HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Depletion of mitochondrial enzyme system in liver, lung, brain, stomach and kidney induced by benzo(a)pyrene.

Abstract
Mitochondrial dysfunction has recently received considerable attention as it plays an important role in adult human pathology caused by various drugs, endogenous agents and environmental agents. Benzo(a)pyrene (BaP), is a ubiquitous environmental contaminant mainly derived from anthropogenic activity during incomplete combustion of organic materials from various sources. The present study aimed to evaluate the effects of benzo(a)pyrene (BaP) on mitochondrial enzymes in the multiple organs including liver, lung, brain, stomach and kidney. ICR mice were exposed to different doses of BaP (2.5, 5 and 10mg/kg body weight) through oral gavage and intraperitoneal injection treatment for 13 weeks consecutively. The induced mitochondrial damage in the examined organs was assayed in terms of significant increase in lipid peroxidation (LPO) and prominent decrease in antioxidant enzymes. Non enzymatic antioxidants and Krebs cycle's enzymes were also significantly decreased in mitochondria. Additionally, BaP induced the body growth retardation and decrease in relative liver weight, increase in relative lung, stomach, kidney and brain weights, and this was further certified through histopathological lesions. Liver and lungs were more prominently damaged by BaP. The mitochondrial depletion increased in BaP dose-dependent manner.
AuthorsXiaoying Ji, Yongfei Li, Jianlong He, Walayat Shah, Xiaochang Xue, Guodong Feng, Huqin Zhang, Meili Gao
JournalEnvironmental toxicology and pharmacology (Environ Toxicol Pharmacol) Vol. 43 Pg. 83-93 (Apr 2016) ISSN: 1872-7077 [Electronic] Netherlands
PMID26970059 (Publication Type: Journal Article)
CopyrightCopyright © 2016 Elsevier B.V. All rights reserved.
Chemical References
  • Hazardous Substances
  • Benzo(a)pyrene
Topics
  • Animals
  • Benzo(a)pyrene (toxicity)
  • Hazardous Substances (toxicity)
  • Humans
  • Kidney (enzymology)
  • Liver (enzymology)
  • Lung (enzymology)
  • Mice
  • Mice, Inbred ICR
  • Mitochondria (drug effects, enzymology)
  • Stomach (enzymology)
  • Toxicity Tests

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: