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Therapeutic Effects of Aldose Reductase Inhibitor on Experimental Diabetic Neuropathy through Synthesis/Secretion of Nerve Growth Factor

We investigated alterations in nerve growth factor (NGF) and ciliary neurotrophic factor (CNTF) contents during treatment with epalrestat, an aldose reductase inhibitor (ARI), on streptozotocin (STZ)-induced diabetic neuropathy in rats. Diabetic rats showed a statistically significant reduction in H...

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Published in:Experimental neurology 1998-06, Vol.151 (2), p.215-220
Main Authors: Ohi, Takekazu, Saita, Kazuko, Furukawa, Shoei, Ohta, Mitsuhiro, Hayashi, Kyozo, Matsukura, Shigeru
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cited_by cdi_FETCH-LOGICAL-c434t-928f58cfbe14ee1b3601ede847b13ed87d3616feedae188e3acd0c3d43bc0af83
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container_issue 2
container_start_page 215
container_title Experimental neurology
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creator Ohi, Takekazu
Saita, Kazuko
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Ohta, Mitsuhiro
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Matsukura, Shigeru
description We investigated alterations in nerve growth factor (NGF) and ciliary neurotrophic factor (CNTF) contents during treatment with epalrestat, an aldose reductase inhibitor (ARI), on streptozotocin (STZ)-induced diabetic neuropathy in rats. Diabetic rats showed a statistically significant reduction in H-wave-related sensory nerve conduction velocity (HSNCV) and in NGF content in sciatic nerves during the experiment of 8 weeks. No reduction in the CNTF content in sciatic nerves was seen in the diabetic rats. The epalrestat treatment, which started 4 weeks after STZ injection, resulted in a significantly greater NGF content and faster HSNCV than those in untreated diabetic rats. But no statistically significant alterations of motor nerve conduction velocity (MNCV) or CNTF content were seen during the treatment. ARI showed the stimulating effect for NGF synthesis/secretion in rat Schwann cell culturein vitro.These findings suggest that decreased levels of NGF in diabetic sciatic nerves may be involved in the pathogenesis of diabetic neuropathy in these rats and further show that epalrestat treatment can be useful for the treatment of diabetic neuropathy through NGF-induction in Schwann cells and/or inhibition of the polyol pathway.
doi_str_mv 10.1006/exnr.1998.6821
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Impaired glucose tolerance</subject><subject>Diabetic Neuropathies - drug therapy</subject><subject>Diabetic Neuropathies - metabolism</subject><subject>diabetic neuropathy</subject><subject>Electrophysiology</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nerve Growth Factors - biosynthesis</subject><subject>Nerve Growth Factors - secretion</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Nerve Tissue Proteins - secretion</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>NGF</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rhodanine - analogs &amp; derivatives</subject><subject>Rhodanine - pharmacology</subject><subject>Schwann cell culture</subject><subject>Schwann Cells - cytology</subject><subject>Schwann Cells - drug effects</subject><subject>Schwann Cells - enzymology</subject><subject>Sciatic Nerve - chemistry</subject><subject>Sciatic Nerve - cytology</subject><subject>Sciatic Nerve - physiology</subject><subject>Thiazolidines</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNp1kE9P4zAQxS0EgsJy3RuSD1zTjmOTOkcE5Y-EuhKw58ixxxujEke2A_Qb7MdeR6247WlGmvfezPwI-clgzgCqBX71Yc7qWs4rWbIDMmNQQ1EKDodkBsBEIaSsTshpjG8AUItyeUyO66qUy6tqRv6-dhjUgGNymq6sRZ0i9ZZeb4yPSJ_RjDqp3D32nWtd8oH6nq6-BgzuHfukNvTWqRYn-xrH4AeVui1NXfDjn46-bPvUYXRx8YI6ZFU25_Q1hg-k98F_po7eKZ1jf5AjqzYRz_f1jPy-W73ePBRPv-4fb66fCi24SEVdSnsltW2RCUTW8goYGpRi2TKORi4Nr1hlEY1CJiVypQ1obgRvNSgr-RmZ73J18DEGtM2QP1Fh2zBoJqLNRLSZiDYT0Wy42BmGsX1H8y3fI8zzy_1cRa02Nqheu_gtKzmUANNeuZNhfu7DYWiidthrNC5k6I3x7n8X_ANzEZZd</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>Ohi, Takekazu</creator><creator>Saita, Kazuko</creator><creator>Furukawa, Shoei</creator><creator>Ohta, Mitsuhiro</creator><creator>Hayashi, Kyozo</creator><creator>Matsukura, Shigeru</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19980601</creationdate><title>Therapeutic