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儿茶酚胺对豚鼠胃电活动的α兴奋作用的证据。

Evidences for alpha excitatory action of catecholamines on the electrical activity of the guinea-pig stomach.

作者信息

Ohkawa H

出版信息

Jpn J Physiol. 1976;26(1):41-52. doi: 10.2170/jjphysiol.26.41.

Abstract

Effects of catecholamines and their inhibitors on the electrical activity of the smooth muscle of the guinea-pig stomach were studied by using pressure electrodes. The spontaneous electrical activity of antrum and corpus preparations consisted of slow waves with or without superimposed spikes. In quiescent fundus preparations, the spike activity and slow waves were generated by TEA. Catecholamines (noradrenaline, isoprenaline and adrenaline) suppressed or blocked the spike discharges and the generation of slow waves. However, the spike activity was enhanced at a higher concentration of phenylephrine in the antrumand fundus preparations. Inhibitory responses of the smooth muscles from whole regions to adrenaline, noradrenaline or isoprenaline were antagonized by propranolol or DCI but not by phentolamine or phenoxybenzamine. Therefore, inhibitory actions of these amines appear to involve beta-adrenoceptors. After treatment with tetrodotoxin, noradrenaline and isoprenaline blocked the spike activity and the generation of slow waves. Phenylephrine or adrenaline potentiated the spike activity in the presence of tetrodotoxin. After treatment with DCI or propranolol, phenylephrine potentiated the spike activity of the antrum and fundus preparations. These excitatory effects were antagonized by phentolamine or phenoxybenzamine. It is concluded that excitatory actions of these amines are mediated by alpha-adrenoceptors rather than via a nervous pathway.

摘要

采用压力电极研究了儿茶酚胺及其抑制剂对豚鼠胃平滑肌电活动的影响。胃窦和胃体标本的自发电活动由伴有或不伴有叠加锋电位的慢波组成。在静止的胃底标本中,TEA可产生锋电位活动和慢波。儿茶酚胺(去甲肾上腺素、异丙肾上腺素和肾上腺素)可抑制或阻断锋电位发放及慢波的产生。然而,在胃窦和胃底标本中,去氧肾上腺素浓度较高时锋电位活动增强。整个区域平滑肌对肾上腺素、去甲肾上腺素或异丙肾上腺素的抑制反应可被普萘洛尔或双氯异丙肾上腺素拮抗,但不能被酚妥拉明或酚苄明拮抗。因此,这些胺类的抑制作用似乎涉及β-肾上腺素能受体。用河豚毒素处理后,去甲肾上腺素和异丙肾上腺素可阻断锋电位活动及慢波的产生。在存在河豚毒素的情况下,去氧肾上腺素或肾上腺素可增强锋电位活动。用双氯异丙肾上腺素或普萘洛尔处理后,去氧肾上腺素可增强胃窦和胃底标本的锋电位活动。这些兴奋作用可被酚妥拉明或酚苄明拮抗。结论是这些胺类的兴奋作用是由α-肾上腺素能受体介导的,而不是通过神经途径。

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