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1.
Antioxid Redox Signal ; 13(5): 607-20, 2010 Sep 01.
Article in English | MEDLINE | ID: mdl-20070240

ABSTRACT

Oxidative stress due to increased epidermal levels of H(2)O(2) with consequent inhibition of catalase activity is generally accepted as a leading cytotoxic mechanism of melanocyte loss in vitiligo. Keratinocyte-derived cytokines are considered key factors in the maintenance of melanocyte structure and functions. We hypothesized that abnormal redox control may lead to impaired cytokine production by keratinocytes, thus causing noncytotoxic defects in melanocyte proliferation and melanogenesis. We found significantly suppressed mRNA and protein expression of glutathione-S-transferase (GST) M1 isoform, and higher-than-normal levels of both 4-hydroxy-2-nonenal (HNE)-protein adducts and H(2)O(2) in the cultures of keratinocytes derived from unaffected and affected skin of vitiligo patients, and in their co-cultures with allogeneic melanocytes. GST and catalase activities, as well as glutathione levels, were dramatically low in erythrocytes, whilst HNE-protein adducts were high in the plasma of vitiligo patients. The broad spectrum of major cytokines, chemokines, and growth factors was dysregulated in both blood plasma and cultured keratinocytes of vitiligo patients, when compared to normal subjects. Exogenous HNE added to normal keratinocytes induced a vitiligo-like cytokine pattern, and H(2)O(2) overproduction accompanied by adaptive upregulation of catalase and GSTM1 genes, and transient inhibition of Erk1/2 and Akt phosphorylation. Based on these results, we suggest a novel GST-HNE-H(2)O(2)-based mechanism of dysregulation of cytokine-mediated keratinocyte-melanocyte interaction in vitiligo.


Subject(s)
Aldehydes/metabolism , Cytokines/metabolism , Glutathione Transferase/metabolism , Hydrogen Peroxide/metabolism , Keratinocytes/metabolism , Vitiligo/blood , Vitiligo/metabolism , Adolescent , Adult , Aged , Aldehydes/blood , Aldehydes/pharmacology , Catalase/genetics , Catalase/metabolism , Child , Coculture Techniques , Cytokines/genetics , Erythrocytes/metabolism , Extracellular Signal-Regulated MAP Kinases/metabolism , Female , Fibroblast Growth Factor 2/genetics , Gene Expression/genetics , Gene Expression/radiation effects , Glutathione/metabolism , Glutathione Disulfide/metabolism , Glutathione Transferase/genetics , Humans , Interleukin-6/genetics , Interleukin-6/metabolism , Keratinocytes/cytology , Keratinocytes/drug effects , Keratinocytes/radiation effects , Male , Melanocytes/cytology , Middle Aged , Nitric Oxide Synthase Type II/genetics , Oxidation-Reduction , Phosphorylation/radiation effects , Proto-Oncogene Proteins c-akt/metabolism , SOXB1 Transcription Factors/genetics , Superoxide Dismutase/metabolism , Tumor Necrosis Factor-alpha/blood , Tumor Necrosis Factor-alpha/genetics , Tumor Suppressor Protein p53/metabolism , Ultraviolet Rays , Young Adult
2.
Cytokine ; 49(2): 163-70, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19879157

ABSTRACT

Psoriasis is a chronic recurrent inflammatory disorder of the skin. Clinical subtypes include psoriasis vulgaris (PV), psoriatic arthropathy, and erythrodermic psoriasis. Aim of this study was to analyse relevant inflammatory mediators in the plasma of patients with distinct subtypes of active psoriasis, and in the scales of mild-to-moderate PV patients, and correlation to disease severity. Compared to healthy controls (n=10), patients affected by very severe forms of psoriasis (n=30) were characterized by increased plasma levels of IL-4, IL-6, MCP-1, VEGF and in particular PDGFbb. Each group with severe psoriasis had distinct characteristic features of plasma cytokine profile. Mild-to-moderate PV patients (n=35) showed higher levels of IL-4, IL-6, IL-10, and IL-13 when compared to healthy controls. No correlation was found between PV severity assessed by PASI (Psoriasis Area and Severity Index) and levels of these mediators. By contrast, disease severity correlated to scale levels of IP-10. For the first time, we found exaggerated circulating levels of the pro-angiogenic PDGFbb and VEGF in severe psoriasis. Evidence that the severity of skin symptoms correlated exclusively with scale levels of IP-10, but not with any up-regulated inflammatory mediator in plasma, suggests that distinct skin-independent processes contribute to the circulating cytokine profile in psoriasis.


Subject(s)
Inflammation Mediators/blood , Psoriasis , Skin , Adult , Biomarkers/metabolism , Female , Humans , Inflammation Mediators/immunology , Male , Middle Aged , Psoriasis/blood , Psoriasis/immunology , Psoriasis/pathology , Skin/immunology , Skin/pathology
3.
Biofactors ; 18(1-4): 245-54, 2003.
Article in English | MEDLINE | ID: mdl-14695940

ABSTRACT

The manual workers of the gas-and-oil extraction industry are exposed to hostile environmental and occupational conditions, resulting in elevated mortality and disability, due to chronic neurological and cardiovascular diseases. We evaluated the degree of oxidative stress, often associated with these pathological features, in the blood of manual and office employees of Russian Siberian extraction plants, and their psycho-physiological conditions. Results showed increased levels of spontaneous (p < 0.05) and PMA-activated (p < 0.01) luminol-dependent chemiluminescence (LDCL) in the white blood cells (WBC), and decreased peroxynitrite levels (p < 0.05) in the group of manual workers, and less markedly in the clerks and technicians working on spot, vs. a control group of city clerks. Superoxide release by WBC, and plasma/WBC membrane ubiquinol levels did not display major differences in the three groups. A relevant percentage of manual/office workers of extraction platforms presented impaired cardiovascular and neurological functions. The short term administration of a nutraceutical formulation based on coenzyme10, vitamin E, selenium, methionine and phospholipids led to significant improvement of cardiovascular parameters and psycho-emotional status, consistent with the normalization of LDCL and peroxynitrite production by WBC, with a good compliance to treatment confirmed by the increased blood levels of ubiquinol.


Subject(s)
Environment , Occupational Exposure , Oxidative Stress , Petroleum , Ubiquinone/analogs & derivatives , Ubiquinone/administration & dosage , Adult , Cardiovascular Diseases/etiology , Cardiovascular Diseases/prevention & control , Coenzymes , Dietary Supplements , Emotions , Female , Humans , Industrial Oils , Leukocytes/physiology , Luminescent Measurements , Luminol/pharmacology , Male , Methionine/administration & dosage , Middle Aged , Nervous System Diseases/etiology , Nervous System Diseases/prevention & control , Peroxynitrous Acid/blood , Phospholipids/administration & dosage , Russia , Selenium/administration & dosage , Siberia , Superoxides/blood , Tetradecanoylphorbol Acetate/pharmacology , Ubiquinone/blood , Vitamin E/administration & dosage
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