Lutein Attenuates Isoproterenol-Induced Cardiac Hypertrophy in Rats

preprint OA: closed CC-BY-4.0
📄 Open PDF Full text JSON View at publisher
AI-generated summary by claude@2026-07+body, 2026-07-05

Lutein treatment attenuated isoproterenol-induced cardiac hypertrophy, fibrosis, inflammation, and mortality in rats, partly via the nitric oxide pathway.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-07, 2026-07-05 · read from full text

The study investigated whether lutein attenuates isoproterenol-induced cardiac hypertrophy in rats, using a hypertrophy model where rats received isoproterenol (4.5 mg/kg/day for 7 days) alongside lutein (20 mg/kg/day for 7 days) or the comparator apocynin, and mechanistically testing involvement of the nitric oxide pathway using the nitric oxide synthase inhibitor L-NAME (20 mg/kg/day for 7 days). Lutein and apocynin reduced isoproterenol-associated morphometric hypertrophy features, fibrosis, inflammatory enhancement, infarct area, mortality, cardiac enzyme markers (CPK-total/CPK-MB/LDH/AST/ALT), and electrocardiographic changes, while also preventing isoproterenol-driven reactive oxygen species production and attenuating Bax protein expression. L-NAME partially reversed lutein’s cardioprotective effects, supporting a partial role for the NO pathway. A major caveat is that the work is a preprint and not peer reviewed. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Purpose: Lutein (LUT) is a carotenoid found in fruits, and green vegetables with potent antioxidant, anti-inflammatory and cardioprotective action. However, the mechanisms involved in the cardioprotection against cardiac hypertrophy (CH) remains unkown. Objectives Investigate the anti-hypertrophic action of LUT in rats using the isoproterenol-induced CH model. Methods For CH induction, isoproterenol (ISO; 4.5 mg/kg/day, 7 days, i.p) was administrated and animals were treated with LUT (20 mg/kg/day, 7 days) or apocynin (APO, 10 mg/kg/day, 7 days). To investigate the participation of the nitric oxide (NO) pathway in the mechanism of action of LUT, the animals were treated with L-NAME (20 mg/kg/day, 7 days), an inhibitor of NO synthase. Results LUT and APO animals showed attenuated morphometric, fibrosis and inflammatory enhancement compared to ISO group, in addition to reducing the infarct area and the mortality rate triggered by ISO. Serum levels of CPK-TOTAL, CPK-MB, LDH, AST and ALT were significantly reduced in animals treated with LUT when compared to the ISO group. LUT attenuated the electrocardiographic changes induced by ISO (increase of QRS and QTc and inversion of T wave) and prevented the reduction of left ventricular pressure and heart rate in the ISO group. ISO increased the production of reactive oxygen species (ROS) in the heart which was prevented by LUT. ISO increased the Bax protein expression, which was attenuated by LUT treatment. Also, L-NAME partially reversed the LUT-mediated cardioprotection. Conclusion The results show that LUT exerts a cardioprotective effect against CH in rats partially related to NO pathway.
Full text 16,147 characters · extracted from preprint-html · click to expand
Lutein Attenuates Isoproterenol-Induced Cardiac Hypertrophy in Rats | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Article Lutein Attenuates Isoproterenol-Induced Cardiac Hypertrophy in Rats Vinícius Cisneiros de Oliveira Santos, Michael Ramon Lima Conceição, and 9 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-3967687/v1 This work is licensed under a CC BY 4.0 License Status: Under Review Version 1 posted 7 You are reading this latest preprint version Abstract Purpose Lutein (LUT) is a carotenoid found in fruits, and green vegetables with potent antioxidant, anti-inflammatory and cardioprotective action. However, the mechanisms involved in the cardioprotection against cardiac hypertrophy (CH) remains unkown. Objectives Investigate the anti-hypertrophic action of LUT in rats using the isoproterenol-induced CH model. Methods For CH induction, isoproterenol (ISO; 4.5 mg/kg/day, 7 days, i.p) was administrated and animals were treated with LUT (20 mg/kg/day, 7 days) or apocynin (APO, 10 mg/kg/day, 7 days). To investigate the participation of the nitric oxide (NO) pathway in the mechanism of action of LUT, the animals were treated with L-NAME (20 mg/kg/day, 7 days), an inhibitor of NO synthase. Results LUT and APO animals showed