Literature DB >> 17637895

Copper deficiency, lead, and paraoxonase.

Leslie M Klevay.   

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Year:  2007        PMID: 17637895      PMCID: PMC1913565          DOI: 10.1289/ehp.10151

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


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Li et al. (2006) measured paraoxonase 1 (PON1) in workers and found an inverse association between lead exposure and enzyme activity. This observation compliments some epidemiology and related experiments with animals, because low paraoxonase activity is associated with diabetes mellitus, familial hypercholesterolemia, ischemic heart disease, and metabolic syndrome (Klevay 2004). Paraoxonase, although studied most extensively because of its ability to detoxify organophosphate insecticides (James 2006; van Himbergen et al. 2006), has drawn increasing attention because it hydrolyzes homocysteine thiolactone, a vascular toxin that inhibits copper enzymes (Klevay 2006). Lead intoxication has many manifestations (Fischbein 1998), lesser-known of which is induction of copper deficiency (Klauder and Petering 1977). Rats deficient in copper have an approximately 28% decrease in paraoxonase activity (Klevay 2004). These observations are consonant with the decrease in superoxide dismutase (SOD) associated with occupational exposure to lead (Ito et al. 1985) because this enzyme also depends on adequate copper nutriture for activity (Linder and Goode 1980; Owen 1981). Thus, SOD is an index of copper nutriture in humans (Uauy et al. 1985). Li et al. (2006) stated that “the mechanism by which heavy metals inhibit serum PON1 activity is still not clear.” It seems likely that lead interferes with copper utilization in the workers, leading to low copper nutritional status (Li et al. 2006). Low copper status has been related to a large variety of adverse cardiovascular phenomena in both animals and people; in this context, the most important are hypercholesterolemia, hypertension, and impaired oxidative defense (Klevay 2000, 2002). Are there unpublished copper data on the workers, or can they be reexamined to test this copper hypothesis? Plasma copper and ceruloplasmin are not likely to be useful because they are increased by inflammation (Pepys 1996) and may be falsely high. Extracellular SOD may be helpful because it is sensitive to low copper status (Johnson et al. 2005), and low values have been associated with atherosclerosis in humans (Landmesser et al. 2000; Wang et al. 1998).
  11 in total

Review 1.  The story of PON1: how an organophosphate-hydrolysing enzyme is becoming a player in cardiovascular medicine.

Authors:  T M van Himbergen; L J H van Tits; M Roest; A F H Stalenhoef
Journal:  Neth J Med       Date:  2006-02       Impact factor: 1.422

2.  Anemia of lead intoxication: a role for copper.

Authors:  D S Klauder; H G Petering
Journal:  J Nutr       Date:  1977-10       Impact factor: 4.798

3.  Serum superoxide dismutase 3 (extracellular superoxide dismutase) activity is a sensitive indicator of Cu status in rats.

Authors:  W Thomas Johnson; Lu Ann K Johnson; Henry C Lukaski
Journal:  J Nutr Biochem       Date:  2005-08-02       Impact factor: 6.048

4.  Vascular extracellular superoxide dismutase activity in patients with coronary artery disease: relation to endothelium-dependent vasodilation.

Authors:  U Landmesser; R Merten; S Spiekermann; K Büttner; H Drexler; B Hornig
Journal:  Circulation       Date:  2000-05-16       Impact factor: 29.690

Review 5.  Ischemic heart disease as deficiency disease.

Authors:  L M Klevay
Journal:  Cell Mol Biol (Noisy-le-grand)       Date:  2004-12       Impact factor: 1.770

6.  Serum lipid peroxide level and blood superoxide dismutase activity in workers with occupational exposure to lead.

Authors:  Y Ito; Y Niiya; H Kurita; S Shima; S Sarai
Journal:  Int Arch Occup Environ Health       Date:  1985       Impact factor: 3.015

7.  Plasma extracellular superoxide dismutase levels in an Australian population with coronary artery disease.

Authors:  X L Wang; T Adachi; A S Sim; D E Wilcken
Journal:  Arterioscler Thromb Vasc Biol       Date:  1998-12       Impact factor: 8.311

8.  Red cell superoxide dismutase activity as an index of human copper nutrition.

Authors:  R Uauy; C Castillo-Duran; M Fisberg; N Fernandez; A Valenzuela
Journal:  J Nutr       Date:  1985-12       Impact factor: 4.798

Review 9.  How dietary deficiency, genes and a toxin can cooperate to produce arteriosclerosis and ischemic heart disease.

Authors:  L M Klevay
Journal:  Cell Mol Biol (Noisy-le-grand)       Date:  2006-12-31       Impact factor: 1.770

10.  Lead exposure is associated with decreased serum paraoxonase 1 (PON1) activity and genotypes.

Authors:  Wan-Fen Li; Mei-Hung Pan; Meng-Chu Chung; Chi-Kung Ho; Hung-Yi Chuang
Journal:  Environ Health Perspect       Date:  2006-08       Impact factor: 9.031

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  2 in total

1.  Changes in serum parameters associated with iron metabolism in male rat exposed to lead.

Authors:  Minoo Moshtaghie; Pedram Malekpouri; Mohammad Reza Dinko; Ali Asghar Moshtaghie
Journal:  J Physiol Biochem       Date:  2012-09-25       Impact factor: 4.158

2.  Reciprocal modulation of Aβ42 aggregation by copper and homocysteine.

Authors:  Salla Keskitalo; Melinda Farkas; Michael Hanenberg; Anita Szodorai; Luka Kulic; Alexander Semmler; Michael Weller; Roger M Nitsch; Michael Linnebank
Journal:  Front Aging Neurosci       Date:  2014-09-08       Impact factor: 5.750

  2 in total

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