Peterson D A, Butterfield J, Garrard J M
Research Service, Veterans Administration Medical Center, Minneapolis, MN 55417.
Med Hypotheses. 1988 May;26(1):73-5. doi: 10.1016/0306-9877(88)90117-x.
We have previously suggested that several intercellular messengers activate their receptors via reductive activation. Adenylate cyclase activation involves exposure of a sulfhydryl group. The dopamine D1 receptor activates this enzyme. Because sulfhydryl exposure could be secondary to reduction of a disulfide group we evaluated dopaminergic D1 agonists and antagonists as reducing agents. The agonists were found to be reducing agents and the antagonists were inactive. These results are consistent with the concept that dopaminergic D1 agonists activate adenylate cyclase via reductive activation.
我们之前曾提出,几种细胞间信使通过还原激活来激活其受体。腺苷酸环化酶的激活涉及巯基的暴露。多巴胺D1受体可激活这种酶。由于巯基的暴露可能是二硫键还原的继发结果,我们评估了多巴胺能D1激动剂和拮抗剂作为还原剂的作用。结果发现激动剂是还原剂,而拮抗剂无活性。这些结果与多巴胺能D1激动剂通过还原激活来激活腺苷酸环化酶这一概念相一致。