Ashby C R, Edwards E, Harkins K, Wang R Y
Department of Psychiatry and Behavioral Science, State University of New York, Stony Brook 11794-8790.
Eur J Pharmacol. 1989 Dec 7;173(2-3):193-6. doi: 10.1016/0014-2999(89)90519-0.
The microiontophoretic application of the selective 5-hydroxytryptamine3 (5-HT3) agonist 2-methylserotonin suppresses medial prefrontal cortex cell firing. This effect is blocked by the 5-HT3 antagonists BRL 43694 and ICS205930, but not by metergoline or (+/-)-pindolol. Continuous microiontophoretic administration of magnesium chloride or the gamma-aminobutyric acidA antagonist SR 95103 did not alter 2-methylserotonin's suppressant action, suggesting that this effect is direct. Our results suggest that 5-HT3 receptors have a functional role in the medial prefrontal cortex.
选择性5-羟色胺3(5-HT3)激动剂2-甲基血清素的微量离子电渗应用可抑制内侧前额叶皮质细胞放电。5-HT3拮抗剂BRL 43694和ICS205930可阻断这种效应,但美替戈林或(±)-吲哚洛尔则不能。持续微量离子电渗给予氯化镁或γ-氨基丁酸A拮抗剂SR 95103不会改变2-甲基血清素的抑制作用,表明这种效应是直接的。我们的结果表明,5-HT3受体在内侧前额叶皮质中具有功能性作用。