Missing protein helps mice on high-fat diet stay slim
April 16th, 2010 - 6:10 pm ICT by ANIWashington, April 16 (ANI): Mice lacking a protein involved in the response to low oxygen stay slim and healthy while on a high-fat diet, a new American research has found.
The study conducted by Randall Johnson, professor of biology at the University of California, San Diego, and his team has appeared in the April 15 issue of the journal Cell Metabolism.
While their normal counterparts gain weight, develop fatty livers and become resistant to insulin on a high fat diet, just like overweight humans do, the mutant mice suffered none of these ill effects.
Johnson said: “They process fat differently.”
The protein, an enzyme called FIH, plays a key role in the physiological response to low levels of oxygen and could be a new target for drugs to help people who struggle with weight gain.
Johnson said: “The enzyme is easily inhibited by drugs.”
Because the protein influences a wide range of genes involved in development, the scientists were surprised that its deletion improved health.
Lead author Na Zhang, a graduate student in Johnson’s lab, said: “We expected them to die as embryos.
‘”Then we saw they can survive for a long time.”
Zhang added: “From the beginning I noticed that these mice are smaller, but not sick. These mice seem to be healthy.”
The lean mice have a high metabolism, and a common check for insulin resistance, a symptom of diabetes, revealed a super sensitivity to insulin.
Zhang added: “We fed the mice with a very high fat diet - 60 percent fat - just to see how they would respond.
“Mutants can eat a lot, but they didn’t gain a lot of weight. They are less fatty around their middles compared with their littermates.”
Obese people develop a “fatty liver,” and so did the wild type littermates.
The fat mice also developed high blood cholesterol with elevated levels of the “bad” type, LDL. In lean mutants, LDL increased much less.
Zhang said: “All of these observations support that the modified mice have better metabolic profiles.”
The genetic manipulations disabled the FIH gene entirely.
Zhang said: “In every tissue, in every cell, the protein is gone.”
But the scientists wanted to know what part of the mouse physiology was responsible for the changes, so they created new mice in which the FIH protein was deleted only in specific tissues: the nervous system or the liver.
Mice that were missing FIH only from their nervous system showed most of the same effects. “But if it was only deleted in the liver, then no.” Zhang pointed out.
Though smaller, the mutant mice eat and drink 30 to 40 percent more than wild-type mice.
Johnson said: “Where do those calories go? To heat generation and an increased heart rate.”
They also breathe heavily compared with normal mice, taking in 20 to 40 per cent more air.
Johnson said: “This deep breathing is like exercise for them.”
The FIH protein is part of a wide system that responds to low levels of oxygen.
The mice behave as if they are breathing thin air. When people travel to higher altitudes, they breathe heavily for a few days, then adjust by producing more oxygen-carrying blood cells.
Johnson said: “These mice never adjust to the apparent low oxygen…They stay in this acute phase of hypoxic response their whole lives.” (ANI)
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Tags: california san diego, cell metabolism, fatty liver, gain weight, high blood cholesterol, high metabolism, ill effects, improved health, insulin resistance, key role, ldl, lean mice, livers, mutant mice, mutants, physiological response, randall johnson, symptom of diabetes, target, university of california san diego