Chilvers E R, Batty I H, Barnes P J, Nahorski S R
Department of Pharmacology, University of Leicester, England.
J Pharmacol Exp Ther. 1990 Feb;252(2):786-91.
The effect of muscarinic-receptor stimulation on [3H]inositol mono-, bis-, tris- and tetrakisphosphate (InsP1, InsP2, InsP3 and InsP4) accumulation was examined in bovine tracheal smooth muscle slices prelabeled with myo-[3H]inositol. Carbachol (0.1 mM) caused a rapid increase in [3H]InsP3 and [3H]InsP2 followed by delayed increases in [3H]InsP1 and [3H]InsP4 accumulation. Analysis of the [3H]InsP3 isomers by HPLC showed an immediate although transient increase in [3H]Ins(1,4,5)P3 with a progressive and sustained accumulation of [3H]Ins(1,3,4)P3. [3H]Ins(1,3,4)P3 was confirmed as the predominant (greater than 80%) [3H]InsP3 isomer present at 1 and 30 min using an enzymatic method which causes selective hydrolysis of Ins(1,3,4)P3. Lithium enhanced markedly the carbachol-stimulated accumulation of [3H]InsP1 and [3H]InsP2 with a lower potency than that observed in other tissues but had no significant influence on [3H]InsP3 or [3H]InsP4 values. These data support a role for Ins(1,4,5)P3 in initiating airway smooth muscle contraction and indicate the importance of the Ins(1,3,4,5)P4/Ins(1,3,4)P4 pathway in this tissue.
在用肌醇-[3H]标记的牛气管平滑肌切片中,研究了毒蕈碱受体刺激对[3H]肌醇单磷酸、双磷酸、三磷酸和四磷酸(InsP1、InsP2、InsP3和InsP4)积累的影响。卡巴胆碱(0.1 mM)导致[3H]InsP3和[3H]InsP2迅速增加,随后[3H]InsP1和[3H]InsP4积累延迟增加。通过高效液相色谱法对[3H]InsP3异构体进行分析,结果显示[3H]Ins(1,4,5)P3立即出现短暂增加,同时[3H]Ins(1,3,4)P3逐渐持续积累。使用能选择性水解Ins(1,3,4)P3的酶法,证实[3H]Ins(1,3,4)P3是1分钟和30分钟时存在的主要(大于80%)[3H]InsP3异构体。锂显著增强了卡巴胆碱刺激的[3H]InsP1和[3H]InsP2积累,但其效力低于在其他组织中观察到的情况,对[3H]InsP3或[3H]InsP4值无显著影响。这些数据支持Ins(1,4,5)P3在引发气道平滑肌收缩中起作用,并表明Ins(1,3,4,5)P4/Ins(1,3,4)P4途径在该组织中的重要性。