Kilinc Leyla, Uz Yesim Hulya
Department of Histology and Embryology, Faculty of Medicine, Trakya University, Edirne, Turkey.
Department of Histology and Embryology, Faculty of Medicine, Akdeniz University, Antalya, Turkey.
Clin Exp Reprod Med. 2021 Sep;48(3):211-220. doi: 10.5653/cerm.2020.04105. Epub 2021 Jul 20.
The present study aimed to investigate the possibility that curcumin (CMN) protects against methotrexate (MTX)-induced testicular damage by affecting the phospho-p38 (p-p38) mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-κB) signaling pathways.
Eighteen male Wistar albino rats were randomly divided into three groups. The control group was given an intragastric administration of dimethyl sulfoxide (DMSO) daily for 14 days, the MTX group was given a single intraperitoneal dose of MTX (20 mg/kg) on the 11th day, and the MTX+CMN group was given intragastric CMN (100 mg/kg/day, dissolved in DMSO) for 14 days and a single intraperitoneal dose of MTX (20 mg/kg) on the 11th day. At the end of the experiment, all animals were sacrificed and the testicular tissues were removed for morphometry, histology, and immunohistochemistry. Body and testicular weights were measured.
Body weights, seminiferous tubule diameter, and germinal epithelium height significantly decreased in the MTX group compared to the control group. Whereas, the number of histologically damaged seminiferous tubules and interstitial space width significantly increased in the MTX group. In addition, the number of p-p38 MAPK immunopositive cells and the immunoreactivity of NF-κB also increased in the MTX group compared to the control group. CMN improved loss of body weight, morphometric values, and histological damage due to MTX. CMN also reduced the number of p-p38 MAPK immunopositive cells and the NF-κB immunoreactivity.
CMN may reduce MTX-induced testicular damage by suppressing the p38 MAPK and NF-κB signaling pathways.
本研究旨在探讨姜黄素(CMN)通过影响磷酸化p38(p-p38)丝裂原活化蛋白激酶(MAPK)和核因子-κB(NF-κB)信号通路来预防甲氨蝶呤(MTX)诱导的睾丸损伤的可能性。
18只雄性Wistar白化大鼠随机分为三组。对照组每天灌胃二甲基亚砜(DMSO),持续14天;MTX组在第11天腹腔注射单次剂量的MTX(20 mg/kg);MTX+CMN组连续14天灌胃CMN(100 mg/kg/天,溶于DMSO),并在第11天腹腔注射单次剂量的MTX(20 mg/kg)。实验结束时,处死所有动物,取出睾丸组织进行形态测量、组织学和免疫组织化学分析。测量体重和睾丸重量。
与对照组相比,MTX组的体重、生精小管直径和生精上皮高度显著降低。然而,MTX组组织学损伤的生精小管数量和间质间隙宽度显著增加。此外,与对照组相比,MTX组中p-p38 MAPK免疫阳性细胞数量和NF-κB免疫反应性也增加。CMN改善了MTX导致的体重减轻、形态学值和组织学损伤。CMN还减少了p-p38 MAPK免疫阳性细胞数量和NF-κB免疫反应性。
CMN可能通过抑制p38 MAPK和NF-κB信号通路来减轻MTX诱导的睾丸损伤。