Chang M C, Grange E, Rabin O, Bell J M, Allen D D, Rapoport S I
Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892-1582, USA.
Neurosci Lett. 1996 Dec 20;220(3):171-4. doi: 10.1016/s0304-3940(96)13264-x.
In vivo rates of incorporation and turnover of palmitate and arachidonate in brain phospholipids were measured in awake rats treated chronically with lithium, following intravenous infusion of radiolabeled palmitate and arachidonate, respectively. Chronic lithium, at a brain level considered to be therapeutic in humans, decreased turnover of arachidonate within brain phosphatidylinositol, phosphatidylcholine and phosphatidylethanolamine by up to 80% (P < 0.001). In contrast, lithium had a minimal effect on turnover of palmitate, causing only a 26% reduction in turnover in phosphatidylcholine (P < 0.01). These results suggest that a major therapeutic effect of lithium is to reduce turnover specifically of arachidonate, possibly by inhibiting phospholipase A2 involved in signal transduction. The effect may be secondary to the known action of lithium on the phosphoinositide cycle, by inhibiting the activity of inositol monophosphatase.
分别静脉输注放射性标记的棕榈酸酯和花生四烯酸酯后,在长期接受锂治疗的清醒大鼠中,测量了脑磷脂中棕榈酸酯和花生四烯酸酯的体内掺入率和周转率。在被认为对人类具有治疗作用的脑水平下,慢性锂使脑磷脂酰肌醇、磷脂酰胆碱和磷脂酰乙醇胺中花生四烯酸酯的周转率降低高达80%(P<0.001)。相比之下,锂对棕榈酸酯的周转率影响极小,仅使磷脂酰胆碱的周转率降低26%(P<0.01)。这些结果表明,锂的主要治疗作用可能是通过抑制参与信号转导的磷脂酶A2来特异性降低花生四烯酸酯的周转率。该作用可能继发于锂对磷酸肌醇循环的已知作用,即抑制肌醇单磷酸酶的活性。