open access

Vol 73, No 2 (2022)
Original paper
Submitted: 2021-12-16
Accepted: 2022-01-25
Published online: 2022-04-13
Get Citation

Effects of ethephon on serum levels of sex hormone, apoptosis, and cell cycle of ovaries in mice

Hongyuan Huang1, Xiaoqiu Zhao2, Xin Shi2, Qiyue Tan2, Ruizhi Zhang2, Mei Yue2, Rongshuang Ma2, Qiang Chen2, Shuhua Zhao2, Li Yang1
·
Pubmed: 35593683
·
Endokrynol Pol 2022;73(2):346-352.
Affiliations
  1. Department of Occupational and Environmental Health, School of Public Health, Guangxi Medical University, Nanning, Guangxi, China
  2. Preventive Medicine Experimental Teaching Centre, School of Public Health, Jilin University, Changchun, Jilin, China

open access

Vol 73, No 2 (2022)
Original Paper
Submitted: 2021-12-16
Accepted: 2022-01-25
Published online: 2022-04-13

Abstract

Introduction: The effects of ethephon on the reproductive systems of mammalian females are still ambiguous. This study was conducted to evaluate the toxic effects of ethephon on the female reproductive system.

Material and methods: Forty female C57 mice were used as experimental subjects and evenly divided into 8 groups, which were fed with mixed ethephon (0, 107.3, 214.5, and 429 mg/kg bw/day) and pure water. After 20 and 40 days of gavage, the mice were weighed and individual organ coefficients of the ovaries were measured. Enzyme-linked immunoassay was used to detect the serum levels of serum sex hormones. The cell cycle distribution and rate of apoptosis of mouse ovarian tissues were examined using flow cytometry.

Results: Ethephon intoxication significantly decreased serum levels of progesterone (P) and oestradiol (E2) and increased the serum levels of luteinizing hormone (LH). The serum levels of follicle-stimulating hormone (FSH) decreased and then increased over time. In addition, ethephon significantly inhibited the apoptosis rate in the ovary and caused G0/G1 and G2/M arrest.

Conclusion: These results indicate that prolonged exposure to ethephon may have negative effects on the female reproductive system.

Abstract

Introduction: The effects of ethephon on the reproductive systems of mammalian females are still ambiguous. This study was conducted to evaluate the toxic effects of ethephon on the female reproductive system.

Material and methods: Forty female C57 mice were used as experimental subjects and evenly divided into 8 groups, which were fed with mixed ethephon (0, 107.3, 214.5, and 429 mg/kg bw/day) and pure water. After 20 and 40 days of gavage, the mice were weighed and individual organ coefficients of the ovaries were measured. Enzyme-linked immunoassay was used to detect the serum levels of serum sex hormones. The cell cycle distribution and rate of apoptosis of mouse ovarian tissues were examined using flow cytometry.

Results: Ethephon intoxication significantly decreased serum levels of progesterone (P) and oestradiol (E2) and increased the serum levels of luteinizing hormone (LH). The serum levels of follicle-stimulating hormone (FSH) decreased and then increased over time. In addition, ethephon significantly inhibited the apoptosis rate in the ovary and caused G0/G1 and G2/M arrest.

Conclusion: These results indicate that prolonged exposure to ethephon may have negative effects on the female reproductive system.

Get Citation

Keywords

ethephon; female mice; cell cycle; apoptosis; serum sex hormone

About this article
Title

Effects of ethephon on serum levels of sex hormone, apoptosis, and cell cycle of ovaries in mice

Journal

Endokrynologia Polska

Issue

Vol 73, No 2 (2022)

Article type

Original paper

Pages

346-352

Published online

2022-04-13

Page views

4900

Article views/downloads

580

DOI

10.5603/EP.a2022.0025

Pubmed

35593683

Bibliographic record

Endokrynol Pol 2022;73(2):346-352.

Keywords

ethephon
female mice
cell cycle
apoptosis
serum sex hormone

Authors

Hongyuan Huang
Xiaoqiu Zhao
Xin Shi
Qiyue Tan
Ruizhi Zhang
Mei Yue
Rongshuang Ma
Qiang Chen
Shuhua Zhao
Li Yang

