Literature DB >> 185045

Acidosis activation of the pituitary-adrenal-renal glutaminase I axis.

T C Welbourne.   

Abstract

Previous studies have demonstrated that the adrenal glands were necessary for acidosis activation of the mitochondrial glutaminase I pathway. The present studies were undertaken to determine if corticosterone levels are elevated in acidotic rats and if so, whether acidosis stimulates the adrenal glands directly or via the pituitary-adrenal axis. Metabolic acidosis induced by NH4Cl, either acute or chronic, increased corticosterone levels 100 to 130% in intact rats. Acute metabolic acidosis did not activate the mitochondrial pathway in adrenalectomized rats; corticosterone levels were not elevated in hypophysectomized rats nor did activation of the mitochondrial pathway occur in response to acidosis. Therefore, acidosis does not stimulate the adrenal gland directly; rather, it requires the intact pituitary. Administering exogenous corticotropin to hypophysectomized rats resulted in elevation of plasma corticosterone levels and activation of the mitochondrial pathway. The pituitary-adrenal cortex-renal glutaminase I axis apparently operates as a functional unit in the homeostatic response to metabolic acidosis.

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Year:  1976        PMID: 185045     DOI: 10.1210/endo-99-4-1071

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  12 in total

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7.  Ammonium chloride metabolic acidosis and the activity of renin-angiotensin-aldosterone system in children.

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8.  Metabolic acidosis stimulates protein degradation in rat muscle by a glucocorticoid-dependent mechanism.

Authors:  R C May; R A Kelly; W E Mitch
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9.  Bicarbonate transport along the loop of Henle. II. Effects of acid-base, dietary, and neurohumoral determinants.

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10.  Glucocorticoids enhance acid activation of the Na+/H+ exchanger 3 (NHE3).

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