Involvement of G-protein in the synaptic transmission at the lobster neuromuscular junction
G 蛋白参与龙虾神经肌肉接头的突触传递
基本信息
- 批准号:63570075
- 负责人:
- 金额:$ 1.22万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for General Scientific Research (C)
- 财政年份:1988
- 资助国家:日本
- 起止时间:1988 至 1989
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The role of GTP binding protein in the presynaptic membrane was investigated by use of intra-axonal recording near the nerve terminal of lobster neuromuscular synapse. L-glutamate activated the presynaptic glutamate receptor. (glutamate B receptor), inducing a hyperpolarizing current carried by K ion. This presynaptic glutamate potential was effectively blocked by pertussis toxin (IAP), indicating mediation by GTP-protein. Injection of GTPYS, a non-hydrolysable analog of GTP, hyperpolarized the presynaptic membrane and mimicked the presynaptic glutamte potential.The effect of GTP_<gamma>S injection on synaptic transmission was studied by recording the excitatory postsynaptic current (EPSC) with macro-patch recording. After injection GTP_<gamma>S in the presynaptic axon, the amplitude of the EPSC was gradually and irreversively diminished. Quantal analysis of EPSCs revealed that after GTP_<gamma>S injection quantal content was much reduced, whereas unit quantal size was unchanged.The results suggest that glutamate B receptor in the presynaptic membrane gives rise to a presynaptic inhibitory effect on transmitter release by activating GTP-binding protein.
在龙虾神经肌肉突触神经末梢附近的轴突内记录,研究了GTP结合蛋白在突触前膜中的作用。L-谷氨酸激活突触前谷氨酸受体。(谷氨酸B受体),诱导K离子携带的超极化电流。这种突触前谷氨酸电位可被百日咳毒素(IAP)有效阻断,提示GTP蛋白参与了这一过程。注射GTP的非水解性类似物GTPYS可使突触前膜超极化,模拟突触前谷氨酸电位。采用大片片记录兴奋性突触后电流的方法,研究了GTP_1、GT、GT、S对突触传递的影响。突触前轴突注射GTP_(lt;)γ>;S后,EPSC的波幅逐渐降低,且不可逆。突触前膜谷氨酸B受体通过激活GTP结合蛋白对递质释放产生突触前抑制作用。
项目成果
期刊论文数量(24)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
T.Toki,et al.: "Isolation and chemical charactrization of a series of new spider toxin(Nephilatoxins)in the venom of Joro spider,Nephila clavata" Biomedical Research. 9. 421-428 (1989)
T.Toki 等人:“Joro 蜘蛛 Nephila clavata 毒液中一系列新型蜘蛛毒素(Nephilatoxins)的分离和化学特性”生物医学研究。
- DOI:
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- 影响因子:0
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NOBUFUMI KAWAI, AKIKO MIWA, YUICHI HASHIMOTO, KOICHI SHUDO, TAIJI ASAMI and TERUMI NAKAJIMA: "Zinc ion enhances the blocking potency of synthetic analogs of spider toxin (JSTX) on the glutamate receptor" Neurosci. Res., vol.6, 358-362, 1989.
NOBUFUMI KAWAI、AKIKO MIWA、YUichi Hashimoto、KOICHI SHUDO、TAIJI ASAMI 和 TERUMI NAKAJIMA:“锌离子增强蜘蛛毒素 (JSTX) 合成类似物对谷氨酸受体的阻断效力” Neurosci。
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- 影响因子:0
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N.Kawai et al.: "Zinc ion enhances the blocking potency of synthetic analogs of spider toxin(JSTX)on the glutamate receptor." Neuroscience Research. 6. 358-362 (1989)
N.Kawai 等人:“锌离子增强了蜘蛛毒素 (JSTX) 合成类似物对谷氨酸受体的阻断效力。”
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- 影响因子:0
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M.Saito et al.: "Effects of a spider toxin(JSTX)on hippocampal CA1 neurons in vitro." Brain Research. 481. 16-24 (1989)
M.Saito 等人:“蜘蛛毒素 (JSTX) 对海马 CA1 神经元的体外影响。”
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- 影响因子:0
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T,Abe,et al.,: "Blocking of repetitive response form a neuromuscular preparation of tenebrio Molitor by phosphotriesters" Comp.Biochoem.Physiol.92C. 309-313 (1989)
T,Abe,et al.,:“通过磷酸三酯阻断黄粉虫神经肌肉制剂的重复反应”Comp.Biochoem.Physiol.92C。
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MIWA Akiko其他文献
MIWA Akiko的其他文献
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{{ truncateString('MIWA Akiko', 18)}}的其他基金
Prevention of medical errors by critical care nurses
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16H07381 - 财政年份:2016
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$ 1.22万 - 项目类别:
Grant-in-Aid for Research Activity Start-up
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