Literature DB >> 28339347

The aging kidney and the nephrotoxic effects of mercury.

Christy C Bridges1, Rudolfs K Zalups1.   

Abstract

Owing to advances in modern medicine, life expectancies are lengthening and leading to an increase in the population of older individuals. The aging process leads to significant alterations in many organ systems, with the kidney being particularly susceptible to age-related changes. Within the kidney, aging leads to ultrastructural changes such as glomerular and tubular hypertrophy, glomerulosclerosis, and tubulointerstitial fibrosis, which may compromise renal plasma flow (RPF) and glomerular filtration rate (GFR). These alterations may reduce the functional reserve of the kidneys, making them more susceptible to pathological events when challenged or stressed, such as following exposure to nephrotoxicants. An important and prevalent environmental toxicant that induces nephrotoxic effects is mercury (Hg). Since exposure of normal kidneys to mercuric ions might induce glomerular and tubular injury, aged kidneys, which may not be functioning at full capacity, may be more sensitive to the effects of Hg than normal kidneys. Age-related renal changes and the effects of Hg in the kidney have been characterized separately. However, little is known regarding the influence of nephrotoxicants, such as Hg, on aged kidneys. The purpose of this review was to summarize known findings related to exposure of aged and diseased kidneys to the environmentally relevant nephrotoxicant Hg.

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Year:  2017        PMID: 28339347      PMCID: PMC6088787          DOI: 10.1080/10937404.2016.1243501

Source DB:  PubMed          Journal:  J Toxicol Environ Health B Crit Rev        ISSN: 1093-7404            Impact factor:   6.393


  264 in total

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3.  Bioaccessibility and bioavailability of methylmercury from seafood commonly consumed in North America: In vitro and epidemiological studies.

Authors:  Maia Siedlikowski; Mark Bradley; Stan Kubow; Jaclyn M Goodrich; Alfred Franzblau; Niladri Basu
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Authors:  M G Cherian; T W Clarkson
Journal:  Chem Biol Interact       Date:  1976-02       Impact factor: 5.192

5.  The molecular basis of age-related kidney disease.

Authors:  Feng Zheng; Anna Rita Plati; Anita Banerjee; Sharon Elliot; Liliane J Striker; Gary E Striker
Journal:  Sci Aging Knowledge Environ       Date:  2003-07-23

6.  Early predictors of 15-year end-stage renal disease in hypertensive patients.

Authors:  H M Perry; J P Miller; J R Fornoff; J D Baty; M P Sambhi; G Rutan; D W Moskowitz; S E Carmody
Journal:  Hypertension       Date:  1995-04       Impact factor: 10.190

7.  Concentration of selenium in the whole blood and the thyroid tissue of patients with various thyroid diseases.

Authors:  M Kucharzewski; J Braziewicz; U Majewska; S Góźdź
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8.  Studies on the pathophysiology of acute renal failure. II. A histochemical study of the proximal tubule of the rat following administration of mercuric chloride.

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Journal:  Virchows Arch B Cell Pathol       Date:  1976-11-24

9.  Luminal and basolateral mechanisms involved in the renal tubular uptake of inorganic mercury.

Authors:  R K Zalups; K H Minor
Journal:  J Toxicol Environ Health       Date:  1995-09

10.  Mercuric chloride-induced nephrotoxicity in the rat following unilateral nephrectomy and compensatory renal growth.

Authors:  R K Zalups; G L Diamond
Journal:  Virchows Arch B Cell Pathol Incl Mol Pathol       Date:  1987
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Journal:  J Toxicol Environ Health A       Date:  2017-07-13

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Journal:  Diagnostics (Basel)       Date:  2020-01-01

9.  The Prevalence of Inorganic Mercury in Human Kidneys Suggests a Role for Toxic Metals in Essential Hypertension.

Authors:  Roger Pamphlett; Philip A Doble; David P Bishop
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10.  Grape-Seed Proanthocyanidin Extract Reverts Obesity-Related Metabolic Derangements in Aged Female Rats.

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