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(Reference retrieved automatically from Google Scholar through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Chronic oral administration of arginine induces GH gene expression and insulin resistance

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Author(s):
de Castro Barbosa‚ T. ; Lourenço Poyares‚ L. ; Fabres Machado‚ U. ; Nunes‚ M.T.
Total Authors: 4
Document type: Journal article
Source: Life Sciences; v. 79, n. 15, p. 1444-1449, 2006.
Abstract

Arginine (Arg) presents a potent growth hormone (GH) releasing activity. in vivo and in vitro studies carried out in our laboratory have demonstrated that acute treatment with Arg also increases GH gene expression. Taking into account the recognizable diabetogenic role of GH and that Arg increases insulin release, this study aimed at evaluating the effects of oral chronic administration of Arg on GH gene expression, by Northern blotting analysis, and on the insulin sensitivity, by means of the Insulin Tolerance Test (ITT), blood glucose decay rate (kitt) and insulin plasma concentration. We demonstrated that rats that consumed Arg (similar to 35 mg/day) in drinking water, during 4 weeks, presented an increase in GH mRNA content (p < 0.01), a decreased peripheral response to insulin, as shown by the reduced blood glucose decay rate (p < 0.05), and a higher insulin plasma concentration (p < 0.01) than control group. Arg treatment did not modify the animals' food and water intake, while it decreased the heart rate and the arterial blood pressure compared to control group (P < 0.05). According to the results presented herein we conclude that chronic oral administration of arginine increases GH gene expression and induces insulin resistance. The arterial blood pressure decrease has already been pointed out in the literature, and seems to occur in response to the dilating effect of nitric oxide generated from Arg, as well as from NO generation in central and peripheral neuronal populations that express NOS and are involved in the autonomic regulation of the cardiac function. (c) 2006 Elsevier Inc. All rights reserved. (AU)

FAPESP's process: 02/07384-4 - Regulation of glucose transporters gene expression in Diabetes Mellitus: Pathophysiological role and potential preventive and therapeutical approaches
Grantee:Ubiratan Fabres Machado
Support Opportunities: Research Projects - Thematic Grants