Literature DB >> 22359123

An in vitro test for measuring cytotoxicity of mercuric chloride to human kidney epithelial cells by specific enzyme release.

D Merlet1, M Mellado, J P Merlet, J Cambar.   

Abstract

Mercuric compound toxicity is well documented in animals and man for practically all organs. The recent development of cell culture techniques appeared as a novel fruitful tool in toxicology, especially in renal toxicology. Heavy metal induced renal cell alterations can be evaluated by membrane permeability damages.The present study evaluates mercuric chloride nephrotoxic effect in human kidney epithelial cells by measuring the release of two specific nephrotoxicity marker enzymes, Gamma Glutamyl Transferase (GGT) and Alkaline Phosphatase (ALP) in the culture medium. Cultured kidney epithelial cells were exposed to different HgCl(2) concentrations (5, 10, 20, and 50 μg). Cultures were examined after 6 and 24 hours exposure. A good correlation between mercury dose and toxic effect, and exposure time and toxic effect was found. Enzymes were significantly released into the culture medium for 5 μg and 10 μg HgCl(2)/ml after 6 hours exposure; and after 24 hours exposure, enzymes were released for 5 μg/ml only.It appears that the specific tubular enzyme release in the culture medium is a good in vitro test for quantification of specific tubular damage.

Entities:  

Year:  1988        PMID: 22359123     DOI: 10.1007/BF00145030

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  24 in total

Review 1.  Urinary enzymes, nephrotoxicity and renal disease.

Authors:  R G Price
Journal:  Toxicology       Date:  1982       Impact factor: 4.221

2.  Comparison of different methods of determining cell viability after exposure to cytotoxic compounds.

Authors:  B K Bhuyan; B E Loughman; T J Fraser; K J Day
Journal:  Exp Cell Res       Date:  1976-02       Impact factor: 3.905

3.  Content of mercury in chromatin and level of metallothionein proteins in kidneys and liver of rats.

Authors:  M Rózalski; E Kuziemska; R Wierzbicki
Journal:  Biochem Pharmacol       Date:  1981-08-01       Impact factor: 5.858

4.  Isolation of a pure suspension of rat proximal tubules.

Authors:  P Vinay; A Gougoux; G Lemieux
Journal:  Am J Physiol       Date:  1981-10

5.  Increase in cis-dichlorodiammineplatinum (II) cytotoxicity upon reversible electropermeabilization of the plasma membrane in cultured human NHIK 3025 cells.

Authors:  J E Melvik; E O Pettersen; P B Gordon; P O Seglen
Journal:  Eur J Cancer Clin Oncol       Date:  1986-12

6.  Tissue culture of human kidney epithelial cells of proximal tubule origin.

Authors:  C J Detrisac; M A Sens; A J Garvin; S S Spicer; D A Sens
Journal:  Kidney Int       Date:  1984-02       Impact factor: 10.612

7.  Lack of cytotoxicity of ticrynafen in primary cultures of rat liver cells.

Authors:  D Acosta; D B Mitchell; K S Santone; A Bock; W Lewis
Journal:  Toxicol Lett       Date:  1982-03       Impact factor: 4.372

8.  Evaluation of the cytotoxicity of tricyclic antidepressants in primary cultures of rat hepatocytes.

Authors:  D B Mitchell; D Acosta
Journal:  J Toxicol Environ Health       Date:  1981-01

9.  Separation of proximal tubule cells from suspensions of rat kidney cells in density gradients of Ficoll in tissue culture medium.

Authors:  J I Kreisberg; A M Pitts; T G Pretlow
Journal:  Am J Pathol       Date:  1977-03       Impact factor: 4.307

10.  Screening of toxic compounds in tissue culture.

Authors:  B Ekwall
Journal:  Toxicology       Date:  1980       Impact factor: 4.221

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