Vatanpour Morvarid, Ebrahimzadeh-Bideskan Alireza, Rajabian Arezoo, Alipour Fatemeh, Raoofi Amir, Ebrahimi Vahid
Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran; Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Tissue Cell. 2024 Dec;91:102550. doi: 10.1016/j.tice.2024.102550. Epub 2024 Aug 30.
This study was designed to examine the effects of selenium nanoparticles (SeNPs) coated with gallic acid (GA) on testis in azoospermic rats. Thirty-six adult Wistar rats were assigned to six groups: control (1 ml intraperitoneal (i.p.) phosphate-buffered saline (PBS) for 7 consecutive days), SHAM (single i.p. injection of 1 ml of 8 % dimethyl sulfoxide (DMSO)), BUS (single i.p. injection of busulfan (BUS) 30 mg/kg body weight), GA (single i.p. injection of BUS 30 mg/kg on day 1, 100 mg/kg body weight GA from days 2-7), SeNPs (single i.p. injection of BUS 30 mg/kg on day 1, 0.5 mg/kg body weight SeNPs from days 2-7), and SeNPs-GA (single i.p. injection of BUS 30 mg/kg on day 1, 0.5 mg/kg body weight SeNPs-GA from days 2-7). Subsequently, serum levels of testosterone and insulin-like growth factor-1 (IGF-1), antioxidant markers, sperm parameters, and histological parameters were evaluated. The results showed that BUS injection induced azoospermia in rats by causing oxidative stress and testicular tissue damage. In contrast, co-administration of SeNPs and GA showed significant improvements in testosterone and IGF-1 levels, antioxidant status, testicular tissue characteristics, and sperm parameters. Overall, the findings suggest that GA-coated SeNPs offer therapeutic potential in BUS-induced azoospermic models.
本研究旨在考察没食子酸(GA)包覆的硒纳米颗粒(SeNPs)对无精子症大鼠睾丸的影响。将36只成年Wistar大鼠分为6组:对照组(连续7天腹腔注射1 ml磷酸盐缓冲盐水(PBS))、假手术组(单次腹腔注射1 ml 8%二甲基亚砜(DMSO))、白消安组(单次腹腔注射白消安(BUS)30 mg/kg体重)、GA组(第1天单次腹腔注射BUS 30 mg/kg,第2 - 7天注射100 mg/kg体重的GA)、SeNPs组(第1天单次腹腔注射BUS 30 mg/kg,第2 - 7天注射0.5 mg/kg体重的SeNPs)和SeNPs - GA组(第1天单次腹腔注射BUS 30 mg/kg,第2 - 7天注射0.5 mg/kg体重的SeNPs - GA)。随后,评估血清睾酮和胰岛素样生长因子-1(IGF - 1)水平、抗氧化标志物、精子参数和组织学参数。结果显示,注射白消安通过引起氧化应激和睾丸组织损伤导致大鼠无精子症。相比之下,联合给予SeNPs和GA可显著改善睾酮和IGF - 1水平、抗氧化状态、睾丸组织特征和精子参数。总体而言,研究结果表明GA包覆的SeNPs在白消安诱导的无精子症模型中具有治疗潜力。