Heme oxygenase-1 induced by desoxo-narchinol-A attenuated the severity of acute pancreatitis via blockade of neutrophil infiltration

Int Immunopharmacol. 2019 Apr:69:225-234. doi: 10.1016/j.intimp.2019.01.051. Epub 2019 Feb 7.

Abstract

Heme oxygenase-1 (HO-1) has an anti-inflammatory action in acute pancreatitis (AP). However, its mechanism of action and natural compounds/drugs to induce HO-1 in pancreas are not well understood. In this study, we investigated the regulatory mechanisms of HO-1 during AP using desoxo-narchinol-A (DN), the natural compound inducing HO-1 in the pancreas. Female C57/BL6 Mice were intraperitoneally injected with supramaximal concentrations of cerulein (50 μg/kg) hourly for 6 h to induce AP. DMSO or DN was administered intraperitoneally, then mice were sacrificed 6 h after the final cerulein injection. Administration of DN increased pancreatic HO-1 expression through activation of activating protein-1, mediated by mitogen-activated protein kinases. Furthermore, DN treatment reduced the pancreatic weight-to-body weight ratio as well as production of digestive enzymes and pro-inflammatory cytokines. Inhibition of HO-1 by tin protoporphyrin IX abolished the protective effects of DN on pancreatic damage. Additionally, DN treatment inhibited neutrophil infiltration into the pancreas via regulation of chemokine (C-X-C motif) ligand 2 (CXCL2) by HO-1. Our results suggest that DN is an effective inducer of HO-1 in the pancreas, and that HO-1 regulates neutrophil infiltration in AP via CXCL2 inhibition.

Keywords: Acute pancreatitis; Chemokine (C-X-C motif) ligand 2; Desoxo-narchinol-A; Heme oxygenase-1; Neutrophils.

MeSH terms

  • Acute Disease
  • Amylases / blood
  • Animals
  • Ceruletide / administration & dosage
  • Chemokine CXCL2 / metabolism*
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Heme Oxygenase-1 / metabolism*
  • Humans
  • Inflammation Mediators / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Naphthols / metabolism
  • Neutrophil Infiltration
  • Neutrophils / physiology*
  • Pancreas / metabolism*
  • Pancreas / pathology
  • Pancreatitis / metabolism*
  • Pancreatitis / pathology

Substances

  • Chemokine CXCL2
  • Cytokines
  • Inflammation Mediators
  • Naphthols
  • desoxonarchinol A
  • Ceruletide
  • Heme Oxygenase-1
  • Amylases