Hamilton C A, Reid J L, Yakubu M A
Department of Materia Medica, Stobhill General Hospital, Glasgow, U.K.
Eur J Pharmacol. 1988 Feb 9;146(2-3):345-8. doi: 10.1016/0014-2999(88)90314-7.
The binding of the alpha 2-adrenoceptor ligands [3H]yohimbine and [3H]idazoxan to rabbit kidney and forebrain membranes was compared. The maximum number of [3H]yohimbine binding sites was higher than the number of [3H]idazoxan binding sites in forebrain and lower in kidney. Large differences were observed in the ability of noradrenaline, adrenaline, idazoxan, rauwolscine, yohimbine and WY 26392 to displace [3H]yohimbine and [3H]idazoxan from their binding sites. These data suggest that [3H]idazoxan and [3H]yohimbine bind to different sites on rabbit tissue membranes.
比较了α2 -肾上腺素能受体配体[3H]育亨宾和[3H]咪唑克生与兔肾和前脑细胞膜的结合情况。[3H]育亨宾结合位点的最大数量在前脑中高于[3H]咪唑克生结合位点的数量,而在肾中则较低。观察到去甲肾上腺素、肾上腺素、咪唑克生、育亨宾碱、育亨宾和WY 26392从其结合位点置换[3H]育亨宾和[3H]咪唑克生的能力存在很大差异。这些数据表明,[3H]咪唑克生和[3H]育亨宾与兔组织细胞膜上的不同位点结合。