Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 296
Filtrar
1.
Toxicol Appl Pharmacol ; 371: 12-19, 2019 05 15.
Artigo em Inglês | MEDLINE | ID: mdl-30928402

RESUMO

The increment of eryptosis in lead-exposed workers has been associated with oxidative stress, having as the main mediator [Ca2+]i. However, other molecules could participate as signals, such as PLA2 and SMase, which have been proposed to increase PGE2 and ceramides, both involved in the increment of PS externalization due to osmotic stress. To study the role of these enzymes in lead intoxication, we studied 30 lead exposed workers and 27 non-lead exposed individuals. We found, compared to non-exposed subjects, lead intoxication characterized by high blood lead concentration (median = 39.1 µg/dL), and low δ-ALAD activity (median = 348 nmol of porphobilinogen/h/mL); oxidative stress with high lipid peroxidation (median = 1.31 nmol of malondialdehyde/mL) and low TAC (median = 370 mM Trolox equivalents); a higher enzymatic activity of PLA2 (median = 518 AFU/mg) and SMase (median = 706 AFU/mg) and higher eryptosis (median = 0.92% PS externalization). Correlation and conditional probability analyses permit to associate oxidative stress and eryptosis with high PLA2 activity. However, high SMase activity was only associated with PLA2 activity. The role of these enzymes in the signal path to eryptosis induced by oxidative stress in lead-exposed workers is discussed.


Assuntos
Poluentes Ambientais/efeitos adversos , Eriptose/efeitos dos fármacos , Eritrócitos/efeitos dos fármacos , Intoxicação por Chumbo/etiologia , Chumbo/efeitos adversos , Exposição Ocupacional/efeitos adversos , Estresse Oxidativo/efeitos dos fármacos , Fosfolipases A2/sangue , Esfingomielina Fosfodiesterase/sangue , Adulto , Biomarcadores/sangue , Estudos de Casos e Controles , Poluentes Ambientais/sangue , Eritrócitos/enzimologia , Eritrócitos/patologia , Humanos , Chumbo/sangue , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Intoxicação por Chumbo/patologia , Peroxidação de Lipídeos/efeitos dos fármacos , Pessoa de Meia-Idade , Sintase do Porfobilinogênio/sangue , Medição de Risco , Transdução de Sinais , Adulto Jovem
2.
Toxicol Lett ; 295: 351-356, 2018 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-30025905

RESUMO

Lead is an environmental hazard with great public health concern and has been known to inhibit delta-aminolevulinate dehydratase (ALAD) activity involved in the heme biosynthetic pathway. The study aimed to investigate the influence of ALAD polymorphism (G177C) on retention of Pb-B levels and ALAD activity on occupationally exposed lead workers. In the present study, we enrolled 561 lead exposed and 317 non-occupationally exposed subjects and performed a comprehensive analysis of Pb-B levels along with ALAD activity and genotyping. The frequency of ALAD variants observed in the total subjects (n = 878) was 70.04% for ALAD 1-1, 27.44% for heterozygous ALAD 1-2 and 2.5% for homozygous mutant ALAD 2-2. Our study revealed that ALAD 1-2 carriers presented higher Pb-B levels compared to wild type ALAD 1-1 carriers. Further, a significant difference was observed in the activity of ALAD between ALAD 1-2/ 2-2 and ALAD 1-1 carriers of non-occupationally exposed group indicating that the polymorphic nature of the enzyme may contribute to altered activity of ALAD irrespective of lead exposure. Hence, ALAD 2 allele might contribute to increased susceptibility to high Pb-B retention, and genotyping of ALAD in lead exposed subjects might be used as a prediction marker to impede tissue/organ damage due to lead toxicity.


Assuntos
Poluentes Ocupacionais do Ar/sangue , Intoxicação por Chumbo/genética , Chumbo/sangue , Polimorfismo Genético , Sintase do Porfobilinogênio/genética , Adolescente , Adulto , Poluentes Ocupacionais do Ar/efeitos adversos , Estudos de Casos e Controles , Estudos Transversais , Feminino , Frequência do Gene , Estudos de Associação Genética , Predisposição Genética para Doença , Heterozigoto , Homozigoto , Humanos , Índia , Chumbo/efeitos adversos , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Masculino , Pessoa de Meia-Idade , Exposição Ocupacional/efeitos adversos , Fenótipo , Sintase do Porfobilinogênio/metabolismo , Medição de Risco , Fatores de Risco , Adulto Jovem
3.
Acta Physiol Hung ; 101(1): 59-66, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24631795

RESUMO

UNLABELLED: This study is to explore the effect of ALAD polymorphism on hematopoietic, hepatic and renal toxicity from lead in occupational exposure workers. METHODS: We conducted a cross-sectional study on 156 workers with occupational exposure to lead between 2002 and 2007. The results of laboratory examinations were analyzed. RESULTS: The authors found that workers with the ALAD 1-1 genotype were associated with higher blood lead level than those with the ALADl-2 genotype. Blood and urine lead levels were much higher in storage battery workers than in cable workers. The urine ALA and blood ZPP levels in workers with the ALAD 1-1 genotype were higher than those with the ALADl-2 genotype. The serum Cr level in workers with the ALADl-1 genotype was much higher than those with the ALADl-2 genotype especially in higher lead exposure level. CONCLUSIONS: The ALAD-2 protein might modify the kinetics of lead in blood at a relatively higher blood lead level and protect against hematopoietic, hepatic and renal toxicity from lead. Urine ALA, blood ZPP and serum Cr levels might be considered as effective biological monitoring partners of lead induced hematopoietic and renal toxicology.


Assuntos
Povo Asiático/genética , Hematopoese/efeitos dos fármacos , Nefropatias/genética , Intoxicação por Chumbo/genética , Hepatopatias/genética , Doenças Profissionais/genética , Polimorfismo Genético , Sintase do Porfobilinogênio/genética , Adulto , Ácido Aminolevulínico/urina , Biomarcadores/sangue , Biomarcadores/urina , China/epidemiologia , Creatinina/sangue , Estudos Transversais , Feminino , Frequência do Gene , Predisposição Genética para Doença , Humanos , Nefropatias/sangue , Nefropatias/enzimologia , Nefropatias/etnologia , Nefropatias/urina , Chumbo/sangue , Chumbo/urina , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Intoxicação por Chumbo/etnologia , Intoxicação por Chumbo/urina , Hepatopatias/sangue , Hepatopatias/enzimologia , Hepatopatias/etnologia , Hepatopatias/urina , Masculino , Pessoa de Meia-Idade , Doenças Profissionais/sangue , Doenças Profissionais/enzimologia , Doenças Profissionais/etnologia , Doenças Profissionais/urina , Exposição Ocupacional , Fenótipo , Sintase do Porfobilinogênio/metabolismo , Protoporfirinas/sangue , Fatores de Risco , Adulto Jovem
4.
J Toxicol Environ Health A ; 76(15): 895-906, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24156693

RESUMO

Lead (Pb) body burden and toxicity may be influenced by genetic polymorphisms. The aim of this study was to investigate the influence of G177C delta-aminolevulinic acid dehydratase (ALAD) polymorphism (rs1800435) on selected Pb exposure biomarkers in a population of workers highly exposed to this metal in the past. A cross-sectional survey was conducted between 2007 and 2009 within the cohort of ex-employees of a smelter in the north of France that closed down in 2003. A questionnaire was completed by each participant and blood samples enabled determination of Pb levels and ALAD polymorphism. Five parameters estimating the Pb body burden and its variations were studied: last blood lead level (BLL) during activity, cumulative blood Pb index, BLL at the time of the study, and absolute and percent changes in BLL after cessation of metal exposure. Multiple regression models were used to evaluate links between ALAD polymorphism and the selected Pb exposure biomarkers. Two hundred and four men were included. At the time of inclusion, the median age was 53.5 yr. The median duration of Pb exposure was 25 yr and the median latency since end of exposure was 5.6 yr. The frequency of ALAD-2 allele was 9.3%, with 34 subjects being heterozygous (ALAD1-2) and 2 homozygous (ALAD2-2). According to genotype, there was no significant difference for any of the five selected Pb exposure biomarkers. These results lend support to the notion that ALAD polymorphism exerts no marked impact on Pb body burden.


Assuntos
Predisposição Genética para Doença , Intoxicação por Chumbo/genética , Metalurgia , Doenças Profissionais/genética , Exposição Ocupacional/efeitos adversos , Polimorfismo Genético , Sintase do Porfobilinogênio/genética , Biomarcadores/sangue , Carga Corporal (Radioterapia) , Estudos de Coortes , Estudos Transversais , Humanos , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Masculino , Pessoa de Meia-Idade , Doenças Profissionais/sangue , Doenças Profissionais/enzimologia , Sintase do Porfobilinogênio/metabolismo , Inquéritos e Questionários , Fatores de Tempo
5.
Biomed Res Int ; 2013: 474963, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23484121

RESUMO

A number of studies suggested that lead is related to the induction of oxidative stress, and alteration of immune response. In addition, modifying these toxic effects varied partly by GST polymorphism. The objectives of this study were to assess the association between the lead-induced alteration in serum hs-CRP, with GSTM1, GSTT1, and GSTP1 Val105Ile genetic variations and the health consequence from environmental lead exposure. The 924 blood samples were analyzed for blood lead, CRP, and genotyping of three genes with real-time PCR. Means of blood lead and serum hs-CRP were 5.45 µ g/dL and 2.07 mg/L. Both CRP and systolic blood pressure levels were significantly higher for individuals with blood lead in quartile 4 (6.48-24.63 µ g/dL) compared with those in quartile 1 (1.23-3.47 µ g/dL, P < 0.01). In particular, in men with blood lead >6.47 µ g/dL the adjusted odds ratio (OR) of CRP levels for individuals with GSTP1 variants allele, GSTM1 null, GSTT1 null, double-null GSTM1, and GSTT1 compared with wild-type allele was 1.46 (95% CI; 1.05-2.20), 1.32 (95% CI; 1.03-1.69), 1.65 (95% CI; 1.17-2.35), and 1.98 (95% CI; 1.47-2.55), respectively. Our findings suggested that lead exposure is associated with adverse changes in inflammatory marker and SBP. GST polymorphisms are among the genetic determinants related to lead-induced inflammatory response.


Assuntos
Exposição Ambiental/efeitos adversos , Glutationa S-Transferase pi/genética , Glutationa Transferase/genética , Intoxicação por Chumbo , Chumbo/farmacocinética , Polimorfismo Genético , Adulto , Alelos , Substituição de Aminoácidos , Biomarcadores/sangue , Pressão Sanguínea/efeitos dos fármacos , Pressão Sanguínea/genética , Proteína C-Reativa/genética , Proteína C-Reativa/metabolismo , Glutationa S-Transferase pi/sangue , Glutationa Transferase/sangue , Humanos , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Intoxicação por Chumbo/genética , Masculino , Pessoa de Meia-Idade , Estresse Oxidativo/efeitos dos fármacos , Estresse Oxidativo/genética
6.
Toxicology ; 306: 68-73, 2013 Apr 05.
Artigo em Inglês | MEDLINE | ID: mdl-23429061

RESUMO

Lead is a renal toxin, and susceptibility to lead varies between individuals. Metallothionein (MT) is known for its metal scavenging role. The aim of the study was to investigate the association of blood lead levels, urinary uric acid (UA) and N-acetyl-beta-d-glucosaminidase (NAG) in chronic occupational lead-exposed workers, and to study whether the association was influenced by MT1A gene polymorphisms. In this cross-sectional study, 412 lead-exposed workers participated. Their annual health examination data and renal function markers were collected after the Institutional Review Broad of Kaohsiung Medical University Hospital approved the study and consent letters were obtained. From the blood samples, DNA was extracted and used for real-time PCR typing of 2 MT1A single nucleotide polymorphisms (SNPs): rs11640851 and rs8052394 on exons 2 and 3. Descriptive analysis, one-way ANOVA, and multiple linear regressions were performed. There was a significant inverted relationship of creatinine-adjusted urine UA concentrations and the time-weighted index of cumulative blood lead levels (TWICL) that may be significantly influenced by the AC genotypes of rs11640851 in exon 2 and rs8052394 in exon 3. After controlling for potential confounding factors, the creatinine-adjusted urine NAG concentrations were shown to be influenced by the GG genotype of rs8052394 in exon 3, and were weakly increased with TWICL. Therefore, we concluded that the variations of MT1A SNPs may influence urine UA and NAG excretion in chronic lead-exposed workers, and urine creatinine-adjusted urine UA as a biomarker of lead toxicity should be considered.


Assuntos
Acetilglucosaminidase/urina , Intoxicação por Chumbo/urina , Metalotioneína/genética , Metalotioneína/metabolismo , Doenças Profissionais/urina , Exposição Ocupacional/efeitos adversos , Ácido Úrico/urina , Adulto , Alelos , Biomarcadores/urina , Estudos Transversais , DNA/química , DNA/genética , Feminino , Genótipo , Humanos , Intoxicação por Chumbo/enzimologia , Intoxicação por Chumbo/genética , Modelos Lineares , Masculino , Doenças Profissionais/induzido quimicamente , Doenças Profissionais/enzimologia , Doenças Profissionais/genética , Reação em Cadeia da Polimerase , Polimorfismo de Nucleotídeo Único , Estudos Prospectivos , Estudos Retrospectivos
7.
J Toxicol Environ Health A ; 75(13-15): 807-18, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22788368

RESUMO

Although adverse health effects produced by lead (Pb) have long been recognized, studies regarding the immunotoxic effects of occupational exposure report conflicting results. In a previous study, alterations in some immunological parameters were noted in 70 Pb-exposed workers. In view of these results, it was of interest to extend this study comprising a larger population and increasing the number of immunological endpoints assessed. Accordingly, in this study the immunotoxic effects of occupational exposure to Pb were assessed by analyzing (1) percentages of lymphocyte subsets (CD3⁺, CD4⁺, CD8⁺, CD19⁺, and CD56⁺/16⁺); (2) concentration of plasma cytokines, namely, interleukin (IL) 2, IL4, IL6, IL10, tumor necrosis factor (TNF) α, and interferon (IFN) γ; and (3) plasma concentrations of neopterin, tryptophan (Trp), and kynurenine (Kyn). In addition, the possible influence of genetic polymorphisms in the vitamin D receptor (VDR) and δ-aminolevulinic acid dehydratase (ALAD) genes on immunotoxicity parameters was studied. Exposed workers showed significant decreases in %CD3⁺, %CD4⁺/%CD8⁺ ratio, IL4, TNFα, IFNγ, and Kyn to Trp ratio (Kyn/Trp), and significant increases in %CD8⁺, IL10, and Trp levels. All these parameters, except Trp, were significantly correlated with exposure biomarkers. No significant influence of genetic polymorphisms was observed. Significant correlation between Kyn/Trp and neopterin concentrations suggests an involvement of indoleamine 2,3-dioxygenase in the Trp metabolic alterations, which may contribute to some of the immune alterations observed. Results obtained suggest that occupational exposure to PB may influence the immune system by impairing several mechanisms, which might ultimately produce deregulation of the immune response and diminish immunosurveillance in exposed individuals.


Assuntos
Imunossupressores/toxicidade , Intoxicação por Chumbo/imunologia , Chumbo/toxicidade , Exposição Ocupacional , Adulto , Biomarcadores/sangue , Citocinas/sangue , Estudos de Associação Genética , Humanos , Imunossupressores/sangue , Indústrias , Cinurenina/sangue , Chumbo/sangue , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Intoxicação por Chumbo/genética , Subpopulações de Linfócitos/efeitos dos fármacos , Subpopulações de Linfócitos/imunologia , Masculino , Pessoa de Meia-Idade , Neopterina/sangue , Polimorfismo Genético , Sintase do Porfobilinogênio/sangue , Sintase do Porfobilinogênio/genética , Portugal , Receptores de Calcitriol/sangue , Receptores de Calcitriol/genética , Fumar/sangue , Espanha , Triptofano/sangue
8.
Toxicol Lett ; 203(1): 48-53, 2011 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-21396434

RESUMO

DNA methylation provides a plausible link between the environment and alterations in gene expression that may lead to disease phenotypes. Lead exposure can change DNA methylation status. Here, we hypothesized that the methylation of the ALAD gene promoter may play an important role in lead toxicity. To determine whether the methylation level of the ALAD promoter is associated with the risk of lead poisoning, we conducted a case-control study of 103 workers from a battery plant and 103 healthy volunteers with matching age and gender distribution. We employed real-time PCR and methylation-specific PCR (MSP) in cell models to determine the relationship between ALAD methylation level and transcription level. We found lead exposure to increase the ALAD gene methylation level and down-regulate ALAD transcription. The difference in methylation frequencies between exposures and controls was statistically significant (p=0.002), and individuals with methylated ALAD gene showed an increased risk of lead poisoning (adjusted OR=3.57, 95% CI, 1.55-8.18). This study suggests that the lead-exposure-induced increases in ALAD methylation may be involved in the mechanism of lead toxicity.


