Loss of NRF2 impairs gastric nitrergic stimulation and function.

Mukhopadhyay S, Sekhar KR, Hale AB, Channon KM, Farrugia G, Freeman ML, Gangula PR
Free Radic Biol Med. 2011 51 (3): 619-25

PMID: 21605664 · PMCID: PMC3129370 · DOI:10.1016/j.freeradbiomed.2011.04.044

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.

Published by Elsevier Inc.

MeSH Terms (20)

Animals Antioxidants Biopterin Chloramphenicol O-Acetyltransferase Disease Models, Animal Down-Regulation Gastric Emptying Gastric Mucosa Gastroparesis Glutamate-Cysteine Ligase Humans Mice Mice, Knockout Muscle Relaxation NF-E2-Related Factor 2 Nitrergic Neurons Stomach Superoxide Dismutase Superoxide Dismutase-1 Vasomotor System

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