MARTEČÍKOVÁ, Soňa and Petr DUBOVÝ. Changes of intraneuronal immunostaining for chondroitin sulphate proteoglycans in the bodies of primary afferent neurons following constriction nerve injury. In Progress in Basic, Applied and Diagnostic Histochemistry. Brno: Vydavatelství MU, 2005, p. 132-132. ISBN 80-210-3793-8.
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Basic information
Original name Changes of intraneuronal immunostaining for chondroitin sulphate proteoglycans in the bodies of primary afferent neurons following constriction nerve injury
Name in Czech Změny v intraneuronální imunolokalizaci chondroitin sulfát proteoglykanu v tělech aferentních neuronů po konstrikčním poškození nervu
Authors MARTEČÍKOVÁ, Soňa and Petr DUBOVÝ.
Edition Brno, Progress in Basic, Applied and Diagnostic Histochemistry, p. 132-132, 1 pp. 2005.
Publisher Vydavatelství MU
Other information
Original language English
Type of outcome Proceedings paper
Field of Study 30000 3. Medical and Health Sciences
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
Organization unit Faculty of Medicine
ISBN 80-210-3793-8
Keywords in English extracellular matrix; inhibitory of axon growth
Tags extracellular matrix, inhibitory of axon growth
Tags International impact
Changed by Changed by: prof. RNDr. Petr Dubový, CSc., učo 698. Changed: 26/6/2009 10:37.
Abstract
Chronic constriction injury is one of the most used experimental models for study of neuropathic pain. The sciatic nerve constriction injury is a partial nerve injury model based on both axotomized and spared neurons. The extracellular matrix molecules have a variety of roles in the nervous system. Chondroitin sulphate proteoglycans (CSPGs) are the most abundant type of proteoglycans in the nervous system that act mainly as barrier forming molecules and belong to major inhibitory regulators of axonal regeneration. Monoclonal antibody CS-56 recognizes both the 4- and 6-sulphated forms of CSPG. The aim of the present study was to investigate an immunofluorescence for CS-56 in the dorsal root ganglion (DRG) neurons of intact rats as well as DRG after constriction of sciatic nerve for 14 and 28 days. The immunostained sections were analyzed by an epifluorescence microscope (Leica DMLB) using a software Lucia to measure intensity (brightness) of immunofluorescence and the size of neuronal bodies. Besides immunostaining in the extracellular matrix of DRG, CS-56 immunofluorescence of different intensities was detected in the bodies of DRG neurons of all size-types. The bodies of largest DRG neurons exhibited higher immunofluorescence intensity than was found in the medium- or small-sized neurons. Significantly increased intensity of immunofluorescence was found only in the medium-sized neurons of ipsilateral DRG 28 days after constriction injury when compared with DRG of naive rats or 14 days after operation. No significant difference of immunofluorescence intensity was measured in the contralateral DRG when compared with those of naive rats or operated side. In conclusion, sciatic nerve constriction used as an experimental model of neuropathic pain stimulated increased immunofluorescence for CS-56 only in the medium-sized neuron bodies. The studies of mechanisms related with elevated CS-56 immunofluorescence in the medium-sized neuronal bodies after sciatic nerve constriction are in progress.
Abstract (in Czech)
Změny v intraneuronální imunolokalizaci chondroitin sulfát proteoglykanu v tělech aferentních neuronů po konstrikčním poškození nervu
Links
GA309/03/1199, research and development projectName: Změny v satelitních gliových buňkách a jejich extracelulární matrix po axotomii - podmínky pro tvorbu sympatických kolaterál ve spinálních gangliích ?
Investor: Czech Science Foundation
MSM0021622404, plan (intention)Name: Vnitřní organizace a neurobiologické mechanismy funkčních systémů CNS
Investor: Ministry of Education, Youth and Sports of the CR, The internal organisation and neurobiological mechanisms of functional CNS systems under normal and pathological conditions.
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