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氰化物对兔离体主动脉制剂中硝血管扩张剂舒张反应的拮抗作用。

Antagonism of relaxing responses to nitrovasodilators by cyanide in rabbit isolated aortic preparation.

作者信息

Nakanishi H, Ariga H, Yamada Y, Ono T, Matsuoka I, Nakahata N

机构信息

Department of Pharmacology, Fukushima Medical College, Japan.

出版信息

Fukushima J Med Sci. 1995 Dec;41(2):125-34.

PMID:8823992
Abstract

Effect of sodium cyanide on the relaxing response (decrease of intraluminal pressure) to sodium nitroprusside, sodium nitrite, nitric oxide and human atrial natriuretic peptide (HANP) was investigated in isolated rabbit aortic preparations in vitro. Cyanide 1 microM approximately 1 mM produced relaxation in norepinephrine (NE) 1 microM-contracted aortic preparation in a concentration dependent manner. Cyanide 100 microM, which was administered approximately 8 min before NE addition, depressed the relaxing response to nitroprusside 0.1 microM in NE 1 microM-contracted aortic preparation. The relaxing responses to nitric oxide 0.3 and 3.3 microM were slightly, but concentration-dependently depressed by cyanide 1-100 microM, which was administered 6-10 min before nitric oxide addition, in NE 1 microM-contracted aortic preparations. Cyanide 100 microM and 1 mM, which was administered 4-10 min after nitroprusside 0.1 microM, reversed the nitroprusside-induced relaxation in NE 1 microM contracted aortic preparation. Namely, relaxing response of NE-contracted aortic preparation to cyanide was converted into contractile response in the presence of nitroprusside. Similar reversal phenomena of the responses to cyanide 100 microM and 1 mM were also observed in the presence of sodium nitrite 0.1 microM or nitric oxide 3.3 microM, but those were less extent than that of nitroprusside 0.1 microM. On the contrary, the relaxing response to cyanide 100 microM was unaffected by pretreatment with HANP 0.37 nM. These findings may indicate that cyanide inhibits soluble guanylate cyclase activated by nitroprusside, sodium nitrite or nitric oxide through interaction with nitric oxide and heme binding site of the enzyme.

摘要

在体外分离的兔主动脉制剂中,研究了氰化钠对硝普钠、亚硝酸钠、一氧化氮和人心房利钠肽(HANP)舒张反应(管腔内压力降低)的影响。1微摩尔至约1毫摩尔的氰化物以浓度依赖的方式使1微摩尔去甲肾上腺素(NE)收缩的主动脉制剂产生舒张。在添加NE前约8分钟给予100微摩尔氰化物,可抑制1微摩尔NE收缩的主动脉制剂对0.1微摩尔硝普钠的舒张反应。在添加一氧化氮前6至10分钟给予1至100微摩尔氰化物,可使1微摩尔NE收缩的主动脉制剂对0.3和3.3微摩尔一氧化氮的舒张反应略有降低,但呈浓度依赖性。在给予0.1微摩尔硝普钠后4至10分钟给予100微摩尔和1毫摩尔氰化物,可逆转1微摩尔NE收缩的主动脉制剂中硝普钠诱导的舒张。也就是说,在硝普钠存在的情况下,NE收缩的主动脉制剂对氰化物的舒张反应转变为收缩反应。在0.1微摩尔亚硝酸钠或3.3微摩尔一氧化氮存在的情况下,也观察到了对100微摩尔和1毫摩尔氰化物反应的类似逆转现象,但程度低于0.1微摩尔硝普钠。相反,0.37纳摩尔HANP预处理对100微摩尔氰化物的舒张反应没有影响。这些发现可能表明,氰化物通过与一氧化氮和该酶的血红素结合位点相互作用,抑制由硝普钠、亚硝酸钠或一氧化氮激活的可溶性鸟苷酸环化酶。

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