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具有人类同源性的小鼠和大鼠扣带回皮质的细胞结构

Cytoarchitecture of mouse and rat cingulate cortex with human homologies.

作者信息

Vogt Brent A, Paxinos George

机构信息

Cingulum Neurosciences Institute, 4435 Stephanie Drive, Manlius, NY, 13104, USA,

出版信息

Brain Struct Funct. 2014 Jan;219(1):185-92. doi: 10.1007/s00429-012-0493-3. Epub 2012 Dec 11.

Abstract

A gulf exists between cingulate area designations in human neurocytology and those used in rodent brain atlases with a major underpinning of the former being midcingulate cortex (MCC). The present study used images extracted from the Franklin and Paxinos mouse atlas and Paxinos and Watson rat atlas to demonstrate areas comprising MCC and modifications of anterior cingulate (ACC) and retrosplenial cortices. The laminar architecture not available in the atlases is also provided for each cingulate area. Both mouse and rat have a MCC with neurons in all layers that are larger than in ACC and layer Va has particularly prominent neurons and reduced neuron densities. An undifferentiated ACC area 33 lies along the rostral callosal sulcus in rat but not in mouse and area 32 has dorsal and ventral subdivisions with the former having particularly large pyramidal neurons in layer Vb. Both mouse and rat have anterior and posterior divisions of retrosplenial areas 29c and 30, although their cytology is different in rat and mouse. Maps of the rodent cingulate cortices provide for direct comparisons with each region in the human including MCC and it is significant that rodents do not have a posterior cingulate region composed of areas 23 and 31 like the human. It is concluded that rodents and primates, including humans, possess a MCC and this homology along with those in ACC and retrosplenial cortices permit scientists inspired by human considerations to test hypotheses on rodent models of human diseases.

摘要

人类神经细胞学中的扣带区命名与啮齿动物脑图谱中使用的命名之间存在差异,前者的主要基础是中扣带回皮质(MCC)。本研究使用从富兰克林和帕西诺斯小鼠图谱以及帕西诺斯和沃森大鼠图谱中提取的图像,来展示构成MCC的区域以及前扣带回(ACC)和压后皮质的变化。还为每个扣带区提供了图谱中未有的分层结构。小鼠和大鼠都有一个MCC,其所有层中的神经元都比ACC中的大,并且第Va层有特别突出的神经元和降低的神经元密度。未分化的ACC区域33位于大鼠的胼胝体沟前部,但小鼠中没有,区域32有背侧和腹侧亚区,前者在第Vb层有特别大的锥体细胞。小鼠和大鼠都有压后区域29c和30的前部和后部划分,尽管它们在大鼠和小鼠中的细胞学不同。啮齿动物扣带皮质的图谱便于与人类的每个区域,包括MCC进行直接比较,重要的是,啮齿动物没有像人类那样由区域23和31组成的后扣带区域。结论是,啮齿动物和灵长类动物,包括人类,都拥有一个MCC,这种同源性以及ACC和压后皮质中的同源性,使受人类因素启发的科学家能够在人类疾病的啮齿动物模型上检验假设。

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