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麻醉大鼠海马CA1区和CA3区中内源性5-羟色胺介导的突触传递的差异特征。

Differential characteristics of endogenous serotonin-mediated synaptic transmission in the hippocampal CA1 and CA3 fields of anaesthetized rats.

作者信息

Matsumoto Machiko, Kojima Taku, Togashi Hiroko, Mori Kiyoshi, Ohashi Satoshi, Ueno Ken-ichi, Yoshioka Mitsuhiro

机构信息

Department of Pharmacology, Hokkaido University Graduate School of Medicine, Kita-15, Nishi-7, Kita-ku, Sapporo 060-8638, Japan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2002 Dec;366(6):570-7. doi: 10.1007/s00210-002-0634-y. Epub 2002 Oct 1.

Abstract

The characteristics of endogenous serotonin (5-HT)-mediated synaptic transmission were investigated in the hippocampal CA1 and CA3 fields of anaesthetized rats. Electrophysiological approaches were used to elucidate the effects of a selective 5-HT reuptake inhibitor, fluvoxamine, on synaptic transmission by determining the population spike amplitude (PSA). Fluvoxamine (10 or 30 mg/kg i.p.) increased the PSA in the CA1 and CA3 fields concentration dependently, whereby this facilitatory response was greater in the CA3 than in the CA1 field. Fluvoxamine (30 mg/kg i.p.)-induced increases in the PSA were augmented by the 5-HT(1A) receptor antagonist NAN 190 (0.5 mg/kg i.p.) and prevented by the 5-HT(4) receptor antagonist GR 113808 (20 micro g/rat i.c.v.) or by the 5-HT(7) receptor antagonist DR 4004 (10 micro g/rat i.c.v.) in the CA1 field. Thus, fluvoxamine-induced facilitatory effects appear to be mediated via 5-HT(1A) and 5-HT(4)/5-HT(7) receptors in an inhibitory and a stimulatory manner, respectively. In the CA3 field, excitability produced by fluvoxamine was abolished by either NAN 190 or DR 4004, but not by GR 113808, suggesting that 5-HT(1A) and 5-HT(7) receptors contribute to this facilitation. These findings were supported in part by the results obtained by exogenously applied 5-HT receptor agonists: the 5-HT(1A) receptor agonist tandospirone (10 mg/kg i.p.) decreased PSA in the CA1 field, whereas the 5-HT(4) receptor agonist SC 53116 (10 micro g/rat i.c.v.) increased it. In contrast, in the CA3 field, tandospirone increased PSA, whereas SC 53116 had no effect. Taken together, the present study revealed that characteristics of synaptic transmission mediated via 5-HT receptors differ between the CA1 and CA3 fields: in the CA1 field, three 5-HT receptors, 5-HT(1A), 5-HT(4) and 5-HT(7), are associated with the endogenous 5-HT-induced facilitation in an opposite and independent manner. In the CA3 field, at least two 5-HT receptors, i.e. 5-HT(1A) and 5-HT(7), are involved in this mediation in a facilitatory manner. 5-HT neurons may modulate pyramidal neuron responses to incoming stimuli by complex mechanisms involving these 5-HT receptors. In other words, the net effects resulting from the differential characteristics in the CA1 and CA3 fields may play an important role in the physiological functions of the hippocampus.

摘要

在麻醉大鼠的海马CA1区和CA3区研究了内源性5-羟色胺(5-HT)介导的突触传递特性。采用电生理学方法,通过测定群体峰电位幅度(PSA)来阐明选择性5-HT再摄取抑制剂氟伏沙明对突触传递的影响。氟伏沙明(腹腔注射10或30mg/kg)浓度依赖性地增加CA1区和CA3区的PSA,其中CA3区的这种促进反应比CA1区更大。腹腔注射30mg/kg氟伏沙明引起的PSA增加被5-HT(1A)受体拮抗剂NAN 190(腹腔注射0.5mg/kg)增强,并被5-HT(4)受体拮抗剂GR 113808(脑室内注射20μg/只大鼠)或5-HT(7)受体拮抗剂DR 4004(脑室内注射10μg/只大鼠)在CA1区阻断。因此,氟伏沙明诱导的促进作用似乎分别通过5-HT(1A)和5-HT(4)/5-HT(7)受体以抑制和刺激的方式介导。在CA3区,氟伏沙明产生的兴奋性被NAN 190或DR 4004消除,但不被GR 113808消除,表明5-HT(1A)和5-HT(7)受体参与了这种促进作用。这些发现部分得到了外源性应用5-HT受体激动剂所得结果的支持:5-HT(1A)受体激动剂坦度螺酮(腹腔注射10mg/kg)降低了CA1区的PSA,而5-HT(4)受体激动剂SC 53116(脑室内注射10μg/只大鼠)则增加了PSA。相反,在CA3区,坦度螺酮增加了PSA,而SC 53116没有作用。综上所述,本研究表明,通过5-HT受体介导的突触传递特性在CA1区和CA3区之间存在差异:在CA1区,三种5-HT受体,即5-HT(1A)、5-HT(4)和5-HT(7),以相反且独立的方式与内源性5-HT诱导的促进作用相关。在CA3区,至少两种5-HT受体,即5-HT(1A)和5-HT(7),以促进的方式参与这种介导。5-HT神经元可能通过涉及这些5-HT受体的复杂机制调节锥体神经元对传入刺激的反应。换句话说,CA1区和CA3区差异特性产生的净效应可能在海马的生理功能中起重要作用。

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