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Current Stem Cell Research & Therapy

Editor-in-Chief

ISSN (Print): 1574-888X
ISSN (Online): 2212-3946

Research Article

Use of Mesenchymal Stem Cells in Experimental Ovarian Damage

Author(s): Hanan Fouad, Ibrahim A Albahlol, Hazim A. Wahab, Eman H Nadwa, Heba M. Galal, Mohamed Abouelkheir*, Ahmed E. Taha, Abdelkarim G. Kamel and Hassan A. Abdelmawlla

Volume 19, Issue 5, 2024

Published on: 04 September, 2023

Page: [725 - 734] Pages: 10

DOI: 10.2174/1574888X18666230713121530

Price: $65

Abstract

Background: Bisphenol-A (BPA) has a well-proven deleterious effect on the hypothalamicpituitary- gonadal axis.

Objectives: The current study investigated the therapeutic potentials of mesenchymal stem cells (MSCs) in a murine model of BPA-induced ovarian damage.

Methods: Fifty adult female rats were divided into: Group 1; control group, Group IIa, IIb: rats were given oral gavage of BPA (25 and 50 mg/Kg body weight respectively) on a daily basis for 15 days, and Group IIIa, IIIb; rats were intravenously treated with of MSCs (106 cells) after receiving the last dose of BPA as in group II. Plasma and ovarian tissue levels of Malondialdehyde (MDA) and gonadal axis hormones were assessed. Apoptosis was evaluated by TUNNEL assay and by apoptosis markers (FAS, FASL, Caspase 3, SLTM). A histological examination of ovarian tissue was also conducted.

Results: BPA resulted in a significant elevation in plasma levels of LH, FSH, and ovarian tissue levels of MDA and a significant decrease in estradiol and progesterone. All genetic and protein markers of apoptosis were elevated in BPA treated group with decreased oestrogen receptor expression in the ovarian tissue. Increased apoptotic cells were confirmed by TUNEL assay. A high dose of BPA was able to increase the number of atretic follicles in the ovarian tissue whereas the numbers of primordial, primary, secondary and Graafian follicles were decreased. All the laboratory and histological abnormalities were ameliorated by treatment with MSCs.

Conclusion: The antioxidant and anti-apoptotic effects of MSCs could possibly explain the ability of this therapeutic modality to ameliorate BPA-induced-ovarian damage.

