Literature DB >> 11405253

Gamma-diketone peripheral neuropathy III. Neurofilament gene expression.

L A Opanashuk1, D K He, E J Lehning, R M LoPachin.   

Abstract

Evidence suggests the morphologic hallmark of gamma-diketone neuropathy is axon atrophy and that this effect is associated with reduced neurofilament (NF) subunit protein content (Toxicol Appl Pharmacol 2000;165:141-7). To investigate the mechanism of diminished NF content, subunit (NF-L, -M and -H) gene expression was quantified in dorsal root ganglion (DRG) of slightly affected and moderately intoxicated groups of rats exposed to 2,5-hexanedione (HD) at one of three daily dosing rates (175, 250 and 400 mg/kg per day). Results show that sensory ganglia from slightly affected rats exhibited no changes in gene expression, whereas at a moderate level of neurotoxicity, each dosing protocol was associated with small but significant reductions (approximately 20%) in mean NF subunit mRNA. This was not a generalized effect on expression of cytoskeletal components in sensory ganglia since tubulin message levels were not affected. Although the observed reduction in NF gene expression might be related to diminished levels of subunit proteins in peripheral nerve, the actual contribution is likely to be minimal. The magnitude of effect was small and did not correspond to the dose-rate dependent effect of HD on respective isotype proteins. The mechanism of gamma-diketone-induced axon atrophy is unknown but might involve local changes in axonal NF phosphorylation and degradation.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11405253     DOI: 10.1016/s0161-813x(00)00011-5

Source DB:  PubMed          Journal:  Neurotoxicology        ISSN: 0161-813X            Impact factor:   4.294


  7 in total

Review 1.  Toxic neuropathies: Mechanistic insights based on a chemical perspective.

Authors:  Richard M LoPachin; Terrence Gavin
Journal:  Neurosci Lett       Date:  2014-09-16       Impact factor: 3.046

Review 2.  Neuroprotein Targets of γ-Diketone Metabolites of Aliphatic and Aromatic Solvents That Induce Central-Peripheral Axonopathy.

Authors:  Peter S Spencer
Journal:  Toxicol Pathol       Date:  2020-03-12       Impact factor: 1.902

3.  Application of the hard and soft, acids and bases (HSAB) theory as a method to predict cumulative neurotoxicity.

Authors:  Fjodor Melnikov; Brian C Geohagen; Terrence Gavin; Richard M LoPachin; Paul T Anastas; Phillip Coish; David W Herr
Journal:  Neurotoxicology       Date:  2020-05-05       Impact factor: 4.294

4.  2,5-Hexanedione induced decrease in cytoskeletal proteins of rat sciatic-tibial nerve.

Authors:  Tianliang Zhang; Xiulan Zhao; Zhenping Zhu; LiHua Yu; Xiaoying Han; Cuili Zhang; Keqin Xie
Journal:  Neurochem Res       Date:  2005-02       Impact factor: 3.996

5.  Probing mechanisms of axonopathy. Part II: Protein targets of 2,5-hexanedione, the neurotoxic metabolite of the aliphatic solvent n-hexane.

Authors:  Desire Tshala-Katumbay; Victor Monterroso; Robert Kayton; Michael Lasarev; Mohammad Sabri; Peter Spencer
Journal:  Toxicol Sci       Date:  2008-11-25       Impact factor: 4.849

6.  Carbon disulfide-induced changes in cytoskeleton protein content of rat cerebral cortex.

Authors:  Fuyong Song; Sufang Yu; Xiulan Zhao; Cuili Zhang; Keqin Xie
Journal:  Neurochem Res       Date:  2006-01       Impact factor: 3.996

7.  Time-dependent alteration of cytoskeletal proteins in cerebral cortex of rat during 2,5-hexanedione-induced neuropathy.

Authors:  Fuyong Song; Cuili Zhang; Sufang Yu; Xiulan Zhao; Lihua Yu; Keqin Xie
Journal:  Neurochem Res       Date:  2007-04-20       Impact factor: 3.996

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.