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去势及给予睾酮后大鼠肝脏环(组氨酸-脯氨酸)结合位点的变化。

Changes in rat liver cyclo(His-Pro) binding sites upon castration and testosterone administration.

作者信息

Sora Y H, Ogawa N, Mori A

出版信息

Regul Pept. 1987 Jul;18(1):1-5. doi: 10.1016/0167-0115(87)90044-9.

Abstract

Histidyl-proline diketopiperazine [cyclo(His-Pro)] binding was compared in livers from male and female rats. Cyclo(His-Pro) binding of female rat liver was very much lower than that of male rat liver. Scatchard analysis showed that the sex difference in cyclo(His-Pro) binding was due to different binding capacity. Cyclo(His-Pro) binding of castrated male rat liver was significantly decreased. Testosterone replacement raised the binding to the control level, and an excess of testosterone increased the specific binding beyond the control level. The testosterone-induced changes in cyclo(His-Pro) binding were also due to variation in the binding capacity. These findings indicate that testosterone is an important factor in the regulation of cyclo(His-Pro) binding in the rat liver.

摘要

对雄性和雌性大鼠肝脏中的组氨酰-脯氨酸二酮哌嗪[环(His-Pro)]结合情况进行了比较。雌性大鼠肝脏的环(His-Pro)结合量远低于雄性大鼠肝脏。Scatchard分析表明,环(His-Pro)结合的性别差异是由于结合能力不同所致。去势雄性大鼠肝脏的环(His-Pro)结合显著降低。睾酮替代使结合量提高到对照水平,而过量的睾酮则使特异性结合超过对照水平。睾酮诱导的环(His-Pro)结合变化也是由于结合能力的改变。这些发现表明,睾酮是调节大鼠肝脏中环(His-Pro)结合的一个重要因素。

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