Batty I, Nahorski S R
J Neurochem. 1985 Nov;45(5):1514-21. doi: 10.1111/j.1471-4159.1985.tb07221.x.
The accumulation of labelled inositol mono-, bis-, and trisphosphate in rat cerebral cortex slices was examined following preincubation with [3H]inositol. The muscarinic receptor agonist carbachol produced a rapid and sustained increased accumulation of each labelled inositol phosphate both in the presence and absence of 5 mM lithium. Lithium potentiated carbachol-stimulated accumulation of inositol monophosphate (EC50 0.5 mM) and inositol bisphosphate (EC50 4 mM) in a concentration-dependent manner. However, exposure to lithium in the presence of the muscarinic agonist produced a concentration- and time-dependent inhibition of inositol trisphosphate accumulation that was not related to receptor desensitisation. Although the present data do suggest that polyphosphoinositides are substrates for agonist-stimulated phospholipase C in brain, these results may not be entirely consistent with the production of inositol mono- and bisphosphate through inositol trisphosphate dephosphorylation. Furthermore, these data suggest site(s) additional to inositol monophosphatase that are affected by lithium.
在用[3H]肌醇预孵育后,检测了大鼠大脑皮层切片中标记的肌醇一磷酸、二磷酸和三磷酸的积累情况。毒蕈碱受体激动剂卡巴胆碱在存在和不存在5 mM锂的情况下,均使每种标记的肌醇磷酸的积累迅速且持续增加。锂以浓度依赖的方式增强了卡巴胆碱刺激的肌醇一磷酸(EC50为0.5 mM)和肌醇二磷酸(EC50为4 mM)的积累。然而,在毒蕈碱激动剂存在的情况下暴露于锂会产生浓度和时间依赖性的肌醇三磷酸积累抑制,这与受体脱敏无关。尽管目前的数据确实表明多磷酸肌醇是大脑中激动剂刺激的磷脂酶C的底物,但这些结果可能并不完全与通过肌醇三磷酸去磷酸化产生肌醇一磷酸和二磷酸一致。此外,这些数据表明除肌醇单磷酸酶外还有其他受锂影响的位点。