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L-色氨酸对大鼠利尿及5-羟吲哚乙酸排泄的影响。

Effect of L-tryptophan on diuresis and 5-hydroxyindoleacetic acid excretion in the rat.

作者信息

BERTACCINI G, NOBILI M B

出版信息

Br J Pharmacol Chemother. 1961 Dec;17(3):519-25. doi: 10.1111/j.1476-5381.1961.tb01138.x.

Abstract

Oral administration of L-tryptophan to rats produced two main biochemical and pharmacological effects: a marked increase in urinary 5-hydroxyindoleacetic acid excretion, and a significant reduction in the urine flow after a water load. Urinary 5-hydroxyindoleacetic acid excretion reached its maximum 2 to 6 hr after the administration of tryptophan, and it increased with the dose of the amino acid. Antidiuresis was seen after the administration of L-tryptophan, 200 mg/kg, or more. The effect appeared promptly and it was roughly proportional to the dose of the amino acid administered. Both antidiuretic effect and increase in urinary 5-hydroxyindoleacetic acid excretion were more intense after oral than after parenteral administration of L-tryptophan. D-Tryptophan, in oral doses up to 1,000 mg/kg, produced neither an increase in urinary 5-hydroxyindoleacetic acid nor a reduction of diuresis. Available evidence suggests that reduction of urine flow is a consequence of biosynthesis and release of 5-hydroxytryptamine by the gastrointestinal mucosa. Tryptamine produced by direct decarboxylation of L-tryptophan does not seem to play any important role.

摘要

给大鼠口服L-色氨酸产生了两种主要的生化和药理作用:尿中5-羟吲哚乙酸排泄量显著增加,以及水负荷后尿流量显著减少。色氨酸给药后2至6小时,尿中5-羟吲哚乙酸排泄量达到最大值,且随氨基酸剂量增加而增加。给予200mg/kg或更高剂量的L-色氨酸后出现抗利尿作用。该作用迅速出现,且大致与所给予氨基酸的剂量成正比。口服L-色氨酸后的抗利尿作用和尿中5-羟吲哚乙酸排泄量的增加比胃肠外给药后更强烈。口服剂量高达1000mg/kg的D-色氨酸既不会使尿中5-羟吲哚乙酸增加,也不会使利尿减少。现有证据表明,尿流量减少是胃肠道黏膜生物合成和释放5-羟色胺的结果。由L-色氨酸直接脱羧产生的色胺似乎未发挥任何重要作用。

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