Histological assessment for investigation of dose-dependent ovarian toxicity of cyclophosphamide in the rat

被引:0
|
作者
Elahi, Narges [1 ,2 ]
Astaneh, Mohammad Ebrahim [3 ]
Ai, Jafar [4 ]
Makoolati, Zohreh [3 ]
机构
[1] Fasa Univ Med Sci, Students Res Comm, Fasa, Iran
[2] Fasa Univ Med Sci, Sch Adv Technol Med, Dept Tissue Engn, Fasa, Iran
[3] Fasa Univ Med Sci, Fac Med, Dept Anat Sci, Fasa, Iran
[4] Univ Tehran Med Sci, Sch Adv Technol Med, Dept Tissue Engn & Appl Cell Sci, Tehran, Iran
关键词
Ovarian toxicity; Cyclophosphamide; Follicle; IN-VITRO FERTILIZATION; CHEMOTHERAPY; FOLLICLES; HORMONE; RESERVE; IMPACT; CELLS;
D O I
10.1016/j.heliyon.2024.e36767
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Cyclophosphamide (CPA) have significant effects on ovarian follicles which lead to ovarian toxicity and impair the normal female reproductive function. This study aimed to evaluate the dose-dependent effects of CPA on rat follicle numbers. Methods: The experimental groups consisted of rats administered a single intraperitoneal injection of CPA at doses of either 50, 75,150, or 200 mg/kg followed by daily doses of 8 mg/kg for 14 days and control group given no treatment. After the treatment period, the histological evaluation was done. Results: Primordial and primary follicles were affected by all doses of CPA, but differential follicle counts revealed that graaf and preantral follicles were most sensitive to CPA, followed by primary and primordial follicles. The greatest reduction in all type of studied follicles caused by CPA doses of 50 mg/kg. Conclusion: Differential follicle counts revealed that CPA-induced ovarian toxicity is exhibited in structural feature of the ovary, particularly in destruction of graaf and preantral follicles in a dose-dependent manner so that the highest decrease in all type of studied follicles caused by 50 mg/kg of CPA and is suggested as the best concentration for ovotoxicity induction. These findings give insight into ovarian response to structural disruption of folliculogenesis.
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页数:9
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