Abramets I I, Komissarov I V, Samoĭlovich I M
Biull Eksp Biol Med. 1988 Aug;106(8):172-4.
Application of 5-hydroxytryptamine (5-HT) (3 x 10(-5) M) on the rat lumbar dorsal ganglia (RDG) induced membrane depolarization with increased input resistance in 30% of neurons, hyperpolarization with decreased input resistance in 30% of neurons and mixed responses in 40% of neurons. Methysergide and amitriptyline (10(-6) M) blocked depolarizing but not hyperpolarizing effects of 5-HT. Propranolol (3 x 10(-6) M) was inactive in respect to both 5-HT responses. 5-HT depolarizing responses of RDG neurons were mediated by 5-HT2 receptors activation and decreased membrane potassium conductivity; 5-HT hyperpolarizing responses were mediated by 5-HT1A receptor activation and increased potassium conductivity. RDG neurons seem to be an interesting model for the investigation of central 5-HT receptor mechanism.
将5-羟色胺(5-HT)(3×10⁻⁵ M)应用于大鼠腰段背根神经节(RDG)时,30%的神经元出现膜去极化且输入电阻增加,30%的神经元出现超极化且输入电阻降低,40%的神经元出现混合反应。麦角新碱和阿米替林(10⁻⁶ M)可阻断5-HT的去极化作用,但不影响其超极化作用。普萘洛尔(3×10⁻⁶ M)对5-HT的两种反应均无作用。RDG神经元的5-HT去极化反应是由5-HT₂受体激活和膜钾电导率降低介导的;5-HT超极化反应是由5-HT₁A受体激活和钾电导率增加介导的。RDG神经元似乎是研究中枢5-HT受体机制的一个有趣模型。