Literature DB >> 2255667

Effect of cyclosporin A and different vehicles on ATP production in mitochondria isolated from the rat kidney cortex.

L Nässberger1.   

Abstract

Isolated rat kidney mitochondria were exposed in vitro to cyclosporin A and three different vehicles, ethanol, DMSO and cremophor. Spontaneous ATP production and oxidative phosphorylation were measured with a bioluminometric method. Both ethanol and cremophor caused a slight (4-7%) decrease in spontaneous ATP production, and also cyclosporin A itself had a minimal effect. On the other hand DMSO had an opposite effect, causing an increase of about 20%. Cyclosporin A showed a dose dependent inhibition of oxidative phosphorylation, being most pronounced when dissolved in ethanol. Cremophor, the castor oil used in commercial preparations caused per se almost a 40% inhibition of the oxidative phosphorylation.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2255667     DOI: 10.1111/j.1600-0773.1990.tb00801.x

Source DB:  PubMed          Journal:  Pharmacol Toxicol        ISSN: 0901-9928


  3 in total

1.  Synaptic Mitochondria Sustain More Damage than Non-Synaptic Mitochondria after Traumatic Brain Injury and Are Protected by Cyclosporine A.

Authors:  Jacqueline R Kulbe; Rachel L Hill; Indrapal N Singh; Juan A Wang; Edward D Hall
Journal:  J Neurotrauma       Date:  2016-10-13       Impact factor: 5.269

2.  Effect of cyclosporin A and its vehicle on cardiac and skeletal muscle mitochondria: relationship to efficacy of the respiratory chain.

Authors:  H Sanchez; J Zoll; X Bigard; V Veksler; B Mettauer; E Lampert; J Lonsdorfer; R Ventura-Clapier
Journal:  Br J Pharmacol       Date:  2001-07       Impact factor: 8.739

3.  Cyclosporine exacerbates ketamine toxicity in zebrafish: Mechanistic studies on drug-drug interaction.

Authors:  Bonnie L Robinson; Melanie Dumas; Syed F Ali; Merle G Paule; Qiang Gu; Jyotshna Kanungo
Journal:  J Appl Toxicol       Date:  2017-06-01       Impact factor: 3.446

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.