Open AccessEffects of morphine,codeine and codeine-epoxide on calcium uptake into the synaptosomes isolated from naive and tolerant rats.
Author(s) -
Fukio Konno,
Issei Takayanagi
Publication year - 1982
Publication title -
japanese journal of pharmacology/japanese journal of pharmacology
Language(s) - English
Resource type - Journals
eISSN - 1347-3506
pISSN - 0021-5198
DOI - 10.1254/jjp.32.1143
Subject(s) - codeine , morphine , chemistry , pharmacology , (+) naloxone , inhibitory postsynaptic potential , calcium , opioid , biochemistry , endocrinology , medicine , receptor , organic chemistry
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.