Angiotensin II induces skeletal muscle wasting through enhanced protein degradation and down-regulates autocrine insulin-like growth factor I

M Brink, SR Price, J Chrast, JL Bailey, A Anwar… - …, 2001 - academic.oup.com
M Brink, SR Price, J Chrast, JL Bailey, A Anwar, WE Mitch, P Delafontaine
Endocrinology, 2001academic.oup.com
We previously showed that angiotensin II (ang II) infusion in the rat produces cachexia and
decreases circulating insulin-like growth factor I (IGF-I). The weight loss derives from an
anorexigenic response and a catabolic effect of ang II. In these experiments we assessed
potential catabolic mechanisms and the involvement of the IGF-I system in these responses
to ang II. Ang II infusion caused a significant decrease in body weight compared with that of
pair-fed control rats. Kidney and left ventricular weights were significantly increased by ang …
Abstract
We previously showed that angiotensin II (ang II) infusion in the rat produces cachexia and decreases circulating insulin-like growth factor I (IGF-I). The weight loss derives from an anorexigenic response and a catabolic effect of ang II. In these experiments we assessed potential catabolic mechanisms and the involvement of the IGF-I system in these responses to ang II. Ang II infusion caused a significant decrease in body weight compared with that of pair-fed control rats. Kidney and left ventricular weights were significantly increased by ang II, whereas fat tissue was unchanged. Skeletal muscle mass was significantly decreased in the ang II-infused rats, and a reduction in lean muscle mass was a major reason for their overall loss of body weight. In skeletal muscles, ang II did not significantly decrease protein synthesis, but overall protein breakdown was accelerated; inhibiting lysosomal and calcium-activated proteases did not reduce the ang II-induced increase in muscle proteolysis. Circulating IGF-I levels were 33% lower in ang II rats vs. control rats, and this difference was reflected in lower IGF-I messenger RNA levels in the liver. Moreover, IGF-I, IGF-binding protein-3, and IGF-binding protein-5 messenger RNAs in the gastrocnemius were significantly reduced. To investigate whether the reduced circulating IGF-I accounts for the loss in muscle mass, we increased circulating IGF-I by coinfusing ang II and IGF-I, but this did not prevent muscle loss. Our data suggest that ang II causes a loss in skeletal muscle mass by enhancing protein degradation probably via its inhibitory effect on the autocrine IGF-I system.
Oxford University Press