2)、及抗繆勒管激素(AMH)水平;實(shí)時(shí)熒光定量PCR(qRT-PCR)法檢測(cè)卵巢組織中血管內(nèi)皮生長(zhǎng)因子(VEGF)、堿性成纖維細(xì)胞生長(zhǎng)因子(bFGF)mRNA的表達(dá)變化。結(jié)果 與對(duì)照組比較,模型組卵巢內(nèi)的始基卵泡、竇前卵泡、竇狀卵泡數(shù)目明顯減少,閉鎖卵泡數(shù)目明顯增多(P<0.05);E2、AMH水平明顯降低(P<0.05),F(xiàn)SH、LH水平明顯升高(P<0.05);VEGF、bFGF mRNA水平均明顯降低(P<0.05)。與模型組比較,坤泰膠囊組卵巢內(nèi)的始基卵泡、竇狀卵泡、竇前卵泡數(shù)目明顯增多,閉鎖卵泡數(shù)目明顯減少(P<0.05);E2、AMH水平明顯升高(P<0.05),F(xiàn)SH、LH水平明顯降低(P<0.05);VEGF、bFGF mRNA水平均明顯升高(P<0.05)。結(jié)論 坤泰膠囊通過調(diào)節(jié)激素水平及上調(diào)VEGF、bFGF mRNA表達(dá),修復(fù)受損的卵巢組織,促進(jìn)卵泡的生長(zhǎng)發(fā)育,從而抑制卵泡過早耗竭。;Objective To explore the effect and mechanism of Kuntai Capsule (KC) on premature ovarian failure in rats. Methods Totally 40 SD female rats were randomly divided into four groups:control group, model group, Kuntai Capsule (KC) group and conjugated estrogens tablets (CET) group. The premature ovarian failure model in rats was made by ig administration of 75 mg/kg tripterygium. After the model was established, rats were continually treated with 0.6 and 0.625 g/kg of KC and CET respectively by ig administration for 36 d. HE staining was used to observe the morphology of ovary and count the number of follicle. The enzyme-linked immunosorbent assay (Elisa) method was used for the detection of follicle stimulating hormone (FSH), luteinizing hormone (LH), serum estradiol (E2), and anti-Mueller tube hormone (AMH) level. The real-time fluorescence quantitative PCR (qRT-PCR) method was used to detect the mRNA expression of vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF). Results Compared with control group, the number of primordial follicles, preantral follicles and antral follicles were significantly reduced, the number of atretic follicles was increased (P<0.05), E2 and AMH significantly decreased (P<0.05), FSH and LH levels increased significantly (P<0.05), and the levels of VEGF and bFGF mRNA in model group were significantly decreased (P<0.05). Compared with model group, the number of primordial follicles, preantral follicles, and antral follicles were significantly increased, the number of atretic follicles was significantly reduced (P<0.05), E2 and AMH significantly increased (P<0.05), FSH and LH levels significantly decreased (P<0.05), and the levels of VEGF and bFGF mRNA in KC group were significantly increased (P<0.05). Conclusion By regulating the level of hormone and up-regulating the expression of VEGF and bFGF, KC can repair the damaged ovarian tissue and promote the growth and development of the follicle, so as to inhibit the premature exhaustion of mRNA."/>