Wu Xue-qing, Li Xiao-feng, Ye Bi-lü
Department of Obstetrics and Gynecology, First Affiliated Hospital of Wenzhou Medical College, China.
Zhonghua Fu Chan Ke Za Zhi. 2011 Jun;46(6):441-5.
To investigate the long-term programming effects on pubertal reproductive function by immunological challenge in early life.
Female Sprague-Dawley rats were administered by endotoxin (lipopolysaccharide, LPS) at a dosage of 50 µg/kg and saline intraperitoneally on postnatal day 3 and 5. Body weight was measured weekly. Puberty onset (vaginal opening) and oestrous cyclicity were monitored from postnatal day 30. At the age of 6 weeks, bilateral ovariectomy was performed. The histological and morphological change of the ovaries (the thickness of the theca interna and the number of different kinds of follicles) were observed and the immunoreactivity of the ovarian sympathetic nerve markers (low affinity receptor of nerve growth factor, p75NGFR) was evaluated by immune staining.
Immunological challenge (exposed to LPS) in early life delayed vaginal opening significantly [LPS-treated (40.6 ± 0.7) days versus controls (38.6 ± 0.5) days, P < 0.05], decreased the percentage of normal oestrous cyclicity (LPS-treated 26.1% versus controls 66.8%, P < 0.05), decreased the total number of different types of follicles (primordial follicles: LPS-treated 610 ± 47 versus controls 1181 ± 57, P < 0.05; primary follicles: LPS-treated 624 ± 41 versus controls 960 ± 30, P < 0.05; preantral follicles: LPS-treated 183 ± 16 versus controls 260 ± 14, P < 0.05; antral follicles: LPS-treated 32 ± 4 versus controls 79 ± 7, P < 0.05) and increased the thickness of the theca interna [LPS-treated (15.8 ± 0.4) µm versus controls (11.4 ± 0.3) µm, P < 0.05]. The immunostaining of p75NGFR was obviously enhanced in the LPS-treated ovaries when compared with that of controls (P < 0.05).
Immunological stress during early critical developmental windows could have long dysfunctional effects on the pubertal reproductive function. It delayed puberty onset, reduced the percentage of the normal oestrous cycles, decreased follicles reserve and increased the thickness of the theca interna which might involve the up-regulation of the local ovarian sympathetic nerve activity.
研究生命早期免疫应激对青春期生殖功能的长期程序化影响。
出生后第3天和第5天,给雌性斯普拉格-道利大鼠腹腔注射剂量为50μg/kg的内毒素(脂多糖,LPS)和生理盐水。每周测量体重。从出生后第30天开始监测青春期启动(阴道开口)和发情周期。6周龄时,进行双侧卵巢切除术。观察卵巢的组织学和形态学变化(内膜厚度和不同类型卵泡的数量),并通过免疫染色评估卵巢交感神经标志物(神经生长因子低亲和力受体,p75NGFR)的免疫反应性。
生命早期的免疫应激(暴露于LPS)显著延迟了阴道开口[LPS处理组(40.6±0.7)天,对照组(38.6±0.5)天,P<0.05],降低了正常发情周期的百分比(LPS处理组26.1%,对照组66.8%,P<0.05),减少了不同类型卵泡的总数(原始卵泡:LPS处理组610±47,对照组1181±57,P<0.05;初级卵泡:LPS处理组624±41,对照组960±30,P<0.05;窦前卵泡:LPS处理组183±16,对照组260±14,P<0.05;窦卵泡:LPS处理组32±4,对照组79±7,P<0.05),并增加了内膜厚度[LPS处理组(15.8±0.4)μm,对照组(11.4±0.3)μm,P<0.05]。与对照组相比,LPS处理组卵巢中p75NGFR的免疫染色明显增强(P<0.05)。
关键发育早期的免疫应激可能对青春期生殖功能产生长期的功能障碍影响。它延迟了青春期启动,降低了正常发情周期的百分比,减少了卵泡储备,并增加了内膜厚度,这可能涉及局部卵巢交感神经活动的上调。