Humulene Inhibits Acute Gastric Mucosal Injury by Enhancing Mucosal Integrity.
Dahee YeoSu-Jung HwangYe-Seul SongHyo-Jong LeePublished in: Antioxidants (Basel, Switzerland) (2021)
This study was designed to determine whether α-humulene, a major constituent in many plants used in fragrances, has a protective role against gastric injury in vivo and in vitro. A rat model of hydrochloric acid (HCl)/ethanol-induced gastritis and human mast cells (HMC-1) were used to investigate the mucosal protective effect of α-humulene. α-Humulene significantly inhibited gastric lesions in HCl/ethanol-induced acute gastritis and decreased gastric acid secretion pyloric ligation-induced gastric ulcers in vivo. In addition, α-humulene reduced the amount of reactive oxygen species and malondialdehyde through upregulation of prostaglandin E2 (PGE2) and superoxide dismutase (SOD). In HMC-1 cells, α-humulene decreased intracellular calcium and increased intracellular cyclic adenosine monophosphate (cAMP) levels, resulting in low histamine levels. α-Humulene also reduced the expression levels of cytokine genes such as interleukin (IL)-1β, IL-6, tumor necrosis factor (TNF) by downregulating nuclear factor-κB (NF-κB) nuclear translocation. Finally, α-humulene upregulated the expression levels of mucin 5AC (Muc5ac), Muc6, trefoil factor 1 (Tff1), trefoil factor 2 (Tff2), and polymeric immunoglobulin receptor (pigr). α-Humulene may attenuate HCl/ethanol-induced gastritis by inhibiting histamine release and NF-κB activation and stimulating antioxidants and mucosal protective factors, particularly Muc5ac and Muc6. Therefore, these data suggest that α-humulene is a potential drug candidate for the treatment of stress-induced or alcoholic gastritis.
Keyphrases
- nuclear factor
- helicobacter pylori
- drug induced
- reactive oxygen species
- helicobacter pylori infection
- stress induced
- signaling pathway
- poor prognosis
- high glucose
- diabetic rats
- liver injury
- endothelial cells
- oxidative stress
- induced apoptosis
- rheumatoid arthritis
- lps induced
- ulcerative colitis
- binding protein
- gene expression
- risk assessment
- respiratory failure
- hydrogen peroxide
- inflammatory response
- immune response
- genome wide
- nitric oxide
- extracorporeal membrane oxygenation
- drug release
- wound healing