Graphical Abstract

[1]
Kawa IA. Akbar masood , Fatima Q, et al. Endocrine disrupting chemical Bisphenol A and its potential effects on female health. Diabetes Metab Syndr 2021; 15(3): 803-11.
[http://dx.doi.org/10.1016/j.dsx.2021.03.031] [PMID: 33839640]
[2]
Wazir U, Mokbel K, Bisphenol A. A Concise review of literature and a discussion of health and regulatory implications. In Vivo 2019; 33(5): 1421-3.
[http://dx.doi.org/10.21873/invivo.11619] [PMID: 31471387]
[3]
Graceli JB, Dettogni RS, Merlo E, et al. The impact of endocrine-disrupting chemical exposure in the mammalian hypothalamic-pituitary axis. Mol Cell Endocrinol 2020; 518: 110997.
[http://dx.doi.org/10.1016/j.mce.2020.110997] [PMID: 32841708]
[4]
Brown J, Roberson M. Novel insights into gonadotropin-releasing hormone action in the pituitary gonadotrope. Semin Reprod Med 2017; 35(2): 130-8.
[http://dx.doi.org/10.1055/s-0037-1599084] [PMID: 28212592]
[5]
Konieczna A, Rutkowska A. Rachoń D. Health risk of exposure to Bisphenol A (BPA). Rocz Panstw Zakl Hig 2015; 66(1): 5-11.
[PMID: 25813067]
[6]
Amjad S, Rahman MS, Pang MG. Role of antioxidants in alleviating Bisphenol A toxicity. Biomolecules 2020; 10(8): 1105.
[http://dx.doi.org/10.3390/biom10081105] [PMID: 32722388]
[7]
Aghajanpour-Mir SM, Zabihi E, Akhavan-Niaki H, et al. The genotoxic and cytotoxic effects of Bisphenol-A (BPA) in MCF-7 cell line and amniocytes. Int J Mol Cell Med 2016; 5(1): 19-29.
[PMID: 27386435]
[8]
Meli R, Monnolo A, Annunziata C, Pirozzi C, Ferrante MC. Oxidative stress and BPA toxicity: An antioxidant approach for male and female reproductive dysfunction. Antioxidants 2020; 9(5): 405.
[http://dx.doi.org/10.3390/antiox9050405] [PMID: 32397641]
[9]
Chen Y, Wang H, Yan Y, Ren M, Yan C, Wang B. Correlation between FAS single nucleotide polymorphisms and breast carcinoma susceptibility in Asia. Medicine (Baltimore) 2019; 98(49): e18240.
[http://dx.doi.org/10.1097/MD.0000000000018240] [PMID: 31804351]
[10]
Lee SG, Kim JY, Chung JY, et al. Bisphenol A exposure during adulthood causes augmentation of follicular atresia and luteal regression by decreasing 17β-estradiol synthesis via downregulation of aromatase in rat ovary. Environ Health Perspect 2013; 121(6): 663-9.
[http://dx.doi.org/10.1289/ehp.1205823] [PMID: 23512349]
[11]
Yan B, Singla DK. Transplanted induced pluripotent stem cells mitigate oxidative stress and improve cardiac function through the Akt cell survival pathway in diabetic cardiomyopathy. Mol Pharm 2013; 10(9): 3425-32.
[http://dx.doi.org/10.1021/mp400258d] [PMID: 23879836]
[12]
Liang W, Chen X, Zhang S, et al. Mesenchymal stem cells as a double-edged sword in tumor growth: focusing on MSC-derived cytokines. Cell Mol Biol Lett 2021; 26(1): 3.
[http://dx.doi.org/10.1186/s11658-020-00246-5] [PMID: 33472580]
[13]
Zhou Y, Xu H, Xu W, et al. Exosomes released by human umbilical cord mesenchymal stem cells protect against cisplatin-induced renal oxidative stress and apoptosis in vivo and in vitro. Stem Cell Res Ther 2013; 4(2): 34.
[http://dx.doi.org/10.1186/scrt194] [PMID: 23618405]
[14]
Jin G, Qiu G, Wu D, et al. Allogeneic bone marrow-derived mesenchymal stem cells attenuate hepatic ischemia-reperfusion injury by suppressing oxidative stress and inhibiting apoptosis in rats. Int J Mol Med 2013; 31(6): 1395-401.
[http://dx.doi.org/10.3892/ijmm.2013.1340] [PMID: 23589072]
[15]
Fouad H, Faruk EM, Alasmari WA, Nadwa EH, Ebrahim UFA. Structural and chemical role of mesenchymal stem cells and resveratrol in regulation of apoptotic -induced genes in Bisphenol-A induced uterine damage in adult female albino rats. Tissue Cell 2021; 70: 101502.
[http://dx.doi.org/10.1016/j.tice.2021.101502] [PMID: 33582552]
[16]
Salem H, Ellakwa DES, Fouad H, Hamid MA. APOA1 AND APOA2 proteins as prognostic markers for early detection of urinary bladder cancer. Gene Rep 2019; 16: 100463.
[http://dx.doi.org/10.1016/j.genrep.2019.100463]
[17]
Zhu X, Tian GG, Yu B, Yang Y, Wu J. Effects of bisphenol A on ovarian follicular development and female germline stem cells. Arch Toxicol 2018; 92(4): 1581-91.
[http://dx.doi.org/10.1007/s00204-018-2167-2] [PMID: 29380011]
[18]
Watson CS, Bulayeva NN, Wozniak AL, Alyea RA. Xenoestrogens are potent activators of nongenomic estrogenic responses. Steroids 2007; 72(2): 124-34.
[http://dx.doi.org/10.1016/j.steroids.2006.11.002] [PMID: 17174995]
[19]
