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大鼠海马体中间神经元上的功能性烟碱型乙酰胆碱受体

Functional nicotinic ACh receptors on interneurones in the rat hippocampus.

作者信息

Jones S, Yakel J L

机构信息

Laboratory of Signal Transduction, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.

出版信息

J Physiol. 1997 Nov 1;504 ( Pt 3)(Pt 3):603-10. doi: 10.1111/j.1469-7793.1997.603bd.x.

DOI:10.1111/j.1469-7793.1997.603bd.x
PMID:9401968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1159964/
Abstract
  1. Neuronal nicotinic ACh receptors (nAChRs) were studied in the rat hippocampal slice preparation using whole-cell patch-clamp recording techniques. 2. Responses to ACh (100 microM) were detected on inhibitory interneurones in the Ca1 field of the hippocampus proper and in the dentate gyrus, but not on principal excitatory neurones in either region. The different neuronal types were identified based on their morphology and location. 3. ACh excited interneurones in the hippocampus and dentate gyrus in current-clamp recordings. In voltage-clamp recordings, ACh-activated inward currents were recorded from interneurones in the presence of blockers of synaptic transmission and the muscarinic ACh receptor antagonist atropine. The zero current potential for this response to ACh was near 0 mV. 4. The effect of ACh was mimicked by the nAChR-selective agonists nicotine (100 microM) and 1,1-dimethyl-4-phenyl-piperazinium iodide (DMPP, 100 microM). The response to ACh was reversibly antagonized by the neuronal nAChR antagonist mecamylamine (10 microM). The nAChR alpha 7 subunit-selective antagonists alpha-bungarotoxin (100 nM) and methyllycaconitine (10 nM) also inhibited the response to ACh. 5. These observations demonstrate the presence of functional nAChRs on inhibitory interneurones in the rat hippocampus. Thus, a novel mechanism by which ACh can regulate neuronal activity in the hippocampus is revealed.
摘要
  1. 使用全细胞膜片钳记录技术,在大鼠海马脑片标本中研究了神经元烟碱型乙酰胆碱受体(nAChRs)。2. 在海马体CA1区和齿状回的抑制性中间神经元上检测到对乙酰胆碱(100微摩尔)的反应,但在这两个区域的主要兴奋性神经元上未检测到。根据不同神经元的形态和位置对其进行了识别。3. 在电流钳记录中,乙酰胆碱使海马体和齿状回中的中间神经元兴奋。在电压钳记录中,在存在突触传递阻滞剂和毒蕈碱型乙酰胆碱受体拮抗剂阿托品的情况下,从中间神经元记录到了乙酰胆碱激活的内向电流。该乙酰胆碱反应的零电流电位接近0毫伏。4. 乙酰胆碱的作用被nAChR选择性激动剂尼古丁(100微摩尔)和碘化1,1 - 二甲基 - 4 - 苯基哌嗪(DMPP,100微摩尔)模拟。神经元nAChR拮抗剂美加明(10微摩尔)可逆性拮抗对乙酰胆碱的反应。nAChRα7亚基选择性拮抗剂α - 银环蛇毒素(100纳摩尔)和甲基lycaconitine(10纳摩尔)也抑制对乙酰胆碱的反应。5. 这些观察结果证明大鼠海马体中的抑制性中间神经元上存在功能性nAChRs。因此,揭示了乙酰胆碱调节海马体神经元活动的一种新机制。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017d/1159964/e010f4803e0f/jphysiol00379-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017d/1159964/e010f4803e0f/jphysiol00379-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/017d/1159964/e010f4803e0f/jphysiol00379-0100-a.jpg

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