Loss of NRF2 impairs gastric nitrergic stimulation and function

Sutapa Mukhopadhyay, Konjeti R. Sekhar, Ashley B. Hale, Keith M. Channon, Gianrico Farrugia, Michael L. Freeman, Pandu R. Gangula

Research output: Contribution to journalArticlepeer-review

18 Scopus citations


Emerging research suggests that antioxidant gene expression has the potential to suppress the development of gastroparesis. However, direct genetic evidence that definitively supports this concept is lacking. We used mice carrying a targeted disruption of Nfe2l2, the gene that encodes the transcription factor NRF2 and directs antioxidant Phase II gene expression, as well as mice with a targeted disruption of Gclm, the modifier subunit for glutamate-cysteine ligase, to test the hypothesis that defective antioxidant gene expression contributes to development of gastroparesis. Although expression of heme oxygenase-1 remained unchanged, expression of GCLC, GCLM, SOD1, and CAT was down-regulated in gastric tissue from Nrf2 -/- mice compared to wild-type animals. Tetrahydrobiopterin oxidation was significantly elevated and nitrergic relaxation was impaired in Nrf2 -/- mouse gastric tissue. In vitro studies showed a significant decrease in NO release in Nrf2 -/- mouse gastric tissue. Nrf2 -/- mice displayed delayed gastric emptying. The use of Gclm -/- mice demonstrated that the loss of glutamate-cysteine ligase function enhanced tetrahydrobiopterin oxidation while impairing nitrergic relaxation. These results provide genetic evidence that loss of antioxidant gene expression can contribute to the development of gastroparesis and suggest that NRF2 represents a potential therapeutic target.

Original languageEnglish (US)
Pages (from-to)619-625
Number of pages7
JournalFree Radical Biology and Medicine
Issue number3
StatePublished - Aug 1 2011


  • Free radicals
  • GCLC
  • GCLM
  • Gastric motility
  • Gastroparesis
  • Mice
  • NRF2
  • Nitric oxide
  • nNOSα

ASJC Scopus subject areas

  • Biochemistry
  • Physiology (medical)


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