Abstract

Presumptive evidence suggests that the brown fat mitochondrial uncoupling protein, thermogenin, is involved in the mechanism of stimulation of respiration by norepinephrine in the intact tissue. Conflicting data have been reported which suggest involvement of either adenine nucleotides, or fatty acids, or long chain acyl-CoA, or protons in the physiological regulation. We measured the electrical potential gradient across the mitochondrial membrane (delta psi m) in control cells and in cells stimulated with norepinephrine, using the accumulation of lipophilic cation, tetraphenylphosphonium, as an indicator of the potential gradient. The value of delta psi m in the cells in the control state is 116 mV, and in the hormonally stimulated state it is 56.6 mV. This supports the view that the protein is involved in the mechanism of hormone action. Other studies were designed to distinguish between the effects of fatty acids and ATP levels on the uncoupling protein in isolated mitochondria and in the adipocytes. ATP levels and fatty acid levels inside intact cells were independently varied using oligomycin or external fatty acids. Their effect on thermogenin was monitored as the capacity of the cells for reverse electron transport from durohydroquinone. The results suggest that ATP modulates the activity of thermogenin, while fatty acids can alter the relationship between ATP and thermogenin activity such that the protein appears to be activated at a higher cellular ATP level in the presence of fatty acids than in their absence.

Highlights

  • The Effects of ATP and FattyAcids on Respiration and A@, of Isolated Mitochondria-Usually, isolated brown fat mitochondria are studied in media containing bovine serum albumin, which depletes the mitochondria membranes of fatty acids

  • The measured levels of intramitochontion. It has been suggested by several laboratories [10,11,47] drial AMP, obtained from isolated mitochondria in the conon the basis of data obtained from isolated brown fat mito- trolled respiration state, were applied in the calculation of chondria depleted of fatty acids

  • The studies carried out designed to measure A*, in brown fat cells (Fig. 2 andTable I) indicate that the uncoupling protein is activated by norepinephrine, as many workers have proposed previously [1, 3, 6, 12]

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Summary

Regulation of the Uncoupling Protein in BrownAdipose Tissue*

This view is supported by the observation protein inisolated mitochondria and in the adipocytes. The mechanism by which the stimulation measure A+,,, have been largely unsuccessful [1].In the presoccurs has been under investigation for a number of years, ent study, we have used tetraphenylphosphonium (TPP+)’to and it is generally accepted that a specialized protein, measure the A+,,, in the intact cells This method has been thermogenin, which occurs only in the inner mitochondrial applied previously to white adipocytes, lymphocytes,and hepmembrane of brown fat mitochondria, is the ultimate target atocytes [19,20,21,22,23].

METHODS
RESIJLTS AND DISCUSSION
Regulation of the UncouplingProtienin Brown Adipose Tissue
Regulation of the UncouplingPrBotirenoinwn
Regulation of the UncouplingPrBotirenoiwn n
CONCLUSIONS
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