Synaptic plasticity in sex steroid-sensitive motoneurons.
Synaptic plasticity in sex steroid-sensitive motoneurons.
批准号:
01540621
负责人:
MATSUMOTO Akira
金额:
$1.28万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1989
资助国家:
日本
项目状态:
已结题
起止时间:
1989 至 1991
中文摘要
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英文摘要
Gap junctions are considered to play an important role in metabolic and electrical coupling between neurons. We studied androgenic influence on the expression of the mRNA for gap junction protein in the androgen-sensitive motoneurons in the spinal nucleus of the bulbocavernosus(SNB)by using in situ hybridization histochemistry. A complementary DNA specific for the mRNA for r liver gap junction protein(connexin 32, a gift from Dr. D. A. Goodenough, Harvard Medical Sch was applied to in situ hybridization.1. Cellular localization of gap junction mRNA was examined in the neonatal male rat brai Autoradiographic signals for connexin 32 mRNA were found to distribute in various regions of the brain such as parietal cortex, hippocampus, thalamus/striatum and hypothalamus. These signals were localized on neuronal cells. Immunohistochemical and ultrastructural observations of the hippocampus supported the presence of gap junctions in the examined region.2. Cellular localization of gap junction m … More RNA was examined in the lumbar spinal cords of adult male rats. Autoradiographic-signals for connexin 32 mRNA were found to be localized on the somata and proximal dendrites of motoneurons in the SNB, dorsolateral nucleus(DLN)and retrodorsolateral nucleus(RDLN).3. Adult male rats were castrated and implanted with Silastic tubes containing testosterone or nothing. Animals were sacrificed 4 weeks later. The removal of androgen by castration dramatically reduced the expression of gap junction mRNA in the androgen-sensitive SNB motoneurons, whereas this change was prevented by testosterone treatment. On the contrary, castration or testosterone treatment did not induce any changes in the expression level of gap junction mRNA in the androgen-insensitive RDLN motoneurons. These results suggest that androgen influences the expression of gap junction gene in the SNB motoneurons and may provide evidence for the molecular mechanisms of hormonally induced synaptic plasticity in the SNB motoneurons. Less
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松本 明: "ギャップ結合の可塑性" 生体の科学. 40. 635-639 (1989)
Akira Matsumoto:“间隙连接的可塑性”生物科学。40。635-639(1989)
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通讯作者:
Matsumoto, A., Arai, Y., Urano, A. and Hyodo, S.: "Androgen regulates gap junction mRNA expression in androgensensitive motoneurons in the rat spinal cord." Neurosci. lett.131. 159-162 (1991)
Matsumoto, A.、Arai, Y.、Urano, A. 和 Hyodo, S.:“雄激素调节大鼠脊髓中雄激素敏感运动神经元的间隙连接 mRNA 表达。”
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通讯作者:
Matsumoto,A.et al.: "Androgen regulates gap junction mRNA expression in androgenーsensitive motoneurons in the rat spinal cord." Neurosci.Lett.131. 159-162 (1991)
Matsumoto, A. 等人:“雄激素调节大鼠脊髓中雄激素敏感运动神经元的间隙连接 mRNA 表达。Neurosci.Lett.131 (1991)。”
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Matsumoto, A., Arnold, A. P. and Micevych, P. E.: "Gap junctions between lateral spinal motoneurons in the rats." Brain Res.495. 362-366 (1989)
Matsumoto, A.、Arnold, A. P. 和 Micevych, P. E.:“大鼠外侧脊髓运动神经元之间的间隙连接。”
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通讯作者:
Matsumoto, A., Arai, Y., Urano, A. and Hyodo, S.: "Cellular localization of gap junction mRNA in the neonatal rat brain." Neurosci. Lett.124. 225-228 (1991)
Matsumoto, A.、Arai, Y.、Urano, A. 和 Hyodo, S.:“新生大鼠脑中间隙连接 mRNA 的细胞定位”。
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