Assuntos
Ilhas de CpG/efeitos dos fármacos , Metilação de DNA/efeitos dos fármacos , Fontes de Energia Elétrica , Poluentes Ambientais/efeitos adversos , Intoxicação por Chumbo/genética , Chumbo/efeitos adversos , Sintase do Porfobilinogênio/genética , Regiões Promotoras Genéticas/efeitos dos fármacos , Transcrição Gênica/efeitos dos fármacos , Estudos de Casos e Controles , Distribuição de Qui-Quadrado , China , DNA (Citosina-5-)-Metiltransferases/genética , DNA (Citosina-5-)-Metiltransferases/metabolismo , Poluentes Ambientais/sangue , Poluentes Ambientais/toxicidade , Repressão Enzimática , Células Hep G2 , Hepatócitos/efeitos dos fármacos , Hepatócitos/enzimologia , Humanos , Chumbo/sangue , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Modelos Logísticos , Exposição Ocupacional , Razão de Chances , Compostos Organometálicos/toxicidade , Reação em Cadeia da Polimerase , Sintase do Porfobilinogênio/biossíntese , RNA Mensageiro/biossíntese , Medição de Risco , Fatores de Risco , Transfecção , DNA Metiltransferase 3B
9.
Biotech Histochem ; 86(6): 436-43, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21039307

RESUMO

Female Wistar-albino rats were given lead acetate (PbAc) for 60 days to investigate the protective effects of L-carnitine (CA) clinically and histopathologically on PbAc-induced tissue damage. Blood samples were obtained from the jugular vein for hemoglobin (HB), hematocrit (HCT), red blood cells (RBC), white blood cells (WBC), platelets (PLT), aspartate aminotransferase (AST), alanine aminotransferase (ALT) and creatinine. PbAc treatment caused a significant decrease in HB, HCT and RBC, a significant increase in WBC, AST, ALT and creatinine compared to controls. Although administration of CA did not reverse HB and HCT values, it reversed both the decrease in RBC and the increase in WBC, AST, ALT and creatinine. After the experimental period, all rats were weighed, then decapitated for pathological examination. Control rat liver, kidney and brain showed normal histological architecture. Lead-induced nephropathic kidneys; degenerative changes, inflammation and portal edema of the liver; and brain neuropil vacuolation, neuronal vacuolation, satellitosis and neuronophagia were observed in experimental groups. All changes were reduced in the PbAc group treated with CA (PbAc + CA). PbAc caused copper/zinc superoxide dismutase (Cu/Zn-SOD) expression in both the hepatocytes and tubular epithelium of the kidney. PbAc + CA exposure caused moderate Cu/Zn-SOD immunoreactivity. While in the brain sections of the PbAc group the degenerative neurons were stained intensely with anti-ubiquitin antibody, PbAc + CA rats showed moderate staining in neurons with anti-ubiquitin antibody. These results show that CA as a food additive reduced the severity of tissue damage caused by PbAc.


Assuntos
Encefalopatias/prevenção & controle , Carnitina/farmacologia , Doença Hepática Induzida por Substâncias e Drogas/patologia , Enzimas/metabolismo , Nefropatias/prevenção & controle , Intoxicação por Chumbo/patologia , Intoxicação por Chumbo/prevenção & controle , Animais , Células Sanguíneas/efeitos dos fármacos , Células Sanguíneas/metabolismo , Encefalopatias/induzido quimicamente , Encefalopatias/patologia , Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Enzimas/sangue , Enzimas/efeitos dos fármacos , Hematologia , Imuno-Histoquímica , Nefropatias/induzido quimicamente , Nefropatias/patologia , Intoxicação por Chumbo/enzimologia , Compostos Organometálicos/toxicidade , Ratos , Ratos Wistar , Superóxido Dismutase/efeitos dos fármacos , Superóxido Dismutase/metabolismo
10.
Wei Sheng Yan Jiu ; 39(5): 643-6, 2010 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-21033449

RESUMO

Lead (Pb) is a toxic heavy metal which exists widely in the environment. Children, pregnant women, the elderly, and other populations, have diverse ways of lead exposure and different toxicokinetics. Moreover, the exposure and effect of lead involve multiple metabolic pathways and mechanisms. Besides ALAD, VDR, HFE genes, the polymorphisms of TF gene and oxidative-stress related genes (Rac2, GPx1, XDH) have been discovered recently to affect lead internal exposure level as well. This review comprehensively describes the characteristics of lead exposure, metabolic characteristics and the lead exposure sensitive markers, of different people groups, and looks forward to the future of the application of Genome-Wide Association Study (GWAS) in this field.


