Mørk A, Geisler A
Pharmacol Toxicol. 1987 Jan;60(1):17-23. doi: 10.1111/j.1600-0773.1987.tb01713.x.
The influence of lithium on calmodulin-stimulated adenylate cyclase activity has been studied in vitro and after chronic treatment. Chronic lithium treatment decreased calcium-calmodulin-stimulated adenylate cyclase activity in rat cortical membranes, while no effect was observed on GTP-stimulated activity. Lithium in vitro inhibited adenylate cyclase activity stimulated by isoprenaline, GTP or calcium-calmodulin. Calcium-calmodulin-stimulated activity was more sensitive to lithium (2 mM) than isoprenaline- and GTP-stimulated activities (5 mM) and activities by these agents combined. Lithium had no effect on the unstimulated enzyme activity. The inhibitory effect of lithium in vitro on calcium-calmodulin-stimulated adenylate cyclase activity was antagonized by magnesium. The inhibition induced by lithium in vitro on the GTP-stimulated adenylate cyclase activity was increased by substituting manganese for magnesium in the assay media. Furthermore, the manganese-stimulated activity was also reduced by lithium. The latter effect was not observed in calmodulin-depleted membranes, but the inhibitory effect of lithium could be restored by addition of exogenous calmodulin. The present results suggest that lithium might influence the interaction of calmodulin with the enzyme and/or interfere with the divalent cation site(s) on the adenylate cyclase system.
锂对钙调蛋白刺激的腺苷酸环化酶活性的影响已在体外和长期治疗后进行了研究。长期锂治疗降低了大鼠皮质膜中钙-钙调蛋白刺激的腺苷酸环化酶活性,而对GTP刺激的活性未观察到影响。体外锂抑制异丙肾上腺素、GTP或钙-钙调蛋白刺激的腺苷酸环化酶活性。钙-钙调蛋白刺激的活性比异丙肾上腺素和GTP刺激的活性(5 mM)以及这些试剂联合刺激的活性对锂(2 mM)更敏感。锂对未刺激的酶活性没有影响。体外锂对钙-钙调蛋白刺激的腺苷酸环化酶活性的抑制作用被镁拮抗。在测定介质中用锰替代镁可增加体外锂对GTP刺激的腺苷酸环化酶活性的抑制作用。此外,锰刺激的活性也被锂降低。在钙调蛋白耗尽的膜中未观察到后一种效应,但添加外源性钙调蛋白可恢复锂的抑制作用。目前的结果表明,锂可能影响钙调蛋白与酶的相互作用和/或干扰腺苷酸环化酶系统上的二价阳离子位点。