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  Vol. 22, No. 22  Previous Table of Contents Home  Next December 1, 2000 

`Fat-proof' Mice Yield New Anti-obesity Drug Target


By JOAN CARTER
Baylor College of Medicine

Forget the fountain of youth. Scientists at Baylor College of Medicine may have found something even more exciting - the secret to effortless weight loss.

The key is outsmarting perilipin, a protein that acts as a "bodyguard" for fat cells. The Baylor researchers discovered the fat-protecting role of perilipin after breeding laboratory mice to eliminate the gene that codes for the protein. The team's findings appear in the December issue of Nature Genetics.

"Perilipin works by coating the surface of fat storage droplets inside fat cells, protecting them from hormone-sensitive lipase, a fat-metabolizing enzyme," said Dr. Lawrence Chan, lead investigator of the study and a Baylor professor in the Departments of Medicine and Molecular and Cellular Biology.

In perilipin-free mice, fat storage is a losing battle because hormone-sensitive lipase metabolizes fat as soon as it is made.

"This process burns a great deal of energy that would otherwise be deposited as fat," Dr. Chan said.

Dr. Chan said the extra calorie-burning capacity of the perilipin-free mice was reflected in their metabolic rate, which was consistently higher than that of their wild-type cagemates. The mice also had eight percent more muscle and only about half as much body fat, despite consuming 25 percent more food and exercising less. And while both groups of mice had the same number of fat cells, those of the perilipin-free mice were only half the size.

Being perilipin-free also benefited db/db mice, so named because they inherit the db gene that predisposes them to obesity from both parents. The mice, though genetically programmed to be obese, grew up lean.

"These results are very exciting because not only is perilipin active in humans, it is made almost exclusively by fat cells," Dr. Chan said.

The latter could be key to the success of anti-perilipin drugs to fight obesity. Dr. Chan said drugs designed to disrupt a very precise target like perilipin in body tissues have potentially fewer side effects than those affecting the brain or multiple organ systems.

Although he believes that perilipin research is very promising, Dr. Chan remains cautious.

"This is an exciting first step, but it will take time to move perilipin research from experiments in mice to helping humans with weight problems," he said.

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