Assuntos
Exposição Ambiental/efeitos adversos , Predisposição Genética para Doença , Intoxicação por Chumbo/genética , Chumbo/toxicidade , Farmacogenética , Biotransformação , Poluentes Ambientais/toxicidade , Expressão Gênica , Humanos , Intoxicação por Chumbo/enzimologia
11.
Food Chem Toxicol ; 48(10): 2688-94, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20600524

RESUMO

Several environmental toxins with toxic effects to the bone marrow have been identified. Pathology associated with lead intoxication is due to the cellular damage mediated by free radicals. In the current study, we examined the effect of Etlingera elatior extract on lead-induced changes in the oxidative biomarkers and histology of bone marrow of rats. Sprague-Dawley rats were exposed to 500 ppm lead acetate in their drinking water for 14 days. E. elatior extract was treated orally (100mg/kg body weight) in combination with, or after lead acetate treatment. The results showed that there was a significant increase in lipid hydroperoxide, protein carbonyl content and a significant decrease in total antioxidants, super oxide dismutase, glutathione peroxidase and glutathione--S-transferase in bone marrow after lead acetate exposure. Treatment with E. elatior decreased lipid hydroperoxides and protein carbonyl contents and significantly increased total antioxidants and antioxidant enzymes. Treatments with E. elatior extract also reduced, lead-induced histopathological damage in bone marrow. In conclusion, these data suggest that E. elatior has a powerful antioxidant effect, and it protects the lead acetate-induced bone marrow oxidative damage in rats.


Assuntos
Medula Óssea/metabolismo , Intoxicação por Chumbo/prevenção & controle , Compostos Organometálicos/toxicidade , Estresse Oxidativo/efeitos dos fármacos , Substâncias Protetoras , Zingiberaceae/química , Fosfatase Alcalina/metabolismo , Animais , Biomarcadores , Medula Óssea/efeitos dos fármacos , Medula Óssea/enzimologia , Etanol , Glutationa Peroxidase/metabolismo , Glutationa Transferase/metabolismo , Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Intoxicação por Chumbo/patologia , Peroxidação de Lipídeos/efeitos dos fármacos , Peróxidos Lipídicos/metabolismo , Masculino , Extratos Vegetais/uso terapêutico , Carbonilação Proteica/efeitos dos fármacos , Ratos , Ratos Sprague-Dawley , Espécies Reativas de Oxigênio/metabolismo , Solventes , Superóxido Dismutase/metabolismo
12.
J Biol Chem ; 284(51): 35807-17, 2009 Dec 18.
Artigo em Inglês | MEDLINE | ID: mdl-19812033

RESUMO

Porphobilinogen synthase (PBGS) catalyzes the first common step in tetrapyrrole (e.g. heme, chlorophyll) biosynthesis. Human PBGS exists as an equilibrium of high activity octamers, low activity hexamers, and alternate dimer configurations that dictate the stoichiometry and architecture of further assembly. It is posited that small molecules can be found that inhibit human PBGS activity by stabilizing the hexamer. Such molecules, if present in the environment, could potentiate disease states associated with reduced PBGS activity, such as lead poisoning and ALAD porphyria, the latter of which is associated with human PBGS variants whose quaternary structure equilibrium is shifted toward the hexamer (Jaffe, E. K., and Stith, L. (2007) Am. J. Hum. Genet. 80, 329-337). Hexamer-stabilizing inhibitors of human PBGS were identified using in silico prescreening (docking) of approximately 111,000 structures to a hexamer-specific surface cavity of a human PBGS crystal structure. Seventy-seven compounds were evaluated in vitro; three provided 90-100% conversion of octamer to hexamer in a native PAGE mobility shift assay. Based on chemical purity, two (ML-3A9 and ML-3H2) were subjected to further evaluation of their effect on the quaternary structure equilibrium and enzymatic activity. Naturally occurring ALAD porphyria-associated human PBGS variants are shown to have an increased susceptibility to inhibition by both ML-3A9 and ML-3H2. ML-3H2 is a structural analog of amebicidal drugs, which have porphyria-like side effects. Data support the hypothesis that human PBGS hexamer stabilization may explain these side effects. The current work identifies allosteric ligands of human PBGS and, thus, identifies human PBGS as a medically relevant allosteric enzyme.


Assuntos
Sintase do Porfobilinogênio/química , Regulação Alostérica/fisiologia , Humanos , Intoxicação por Chumbo/enzimologia , Ligantes , Sintase do Porfobilinogênio/metabolismo , Porfirias/enzimologia , Estrutura Quaternária de Proteína/fisiologia
13.
Georgian Med News ; (172-173): 92-6, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19644200

RESUMO

Lead is a ubiquitous environmental toxin that is capable of causing numerous acute and chronic circulatory, neurological, hematological, gastrointestinal, reproductive and immunological pathologies. The mechanism of lead induced toxicity is not fully understood. The prime targets to lead toxicity are the heme synthesis enzymes, thiol-containing antioxidants and enzymes (superoxide dismutase, catalase, glutathione peroxidase, glucose 6-phosphate dehydrogenase and antioxidant molecules like GSH). The low blood lead levels are sufficient to inhibit the activity of these enzymes and induce generation of reactive oxygen species and intensification oxidative stress. Oxidative stress plays important role in pathogenesis of lead-induced toxicity and pathogenesis of coupled disease. The primary target of lead toxicity is the central nervous system. There are different cellular, intracellular and molecular mechanisms of lead neurotoxicity: such as induction of oxidative stress, intensification of apoptosis of neurocites, interfering with Ca(2+) dependent enzyme like nitric oxide synthase. Population studies have demonstrated a link between lead exposure and subsequent development of hypertension and cardiovascular disease. The vascular endothelium is now regarded as the main target organ for the toxic effect of lead. Lead affects the vasoactive function of endothelium through the increased production of reactive oxygen species, inactivation of endogenous nitric oxide and downregulation of soluble guanylate cyclase by reactive oxygen species, leading to a limiting nitric oxide availability, impairing nitric oxide signaling. This review summarizes recent findings of the mechanism of the lead-induced toxicity and possibilities of its prevention.


