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Cholinergic activity regulates muscarinic receptors in central nervous system cultures.

机译:胆碱能活性调节中枢神经系统培养物中的毒蕈碱受体。

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摘要

Muscarinic acetylcholine receptor activation induces a loss of muscarinic receptors from cultured neuroblastoma and embryonic chicken cerebrum cells. As measured by specific binding of [3H]quinuclidinyl benzilate, steady-state receptor concentrations decrease 75% in response to receptor-saturating concentrations of cholinomimetic drugs. Both the degree and duration of activation determine the extent of receptor loss. A method for analyzing receptor turnover, which does not rely upon protein synthesis inhibitors, shows that activated receptors have a half-life of 1.6 hr. The regulated rate of receptor disappearance begins as soon as activators are added, and the rate is maintained as long as activators are present. The receptor blocker atropine causes an increase in receptor levels in central nervous system cultures but has no effect on receptors in cultures of adrenergic neuroblastoma cells. Because spontaneous cholinergic activity is expected only in the central nervous system cultures, the increase likely reflects blockade of endogenous regulation. Cytochalasin B blocks receptor regulation, suggesting that regulation may be mediated by a process involving microfilaments.
机译:毒蕈碱型乙酰胆碱受体激活可诱导培养的神经母细胞瘤和胚胎鸡大脑细胞中毒蕈碱受体的损失。如通过[3 H]喹啉基苄基苯甲酸酯的特异性结合所测量的,响应于饱和受体的拟胆碱药物浓度,稳态受体浓度降低了75%。激活的程度和持续时间均决定受体损失的程度。一种不依赖蛋白质合成抑制剂的分析受体更新的方法表明,活化的受体的半衰期为1.6小时。加入激活剂后,受体消失的调节速率就开始了,只要存在激活剂,受体消失的速率就保持不变。受体阻滞剂阿托品引起中枢神经系统培养物中受体水平的增加,但对肾上腺能神经母细胞瘤细胞培养物中的受体没有影响。因为仅在中枢神经系统培养物中会预期自发胆碱能活性,所以这种增加可能反映了内源性调节的阻滞。细胞松弛素B阻断受体调节,提示调节可能是由涉及微丝的过程介导的。

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  • 作者

    Siman, R G; Klein, W L;

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  • 年度 1979
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  • 原文格式 PDF
  • 正文语种 en
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