oxidative stress and excessive autophagy in severe acute pancreatitis-related acute lung injury. Cell Death Dis., 2021, 12(10), 928. [http://dx.doi.org/10.1038/s41419-021-04227-0] [PMID: 34635643] [http://dx.doi.org/10.1038/s41419-021-04227-0] [PMID: 34635643] [35] Ebrahimnezhad, N.; Nayebifar, S.; Soltani, Z.; Khoramipour, K. High-intensity interval training reduced oxidative stress and apoptosis in the hippocampus of male rats with type 2 diabetes: The role of the PGC1α-Keap1-Nrf2 signaling pathway. Iran. J. Basic Med. Sci., 2023, 26(11), 1313-1319. [PMID: 37885999] [PMID: 37885999] [36] Ushimoto, C.; Sugiki, S.; Kunii, K. Dynamic change and preventive role of stress response via Keap1-Nrf2 during renal crystal formation. Free Radic. Biol. Med., 2023, 207, 120-132. [http://dx.doi.org/10.1016/j.freeradbiomed.2023.07.013] [PMID: 37451369] [http://dx.doi.org/10.1016/j.freeradbiomed.2023.07.013] [PMID: 37451369] [37] Baird, L.; Taguchi, K.; Zhang, A. A NRF2-induced secretory phenotype activates immune surveillance to remove irreparably damaged cells. Redox Biol., 2023, 66, 102845. [http://dx.doi.org/10.1016/j.redox.2023.102845] [PMID: 37597423] [http://dx.doi.org/10.1016/j.redox.2023.102845] [PMID: 37597423] [38] Fuertes-Agudo, M.; Luque-Tévar, M.; Cucarella, C.; Martín-Sanz, P.; Casado, M. Advances in understanding the role of NRF2 in liver pathophysiology and its relationship with hepatic-specific cyclooxygenase-2 expression. Antioxidants, 2023, 12(8), 1491. [http://dx.doi.org/10.3390/antiox12081491] [PMID: 37627486] [http://dx.doi.org/10.3390/antiox12081491] [PMID: 37627486] [39] Palomino-Antolín, A.; Decouty-Pérez, C.; Farré-Alins, V. Redox regulation of microglial inflammatory response: Fine control of NLRP3 inflammasome through Nrf2 and NOX4. Antioxidants, 2023, 12(9), 1729. [http://dx.doi.org/10.3390/antiox12091729] [PMID: 37760032] [http://dx.doi.org/10.3390/antiox12091729] [PMID: 37760032] [40] Cai, C.; Ma, H.; Peng, J. USP25 regulates KEAP1-NRF2 anti-oxidation axis and its inactivation protects acetaminophen-induced liver injury in male mice. Nat. Commun., 2023, 14(1), 3648. [http://dx.doi.org/10.1038/s41467-023-39412-6] [PMID: 37339955] [http://dx.doi.org/10.1038/s41467-023-39412-6] [PMID: 37339955] [41] Fadoul, G.; Ikonomovic, M.; Zhang, F.; Yang, T. The cell-specific roles of Nrf2 in acute and chronic phases of ischemic stroke. CNS Neurosci. Ther., 2024, 30(3), e14462. [PMID: 37715557] [PMID: 37715557] [42] Wang, Z.; Liu, J.; Li, F. Mechanisms of qingyi decoction in severe acute pancreatitis-associated acute lung injury via gut microbiota: Targeting the short-chain fatty acids-mediated AMPK/] NF-κB/NLRP3 pathway. Microbiol. Spectr., 2023, 11(4), e03664-e22. [http://dx.doi.org/10.1128/spectrum.03664-22] [http://dx.doi.org/10.1128/spectrum.03664-22] [43] Neves, R.P.P.; Cunha, A.V.; Fernandes, P.A.; Ramos, M.J. Towards the accurate thermodynamic characterization of enzyme reaction mechanisms. ChemPhysChem, 2022, 23(13), e202200159. [http://dx.doi.org/10.1002/cphc.202200159] [PMID: 35499146] [http://dx.doi.org/10.1002/cphc.202200159] [PMID: 35499146] [44] Damasceno, R.O.S.; Soares, P.M.G.; Barbosa, A.L.R.; Nicolau, L.A.D.; Medeiros, J.V.R.; Souza, M.H.L.P. Modulatory role of carbon monoxide on the inflammatory response and oxidative stress linked to gastrointestinal disorders. Antioxid. Redox Signal., 2022, 37(1-3), 98-114. [http://dx.doi.org/10.1089/ars.2020.8223] [PMID: 34806398] [http://dx.doi.org/10.1089/ars.2020.8223] [PMID: 34806398] [45] Li, X-J.; Liu, T.; Wang, Y. Allicin ameliorates sepsis-induced acute kidney injury through Nrf2/HO-1 signaling pathway. J. Nat. Med., 2024, 78(1), 53-67. [PMID: 37668824] [PMID: 37668824] [46] Liu, Y.; Wang, X.; Xu, X.; Qin, W.; Sun, B. Carbon monoxide releasing molecule 2 (CORM 2) liberated CO ameliorates acute pancreatitis. Mol. Med. Rep., 2019, 19(6), 5142-5152. [http://dx.doi.org/10.3892/mmr.2019.10173] [PMID: 31059081] [http://dx.doi.org/10.3892/mmr.2019.10173] [PMID: 31059081] [47] Puentes-Pardo, J.D.; Moreno-SanJuan, S.; Carazo, Á.; León, J. Heme oxygenase-1 in gastrointestinal tract health and disease. Antioxidants, 2020, 9(12), 1214. [http://dx.doi.org/10.3390/antiox9121214] [PMID: 33276470] [http://dx.doi.org/10.3390/antiox9121214] [PMID: 33276470] [48] Mao, X.; Mao, S.; Wang, L. Single-cell transcriptomic analysis of the mouse pancreas: Characteristic features of pancreatic ductal cells in chronic pancreatitis. Genes, 2022, 13(6), 1015. [http://dx.doi.org/10.3390/genes13061015] [PMID: 35741777] [http://dx.doi.org/10.3390/genes13061015] [PMID: 35741777] [49] Yao, Q.; Jiang, X.; Zhai, Y.Y. Protective effects and mechanisms of bilirubin nanomedicine against acute pancreatitis. J. Control. Release, 2020, 322, 312-325. [http://dx.doi.org/10.1016/j.jconrel.2020.03.034] [PMID: 32243974] [http://dx.doi.org/10.1016/j.jconrel.2020.03.034] [PMID: 32243974] [50] Jiang, X.; Zheng, Y.W.; Bao, S. Drug discovery and formulation development for acute pancreatitis. Drug Deliv., 2020, 27(1), 1562-1580. [http://dx.doi.org/10.1080/10717544.2020.1840665] [PMID: 33118404] [http://dx.doi.org/10.1080/10717544.2020.1840665] [PMID: 33118404] [51] Guo, W.; Huang, D.; Li, S. Lycopene alleviates oxidative stress-induced cell injury in human vascular endothelial cells by encouraging the SIRT1/Nrf2/HO-1 pathway. Clin. Exp. Hypertens., 2023, 45(1), 2205051. [http://dx.doi.org/10.1080/10641963.2023.2205051] [PMID: 37120838] [http://dx.doi.org/10.1080/10641963.2023.2205051] [PMID: 37120838] [52] Hsieh, CY; Jayakumar, T; Lin, KC Morin hydrate suppresses lipoteichoic acid-induced oxidative stress-mediated inflammatory events in macrophages via augmenting Nrf2/HO-1 and antioxidant defense molecules. Eur J Inflamm, 2023, 21, 1721727X231199414. [http://dx.doi.org/10.1177/1721727X231199414] [http://dx.doi.org/10.1177/1721727X231199414] [53] Zhang, F.; Liu, Y.; Dong, X. Shenmai injection upregulates heme oxygenase-1 to confer protection against severe acute pancreatitis. J. Surg. Res., 2020, 256, 295-302. [http://dx.doi.org/10.1016/j.jss.2020.06.035] [PMID: 32712444] [http://dx.doi.org/10.1016/j.jss.2020.06.035] [PMID: 32712444] [54] Batran, R.Z.; Ahmed, E.Y.; Awad, H.M.; Ali, K.A.; Abdel Latif, N.A. EGFR and PI3K/m-TOR inhibitors: Design, microwave assisted synthesis and anticancer activity of thiazole–coumarin hybrids. RSC Advances, 2023, 13(42), 29070-29085. [http://dx.doi.org/10.1039/D3RA03483F] [PMID: 37800132] [http://dx.doi.org/10.1039/D3RA03483F] [PMID: 37800132] [55] DeBlasi, J.M.; Falzone, A.; Caldwell, S. Distinct Nrf2 signaling thresholds mediate lung tumor initiation and progression. Cancer Res., 2023, 83(12), 1953-1967. [http://dx.doi.org/10.1158/0008-5472.CAN-22-3848] [PMID: 37062029] [http://dx.doi.org/10.1158/0008-5472.CAN-22-3848] [PMID: 37062029] [56] Arab, H.H.; Al-Shorbagy, M.Y.; Saad, M.A. Activation of autophagy and suppression of apoptosis