Assuntos
Exposição Ambiental , Intoxicação por Chumbo/enzimologia , Chumbo/toxicidade , Doenças Profissionais/enzimologia , Endotélio Vascular/efeitos dos fármacos , Humanos , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/prevenção & controle , Doenças Profissionais/sangue , Doenças Profissionais/prevenção & controle , Estresse Oxidativo
14.
Artigo em Chinês | MEDLINE | ID: mdl-19351468

RESUMO

OBJECTIVE: To establish the methods of calculating and analyzing the multi-coefficient of variation significance test for the toxicology study. METHODS: The paper aimed to confirm the significance level with the method of Bonferroni and then compared the methods of calculating and analyzing of the experiment groups with the control group respectively. RESULTS: The significance level of multi-coefficient of variation significance test was confirmed as alpha1=0.0167. Compared with the control groups, the activity of ALT in serum both in 30 mg/kg and 60 mg/kg groups did not change in the average significance test, which was not statistically significant (P>0.05), while it changed in the variation significance test, which was of statistical significance (P<0.0167). The activity of AST in serum in 60 mg/kg group did not change in the average significance test (P>0.05), while it changed in the variation significance test (P<0.0167). CONCLUSION: The complete changes of the indexes can only be shown by use of both the average significance test and the variation significance test together.


Assuntos
Intoxicação por Chumbo/enzimologia , Distribuições Estatísticas , Alanina Transaminase/sangue , Animais , Aspartato Aminotransferases/sangue , Modelos Animais de Doenças , Feminino , Ratos , Ratos Wistar
15.
Biol Trace Elem Res ; 130(2): 95-106, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19183866

RESUMO

UNLABELLED: The study population included employees of metal works, with significant exposure to lead (Pb) for about 20 years (mean blood lead level PbB = 43 microg/dl), divided into four groups: normotensive (Pb-normotensive), high-normotensive, first (HT-1), and second degree (HT-2) of hypertension. The control group comprised of 30 office workers with normal blood pressure and no history of occupational exposure to lead. In erythrocytes, the activity of antioxidant enzymes and lipid peroxidation (measured as concentration of malondialdehyde (MDA)) was estimated. MDA concentration, glutathione peroxide (GPx), and superoxide dimutase (SOD) activities were significantly higher in Pb-normotensive group when compared to the normotensive control. Body mass index, age, duration of exposure to lead, and PbB were higher in both hypertensive groups than in Pb-normotensive or high-normotensive groups. MDA increased in HT-1 group by 48% and in HT-2 by 72%, and the activity of GPx decreased significantly in HT-1 group, by 30% and in HT-2 by 43%. No significant differences were observed in their activity of SOD, catalase, and glutathione reductase in erythrocytes. Arterial blood pressure (both systolic and diastolic) positively correlated with body mass index (BMI), age, lead exposure duration, PbB, MDA, and negatively correlated with GPx. There was no significant correlation between BMI and MDA, BMI and GPx, age and MDA, AND age and GPx. IN CONCLUSION: (1) lead increases erythrocyte MDA concentration and the activity of GPx as well as SOD in normotensive subjects. (2) Among individuals exposed to lead, with arterial hypertension diagnosed, higher body mass index, age, values of blood lead level, and prolonged exposure to lead have been noticed, accompanied by intensified oxidative stress and the decrease in the activity of glutathione peroxidase in erythrocytes. The reasons for increase of blood pressure in lead exposure remain unrecognized.


Assuntos
Eritrócitos/enzimologia , Hipertensão/etiologia , Intoxicação por Chumbo/enzimologia , Chumbo/toxicidade , Exposição Ocupacional , Adulto , Antioxidantes/análise , Catalase/análise , Catalase/metabolismo , Glutationa Peroxidase/análise , Glutationa Redutase/análise , Glutationa Redutase/metabolismo , Humanos , Hipertensão/sangue , Hipertensão/enzimologia , Chumbo/sangue , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/complicações , Malondialdeído/sangue , Pessoa de Meia-Idade , Protoporfirinas/sangue , Superóxido Dismutase/análise , Superóxido Dismutase/metabolismo
16.
C R Biol ; 330(8): 581-8, 2007 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-17637439

RESUMO

Lead toxicity is closely related to its accumulation in several tissues and its interference with bioelements, whose role is critical for several biological processes. Recently, oxidative stress has been proposed as a possible mechanism involved in lead toxicity. This study was carried out to investigate the effect of dose-dependent lead exposure on haematological and oxidative stress parameters. Adult male 'Wistar' rats (150-200 g) were divided into three groups: group [Pb 5] and group [Pb 15] received respectively 5 mg Pb(2+) (n=16) and 15 mg Pb(2+)/kg b.w. (n=16) as lead acetate solution i.p. for a period of seven days. Group [T] (n= 16) served as control and received 15 mg Na(+)/kg b.w. as sodium acetate solution i.p. for the same period. All animals were sacrificed 24 h after the last injection. Blood superoxide dismutase (SOD) and blood glutathione peroxidase (GPx) activities and plasma bilirubin level were measured. Liver was quickly excised for the estimation of alteration in lipid peroxidation indices (MDA). Lead exposure induces, in both treated groups, a marked decline in haematocrit and haemoglobin levels (p<0.01) when compared to control. The results show also a significant decrease (p<0.01) in SOD activity, but only in group [Pb 15]. SOD activity did not decrease in group [Pb 5] in comparison with control (p>0.05). However, lead exposure caused a light increase in GPx activity in group [Pb 15], which remains non-significant (p>0.05) compared to control. Group [Pb 5] did not record significant changes in the activity of GPx. Lead exposure for a period of seven days resulted in a significant (p<0.05) increase in bilirubin level in group [Pb 15] compared to control. The bilirubin level from rats of group [Pb 5] did not reach a statistical significance. Changes in liver MDA content in lead-exposed rats from [Pb 5] and [Pb 15] groups did not reach a statistical (p<0.05) significance. It is concluded that lead induces oxidative stress in a dose-dependent manner. No dose-dependent response was observed in blood GPx activity and liver MDA content. These results could be due to the short duration of the treatment.


