Dendritic spine formation in response to progesterone synthesized de novo in the developing Purkinje cell in rats

被引:69
作者
Sakamoto, H
Ukena, K
Tsutsui, K [1 ]
机构
[1] Hiroshima Univ, Fac Integrated Arts & Sci, Lab Brain Sci, Higashihiroshima 7398521, Japan
[2] Japan Sci & Technol Corp, CREST, Tokyo 1500002, Japan
基金
日本学术振兴会;
关键词
neurosteroids; progesterone; 3; alpha; 5; alpha-tetrahydroprogesterone; dendritic spine formation; Purkinje cell; cerebellar development;
D O I
10.1016/S0304-3940(02)00077-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The cerebellar Purkinje cell (PC) is a typical site for neurosteroid formation. We have demonstrated that this neuron possesses intranuclear receptor for progesterone and actively synthesizes progesterone de novo from cholesterol only during rat neonatal life, when the formation of the cerebellar cortex occurs dramatically. In this study, we therefore analyzed the effect of progesterone on dendritic spine formation of the PC. In vitro studies using cerebellar slice cultures from newborn rats showed that progesterone increases the density of PC dendritic spines in a dose-dependent manner. This effect was blocked by the progesterone receptor antagonist, RU486. Furthermore, trilostane, a specific inhibitor of progesterone synthesis, inhibited the increase of spine density. These results suggest that progesterone can promote dendritic spine formation, and endogenous progesterone synthesized de novo in the developing PC may induce such an effect. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:111 / 115
页数:5
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