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补肾方对自然衰老大鼠睾酮调节作用及机制研究
引用本文:Jin HQ,Jiang F,Deng DM,Chen WX,Yang GZ,Zhuang TQ. 补肾方对自然衰老大鼠睾酮调节作用及机制研究[J]. 中华男科学杂志, 2011, 17(8): 758-762
作者姓名:Jin HQ  Jiang F  Deng DM  Chen WX  Yang GZ  Zhuang TQ
作者单位:1. 苏州市相城区中医院男科,江苏,苏州,215155
2. 上海中医药大学研究生院,上海,201203
3. 苏州市中医院男科,江苏,苏州,215003
摘    要:目的:探讨补肾方对自然衰老大鼠睾酮调节作用及机制,为临床治疗迟发性睾丸功能减退提供理论和实验依据。方法:将32只18月龄老年雄性SD大鼠随机分为4组,自然衰老模型组,补肾方低、中、高剂量组,每组8只;另选4月龄青年雄性SD大鼠8只作为正常对照。正常对照组、自然衰老模型组予生理盐水,补肾方低剂量、中剂量、高剂量组分别按生药量3.25、7.5、15.0 g/kg体重予中药复方连续灌胃,各组给药3周后处死。采用苏木精-伊红(HE)染色观察大鼠睾丸组织形态,放免法检测大鼠血清睾酮水平,RT-PCR法检测大鼠类固醇合成急性调节蛋白(StAR)、细胞色素胆固醇侧链裂解酶(P450 scc)、3β-羟类固醇脱氢酶Ⅰ(3β-HSDⅠ)mRNA的相对表达。结果:睾丸组织病理切片显示补肾方干预后大鼠睾丸间质细胞数目增多,补肾方低、中、高剂量组血清睾酮水平[(6.74±1.56)、(8.50±1.99)、(12.41±2.91)nmol/L]与自然衰老模型组[(3.48±0.75)nmol/L]比较显著提高(P<0.05),睾酮合成相关酶StAR、P450 scc、3β-HSDⅠmRNA相对表达(StAR:0.74±0.29、0.83±0.32、1.35±0.50;P450 scc:0.72±0.36、1.02±0.30、1.41±0.37;3β-HSDⅠ:0.58±0.14、0.72±0.07、0.85±0.18)与自然衰老模型组(StAR:0.44±0.09;P450 scc:0.33±0.05;3β-HSDⅠ:0.34±0.02)比较均提高,其中高剂量组StAR,中、高剂量组P450 scc、3β-HSDⅠ的表达与自然衰老模型组比较差异有显著性(P<0.05)。结论:改善睾丸组织衰老的病理状态,提高睾酮合成酶表达可能是补肾方调节自然衰老大鼠睾酮水平的作用机制。

关 键 词:迟发性睾丸功能减退  睾酮  睾酮合成酶  补肾方  大鼠

Regulatory effect of Bushenfang on the serum testosterone level of naturally aging rats and its mechanism
Jin Hui-Qing,Jiang Fei,Deng Dong-Mei,Chen Wei-Xiang,Yang Guang-Zhao,Zhuang Tian-Qu. Regulatory effect of Bushenfang on the serum testosterone level of naturally aging rats and its mechanism[J]. National journal of andrology, 2011, 17(8): 758-762
Authors:Jin Hui-Qing  Jiang Fei  Deng Dong-Mei  Chen Wei-Xiang  Yang Guang-Zhao  Zhuang Tian-Qu
Affiliation:JIN Hui-qing1,JIANG Fei1,DENG Dong-mei2,CHEN Wei-xiang2,YANG Guang-zhao3,ZHUANG Tian-qu31.Department of Andrology,Xiangcheng Hospital of Traditional Chinese Medicine,Suzhou,Jiangsu 215155,China,2.Graduate School,Shanghai University of Traditional Chinese Medicine,Shanghai 201203,3.Department of Andrology,Suzhou Hospital of Traditional Chinese Medicine,Jiangsu 215003
Abstract:Objective: To study the regulatory effect of Bushenfang on the serum testosterone(T) level of naturally aging rats and its mechanism,in order to provide a theoretical and experimental basis for the clinical treatment of late onset hypogonadism(LOH) in males.Methods: Thirty-two 18-month-old male SD rats were randomly divided into four groups of equal number,naturally aging model and low-,medium-and high-dose Bushenfang groups,and another eight 4-month-old rats were taken as normal controls.The rats of the ag...
Keywords:late onset hypogonadism in males  testosterone  synthetase  Bushenfang  rat  
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