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首页> 外文期刊>Biomedical Research >BmK AS, an active scorpion polypeptide, enhances [H-3]noradrenaline release from rat hippocampal slices
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BmK AS, an active scorpion polypeptide, enhances [H-3]noradrenaline release from rat hippocampal slices

机译:活性蝎多肽BmK AS增强大鼠海马切片中[H-3]去甲肾上腺素的释放

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摘要

Slices of rat hippocampus were preincubated with [H-3]noradrenaline ([H-3]NA) and superfused with a medium containing desipramine (1 mM) to prevent the reuptake of NA. Addition of BmK AS (0.4 mM), a polypeptide activator of skeletal muscle ryanodine receptor isolated from Chinese scorpion Buthus martensi Karsch, to the superfusion medium significantly increased [H-3]NA release. The response curve showed a bell-shaped dose-response relationship (0.05-1 mM) with the maximal response at 0.4 mM. Further experiments showed that the increase of [H-3]NA release was dependent on the presence of extracellular Ca2+, and inhibited completely by tetrodotoxin (0.3 mM) and strongly by omega-conotoxin GVIA (0.1 mM). The results observed in this study suggest that BmK AS may induce noradrenaline release by increasing Naf influx.
机译:将大鼠海马切片与[H-3]去甲肾上腺素([H-3] NA)预孵育,并与含有地昔帕明(1 mM)的培养基超融合以防止NA的再摄取。将BmK AS(0.4 mM)(一种从中华蝎子Buthus martensi Karsch分离的骨骼肌ryanodine受体的多肽激活剂)添加到超融合培养基中会显着增加[H-3] NA的释放。响应曲线显示出钟形剂量-反应关系(0.05-1 mM),最大响应为0.4 mM。进一步的实验表明,[H-3] NA释放的增加取决于细胞外Ca2 +的存在,并被河豚毒素(0.3 mM)完全抑制,并被ω-芋螺毒素GVIA(0.1 mM)强烈抑制。在这项研究中观察到的结果表明,BmK AS可能通过增加Naf流入而诱导去甲肾上腺素释放。

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