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Cell Biology International
Volume 30, Issue 6, June 2006, Pages 500-504
 
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doi:10.1016/j.cellbi.2005.12.012    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2006 International Federation for Cell Biology Published by Elsevier Ltd.

Effects of Ginkgolide on the development of NOS and AChE positive neurons in the embryonic basal forebrain

Guo-Hua Jina, Corresponding Author Contact Information, E-mail The Corresponding Author, Zhen Huanga, Xue-Feng Tana, Mei-Ling Tiana, Xin-Hua Zhanga, Jian-Bing Qina, Hui-Jun Xua, D.T. Yewb and Y.T. Makb

aDepartment of Anatomy and Neurobiology, School of Basic Medical Sciences, Nantong University, Nantong 226001, China bDepartment of Anatomy, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China

Received 22 June 2005; 
revised 24 September 2005; 
accepted 10 December 2005. 
Available online 23 May 2006.

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Abstract

Extract of Ginkgo biloba (EGb) has been therapeutically used for several decades to increase peripheral and cerebral blood flow so as to prevent cardiovascular and neurovascular diseases. However, the role of EGb in neuroprotective effects has received much attention recently. In this study, we investigated the effect of EGb on the development of NOS and AChE positive neurons in the rat embryonic basal forebrain. The results showed that treated with EGb, the OD of MTT staining analysis, and the numbers, the cell sizes and circumferences of NOS and AChE positive neurons were greatly promoted. These data suggest that EGb had similar effects of the neurotrophins such as NGF and BDNF in promoting the development of NOS and AChE positive neurons in the rat embryonic basal forebrain.

Keywords: EGb; Embryonic basal forebrain; NOS positive neurons; AChE positive neurons; Rat

Article Outline

1. Introduction
2. Materials and methods
2.1. Rat embryonic basal forebrain neuron culture
2.2. MTT colorimetric analysis
2.3. NADPH-d and AChE histochemistry
2.4. Neuron counting and image analysis
2.5. Data analysis
3. Results
3.1. MTT colorimetric analysis
3.2. NADPH-d histochemistry
3.3. AChE histochemistry
4. Discussion
Acknowledgements
References


 
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