Literature DB >> 3350234

Nephrotoxicity of intravenously injected cadmium-metallothionein: critical concentration and tolerance.

T Maitani1, F E Cuppage, C D Klaassen.   

Abstract

The nephrotoxicity of Cd-metallothionein (Cd-MT) was examined after iv administration of various dosages to mice. The lowest dosage of Cd-MT that produced renal injury was 0.2 mg Cd/kg. This dosage of Cd-MT resulted in 10 micrograms Cd/g in the kidneys 24 hr after administration. A time-course experiment utilizing a higher (0.3 mg Cd/kg) nephrotoxic dose of Cd-MT demonstrated that the renal Cd concentration at 4 and 12 hr was much higher than the critical concentration, but thereafter decreased to about 10 micrograms Cd/g wet tissue by 24 hr. Thus, Cd in excess of 10 micrograms/g appears to damage the kidney and then distributes to other tissues and/or is excreted into urine. When a total of 0.3, 0.4, and 0.8 mg of Cd/kg as Cd-MT was administered in divided dosages over 4 days, as much as 30 micrograms Cd/g was detected in the kidney but no renal injury was observed. Thus, the critical concentration for producing renal injury after acute administration of Cd-MT is estimated to be approximately 10 micrograms Cd/g wet weight. However, with repeated exposure to Cd-MT, this acute critical concentration can be exceeded without producing renal injury, as tolerance to the nephrotoxic effects of Cd-MT develops.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3350234     DOI: 10.1016/0272-0590(88)90255-2

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  3 in total

1.  Mercury distribution and renal metallothionein induction after subchronic oral exposure in rats.

Authors:  M A Morcillo; J Santamaria
Journal:  Biometals       Date:  1996-07       Impact factor: 2.949

2.  The influence of aging on renal response to cadmium in Syrian hamsters.

Authors:  T Shibasaki; Q Y Xu; I Ohno; F Ishimoto; O Sakai
Journal:  Biol Trace Elem Res       Date:  1996-07       Impact factor: 3.738

3.  Cadmium exposure enhances organic cation transporter 2 trafficking to the kidney membrane and exacerbates cisplatin nephrotoxicity.

Authors:  Hong Yang; Jie Tang; Dong Guo; Qingqing Zhao; Jiagen Wen; Yanjuan Zhang; Obinna N Obianom; Shiwei Zhou; Wei Zhang; Yan Shu
Journal:  Kidney Int       Date:  2019-11-26       Impact factor: 10.612

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.