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

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.

Administration, Oral↗

The urinary excretion of 5-hydroxyndoleacetic acid in patients with menopausal flushing.

The 24-hour urinary excretion of 5-hydroxyindoleacetic acid in women with post-menopausal flushing attacks was compared with that of a control group of post-menopausal women without flushing attacks. The results were normal in the women with post-menopausal flushing, and it is concluded that 5-hydroxytryptamine is not a factor in the pathogenesis of post-menopausal flushing.

Female↗

Karzinoid.

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Carcinoid Tumor↗