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1. 上海中医药大学附属岳阳临床医学院
2. 上海市针灸经络研究所
3. 中国中医科学院针灸研究所
纸质出版日期:2013
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孙洁, 赵继梦, 季蓉, 等. 电针对多囊卵巢综合征大鼠卵巢高雄激素症的影响[J]. 针刺研究, 2013,38(6):465-472.
SUN Jie, ZHAO Ji-meng, JI Rong, et al. Effects of Electroacupuncture of“Guanyuan”(CV 4)-“Zhongji”(CV 3)on Ovarian P 450arom and P 450c17αExpression and Relevant Sex Hormone Levels in Rats with Polycystic Ovary Syndrome[J]. Acupuncture research, 2013, 38(6): 465-472.
孙洁, 赵继梦, 季蓉, 等. 电针对多囊卵巢综合征大鼠卵巢高雄激素症的影响[J]. 针刺研究, 2013,38(6):465-472. DOI: 10.13702/j.1000-0607.2013.06.008.
SUN Jie, ZHAO Ji-meng, JI Rong, et al. Effects of Electroacupuncture of“Guanyuan”(CV 4)-“Zhongji”(CV 3)on Ovarian P 450arom and P 450c17αExpression and Relevant Sex Hormone Levels in Rats with Polycystic Ovary Syndrome[J]. Acupuncture research, 2013, 38(6): 465-472. DOI: 10.13702/j.1000-0607.2013.06.008.
目的:观察电针对来曲唑诱导的多囊卵巢综合征(PCOS)大鼠卵巢P 450芳香化酶(arom)和P450 17α羟化酶(c 17α)表达及相关性激素的影响。方法:将30只雌性SD大鼠随机分成正常组、模型组、电针组各10只
模型组和电针组采用来曲唑灌胃复制PCOS模型。电针组选取"关元""中极"给予电针治疗
每日1次
治疗14d。观察大鼠卵巢质量、卵巢组织形态学及超微结构变化;免疫组化法观察卵泡颗粒细胞层P 450arom和卵泡膜细胞层P 450c17α的表达;ELISA法检测卵巢组织相关性激素雌二醇(E 2)、雌酮(E 1)、雄烯二酮(ASD)、睾酮(T)、促卵泡刺激素(FSH)、促黄体生成素(LH)含量变化。结果:与正常组相比
模型组大鼠左、右卵巢组织质量均有显著增加(P<0.01)
电针组较模型组则显著降低(P<0.01);同时模型组大鼠卵巢组织形态学及超微结构也出现异常改变
而经电针治疗后大鼠卵巢组织形态学及超微结构均有明显改善。与正常组比较
模型组大鼠卵巢颗粒细胞层P 450arom表达降低(P<0.01)
卵泡膜细胞层P 450c17α表达显著增高(P<0.01);电针组P 450arom表达较模型组增高(P<0.05)
P 450c17α表达则降低(P<0.01)。与正常组比较
模型组大鼠卵巢组织ASD、T、LH水平显著升高(P<0.01)
E 1、E 2水平显著降低(P<0.01);而电针组大鼠ASD、T、LH水平较模型组显著降低(P<0.05
P<0.01)
E 1、E 2水平显著升高(P<0.01)。结论:电针可通过促进/增加PCOS大鼠卵巢颗粒细胞层P 450arom表达、抑制/减弱卵泡膜细胞层P 450c17α表达
促使卵巢内雄激素能向雌激素正常转化
由此改善PCOS卵巢局部内分泌环境紊乱
达到恢复或改善其卵泡发育及排卵异常的作用。
Objective To observe the effect of electroacupuncture(EA)on ovarian P 450arom and P 450c17α(aromatases)expression and related sex hormone levels in polycystic ovary syndrome(PCOS)rats.Methods Thirty SD rats were randomly divided into normal control group
model group and EA group(10rats/group).PCOS model was made by intragastric administration of letrozole at 1mg/kg per day for consecutive 21days."Guanyuan"(CV 4)and"Zhongji"(CV 3)acupoints were stimulated 20min by EA(2mA
2Hz)
once daily for consecutive 14days.The damp ovarian weight was weighed and the pathological changes of the ovarian tissue were observed after H.E.staining.Ultrastructural changes of the ovarian tissue were observed by transmission electron microscope.Immunohistochemical staining was adopted to detect ovarian follicle granulosa cell P 450arom and follicle membrane cell P 450c17αexpression.The contents of estradiol(E 2)
estrone(E 1)
androstenedione(ASD)
testosterone(T)
follicle-stimulating hormone(FSH)and luteinizing hormone(LH)in the ovarian tissue were measured by ELISA.Results Compared with the normal group
there was a significant increase in the damp weight of both left and right ovarian tissues in the model group(P<0.01).After EA
the ovarian weight was remarkably reduced(P<0.01).Pathological changes of the ovarian tissue such as thickening of the superficial albugineous coat of the ovary
thinning of the granular cell layer
and disappearance of the intraovular oocytes and coronaradiata under light microscope
and mitochondrion swelling
fracture or disappearance of mitochondrial cristae
and enlargement of the endoplasmic reticulum
etc.after modeling were obviously improved in the EA group.In comparison to the control group
the expression of the follicle granulosa cell P 450arom was significantly down-regulated and that of follicle membrane cell P 450c 17αwas significantly upregulated in the model group(P<0.01).After EA intervention these changes were obviously reversed(P<0.05
P<0.01).In the model group
there was a significant increase in the levels of ASD
T and LH in the ovarian tissues(P<0.01)and a marked decrease in the contents of ovarian E 1and E 2(P<0.01)in comparison to the control group.After EA
the ovarian ASD
T and LH levels were notably decreased(P<0.05
P<0.01)and the E 1and E 2levels apparently increased(P<0.01)compared with the model group.Conclusion EA can improve letrozole-induced pathological changes of ovarian morphology and ultrastructure and obviously promote P 450arom expression in the follicle granulosa cell layer and inhibit P 450c17αexpression in the follicle membrane cell layer
as well as regulate sex hormone levels in PCOS rats
facilitating the normal transformation of ovarian androgen to estrogen and restoring the local endocrine disorders.
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