HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Monosodium glutamate-induced obesity changed the expression and activity of glutathione S-transferases in mouse heart and kidney.

Abstract
Obesity may affect activity and/or expression of enzymes participating in xenobiotics' detoxification and antioxidant defense. This study sought to investigate the activities and expression of cardiac and renal glutathione S-transferase (GST) isoforms in order to reveal possible differences between obese and control mice. For this purpose, mice with monosodium glutamate (MSG)-induced obesity were used as an experimental model. Obesity was induced in newborn male mice by repeated s.c. administration of MSG. At 8 months of age, mice were sacrificed and specific activity, protein and mRNA expressions levels of GSTs were analyzed in their heart and kidney. In hearts of obese mice, specific activity of GST was decreased by 51% compared to control. This reduction was accompanied by a decline in GSTP-class protein and Gstp1/2 mRNA expression levels. In contrast, specific activity of GST was elevated by 31% in kidney of obese mice and this increase was accompanied by upregulation of GSTA-class protein and Gsta1/2 mRNA expressions. Increased capacity of renal GSTs together with GSTA upregulation may serve as compensatory mechanism against elevated oxidative stress, which accompanies obesity. On the other hand, decreased cardiac GST activity in obese mice and GSTP downregulation may worsen the defense against oxidative stress and harmful xenobiotics.
AuthorsI Boušová, Š Košťáková, P Matoušková, H Bártíková, B Szotáková, L Skálová
JournalDie Pharmazie (Pharmazie) Vol. 72 Issue 5 Pg. 257-259 (May 01 2017) ISSN: 0031-7144 [Print] Germany
PMID29441869 (Publication Type: Journal Article)
Chemical References
  • Isoenzymes
  • RNA, Messenger
  • GSTA2 protein, mouse
  • Glutathione Transferase
  • glutathione S-transferase alpha
  • Sodium Glutamate
Topics
  • Animals
  • Animals, Newborn
  • Disease Models, Animal
  • Glutathione Transferase (genetics, metabolism)
  • Isoenzymes (genetics, metabolism)
  • Kidney (enzymology)
  • Male
  • Mice
  • Myocardium (enzymology)
  • Obesity (metabolism, physiopathology)
  • Oxidative Stress
  • RNA, Messenger (metabolism)
  • Sodium Glutamate
  • Up-Regulation

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: