Protective effect of astragaloside IV on cadmium-induced spermatogenesis microenvironment damage in rats.

IF 2.1 4区 医学 Q3 ANDROLOGY
Wei Ning, Xiaogang Liao, Xingyou Dong, Yangcai Wang, Xingliang Yang, Jie Xu, Shanhong Yi, Zhenxing Yang
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引用次数: 1

Abstract

The previous study using Sertoli cells cultured in vitro has shown that the protective effects of astragaloside IV (AsIV) on cadmium (Cd)-induced damage to Sertoli cells and its membrane proteins. Yet, it is not known if AsIV has an equivalent effect on Cd-induced damage to the spermatogenesis microenvironment in rats. Using an in vivo model, Cd-induced damage to the spermatogenesis microenvironment and the protective effects of AsIV were studied. Eighteen male Sprague Dawley (SD) rats were randomly divided into three groups (n = 6/group): Cd group, Cd&AsIV group, and control group. Cd was administered to the rats in the Cd group via i.p. at 1 mg/kg body weight once daily, Cd and AsIV was administered to the rats in the Cd&AsIV group via i.p. at 1 mg/kg body weight and 10 mg/kg body weight respectively once daily, and the same volume of saline was administered to the rats in control group via i.p. once daily. The rats in the three groups were injected continuously for 5 days. Vesicular formation in the seminiferous tubules was observed in the Cd treatment group. The average optical density of claudin-11, zonal occludin-1 (ZO-1), and connexin 43 (Cx43) decreased significantly in the Cd treatment group. The ultrastructural damage of the Sertoli cells and tight junctions were also observed by electron microscopy. AsIV treatment rescued the morphologic changes of the seminiferous tubules of the testis and the ultrastructural damage of the Sertoli cells and tight junctions. The average optical density of claudin-11, ZO-1, and Cx43 also increased significantly after AsIV treatment. Cd damages the spermatogenesis microenvironment in rats, which can be rescued by AsIV treatment. These results illustrate that AsIV may also have a protective effect on Cd-induced damage to the spermatogenesis microenvironment in rats.Abbreviations: AsIV: astragaloside IV; Cd: cadmium; SD: Sprague Dawley; ZO-1: zonal occludin-1; Cx43: connexin 43; BTB: blood-testis barrier; MAPKs: mitogen-activated protein kinases; OSP: oligodendrocyte-specific protein; Cxs: connexins; GJIC: gap junctional intercellular communication; ROS: reactive oxygen species; MDA: malondialdehyde; TGF: tumor growth factor; PBS: phosphate buffer saline; BSA: bovine serum albumin.

黄芪甲苷对镉致大鼠精子发生微环境损伤的保护作用。
体外培养的支持细胞研究表明,黄芪甲苷(astragaloside IV, AsIV)对镉(Cd)诱导的支持细胞及其膜蛋白损伤具有保护作用。然而,目前尚不清楚asv是否对cd诱导的大鼠精子发生微环境损伤具有同等作用。通过体内模型,研究cd诱导的精子发生微环境损伤及asv的保护作用。雄性SD大鼠18只,随机分为3组(n = 6/组):Cd组、cd&asv组和对照组。Cd组大鼠按1 mg/kg体重每日1次腹腔注射Cd, Cd&AsIV组大鼠分别按1 mg/kg体重和10 mg/kg体重每日1次腹腔注射Cd和AsIV,对照组大鼠等量生理盐水每日1次腹腔注射。三组大鼠连续注射5 d。Cd治疗组精子小管出现囊泡形成。Cd治疗组claudin-11、带状闭塞蛋白1 (ZO-1)、连接蛋白43 (Cx43)的平均光密度显著降低。电镜观察到支持细胞的超微结构损伤和紧密连接。asv治疗恢复了睾丸精小管的形态改变和支持细胞和紧密连接的超微结构损伤。asv处理后,claudin-11、ZO-1和Cx43的平均光密度也显著升高。Cd破坏大鼠精子发生微环境,可通过asv治疗恢复。这些结果表明,asv也可能对cd诱导的大鼠精子发生微环境损伤具有保护作用。缩写:AsIV:黄芪甲苷;Cd:镉;SD:斯普拉格·道利;ZO-1:区域闭塞素-1;Cx43: connexin 43;BTB:血睾丸屏障;MAPKs:丝裂原活化蛋白激酶;OSP:少突胶质细胞特异性蛋白;Cxs:连接素;GJIC:间隙连接细胞间通讯;ROS:活性氧;MDA:丙二醛;TGF:肿瘤生长因子;PBS:磷酸盐缓冲盐水;牛血清白蛋白。
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来源期刊
CiteScore
4.30
自引率
4.20%
发文量
27
审稿时长
>12 weeks
期刊介绍: Systems Biology in Reproductive Medicine, SBiRM, publishes Research Articles, Communications, Applications Notes that include protocols a Clinical Corner that includes case reports, Review Articles and Hypotheses and Letters to the Editor on human and animal reproduction. The journal will highlight the use of systems approaches including genomic, cellular, proteomic, metabolomic, bioinformatic, molecular, and biochemical, to address fundamental questions in reproductive biology, reproductive medicine, and translational research. The journal publishes research involving human and animal gametes, stem cells, developmental biology and toxicology, and clinical care in reproductive medicine. Specific areas of interest to the journal include: male factor infertility and germ cell biology, reproductive technologies (gamete micro-manipulation and cryopreservation, in vitro fertilization/embryo transfer (IVF/ET) and contraception. Research that is directed towards developing new or enhanced technologies for clinical medicine or scientific research in reproduction is of significant interest to the journal.
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