Cao H, Wang L, Cao M, Ye T, Sun Y. Computational insights on agonist and antagonist mechanisms of estrogen receptor α induced by bisphenol A analogues. Environ Pollut 2019; 248: 536-45.
[http://dx.doi.org/10.1016/j.envpol.2019.02.058] [PMID: 30831350]
[20]
Li Y, Burns KA, Arao Y, Luh CJ, Korach KS. Differential estrogenic actions of endocrine-disrupting chemicals bisphenol A, bisphenol AF, and zearalenone through estrogen receptor α and β in vitro. Environ Health Perspect 2012; 120(7): 1029-35.
[http://dx.doi.org/10.1289/ehp.1104689] [PMID: 22494775]
[21]
Watson CS, Koong L, Jeng YJ, Vinas R. Xenoestrogen interference with nongenomic signaling actions of physiological estrogens in endocrine cancer cells. Steroids 2019; 142: 84-93.
[http://dx.doi.org/10.1016/j.steroids.2018.06.014] [PMID: 30012504]
[22]
Liang H, Xu W, Chen J, et al. The Association between exposure to environmental Bisphenol A and gonadotropic hormone levels among men. PLoS One 2017; 12(1): e0169217.
[http://dx.doi.org/10.1371/journal.pone.0169217] [PMID: 28085949]
[23]
Rodríguez HA, Santambrosio N, Santamaría CG, Muñoz-de-Toro M, Luque EH. Neonatal exposure to bisphenol A reduces the pool of primordial follicles in the rat ovary. Reprod Toxicol 2010; 30(4): 550-7.
[http://dx.doi.org/10.1016/j.reprotox.2010.07.008] [PMID: 20692330]
[24]
Huang M, Huang M, Li X, et al. Bisphenol A induces apoptosis through GPER-dependent activation of the ROS/Ca2+-ASK1-JNK pathway in human granulosa cell line KGN. Ecotoxicol Environ Saf 2021; 208: 111429.
[http://dx.doi.org/10.1016/j.ecoenv.2020.111429] [PMID: 33039870]
[25]
Khalaf AA, Ahmed WMS, Moselhy WA, Abdel-Halim BR, Ibrahim MA. Protective effects of selenium and nano-selenium on bisphenol-induced reproductive toxicity in male rats. Hum Exp Toxicol 2019; 38(4): 398-408.
[http://dx.doi.org/10.1177/0960327118816134] [PMID: 30526071]
[26]
Shi J, Liu C, Chen M, et al. The interference effects of bisphenol A on the synthesis of steroid hormones in human ovarian granulosa cells. Environ Toxicol 2021; 36(4): 665-74.
[http://dx.doi.org/10.1002/tox.23070] [PMID: 33258555]
[27]
Bloom MS, Mok-Lin E, Fujimoto VY. Bisphenol A and ovarian steroidogenesis. Fertil Steril 2016; 106(4): 857-63.
[http://dx.doi.org/10.1016/j.fertnstert.2016.08.021] [PMID: 27543890]
[28]
Feng Y, Yin J, Jiao Z, Shi J, Li M, Shao B. Bisphenol AF may cause testosterone reduction by directly affecting testis function in adult male rats. Toxicol Lett 2012; 211(2): 201-9.
[http://dx.doi.org/10.1016/j.toxlet.2012.03.802] [PMID: 22504055]
[29]
Ruffinatti FA, Gilardino A, Secchi V, Cottone E, Lovisolo D, Bovolin P. Bisphenol A activates calcium influx in immortalized GnRH neurons. Int J Mol Sci 2019; 20(9): 2160.
[http://dx.doi.org/10.3390/ijms20092160] [PMID: 31052388]
[30]
Adewale HB, Jefferson WN, Newbold RR, Patisaul HB. Neonatal bisphenol-a exposure alters rat reproductive development and ovarian morphology without impairing activation of gonadotropin-releasing hormone neurons. Biol Reprod 2009; 81(4): 690-9.
[http://dx.doi.org/10.1095/biolreprod.109.078261] [PMID: 19535786]
[31]
vom Saal FS, Akingbemi BT, Belcher SM, et al. Chapel Hill bisphenol A expert panel consensus statement: Integration of mechanisms, effects in animals and potential to impact human health at current levels of exposure. Reprod Toxicol 2007; 24(2): 131-8.
[http://dx.doi.org/10.1016/j.reprotox.2007.07.005] [PMID: 17768031]
[32]
Stavely R, Nurgali K. The emerging antioxidant paradigm of mesenchymal stem cell therapy. Stem Cells Transl Med 2020; 9(9): 985-1006.
[http://dx.doi.org/10.1002/sctm.19-0446] [PMID: 32497410]
[33]
He Y, Chen D, Yang L, Hou Q, Ma H, Xu X. The therapeutic potential of bone marrow mesenchymal stem cells in premature ovarian failure. Stem Cell Res Ther 2018; 9(1): 263.
[http://dx.doi.org/10.1186/s13287-018-1008-9] [PMID: 30286808]
[34]
Jalalie L, Rezaee MA, Rezaie MJ, Jalili A, Raoofi A, Rustamzade A. Human umbilical cord mesenchymal stem cells improve morphometric and histopathologic changes of cyclophosphamide-injured ovarian follicles in mouse model of premature ovarian failure. Acta Histochem 2021; 123(1): 151658.
[http://dx.doi.org/10.1016/j.acthis.2020.151658] [PMID: 33249312]
[35]
Kossl J, Bohacova P, Hermankova B, Javorkova E, Zajicova A, Holan V. Antiapoptotic properties of mesenchymal stem cells in a mouse model of corneal inflammation. Stem Cells Dev 2021; 30(8): 418-27.
[http://dx.doi.org/10.1089/scd.2020.0195] [PMID: 33607933]

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