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2-烟酰胺基乙基硝酸盐对豚鼠和猪肠系膜动脉平滑肌细胞及肾上腺素能传递的影响。

Effects of 2-nicotinamidoethyl nitrate on smooth muscle cells and on adrenergic transmission in the guinea-pig and porcine mesenteric arteries.

作者信息

Itoh T, Furukawa K, Kajiwara M, Kitamura K, Suzuki H, Ito Y, Kuriyama H

出版信息

J Pharmacol Exp Ther. 1981 Jul;218(1):260-70.

PMID:6264070
Abstract

Muscle membranes of the porcine but not guinea-pig mesenteric artery wee hyperpolarized by applications of over 10(-6) M 2-nicotinamidoethyl nitrate (SG 75; 2-NN) dose-dependently from -53 to -72 mV, due to an increase in the ionic conductance of the membrane. In the porcine mesenteric artery but not guinea-pig, 2-NN suppressed the K-induced contraction in concentrations below 20 mM [K]0. The suppression of the K-induced contraction depended on the degree of hyperpolarization and the level of the resting membrane potential. The norepinephrine-induced contraction was suppressed by 2-NN with hyperpolarization of the membrane in the porcine mesenteric artery, but with no change in the membrane potential in the guinea-pig mesenteric artery, presumably due to suppression of the Ca-mobilization in the cell. The excitatory junction potential (ejp) could be recorded by perivascular nerve stimulation in both mesenteric arteries. Whether or not the membrane was hyperpolarized, 2-NN increased the amplitude of ejp in both tissues and increased the appearances of miniature ejp in the guinea-pig mesenteric artery. Nitroglycerin did not modify the membrane potential, the amplitude of ejp, electrical threshold and spike superimposed on the ejp, while sodium nitroprusside suppressed the amplitude of ejp, the facilitation process produced by repetitive stimulation and the spike superimposed on the ejp. Specific features of 2-NN actions on the muscle cell and adrenergic transmission of the mesenteric arteries in both species were discussed in relation to vasodilating actions, species differences and also in relation to other nitrite compounds.

摘要

超过10⁻⁶ M的2-烟酰胺基乙基硝酸盐(SG 75;2-NN)作用于猪肠系膜动脉而非豚鼠肠系膜动脉的肌膜时,可使其超极化,超极化幅度从-53 mV剂量依赖性地增加到-72 mV,这是由于膜离子电导增加所致。在猪肠系膜动脉而非豚鼠肠系膜动脉中,2-NN在低于20 mM [K]₀的浓度下可抑制钾诱导的收缩。钾诱导收缩的抑制取决于超极化程度和静息膜电位水平。在猪肠系膜动脉中,2-NN可抑制去甲肾上腺素诱导的收缩并使膜超极化,但在豚鼠肠系膜动脉中,2-NN抑制去甲肾上腺素诱导的收缩时膜电位无变化,推测这是由于其抑制了细胞内钙的动员。在两种肠系膜动脉中,通过血管周围神经刺激均可记录到兴奋性接头电位(ejp)。无论膜是否超极化,2-NN均可增加两种组织中ejp的幅度,并增加豚鼠肠系膜动脉中微小ejp的出现频率。硝酸甘油不改变膜电位、ejp幅度、电阈值以及叠加在ejp上的锋电位,而硝普钠则抑制ejp幅度、重复刺激产生的易化过程以及叠加在ejp上的锋电位。本文结合血管舒张作用、种属差异以及与其他亚硝酸盐化合物的关系,讨论了2-NN对两种动物肠系膜动脉肌细胞和肾上腺素能传递的特异性作用。

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