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鱼精蛋白对培养的牛肾上腺髓质细胞儿茶酚胺分泌和离子内流的抑制作用。

Inhibition by protamine of catecholamine secretion and ion influxes in bovine adrenal medullary cells in culture.

作者信息

Minami K, Yanagihara N, Segawa K, Sata T, Tsutsui M, Shigematsu A, Izumi F

机构信息

Department of Anesthesiology, University of Occupational and Environmental Health, School of Medicine, Fukuoka, Japan.

出版信息

J Pharmacol Exp Ther. 1996 Nov;279(2):838-43.

PMID:8930191
Abstract

To elucidate the mechanism of protamine-induced hypotension, we examined the effects of protamine on catecholamine secretion in bovine adrenal medullary cells and on the serum norepinephrine in the rat. 1) in bovine adrenal medullary cells in culture, protamine at concentrations of 10 to 100 micrograms/ml inhibited catecholamine secretion stimulated by carbachol. The inhibitory effect of protamine was diminished by heparin at concentrations of 3.5 to 14 U/ml. Protamine suppressed carbachol-stimulated 22Na+ influx and 45Ca++2 influx at a concentration similar to that which inhibited catecholamine secretion. Protamine (10-100 micrograms/ml) also inhibited veratridine-induced 22Na+ influx and 45Ca++ influx and 56 mM K(+)-evoked 45Ca++ influx. The inhibition of these ion influxes by protamine was closely correlated with that of catecholamine secretion. 2) In rats, i.v. administration of protamine (10 mg/kg) attenuated the arterial blood pressure and the serum norepinephrine. There was a high correlation (r = 0.96) between the serum norepinephrine and the arterial blood pressure in protaminetreated rats. Furthermore, pretreatment with heparin (1000 U/kg) abolished the protamine-induced decreases in arterial blood pressure and serum norepinephrine. Because protamine seems to inhibit catecholamine secretion by interfering with Na+ influx and Ca++ influx to adrenal medullary cells, the protamine-induced hypotension may be, at least in part, due to inhibition of norepinephrine release and ion channel activities of sympathetic nerve terminals in rats.

摘要

为阐明鱼精蛋白诱导低血压的机制,我们研究了鱼精蛋白对牛肾上腺髓质细胞儿茶酚胺分泌及大鼠血清去甲肾上腺素的影响。1)在培养的牛肾上腺髓质细胞中,浓度为10至100微克/毫升的鱼精蛋白可抑制卡巴胆碱刺激的儿茶酚胺分泌。浓度为3.5至14单位/毫升的肝素可减弱鱼精蛋白的抑制作用。鱼精蛋白抑制卡巴胆碱刺激的22Na+内流和45Ca++2内流的浓度与抑制儿茶酚胺分泌的浓度相似。鱼精蛋白(10 - 100微克/毫升)还可抑制藜芦碱诱导的22Na+内流和45Ca++内流以及56毫摩尔/升钾诱发的45Ca++内流。鱼精蛋白对这些离子内流的抑制作用与儿茶酚胺分泌的抑制作用密切相关。2)在大鼠中,静脉注射鱼精蛋白(10毫克/千克)可使动脉血压和血清去甲肾上腺素降低。在接受鱼精蛋白治疗的大鼠中,血清去甲肾上腺素与动脉血压之间存在高度相关性(r = 0.96)。此外,预先注射肝素(1000单位/千克)可消除鱼精蛋白诱导的动脉血压和血清去甲肾上腺素降低。由于鱼精蛋白似乎通过干扰肾上腺髓质细胞的Na+内流和Ca++内流来抑制儿茶酚胺分泌,鱼精蛋白诱导的低血压可能至少部分是由于抑制了大鼠交感神经末梢的去甲肾上腺素释放和离子通道活性。

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