by dapagliflozin attenuates experimental inflammatory bowel disease in rats: Targeting AMPK/] mTOR, HMGB1/RAGE and Nrf2/HO-1 pathways. Chem. Biol. Interact., 2021, 335, 109368. [http://dx.doi.org/10.1016/j.cbi.2021.109368] [PMID: 33412153] [http://dx.doi.org/10.1016/j.cbi.2021.109368] [PMID: 33412153] [57] Dodson, M.; de la Vega, M.R.; Cholanians, A.B.; Schmidlin, C.J.; Chapman, E.; Zhang, D.D. Modulating NRF2 in disease: Timing is everything. Annu. Rev. Pharmacol. Toxicol., 2019, 59, 555-575. [58] Hu, Y.; Yang, W. Paeoniflorin can improve acute lung injury caused by severe acute pancreatitis through Nrf2/ARE pathway. Comput. Math. Methods Med., 2022, 2022, 5712219. [59] Li, Y.; Wang, K.; Zhu, X. Ginkgo biloba extracts protect human retinal Müller glial cells from t -BHP induced oxidative damage by activating the AMPK-Nrf2-NQO-1 axis. J. Pharm. Pharmacol., 2023, 75(3), 385-396. [http://dx.doi.org/10.1093/jpp/rgac095] [PMID: 36583518] [http://dx.doi.org/10.1093/jpp/rgac095] [PMID: 36583518] [60] Guzel Tanoglu, E.; Tanoglu, A.; Guven, B.B. mir‐221, mir‐190b, mir‐363‐3p, mir‐200c are involved in rat liver ischaemia‐reperfusion injury through oxidative stress, apoptosis and endoplasmic reticulum stress. Int. J. Clin. Pract., 2021, 75(11), e14848. [http://dx.doi.org/10.1111/ijcp.14848] [PMID: 34519137] [http://dx.doi.org/10.1111/ijcp.14848] [PMID: 34519137] [61] Xia, Q.; Li, Y.; Xu, W. Enhanced liquidity of p62 droplets mediated by Smurf1 links Nrf2 activation and autophagy. Cell Biosci., 2023, 13(1), 37. [http://dx.doi.org/10.1186/s13578-023-00978-9] [PMID: 36810259] [http://dx.doi.org/10.1186/s13578-023-00978-9] [PMID: 36810259] [62] Zhu, D.; Xia, Y.; Li, S. Iso-seco-tanapartholide activates Nrf2 signaling pathway through Keap1 modification and oligomerization to exert anti-inflammatory effects. Free Radic. Biol. Med., 2022, 178, 398-412. [http://dx.doi.org/10.1016/j.freeradbiomed.2021.12.259] [PMID: 34923099] [http://dx.doi.org/10.1016/j.freeradbiomed.2021.12.259] [PMID: 34923099] [63] Zhang, H.; Zeng, J.; Li, J. Sivelestat sodium attenuates acute lung injury by inhibiting JNK/NF-κB and activating Nrf2/HO-1 signaling pathways. Biomolecules and Biomedicine, 2023, 23(3), 457-470. [http://dx.doi.org/10.17305/bb.2022.8549] [PMID: 36724020] [http://dx.doi.org/10.17305/bb.2022.8549] [PMID: 36724020] [64] Oeckinghaus, A.; Hayden, M.S.; Ghosh, S. Crosstalk in NF-κB signaling pathways. Nat. Immunol., 2011, 12(8), 695-708. [http://dx.doi.org/10.1038/ni.2065] [PMID: 21772278] [http://dx.doi.org/10.1038/ni.2065] [PMID: 21772278] [65] Wu, X-l. Paeoniflorin inhibits pancreatitis-induced oxidative stress and endoplasmic reticulum stress through NF-κB/MAPK pathway. J. Biol. Regul. Homeost. Agents, 2023, 37(4), 2043-2054. [66] Yin, H.; Zhang, Z.; Zhang, D. A new method for treating chronic pancreatitis and preventing fibrosis using bioactive calcium silicate ion solution. J. Mater. Chem. B Mater. Biol. Med., 2023, 11(38), 9163-9178. [http://dx.doi.org/10.1039/D3TB01287E] [PMID: 37642526] [http://dx.doi.org/10.1039/D3TB01287E] [PMID: 37642526] [67] Cai, J.; Yao, S.; Wang, H.; Rong, W. Kaempferol protects rats with severe acute pancreatitis through regulating NF-κB and Keap1–Nrf2 signaling pathway. Ital. J. Food Sci., 2021, 33(3), 25-32. [http://dx.doi.org/10.15586/ijfs.v33i3.2100] [http://dx.doi.org/10.15586/ijfs.v33i3.2100] [68] Zhou, X.; Wang, W.; Wang, C.; Zheng, C.; Xu, X.; Ni, X. DPP4 inhibitor attenuates severe acute pancreatitis-associated intestinal inflammation via Nrf2 signaling. Oxid. Med. Cell. Longev., 2019, 2019, 6181754. [http://dx.doi.org/10.1155/2019/6181754] [http://dx.doi.org/10.1155/2019/6181754] [69] Yi, W.; Lan, H.; Wen, Y. Retracted: HO‐1 overexpression alleviates senescence by inducing autophagy via the mitochondrial route in human nucleus pulposus cells. J. Cell. Physiol., 2020, 235(11), 8402-8415. [http://dx.doi.org/10.1002/jcp.29684] [PMID: 32239675] [http://dx.doi.org/10.1002/jcp.29684] [PMID: 32239675] [70] Reuter, S.; Gupta, S.C.; Chaturvedi, M.M.; Aggarwal, B.B. Oxidative stress, inflammation, and cancer: How are they linked? Free Radic. Biol. Med., 2010, 49(11), 1603-1616. [http://dx.doi.org/10.1016/j.freeradbiomed.2010.09.006] [PMID: 20840865] [http://dx.doi.org/10.1016/j.freeradbiomed.2010.09.006] [PMID: 20840865] [71] Zhou, Z.; Chen, Y.; Dong, W.; An, R.; Liang, K.; Wang, X. Da cheng qi decoction alleviates cerulein-stimulated AR42J pancreatic acinar cell injury via the JAK2/STAT3 signaling pathway. Evid. Based Complement. Alternat. Med., 2021, 2021, 6657036. [72] Li, C.; Cui, L.; Zhang, L. Saikosaponin D attenuates pancreatic injury through suppressing the apoptosis of acinar cell via modulation of the MAPK signaling pathway. Front. Pharmacol., 2021, 12, 735079. [http://dx.doi.org/10.3389/fphar.2021.735079] [PMID: 34744719] [http://dx.doi.org/10.3389/fphar.2021.735079] [PMID: 34744719] [73] Zhu, X.; Guo, S.; Zhang, M.; Bai, X. Emodin protects against apoptosis and inflammation by regulating reactive oxygen species-mediated NF-κB signaling in interleukin-1 β-stimulated human nucleus pulposus cells. Hum. Exp. Toxicol., 2023, 42. [http://dx.doi.org/10.1177/09603271221138552] [http://dx.doi.org/10.1177/09603271221138552] [74] Ghany, L.M.A.A.; Beshay, B.Y.; Youssef Moustafa, A.M. Design, synthesis, anti-inflammatory evaluation, and molecular modelling of new coumarin-based analogs combined curcumin and other heterocycles as potential TNF-α production inhibitors via upregulating Nrf2/HO-1, downregulating AKT/mTOR signalling pathways and downregulating NF-κB in LPS induced macrophages. J. Enzyme Inhib. Med. Chem., 2023, 38(1), 2243551. [http://dx.doi.org/10.1080/14756366.2023.2243551] [PMID: 37558232] [http://dx.doi.org/10.1080/14756366.2023.2243551] [PMID: 37558232] [75] Huang, L.; Lu, S.; Bian, M. Punicalagin attenuates TNF-α-induced oxidative damage and promotes osteogenic differentiation of bone mesenchymal stem cells by activating the Nrf2/HO-1 pathway. Exp. Cell Res., 2023, 430(1), 113717. [http://dx.doi.org/10.1016/j.yexcr.2023.113717] [PMID: 37429372] [http://dx.doi.org/10.1016/j.yexcr.2023.113717] [PMID: 37429372] [76] Li, X.; Qin, H.; Anwar, A. Molecular mechanism analysis of m6A modification-related lncRNA-miRNA-mRNA network in regulating autophagy in acute pancreatitis. Islets, 2022, 14(1), 184-199. [http://dx.doi.org/10.1080/19382014.2022.2132099] [PMID: 36218109] [http://dx.doi.org/10.1080/19382014.2022.2132099] [PMID: 36218109] [77] Kong, L.; Zhang, H.; Lu, C. AICAR, an AMP-activated protein kinase activator, ameliorates acute pancreatitis-associated liver injury partially through Nrf2-mediated antioxidant effects and inhibition of NLRP3 inflammasome activation. Front. Pharmacol., 2021, 12, 724514. [http://dx.doi.org/10.3389/fphar.2021.724514] [PMID: 34531748] [http://dx.doi.org/10.3389/fphar.2021.724514] [PMID: 34531748] [78] Hur, Y.; Huynh, J.; Leong, E. The