HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Co-exposure to aluminum and acrylamide disturbs expression of metallothionein, proinflammatory cytokines and induces genotoxicity: Biochemical and histopathological changes in the kidney of adult rats.

Abstract
The individual toxic effects of aluminum and acrylamide are known but there is no data on their combined effects. The present study investigates the toxic effects after combined exposure to these toxicants on: (i) oxidative stress during combined chronic exposure to aluminum and acrylamide on kidney function (ii) correlation of oxidative stress with metallothionein (MT) and inflammatory cytokines expression, DNA damage, and histopathological changes. Rats were exposed to aluminum (50 mg/kg body weight) in drinking water and acrylamide (20 mg/kg body weight) by gavage either individually or in combination for 3 weeks. Exposure rats to aluminum chloride or acrylamide alone and in combination induced nephrotoxicity, as evidenced by a decrease in the 24-h urine volume and uric acid levels in plasma and an increase of plasma creatinine, urea, and blood urea nitrogen levels. Nephrotoxicity was objectified by a significant increase in malondialdehyde level, advanced oxidation protein, and protein carbonyl contents, whereas reduced glutathione, nonprotein thiol, vitamin C levels, catalase, and glutathione peroxidase activities showed a significant decline. Superoxide dismutase activity and its gene expression were increased. Aluminum and acrylamide co-exposure exhibited synergism in various biochemical variables and also in DNA damage. Kidney total MT levels and genes expression of MT1, MT2, and proinflammatory cytokines were increased. All these changes were supported by histopathological observations. Co-exposure to aluminum and acrylamide exhibited synergism and more pronounced toxic effects compared with their individual effects based on various biochemical variables, genotoxic, and histopathological changes. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 1044-1058, 2016.
AuthorsImen Ghorbel, Sameh Maktouf, Nesrine Fendri, Kamel Jamoussi, Semia Ellouze Chaabouni, Tahia Boudawara, Najiba Zeghal
JournalEnvironmental toxicology (Environ Toxicol) Vol. 31 Issue 9 Pg. 1044-58 (Sep 2016) ISSN: 1522-7278 [Electronic] United States
PMID25858877 (Publication Type: Journal Article)
Copyright© 2015 Wiley Periodicals, Inc.
Chemical References
  • Aluminum Compounds
  • Biomarkers
  • Chlorides
  • Cytokines
  • Drinking Water
  • Acrylamide
  • Uric Acid
  • Aluminum Chloride
  • Malondialdehyde
  • Metallothionein
  • Creatinine
  • Catalase
  • Superoxide Dismutase
  • Glutathione
Topics
  • Acrylamide (toxicity)
  • Aluminum Chloride
  • Aluminum Compounds (toxicity)
  • Animals
  • Biomarkers (blood, urine)
  • Blood Urea Nitrogen
  • Catalase (metabolism)
  • Chlorides (toxicity)
  • Creatinine (blood)
  • Cytokines (metabolism)
  • DNA Damage (drug effects)
  • Drinking Water (chemistry)
  • Female
  • Glutathione (metabolism)
  • Kidney (drug effects, metabolism, pathology)
  • Malondialdehyde (metabolism)
  • Metallothionein (metabolism)
  • Oxidation-Reduction
  • Oxidative Stress (drug effects)
  • Protein Carbonylation (drug effects)
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase (genetics, metabolism)
  • Uric Acid (blood)

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: