Boyer J L, García A, Posadas C, García-Sáinz J A
J Biol Chem. 1984 Jul 10;259(13):8076-9.
The effect of pertussis toxin treatment on the guanine nucleotide-induced modulation of the affinity of renal alpha 1- and alpha 2-adrenergic receptors was investigated. Pretreatment of rats with pertussis toxin did not induce any change in the number of or affinity for antagonists of alpha 1- or alpha 2-receptors studied using [3H]prazosin and [3H]yohimbine, respectively. Guanyl-5'-yl imidodiphosphate induced an "up-shift" in the number of alpha 2-adrenergic receptors; this up-shift was not observed for alpha 1-adrenergic receptors. Pertussis toxin treatment decreased the affinity of epinephrine for the [3H]yohimbine-binding sites and reduced the ability of guanine nucleotides to modulate alpha 2-adrenoceptor agonist affinity. The regulation by guanine nucleotides of alpha 1-adrenoceptor affinity for agonists was not altered. These results suggest that the modulation of alpha 1- and alpha 2-adrenoceptors by guanine nucleotides is probably exerted through different molecular entities.
研究了百日咳毒素处理对鸟嘌呤核苷酸诱导的肾α1和α2肾上腺素能受体亲和力调节的影响。分别用[3H]哌唑嗪和[3H]育亨宾研究发现,用百日咳毒素预处理大鼠后,α1或α2受体拮抗剂的数量或亲和力未发生任何变化。鸟苷-5'-基亚氨基二磷酸诱导α2肾上腺素能受体数量“上移”;α1肾上腺素能受体未观察到这种上移。百日咳毒素处理降低了肾上腺素对[3H]育亨宾结合位点的亲和力,并降低了鸟嘌呤核苷酸调节α2肾上腺素能受体激动剂亲和力的能力。鸟嘌呤核苷酸对α1肾上腺素能受体激动剂亲和力的调节未改变。这些结果表明,鸟嘌呤核苷酸对α1和α2肾上腺素能受体的调节可能是通过不同的分子实体实现的。