attenuated morphometric, fibrosis and inflammatory enhancement compared to ISO group, in addition to reducing the infarct area and the mortality rate triggered by ISO. Serum levels of CPK-TOTAL, CPK-MB, LDH, AST and ALT were significantly reduced in animals treated with LUT when compared to the ISO group. LUT attenuated the electrocardiographic changes induced by ISO (increase of QRS and QTc and inversion of T wave) and prevented the reduction of left ventricular pressure and heart rate in the ISO group. ISO increased the production of reactive oxygen species (ROS) in the heart which was prevented by LUT. ISO increased the Bax protein expression, which was attenuated by LUT treatment. Also, L-NAME partially reversed the LUT-mediated cardioprotection. Conclusion The results show that LUT exerts a cardioprotective effect against CH in rats partially related to NO pathway. Lutein carotenoid cardiac hypertrophy antioxidant isoproterenol rat Full Text Additional Declarations No competing interests reported. Supplementary Files DataAvailabilitydeclaration.xlsx SuplementaryBlot.tif Cite Share Download PDF Status: Under Review Version 1 posted Editorial decision: Revision requested 27 Mar, 2024 Reviews received at journal 25 Mar, 2024 Reviewers agreed at journal 16 Mar, 2024 Reviewers invited by journal 14 Mar, 2024 Editor assigned by journal 13 Mar, 2024 Submission checks completed at journal 13 Mar, 2024 First submitted to journal 18 Feb, 2024 You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. Our growing team is made up of researchers and industry professionals working together to solve the most critical problems facing scientific publishing. Also discoverable on Platform About Our Team In Review Editorial Policies Advisory Board Help Center Resources Author Services Accessibility API Access RSS feed Manage Cookie Preferences © Research Square 2026 | ISSN 2693-5015 (online) Privacy Policy Terms of Service Do Not Sell My Personal Information {"props":{"pageProps":{"initialData":{"identity":"rs-3967687","acceptedTermsAndConditions":true,"allowDirectSubmit":false,"archivedVersions":[],"articleType":"Research Article","associatedPublications":[],"authors":[{"id":279631482,"identity":"a03eb23f-8530-49e1-b808-a9f7d160799a","order_by":0,"name":"Vinícius Cisneiros de Oliveira Santos","email":"","orcid":"","institution":"Universidade Federal de Sergipe","correspondingAuthor":false,"prefix":"","firstName":"Vinícius","middleName":"Cisneiros de Oliveira","lastName":"Santos","suffix":""},{"id":279631483,"identity":"069e2422-9772-4f1a-a664-ebdb33f313fc","order_by":1,"name":"Michael Ramon Lima Conceição","email":"","orcid":"","institution":"Federal University of São Paulo","correspondingAuthor":false,"prefix":"","firstName":"Michael","middleName":"Ramon Lima","lastName":"Conceição","suffix":""},{"id":279631484,"identity":"11d90b8c-57e7-4f58-8a7b-e6f0665c4aad","order_by":2,"name":"Diego Santos de Souza","email":"","orcid":"","institution":"Universidade Federal de Sergipe","correspondingAuthor":false,"prefix":"","firstName":"Diego","middleName":"Santos","lastName":"de Souza","suffix":""},{"id":279631485,"identity":"6750528f-c6e4-4e91-87ea-4cb41b90a09c","order_by":3,"name":"Ricardo Luiz Cavalcanti Albuquerque-Júnior","email":"","orcid":"","institution":"Universidade Federal de Santa Catarina","correspondingAuthor":false,"prefix":"","firstName":"Ricardo","middleName":"Luiz Cavalcanti","lastName":"Albuquerque-Júnior","suffix":""},{"id":279631486,"identity":"f68b25c7-0ba1-4949-861c-181c1a1d9bed","order_by":4,"name":"Thallita Kelly Rabelo","email":"","orcid":"","institution":"Universidade Federal de Sergipe","correspondingAuthor":false,"prefix":"","firstName":"Thallita","middleName":"Kelly","lastName":"Rabelo","suffix":""},{"id":279631487,"identity":"65b0a02a-c1e4-4017-a3f4-a8c6d08b2087","order_by":5,"name":"Júlio Alves da Silva-Neto","email":"","orcid":"","institution":"Universidade Federal de Sergipe","correspondingAuthor":false,"prefix":"","firstName":"Júlio","middleName":"Alves da","lastName":"Silva-Neto","suffix":""},{"id":279631488,"identity":"00a8b9d2-02f6-4522-b431-298d15847699","order_by":6,"name":"Andreza Melo de Araújo","email":"","orcid":"","institution":"Universidade Federal de Sergipe","correspondingAuthor":false,"prefix":"","firstName":"Andreza","middleName":"Melo","lastName":"de Araújo","suffix":""},{"id":279631489,"identity":"c9aaba2a-272e-44cf-b687-a2a6cf03ab9e","order_by":7,"name":"Diego