According to a report in the June issue of the journal Cell Metabolism, published by Cell Press People with a low-carbohydrate, high-fat diet may result in increased levels of a newly identified 'starvation hormone' produced by the liver. Two studies in the issue show that the hormone plays a critical role in the metabolic shift seen in animals after a period of fasting and in those fed an Atkins-like diet.
That shift is characterized by an increased reliance on fat stores as an alternative source of fuel when glucose, the body's primary energy source, plummets. A team led by Eleftheria Maratos-Flier of Harvard University reports evidence that increased blood levels of liver-derived 'fibroblast growth factor 21' (FGF21) are required for fasted mice and mice on a carbohydrate-restricted diet to switch gears and begin burning fat.
AdvertisementLikewise, an accompanying study led by Steven Kliewer of the University of Texas Southwestern Medical Center found that FGF21 mobilizes fat in food-restricted animals and those with chronically elevated concentrations of the liver hormone.
'We think these findings would increase the desirability of a drug that [might work through this mechanism] to increase fat oxidation in the liver,' said Maratos-Flier, noting that the rise in obesity has contributed to a growing epidemic of nonalcoholic fatty liver disease. Mammals survive periods of nutrient deprivation by shifting from carbohydrates to so-called ketone bodies as a primary fuel source.
Ketone bodies are produced from fatty acids transferred from storage in fat tissue to the liver when carbohydrates are scarce. During prolonged fasts, ketone bodies can provide nearly half of baseline energy requirements and up to 70% of the energy required by the brain. Maratos-Flier's team examined changes in gene activity occurring in mice fed a high-fat, low-carb diet for 30 days. Their comprehensive genetic screen of the animals, which lost weight on the special diet, turned up FGF21.'We saw a dramatic increase in FGF21 in the livers of the mice [on the diet],' she said.
Kliewer's group showed that FGF21 is induced directly by PPAR (peroxisome proliferator-activated receptor) in liver in response to fasting in mice. Scientists have known that PPAR controls fats' use as an energy source during starvation. In addition, some drugs that lower 'bad' cholesterol work by targeting PPAR. FGF21 in turn stimulates lipid breakdown in white adipose tissue and ketone body production in the liver. They unexpectedly also found that FGF21 led the animals to reduce their physical activity and made them more sensitive to entering torpor, a short-term, hibernation-like state.
'During fasting, the liver hormone communicates with adipose tissue to send fat to the liver. It turns on the metabolism of fat into ketone bodiesand at the same time, it sensitizes the animals to going into torpor to conserve energy. It's clear that FGF21 is a principal component of the fasting.' she added.
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