小鸡和啮齿动物神经元生物传感器的功能相似吗?

Serena Y. Kuang, Xiaoqi Yang, Lina Wei, Ting Huang, Zhonghai Wang, Tingfei Xi, Bruce Z. Gao
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引用次数: 3

摘要

越来越多的研究论文报道了小鸡和啮齿动物皮层组织在细胞类型、神经元连接和信息处理原理上的相似性,它们的结构非常不同。本文将这些比较扩展到皮层组织之外。利用微电极阵列技术,我们报告了原始小鸡数据和文献中啮齿动物数据之间三个显著的功能相似性:(a)小鸡脊髓神经元生物传感器的自发尖峰活动模式与啮齿动物脊髓神经元生物传感器非常相似(即啮齿动物)。(b)鸡前脑神经元生物传感器的自发尖峰活动模式与啮齿动物皮质神经元生物传感器非常相似,但鸡前脑神经元生物传感器不仅包含皮质神经元,还包含间脑神经元。换句话说,鸡前脑神经元生物传感器不能被认为是啮齿类动物皮层神经元生物传感器的对应物。(c)小鸡前脑神经元生物传感器对几种经典神经活性药物的反应方式与啮齿动物皮质神经元生物传感器类似,这反映在它们的药物特异性浓度-反应曲线和它们的EC50值(引起药物最大作用的50%的有效浓度)上。如果小鸡和啮齿动物之间的神经元来源是同源的,那么这些初步发现为标题中的重大研究问题“小鸡和啮齿动物的神经元生物传感器功能相似吗”提供了直接和间接的支持。我们的发现对比较生物学/生理学、药理学、神经毒理学和生物工程以及研究鸡神经元生物传感器的更经济有效的扩展应用具有特别的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Do chick and rodent neuron biosensors function similarly?

Do chick and rodent neuron biosensors function similarly?

A growing number of research papers report similarities in cell types, neuronal connections and information-processing principles between chick and rodent cortical tissues, which have very different architectures. This paper extends these comparisons beyond the cortical tissues. Using microelectrode array technology, we report three remarkable functional similarities between our original chick data and rodent data from the literature: (a) the pattern of spontaneous spiking activity from chick spinal cord neuron biosensors is very similar to that of rodent spinal cord neuron biosensors (i.e. rodent counterparts). (b) The spontaneous spiking activity pattern of the chick forebrain neuron biosensors is very similar to that of the rodent cortical neuron biosensors, but chick forebrain neuron biosensors contain not only cortical neurons, but also diencephalic neurons. In other words, chick forebrain neuron biosensors cannot be considered the counterparts of rodent cortical neuron biosensors. (c) Chick forebrain neuron biosensors respond to several classical neuroactive agents in a way similar to rodent cortical neuron biosensors as reflected in their agent-specific concentration–response curves and their values of EC50 (the effective concentration that causes 50% of the maximal effect of an agent). These preliminary findings provide both direct and indirect support for a positive answer to the big research question in the title: ‘Do chick and rodent neuron biosensors function similarly’ if the sources of the neurons are homologous between chick and rodent? Our findings are of particular value to comparative biology/physiology, pharmacology, neurotoxicology and bioengineering and to research on the more cost-effective extended application of chick neuron biosensors.

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