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大补阴丸对雌性大鼠真性性早熟治疗作用的实验研究

[Experimental study on therapeutic effect of Dabuyin Wan on true precocious puberty in female rats].

作者信息

Cheng Min, Ye Xiao-Di, Miao Yun-Ping, Chen Ai-Ying, Zheng Gao-Li

机构信息

Institute of Materia Medica, Zhejiang Academy of Medical Sciences, Hangzhou 310013, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2013 Feb;38(3):386-90.

Abstract

OBJECTIVE

To study the therapeutic effect of Dabuyin Wan on true precocious puberty of female rats and its possible mechanism.

METHOD

Twenty-two-day-old female SD rats were subcutaneously injected with 40 mg x kg(-1) N-methyl-DL-aspartic acid (NMA) at 14:00 and 16:00 every day; meanwhile, the rats were given Dabuyin Wan for intervention. Visual inspection was conducted for the time of vaginal opening. The first estrus was observed by yaginal smear test. Their ovaries and uterus were weighed to calculate organ coefficients. Conventional pathological slices were made to observe morphological changes in ovaries and uterus and calculate the thickness of uterine walls and the number of corpus luteums. The level of E2 in serum was detected to assess the therapeutic effect of Dabuyin Wan on NMA precocious puberty in rats. expressions of GnRH, GPR54 and Kiss-1 mRNA in hypothalamus were measured by semi-quantitative RT-PCR to investigate the possible mechanism of Dabuyin Wan.

RESULT

Dabuyin Wan at 3.24 g x kg(-1) and 1.62 g x kg(-1) significantly decreased the organ coefficients in rats with precocious puberty (P < 0.05), decrease the number of vaginal openings in rats (P < 0.01) and the thickness of uterine walls and the number of corpus luteums (P < 0.05), and notably down-regulated expressions of GnRH, GPR54 and Kiss-1 mRNA in hypothalamus (P < 0.05), without significant impact on E2 in serum.

CONCLUSION

Dabuyin Wan may inhibit GnRH synthesis and release as well as startup of hypothalamic-pituitary-gonadal axis by down-regulating Kiss-1/GPR54 mRNA expression in hypothalamus, in order to realize the therapeutic effect on true precocious puberty.

摘要

目的

研究大补阴丸对雌性大鼠真性性早熟的治疗作用及其可能机制。

方法

22日龄雌性SD大鼠每天14:00和16:00皮下注射40mg·kg⁻¹N-甲基-DL-天冬氨酸(NMA);同时给予大鼠大补阴丸进行干预。肉眼观察阴道开口时间。通过阴道涂片检查观察首次发情情况。称量其卵巢和子宫重量以计算脏器系数。制作常规病理切片观察卵巢和子宫的形态变化,并计算子宫壁厚度和黄体数量。检测血清中E2水平以评估大补阴丸对大鼠NMA性早熟的治疗效果。采用半定量RT-PCR法检测下丘脑GnRH、GPR54和Kiss-1mRNA的表达,以探讨大补阴丸的可能作用机制。

结果

3.24g·kg⁻¹和1.62g·kg⁻¹大补阴丸可显著降低性早熟大鼠的脏器系数(P<0.05),减少大鼠阴道开口数量(P<0.01)以及子宫壁厚度和黄体数量(P<0.05),并显著下调下丘脑GnRH、GPR54和Kiss-1mRNA的表达(P<0.05),对血清E2无明显影响。

结论

大补阴丸可能通过下调下丘脑Kiss-1/GPR54mRNA表达,抑制GnRH合成与释放以及下丘脑-垂体-性腺轴的启动,从而实现对真性性早熟的治疗作用。

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