Konno F, Takayanagi I
Jpn J Pharmacol. 1983 Jun;33(3):619-26. doi: 10.1254/jjp.33.619.
We studied the relationship between inhibition of 45Ca2+ uptake and the antinociceptive action induced by morphine and effects of papaverine and 1,1-diphenyl-3-piperidinobutanol hydrochloride (Aspaminol) on both these actions of morphine. Addition of these drugs in the incubation medium significantly inhibited glutamate-stimulated synaptosomal 45Ca2+ uptake. The inhibition curves of morphine and Aspaminol on glutamate-stimulated synaptosomal 45Ca2+ uptake were linear, but that of papaverine was not. The inhibition of morphine on synaptosomal 45Ca2+ uptake was reversed by addition of naloxone. The inhibition of synaptosomal 45Ca2+ uptake induced by morphine was increased by the simultaneous addition of Aspaminol, but the inhibition induced by both morphine and papaverine was not increased to more than that by papaverine alone. Since morphine-antinociception was potentiated by Aspaminol and blocked by papaverine, these results support that the inhibition of synaptosomal calcium uptake plays an important role in the production of morphine-antinociception. However, since the inhibition of synaptosomal 45Ca2+ uptake by morphine was less than that by both Aspaminol and papaverine, and papaverine blocked morphine-antinociception, notwithstanding that 10(-4) M of papaverine alone completely inhibited glutamate-stimulated 45Ca2+ uptake into synaptosomes, it may be difficult to account for the antinociceptive action of morphine by the inhibition of 45Ca2+ uptake only.
我们研究了45Ca2+摄取抑制与吗啡诱导的抗伤害感受作用之间的关系,以及罂粟碱和1,1 - 二苯基 - 3 - 哌啶基丁醇盐酸盐(阿斯帕明醇)对吗啡这两种作用的影响。在孵育培养基中添加这些药物可显著抑制谷氨酸刺激的突触体45Ca2+摄取。吗啡和阿斯帕明醇对谷氨酸刺激的突触体45Ca2+摄取的抑制曲线呈线性,而罂粟碱的抑制曲线则不然。添加纳洛酮可逆转吗啡对突触体45Ca2+摄取的抑制作用。同时添加阿斯帕明醇可增强吗啡对突触体45Ca2+摄取的抑制作用,但吗啡和罂粟碱共同诱导的抑制作用并未增强至超过单独使用罂粟碱时的抑制作用。由于阿斯帕明醇可增强吗啡的抗伤害感受作用,而罂粟碱可阻断该作用,这些结果支持突触体钙摄取的抑制在吗啡抗伤害感受作用的产生中起重要作用。然而,由于吗啡对突触体45Ca2+摄取的抑制作用小于阿斯帕明醇和罂粟碱,且尽管单独使用10(-4) M罂粟碱可完全抑制谷氨酸刺激的45Ca2+摄取进入突触体,但罂粟碱仍可阻断吗啡的抗伤害感受作用,因此仅通过抑制45Ca2+摄取来解释吗啡的抗伤害感受作用可能存在困难。