Mita H, Yui Y, Suzuki M, Yasueda H, Shida T
Int Arch Allergy Appl Immunol. 1982;69(2):169-73. doi: 10.1159/000233166.
After intraperitoneal injection of Bordetella pertussis vaccine to guinea pigs, the alpha 1- and beta-adrenergic and cholinergic muscarinic receptors of the whole lung were measured by binding assays with the radioisotope-labeled antagonists, 3H-prazosin, 1-(3)H-dihydroalprenolol and 1-(3)H-quinuclidinyl benzilate, respectively. Injection of guinea pigs with pertussis vaccine resulted in an increase in the maximum binding (Bmax) of 3H-prazosin, while there was about a 30% reduction in 1-(3)H-dihydroalprenolol binding to beta-adrenergic receptors. No difference was observed in the dissociation constant (KD) for binding of each ligand to alpha 1- and beta-adrenergic receptors. 1-(3)H-quinuclidinyl benzilate binding indicated that the Bmax and KD for cholinergic muscarinic receptor in pertussis-sensitized guinea pigs were not significantly different from those normal control animals.
给豚鼠腹腔注射百日咳疫苗后,分别用放射性同位素标记的拮抗剂3H-哌唑嗪、1-(3)H-二氢阿普洛尔和1-(3)H-喹核醇苯甲酸酯通过结合试验测定全肺的α1-肾上腺素能、β-肾上腺素能和胆碱能毒蕈碱受体。给豚鼠注射百日咳疫苗导致3H-哌唑嗪的最大结合量(Bmax)增加,而1-(3)H-二氢阿普洛尔与β-肾上腺素能受体的结合减少了约30%。未观察到每种配体与α1-和β-肾上腺素能受体结合的解离常数(KD)有差异。1-(3)H-喹核醇苯甲酸酯结合表明,百日咳致敏豚鼠中胆碱能毒蕈碱受体的Bmax和KD与正常对照动物无显著差异。