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DOI: 10.1677/jme.0.0250287

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Journal of Molecular Endocrinology, Vol 25, Issue 3, 287-298
Copyright © 2000 by Society for Endocrinology


Articles

Molecular and cellular actions of a structural domain of human growth hormone (AOD9401) on lipid metabolism in Zucker fatty rats

FM Ng, WJ Jiang, R Gianello, S Pitt, and P Roupas


A lipolytic domain (AOD9401) of human growth hormone (hGH) which resides in the carboxyl terminus of the molecule and contains the amino acid residues 177-191, has been synthesized using solid-phase peptide synthesis techniques. AOD9401 stimulated hormone-sensitive lipase and inhibited acetyl coenzyme A carboxylase (acetyl CoA carboxylase) in isolated rat adipose tissues, in a similar manner to the actions of the intact hGH molecule. The synthetic lipolytic domain mimicked the effect of the intact growth hormone on diacylglycerol release in adipocytes. Chronic treatment of obese Zucker rats with AOD9401 for 20 days reduced the body weight gain of the animals, and the average cell size of the adipocytes of the treated animals decreased from 110 to 80 microm in diameter. Unlike hGH, synthetic AOD9401 did not induce insulin resistance or glucose intolerance in the laboratory animals after chronic treatment. The results suggest that AOD9401 has the potential to be developed into a therapeutic agent for the control of obesity.


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M. Heffernan, R. J. Summers, A. Thorburn, E. Ogru, R. Gianello, W.-J. Jiang, and F. M. Ng
The Effects of Human GH and Its Lipolytic Fragment (AOD9604) on Lipid Metabolism Following Chronic Treatment in Obese Mice and {beta}3-AR Knock-Out Mice
Endocrinology, December 1, 2001; 142(12): 5182 - 5189.
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