Narayanan T K, Aronstam R S
Neurochem Res. 1986 Oct;11(10):1397-406. doi: 10.1007/BF00966219.
Gallamine interacts with an allosteric site on muscarinic acetylcholine receptor complexes in rat brain membranes, thereby slowing the dissociation of a radiolabelled ligand ([3H]N-methylscopolamine) from the receptor complex. This effect involves the elimination of the fast component of the biphasic dissociation curve. The allosteric effect of gallamine is equally prominent in membranes containing predominantly M1 (cerebral cortex) and M2 (brainstem) subtypes of muscarinic receptor. Gallamine's action is not affected by a variety of treatments which influence the conformational state of the receptor as reflected by agonist binding affinity, including treatments with heat, N-ethylmaleimide and trypsin. A guanine nucleotide (5'-guanylylimidodiphosphate), however, moderates the effects of gallamine on muscarinic receptors in brainstem, but not in cortical, membranes.
加拉明与大鼠脑膜中毒蕈碱型乙酰胆碱受体复合物上的变构位点相互作用,从而减缓放射性标记配体([3H]N-甲基东莨菪碱)从受体复合物上的解离。这种效应涉及消除双相解离曲线的快速成分。加拉明的变构效应在主要含有毒蕈碱受体M1亚型(大脑皮层)和M2亚型(脑干)的膜中同样显著。加拉明的作用不受多种影响受体构象状态(以激动剂结合亲和力反映)的处理的影响,包括加热、N-乙基马来酰亚胺和胰蛋白酶处理。然而,一种鸟嘌呤核苷酸(5'-鸟苷酰亚胺二磷酸)会减弱加拉明对脑干膜中毒蕈碱受体的作用,但对皮层膜中的受体没有影响。