Quantitative study of neurons and synapses in rat hippocampus by new stereological methods

师晓燕; 赵圆宇; 卢伟; 陈林; 张蕾; 姜蓉; 唐勇

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Quantitative study of neurons and synapses in rat hippocampus by new stereological methods

更新时间：2026-01-09

- Quantitative study of neurons and synapses in rat hippocampus by new stereological methods
- Journal of Army Medical University Vol. 33, Issue 13, Pages: 1328-1332(2011)
- 作者机构：
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  CLC： R329-33;R322.81
- Published：2011
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师晓燕,赵圆宇,卢伟,陈林,张蕾,姜蓉,唐勇.运用新的体视学方法定量研究大鼠海马结构神经元和突触数目[J].陆军军医大学学报(原第三军医大学学报),2011,33(13):1328-1332.

　Shi Xiaoyan,Zhao Yuanyu,Lu Wei,Chen Lin,Zhang Lei,Jiang Rong,Tang Yong.Quantitative study of neurons and synapses in rat hippocampus by new stereological methods[J].J Amry Med Univ (J Third Mil Med Univ),2011,33(13):1328-1332.
师晓燕,赵圆宇,卢伟,陈林,张蕾,姜蓉,唐勇.运用新的体视学方法定量研究大鼠海马结构神经元和突触数目[J].陆军军医大学学报(原第三军医大学学报),2011,33(13):1328-1332. DOI：

　Shi Xiaoyan,Zhao Yuanyu,Lu Wei,Chen Lin,Zhang Lei,Jiang Rong,Tang Yong.Quantitative study of neurons and synapses in rat hippocampus by new stereological methods[J].J Amry Med Univ (J Third Mil Med Univ),2011,33(13):1328-1332. DOI：

摘要

目的建立定量研究海马结构神经元数目和突触数目的无偏体视学方法。方法选择18月龄正常雌性Long-Evans大鼠5只

取一侧大脑半球进行石蜡包埋后切取14 μm厚的冠状连续切片。根据均匀系统随机抽样的原则，在包含海马结构的连续切片中均匀随机地抽取切片。将抽取的一组切片进行神经元的组织化学染色，以计数神经元的数目；将抽取的另外一组切片进行突触的免疫组织化学染色，以计数突触的数目。在体视学设备下，计数大鼠海马结构CA

和DG的神经元数目和大鼠海马结构CA

、CA

放射层（CA

sr）、齿状回内分子层（DGiml）和齿状回外分子层（DGoml）的突触数目。结果得到大鼠海马结构CA

和DG的神经元数目分别为[(3.17×10

)±(2.23×10

)

]

和[(1.70×10

)±(1.87×10

)

]

。大鼠海马结构CA

、CA

sr、DGiml和 DGoml的突触数目分别为[(1.04×10

)±(5.39×10

)

]

、[(4.36×10

)±(3.78×10

)

]

、[(1.87×10

)±(1.81×10

)

]

和[(4.48×10

)±(7.29×10

)

]

。结论本研究建立了定量研究海马结构各区域内神经元数目和突触数目的方法，可为定量研究正常老年及各种神经系统退行性疾病状态下海马结构各区域内神经元数目、突触数目及神经元与突触数目关系的改变提供方法学依据。

Abstract

Objective To establish stereological methods for the quantitative studies of neurons and synapses in the hippocampus. Methods After five 18-month female Long-Evans rats were anesthesized

one of the two hemispheres was sampled randomly after fixatio

n with paraformaldehyde perfusion

and then embedded in paraffin blocks. Serial coronal sections in thickness of 14 μm were cut. The sections were uniformly and randomly sampled from the consecutive sections through hippocampus according to the principles of systematic

uniform and random sampling. One series of sections were stained for Nissl substance for the quantification of neuron number

and another series of sections were stained for the quantification of synaptophysin-positive bouton number. The number of neurons in CA

and DG and the number of synaptophysin-positive boutons in CA

DGiml

and DGoml were estimated with the unbiased stereological technique

the optical fractionator. Results The total number of the neurons in CA

and DG was 3.17×10

±2.23×10

and 1.70×10

±1.87×10

respectively. The total number of the synapses in CA

DGiml

and DGoml was 1.04×10

±5.39×10

4.36×10

±3.78×10

1.87×10

±1.81×10

and 4.48×10

±7.29×10

respectively. Conclusion Our established methods can quantitatively study the neuron and synapse changes during hippocampal formation in normal aging process and in various neurodegenerative diseases.

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