Tack J F, Janssens J, Vantrappen G, Wood J D
Department of Physiology, College of Medicine, Ohio State University, Columbus 43210.
Am J Physiol. 1992 Dec;263(6 Pt 1):G838-46. doi: 10.1152/ajpgi.1992.263.6.G838.
Intracellular recording methods were used to study the actions of 5-hydroxytryptamine (5-HT) on 257 myenteric neurons in the guinea pig gastric antrum. Application of 5-HT caused three types of postsynaptic responses. A fast-activating depolarizing response was accompanied by a decreased input resistance and desensitized quickly to repeated applications. It was mediated by a 5-HT3 receptor. A slowly activating depolarization, accompanied by an increase in the input resistance and enhancement of the excitability, was mainly observed in after hyperpolarizing/type 2 neurons. It was suppressed by the prokinetic benzamide compound renzapride, while classical 5-HT1-4 receptor antagonists had no effect, suggesting the involvement of a 5-HT1p receptor as described in small intestinal neurons. A long-lasting hyperpolarizing response, accompanied by a decreased input resistance, was observed in a small subset of neurons. This response seemed to be mediated by a 5-HT1a receptor. Superfusion of 5-HT caused a dose-dependent inhibition of the stimulus-evoked nicotinic cholinergic fast excitatory postsynaptic potential (EPSP), which was mediated by a presynaptic 5-HT1a receptor. 5-HT also presynaptically inhibited the slow EPSP.
采用细胞内记录方法研究了5-羟色胺(5-HT)对豚鼠胃窦257个肌间神经元的作用。应用5-HT引起三种类型的突触后反应。一种快速激活的去极化反应伴有输入电阻降低,并对重复应用快速脱敏。它由5-HT3受体介导。一种缓慢激活的去极化,伴有输入电阻增加和兴奋性增强,主要在超极化后/2型神经元中观察到。它被促动力苯甲酰胺化合物伦扎必利抑制,而经典的5-HT1-4受体拮抗剂则无作用,提示如在小肠神经元中所描述的5-HT1p受体参与其中。在一小部分神经元中观察到一种持久的超极化反应,伴有输入电阻降低。这种反应似乎由5-HT1a受体介导。5-HT的灌流引起刺激诱发的烟碱型胆碱能快速兴奋性突触后电位(EPSP)的剂量依赖性抑制,这由突触前5-HT1a受体介导。5-HT还对慢EPSP进行突触前抑制。