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毒蕈碱激活在豚鼠肾上腺髓质细胞中的机制和作用。

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

机构信息

Dept. of Cell and Systems Physiology, Univ. of Occupational and Environmental Health School of Medicine, Kitakyushu, Japan.

出版信息

Am J Physiol Cell Physiol. 2012 Sep 15;303(6):C635-44. doi: 10.1152/ajpcell.00147.2012. Epub 2012 Jun 27.

Abstract

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 quinine-insensitive component of muscarine-induced currents changed the polarity at -78 mV and was inhibited by bupivacaine, a TWIK-related 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.

摘要

毒蕈碱受体存在于各种哺乳动物的肾上腺髓质 (AM) 细胞中,但它们的生理作用仍存在争议。因此,本研究在分离的豚鼠 AM 细胞和灌流的豚鼠肾上腺中,研究了毒蕈碱受体介导的去极化的离子机制以及毒蕈碱受体在神经元传递中的作用。在 -60 mV 时,毒蕈碱灌流可诱导内向电流。该内向电流可被奎宁部分抑制,IC50 为 6.1 μM。毒蕈碱诱导电流的奎宁不敏感成分在 -78 mV 时改变极性,并被布比卡因抑制,布比卡因是 TWIK 相关酸敏感钾 (TASK) 通道抑制剂。相反,布比卡因不敏感成分的电流-电压关系显示反转电位为 -5 mV,低于 -40 mV 时斜率为负。La(3+) 对毒蕈碱电流既有增强作用又有抑制作用。免疫印迹和免疫细胞化学显示豚鼠 AM 细胞表达 TASK1 通道和经典瞬时受体电位通道 1、4、5 和 7。阿托品逆行给药可可逆地抑制从肾上腺传出的神经递质去甲肾上腺素的分泌。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来自内脏神经的神经元传递。

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Mechanisms and roles of muscarinic activation in guinea-pig adrenal medullary cells.毒蕈碱激活在豚鼠肾上腺髓质细胞中的机制和作用。
Am J Physiol Cell Physiol. 2012 Sep 15;303(6):C635-44. doi: 10.1152/ajpcell.00147.2012. Epub 2012 Jun 27.

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