Assuntos
Antioxidantes/metabolismo , Bilirrubina/sangue , Intoxicação por Chumbo/metabolismo , Animais , Peso Corporal/efeitos dos fármacos , Eritrócitos/efeitos dos fármacos , Eritrócitos/enzimologia , Glutationa Peroxidase/sangue , Glutationa Peroxidase/efeitos dos fármacos , Hemoglobinas/metabolismo , Intoxicação por Chumbo/enzimologia , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/efeitos dos fármacos , Fígado/fisiopatologia , Masculino , Estresse Oxidativo , Ratos , Ratos Wistar , Superóxido Dismutase/sangue , Superóxido Dismutase/efeitos dos fármacos
17.
Int J Environ Res Public Health ; 3(4): 329-37, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17159274

RESUMO

The aim of this study was to estimate the activity of superoxide dismutase (SOD) and catalase in erythrocytes and malondialdehyde (MDA) in plasma of battery manufacturing workers (BMW) of Western Maharashtra (India) who were occupationally exposed to lead (Pb) over a long period of time (about 15 years). This study was also aimed to determine the Pb intoxication resulted in a disturbance of heme biosynthesis in BMW group. The blood Pb level of BMW group (n = 28) was found to be in the range of 25.8 - 78.0 microg/dL (mean + SD, 53.63 + 16.98) whereas in Pb unexposed control group (n = 35) the range was 2.8 - 22.0 microg/dL (mean + SD, 12.52 + 4.08). The blood level (Pb-B) and urinary lead level (Pb-U) were significantly increased in BMW group as compared to unexposed control. Though activated d- aminolevulinic acid dehydratase (ALAD) activities in BMW group did not show any significant change when compared to control group but activated / non activated erythrocyte - ALAD activities in BMW group showed a significant increase. Erythrocyte- zinc protoporphyrin (ZPP), urinary daminolevulinic acid (ALA-U) and porphobilinogen (PBG-U) of BMW groups elevated significantly as compared to control. A positive correlation (r = 0.66, p < 0.001) between Pb-B and ALA-U were found in BMW group but no such significant correlation (r = 0.02, p> 1.0) were observed in control group. Hematological study revealed a significant decrease of hemoglobin concentration, packed cell volume (%) and other blood indices and a significant increase of total leucocytes count in BMW group in comparison to control group. The serum MDA content was significantly increased (p < 0.001) and the activities of antioxidant enzymes such as erythrocyte- SOD (p < 0.001) and erythrocytecatalase (p < 0.001) were significantly reduced in BMW group as compared to control group. A positive correlation (r = 0.45, p < 0.02) between Pb-B and serum MDA level was observed in BMW group (Pb-B range 25.8 - 78.0 microg / dL) but such significant correlation did not notice in control group (Pb-B range 2.8 - 22.0 microg / dL). The study clearly showed an adverse effect of heme biosynthesis and imbalance of pro-oxidant / antioxidant status in lead exposed battery manufacturing workers resulting in increase in lipid peroxidation associated with decrease in erythrocyte-SOD and erythrocyte-catalase activities.


Assuntos
Catalase/metabolismo , Heme/biossíntese , Chumbo/sangue , Chumbo/toxicidade , Exposição Ocupacional/análise , Superóxido Dismutase/metabolismo , Adulto , Estudos de Casos e Controles , Catalase/sangue , Eritrócitos/química , Eritrócitos/enzimologia , Humanos , Índia , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/enzimologia , Masculino , Malondialdeído/sangue , Metalurgia , Doenças Profissionais/sangue , Doenças Profissionais/enzimologia , Superóxido Dismutase/sangue
18.
Hum Exp Toxicol ; 25(9): 547-53, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17017008

RESUMO

To explore lead-induced oxidative stress among urban adolescents, the present study, the first from India, was designed to determine the proportion of urban adolescents with blood lead >10 microg/dL and its impact on selected oxidative stress parameters and delta-aminolevulinic acid dehydratase (delta-ALAD) inhibition, which could be used as biomarkers of lead intoxication. A total of 39, urban, male adolescents, drawn from Lucknow and adjoining areas, were recruited to determine lead, delta-ALAD, malondialdehyde (MDA) and glutathione (GSH) in blood and catalase (CAT) in RBCs. Mean level of blood lead was 9.96 +/- 3.63 microg/dL (4.62-18.64); 43% of adolescents crossed the Centre for Disease Control (CDC) intervention level of 10 pg/dL blood lead. On the basis of blood lead levels (BLLs), adolescents were categorized into two groups: Group I and Group II had a blood lead <10 microg/dL (7.40 +/- 1.62) and >10 microg/dL (13.27 +/- 2.67), respectively, with significantly different mean values (P <0.001). Age, sex, body mass index (BMI), Hb level (malnutrition), and area of living as confounders of lead exposure and toxicity were not statistically different between the two groups. However, delta-ALAD activity was significantly lower (P <0.001), while CAT activity was higher in Group II than in Group I (P <0.01). MDA level was also significantly higher in Group II compared to Group I (P <0.001). There were significant negative correlation of BLL with 6-ALAD (r= -0.592, P <0.001), and positive correlations with CAT (r=0.485, P <0.01) and MDA (r=0.717, P <0.001). Interestingly, delta-ALAD, in turn, had significant negative correlations with CAT (r= -0.456, P <0.01) and MDA (r= -0.507, P <0.01). Results of the present pilot study provide clues to the possible low level of lead-induced oxidative stress in urban adolescents, suggesting that lead-induced 6-ALAD inhibition can also be an indicator of oxidative stress. The potential of oxidative stress parameters to be used as biomarkers of lead toxicity warranted further investigation.


