Muraki T, Nomoto T, Kato R
Department of Pharmacology, Tokyo Women's Medical College, Japan.
Can J Physiol Pharmacol. 1989 Oct;67(10):1283-7. doi: 10.1139/y89-204.
It is considered that carbachol increases plasma cGMP levels by acting on muscarinic receptors and morphine increases these levels by acting on opioid receptors, followed by stimulation of muscarinic receptors. We investigated the ability of carbachol and morphine to increase cGMP contents of plasma, heart, and lung and the guanylate cyclase activity of heart and lung homogenate in 1-, 2-, 3-, and 7-week-old mice. The increase in plasma cGMP levels induced by carbachol showed a peak at 2 and 3 weeks of age. The basal cGMP contents in heart and lung and their rise induced by carbachol, as well as the guanylate cyclase activity of these organs, were decreased in 7-week-old mice. The effects of morphine on the cGMP contents showed a similar developmental change, except for no effect in 1-week-old mice. These changes in the effects of carbachol and morphine may be the result of developmental changes of the muscarinic receptor--guanylate cyclase system and opioid receptors.
据认为,卡巴胆碱通过作用于毒蕈碱受体来增加血浆环鸟苷酸(cGMP)水平,而吗啡则通过作用于阿片受体,随后刺激毒蕈碱受体来增加这些水平。我们研究了卡巴胆碱和吗啡在1周龄、2周龄、3周龄和7周龄小鼠中增加血浆、心脏和肺中cGMP含量以及心脏和肺匀浆中环鸟苷酸酶活性的能力。卡巴胆碱诱导的血浆cGMP水平升高在2周龄和3周龄时达到峰值。7周龄小鼠心脏和肺中的基础cGMP含量及其由卡巴胆碱诱导的升高,以及这些器官的环鸟苷酸酶活性均降低。吗啡对cGMP含量的影响呈现出类似的发育变化,但在1周龄小鼠中无影响。卡巴胆碱和吗啡作用的这些变化可能是毒蕈碱受体-环鸟苷酸酶系统和阿片受体发育变化的结果。