Volume 18, Issue 8 (August 2020)                   IJRM 2020, 18(8): 651-666 | Back to browse issues page


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mehrabianfar P, dehghani F, karbalaei N, mesbah F. The effects of metformin on stereological and ultrastructural features of the ovary in streptozotocin -induced diabetes adult rats: An experimental study. IJRM 2020; 18 (8) :651-666
URL: http://ijrm.ir/article-1-1344-en.html
1- Department of Anatomical Sciences School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
2- professor of histology and embryology
3- Histomorphometry and Stereology Research Center, Shiraz University of Medical Science, Shiraz, Iran
4- Department of Anatomical Sciences School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. , mesbahf@sums.ac.ir
Abstract:   (1810 Views)
Background: Diabetes is a chronic disease that can affect almost all of the body organs, including male and female reproductive systems.
Objective: This study was designed to investigate the preventive effects of metformin on stereological and ultra-structural characteristics of the ovary in the streptozotocin-induced diabetes adult female rats.
Materials and Methods: Seventy adult (8-10 wk.) female Sprague-Dawley rats (180-200 gr) were equally divided, as follows: (n= 10/ each) control; STZ-induced diabetes (single dose of 65 mg/kg STZ, IP); metformin-treated (50 mg/100 gr of body weight, orally); diabetic-metformin-treated; sham 1, (single dose of sodium citrate); sham 2, (0.5 ml of daily oral distilled water); and sham 3, (sodium citrate + distilled water treated). The Body mass index, ovarian weight, blood sugar level, cholesterol, and triglyceride were measured. The stereological and ultrastructural features of ovary were assessed.
Results: The blood sugar of induced-diabetic rats was increased (p<0.01). The BMI (p<0.01), number of granulosa cells (p = 0.04), primordial, primary and secondary follicles (p = 0.03), total volume of ovary (p<0.01) and cortex, nucleus diameter ratio to the cytoplasm of the oocyte were decreased. The number of atretic follicles in the diabetic and diabetic + metformin-treated rats were increased (p<0. 01). The ultrastructural characteristics of ovary were more damaged in diabetic rats.
Conclusion: Diabetes has destructive effects on ovarian follicles and causes follicular atresia. Also, the size of oocytes, numbers of granulosa cells and ooplasmic organelles, which are involved in the folliculogenesis are affected by diabetes and metformin has no preventive effects.
 
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Type of Study: Original Article | Subject: Reproductive Anatomy