Assuntos
Catalase/metabolismo , Intoxicação por Chumbo/sangue , Chumbo/sangue , Estresse Oxidativo/fisiologia , Sintase do Porfobilinogênio/metabolismo , Adolescente , Biomarcadores/sangue , Catalase/efeitos dos fármacos , Inibidores Enzimáticos/sangue , Eritrócitos/efeitos dos fármacos , Eritrócitos/enzimologia , Glutationa/sangue , Humanos , Índia , Intoxicação por Chumbo/enzimologia , Masculino , Malondialdeído/sangue , Sintase do Porfobilinogênio/efeitos dos fármacos , Estatísticas não Paramétricas , População Urbana
19.
J Biol Chem ; 281(29): 20521-9, 2006 Jul 21.
Artigo em Inglês | MEDLINE | ID: mdl-16672222

RESUMO

Eukaryotic pyrimidine 5'-nucleotidase type 1 (P5N-1) catalyzes dephosphorylation of pyrimidine 5'-mononucleotides. Deficiency of P5N-1 activity in red blood cells results in nonspherocytic hemolytic anemia. The enzyme deficiency is either familial or can be acquired through lead poisoning. We present the crystal structure of mouse P5N-1 refined to 2.35 A resolution. The mouse P5N-1 has a 92% sequence identity to its human counterpart. The structure revealed that P5N-1 adopts a fold similar to enzymes of the haloacid dehydrogenase superfamily. The active site of this enzyme is structurally highly similar to those of phosphoserine phosphatases. We propose a catalytic mechanism for P5N-1 that is also similar to that of phosphoserine phosphatases and provide experimental evidence for the mechanism in the form of structures of several reaction cycle states, including: 1) P5N-1 with bound Mg(II) at 2.25 A, 2) phosphoenzyme intermediate analog at 2.30 A, 3) product-transition complex analog at 2.35 A, and 4) product complex at 2.1A resolution with phosphate bound in the active site. Furthermore the structure of Pb(II)-inhibited P5N-1 (at 2.35 A) revealed that Pb(II) binds within the active site in a way that compromises function of the cationic cavity, which is required for the recognition and binding of the phosphate group of nucleotides.


Assuntos
5'-Nucleotidase/química , Intoxicação por Chumbo/enzimologia , Intoxicação por Chumbo/prevenção & controle , 5'-Nucleotidase/antagonistas & inibidores , Animais , Sítios de Ligação , Domínio Catalítico , Humanos , Chumbo/farmacologia , Camundongos , Modelos Moleculares , Conformação Proteica , Dobramento de Proteína , Estrutura Secundária de Proteína , Difração de Raios X
20.
Environ Toxicol Chem ; 24(6): 1483-95, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16117126

RESUMO

We assessed the exposure of fish from the Spring and Neosho Rivers in northeast Oklahoma, USA, to lead, zinc, and cadmium from historical mining in the Tri-States Mining District (TSMD). Fish (n = 74) representing six species were collected in October 2001 from six sites on the Spring and Neosho Rivers influenced to differing degrees by mining. Additional samples were obtained from the Big River, a heavily contaminated stream in eastern Missouri, USA, and from reference sites. Blood from each fish was analyzed for Pb, Zn, Cd, Fe, and hemoglobin (Hb). Blood also was analyzed for delta-aminolevulinic acid dehydratase (ALA-D) activity. The activity of ALA-D, an enzyme involved in heme synthesis, is inhibited by Pb. Concentrations of Fe and Hb were highly correlated (r = 0.89, p < 0.01) across all species and locations and typically were greater in common carp (Cyprinus carpio) than in other taxa. Concentrations of Pb, Zn, and Cd typically were greatest in fish from sites most heavily affected by mining and lowest in reference samples. The activity of ALA-D, but not concentrations of Hb or Fe, also differed significantly (p < 0.01) among sites and species. Enzyme activity was lowest in fish from mining-contaminated sites and greatest in reference fish, and was correlated negatively with Pb in most species. Statistically significant (p < 0.01) linear regression models that included negative terms for blood Pb explained as much as 68% of the total variation in ALA-D activity, but differences among taxa were highly evident. Positive correlations with Zn were documented in the combined data for channel catfish (Icralurus punctatus) and flathead catfish (Pylodictis olivaris), as has been reported for other taxa, but not in bass (Micropterus spp.) or carp. In channel catfish, ALA-D activity appeared to be more sensitive to blood Pb than in the other species investigated (i.e., threshold concentrations for inhibition were lower). Such among-species differences are consistent with previous studies. Enzyme activity was inhibited by more than 50% relative to reference sites in channel catfish from several TSMD sites. Collectively, our results indicate that Pb is both bioavailable and active biochemically in the Spring-Neosho River system.


Assuntos
Intoxicação por Cádmio/sangue , Doenças dos Peixes/induzido quimicamente , Peixes/sangue , Intoxicação por Chumbo/sangue , Poluentes Químicos da Água/intoxicação , Animais , Cádmio/sangue , Cádmio/farmacocinética , Intoxicação por Cádmio/enzimologia , Exposição Ambiental , Monitoramento Ambiental/métodos , Doenças dos Peixes/sangue , Doenças dos Peixes/enzimologia , Hemoglobinas/metabolismo , Chumbo/sangue , Chumbo/farmacocinética , Intoxicação por Chumbo/enzimologia , Mineração , Oklahoma , Sintase do Porfobilinogênio/metabolismo , Temperatura , Poluentes Químicos da Água/sangue , Zinco/sangue , Zinco/farmacocinética , Zinco/intoxicação
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...