HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Drug-metabolizing and antioxidant enzymes in monosodium L-glutamate obese mice.

Abstract
The prevalence of obesity is rapidly increasing across the world. Physiologic alterations associated with obesity are known to alter enzyme expression and/or activities. As drug-metabolizing and antioxidant enzymes serve as defense system against potentially toxic compounds, their modulation might have serious consequences. In this work, we studied selected antioxidant and drug-metabolizing enzymes (DME) in monosodium glutamate-mouse model of obesity. Specific activities, protein, and mRNA expressions of these enzymes in liver as well as in small intestine were compared in obese male mice and in their lean counterparts. Furthermore, expression of the NF-E2-related factor 2 (Nrf2) and its relation to obesity were tested. Obtained results showed that obesity affects expression and/or activities of some DME and antioxidant enzymes. In obese mice, upregulation of UDP-glucuronosyltransferases 1A (UGT1A), NAD(P)H:quinone oxidoreductase 1 (NQO1), nuclear transcription factor Nrf2, and downregulation of some isoforms of glutathione S-transferases (GST) were observed. Most of these changes were tissue and/or isoform specific. NQO1 seems to be regulated transcriptionally via Nrf2, but other enzymes might be regulated post-transcriptionally and/or post-translationally. Enhanced expression of Nrf2 in livers of obese mice is expected to play a role in protective adaptation. In contrast, elevated activities of NQO1 and UGT1A may cause alterations in drug pharmacokinetics in obese individuals. Moreover, decreased capacity of GST in obese animals indicates potentially reduced antioxidant defense and weaker chemoprotection.
AuthorsPetra Matoušková, Hana Bártíková, Iva Boušová, Lucie Levorová, Barbora Szotáková, Lenka Skálová
JournalDrug metabolism and disposition: the biological fate of chemicals (Drug Metab Dispos) Vol. 43 Issue 2 Pg. 258-65 (Feb 2015) ISSN: 1521-009X [Electronic] United States
PMID25473020 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014 by The American Society for Pharmacology and Experimental Therapeutics.
Chemical References
  • Isoenzymes
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • RNA, Messenger
  • NAD(P)H Dehydrogenase (Quinone)
  • Nqo1 protein, mouse
  • UGT1A1 enzyme
  • Glucuronosyltransferase
  • Glutathione Transferase
  • Sodium Glutamate
Topics
  • Animals
  • Animals, Newborn
  • Disease Models, Animal
  • Gene Expression Regulation, Enzymologic
  • Glucuronosyltransferase (genetics, metabolism)
  • Glutathione Transferase (genetics, metabolism)
  • Intestinal Mucosa (enzymology, metabolism)
  • Intestine, Small (enzymology, metabolism)
  • Isoenzymes (genetics, metabolism)
  • Liver (enzymology, metabolism)
  • Male
  • Mice, Inbred Strains
  • NAD(P)H Dehydrogenase (Quinone) (genetics, metabolism)
  • NF-E2-Related Factor 2 (genetics, metabolism)
  • Obesity (enzymology, metabolism)
  • Organ Specificity
  • RNA, Messenger (metabolism)
  • Sodium Glutamate

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: