Literature DB >> 11520028

A quantitative histochemistry technique for measuring regional distribution of acetylcholinesterase in the brain using digital scanning densitometry.

T Ma1, Z Cai, S E Wellman, I K Ho.   

Abstract

Studies of brain acetylcholinesterase (AChE) are traditionally based on biochemical assays, immunoreactivity, and histochemistry. Conventional histochemistry yields rich morphological data from tissue sections but yields quantitative results only with great difficulty. Several histochemical methods developed in recent years, including microdensitometry, microphotometry, and video-based histochemistry, are effective in quantitative and detailed study of AChE in tissue sections. However, they are usually time-consuming. As we report here, we adapted digital scanning densitometry to quantitate AChE histochemical staining in brain sections. The AChE and butyrylcholinesterase (BuChE), as measured by the method, were heterogeneously distributed throughout the brain, results that are consistent with those obtained by biochemical methods. The staining intensity is dependent on section thickness, substrate concentration, and reaction time. The cholinesterase inhibitor methyl paraoxon significantly decreased AChE staining intensity. Furthermore, data acquired from densitometry are similar to those obtained by video-based microscopy or by spectrophotometry. The advantage of the densitometric measurements compared to other quantitative histochemical methods is that it is very rapid while collecting data that are equivalent in quality. Because the digital scanning densitometers provide high quality and sensitive imaging, wide dynamic ranges, and convenient image analysis software, they are very useful tools in quantitative histochemistry. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11520028     DOI: 10.1006/abio.2001.5208

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  4 in total

1.  Efficient measurement of endogenous neurotransmitters in small localized regions of central nervous systems in vitro with HPLC.

Authors:  Xuesi M Shao; Jack L Feldman
Journal:  J Neurosci Methods       Date:  2006-11-07       Impact factor: 2.390

2.  Changes in acetylcholinesterase activity and muscarinic receptor bindings in mu-opioid receptor knockout mice.

Authors:  Lu-Tai Tien; Lir-Wan Fan; Chiharu Sogawa; Tangeng Ma; Horance H Loh; Ing-Kang Ho
Journal:  Brain Res Mol Brain Res       Date:  2004-07-05

3.  Substitution of natural sensory input by artificial neurostimulation of an amputated trigeminal nerve does not prevent the degeneration of basal forebrain cholinergic circuits projecting to the somatosensory cortex.

Authors:  Celia Herrera-Rincon; Fivos Panetsos
Journal:  Front Cell Neurosci       Date:  2014-11-14       Impact factor: 5.505

4.  Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo.

Authors:  Qiping Zheng; Guang Zhou; Roy Morello; Yuqing Chen; Xavier Garcia-Rojas; Brendan Lee
Journal:  J Cell Biol       Date:  2003-09-01       Impact factor: 10.539

  4 in total

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