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神经降压素对大鼠海马体中乙酰胆碱和γ-氨基丁酸释放的调节:一项体内微透析研究。

Neurotensin modulation of acetylcholine and GABA release from the rat hippocampus: an in vivo microdialysis study.

作者信息

Rakovska A, Giovannini M G, Della Corte L, Kalfin R, Bianchi L, Pepeu G

机构信息

Institute of Physiology, Bulgarian Academy of Sciences, Sofia.

出版信息

Neurochem Int. 1998 Oct;33(4):335-40. doi: 10.1016/s0197-0186(98)00036-9.

Abstract

The effects of neurotensin (NT) on the release of acetylcholine (ACh), aspartate (Asp), glutamate (Glu) and gamma-aminobutyric acid (GABA) from the hippocampus of freely moving rats were studied by transversal microdialysis. ACh was detected by High Performance Liquid Chromatography (HPLC) with electrochemical detection while GABA, glutamate and aspartate were measured using HPLC with fluorometric detection. Neurotensin (0.2 and 0.5 microM) administered locally through the microdialysis probe to the hippocampus produced a long-lasting and concentration-dependent increase in the basal extracellular levels of GABA and ACh but not of glutamate and aspartate. The increase in the extracellular levels of GABA and ACh produced by 0.5 microM neurotensin in the hippocampus reached a maximum of about 310% for GABA and 250% for ACh. This stimulant effect of NT was antagonized by the NT receptor antagonist SR 48692 (100 microg/kg, i.p.). Local infusion of tetrodotoxin (1 microM) decreased the basal release of ACh, GABA, Asp, Glu and prevented the 0.2 microM NT-induced increase in GABA and ACh release. The effect of NT on the release of ACh was blocked by the GABA(A) receptor antagonist bicuculline (2-10 microM). Our findings indicate for the first time that neurotensin plays a neuromodulatory role in the regulation of GABAergic and cholinergic neuronal activity in the hippocampus of awake and freely moving rats. The potentiating effects of neurotensin on GABA and ACh release in the hippocampus are probably mediated by (i) NT receptors located on GABAergic cell bodies and (ii) through GABA(A) receptors located on cholinergic nerve terminals.

摘要

采用横向微透析技术研究了神经降压素(NT)对自由活动大鼠海马中乙酰胆碱(ACh)、天冬氨酸(Asp)、谷氨酸(Glu)和γ-氨基丁酸(GABA)释放的影响。ACh通过高效液相色谱(HPLC)结合电化学检测进行检测,而GABA、谷氨酸和天冬氨酸则使用HPLC结合荧光检测进行测定。通过微透析探针向海马局部给予神经降压素(0.2和0.5微摩尔)可使GABA和ACh的基础细胞外水平产生持久且浓度依赖性的升高,但对谷氨酸和天冬氨酸则无此作用。海马中0.5微摩尔神经降压素引起的GABA和ACh细胞外水平升高,GABA最高可达约310%,ACh最高可达250%。NT的这种刺激作用被NT受体拮抗剂SR 48692(100微克/千克,腹腔注射)所拮抗。局部注射河豚毒素(1微摩尔)可降低ACh、GABA、Asp、Glu的基础释放,并阻止0.2微摩尔NT诱导的GABA和ACh释放增加。NT对ACh释放的作用被GABA(A)受体拮抗剂荷包牡丹碱(2 - 10微摩尔)所阻断。我们的研究结果首次表明,神经降压素在清醒且自由活动大鼠海马的GABA能和胆碱能神经元活动调节中发挥神经调节作用。神经降压素对海马中GABA和ACh释放的增强作用可能是通过(i)位于GABA能细胞体上的NT受体和(ii)位于胆碱能神经末梢上的GABA(A)受体介导的。

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