Aguilar J S, Fonseca M I, De Robertis E
Neurochem Res. 1986 May;11(5):745-52. doi: 10.1007/BF00965342.
The injection of Bordetella pertussis, inactivated by merthiolate, causes a 2-fold increase in the IC50 of carbamylcholine (carbachol) in displacing [3H];-L(-) quinuclidinyl benzilate binding ([3H]QNB) to the receptor. In control animals, 50 microM Gpp(NH)p causes a 6-fold decrease in the affinity of carbachol binding, whereas after vaccination the reduction is only 1.6-fold. After pertussis treatment there is no alteration in the affinity and number of [3H]QNB binding sites of to the muscarinic receptor.
用硫柳汞灭活的百日咳博德特氏菌注射后,在将[3H]-L(-)喹核醇基苯甲酸酯([3H]QNB)置换到受体上时,氨基甲酰胆碱(卡巴胆碱)的IC50增加了2倍。在对照动物中,50 microM Gpp(NH)p使卡巴胆碱结合亲和力降低6倍,而接种疫苗后降低仅1.6倍。百日咳治疗后,[3H]QNB与毒蕈碱受体结合位点的亲和力和数量没有改变。