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Mechanisms and roles of muscarinic activation in guinea-pig adrenal medullary cells

机译:毒蕈碱激活在豚鼠肾上腺髓质细胞中的机制和作用

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摘要

Muscarinic receptors are expressed in the adrenal medullary (AM) cells of various mammals, but their physiological roles are controversial. Therefore, the ionic mechanism for muscarinic receptor-mediated depolarization and the role of muscarinic receptors in neuronal transmission were investigated in dissociated guinea-pig AM cells and in the perfused guinea-pig adrenal gland. Bath application of muscarine induced an inward current at -60 mV. This inward current was partially suppressed by quinine with an IC 50 of 6.1 μM. The quinineinsensitive component of muscarine-induced currents changed the polarity at -78 mV and was inhibited by bupivacaine, a TWIKrelated acid-sensitive K + (TASK) channel inhibitor. Conversely, the current-voltage relationship for the bupivacaine-insensitive component of muscarine currents showed a reversal potential of -5 mV and a negative slope below -40 mV. External application of La 3+ had a double action on muscarine currents of both enhancement and suppression. Immunoblotting and immunocytochemistry revealed expression of TASK1 channels and cononical transient receptor potential channels 1, 4, 5, and 7 in guinea-pig AM cells. Retrograde application of atropine reversibly suppressed transsynaptically evoked catecholamine secretion from the adrenal gland. The results indicate that muscarinic receptor stimulation in guinea-pig AM cells induces depolarization through inhibition of TASK channels and activation of nonselective cation channels and that muscarinic receptors are involved in neuronal transmission from the splanchnic nerve.
机译:毒蕈碱受体在各种哺乳动物的肾上腺髓质(AM)细胞中表达,但它们的生理作用是有争议的。因此,在解离的豚鼠AM细胞和灌注的豚鼠肾上腺中研究了毒蕈碱受体介导的去极化的离子机制和毒蕈碱受体在神经元传递中的作用。在浴液中施用毒蕈碱会在-60 mV感应到内向电流。奎宁部分抑制了该流入电流,IC 50为6.1μM。毒蕈碱感应电流的奎宁不敏感成分在-78 mV时改变了极性,并被TWIK相关的酸敏感K +(TASK)通道抑制剂布比卡因抑制。相反,毒蕈碱电流中对布比卡因不敏感的成分的电流-电压关系显示出-5 mV的反向电位和低于-40 mV的负斜率。 La 3+的外用对毒蕈碱电流的增强和抑制都有双重作用。免疫印迹和免疫细胞化学揭示了豚鼠AM细胞中TASK1通道和圆锥形瞬时受体电位通道1、4、5和7的表达。逆行应用阿托品可逆地抑制肾上腺经突触诱发的儿茶酚胺分泌。结果表明,豚鼠AM细胞中的毒蕈碱受体刺激通过抑制TASK通道和激活非选择性阳离子通道诱导去极化,并且毒蕈碱受体参与了从内脏神经的神经元传递。

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