{"title":"中枢神经系统乙酰胆碱释放:50年回顾。","authors":"John W Phillis","doi":"10.1615/critrevneurobiol.v17.i3-4.30","DOIUrl":null,"url":null,"abstract":"<p><p>Some 50 years have elapsed since Elliot et al. and MacIntosh & Oborin first reported a release of acetylcholine (ACh) from canine and feline cerebral cortices, respectively. In this review, subsequent developments in the field during the succeeding five decades are explored. The arrangement of material in the review is outlined in this abstract, concluding with some suggestions as to its potential significance. A number of technical advances during this period have contributed to a greater understanding of the role that ACh may play in the central nervous system. These include the relatively recent evolution of the microdialysis and transverse dialysis techniques that enabled investigators to explore ACh release in deep regions of the brain. Future studies will likely be refined with the use of microelectrode biosensors, which should allow real-time measurements of ACh concentrations at the synaptic level. Controversies arising from the use of cholinesterase inhibitors and muscarinic receptor antagonists to enhance release are being resolved as a result of a better understanding of the presynaptic actions of these agents. Future studies will also benefit from the recent development of clostridial and other neurotoxins to reduce ACh release in areas of the brain. The likelihood that ACh may act as a cotransmitter at synapses in conjunction with glutamic acid, nitric oxide, and adenosine triphosphate is also explored. Attention is focused on the elucidation of choline acetyl-transferase (ChAT)-containing pathways in the central nervous system using techniques such as immunohistochemistry, in situ hybridization, histochemistry of ChAT mRNA, acetylcholinesterase histochemistry, and the distribution of the vesicular ACh transporter. Such studies have defined several major groupings of cholinergic neurons in the brain, which provide ascending or descending projections to higher and lower central structures. A major section of the review is devoted to actual studies on ACh release in the brain and spinal cord. This presentation is in two sections. The text details some of the material that has been obtained in experiments over the past 50 years. In five Tables, the results obtained in the majority of release studies to date are summarized. Although the data obtained to date clearly support the hypothesis that ACh is involved in electroencephalographic activation associated with cerebral cortical arousal, this occurs while the animals appear to be awake with full postural control, suggesting that noncholinergic pathways to the cerebral cortex are also involved in such behavioral manifestations. The roles of acetylcholine in cognitive processes such as attention, learning, memory, responses to environmental changes, and motor activity still remain to be defined.</p>","PeriodicalId":10778,"journal":{"name":"Critical reviews in neurobiology","volume":"17 3-4","pages":"161-217"},"PeriodicalIF":0.0000,"publicationDate":"2005-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"61","resultStr":"{\"title\":\"Acetylcholine release from the central nervous system: a 50-year retrospective.\",\"authors\":\"John W Phillis\",\"doi\":\"10.1615/critrevneurobiol.v17.i3-4.30\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Some 50 years have elapsed since Elliot et al. and MacIntosh & Oborin first reported a release of acetylcholine (ACh) from canine and feline cerebral cortices, respectively. In this review, subsequent developments in the field during the succeeding five decades are explored. The arrangement of material in the review is outlined in this abstract, concluding with some suggestions as to its potential significance. A number of technical advances during this period have contributed to a greater understanding of the role that ACh may play in the central nervous system. These include the relatively recent evolution of the microdialysis and transverse dialysis techniques that enabled investigators to explore ACh release in deep regions of the brain. Future studies will likely be refined with the use of microelectrode biosensors, which should allow real-time measurements of ACh concentrations at the synaptic level. Controversies arising from the use of cholinesterase inhibitors and muscarinic receptor antagonists to enhance release are being resolved as a result of a better understanding of the presynaptic actions of these agents. Future studies will also benefit from the recent development of clostridial and other neurotoxins to reduce ACh release in areas of the brain. The likelihood that ACh may act as a cotransmitter at synapses in conjunction with glutamic acid, nitric oxide, and adenosine triphosphate is also explored. Attention is focused on the