Konno F, Takayanagi I
Jpn J Pharmacol. 1982 Dec;32(6):1143-50. doi: 10.1254/jjp.32.1143.
We studied the effects of morphine, codeine and codeine-7,8-oxide (codeine-epoxide) on the stimuli-induced 45Ca2+ uptake into the synaptosomes isolated from naive and tolerant rats and clarified the relationship between pharmacological responses of opiates and synaptosomal 45Ca2+ uptake. In vitro additions of morphine and codeine-epoxide inhibited the synaptosomal 45Ca2+ uptakes induced by two stimuli, that is, high KCl and veratrine in a concentration-dependent manner; and the inhibitions could be reversed by naloxone. However, the inhibitory action of codeine was less than that of morphine and codeine-epoxide. Since the potency ratios of the anti-nociceptive action of opiates are higher in the order of morphine greater than codeine-epoxide greater than codeine, the inhibitory effect of opiates on synaptosomal 45Ca2+ uptake may partly relate to their antinociceptive action. On the other hand, opiates significantly increased synaptosomal 45Ca2+ uptake when animals were rendered tolerant to their antinociceptive action, and data showed that the elevation of stimuli-induced 45Ca2+ uptake into the synaptosomes isolated from tolerant animals may reflect the degree of antinociceptive tolerance. Our results support the hypothesis that some of the pharmacological effects of opiates may be attributable to its ability to affect calcium accumulation in synaptosomes.
我们研究了吗啡、可待因和可待因 -7,8 - 氧化物(可待因环氧化物)对从未接触过药物和产生耐受性的大鼠分离出的突触体中刺激诱导的45Ca2+摄取的影响,并阐明了阿片类药物的药理反应与突触体45Ca2+摄取之间的关系。体外添加吗啡和可待因环氧化物以浓度依赖性方式抑制了由高钾离子(KCl)和藜芦碱这两种刺激诱导的突触体45Ca2+摄取;并且这些抑制作用可被纳洛酮逆转。然而,可待因的抑制作用小于吗啡和可待因环氧化物。由于阿片类药物的抗伤害感受作用的效价顺序为吗啡大于可待因环氧化物大于可待因,阿片类药物对突触体45Ca2+摄取的抑制作用可能部分与其抗伤害感受作用有关。另一方面,当动物对阿片类药物的抗伤害感受作用产生耐受性时,阿片类药物会显著增加突触体45Ca2+摄取,并且数据表明,从耐受性动物分离出的突触体中刺激诱导的45Ca2+摄取的升高可能反映了抗伤害感受耐受性的程度。我们的结果支持这样一种假设,即阿片类药物的某些药理作用可能归因于其影响突触体中钙积累的能力。