Mizushima A, Uchida S, Matsumoto K, Osugi T, Kagiya T, Zhou X M, Higuchi H, Yoshida H
Eur J Pharmacol. 1985 Dec 17;119(3):177-82. doi: 10.1016/0014-2999(85)90293-6.
The Kd values of the multiple agonist binding sites in cardiac muscarinic receptors (mAChR) and pD2 values for negative inotropic actions were determined independently and their relation was examined. The guinea-pig cardiac mAChR is known to have three agonist binding sites (super-high (SH), high (H) and low (L) affinity agonist binding sites) for carbachol (CCh). Pilocarpine (Pilo) and oxotremorine (Oxo) distinguished two sites (higher (Ho/p) with pKd of 5.88 and 8.20, respectively, and lower (Lo/p) affinity agonist binding sites with pKd of 5.08 and 6.17, respectively). The effects of guanine nucleotide and sulfhydryl reagent indicated that the Ho/p site corresponded with the SH site for carbachol, and the Lo/p site with the H + L sites for carbachol. The pD2 values of CCh, Pilo and Oxo for negative inotropic actions on autocontraction of right atria were 5.38, 5.30 and 6.80, respectively. The pD2 values of CCh and Oxo on electrically stimulated contraction of left atria in the presence of isoproterenol were 5.80 and 6.46, respectively, thus being closely related to H or Lo/p agonist binding sites of mAChR.
测定了心肌毒蕈碱受体(mAChR)中多个激动剂结合位点的解离常数(Kd值)以及负性变力作用的亲和力指数(pD2值),并研究了它们之间的关系。已知豚鼠心肌mAChR对卡巴胆碱(CCh)有三个激动剂结合位点(超高亲和力(SH)、高亲和力(H)和低亲和力(L)激动剂结合位点)。毛果芸香碱(Pilo)和氧化震颤素(Oxo)区分出两个位点(较高亲和力(Ho/p)位点,其pKd分别为5.88和8.20,以及较低亲和力激动剂结合位点(Lo/p),其pKd分别为5.08和6.17)。鸟嘌呤核苷酸和巯基试剂的作用表明,Ho/p位点对应于卡巴胆碱的SH位点,而Lo/p位点对应于卡巴胆碱的H + L位点。CCh、Pilo和Oxo对右心房自收缩负性变力作用的pD2值分别为5.38、5.30和6.80。在异丙肾上腺素存在下,CCh和Oxo对左心房电刺激收缩的pD2值分别为5.80和6.46,因此与mAChR的H或Lo/p激动剂结合位点密切相关。