|国家科技期刊平台
首页|期刊导航|中国比较医学杂志|雷公藤多苷致小鼠早发性卵巢功能不全模型的不同时间点进展研究

雷公藤多苷致小鼠早发性卵巢功能不全模型的不同时间点进展研究OACSTPCD

Progression of Tripterygium wilfordii polyglycoside in mice with premature ovarian insufficiency at various time points

中文摘要英文摘要

目的 探讨雷公藤多苷致早发性卵巢功能不全(POI)小鼠模型相关指标的变化,确定采取干预措施的最佳时间点.方法 将40只ICR雌性小鼠随机分为对照组、A、B、C、D模型组,每组8只.对照组灌胃纯水14 d(0.01 mL/10 g),其余各组给予雷公藤多苷混悬液(80 mg/kg,0.01 mL/10 g)分别连续灌胃1 d(A模型组)、3 d(B模型组)、7 d(C模型组)、14 d(D模型组),并分批次取材.称量各组小鼠体重、湿重子宫和双侧卵巢;酶联免疫法检测各组小鼠血清FSH、LH、E2、P、AMH、INH-B、T含量;HE染色观察各组小鼠各级卵泡、黄体的数量及发育状态;TUNEL荧光染色法检测各组小鼠卵巢内凋亡面积;IHC法检测各组小鼠卵巢中VEGFA、CD34、EPO蛋白阳性表达;PCR法检测各组小鼠HIF-1α、SDF-1、CXCR4的mRNA表达量.结果 与对照组比较,A模型组各指标变化不符合POI成模标准;B模型组小鼠卵巢指数、子宫指数、体重显著降低(P<0.01),C模型组体重显著下降(P<0.01),D模型组卵巢指数明显下降(P<0.05);B、C、D模型组血清指标FSH、LH含量升高(P<0.05,P<0.01),E2、PROG、AMH、INH-B、T含量下降(P<0.01);B、C、D模型组始基卵泡、窦前卵泡、窦状卵泡、排卵前卵泡及黄体数量明显减少(P<0.05,P<0.01),闭锁卵泡数量显著增多(P<0.01);A、B、C、D模型组TUNEL荧光染色凋亡面积明显增加(P<0.05,P<0.01);B、C、D 模型组 CD34、VEGFA、EPO 阳性表达明显下降(P<0.05,P<0.01);A、B 模型组 HIF-1α、SDF-1、CXCR4的mRNA表达量明显升高(P<0.05,P<0.01).与B模型组相比,C、D模型组相关指标发生明显变化,提示C、D模型较严重,趋向POF发展.结论 B模型组是卵巢功能从受损状态POI发展到不可逆卵巢早衰(POF)的转折点,提示雷公藤多苷给药3 d是诱导POI疾病模型及药物有效干预的最佳时间.

Objective Changes in relevant indexes in the mouse model of early-onset ovarian insufficiency caused by Tripterygium wilfordii polyglycoside were analyzed,and the optimal time point for intervention was determined.Methods Forty female ICR mice were randomly divided into control and A,B,C,and D model groups with eight mice in each group.The control group was gavaged with purified water for 14 days(0.01 mL/10 g),and the remaining groups were administered a Tripterygium wilfordii polyglycoside suspension(80 mg/kg,0.01 mL/10 g)for 1 day(A model group),3 days(B model group),7 days(C model group),or 14 days(D model group),and samples were collected.Body weight and wet weights of the uterus and bilateral ovaries of mice were determined in each group.Serum FSH,LH,E2,P,AMH,INH-B,and T contents were measured using enzyme-linked immunoassays.HE staining was used to observe the number and developmental status of follicles and corpus luteum at all levels in mice of each group.TUNEL staining was used to detect the apoptosis in the ovaries of mice in each group.IHC detected expression of VEGFA,CD34,and EPO proteins in the ovaries of mice in each group.mRNA expression of HIF-1α,SDF-1,and CXCR4 in each group of mice was detected by PCR.Results Compared with the control group,changes in indicators in model A mice did not meet the POI modeling standard.The ovarian index,uterine index,and body weight of mice in the B model group were decreased significantly(P<0.01),the weight of the C model group was decreased significantly(P<0.01),and the ovarian index of the D model group was decreased significantly(P<0.05).Serum contents of FSH and LH in B,C,and D model groups were increased(P<0.05,P<0.01),the E2,PROG,AMH,INH-B,and T contents were decreased(P<0.01).The numbers of basal follicles,pre-sinus follicles,sinusoidal follicles,antral follicles,preovulatory follicles,and corpus luteum were decreased significantly(P<0.05,P<0.01)and the number of atresia follicles was increased significantly(P<0.01)in B,C,and D model groups.The apoptotic area of TUNEL staining in A,B,C,and D model groups was increased significantly(P<0.05,P<0.01).Expression of CD34,VEGFA,and EPO in B,C,and D model groups was decreased significantly(P<0.05,P<0.01).mRNA expression of HIF-1α,SDF-1,and CXCR4 in A and B model groups was significantly increased(P<0.05,P<0.01).Compared with the B model group,the relevant indexes of C and D model groups were changed significantly,indicating that C and D models were more serious and tended to develop POF.Conclusions The B model group is the turning point of ovarian function from impaired POI to irreversible POF,suggesting that 3 days of administrating Tripterygium wilfordii polyglycoside is optimal to induce a POI disease model for effective drug intervention.

马林纳;马堃;范晓迪;罗洁;高山凤;李佳妮;张涵

天津中医药大学,天津 301617中国中医科学院西苑医院,北京 100091中国中医科学院西苑医院基础医学研究所,北京 100091

早发性卵巢功能不全雷公藤多苷颗粒细胞血管新生病理性缺氧

premature ovarian insufficiencyTripterygium wilfordii polyglycosidegranule cellsangiogenesispathological hypoxia

《中国比较医学杂志》 2024 (002)

35-44,153 / 11

中国中医科学院科技创新工程项目(CI2021A02406);北京市自然科学基金(7212193);北京市科技计划(Z171100001017104).

10.3969/j.issn.1671-7856.2024.02.005

评论