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肝肠是否会显著降解人体内循环的内源性P物质?

Does liver-intestine significantly degrade circulating endogenous substance P in man?

作者信息

Henriksen J H, Schaffalitzky de Muckadell O B, Bülow J B

出版信息

Scand J Gastroenterol. 1986 Apr;21(3):300-4. doi: 10.3109/00365528609003079.

Abstract

Elevated concentrations of circulating substance P in patients with liver insufficiency have been ascribed to decreased hepatic degradation. To establish a possible biodegradation of the peptide in liver-intestine and kidneys, the concentration of endogenous immunoreactive substance P was determined in various vascular beds during a right-sided catheterization in 13 subjects without liver insufficiency. All subjects had normal values of circulating substance P, and no significant difference was found between systemic plasma and hepatic venous or renal venous concentrations of substance P. The results indicate that degradation of circulating endogenous substance P in man is not confined to liver-intestine or kidney but may take place in many tissues.

摘要

肝功能不全患者循环中P物质浓度升高被归因于肝脏降解减少。为了确定该肽在肝肠和肾脏中的可能生物降解情况,在13名无肝功能不全的受试者右侧插管期间,测定了不同血管床中内源性免疫反应性P物质的浓度。所有受试者循环中P物质的值均正常,全身血浆与肝静脉或肾静脉中P物质的浓度之间未发现显著差异。结果表明,人体内循环内源性P物质的降解不仅限于肝肠或肾脏,还可能发生在许多组织中。

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