differing effects of a dual acting regulator on SIRT1. Front. Mol. Biosci., 2023, 10, 1260489. [http://dx.doi.org/10.3389/fmolb.2023.1260489] [PMID: 37711385] [http://dx.doi.org/10.3389/fmolb.2023.1260489] [PMID: 37711385] [79] Chen, H.H.; Zhang, Y.X.; Lv, J.L. Role of sirtuins in metabolic disease-related renal injury. Biomed. Pharmacother., 2023, 161, 114417. [http://dx.doi.org/10.1016/j.biopha.2023.114417] [PMID: 36812714] [http://dx.doi.org/10.1016/j.biopha.2023.114417] [PMID: 36812714] [80] Abdelmageed, N.; Twafik, W.A.A.; Morad, O.A.R. Vinpocetine protects against chloroquine-induced cardiotoxicity by mitigating oxidative stress. Arch. Toxicol., 2023, 97(10), 2763-2770. [http://dx.doi.org/10.1007/s00204-023-03546-9] [PMID: 37401952] [http://dx.doi.org/10.1007/s00204-023-03546-9] [PMID: 37401952] [81] Ansari, M.A.; Iqubal, A.; Ekbbal, R.; Haque, S.E. Effects of nimodipine, vinpocetine and their combination on isoproterenol-induced myocardial infarction in rats. Biomed. Pharmacother., 2019, 109, 1372-1380. [http://dx.doi.org/10.1016/j.biopha.2018.10.199] [PMID: 30551388] [http://dx.doi.org/10.1016/j.biopha.2018.10.199] [PMID: 30551388] [82] Abdelzaher, W.Y.; Ahmed, S.M.; Welson, N.N.; Marraiki, N.; Batiha, G.E.S.; Kamel, M.Y. Retracted: Vinpocetine ameliorates L-arginine induced acute pancreatitis via Sirt1/Nrf2/TNF pathway and inhibition of oxidative stress, inflammation, and apoptosis. Biomed. Pharmacother., 2021, 133, 110976. [http://dx.doi.org/10.1016/j.biopha.2020.110976] [PMID: 33202281] [http://dx.doi.org/10.1016/j.biopha.2020.110976] [PMID: 33202281] [83] Saha, S.; Buttari, B.; Panieri, E.; Profumo, E.; Saso, L. An overview of Nrf2 signaling pathway and its role in inflammation. Molecules, 2020, 25(22), 5474. [http://dx.doi.org/10.3390/molecules25225474] [PMID: 33238435] [http://dx.doi.org/10.3390/molecules25225474] [PMID: 33238435] [84] Chen, Z.; Zhong, H.; Wei, J. Inhibition of Nrf2/HO-1 signaling leads to increased activation of the NLRP3 inflammasome in osteoarthritis. Arthritis Res. Ther., 2019, 21(1), 300. [http://dx.doi.org/10.1186/s13075-019-2085-6] [PMID: 31870428] [http://dx.doi.org/10.1186/s13075-019-2085-6] [PMID: 31870428] [85] Li, L.Y.; Liu, Q.; Le, C.Y.; Zhang, H.C.; Liu, W.F.; Gu, Y. Toll-like receptor 2 deficiency alleviates acute pancreatitis by inactivating the NF-xB/NLRP3 pathway. Int. Immunopharmacol., 2023, 121. [86] Chen, P.; Zhao, L.J.; Huang, L. Nafamostat mesilate prevented caerulein-induced pancreatic injury by targeting HDAC6-mediated NLRP3 inflammasome activation. Inflamm. Res., 2023, 72(9), 1919-1932. [http://dx.doi.org/10.1007/s00011-023-01794-0] [PMID: 37725105] [http://dx.doi.org/10.1007/s00011-023-01794-0] [PMID: 37725105] [87] Gao, Z.; Sui, J.; Fan, R.; Qu, W.; Dong, X.; Sun, D. Emodin protects against acute pancreatitis-associated lung injury by inhibiting NLPR3 inflammasome activation via Nrf2/HO-1 signaling. Drug Des. Devel. Ther., 2020, 14, 1971-1982. [http://dx.doi.org/10.2147/DDDT.S247103] [PMID: 32546964] [http://dx.doi.org/10.2147/DDDT.S247103] [PMID: 32546964] [88] Qiang, R.; Li, Y.; Dai, X.; Lv, W. NLRP3 inflammasome in digestive diseases: From mechanism to therapy. Front. Immunol., 2022, 13, 978190. [http://dx.doi.org/10.3389/fimmu.2022.978190] [PMID: 36389791] [http://dx.doi.org/10.3389/fimmu.2022.978190] [PMID: 36389791] [89] Swanson, K.V.; Deng, M.; Ting, J.P.Y. The NLRP3 inflammasome: Molecular activation and regulation to therapeutics. Nat. Rev. Immunol., 2019, 19(8), 477-489. [http://dx.doi.org/10.1038/s41577-019-0165-0] [PMID: 31036962] [http://dx.doi.org/10.1038/s41577-019-0165-0] [PMID: 31036962] [90] Lamichhane, P.P.; Samir, P. Cellular stress: Modulator of regulated cell death. Biology, 2023, 12(9), 1172. [http://dx.doi.org/10.3390/biology12091172] [PMID: 37759572] [http://dx.doi.org/10.3390/biology12091172] [PMID: 37759572] [91] Shi, W.; Liu, T.; Yang, H. Isomaculosidine facilitates NLRP3 inflammasome activation by promoting mitochondrial reactive oxygen species production and causes idiosyncratic liver injury. J. Ethnopharmacol., 2024, 319(Pt 1), 117063. [http://dx.doi.org/10.1016/j.jep.2023.117063] [PMID: 37598766] [http://dx.doi.org/10.1016/j.jep.2023.117063] [PMID: 37598766] [92] Xie, D.; Guo, H.; Li, M. Splenic monocytes mediate inflammatory response and exacerbate myocardial ischemia/reperfusion injury in a mitochondrial cell-free DNA-TLR9-NLRP3-dependent fashion. Basic Res. Cardiol., 2023, 118(1), 44. [http://dx.doi.org/10.1007/s00395-023-01014-0] [PMID: 37814087] [http://dx.doi.org/10.1007/s00395-023-01014-0] [PMID: 37814087] [93] Chen, M.; Yu, S.; Gao, Y. TRAF6-TAK1-IKKβ pathway mediates TLR2 agonists activating “one-step” NLRP3 inflammasome in human monocytes. Cytokine, 2023, 169, 156302. [http://dx.doi.org/10.1016/j.cyto.2023.156302] [http://dx.doi.org/10.1016/j.cyto.2023.156302] [94] Xu, Y.; Biby, S.; Kaur, B.; Zhang, S. A patent review of NLRP3 inhibitors to treat autoimmune diseases. Expert Opin. Ther. Pat., 2023, 33(6), 455-470. [http://dx.doi.org/10.1080/13543776.2023.2239502] [PMID: 37470439] [http://dx.doi.org/10.1080/13543776.2023.2239502] [PMID: 37470439] [95] Dixon, S.J.; Lemberg, K.M.; Lamprecht, M.R. Ferroptosis: An iron-dependent form of nonapoptotic cell death. Cell, 2012, 149(5), 1060-1072. [http://dx.doi.org/10.1016/j.cell.2012.03.042] [PMID: 22632970] [http://dx.doi.org/10.1016/j.cell.2012.03.042] [PMID: 22632970] [96] Jin, S.K.; Liu, P.S.; Zheng, D.H.; Xie, X. The interplay of miRNAs and ferroptosis in diseases related to iron overload. Apoptosis, 2023, 29(1-2), 45-65. [PMID: 37758940] [PMID: 37758940] [97] Malekzadeh, R.; Mortezazadeh, T.; Abdulsahib, W.K. Nanoarchitecture-based photothermal ablation of cancer: A systematic review. Environ. Res., 2023, 236(Pt 1), 116526. [http://dx.doi.org/10.1016/j.envres.2023.116526] [PMID: 37487920] [http://dx.doi.org/10.1016/j.envres.2023.116526] [PMID: 37487920] [98] Liang, C.; Zhang, X.; Yang, M.; Dong, X. Recent progress in ferroptosis inducers for cancer therapy. Adv. Mater., 2019, 31(51), 1904197. [http://dx.doi.org/10.1002/adma.201904197] [PMID: 31595562] [http://dx.doi.org/10.1002/adma.201904197] [PMID: 31595562] [99] Bersuker, K.; Hendricks, J.M.; Li, Z. The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis. Nature, 2019, 575(7784), 688-692. [http://dx.doi.org/10.1038/s41586-019-1705-2] [PMID: 31634900] [http://dx.doi.org/10.1038/s41586-019-1705-2] [PMID: 31634900] [100] Evans, J.A.; Mendonca, P.; Soliman, K.F.A. Involvement of Nrf2 activation and NF-kB pathway inhibition in the antioxidant and anti-inflammatory effects of hesperetin in activated BV-2 microglial cells. Brain Sci., 2023, 13(8), 1144. [http://dx.doi.org/10.3390/brainsci13081144] [PMID: 37626501] [http://dx.doi.org/10.3390/brainsci13081144] [PMID: 37626501] [101] Lee, J.; Roh, J.L. Targeting Nrf2 for ferroptosis-based therapy: Implications for overcoming