Effects of Aldose Reductase Inhibitor on Experimental Diabetic Neuropathy through Synthesis/Secretion of Nerve Growth Factor</title><author>Ohi, Takekazu ; Saita, Kazuko ; Furukawa, Shoei ; Ohta, Mitsuhiro ; Hayashi, Kyozo ; Matsukura, Shigeru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-928f58cfbe14ee1b3601ede847b13ed87d3616feedae188e3acd0c3d43bc0af83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Aldehyde Reductase - antagonists &amp; inhibitors</topic><topic>aldose reductase inhibitor</topic><topic>Animals</topic><topic>Associated diseases and complications</topic><topic>Biological and medical sciences</topic><topic>Catechols - pharmacology</topic><topic>Cells, Cultured</topic><topic>Ciliary Neurotrophic Factor</topic><topic>CNTF</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Diabetic Neuropathies - drug therapy</topic><topic>Diabetic Neuropathies - metabolism</topic><topic>diabetic neuropathy</topic><topic>Electrophysiology</topic><topic>Endocrine pancreas. 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Diabetic rats showed a statistically significant reduction in H-wave-related sensory nerve conduction velocity (HSNCV) and in NGF content in sciatic nerves during the experiment of 8 weeks. No reduction in the CNTF content in sciatic nerves was seen in the diabetic rats. The epalrestat treatment, which started 4 weeks after STZ injection, resulted in a significantly greater NGF content and faster HSNCV than those in untreated diabetic rats. But no statistically significant alterations of motor nerve conduction velocity (MNCV) or CNTF content were seen during the treatment. ARI showed the stimulating effect for NGF synthesis/secretion in rat Schwann cell culturein vitro.These findings suggest that decreased levels of NGF in diabetic sciatic nerves may be involved in the pathogenesis of diabetic neuropathy in these rats and further show that epalrestat treatment can be useful for the treatment of diabetic neuropathy through NGF-induction in Schwann cells and/or inhibition of the polyol pathway.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>9628756</pmid><doi>10.1006/exnr.1998.6821</doi><tpages>6</tpages></addata></record>
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identifier ISSN: 0014-4886
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1090-2430
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source Elsevier
subjects Aldehyde Reductase - antagonists & inhibitors
aldose reductase inhibitor
Animals
Associated diseases and complications
Biological and medical sciences
Catechols - pharmacology
Cells, Cultured
Ciliary Neurotrophic Factor
CNTF
Diabetes. Impaired glucose tolerance
Diabetic Neuropathies - drug therapy
Diabetic Neuropathies - metabolism
diabetic neuropathy
Electrophysiology
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Enzyme Inhibitors - pharmacology
Male
Medical sciences
Nerve Growth Factors - biosynthesis
Nerve Growth Factors - secretion
Nerve Tissue Proteins - biosynthesis
Nerve Tissue Proteins - secretion
Neuroprotective Agents - pharmacology
NGF
Rats
Rats, Sprague-Dawley
Rhodanine - analogs & derivatives
Rhodanine - pharmacology
Schwann cell culture
Schwann Cells - cytology
Schwann Cells - drug effects
Schwann Cells - enzymology
Sciatic Nerve - chemistry
Sciatic Nerve - cytology
Sciatic Nerve - physiology
Thiazolidines
title Therapeutic Effects of Aldose Reductase Inhibitor on Experimental Diabetic Neuropathy through Synthesis/Secretion of Nerve Growth Factor
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