Wang Shao-jun, Tan Lian-hong, Yang Yong-sheng
Department of Biochemistry and Molecular Biology, Institute of Acu-moxibustion, China Academy of Chinese Medical Sciences, Beiing 100700, China.
Zhen Ci Yan Jiu. 2011 Feb;36(1):1-6, 39.
To observe the effect of electroacupuncture (EA) on the efficacy of estrogen-induced regulation of reproductive endocrine in ovariectomized (OVX) rats.
Thirty SD rats were randomly divided into control, model (OVX), EA-Guanyuan(CV 4), Estrogen (E) and EA+ E groups (n = 6 in each group). OVX model was duplicated by removing the bilateral ovaries. EA (5 Hz/20 Hz, 1- 2 mA) was applied to "Guanyuan" (CV 4) for 30 min, once every other day and for 3 sessions. Estrogen at doses of 0.5 mg/kg and 0. 25 mg/kg was intraperitonealy given to rats in the E group and EA+ E group, respectively. Serum estrogen and cortisol contents were assayed by enzyme linked immunosorbent assay and the expression of hypothalamic gonadotrophin releasing hormone(GnRH)mRNA, G protein-coupled receptor 54(GPR 54)mRNA, kisspeptin-1 (Kiss-l) mRNA and corticotropin releasing hormone (CRH) mRNA were detected by using real time polymerase chain reaction (RT-PCR).
Compared with the control group, the expression levels of GnRH mRNA, GPR 54 mRNA and Kiss-1 mRNA in hypothalamus in the model group were increased significantly (P<0. 05), while the expression of hypothalamic CRH mRNA was down-regulated obviously (P<0. 05), and serum cortisol and estrogen levels were reduced significantly (P<0. 05). In comparison with the model group, the expression levels of hypothalamic GnRH mRNA in the EA, E and EA+ E groups, and those of hypothalamic GPR 54 mRNA and Kiss-1 mRNA in the E and EA+ E groups were down-regulated considerably (P<0. 05); whereas hypothalamic CRH mRNA expression levels in the E and EA+ E groups were up-regulated obviously (P<0. 05),and serum cortisol and estrogen contents in the E and EA+ E groups were increased remarkably (P<0.05). Comparison among the EA and EA+ E groups showed that the effects of EA+ E group were significantly superior to those of EA group in down-regulating hypothalalmic GnRH mRNA and GPR 54 mRNA expression, and in up-regulating hypothalamic CRH mRNA expression and serum cortisol and estrogen contents (P<0.05). No significant differences were found between E and EA + E groups in down-regulating hypothalamic GnRH mRNA, GPR 54 mRNA and Kiss-1 mRNA expression, and in up-regulating hypothalamic CRH mRNA expression and serum cortisol and estrogen levels (P>0. 05).
EA-CV 4 is able to potentiate the effects of low-dose of estrogen in down-regulating hypothalamic GnRH mRNA,GPR 54 mRNA and Kiss-1 mRNA expression, and up-regulating hypothalamic CRH mRNA expression and raising serum cortisol and estrogen contents in OVX rats, showing a favorable modulation effect on reproductive endocrine activity.
观察电针(EA)对雌激素诱导去卵巢(OVX)大鼠生殖内分泌调节作用的影响。
将30只SD大鼠随机分为对照组、模型组(OVX)、电针关元组(CV 4)、雌激素组(E)和电针+雌激素组(EA+ E),每组6只。通过切除双侧卵巢建立OVX模型。将电针(5 Hz/20 Hz,1 - 2 mA)施加于“关元”(CV 4)30分钟,隔日1次,共3次。E组和EA+ E组大鼠分别腹腔注射0.5 mg/kg和0.25 mg/kg的雌激素。采用酶联免疫吸附测定法检测血清雌激素和皮质醇含量,运用实时聚合酶链反应(RT-PCR)检测下丘脑促性腺激素释放激素(GnRH)mRNA、G蛋白偶联受体54(GPR 54)mRNA、亲吻素-1(Kiss-1)mRNA和促肾上腺皮质激素释放激素(CRH)mRNA的表达。
与对照组相比,模型组下丘脑GnRH mRNA、GPR 54 mRNA和Kiss-1 mRNA的表达水平显著升高(P<0.05),而下丘脑CRH mRNA的表达明显下调(P<0.05),血清皮质醇和雌激素水平显著降低(P<0.05)。与模型组相比,EA组、E组和EA+ E组下丘脑GnRH mRNA的表达水平,以及E组和EA+ E组下丘脑GPR 54 mRNA和Kiss-1 mRNA的表达水平均显著下调(P<0.05);而E组和EA+ E组下丘脑CRH mRNA的表达水平明显上调(P<0.05),E组和EA+ E组血清皮质醇和雌激素含量显著增加(P<0.05)。EA组与EA+ E组比较,EA+ E组在下调下丘脑GnRH mRNA和GPR 54 mRNA表达,以及上调下丘脑CRH mRNA表达和血清皮质醇及雌激素含量方面的作用明显优于EA组(P<0.05)。E组与EA + E组在下调下丘脑GnRH mRNA、GPR 54 mRNA和Kiss-1 mRNA表达,以及上调下丘脑CRH mRNA表达和血清皮质醇及雌激素水平方面无显著差异(P>0.05)。
电针关元能增强低剂量雌激素对OVX大鼠下丘脑GnRH mRNA、GPR 54 mRNA和Kiss-1 mRNA表达的下调作用,以及对下丘脑CRH mRNA表达的上调作用,并提高血清皮质醇和雌激素含量,对生殖内分泌活动具有良好的调节作用。