ferroptosis evasion and therapy resistance in cancer. Biochim. Biophys. Acta Mol. Basis Dis., 2023, 1869(7), 166788. [http://dx.doi.org/10.1016/j.bbadis.2023.166788] [PMID: 37302427] [http://dx.doi.org/10.1016/j.bbadis.2023.166788] [PMID: 37302427] [102] Cubas-Gaona, L.L.; de Francisco, P.; Martín-González, A.; Gutiérrez, J.C. Tetrahymena glutathione peroxidase family: A comparative analysis of these antioxidant enzymes and differential gene expression to metals and oxidizing agents. Microorganisms, 2020, 8(7), 1008. [http://dx.doi.org/10.3390/microorganisms8071008] [PMID: 32635666] [http://dx.doi.org/10.3390/microorganisms8071008] [PMID: 32635666] [103] Liu, Y.; Wan, Y.; Jiang, Y.; Zhang, L.; Cheng, W. GPX4: The hub of lipid oxidation, ferroptosis, disease and treatment. Biochim. Biophys. Acta Rev. Cancer, 2023, 1878(3), 188890. [http://dx.doi.org/10.1016/j.bbcan.2023.188890] [PMID: 37001616] [http://dx.doi.org/10.1016/j.bbcan.2023.188890] [PMID: 37001616] [104] Forcina, G.C.; Dixon, S.J. GPX4 at the crossroads of lipid homeostasis and ferroptosis. Proteomics, 2019, 19(18), 1800311. [http://dx.doi.org/10.1002/pmic.201800311] [PMID: 30888116] [http://dx.doi.org/10.1002/pmic.201800311] [PMID: 30888116] [105] Li, Y.; Li, M.; Feng, S. Ferroptosis and endoplasmic reticulum stress in ischemic stroke. Neural Regen. Res., 2024, 19(3), 611-618. [http://dx.doi.org/10.4103/1673-5374.380870] [PMID: 37721292] [http://dx.doi.org/10.4103/1673-5374.380870] [PMID: 37721292] [106] Dar, N.J.; John, U.; Bano, N.; Khan, S.; Bhat, S.A. Oxytosis/ferroptosis in neurodegeneration: The underlying role of master regulator glutathione peroxidase 4 (GPX4). Mol. Neurobiol., 2023, 61(3), 1507-1526. [PMID: 37725216] [PMID: 37725216] [107] Liang, B.; Wu, Y. Hsa-miR-26a-5p improves OSCC sensitivity to ferroptosis by inhibiting SLC7A11. Arch. Oral Biol., 2023, 156, 105807. [http://dx.doi.org/10.1016/j.archoralbio.2023.105807] [PMID: 37776596] [http://dx.doi.org/10.1016/j.archoralbio.2023.105807] [PMID: 37776596] [108] Li, J.; Zhang, S.; Zhou, R.; Zhang, J.; Li, Z.F. Perspectives of traditional Chinese medicine in pancreas protection for acute pancreatitis. World J. Gastroenterol., 2017, 23(20), 3615-3623. [http://dx.doi.org/10.3748/wjg.v23.i20.3615] [PMID: 28611514] [http://dx.doi.org/10.3748/wjg.v23.i20.3615] [PMID: 28611514] [109] Tang, Y.; Sun, M.; Liu, Z. Phytochemicals with protective effects against acute pancreatitis: A review of recent literature. Pharm. Biol., 2022, 60(1), 479-490. [http://dx.doi.org/10.1080/13880209.2022.2039723] [PMID: 35180016] [http://dx.doi.org/10.1080/13880209.2022.2039723] [PMID: 35180016] [110] Jung, K.H.; Hong, S.W.; Zheng, H.M. Melatonin ameliorates cerulein‐induced pancreatitis by the modulation of nuclear erythroid 2‐related factor 2 and nuclear factor‐kappaB in rats. J. Pineal Res., 2010, 48(3), 239-250. [http://dx.doi.org/10.1111/j.1600-079X.2010.00748.x] [PMID: 20210857] [http://dx.doi.org/10.1111/j.1600-079X.2010.00748.x] [PMID: 20210857] [111] Ma, J.A.; Liu, X.M.; Deng, J.F.; Liu, J. Protective effect of geniposide against myocardial ischemia reperfusion injuries and itsrelationship with Pl3K/Akt signaling pathway in rats. Int. J. Clin. Exp. Med., 2018, 17(20), 2152-2155. [112] Wang, D.; Liu, J.; Zhang, X.Y.; Liu, P.; Peng, H.M. Geniposide alleviates liver injuries in rats with severe pancreatitis through the Nrf2/Keap1/ARE pathway. J Changchun Univ Chin Med, 2022, 38(06), 631-635. [113] Zhang, Y.G.; Zhang, S.J.; Bian, T.T.; Si, X.L.; Niu, J.T.; Xin, E.D. New progress in pharmacological action of paeoniflorin. Chin. Tradit. Herbal Drugs, 2019, 50(15), 3735-3740. [114] Liu, Yuan; Liu, LongZhong; Xu, YaSha; Xie, X.ueli; Li, LiSheng; Xu, ShangFu Effects of OingYi II on Nrf2 sianaling pathway in cerulein-induced acute pancreatitis mice. J Zunyi Med Univ, 2017, 40(01), 33-37. [115] Yang, X.; Yao, L.; Yuan, M. Transcriptomics and network pharmacology reveal the protective effect of chaiqin chengqi decoction on obesity-related alcohol-induced acute pancreatitis via oxidative stress and PI3K/Akt signaling pathway. Front. Pharmacol., 2022, 13, 896523. [http://dx.doi.org/10.3389/fphar.2022.896523] [PMID: 35754467] [http://dx.doi.org/10.3389/fphar.2022.896523] [PMID: 35754467] [116] Du, D.; Yao, L.; Zhang, R. Protective effects of flavonoids from Coreopsis tinctoria Nutt. on experimental acute pancreatitis via Nrf-2/ARE-mediated antioxidant pathways. J. Ethnopharmacol., 2018, 224, 261-272. [http://dx.doi.org/10.1016/j.jep.2018.06.003] [PMID: 29870787] [http://dx.doi.org/10.1016/j.jep.2018.06.003] [PMID: 29870787] [117] Li, Z.; Jiang, H.; Jiang, X.; Zhang, L.; Qin, Y. Integrated physiological, transcriptomic, and metabolomic analyses reveal that low-nitrogen conditions improve the accumulation of flavonoids in snow chrysanthemum. Ind. Crops Prod., 2023, 197, 116574. [http://dx.doi.org/10.1016/j.indcrop.2023.116574] [http://dx.doi.org/10.1016/j.indcrop.2023.116574] [118] Yao, L.B.; Xia, Q.; Du, D. Protective effect of a dihydroflavonol glycoside from Coreopsis tinctoria Nutt. in mouse model of alcoholic acute pancreatitis. Sichuan Da Xue Xue Bao Yi Xue Ban, 2019, 50(4), 533-539. [Medical Edition] [PMID: 31642231] [PMID: 31642231] [119] Li, J; Han, J; Lv, J; Wang, S; Qu, L; Jiang, Y. Saikosaponin A-induced gut microbiota changes attenuate severe acute pancreatitis through the activation of Keap1/Nrf2-are antioxidant signaling Oxid Med Cell Longev, 2020, 2020, 9217219. [http://dx.doi.org/10.1155/2020/9217219] [PMID: 33204401] [http://dx.doi.org/10.1155/2020/9217219] [PMID: 33204401] [120] Songohoutou, E.E.; Daniel, L.; Nouga, A.B.; Palé, W.Y.; Owono, L.C.; Kenfack, C.A. Monitoring the thermal oxidation of local edible oils by fluorescence spectroscopy technique coupled to chemometric methods. Food Anal. Methods, 2023, 16(8), 1422-1436. [http://dx.doi.org/10.1007/s12161-023-02491-8] [http://dx.doi.org/10.1007/s12161-023-02491-8] [121] Leri, M.; Scuto, M.; Ontario, M.L. Healthy effects of plant polyphenols: Molecular mechanisms. Int. J. Mol. Sci., 2020, 21(4), 1250. [http://dx.doi.org/10.3390/ijms21041250] [PMID: 32070025] [http://dx.doi.org/10.3390/ijms21041250] [PMID: 32070025] [122] Fusco, R.; Cordaro, M.; Siracusa, R. Biochemical evaluation of the antioxidant effects of hydroxytyrosol on pancreatitis-associated gut injury. Antioxidants, 2020, 9(9), 781. [http://dx.doi.org/10.3390/antiox9090781] [PMID: 32842687] [http://dx.doi.org/10.3390/antiox9090781] [PMID: 32842687] [123] Liu, X; Zhu, Q; Zhang, M; Yin, T; Xu, R; Xiao, W Isoliquiritigenin ameliorates acute pancreatitis in mice via inhibition of oxidative stress and modulation of the Nrf2/HO-1 pathway. OXID MED CELL LONGEV, 2018, 2018 [124] Yuan Hsieh, D.; Islam, M.N.; Kuo, W.W. A combination of isoliquiritigenin with Artemisia argyi and Ohwia caudata water extracts attenuates oxidative stress, inflammation, and apoptosis by