Metformin regresses endometriotic implants in rats by improving implant levels of superoxide dismutase, vascular endothelial growth factor, tissue inhibitor of metalloproteinase-2, and matrix metalloproteinase-9

Yilmaz B, Bulent Yilmaz, Bülent Yılmaz, Sucak A, Ayhan Sucak, Sevtap Kılıç, Kilic S, Sevtap Kilic, Aksakal O, Orhan Aksakal, Aksoy Y, Yasemin Aksoy, Nese Lortlar, Neşe Lortlar, Lortlar N, Necdet Süt, Necdet Sut, Sut N, Tayfun Gungor, Gungor T
American journal of obstetrics and gynecology · 2009 · vol. 202(4) , pp. 368.e1–368.e8 · doi:10.1016/j.ajog.2009.10.873 · PMID:20035912 · W2040619536
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Metformin treatment in rats led to regression of endometriotic implants by modulating key molecules involved in oxidative stress, angiogenesis, and extracellular matrix remodeling.

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Abstract

OBJECTIVE: We sought to test if metformin could regress endometriotic explants in rats. STUDY DESIGN: After inducing endometriotic implants and randomization of female Wistar albino rats, they were given 25 and 50 mg/kg/day of oral metformin in group A (n = 9) and B (n = 8), respectively, for 28 days. Group C (n = 9) was given saline as placebo. RESULTS: Mean volume, weight, and histologic score of implants in groups A (P < .01, P < .05, and P < .05, respectively) and B (P < .01, P < .05, and P < .05, respectively) were significantly lower than in group C. The activity of superoxide dismutase and tissue inhibitor of metalloproteinase-2 staining in groups A (P < .05 and P < .01, respectively) and B (P < .01 and P < .01, respectively) was significantly higher than in the control group. Moreover, there were more significant reductions in implant levels of vascular endothelial growth factor and matrix metalloproteinase-9 in groups A (both P < .001) and B (both P < .001) than in group C. CONCLUSION: Metformin causes regression of endometriotic implants in rats.

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Condition tags

endometriosis

MeSH descriptors

Endometriosis Endometriosis Matrix Metalloproteinase 9 Metformin Superoxide Dismutase Tissue Inhibitor of Metalloproteinase-2 Vascular Endothelial Growth Factor A Animals Animals Disease Models, Animal Disease Models, Animal Endometriosis Endometriosis Endometriosis Endometrium Endometrium Endometrium Endometrium Endometrium Female

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

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