Literature DB >> 11441915

Effect of cadmium on gap junctional intercellular communication in primary cultures of rat renal proximal tubular cells.

M Fukumoto1, T Kujiraoka, M Hara, T Shibasaki, T Hosoya, M Yoshida.   

Abstract

Cadmium mainly accumulates in the kidney and causes renal injury. To clarify the mechanism of Cd nephrotoxicity, we investigated the effects of this element on intercellular communication through gap junction channels in primary cultures of rat renal proximal tubular cells. Sixty minutes after exposure to 100 microM Cd, dye coupling experiments showed that gap junctional intercellular communication (GJIC) was significantly inhibited. This inhibition occurred before the appearance of cytotoxicity. Intracellular calcium concentrations [Ca2+]i, which modulate the function of gap junctions, gradually increased after exposure to Cd and reached a maximum after 60 minutes. These results suggest that the inhibition of GJIC as a result of Cd exposure is related to an increase in [Ca2+]i, and that GJIC inhibition may be an indicator of nephrotoxicity.

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Year:  2001        PMID: 11441915     DOI: 10.1016/s0024-3205(01)01063-3

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  3 in total

Review 1.  The blood-testis barrier and its implications for male contraception.

Authors:  C Yan Cheng; Dolores D Mruk
Journal:  Pharmacol Rev       Date:  2011-10-28       Impact factor: 25.468

2.  Connexin43 hemichannels contribute to cadmium-induced oxidative stress and cell injury.

Authors:  Xin Fang; Tao Huang; Ying Zhu; Qiaojing Yan; Yuan Chi; Jean X Jiang; Peiyu Wang; Hiroyuki Matsue; Masanori Kitamura; Jian Yao
Journal:  Antioxid Redox Signal       Date:  2011-03-31       Impact factor: 8.401

Review 3.  Cell adhesion molecules in chemically-induced renal injury.

Authors:  Walter C Prozialeck; Joshua R Edwards
Journal:  Pharmacol Ther       Date:  2007-01-23       Impact factor: 12.310

  3 in total

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