DISTRIBUTION OF PYY RECEPTORS IN HUMAN FAT-CELLS - AN ANTILIPOLYTIC SYSTEM ALONGSIDE THE ALPHA(2)-ADRENERGIC SYSTEM

被引:48
作者
CASTAN, I
VALET, P
LARROUY, D
VOISIN, T
REMAURY, A
DAVIAUD, D
LABURTHE, M
LAFONTAN, M
机构
[1] UNIV PAUL SABATIER, INST LOUIS BUGNARD, INSERM, U317, BAT L3, F-31054 TOULOUSE, FRANCE
[2] UNIV PARIS 07, FAC MED XAVIER BICHAT, INSERM, U239, F-75018 PARIS, FRANCE
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 01期
关键词
PEPTIDE-YY; NEUROPEPTIDE-Y; ALPHA(2)-ADRENOCEPTOR; LIPOLYSIS; G(I)-PROTEINS;
D O I
10.1152/ajpendo.1993.265.1.E74
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The antilipolytic effect of peptide YY (PYY) and neuropeptide Y has recently been shown in human adipocytes. PYY receptors were investigated in three human adipose deposits. A greater number of I-125-labeled PYY binding sites was found in femoral adipocyte membranes (maximal binding = 40 +/- 4 fmol/mg protein; dissociation constant = 0.3 +/- 0.1 nM) when compared with mammary and pericolonic adipose tissue. PYY receptors, like alpha2-adrenergic sites, were largely expressed in femoral fat cells. Such a distribution was not specific either to inhibitory or to stimulating adenylyl cyclase systems since adenosine A1 and beta-adrenergic receptors were more numerous in pericolonic adipocytes. On isolated adipocytes, PYY (10(-7) M) inhibited lipolysis by 58 +/- 2% in femoral and 14 +/- 4% in pericolonic fat cells; epinephrine had the following similar response: 62 +/- 5 and 26 +/- 8%, respectively. A close relationship between the number Of alpha2-Sites and PYY sites and the antilipolytic effects initiated by PYY and an alpha2-agonist was observed. No significant differences were noted in the amount of G(i) proteins in femoral and pericolonic adipocyte membranes.
引用
收藏
页码:E74 / E80
页数:7
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