metallothionein has been researched along with Polyneuropathies* in 3 studies
2 review(s) available for metallothionein and Polyneuropathies
Article | Year |
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Hyperzincemia from ingestion of denture adhesives.
The purpose of this article is to review the recent literature that documents the serious adverse systemic effects of prolonged, excessive zinc ingestion from the overuse of denture adhesives. This condition causes elevation of serum zinc levels that result in depression of serum copper. The low serum copper levels cause bone marrow depression and widespread sensory and motor neuropathies. Epidemiologic studies revealed the source of excessive zinc intake to be from overuse of denture adhesives. Denture patients must be advised of the risks of prolonged overuse of denture adhesives. Topics: Adhesives; Copper; Denture Retention; Humans; Metallothionein; Polyneuropathies; Zinc | 2010 |
[Mechanisms of amyloid deposition].
Topics: Amyloid; Amyloidosis; Animals; Humans; Metallothionein; Mice; Mice, Transgenic; Polyneuropathies; Prealbumin; Serum Amyloid P-Component | 1991 |
1 other study(ies) available for metallothionein and Polyneuropathies
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Role of matrix metalloproteinases, proinflammatory cytokines, and oxidative stress-derived molecules in hepatitis C virus-associated mixed cryoglobulinemia vasculitis neuropathy.
Mixed cryoglobulinemia (MC) is a systemic vasculitis, usually associated with hepatitis C virus (HCV) infection. The molecular mechanisms responsible for HCV-associated MC (HCV-MC) vasculitis are largely unknown. This study was undertaken to assess the expression profile of selected genes involved in inflammatory vascular damage in patients with HCV-MC vasculitis, patients with polyarteritis nodosa (PAN), and patients with noninflammatory idiopathic neuropathy.. The quantitative expression levels of 42 selected genes involved in inflammatory vascular damage were assessed in nerve lesions of patients with HCV-MC vasculitis, PAN (rheumatic disease controls), and noninflammatory idiopathic neuropathy (noninflammatory neuropathy controls), using real-time reverse transcriptase-polymerase chain reaction. Genes were considered to be differentially expressed when there was a >2-fold difference in mean expression levels between groups and the P value was less than 0.05.. Expression levels of 8 genes were significantly increased in HCV-MC patients versus control patients with noninflammatory idiopathic neuropathy, with the highest increase for metallothionein 1 H (MT1H), a hypoxic and oxidative stress protein. Compared with PAN patients, HCV-MC patients had higher expression levels of genes encoding oxidative stress-derived molecules (MT1H, endothelial cell nitric oxide synthase 3, Hsp70, and Hsp90) and tissue plasminogen activator and lower expression levels of matrix metalloproteinase 7 (MMP-7). HCV-MC neuropathies were classified according to their morphologic pattern and the presence or absence of necrotizing arteritis. MMP-1, MMP-7, MMP-9, and interleukin-1beta were up-regulated in patients with necrotizing arteritis.. This comprehensive molecular study of HCV-MC vasculitis provides strong evidence that MMPs, proinflammatory cytokines, and oxidative stress-derived molecules have a role in the pathogenesis of HCV-MC vasculitis neuropathy. Topics: Adult; Aged; Chemokines; Cryoglobulinemia; Female; Gene Expression Profiling; Hepatitis C; HSP72 Heat-Shock Proteins; HSP90 Heat-Shock Proteins; Humans; Male; Metalloproteases; Metallothionein; Middle Aged; Nitric Oxide Synthase Type III; Oxidative Stress; Peroneal Nerve; Polyarteritis Nodosa; Polyneuropathies; Tissue Plasminogen Activator; Up-Regulation | 2007 |