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大鼠脊髓中毒蕈碱型乙酰胆碱受体的激动剂调节

Agonist regulation of muscarinic acetylcholine receptors in rat spinal cord.

作者信息

Taylor J E, Yaksh T L, Richelson E

出版信息

J Neurochem. 1982 Aug;39(2):521-4. doi: 10.1111/j.1471-4159.1982.tb03975.x.

Abstract

In vitro studies with cultured cells originating from nervous tissue have shown that chronic exposure to muscarinic agonists results in a loss of muscarinic receptors. To determine whether this type of regulation of muscarinic receptor number also occurs in vivo, we infused carbachol into the spinal cords of rats. A single carbachol injection into the lumbar spinal cord caused a significant increase in the nociceptive threshold. This effect of carbachol diminished to control levels after 12 h of repeated agonist injections every 4 h and was blocked by atropine. The desensitization to the antinociceptive effects of carbachol was associated with a loss of muscarinic receptors as determined by the binding of the muscarinic antagonist [3H]quinuclidinyl benzilate. After a 24-h exposure to carbachol given every 4h, there was about a 60% loss of binding sites. The loss of muscarinic receptors was also blocked by atropine and was reversible. These results represent direct evidence that a muscarinic agonist can regulate receptor number in the central nervous system and suggest that this loss of receptors is associated with a desensitization to the antinociceptive effects of carbachol injected into the spinal cord.

摘要

对源自神经组织的培养细胞进行的体外研究表明,长期暴露于毒蕈碱激动剂会导致毒蕈碱受体丧失。为了确定这种毒蕈碱受体数量的调节类型在体内是否也会发生,我们将卡巴胆碱注入大鼠脊髓。向腰段脊髓单次注射卡巴胆碱会导致伤害性感受阈值显著升高。在每4小时重复注射激动剂12小时后,卡巴胆碱的这种作用减弱至对照水平,并被阿托品阻断。对卡巴胆碱抗伤害感受作用的脱敏与毒蕈碱受体的丧失有关,这是通过毒蕈碱拮抗剂[3H]喹核醇基苯甲酸酯的结合来确定的。在每4小时给予卡巴胆碱24小时后,结合位点约有60%的丧失。毒蕈碱受体的丧失也被阿托品阻断且是可逆的。这些结果代表了毒蕈碱激动剂可调节中枢神经系统中受体数量的直接证据,并表明这种受体丧失与对注入脊髓的卡巴胆碱抗伤害感受作用的脱敏有关。

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