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大鼠海马CA1、CA3和齿状回区域胆碱能和肾上腺素能传入神经释放乙酰胆碱和去甲肾上腺素。

Release of acetylcholine and noradrenaline from the cholinergic and adrenergic afferents in rat hippocampal CA1, CA3 and dentate gyrus regions.

作者信息

Milusheva E, Baranyi M, Zelles T, Mike A, Vizi E S

机构信息

Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest.

出版信息

Eur J Neurosci. 1994 Feb 1;6(2):187-92. doi: 10.1111/j.1460-9568.1994.tb00260.x.

Abstract

An attempt was made to study the release of acetylcholine (ACh) and noradrenaline and their presynaptic modulation in isolated slice preparations dissected from different subfields of the hippocampus: CA1, CA3 and the dentate gyrus. The slices were perfused and loaded with [3H]choline or with [3H]noradrenaline. The release in response to field stimulation was determined radiochemically and the content of transmitters was assayed by a chemiluminescent method or by HPLC combined with electrochemical detection. After 30 min of loading with [3H]choline there were marked subregional differences in the specific activity of [3H]ACh content. The highest concentration was measured in the dentate gyrus and the lowest in CA3. Evidence was obtained that in all three subfields the cholinergic axon terminals are equipped with inhibitory muscarinic autoreceptors and the noradrenergic terminals with alpha 2-autoreceptors, as indicated by an increase in transmitter release when the tissue was exposed to selective muscarinic or alpha 2-adrenoceptor antagonists. In contrast, the cholinergic boutons are not equipped with alpha 2-adrenoceptors, and noradrenergic terminals do not possess inhibitory muscarinic receptors. It is therefore concluded that while the release of both ACh and noradrenaline is controlled by negative feedback modulation, there is no possibility of establishing a presynaptic inhibitory interaction between the two.

摘要

研究人员尝试在从海马体不同亚区(CA1、CA3和齿状回)分离出的离体脑片标本中,研究乙酰胆碱(ACh)和去甲肾上腺素的释放及其突触前调节。脑片经灌注并加载[3H]胆碱或[3H]去甲肾上腺素。通过放射化学方法测定电场刺激后的释放量,并通过化学发光法或高效液相色谱结合电化学检测法测定递质含量。加载[3H]胆碱30分钟后,[3H]ACh含量的比活性存在明显的亚区差异。齿状回中的浓度最高,CA3中的浓度最低。有证据表明,在所有三个亚区中,胆碱能轴突终末都配备有抑制性毒蕈碱自身受体,去甲肾上腺素能终末配备有α2自身受体,当组织暴露于选择性毒蕈碱或α2肾上腺素能受体拮抗剂时,递质释放增加即表明了这一点。相反,胆碱能终扣不配备α2肾上腺素能受体,去甲肾上腺素能终末不具有抑制性毒蕈碱受体。因此得出结论,虽然ACh和去甲肾上腺素的释放均受负反馈调节控制,但两者之间不可能建立突触前抑制性相互作用。

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