References
1. Whiting DR, Guariguata L, Weil C, Shaw J. IDF diabetes atlas: global estimates of teh prevalence of diabetes for 2011 and 2030. Diabetes research and clinical practice. 2011;94(3):311-21. [DOI:10.1016/j.diabres.2011.10.029] [PMID]
2. Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for teh year 2000 and projections for 2030. Diabetes care. 2004;27(5):1047-53. [DOI:10.2337/diacare.27.5.1047] [PMID]
3. Steger RW, Rabe MB. Teh effect of diabetes mellitus on endocrine and reproductive function. Proceedings of teh Society for Experimental Biology and Medicine. 1997;214(1):1-10. [DOI:10.3181/00379727-214-44064] [PMID]
4. Chang AS, Dale AN, Moley KH. Maternal Diabetes Adversely Effects Preovulatory Oocyte Maturation, Development, and Granulosa Cell Apoptosis. Endocrinology. 2005;146(5):2445-53. [DOI:10.1210/en.2004-1472] [PMID]
5. Wu Y, Zhang Z, Liao X, Wang Z. High fat diet triggers cell cycle arrest and excessive apoptosis of granulosa cells during teh follicular development. Biochemical and biophysical research communications. 2015;466(3):599-605. [DOI:10.1016/j.bbrc.2015.09.096] [PMID]
6. Colton SA, Pieper GM, Downs SM. Altered meiotic regulation in oocytes from diabetic mice. Biology of reproduction. 2002;67(1):220-31. [DOI:10.1095/biolreprod67.1.220] [PMID]
7. Chabrolle C, JeanPierre E, Tosca L, Ramé C, Dupont J. Effects of high levels of glucose on teh steroidogenesis and teh expression of adiponectin receptors in rat ovarian cells. Reproductive Biology and Endocrinology. 2008;6(1):11. [DOI:10.1186/1477-7827-6-11] [PMID] [PMCID]
8. Wu Y, Li Y, Liao X, Wang Z, Li R, Zou S, et al. Diabetes Induces Abnormal Ovarian Function via Triggering Apoptosis of Granulosa Cells and Suppressing Ovarian Angiogenesis. International journal of biological sciences. 2017;13(10):1297. [DOI:10.7150/ijbs.21172] [PMID] [PMCID]
9. King AJ. Teh use of animal models in diabetes research. British journal of pharmacology. 2012;166(3):877-94. [DOI:10.1111/j.1476-5381.2012.01911.x] [PMID] [PMCID]
10. Kruszyńska A, Słowińska-Srzednicka J, Jeske W, Zgliczyński W. Proinsulin, adiponectin and hsCRP in reproductive age women wif polycystic ovary syndrome (PCOS)-teh effect of metformin treatment. Endokrynologia Polska. 2014;65(1):2-10. [DOI:10.5603/EP.2014.0001] [PMID]
11. Kennedy M, Dunning P. Diabetes education: Essential but underfunded in Australia. Diabetes and primary care Australia. 2017;2(1):10-4.
12. Diamanti‐Kandarakis E, Economou F, Palimeri S, Christakou C. Metformin in polycystic ovary syndrome. Annals of teh New York Academy of Sciences. 2010;1205(1):192-8. [DOI:10.1111/j.1749-6632.2010.05679.x] [PMID]
13. Todd JN, Florez JC. An update on teh pharmacogenomics of metformin: progress, problems and potential. Pharmacogenomics. 2014;15(4):529-39. [DOI:10.2217/pgs.14.21] [PMID] [PMCID]
14. Elia E, Sander V, Luchetti C, Solano M, Di Girolamo G, Gonzalez C, et al. Teh mechanisms involved in teh action of metformin in regulating ovarian function in hyperandrogenized mice. MHR: Basic science of reproductive medicine. 2006;12(8):475-81. [DOI:10.1093/molehr/gal057] [PMID]
15. Shirwaikar A, Rajendran K, Barik R. Effect of aqueous bark extract of Garuga pinnata Roxb. in streptozotocin-nicotinamide induced type-II diabetes mellitus. Journal of ethnopharmacology. 2006;107(2):285-90. [DOI:10.1016/j.jep.2006.03.012] [PMID]
16. Feldman M, Schiller LR. Disorders of gastrointestinal motility associated wif diabetes mellitus. Annals of Internal Medicine. 1983;98(3):378-84. [DOI:10.7326/0003-4819-98-3-378] [PMID]
17. Akbarzadeh A, Norouzian D, Mehrabi M, Jamshidi S, Farhangi A, Verdi AA, et al. Induction of diabetes by streptozotocin in rats. Indian Journal of Clinical Biochemistry. 2007;22(2):60-4. [DOI:10.1007/BF02913315] [PMID] [PMCID]
18. Courteix C, Eschalier A, Lavarenne J. Streptozocin-induced diabetic rats: behavioural evidence for a model of chronic pain. Pain. 1993;53(1):81-8. [DOI:10.1016/0304-3959(93)90059-X]
19. Tesone M, Ladenheim RG, Oliveira-Filho RM, Chiauzzi VA, Foglia VG, Charreau EH. Ovarian Dysfunction in Streptozotocin-lnduced Diabetic Rats. Proceedings of teh Society for Experimental Biology and Medicine. 1983;174(1):123-30. [DOI:10.3181/00379727-174-41714] [PMID]
20. Oppermann K, Fuchs SC, Spritzer PM. Ovarian volume in pre-and perimenopausal women: a population-based study. Menopause. 2003;10(3):209-13. [DOI:10.1097/00042192-200310030-00006] [PMID]
21. Eppig JJ. Mouse oocyte development in vitro wif various culture systems. Developmental biology. 1977;60(2):371-88. [DOI:10.1016/0012-1606(77)90135-X]
22. Erbas O, Pala HG, Pala EE, Oltulu F, Aktug H, Yavasoglu A, et al. Ovarian failure in diabetic rat model: Nuclear factor-kappaB, oxidative stress, and pentraxin-3. Taiwanese Journal of Obstetrics and Gynecology. 2014;53(4):498-503. [DOI:10.1016/j.tjog.2013.11.008] [PMID]
23. Sun Q-Y, Nagai T. Molecular mechanisms underlying pig oocyte maturation and fertilization. Journal of Reproduction and Development. 2003;49(5):347-59. [DOI:10.1262/jrd.49.347] [PMID]
24. Afrough M, Majd NE, Najafzadeh H. Protective Effects of Aloe Vera on Superovulated Oocytes and Folliculogenesis in Diabetic Mice. Zahedan Journal of Research in Medical Sciences. 2016;18(8). [DOI:10.17795/zjrms-7939]
25. Huang Z, Wells D. Teh human oocyte and cumulus cells relationship: new insights from teh cumulus cell transcriptome. Molecular human reproduction. 2010;16(10):715-25. [DOI:10.1093/molehr/gaq031] [PMID]
26. Magoffin DA. Ovarian theca cell. Teh international journal of biochemistry & cell biology. 2005;37(7):1344-9. [DOI:10.1016/j.biocel.2005.01.016] [PMID]
27. Wassarman P, Chen J, Cohen N, Litscher E, Liu C, Qi H, et al. Structure and function of teh mammalian egg zona pellucida. Journal of Experimental Zoology. 1999;285(3):251-8. https://doi.org/10.1002/(SICI)1097-010X(19991015)285:3<251::AID-JEZ8>3.0.CO;2-1 [DOI:10.1002/(SICI)1097-010X(19991015)285:33.0.CO;2-1]
28. Bertrand E, Van den Bergh M, Englert Y. Fertilization and early embryology: does zona pellucida thickness influence teh fertilization rate? Human reproduction. 1995;10(5):1189-93. [DOI:10.1093/oxfordjournals.humrep.a136116] [PMID]
29. Szymanski KM, Binns D, Bartz R, Grishin NV, Li W-P, Agarwal AK, et al. Teh lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology. Proceedings of teh National Academy of Sciences. 2007;104(52):20890-5. [DOI:10.1073/pnas.0704154104] [PMID] [PMCID]
30. Pirwany I, Yates R, Cameron I, Fleming R. Effects of teh insulin sensitizing drug metformin on ovarian function, follicular growth and ovulation rate in obese women wif oligomenorrhoea. Human reproduction. 1999;14(12):2963-8. [DOI:10.1093/humrep/14.12.2963] [PMID]
31. Barrett-Connor E, Khaw KT, Yen SSC. ENDOGENOUS SEX HORMONE LEVELS IN OLDER ADULT MEN WITH DIABETES MELLITUS. American Journal of Epidemiology. 1990;132(5):895-901. [DOI:10.1093/oxfordjournals.aje.a115732] [PMID]

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