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对成年早期和中年大鼠模型进行乙醇提取物处理后海马神经元密度(CA1和CA3)的分析。

The analysis of hippocampus neuronal density (CA1 and CA3) after ethanolic extract treatment on the young adulthood and middle age rat model.

作者信息

Kusindarta Dwi Liliek, Wihadmadyatami Hevi, Haryanto Aris

机构信息

Department of Anatomy, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia.

Department of Biochemistry, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia.

出版信息

Vet World. 2018 Feb;11(2):135-140. doi: 10.14202/vetworld.2018.135-140. Epub 2018 Feb 8.

Abstract

AIM

This study aimed to assess the changes in neuronal density in CA1 and CA3 regions in the hippocampus of young adulthood and middle age rat model after feeding by ethanolic extract.

MATERIALS AND METHODS

In this research, 30 male Wistar rats consist of young to middle-aged rats were divided into three groups (3, 6, and 9 months old) and treated with a different dosage of ethanolic extract (0, 50, and 100 mg/kg b.w.) for 45 days. Furthermore, cresyl violet staining was performed to analyze hippocampus formation mainly in CA1 and CA3 area. The concentrations of acetylcholine (Ach) in brain tissues were analyzed by enzyme-linked immunosorbent assay.

RESULTS

In our models using rat model, we found that the administration of ethanolic extract with a dosage of 100 mg/kg b.w. for 45 days induced the density of pyramidal cells significantly in CA1 and CA3 of the hippocampus. These results were supported by an increase of Ach concentrations on the brain tissue.

CONCLUSIONS

The administration of ethanolic extract may promote the density of the pyramidal cells in the CA1 and CA3 mediated by the up-regulated concentration of Ach.

摘要

目的

本研究旨在评估用乙醇提取物喂养青年期和中年期大鼠模型后,海马体CA1区和CA3区神经元密度的变化。

材料与方法

在本研究中,30只雄性Wistar大鼠(包括青年到中年大鼠)被分为三组(3、6和9月龄),并用不同剂量的乙醇提取物(0、50和100毫克/千克体重)处理45天。此外,进行甲酚紫染色以主要分析CA1区和CA3区的海马体形成。通过酶联免疫吸附测定法分析脑组织中乙酰胆碱(Ach)的浓度。

结果

在我们使用大鼠模型的实验中,我们发现以100毫克/千克体重的剂量给予乙醇提取物45天,可显著诱导海马体CA1区和CA3区锥体细胞的密度。脑组织中Ach浓度的增加支持了这些结果。

结论

给予乙醇提取物可能通过上调Ach浓度来促进CA1区和CA3区锥体细胞的密度。

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