Jose Belato Orts","email":"","orcid":"","institution":"Federal University of São Paulo","correspondingAuthor":false,"prefix":"","firstName":"Diego","middleName":"Jose Belato","lastName":"Orts","suffix":""},{"id":279631490,"identity":"e8473da2-43f2-4f40-a2c9-4663bce5dc42","order_by":8,"name":"Polyana Leal da Silva","email":"","orcid":"","institution":"Federal University of São Paulo","correspondingAuthor":false,"prefix":"","firstName":"Polyana","middleName":"Leal da","lastName":"Silva","suffix":""},{"id":279631491,"identity":"1092da88-2234-4a9f-8fa7-eaa3fd9e0257","order_by":9,"name":"Danilo Roman-Campos","email":"","orcid":"","institution":"Federal University of São Paulo","correspondingAuthor":false,"prefix":"","firstName":"Danilo","middleName":"","lastName":"Roman-Campos","suffix":""},{"id":279631492,"identity":"02d50008-bd19-4f03-aaa3-725d49117b5b","order_by":10,"name":"Carla Maria Lins de Vasconcelos","email":"data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAZAAAAAyAQMAAABI0h/eAAAABlBMVEX///8AAABVwtN+AAAACXBIWXMAAA7EAAAOxAGVKw4bAAAA2UlEQVRIie3PMQuCQBTA8eeiy8WtLyg/gyGIQ19Ggms5v0FEINRUrUJfIgicFcmW2g9qqAa3piBoKLpcC7Wt4f7THdyP9w5ApfrPtBjABYrFBVu1jCQIzRC0kTyQ+sQSBYFqQie7Y3zn6K32weYsBi4BI10vywhu+1YyjdCLDpkX8EwuRhgTZcQCBnEjQtsRvBNwXRIkTjmhOSQPSezwTZ51CDJI5RTTQkn8cQ2CIoe0LQkK5i38GRK96i90zrTTJeoSGvbiK78NTWqkWSn5TP/tuUqlUqm+9QK/m0Vyt8gT/QAAAABJRU5ErkJggg==","orcid":"","institution":"Universidade Federal de Sergipe","correspondingAuthor":true,"prefix":"","firstName":"Carla","middleName":"Maria Lins","lastName":"de Vasconcelos","suffix":""}],"badges":[],"createdAt":"2024-02-18 18:17:45","currentVersionCode":1,"declarations":"","doi":"10.21203/rs.3.rs-3967687/v1","doiUrl":"https://doi.org/10.21203/rs.3.rs-3967687/v1","draftVersion":[],"editorialEvents":[],"editorialNote":"","failedWorkflow":false,"files":[{"id":52797211,"identity":"d161d403-f195-4907-84fc-43cab65f03fe","added_by":"auto","created_at":"2024-03-15 22:57:00","extension":"pdf","order_by":1,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":921896,"visible":true,"origin":"","legend":"","description":"","filename":"ManuscriptLuteinNew.pdf","url":"https://assets-eu.researchsquare.com/files/rs-3967687/v1_covered_ddf3dd65-59ea-43f6-8d6f-2ee42e5bd55c.pdf"},{"id":52797150,"identity":"d419de07-9f8d-466f-a007-85117b532853","added_by":"auto","created_at":"2024-03-15 22:48:56","extension":"xlsx","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":25062,"visible":true,"origin":"","legend":"","description":"","filename":"DataAvailabilitydeclaration.xlsx","url":"https://assets-eu.researchsquare.com/files/rs-3967687/v1/868d68297720e49bc31b7e85.xlsx"},{"id":52797151,"identity":"ce7152e0-8fe6-4133-990b-acebf934d1c4","added_by":"auto","created_at":"2024-03-15 22:48:56","extension":"tif","order_by":2,"title":"","display":"","copyAsset":false,"role":"supplement","size":533728,"visible":true,"origin":"","legend":"","description":"","filename":"SuplementaryBlot.tif","url":"https://assets-eu.researchsquare.com/files/rs-3967687/v1/8eed4121de69b5235c083144.tif"}],"financialInterests":"No competing interests reported.","formattedTitle":"\u003cp\u003eLutein Attenuates Isoproterenol-Induced Cardiac Hypertrophy in Rats\u003c/p\u003e","fulltext":[],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":false,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":false,"highlight":"","institution":"","isAcceptedByJournal":false,"isAuthorSuppliedPdf":true,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":true,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"naunyn-schmiedebergs-archives-of-pharmacology","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":false,"externalIdentity":"nsap","sideBox":"Learn more about [Naunyn-Schmiedeberg's Archives of Pharmacology](https://www.springer.com/journal/210)","snPcode":"210","submissionUrl":"https://submission.nature.com/new-submission/210/3","title":"Naunyn-Schmiedeberg's Archives of Pharmacology","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"em","reportingPortfolio":"Springer Hybrid","inReviewEnabled":true,"inReviewRevisionsEnabled":false},"keywords":"Lutein, carotenoid, cardiac hypertrophy, antioxidant, isoproterenol, rat","lastPublishedDoi":"10.21203/rs.3.rs-3967687/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-3967687/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003ch2\u003ePurpose\u003c/h2\u003e \u003cp\u003eLutein (LUT) is a carotenoid found in fruits, and green vegetables with potent antioxidant, anti-inflammatory and cardioprotective action. However, the mechanisms involved in the cardioprotection against cardiac hypertrophy (CH) remains unkown.