Literature DB >> 1949014

Urinary porphyrin profiles as biomarkers of trace metal exposure and toxicity: studies on urinary porphyrin excretion patterns in rats during prolonged exposure to methyl mercury.

J S Woods1, M A Bowers, H A Davis.   

Abstract

Studies were conducted to define the specific changes in the urinary porphyrin excretion pattern (porphyrin profile) and the time course of those changes in rats exposed to mercury as methyl mercury hydroxide (MMH) at 5 or 10 ppm in the drinking water for up to 30 weeks. The urinary porphyrin profile elicited by MMH is uniquely characterized by highly elevated levels of 4- and 5-carboxyl porphyrins, and of a third atypical porphyrin with as yet undetermined chemical characteristics. Changes in the porphyrin profile were observed as early as 1 or 2 weeks following initiation of exposure to MMH at 10 or 5 ppm, respectively, and were sustained as long as 40 weeks following cessation of MMH treatment. The magnitude of the urinary porphyrin profile at either MMH dose level increased progressively during the course of mercury treatment and was highly correlated with the renal mercury concentration. A subsequent decline in the magnitude of the urinary porphyrin profile in animals exposed to 10 ppm MMH for more than 10 weeks was associated with the accumulation of high levels of Hg2+ in kidney cells and loss of renal functional status. These findings demonstrate that mercury elicits a unique change in the urinary porphyrin excretion pattern which is related to the dose and duration of mercury treatment. The association of urinary porphyrin excretion rates with renal mercury content and functional status suggests that urinary porphyrin profiles may serve as a useful biomarker of mercury accumulation and nephrotoxicity during prolonged mercury exposure.

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Year:  1991        PMID: 1949014     DOI: 10.1016/0041-008x(91)90047-i

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  10 in total

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Authors:  Nicholas J Heyer; Diana Echeverria; James S Woods
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Review 2.  Biomarkers of mercury toxicity: Past, present, and future trends.

Authors:  Vasco Branco; Sam Caito; Marcelo Farina; João Teixeira da Rocha; Michael Aschner; Cristina Carvalho
Journal:  J Toxicol Environ Health B Crit Rev       Date:  2017-04-05       Impact factor: 6.393

3.  Multibiomarker approach to assess the magnitude of occupational exposure and effects induced by a mixture of metals.

Authors:  V Lopes de Andrade; D Serrazina; M L Mateus; C Batoréu; M Aschner; A P Marreilha Dos Santos
Journal:  Toxicol Appl Pharmacol       Date:  2021-08-23       Impact factor: 4.460

4.  Urinary porphyrin excretion in normal children and adolescents.

Authors:  James S Woods; Michael D Martin; Brian G Leroux; Timothy A DeRouen; Mario F Bernardo; Henrique S Luis; Jorge G Leitão; P Lynne Simmonds; Tessa C Rue
Journal:  Clin Chim Acta       Date:  2009-04-24       Impact factor: 3.786

5.  Cloning, expression, and biochemical properties of CPOX4, a genetic variant of coproporphyrinogen oxidase that affects susceptibility to mercury toxicity in humans.

Authors:  Tingting Li; James S Woods
Journal:  Toxicol Sci       Date:  2009-04-01       Impact factor: 4.849

6.  Urinary porphyrin excretion in neurotypical and autistic children.

Authors:  James S Woods; Sarah E Armel; Denise I Fulton; Jason Allen; Kristine Wessels; P Lynne Simmonds; Doreen Granpeesheh; Elizabeth Mumper; J Jeffrey Bradstreet; Diana Echeverria; Nicholas J Heyer; James P K Rooney
Journal:  Environ Health Perspect       Date:  2010-06-24       Impact factor: 9.031

7.  The plausibility of a role for mercury in the etiology of autism: a cellular perspective.

Authors:  Matthew Garrecht; David W Austin
Journal:  Toxicol Environ Chem       Date:  2011-05-20       Impact factor: 1.437

Review 8.  Biomarker research in neurotoxicology: the role of mechanistic studies to bridge the gap between the laboratory and epidemiological investigations.

Authors:  L G Costa
Journal:  Environ Health Perspect       Date:  1996-03       Impact factor: 9.031

9.  Interaction of blood lead and delta-aminolevulinic acid dehydratase genotype on markers of heme synthesis and sperm production in lead smelter workers.

Authors:  B H Alexander; H Checkoway; P Costa-Mallen; E M Faustman; J S Woods; K T Kelsey; C van Netten; L G Costa
Journal:  Environ Health Perspect       Date:  1998-04       Impact factor: 9.031

10.  Quantitative analyses of the hepatic proteome of methylmercury-exposed Atlantic cod (Gadus morhua) suggest oxidative stress-mediated effects on cellular energy metabolism.

Authors:  Fekadu Yadetie; Silje Bjørneklett; Hilde Kristin Garberg; Eystein Oveland; Frode Berven; Anders Goksøyr; Odd André Karlsen
Journal:  BMC Genomics       Date:  2016-08-05       Impact factor: 3.969

  10 in total

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