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哺乳动物黑质神经元中乙酰胆碱酯酶树突状释放的在线可视化。

On-line visualization of dendritic release of acetylcholinesterase from mammalian substantia nigra neurons.

作者信息

Llinás R R, Greenfield S A

出版信息

Proc Natl Acad Sci U S A. 1987 May;84(9):3047-50. doi: 10.1073/pnas.84.9.3047.

Abstract

This study presents, to our knowledge, the first on-line measurement of acetylcholinesterase (AcChoEase) release from brain tissue. It is now well established that a soluble form of the enzyme is released from central nervous system neurons, and it has been proposed on indirect grounds that such release may occur not only from presynaptic terminals but also from the dendrites of dopamine-containing nigrostriatal neurons. We have used a chemiluminescent reaction to examine the real-time release of AcChoEase from the substantia nigra in vitro in brainstem slices. The light emission was captured by two fiber optic systems, one in direct contact with the brain slice from below and the second 4-mm above the slice, allowing simultaneous imaging of the emitted light and quantitative photometry. It was determined that the light signals are not due to the spontaneous hydrolysis of acetylcholine or the presence of free choline, but are caused by the enzymatic action of AcChoEase. Using this technique, it can be directly shown that AcChoEase is spontaneously released from the soma or dendrites of nigral neurons. The release of the enzyme, which is stored in the subcisternal dendritic compartment, is resistant to blockade of voltage-dependent sodium conductances, is calcium dependent, and can be increased by addition of potassium to the bathing solution. The procedure we describe here will make it possible to study the release of endogenous AcChoEase on a time-scale close to that over which it functions.

摘要

据我们所知,本研究首次对脑组织中乙酰胆碱酯酶(AcChoEase)的释放进行了在线测量。现已明确,该酶的可溶性形式是从中枢神经系统神经元释放出来的,并且基于间接证据提出,这种释放不仅可能发生在突触前终末,还可能发生在含多巴胺的黑质纹状体神经元的树突上。我们利用化学发光反应,在体外脑干切片中检测了黑质中AcChoEase的实时释放情况。发光由两个光纤系统捕获,一个从下方直接与脑切片接触,另一个在切片上方4毫米处,从而能够同时对发射光进行成像和定量光度测量。已确定光信号并非由乙酰胆碱的自发水解或游离胆碱的存在所致,而是由AcChoEase的酶促作用引起的。使用该技术可以直接表明,AcChoEase是从黑质神经元的胞体或树突中自发释放的。储存在树突池下隔室中的该酶的释放对电压依赖性钠电导的阻断具有抗性,依赖于钙,并且通过向浴液中添加钾可使其增加。我们在此描述的方法将使得有可能在接近其发挥功能的时间尺度上研究内源性AcChoEase的释放。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2f4/304799/9d24d3555a99/pnas00274-0493-a.jpg

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