elucidation of choline acetyl-transferase (ChAT)-containing pathways in the central nervous system using techniques such as immunohistochemistry, in situ hybridization, histochemistry of ChAT mRNA, acetylcholinesterase histochemistry, and the distribution of the vesicular ACh transporter. Such studies have defined several major groupings of cholinergic neurons in the brain, which provide ascending or descending projections to higher and lower central structures. A major section of the review is devoted to actual studies on ACh release in the brain and spinal cord. This presentation is in two sections. The text details some of the material that has been obtained in experiments over the past 50 years. In five Tables, the results obtained in the majority of release studies to date are summarized. Although the data obtained to date clearly support the hypothesis that ACh is involved in electroencephalographic activation associated with cerebral cortical arousal, this occurs while the animals appear to be awake with full postural control, suggesting that noncholinergic pathways to the cerebral cortex are also involved in such behavioral manifestations. 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引用次数: 61
摘要
自Elliot et al.和MacIntosh & Oborin首次报道分别从犬和猫的大脑皮层释放乙酰胆碱(ACh)以来,大约50年过去了。在这篇综述中,探讨了在随后的五十年中该领域的后续发展。摘要概述了综述中材料的安排,并就其潜在意义提出了一些建议。这一时期的一些技术进步有助于更好地理解乙酰胆碱在中枢神经系统中可能发挥的作用。其中包括相对较新的微透析和横向透析技术的发展,使研究人员能够探索大脑深部区域的乙酰胆碱释放。未来的研究可能会使用微电极生物传感器进行改进,这将允许在突触水平实时测量ACh浓度。由于对胆碱酯酶抑制剂和毒蕈碱受体拮抗剂的突触前作用有了更好的了解,使用这些药物来增强释放所引起的争议正在得到解决。未来的研究也将受益于梭状芽孢杆菌和其他神经毒素的最新发展,以减少大脑区域的乙酰胆碱释放。乙酰胆碱在与谷氨酸、一氧化氮和三磷酸腺苷结合的突触中作为共递质的可能性也进行了探讨。重点是利用免疫组织化学、原位杂交、ChAT mRNA组织化学、乙酰胆碱酯酶组织化学和囊泡ACh转运体分布等技术阐明中枢神经系统中含有胆碱乙酰转移酶(ChAT)的途径。这些研究已经确定了大脑中几种主要的胆碱能神经元群,它们向较高和较低的中枢结构提供上升或下降的投射。这篇综述的一个主要部分是关于乙酰胆碱在大脑和脊髓中释放的实际研究。本演讲分为两个部分。这篇文章详细介绍了过去50年来在实验中获得的一些材料。在五个表中,总结了迄今为止在大多数释放研究中获得的结果。尽管迄今为止获得的数据清楚地支持ACh参与与大脑皮层觉醒相关的脑电图激活的假设,但这种情况发生在动物似乎清醒并完全控制姿势的情况下,这表明通往大脑皮层的非胆碱能通路也参与了这种行为表现。乙酰胆碱在诸如注意力、学习、记忆、对环境变化的反应和运动活动等认知过程中的作用仍有待确定。
Acetylcholine release from the central nervous system: a 50-year retrospective.
Some 50 years have elapsed since Elliot et al. and MacIntosh & Oborin first reported a release of acetylcholine (ACh) from canine and feline cerebral cortices, respectively. In this review, subsequent developments in the field during the succeeding five decades are explored. The arrangement of material in the review is outlined in this abstract, concluding with some suggestions as to its potential significance. A number of technical advances during this period have contributed to a greater understanding of the role that ACh may play in the central nervous system. These include the relatively recent evolution of the microdialysis and transverse dialysis techniques that enabled investigators to explore ACh release in deep regions of the brain. Future studies will likely be refined with the use of microelectrode biosensors, which should allow real-time measurements of ACh concentrations at the synaptic level. Controversies arising from the use of cholinesterase inhibitors and muscarinic receptor antagonists to enhance release are being resolved as a result of a better understanding of the presynaptic actions of these agents. Future studies will also benefit from the recent development of clostridial and other neurotoxins to reduce ACh release in areas of the brain. The likelihood that ACh may act as a cotransmitter at synapses in conjunction with glutamic acid, nitric oxide, and adenosine triphosphate is also explored. Attention is focused on the elucidation of choline acetyl-transferase (ChAT)-containing pathways in the central nervous system using techniques such as immunohistochemistry, in situ hybridization, histochemistry of ChAT mRNA, acetylcholinesterase histochemistry, and the distribution of the vesicular ACh transporter. Such studies have defined several major groupings of cholinergic neurons in the brain, which provide ascending or descending projections to higher and lower central structures. A major section of the review is devoted to actual studies on ACh release in the brain and spinal cord. This presentation is in two sections. The text details some of the material that has been obtained in experiments over the past 50 years. In five Tables, the results obtained in the majority of release studies to date are summarized. Although the data obtained to date clearly support the hypothesis that ACh is involved in electroencephalographic activation associated with cerebral cortical arousal, this occurs while the animals appear to be awake with full postural control, suggesting that noncholinergic pathways to the cerebral cortex are also involved in such behavioral manifestations. The roles of acetylcholine in cognitive processes such as attention, learning, memory, responses to environmental changes, and motor activity still remain to be defined.