Gillin J C, Hong J S, Yang H Y, Costa E
Proc Natl Acad Sci U S A. 1978 Jun;75(6):2991-3. doi: 10.1073/pnas.75.6.2991.
In rats, chronic treatment with lithium elicits a dose-dependent increase in the [Met5]enkephalin content of nucleus caudatus and globus pallidus. A single injection of lithium fails to change the striatal [Met5]enkephalin content. The increase in [Met5]enkephalin caused by chronic lithium is proportional to the serum lithium level. The extent of the increase in striatal [Met5]enkephalin content levels off at a value of about 250% that of untreated rats. This increase has a time latency of 2--3 days and reaches a plateau at 5 days. The increase that was present at 5 days was no longer evident if the treatment was continued for 2 weeks. Lithium also increases striatal [Leu5]enkephalin content by an extent equal to the increase of [Met 5]enkephalin. Based on the characteristics of the lithium-induced increase in [Met6]enkephalin content, it is proposed that lithium may reduce the rate of release of [Met5]enkephalin from the small enkephalinergic neurons that are intrinsic to the striatum; this action may be related to a change in the regulation of striatal neurons.
在大鼠中,长期用锂治疗会引起尾状核和苍白球中[Met5]脑啡肽含量呈剂量依赖性增加。单次注射锂不会改变纹状体中[Met5]脑啡肽的含量。慢性锂引起的[Met5]脑啡肽增加与血清锂水平成正比。纹状体中[Met5]脑啡肽含量增加的程度在约为未治疗大鼠的250%时趋于平稳。这种增加有2至3天的时间潜伏期,并在5天时达到平台期。如果治疗持续2周,5天时出现的增加不再明显。锂还会使纹状体中[Leu5]脑啡肽含量增加,增加程度与[Met5]脑啡肽的增加程度相同。基于锂诱导的[Met5]脑啡肽含量增加的特征,有人提出锂可能会降低纹状体内源性小脑啡肽能神经元释放[Met5]脑啡肽的速率;这种作用可能与纹状体神经元调节的变化有关。