modulating Nrf2/Ho-1 signaling pathways in SD rats with doxorubicin-induced acute cardiotoxicity. Environ. Toxicol., 2023, 38(12), 3026-3042. [http://dx.doi.org/10.1002/tox.23936] [PMID: 37661764] [http://dx.doi.org/10.1002/tox.23936] [PMID: 37661764] [125] Chen, X.; Cai, X.; Le, R. Isoliquiritigenin protects against sepsis-induced lung and liver injury by reducing inflammatory responses. Biochem. Biophys. Res. Commun., 2018, 496(2), 245-252. [http://dx.doi.org/10.1016/j.bbrc.2017.11.159] [PMID: 29180018] [http://dx.doi.org/10.1016/j.bbrc.2017.11.159] [PMID: 29180018] [126] Zhao, T.T.; Xu, Y.Q.; Hu, H.M.; Gong, H.B.; Zhu, H.L. Isoliquiritigenin (ISL) and its formulations: Potential antitumor agents. Curr. Med. Chem., 2019, 26(37), 6786-6796. [http://dx.doi.org/10.2174/0929867325666181112091700] [PMID: 30417769] [http://dx.doi.org/10.2174/0929867325666181112091700] [PMID: 30417769] [127] Zhang, M.; Wu, Y.Q.; Xie, L. Isoliquiritigenin protects against pancreatic injury and intestinal dysfunction after severe acute pancreatitis via Nrf2 signaling. Front. Pharmacol., 2018, 9, 936. [http://dx.doi.org/10.3389/fphar.2018.00936] [PMID: 30174606] [http://dx.doi.org/10.3389/fphar.2018.00936] [PMID: 30174606] [128] Yuan, C.C.; Zhu, Q.T.; Shen, Q.H. Isoliquiritigenin ameliorates doxorubicin-induced acute pancreatitis by inhibiting ROS production via modulation of Nrf2/HO-1 oxidative stress pathway. World Chin. J. Digestology, 2021, 29(6), 282-290. [http://dx.doi.org/10.11569/wcjd.v29.i6.282] [http://dx.doi.org/10.11569/wcjd.v29.i6.282] [129] Zheng, M.; He, X.L.; Yin, Y.; Lan, Y.H.; Wang, J.H.; Sun, H.Y. Mechanism of isoliguiritigenin underlying severe acute pancreatitis-induced myocardial injury in mice. Chin J Geriatr Heart. Brain Vessel Dis, 2019, 21(02), 177-180. [130] Zhou, H-C.; Du, R.; Wang, H. Advance in studies on pharmacokinetics of baicalin. Zhongguo Zhongyao Zazhi, 2018, 43(4), 684-688. [PMID: 29600641] [PMID: 29600641] [131] Wang, Xin; Zhou, WenYong; Sun, Yue Study on the effect of astragalus saponins on oxidative damage of L-arginine induced acute pancreatitis in mice by activating Nrf2/HO-1 signaling pathway. 2022, 36(03), 38-42. [132] Zhang, P.; Li, Y.F.; Wu, S.Z.; Jin, S.Q.; Wang, J.Q.; Пaвлoвнa, K.И. Effects of paeonol on the oxidative damage of acute pancreatitis in mice induced by L.arginine. J VET ZOOTECH SIN, 2021, 52(07), 1983-1990. [133] Li, Y; Pan, Y; Gao, L; Zhang, J; Xie, X; Tong, Z Naringenin protects against acute pancreatitis in two experimental models in mice by NLRP3 and Nrf2/HO-1 pathways. Mediators Inflamm, 2018, 2018 [134] Nisar, A.; Jagtap, S.; Vyavahare, S. Phytochemicals in the treatment of inflammation-associated diseases: The journey from preclinical trials to clinical practice. Front. Pharmacol., 2023, 14, 1177050. [http://dx.doi.org/10.3389/fphar.2023.1177050] [PMID: 37229273] [http://dx.doi.org/10.3389/fphar.2023.1177050] [PMID: 37229273] [135] Rong, Y.; Ren, J.; Song, W.; Xiang, R.; Ge, Y.; Lu, W. Resveratrol suppresses severe acute pancreatitis-induced microcirculation disturbance through targeting SIRT1-FOXO1 axis. Oxid. Med. Cell. Longev., 2021, 2021, 8891544. [http://dx.doi.org/10.1155/2021/8891544] [http://dx.doi.org/10.1155/2021/8891544] [136] Hu, S.; Zhu, Y.; Xia, X.; Xu, X.; Chen, F.; Miao, X. Ginsenoside Rg3 prolongs survival of the orthotopic hepatocellular carcinoma model by inducing apoptosis and inhibiting angiogenesis. Anal. Cell. Pathol., 2019, 2019, 3815786. [http://dx.doi.org/10.1155/2019/3815786] [http://dx.doi.org/10.1155/2019/3815786] [137] Zou, J.; Su, H.; Zou, C.; Liang, X.; Fei, Z. Ginsenoside Rg3 suppresses the growth of gemcitabine‐resistant pancreatic cancer cells by upregulating lncRNA‐CASC2 and activating PTEN signaling. J. Biochem. Mol. Toxicol., 2020, 34(6), e22480. [http://dx.doi.org/10.1002/jbt.22480] [PMID: 32104955] [http://dx.doi.org/10.1002/jbt.22480] [PMID: 32104955] [138] Xu, J.; Fan, X.; Zhu, M. Ginsenoside Rg3 protects mouse islet β-cells injured by high glucose. Indian J. Microbiol., 2023, 63(2), 173-180. [http://dx.doi.org/10.1007/s12088-023-01065-w] [PMID: 37325021] [http://dx.doi.org/10.1007/s12088-023-01065-w] [PMID: 37325021] [139] Shan, Y.; Li, J.; Zhu, A.; Kong, W.; Ying, R.; Zhu, W. Ginsenoside Rg3 ameliorates acute pancreatitis by activating the NRF2/HO-1-mediated ferroptosis pathway. Int. J. Mol. Med., 2022, 50(1), 89. [http://dx.doi.org/10.3892/ijmm.2022.5144] [PMID: 35582998] [http://dx.doi.org/10.3892/ijmm.2022.5144] [PMID: 35582998] [140] Chang, J.S.; Lee, Y.J.; Wilkie, D.A.; Lin, C.T. The Neuroprotective and antioxidative effects of submicron and blended Lycium barbarum in experimental retinal degeneration in rats. J. Vet. Med. Sci., 2018, 80(7), 1108-1115. [http://dx.doi.org/10.1292/jvms.17-0623] [PMID: 29760314] [http://dx.doi.org/10.1292/jvms.17-0623] [PMID: 29760314] [141] Li, G.; Wang, F.; Fang, J.; Zha, H.; Zhao, Q. Risk factors for post-endoscopic retrograde cholangiopancreatography pancreatitis: Evidence from 1786 cases. Med. Sci. Monit., 2018, 24, 8544-8552. [http://dx.doi.org/10.12659/MSM.913314] [PMID: 30475792] [http://dx.doi.org/10.12659/MSM.913314] [PMID: 30475792] [142] Wang, J.; Shen, Y.; Zhong, Z.; Wu, S.; Zheng, L. Risk factors for post-endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis and the effect of octreotide combined with nonsteroidal anti-inflammatory drugs on preventing its occurrence. Med. Sci. Monit., 2018, 24, 8964-8969. [http://dx.doi.org/10.12659/MSM.911914] [PMID: 30531679] [http://dx.doi.org/10.12659/MSM.911914] [PMID: 30531679] [143] Yao, J.Q.; Zhu, L.; Miao, Y.F. Optimal dosing time of Dachengqi decoction for protection of extrapancreatic organs in rats with experimental acute pancreatitis. World J. Gastroenterol., 2020, 26(22), 3056-3075. [http://dx.doi.org/10.3748/wjg.v26.i22.3056] [PMID: 32587448] [http://dx.doi.org/10.3748/wjg.v26.i22.3056] [PMID: 32587448] [144] Yang, C.; Wang, T.; Chen, J. Traditional Chinese Medicine formulas alleviate acute pancreatitis. Pancreas, 2021, 50(10), 1348-1356. [http://dx.doi.org/10.1097/MPA.0000000000001931] [PMID: 35041332] [http://dx.doi.org/10.1097/MPA.0000000000001931] [PMID: 35041332] [145] Ren, X.Y.; Gong, H.L.; Tang, W-F.; Wan, M.H.; Zhao, J.L.; Huang, X. Dachengqi decoction induces pancreatic acinar cell apoptosis in experimental acute pancreatitis in rats. J. Chin. Integr. Med., 2009, 7(7), 651-656. [http://dx.doi.org/10.3736/jcim20090709] [PMID: 19615319] [http://dx.doi.org/10.3736/jcim20090709] [PMID: 19615319] [146] Wang, J.; Zou, Y.; Chang, D.; Hong, D.Q.; Zhang, J. Protective effect of Dachengqi decoction on the pancreatic microcirculatory system in severe acute pancreatitis by down-regulating HMGB-TLR-4-IL-23-IL-17A mediated neutrophil activation by targeting SIRT1. Gland Surg., 2021, 10(10), 3030-3044. [http://dx.doi.org/10.21037/gs-21-655] [PMID: 34804889] [http://dx.doi.org/10.21037/gs-21-655] [PMID: 