References (30)
  1. Perera PMS, Jayamanna SF, Hettiarachchi R, et al. A phase II clinical trial to assess the safety of clonidine in acute organophosphorus pesticide poisoning. Trials. 2009; 10: 73.
  2. Galloway T, Handy R. Immunotoxicity of organophosphorous pesticides. Ecotoxicology. 2003; 12(1-4): 345–363.
  3. Abdo W, Elmadawy MA, Abdelhiee EY, et al. Protective effect of thymoquinone against lung intoxication induced by malathion inhalation. Sci Rep. 2021; 11(1): 2498.
  4. Bhadoria P, Nagar M, Bharihoke V, et al. Ethephon, an organophosphorous, a Fruit and Vegetable Ripener: Has potential hepatotoxic effects? J Family Med Prim Care. 2018; 7(1): 179–183.
  5. Huang C, Wang D, Li Na, et al. Exposure to ethephon compromises endometrial decidualization in mice during early pregnancy via GPR120. Ecotoxicol Environ Saf. 2021; 220: 112361.
  6. El-Okazy AM. The Effects of Combination of Gibberellic Acid - 3 (GA3) and Ethephon (2-Chloroethyl Phosphonic Acid) (Plant Growth Regulators) on Some Physiological Parameters in Mice. J Egypt Public Health Assoc. 2008; 83(1-2): 67–86.
  7. Bhadoria P, Nagar M, Bahrioke V, et al. Effect of ethephon on the liver in albino rats: A histomorphometric study. Biomed J. 2015; 38(5): 421–427.
  8. Bahr HI, Hamad R, Ismail SAa. The impact of on hepatic and colonic fibrosis induced by ethephon in a rat model. Iran J Basic Med Sci. 2019; 22(8): 956–962.
  9. Mokhtari T, Hussein Osman HE, El-Meghawry El-Kenawy A, et al. Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats. J Tradit Complement Med. 2020; 10(5): 487–495.
  10. Abou-Zeid SM. Ameliorating Effects of Green Tea on Ethephon-Induced Immunotoxicity and Oxidative Stress In Mice. Int J Pharm Sci Sci Res. 2018; 4(1): 01–09.
  11. Hodjat M, Baeeri M, Rezvanfar MA, et al. On the mechanism of genotoxicity of ethephon on embryonic fibroblast cells. Toxicol Mech Methods. 2017; 27(3): 173–180.
  12. Abd Eldaim MA, Tousson E, El Sayed IE, et al. Ameliorative effects of Saussurea lappa root aqueous extract against Ethephon-induced reproductive toxicity in male rats. Environ Toxicol. 2019; 34(2): 150–159.
  13. Yan J, Song C, Zhang H, et al. Effects of Ethephon on spermatogenic cells and sex hormone levels of adolescent male rats. Chin J Applied Clin Ped. 2016; 31: 792–794.
  14. Chathuranga TT, Peiris LD. Chronic (90 days) oral toxicity assessment of ethephon, a commercially available fruit ripener in male wistar rats. Int J Multidiscip Res Dev. 2019; 6(3): 117–120.
  15. Li Na, Liu Te, Zhou L, et al. Di-(2-ethylhcxyl) phthalate reduces progesterone levels and induces apoptosis of ovarian granulosa cell in adult female ICR mice. Environ Toxicol Pharmacol. 2012; 34(3): 869–875.
  16. Xian Y, Liang L, Qi S, et al. Antioxidants retard the ageing of mouse oocytes. Mol Med Rep. 2018; 18(2): 1981–1986.
  17. Mei Y, Rongshuang Ma, Ruizhi Z, et al. Effects of Dimethyl Phthalate (DMP) on Serum Sex Hormone Levels and Apoptosis in C57 Female Mice. Int J Endocrinol Metab. 2019; 17(2): e82882.
  18. Collins JSP, Marshall JC, McCartney CR. Differential sleep-wake sensitivity of gonadotropin-releasing hormone secretion to progesterone inhibition in early pubertal girls. Neuroendocrinology. 2012; 96(3): 222–227.
  19. Robertson DM, Lee CH, Baerwald A. Interrelationships among reproductive hormones and antral follicle count in human menstrual cycles. Endocr Connect. 2016; 5(6): 98–107.
  20. Zhu Q, Ge F, Li X, et al. Dehydroepiandrosterone Antagonizes Pain Stress-Induced Suppression of Testosterone Production in Male Rats. Front Pharmacol. 2018; 9: 322.
  21. Fatahi E, Parivar K, Ali Jorsaraei SG. The effects of diazinon on testosterone, FSH and LH levels and testicular tissue in mice. IJRM. 2009; 7(2): 59–64.
  22. Alaa-Eldin EA, El-Shafei DA, Abouhashem NS. Individual and combined effect of chlorpyrifos and cypermethrin on reproductive system of adult male albino rats. Environ Sci Pollut Res Int. 2017; 24(2): 1532–1543.
  23. Jiao X, Meng T, Zhai Y, et al. Ovarian Reserve Markers in Premature Ovarian Insufficiency: Within Different Clinical Stages and Different Etiologies. Front Endocrinol (Lausanne). 2021; 12: 601752.
  24. Boppana NB, Stochaj U, Kodiha M, et al. Enhanced killing of SCC17B human head and neck squamous cell carcinoma cells after photodynamic therapy plus fenretinide via the de novo sphingolipid biosynthesis pathway and apoptosis. Int J Oncol. 2015; 46(5): 2003–2010.
  25. Li Y, Xu X, Deng M, et al. Identification of mRNAs and lncRNAs Involved in the Regulation of Follicle Development in Goat. Front Genet. 2020; 11: 589076.
  26. Kim H, Kim DH, Park SB, et al. Induction of Ski Protein Expression upon Luteinization in Rat Granulosa Cells. Asian-Australas J Anim Sci. 2012; 25(5): 635–641.
  27. Mertens-Walker I, Baxter RC, Marsh DJ. Gonadotropin signalling in epithelial ovarian cancer. Cancer Lett. 2012; 324(2): 152–159.
  28. Xia L, Wen H, Han X, et al. Luteinizing hormone inhibits cisplatin-induced apoptosis in human epithelial ovarian cancer cells. Oncol Lett. 2016; 11(3): 1943–1947.
  29. Huang K, Chen L, Zhang J, et al. Elevated p53 expression levels correlate with tumor progression and poor prognosis in patients exhibiting esophageal squamous cell carcinoma. Oncol Lett. 2014; 8(4): 1441–1446.
  30. Milicevic Z, Kasapovic J, Gavrilovic L, et al. Mutant p53 protein expression and antioxidant status deficiency in breast cancer. EXCLI J. 2014; 13: 691–708.

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