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Alpha 1-adrenergic stimulation of phosphatidylinositol turnover and respiration of brown fat cells

Journal Article · · Mol. Pharmacol.; (United States)
OSTI ID:6834561
The alpha-adrenergic agonist phenylephrine (in the presence of the beta-adrenergic antagonist alprenolol) stimulated respiration and incorporation of (/sup 3/H)glycerol and (/sup 32/P) P/sub i/ into phosphatidylinositol of hamster brown fat cells in a concentration-dependent manner. Both responses were preferentially inhibited by prazosin as compared with yohimbine, indicating alpha 1 specificity. Uniquely, prazosin inhibition of phenylephrine-stimulated phosphatidylinositol metabolism had two components, since 30% of the response was inhibited by less than 1 nM prazosin, 10 nM gave no further inhibition, and 100 nM prazosin completely inhibited the response. The phosphatidylinositol response was still present in Ca/sup 2/+-free buffer, although reduced in magnitude. The concentration relationships of the effects of agonists and antagonists were compared with those of previous results of (/sup 3/H)prazosin binding and with phenylephrine potency to compete for binding. On the basis of these comparisons, it is suggested that the highly prazosin-sensitive part of the phosphatidylinositol response may be closely associated with receptor occupation.
Research Organization:
Section of Biochemistry, Brown University, Providence, Rhode Island
OSTI ID:
6834561
Journal Information:
Mol. Pharmacol.; (United States), Journal Name: Mol. Pharmacol.; (United States) Vol. 25:1; ISSN MOPMA
Country of Publication:
United States
Language:
English