Lin C J, Cheng J T
Neurosci Lett. 1986 Aug 4;68(3):288-92. doi: 10.1016/0304-3940(86)90504-5.
Picric acid stimulated, in a dose-dependent manner, the release of [14C]acetylcholine (ACh) from isolated synaptosomes of rat cerebral cortex pre-loaded with labelled choline. Radioactive ACh was separated for counting from choline in the synaptosomal supernatants by a liquid cation-exchange method. Neither the nicotinic antagonist (hexamethonium) nor the muscarinic antagonists (atropine and scopolamine) affected the effectiveness of picric acid, suggesting that the action of picric acid does not occur through a cholinoceptor-mediated mechanism. Moreover, oxotremorine, but not pilocarpine, inhibited ACh release in a concentration-dependent manner in either basal- or picric acid-evoked conditions, indicating the presence of muscarinic M2-receptors for auto-regulation of ACh release. The effect of picric acid was compared with high-K+ depolarization which also initiated a non-receptor-mediated release of ACh. Deletion of calcium ion from the medium negated the effects of both drugs. The ACh-releasing effect of picric acid was totally abolished, whereas high-K+ depolarization was reduced to some extent, when tetrodotoxin was added to the medium. These results indicate that picric acid acts as a releaser of ACh in the cerebrocortex of rat.
苦味酸以剂量依赖的方式刺激了预先加载有标记胆碱的大鼠大脑皮层分离突触体中[14C]乙酰胆碱(ACh)的释放。通过液体阳离子交换法从突触体上清液中的胆碱中分离出放射性ACh进行计数。烟碱拮抗剂(六甲铵)和毒蕈碱拮抗剂(阿托品和东莨菪碱)均不影响苦味酸的作用效果,这表明苦味酸的作用并非通过胆碱能受体介导的机制发生。此外,氧化震颤素而非毛果芸香碱,在基础或苦味酸诱发的条件下均以浓度依赖的方式抑制ACh释放,表明存在毒蕈碱M2受体用于ACh释放的自身调节。将苦味酸的作用与高钾去极化的作用进行了比较,高钾去极化也引发了非受体介导的ACh释放。从培养基中去除钙离子消除了两种药物的作用。当向培养基中加入河豚毒素时,苦味酸的ACh释放作用完全消失,而高钾去极化则在一定程度上减弱。这些结果表明苦味酸在大鼠脑皮层中作为ACh的释放剂起作用。