34804889] [147] Yao, J.; Miao, Y.; Zhang, Y. Dao-chi powder ameliorates pancreatitis-induced intestinal and cardiac injuries via regulating the Nrf2-HO-1-HMGB1 signaling pathway in rats. Front. Pharmacol., 2022, 13, 922130. [http://dx.doi.org/10.3389/fphar.2022.922130] [PMID: 35899121] [http://dx.doi.org/10.3389/fphar.2022.922130] [PMID: 35899121] [148] Zhou, Z.; Choi, J.W.; Shin, J.Y. Betulinic acid ameliorates the severity of acute pancreatitis via inhibition of the NF-κB signaling pathway in mice. Int. J. Mol. Sci., 2021, 22(13), 6871. [http://dx.doi.org/10.3390/ijms22136871] [http://dx.doi.org/10.3390/ijms22136871] [149] Fu, X.; Zhong, X.; Chen, X.; Yang, D.; Zhou, Z.; Liu, Y. GSK-3β activates NF-κB to aggravate caerulein-induced early acute pancreatitis in mice. Ann. Transl. Med., 2021, 9(22), 1695. [http://dx.doi.org/10.21037/atm-21-5701] [PMID: 34988204] [http://dx.doi.org/10.21037/atm-21-5701] [PMID: 34988204] [150] Gao, W.; Guo, L.; Yang, Y. Dissecting the crosstalk between Nrf2 and NF-κB response pathways in drug-induced toxicity. Front. Cell Dev. Biol., 2022, 9, 809952. [http://dx.doi.org/10.3389/fcell.2021.809952] [http://dx.doi.org/10.3389/fcell.2021.809952] [151] Özkan, E.; Akyüz, C.; Dulundu, E. Protective effects of lycopene on cerulein-induced experimental acute pancreatitis in rats. J. Surg. Res., 2012, 176(1), 232-238. [http://dx.doi.org/10.1016/j.jss.2011.09.005] [PMID: 22079843] [http://dx.doi.org/10.1016/j.jss.2011.09.005] [PMID: 22079843] [152] Su, C.; Meng, W.; Liu, Z.; Zhang, W.; Chen, G.; Zhao, X. Protective effects of panaxadiolsaponins on liver and kidney injury in rats with severe acute pancreatitis. Int. J. Clin. Exp. Med., 2016, 9(7), 12811-12817. [153] Ren, J.; Fu, L.; Nile, S.H.; Zhang, J.; Kai, G. Salvia miltiorrhiza in treating cardiovascular diseases: A review on its pharmacological and clinical applications. Front. Pharmacol., 2019, 10, 753. [http://dx.doi.org/10.3389/fphar.2019.00753] [PMID: 31338034] [http://dx.doi.org/10.3389/fphar.2019.00753] [PMID: 31338034] [154] Shi, M-J.; Dong, B-S.; Yang, W-N.; Su, S-B.; Zhang, H. Preventive and therapeutic role of Tanshinone IIA in hepatology. Biomed. Pharmacother., 2019, 112. [155] Xu, Z.; Chen, L.; Xiao, Z. Potentiation of the anticancer effect of doxorubicinin drug-resistant gastric cancer cells by tanshinone IIA. Phytomedicine, 2018, 51, 58-67. [http://dx.doi.org/10.1016/j.phymed.2018.05.012] [PMID: 30466628] [http://dx.doi.org/10.1016/j.phymed.2018.05.012] [PMID: 30466628] [156] Peng, G.; Zhang, X.Y. Effects of Salvia miltiorrhiza on serum levels of inflammatory cytokines in patients with severe acute pancreatitis. J. Chin. Integr. Med., 2007, 5(1), 28-31. [http://dx.doi.org/10.3736/jcim20070106] [PMID: 17214932] [http://dx.doi.org/10.3736/jcim20070106] [PMID: 17214932] [157] Liu, M-d.; Shen, Y-h. Effect of tanshinone II A on cytokines of rats with severe acute pancreatitis lung injury. Chin. J. Integr. Med., 2015, 35(11), 1361-1366. [158] Xiao, Z.; Liu, W.; Mu, Y. Pharmacological effects of salvianolic acid B against oxidative damage. Front. Pharmacol., 2020, 11, 572373. [http://dx.doi.org/10.3389/fphar.2020.572373] [PMID: 33343348] [http://dx.doi.org/10.3389/fphar.2020.572373] [PMID: 33343348] [159] Liu, T.; Liu, S.; Yu, X.; Song, N.; Xu, X.; Hu, J. Salvianolic acid B prevents iodinated contrast media-induced acute renal injury in rats via the PI3K/Akt/Nrf2 pathway. Oxid. Med. Cell. Longev., 2016, 2016, 7079487. [160] Zhang, S.; Shi, Y.; Tang, L. Evaluation of brain targeting in rats of Salvianolic acid B nasal delivery by the microdialysis technique. Xenobiotica, 2018, 48(8), 851-859. [http://dx.doi.org/10.1080/00498254.2017.1373207] [PMID: 29027831] [http://dx.doi.org/10.1080/00498254.2017.1373207] [PMID: 29027831] [161] Zhao, D.H.; Wu, Y.J.; Liu, S.T.; Liu, R.Y. Salvianolic acid B attenuates lipopolysaccharide-induced acute lung injury in rats through inhibition of apoptosis, oxidative stress and inflammation. Exp. Ther. Med., 2017, 14(1), 759-764. [http://dx.doi.org/10.3892/etm.2017.4534] [PMID: 28672996] [http://dx.doi.org/10.3892/etm.2017.4534] [PMID: 28672996] [162] Ling, W.C.; Liu, J.; Lau, C.W.; Murugan, D.D.; Mustafa, M.R.; Huang, Y. Treatment with salvianolic acid B restores endothelial function in angiotensin II-induced hypertensive mice. Biochem. Pharmacol., 2017, 136, 76-85. [http://dx.doi.org/10.1016/j.bcp.2017.04.007] [PMID: 28396195] [http://dx.doi.org/10.1016/j.bcp.2017.04.007] [PMID: 28396195] [163] Wang, R.; Yu, X.Y.; Guo, Z.Y.; Wang, Y.J.; Wu, Y.; Yuan, Y.F. Inhibitory effects of salvianolic acid B on CCl4-induced hepatic fibrosis through regulating NF-κB/IκBα signaling. J. Ethnopharmacol., 2012, 144(3), 592-598. [http://dx.doi.org/10.1016/j.jep.2012.09.048] [PMID: 23041223] [http://dx.doi.org/10.1016/j.jep.2012.09.048] [PMID: 23041223] [164] Wang, Y.; Chen, G.; Yu, X. Salvianolic acid B ameliorates cerebral ischemia/reperfusion injury through inhibiting TLR4/] MyD88 signaling pathway. Inflammation, 2016, 39(4), 1503-1513. [http://dx.doi.org/10.1007/s10753-016-0384-5] [PMID: 27255374] [http://dx.doi.org/10.1007/s10753-016-0384-5] [PMID: 27255374] [165] Ren, Z.; Li, H.; Zhang, M. A novel derivative of the natural product danshensu suppresses inflammatory responses to alleviate caerulein-induced acute pancreatitis. Front. Immunol., 2018, 9, 2513. [http://dx.doi.org/10.3389/fimmu.2018.02513] [PMID: 30425719] [http://dx.doi.org/10.3389/fimmu.2018.02513] [PMID: 30425719] [166] Malkawi, A.K.; Alzoubi, K.H.; Jacob, M. Metabolomics based profiling of dexamethasone side effects in rats. Front. Pharmacol., 2018, 9, 46. [http://dx.doi.org/10.3389/fphar.2018.00046] [PMID: 29503615] [http://dx.doi.org/10.3389/fphar.2018.00046] [PMID: 29503615] [167] Alam, W.; Khan, H.; Shah, M.A.; Cauli, O.; Saso, L. Kaempferol as a dietary anti-inflammatory agent: Current therapeutic standing. Molecules, 2020, 25(18), 4073. [http://dx.doi.org/10.3390/molecules25184073] [PMID: 32906577] [http://dx.doi.org/10.3390/molecules25184073] [PMID: 32906577] [168] Kim, S.H.; Park, J.G.; Sung, G.H. Kaempferol, a dietary flavonoid, ameliorates acute inflammatory and nociceptive symptoms in gastritis, pancreatitis, and abdominal pain. Mol. Nutr. Food Res., 2015, 59(7), 1400-1405. [http://dx.doi.org/10.1002/mnfr.201400820] [PMID: 25917334] [http://dx.doi.org/10.1002/mnfr.201400820] [PMID: 25917334] [169] Pasari, L.P.; Khurana, A.; Anchi, P.; Aslam Saifi, M.; Annaldas, S.; Godugu, C. Visnagin attenuates acute pancreatitis via Nrf2/NFκB pathway and abrogates associated multiple organ dysfunction. Biomed. Pharmacother., 2019, 112, 108629. [http://dx.doi.org/10.1016/j.biopha.2019.108629] [PMID: 30798137] [http://dx.doi.org/10.1016/j.biopha.2019.108629] [PMID: 30798137] [170] Yang, J.; Tang, X.; Ke, X.; Dai, Y.; Shi, J. Triptolide suppresses nf-κb-mediated inflammatory responses and activates expression of