AT1 receptor blockade and the sympathoadrenal response to insulin-induced hypoglycemia in humans.

Article Details

Citation

Worck RH, Ibsen H, Frandsen E, Dige-Petersen H

AT1 receptor blockade and the sympathoadrenal response to insulin-induced hypoglycemia in humans.

Am J Physiol. 1997 Mar;272(3 Pt 1):E415-21.

PubMed ID
9124547 [ View in PubMed
]
Abstract

An important facilitating effect of angiotensin II on adrenal catecholamine release has been demonstrated in several species. To determine whether specific AT1 receptor blockade affects medullary epinephrine secretion and musculocutaneous norepinephrine release during insulin-induced hypoglycemia, 16 healthy volunteers received losartan vs. placebo followed by an intravenous insulin bolus and measurement of effect variables at short intervals for 150 min. AT1 receptor blockade was effective, as evidenced by substantially increased circulating renin and angiotensin II levels, a 60% inhibition of circulating aldosterone, and an 8.5% decrease of mean arterial pressure over time compared with placebo. Arterial glucose concentration fell to a nadir of 1.9 mM, arterial epinephrine concentration increased 23-fold, forearm musculocutaneous norepinephrine release increased 4-fold, heart rate increased 40%, and forearm blood flow increased 3-fold. All absolute values and the time course of these changes were independent of AT1 receptor blockade. It is concluded that a putative interaction between angiotensin II and the sympathoadrenal axis may not be mediated by AT1 receptors in humans.

DrugBank Data that Cites this Article

Pharmaco-proteomics
DrugDrug GroupsGeneGene IDChangeInteractionChromosome
LosartanApprovedREN5972
increased
[Losartan results in decreased activity of AGTR1 protein] which results in increased expression of REN protein1q32.1