Ahdieh H B, Feder H H
Institute of Animal Behavior, Rutgers University, Newark, NJ 07102.
Brain Res. 1988 Jul 26;456(2):275-9. doi: 10.1016/0006-8993(88)90228-4.
The binding of the synthetic androgen, [3H]methyltrienolone (R1881) to nuclear androgen receptors (NAR) was studied in various brain areas of gonadectomized male and female guinea pigs treated for 3 days with 2 mg testosterone propionate. The Scatchard analysis of salt-extracted NAR showed a single, high-affinity receptor with a Kd of 0.152 nM and maximum binding sites (Bmax) of 161.9 fmol/mg DNA. The concentration of NAR was highest in the hypothalamus (HYPO) and preoptic area (POA) in both males and females. Lower receptor levels were detected in the amygdala and cortex. NAR levels were significantly lower in the POA of females than in males. Systemic injection of prazosin, an alpha 1-adrenergic antagonist had no effect on NAR concentrations, but an alpha 2-antagonist, idazoxan, significantly reduced the binding of [3H]R1881 to NAR in both HYPO and POA. The reduction in binding of the ligand to receptor was not due to alterations in affinity of NAR, but rather to the decline in the number of receptors.
在经3天2mg丙酸睾酮处理的去势雄性和雌性豚鼠的不同脑区,研究了合成雄激素[3H]甲基三烯olone(R1881)与核雄激素受体(NAR)的结合。对盐提取的NAR进行Scatchard分析显示,存在一种单一的高亲和力受体,解离常数(Kd)为0.152 nM,最大结合位点(Bmax)为161.9 fmol/mg DNA。雄性和雌性的下丘脑(HYPO)和视前区(POA)中NAR的浓度最高。杏仁核和皮层中的受体水平较低。雌性POA中的NAR水平显著低于雄性。全身注射α1肾上腺素能拮抗剂哌唑嗪对NAR浓度没有影响,但α2拮抗剂咪唑克生显著降低了[3H]R1881与HYPO和POA中NAR的结合。配体与受体结合的减少不是由于NAR亲和力的改变,而是由于受体数量的下降。