Nrf2-mediated antioxidant genes to alleviate caerulein-induced acute pancreatitis. Int. J. Mol. Sci., 2022, 23(3), 1252. [http://dx.doi.org/10.3390/ijms23031252] [http://dx.doi.org/10.3390/ijms23031252] [171] Yang, Y.; Ding, Z.; Wang, Y. Systems pharmacology reveals the mechanism of activity of Physalis alkekengi L. var. franchetii against lipopolysaccharide‐induced acute lung injury. J. Cell. Mol. Med., 2020, 24(9), 5039-5056. [http://dx.doi.org/10.1111/jcmm.15126] [PMID: 32220053] [http://dx.doi.org/10.1111/jcmm.15126] [PMID: 32220053] [172] Dong, Z.; Shang, H.; Chen, Y.Q.; Pan, L-L.; Bhatia, M.; Sun, J. Sulforaphane protects pancreatic acinar cell injury by modulating nrf2-mediated oxidative stress and NLRP3 inflammatory pathway. Oxid. Med. Cell. Longev., 2016, 2016, 7864150. [http://dx.doi.org/10.1155/2016/7864150] [http://dx.doi.org/10.1155/2016/7864150] [173] Cordaro, M.; Fusco, R.; D’Amico, R. Cashew (Anacardium occidentale L.) nuts modulate the Nrf2 and NLRP3 pathways in pancreas and lung after induction of acute pancreatitis by cerulein. Antioxidants, 2020, 9(10), 992. [http://dx.doi.org/10.3390/antiox9100992] [PMID: 33066525] [http://dx.doi.org/10.3390/antiox9100992] [PMID: 33066525] [174] Wang, Y.; Bu, C.; Wu, K.; Wang, R.; Wang, J. Curcumin protects the pancreas from acute pancreatitis via the mitogen activated protein kinase signaling pathway. Mol. Med. Rep., 2019, 20(4), 3027-3034. [http://dx.doi.org/10.3892/mmr.2019.10547] [PMID: 31432122] [http://dx.doi.org/10.3892/mmr.2019.10547] [PMID: 31432122] [175] Niu, W.; Guo, L.Y. Therapeutic efficacy of rheum palmatum and salvia miltiorrhiza on patients with severe acute pancreatitis. China Pharmacy, 2013, 24(19), 1801-1803. [176] Li, Z.L.; Zhang, D.; Liu, J.W.; Wang, H. Effects of emodin on the expression of hypoxia inducible factor-1a protein in rats with severeacute pancreatitis-associated renal lnjury. West Chin Med J, 2015, 30(04), 640-644. [177] Jin, Y.; Liu, L.; Chen, B.; Bai, Y.; Zhang, F.; Li, Q. Involvement of the PI3K/Akt/NF-κB signaling pathway in the attenuation of severe acute pancreatitis-associated acute lung injury by Sedum sarmentosum bunge extract. BioMed Res. Int., 2017, 2017, 9698410. [178] Li, H.Y.; Zhao, S.G.; Zhao, B.M.; Wang, X.X.; Tang, H.; Feng, G.H. Effects of baicalin on TNF-a,lL-6 and lL-10 in rats with severe acute pancreatitis. Xinan Goufang Yiyao, 2009, 19(01), 26-29. [179] Li, D.; Zheng, G.M. Study on protective effect of baicalin on renal lnjury in rats with severe acute pancreatitis. Zhonghua Zhongyiyao Xuekan, 2015, 33(10), 2476-2478. [180] Li, H.Y.; Zhang, C.; Zhang, S.; Xu, H.; Liu, J.; Li, F. Effects of emodin combined with baicalin on Akt/Nrf2 pathway in acute pancreatitis model rats. China Pharmacy, 2018, 29(13), 1754-1759. [181] Yuan, X.; Zheng, J.; Jiao, S. A review on the preparation of chitosan oligosaccharides and application to human health, animal husbandry and agricultural production. Carbohydr. Polym., 2019, 220, 60-70. [http://dx.doi.org/10.1016/j.carbpol.2019.05.050] [PMID: 31196551] [http://dx.doi.org/10.1016/j.carbpol.2019.05.050] [PMID: 31196551] [182] Junyuan, Z.; Hui, X.; Chunlan, H. Quercetin protects against intestinal barrier disruption and inflammation in acute necrotizing pancreatitis through TLR4/MyD88/p38 MAPK and ERS inhibition. Pancreatology, 2018, 18(7), 742-752. [http://dx.doi.org/10.1016/j.pan.2018.08.001] [PMID: 30115563] [http://dx.doi.org/10.1016/j.pan.2018.08.001] [PMID: 30115563] [183] Tao, W.; Sun, W.; Liu, L. Chitosan oligosaccharide attenuates nonalcoholic fatty liver disease induced by high fat diet through reducing lipid accumulation, inflammation and oxidative stress in C57BL/6 mice. Mar. Drugs, 2019, 17(11), 645. [http://dx.doi.org/10.3390/md17110645] [PMID: 31744059] [http://dx.doi.org/10.3390/md17110645] [PMID: 31744059] [184] Mei, Q.; Hu, J.; Huang, Z. Pretreatment with chitosan oligosaccharides attenuate experimental severe acute pancreatitis via inhibiting oxidative stress and modulating intestinal homeostasis. Acta Pharmacol. Sin., 2021, 42(6), 942-953. [http://dx.doi.org/10.1038/s41401-020-00581-5] [PMID: 33495520] [http://dx.doi.org/10.1038/s41401-020-00581-5] [PMID: 33495520] [185] Mei, QX; Deng, GY; Huang, ZH; Yin, Y; Li, CL; Hu, JH Porous COS@SiO2 nanocomposites ameliorate severe acute pancreatitis and associated lung injury by regulating the Nrf2 signaling pathway in mice. Front Chem, 2020, 8, 720. eCollection 2020 [http://dx.doi.org/10.3389/fchem.2020.00720.] [http://dx.doi.org/10.3389/fchem.2020.00720.] [186] Zhao, D.; Yu, W.; Xie, W.; Ma, Z.; Hu, Z.; Song, Z. Bone marrow-derived mesenchymal stem cells ameliorate severe acute pancreatitis by inhibiting oxidative stress in rats. Mol. Cell. Biochem., 2022, 477(12), 2761-2771. [http://dx.doi.org/10.1007/s11010-022-04476-3] [PMID: 35622186] [http://dx.doi.org/10.1007/s11010-022-04476-3] [PMID: 35622186] [187] Severino, A.; Varca, S.; Airola, C. Antibiotic utilization in acute pancreatitis: A narrative review. Antibiotics, 2023, 12(7), 1120. [http://dx.doi.org/10.3390/antibiotics12071120] [PMID: 37508216] [http://dx.doi.org/10.3390/antibiotics12071120] [PMID: 37508216] [188] Singh, V.K.; Yadav, D.; Garg, P.K. Diagnosis and management of chronic pancreatitis. JAMA, 2019, 322(24), 2422-2434. [http://dx.doi.org/10.1001/jama.2019.19411] [PMID: 31860051] [http://dx.doi.org/10.1001/jama.2019.19411] [PMID: 31860051] [189] Liu, Y.; Wan, Z.; Liao, D. Efficacy of enteral nutrition for patients with acute pancreatitis: A systematic review and meta analysis of 17 studies. Exp. Ther. Med., 2023, 25(4), 184. [http://dx.doi.org/10.3892/etm.2023.11883] [PMID: 37021072] [http://dx.doi.org/10.3892/etm.2023.11883] [PMID: 37021072] [190] Choi, S.; Kim, H. The remedial potential of lycopene in pancreatitis through regulation of autophagy. Int. J. Mol. Sci., 2020, 21(16), 5775. [http://dx.doi.org/10.3390/ijms21165775] [PMID: 32806545] [http://dx.doi.org/10.3390/ijms21165775] [PMID: 32806545] [191] Tazeoğlu, D.; Akyüz, C.; Gökçeimam, M.; Harman Kamalı, G.; Özsoy, A.; Karahan, S.R. Effect of alpha-tocopherol and dose sensitivity on pancreatitis formation in rats with experimental pancreatitis. National Trauma and Emergency Surgery Dergisi-Turkish Journal of Trauma & Emergency Surgery, 2021, 27(6), 605-612. [PMID: 34710231] [PMID: 34710231] [192] Burzyński, J.; Fichna, J.; Tarasiuk, A. Putative molecular targets for vitamin A in neutralizing oxidative stress in acute and chronic pancreatitis — A systematic review. Naunyn Schmiedebergs Arch. Pharmacol., 2023, 396(7), 1361-1370. [http://dx.doi.org/10.1007/s00210-023-02442-4] [PMID: 36843131] [http://dx.doi.org/10.1007/s00210-023-02442-4] [PMID: 36843131] [193] Deng, J.; Song, Z.; Li, X.; Shi, H.; Huang, S.; Tang, L. Role of lncRNAs in acute pancreatitis: Pathogenesis, diagnosis, and therapy. Front. Genet., 2023, 14, 1257552. [http://dx.doi.org/10.3389/fgene.2023.1257552] [PMID: 