[Electroacupuncture promotes expression of glutathione related regulatory enzymes in ovary tissue of rats with diminished ovarian reserve].

Ling Shi, Ge Lu, Hong-Xiao Li, Mei-Hong Shen
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Abstract

Objective: To observe the effect of electroacupuncture (EA) on ovarian function and expression of glutathione (GSH) related regulatory enzymes γ-glutamylcysteine synthetase (γ-GCS), glutathione reductase (GR) protein and gene in rats with diminished ovarian reserve (DOR), so as to explore its mechanisms underlying up-regulation of antioxidant stress ability.

Methods: A total of 30 female SD rats with normal estrous cycle were randomly divided into blank control, model and EA groups, with 10 rats in each group. The DOR model was established by gavage of tripterygium wilfordii polyglycoside suspension (50 mg·kg-1·d-1) for 14 consecutive days, while the rats in the blank group were given equal volume of 0.9% sodium chloride solution. One hour after daily gavage, EA (1.0 mA, 100 Hz) was applied alternately to bilateral "Shenshu"(BL23), and "Zhongwan"(CV12)+"Guanyuan"(CV4) for 10 min, for 14 consecutive days. Estrous cycles of rats in each group were observed and recorded daily during intervention.After the intervention, H.E.staining was used to observe histopathological changes of the ovarian tissue. The contents of serum sex hormones [follicle stimulating hormone (FSH), anti-mullerian hormone (AMH), estradiol (E2)] and oxidative damage markers [8-hydroxydeoxyguanosine (8-OHDG) and nitrotyrosine (NTY)] were determined by ELISA. The contents of GSH and oxidized glutathione (GSSG) in the liver tissue were determined by colorimetry, and their ratios were calculated. Immunohistochemistry and real-time fluorescence quantitative PCR were used to detect the immunoactivity and gene expression levels of γ-GCS and GR in the ovarian tissues, respectively.

Results: Compared with the blank group, the model group had a marked increase in the disorder rate of estrous cycle, serum FSH, 8-OHDG and NTY contents (P<0.01) and a considerable decrease in the levels of serum AMH and E2, liver GSH and GSSG contents and GSH/GSSG ratio, ovarian optical density and cell number as well as the expression of γ-GCS and GR mRNAs (P<0.05, P<0.01). After EA intervention, the increase of the disorder rate of estrous cycle, serum FSH, 8-OHDG and NTY contents and the decrease of serum AMH and E2, liver GSH and GSSG contents and GSH/GSSG ratio, ovarian optical density and cell number of γ-GCS and GR as well as the expression of γ-GCS genes were all reversed (P<0.01, P<0.05). H.E. staining showed degenerative changes of the ovarian tissue, fewer follicles at every level and increase of atretic follicles, disarrangement and layer number decrease of granulosa cells, and atrophy of corpus luteum in the model group, which were relatively milder in the EA group.

Conclusion: EA can improve ovarian function, and reduce oxidative stress damage in DOR rats, which may be associated with its functions in up-regulating the expression of γ-GCS and GR protein and gene in the ovarian tissue.

[电针促进卵巢储备功能减退大鼠卵巢组织谷胱甘肽相关调节酶的表达]。
目的:观察电针(EA)对卵巢储备功能减退(DOR)大鼠卵巢功能及谷胱甘肽(GSH)相关调节酶γ-谷氨酰半胱氨酸合成酶(γ-GCS)、谷胱甘肽还原酶(GR)蛋白及基因表达的影响,探讨其上调抗氧化应激能力的机制。方法:取30只雌性SD大鼠,月经周期正常,随机分为空白对照组、模型组和EA组,每组10只。采用雷公藤多苷混悬液(50 mg·kg-1·d-1)连续灌胃14 d建立DOR模型,空白组给予等体积0.9%氯化钠溶液。每日灌胃1小时后,将EA (1.0 mA, 100 Hz)交替应用于双侧“肾俞”(BL23)、“中脘”(CV12)+“冠源”(CV4),持续10 min,连续14天。干预期间每天观察记录各组大鼠的动情周期。干预后,采用h.e.染色观察卵巢组织病理变化。采用ELISA法测定大鼠血清性激素[促卵泡激素(FSH)、抗苗勒管激素(AMH)、雌二醇(E2)]和氧化损伤标志物[8-羟基脱氧鸟苷(8-OHDG)、硝基酪氨酸(NTY)]含量。采用比色法测定肝组织中谷胱甘肽和氧化谷胱甘肽(GSSG)的含量,并计算其比值。采用免疫组织化学和实时荧光定量PCR分别检测卵巢组织中γ-GCS和GR的免疫活性和基因表达水平。结果:与空白组比较,模型组大鼠发情周期紊乱率明显升高,血清FSH、8-OHDG、NTY含量(PPP2)、肝脏GSH、GSSG含量及GSH/GSSG比值、卵巢光密度、γ-GCS、GR细胞数及γ-GCS基因表达均逆转(ppp)。EA能改善DOR大鼠卵巢功能,减轻氧化应激损伤,这可能与其上调卵巢组织γ-GCS和GR蛋白及基因的表达有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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