The Chronic Use of Magnesium Decreases VEGF Levels in the Uterine Tissue in Rats

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Chronic magnesium sulfate administration to rats decreased uterine tissue VEGF, SOD, GPx, and MDA levels, correlating negatively with increased magnesium levels.

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The study examined whether chronic magnesium sulfate administration alters uterine vascular endothelial growth factor (VEGF) levels and oxidative status in rats. Rats received magnesium sulfate intramuscularly at 30 mg/kg for 2 weeks, and uterine VEGF, SOD, GPx, and MDA were quantified by ELISA at the metoestrus phase, alongside histologic assessment of uterine vascular and cellular changes. Magnesium levels increased while VEGF, antioxidant enzyme activities (SOD, GPx), and oxidative stress marker (MDA) all decreased, with negative correlations between uterine magnesium and each measured analyte, and no histological changes were observed. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Vascular endothelial growth factor (VEGF) is the most important regulator of angiogenesis which serves to provide sufficient blood supply, and can trigger both physiological and pathological angiogenesis. Recent studies have shown that VEGF increases in gynecological diseases (such as endometriosis, ovarian, and endometrial cancers) and is a prognostic factor in these pathologies. Therefore, VEGF should be maintained at appropriate levels. Magnesium is used in many gynecological practices (such as eclampsia, preeclampsia, dysmenorrhea, and climacteric symptoms) and the mechanisms of action are still under investigation. Redox status, which can be regulated by magnesium, was shown to affect VEGF expression. The aim of this study was to evaluate the effects of chronic magnesium use on VEGF and oxidative status in the uterus. Magnesium sulfate was administered to rats at doses of 30 mg/kg (intramuscular) for 2 weeks. VEGF, Superoxide dismutase (SOD), Glutathione peroxidase (GPx), and Malondialdehyde (MDA) levels were measured using ELISA; vascular and cellular alterations were determined by histology in the uterine tissue at the metoestrus phase. In the uterine tissue of Mg-treated subjects, magnesium levels increased while VEGF, SOD, GPx, and MDA levels decreased without histological changes. There was a negative correlation between uterine tissue magnesium levels and VEGF, SOD, GPx, and MDA levels. Consequently, the results of this study demonstrated that regular magnesium use decreased VEGF levels in uterus. Decreased VEGF levels were associated with decreased uterine oxidative stress. Chronic magnesium usage may protect the uterine tissue from certain diseases in which angiogenesis is critical.
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Abstract

Vascular endothelial growth factor (VEGF) is the most important regulator of angiogenesis which serves to provide sufficient blood supply, and can trigger both physiological and pathological angiogenesis. Recent studies have shown that VEGF increases in gynecological diseases (such as endometriosis, ovarian, and endometrial cancers) and is a prognostic factor in these pathologies. Therefore, VEGF should be maintained at appropriate levels. Magnesium is used in many gynecological practices (such as eclampsia, preeclampsia, dysmenorrhea, and climacteric symptoms) and the mechanisms of action are still under investigation. Redox status, which can be regulated by magnesium, was shown to affect VEGF expression. The aim of this study was to evaluate the effects of chronic magnesium use on VEGF and oxidative status in the uterus. Magnesium sulfate was administered to rats at doses of 30 mg/kg (intramuscular) for 2 weeks. VEGF, Superoxide dismutase (SOD), Glutathione peroxidase (GPx), and Malondialdehyde (MDA) levels were measured using ELISA; vascular and cellular alterations were determined by histology in the uterine tissue at the metoestrus phase. In the uterine tissue of Mg-treated subjects, magnesium levels increased while VEGF, SOD, GPx, and MDA levels decreased without histological changes. There was a negative correlation between uterine tissue magnesium levels and VEGF, SOD, GPx, and MDA levels. Consequently, the results of this study demonstrated that regular magnesium use decreased VEGF levels in uterus. Decreased VEGF levels were associated with decreased uterine oxidative stress. Chronic magnesium usage may protect the uterine tissue from certain diseases in which angiogenesis is critical. Similar content being viewed by others

References

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Conflict of Interest The authors declare that they have no conflict of interest. Additional information Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Rights and permissions About this article Cite this article Hoşgörler, F., Kızıldağ, S., Ateş, M. et al. The Chronic Use of Magnesium Decreases VEGF Levels in the Uterine Tissue in Rats. Biol Trace Elem Res 196, 545–551 (2020). https://doi.org/10.1007/s12011-019-01944-8 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s12011-019-01944-8

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MeSH descriptors

Magnesium Sulfate Magnesium Sulfate Uterus Uterus Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factor A Animals Female Injections, Intramuscular Magnesium Sulfate Oxidative Stress Oxidative Stress Rats Rats, Sprague-Dawley Uterus Uterus Vascular Endothelial Growth Factor A

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