37842644] [http://dx.doi.org/10.3389/fgene.2023.1257552] [PMID: 37842644] [194] Zhang, D.; Li, L.; Li, J. Colchicine improves severe acute pancreatitis-induced acute lung injury by suppressing inflammation, apoptosis and oxidative stress in rats. Biomed. Pharmacother., 2022, 153, 113461. [http://dx.doi.org/10.1016/j.biopha.2022.113461] [PMID: 36076491] [http://dx.doi.org/10.1016/j.biopha.2022.113461] [PMID: 36076491] [195] Hey-Hadavi, J.; Velisetty, P.; Mhatre, S. Trends and recent developments in pharmacotherapy of acute pancreatitis. Postgrad. Med., 2023, 135(4), 334-344. [http://dx.doi.org/10.1080/00325481.2022.2136390] [PMID: 36305300] [http://dx.doi.org/10.1080/00325481.2022.2136390] [PMID: 36305300] [196] Bolourani, S.; Diao, L.; Thompson, D.A. Risk factors for early readmission after acute pancreatitis: Importance of timely interventions. J. Surg. Res., 2020, 252, 96-106. [http://dx.doi.org/10.1016/j.jss.2020.03.003] [PMID: 32278975] [http://dx.doi.org/10.1016/j.jss.2020.03.003] [PMID: 32278975] [197] Yang, F.Y.; Qi, X.Z.; Du, Y.Q.; Chen, Y.; Wang, M.T.; Huang, H.T. Coloclyster of red peony root granules alleviates moderately severe acute pancreatitis: A double-blinded, placebo-controlled, randomized clinical trial. Evid. Based Complement. Alternat. Med., 2020, 2020, 8401239. [198] Zhou, Y.; Liu, D.; Chen, S. Nrf2 activation ameliorates mechanical allodynia in paclitaxel-induced neuropathic pain. Acta Pharmacol. Sin., 2020, 41(8), 1041-1048. [http://dx.doi.org/10.1038/s41401-020-0394-6] [PMID: 32203087] [http://dx.doi.org/10.1038/s41401-020-0394-6] [PMID: 32203087] [199] Jeon, S.; Lee, Y.; Oh, S.R. Recent advances in endocrine organoids for therapeutic application. Adv. Drug Deliv. Rev., 2023, 199, 114959. [http://dx.doi.org/10.1016/j.addr.2023.114959] [PMID: 37301512] [http://dx.doi.org/10.1016/j.addr.2023.114959] [PMID: 37301512] [200] Scholz, O.; Huß, E.; Otter, S. Protection of pancreatic islets from oxidative cell death by a peripherally-active morphinan with increased drug safety. Mol. Metab., 2023, 75, 101775. [http://dx.doi.org/10.1016/j.molmet.2023.101775] [PMID: 37451343] [http://dx.doi.org/10.1016/j.molmet.2023.101775] [PMID: 37451343] [201] Robertson, R.P. Nrf2 and antioxidant response in animal models of type 2 diabetes. Int. J. Mol. Sci., 2023, 24(4), 3082. [http://dx.doi.org/10.3390/ijms24043082] [PMID: 36834496] [http://dx.doi.org/10.3390/ijms24043082] [PMID: 36834496] [202] Sauerland, M.B.; Davies, M.J. Electrophile versus oxidant modification of cysteine residues: Kinetics as a key driver of protein modification. Arch. Biochem. Biophys., 2022, 727, 109344. [http://dx.doi.org/10.1016/j.abb.2022.109344] [PMID: 35777524] [http://dx.doi.org/10.1016/j.abb.2022.109344] [PMID: 35777524] [203] Baumel-Alterzon, S.; Scott, D.K. Regulation of Pdx1 by oxidative stress and Nrf2 in pancreatic beta-cells. Front. Endocrinol., 2022, 13, 1011187. [http://dx.doi.org/10.3389/fendo.2022.1011187] [PMID: 36187092] [http://dx.doi.org/10.3389/fendo.2022.1011187] [PMID: 36187092] [204] Kwak, M.S.; Lim, J.W.; Kim, H. Astaxanthin inhibits interleukin-6 expression in cerulein/resistin-stimulated pancreatic acinar cells. Mediators Inflamm., 2021, 2021, 5587297. [205] Zhang, F.; Cui, S.; Yuan, Y.; Li, C.; Li, R. Dissection of the potential anti‐diabetes mechanism of salvianolic acid B by metabolite profiling and network pharmacology. Rapid Commun. Mass Spectrom., 2022, 36(1), e9205. [http://dx.doi.org/10.1002/rcm.9205] [PMID: 34636119] [http://dx.doi.org/10.1002/rcm.9205] [PMID: 34636119] [206] Saha, S.; Ali, M.R.; Khaleque, M.A.; Bacchu, M.S.; Aly Saad Aly, M.; Khan, M.Z.H. Metal oxide nanocarrier for targeted drug delivery towards the treatment of global infectious diseases: A review. J. Drug Deliv. Sci. Technol., 2023, 86, 104728. [http://dx.doi.org/10.1016/j.jddst.2023.104728] [http://dx.doi.org/10.1016/j.jddst.2023.104728] [207] Tirumala, M.G.; Anchi, P.; Raja, S.; Rachamalla, M.; Godugu, C. Novel methods and approaches for safety evaluation of nanoparticle formulations: A focus towards in vitro models and adverse outcome pathways. Front. Pharmacol., 2021, 12, 612659. [http://dx.doi.org/10.3389/fphar.2021.612659] [PMID: 34566630] [http://dx.doi.org/10.3389/fphar.2021.612659] [PMID: 34566630] [208] Khurana, A.; Tekula, S.; Saifi, M.A.; Venkatesh, P.; Godugu, C. Therapeutic applications of selenium nanoparticles. Biomed. Pharmacother., 2019, 111, 802-812. [http://dx.doi.org/10.1016/j.biopha.2018.12.146] [PMID: 30616079] [http://dx.doi.org/10.1016/j.biopha.2018.12.146] [PMID: 30616079] [209] Zewail, M.B.; El-Gizawy, S.A.; Asaad, G.F.; Shabana, M.E.; El-Dakroury, W.A. Chitosan coated clove oil-based nanoemulsion: An attractive option for oral delivery of leflunomide in rheumatoid arthritis. Int. J. Pharm., 2023, 643, 123224. [http://dx.doi.org/10.1016/j.ijpharm.2023.123224] [PMID: 37451327] [http://dx.doi.org/10.1016/j.ijpharm.2023.123224] [PMID: 37451327] [210] Liu, Y.; Shangguan, L.; Zhao, B.; Chen, B.; Shi, B.; Wang, Y. Cross-linked supramolecular polymer networks constructed by pillar[5]arene-based host–guest recognition and coordination/oxidation of catechol. Polym. Chem., 2022, 13(25), 3763-3767. [http://dx.doi.org/10.1039/D2PY00476C] [http://dx.doi.org/10.1039/D2PY00476C] [211] Mozafari, M.R.; Torkaman, S.; Karamouzian, F.M.; Rasti, B.; Baral, B. Antimicrobial applications of nanoliposome encapsulated silver nanoparticles: A potential strategy to overcome bacterial resistance. Curr. Nanosci., 2021, 17(1), 26-40. [http://dx.doi.org/10.2174/18756786MTA4iMTAi3] [http://dx.doi.org/10.2174/18756786MTA4iMTAi3] [212] Lin, S.; Cui, L.; Chen, G. PLGA/β-TCP composite scaffold incorporating salvianolic acid B promotes bone fusion by angiogenesis and osteogenesis in a rat spinal fusion model. Biomaterials, 2019, 196, 109-121. [http://dx.doi.org/10.1016/j.biomaterials.2018.04.004] [PMID: 29655516] [http://dx.doi.org/10.1016/j.biomaterials.2018.04.004] [PMID: 29655516] [213] Mo, X.; Zhang, D.; Liu, K.; Zhao, X.; Li, X.; Wang, W. Nano-hydroxyapatite composite scaffolds loaded with bioactive factors and drugs for bone tissue engineering. Int. J. Mol. Sci., 2023, 24(2), 1291. [http://dx.doi.org/10.3390/ijms24021291] [PMID: 36674810] [http://dx.doi.org/10.3390/ijms24021291] [PMID: 36674810] [214] Liu, M.; Liu, S.; Zhu, X. Tanshinone IIA-loaded micelles functionalized with rosmarinic acid: A novel synergistic anti-inflammatory strategy for treatment of atherosclerosis. J. Pharm. Sci., 2022, 111(10), 2827-2838. [http://dx.doi.org/10.1016/j.xphs.2022.05.007] [PMID: 35580692] [http://dx.doi.org/10.1016/j.xphs.2022.05.007] [PMID: 35580692] 32 2

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2024) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

References (100)

Source provenance

openalex
last seen: 2026-06-10T17:14:06.276822+00:00
License: CC0 · commercial use OK