White H L
Department of Pharmacology, Wellcome Research Laboratories, Research Triangle Park, North Carolina 27709.
J Neurosci Res. 1988 May;20(1):122-8. doi: 10.1002/jnr.490200117.
Experimental conditions are described which permit effects of various agents on polyphosphoinositides and phosphatidic acid (PA) to be evaluated simultaneously in crude nerve-ending preparations from rat brain. Acetylcholine (3-100 microM) or carbachol (30-1,000 microM) induced the hydrolysis of prelabeled polyphosphoinositides and, at the same time, stimulated the net label incorporated in phosphatidic acid. All muscarinic effects were blocked by atropine or pirenzepine. Non-muscarinic agonists (glutamate, adenosine, norepinephrine) stimulated polyphosphoinositide hydrolysis in this preparation, but of these only norepinephrine affected phosphatidic acid turnover. A potentiation of acetylcholine-induced phosphoinositide turnover by KCl was observed, as well as an apparent selective inhibition of PIP2 hydrolysis by LiCl. Acetylcholine-stimulated turnover of PA was not necessarily coupled to phosphoinositide hydrolysis.
本文描述了实验条件,该条件允许在大鼠脑粗神经末梢制剂中同时评估各种试剂对多磷酸肌醇和磷脂酸(PA)的影响。乙酰胆碱(3 - 100微摩尔)或卡巴胆碱(30 - 1000微摩尔)诱导预先标记的多磷酸肌醇水解,同时刺激掺入磷脂酸中的净标记。所有毒蕈碱样作用均被阿托品或哌仑西平阻断。非毒蕈碱激动剂(谷氨酸、腺苷、去甲肾上腺素)刺激该制剂中的多磷酸肌醇水解,但其中只有去甲肾上腺素影响磷脂酸周转。观察到氯化钾增强了乙酰胆碱诱导的磷酸肌醇周转,以及氯化锂对PIP2水解的明显选择性抑制。乙酰胆碱刺激的PA周转不一定与磷酸肌醇水解相关联。