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突触传递与可塑性研究中的方法与局限性

Approaches and Limitations in the Investigation of Synaptic Transmission and Plasticity.

作者信息

Glasgow Stephen D, McPhedrain Ryan, Madranges Jeanne F, Kennedy Timothy E, Ruthazer Edward S

机构信息

Department of Neurology & Neurosurgery, Montreal Neurological Institute-Hospital, McGill University, Montreal, QC, Canada.

出版信息

Front Synaptic Neurosci. 2019 Jul 24;11:20. doi: 10.3389/fnsyn.2019.00020. eCollection 2019.

Abstract

The numbers and strengths of synapses in the brain change throughout development, and even into adulthood, as synaptic inputs are added, eliminated, and refined in response to ongoing neural activity. A number of experimental techniques can assess these changes, including single-cell electrophysiological recording which offers measurements of synaptic inputs with high temporal resolution. Coupled with electrical stimulation, photoactivatable opsins, and caged compounds, to facilitate fine spatiotemporal control over release of neurotransmitters, electrophysiological recordings allow for precise dissection of presynaptic and postsynaptic mechanisms of action. Here, we discuss the strengths and pitfalls of various techniques commonly used to analyze synapses, including miniature excitatory/inhibitory (E/I) postsynaptic currents, evoked release, and optogenetic stimulation. Together, these techniques can provide multiple lines of convergent evidence to generate meaningful insight into the emergence of circuit connectivity and maturation. A full understanding of potential caveats and alternative explanations for findings is essential to avoid data misinterpretation.

摘要

在整个发育过程中,甚至到成年期,随着突触输入根据持续的神经活动而增加、消除和完善,大脑中突触的数量和强度都会发生变化。许多实验技术可以评估这些变化,包括单细胞电生理记录,它能以高时间分辨率测量突触输入。结合电刺激、光激活视蛋白和笼形化合物,以促进对神经递质释放的精细时空控制,电生理记录允许精确剖析突触前和突触后作用机制。在这里,我们讨论了常用于分析突触的各种技术的优点和缺陷,包括微小兴奋性/抑制性(E/I)突触后电流、诱发释放和光遗传学刺激。这些技术共同提供了多条相互印证的证据,以深入了解电路连接性和成熟的出现。充分理解研究结果的潜在注意事项和其他解释对于避免数据误解至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5611/6667546/eef1c5b1a025/fnsyn-11-00020-g0001.jpg

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