\u003c/p\u003e\u003ch2\u003eObjectives\u003c/h2\u003e \u003cp\u003eInvestigate the anti-hypertrophic action of LUT in rats using the isoproterenol-induced CH model.\u003c/p\u003e\u003ch2\u003eMethods\u003c/h2\u003e \u003cp\u003eFor CH induction, isoproterenol (ISO; 4.5 mg/kg/day, 7 days, i.p) was administrated and animals were treated with LUT (20 mg/kg/day, 7 days) or apocynin (APO, 10 mg/kg/day, 7 days). To investigate the participation of the nitric oxide (NO) pathway in the mechanism of action of LUT, the animals were treated with L-NAME (20 mg/kg/day, 7 days), an inhibitor of NO synthase.\u003c/p\u003e\u003ch2\u003eResults\u003c/h2\u003e \u003cp\u003eLUT and APO animals showed attenuated morphometric, fibrosis and inflammatory enhancement compared to ISO group, in addition to reducing the infarct area and the mortality rate triggered by ISO. Serum levels of CPK-TOTAL, CPK-MB, LDH, AST and ALT were significantly reduced in animals treated with LUT when compared to the ISO group. LUT attenuated the electrocardiographic changes induced by ISO (increase of QRS and QTc and inversion of T wave) and prevented the reduction of left ventricular pressure and heart rate in the ISO group. ISO increased the production of reactive oxygen species (ROS) in the heart which was prevented by LUT. ISO increased the Bax protein expression, which was attenuated by LUT treatment. Also, L-NAME partially reversed the LUT-mediated cardioprotection.\u003c/p\u003e\u003ch2\u003eConclusion\u003c/h2\u003e \u003cp\u003eThe results show that LUT exerts a cardioprotective effect against CH in rats partially related to NO pathway.\u003c/p\u003e","manuscriptTitle":"Lutein Attenuates Isoproterenol-Induced Cardiac Hypertrophy in Rats","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2024-03-15 22:48:51","doi":"10.21203/rs.3.rs-3967687/v1","editorialEvents":[{"type":"communityComments","content":0},{"type":"decision","content":"Revision requested","date":"2024-03-27T09:42:08+00:00","index":"","fulltext":""},{"type":"editorInvitedReview","content":"","date":"2024-03-25T09:17:40+00:00","index":"hide","fulltext":""},{"type":"reviewerAgreed","content":"c3198d05-7756-4af6-bfb8-4d5f2b9f6c32","date":"2024-03-16T16:38:23+00:00","index":"hide","fulltext":""},{"type":"reviewersInvited","content":"","date":"2024-03-14T13:43:39+00:00","index":"","fulltext":""},{"type":"editorAssigned","content":"","date":"2024-03-13T07:26:49+00:00","index":"","fulltext":""},{"type":"checksComplete","content":"","date":"2024-03-13T07:26:48+00:00","index":"","fulltext":""},{"type":"submitted","content":"Naunyn-Schmiedeberg's Archives of Pharmacology","date":"2024-02-18T18:09:51+00:00","index":"","fulltext":""}],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"naunyn-schmiedebergs-archives-of-pharmacology","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":false,"externalIdentity":"nsap","sideBox":"Learn more about [Naunyn-Schmiedeberg's Archives of Pharmacology](https://www.springer.com/journal/210)","snPcode":"210","submissionUrl":"https://submission.nature.com/new-submission/210/3","title":"Naunyn-Schmiedeberg's Archives of Pharmacology","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"em","reportingPortfolio":"Springer Hybrid","inReviewEnabled":true,"inReviewRevisionsEnabled":false}}],"origin":"","ownerIdentity":"b55147a9-52d1-4953-8368-871b20221006","owner":[],"postedDate":"March 15th, 2024","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"under-review","subjectAreas":[],"tags":[],"updatedAt":"2024-04-25T03:55:24+00:00","versionOfRecord":[],"versionCreatedAt":"2024-03-15 22:48:51","video":"","vorDoi":"","vorDoiUrl":"","workflowStages":[]},"version":"v1","identity":"rs-3967687","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-3967687","identity":"rs-3967687","version":["v1"]},"buildId":"J0_U0BvcaRcwD8yVFaRlm","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}

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: preprint-html

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.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
unpaywall
last seen: 2026-05-20T11:00:21.680559+00:00
License: CC-BY-4.0