Effect of biologically active fraction of Nardostachys jatamansi on cerulein-induced acute pancreatitis

World J Gastroenterol. 2012 Jul 7;18(25):3223-34. doi: 10.3748/wjg.v18.i25.3223.

Abstract

Aim: To determine if the fraction of Nardostachys jatamansi (NJ) has the potential to ameliorate the severity of acute pancreatitis (AP).

Methods: Mice were administered the biologically active fraction of NJ, i.e., the 4th fraction (NJ4), intraperitoneally, and then injected with the stable cholecystokinin analogue cerulein hourly for 6 h. Six hours after the last cerulein injection, the pancreas, lung, and blood were harvested for morphological examination, measurement of cytokine expression, and examination of neutrophil infiltration.

Results: NJ4 administration attenuated the severity of AP and lung injury associated with AP. It also reduced cytokine production and neutrophil infiltration and resulted in the in vivo up-regulation of heme oxygenase-1 (HO-1). Furthermore, NJ4 and its biologically active fraction, NJ4-2 inhibited the cerulein-induced death of acinar cells by inducing HO-1 in isolated pancreatic acinar cells.

Conclusion: These results suggest that NJ4 may be a candidate fraction offering protection in AP and NJ4 might ameliorate the severity of pancreatitis by inducing HO-1 expression.

Keywords: Acute pancreatitis; Cytokines; Heme oxygenase-1; Nardostachys jatamansi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Cell Death / drug effects
  • Ceruletide*
  • Cytokines / metabolism
  • Cytoprotection
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Enzymes / blood
  • Female
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / metabolism
  • Inflammation Mediators / metabolism
  • Lung / drug effects
  • Lung / pathology
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nardostachys* / chemistry
  • Neutrophil Infiltration / drug effects
  • Pancreas / drug effects*
  • Pancreas / metabolism
  • Pancreas / pathology
  • Pancreatitis / chemically induced
  • Pancreatitis / genetics
  • Pancreatitis / metabolism
  • Pancreatitis / pathology
  • Pancreatitis / prevention & control*
  • Plant Extracts / pharmacology*
  • Plant Roots
  • Severity of Illness Index
  • Time Factors
  • Up-Regulation

Substances

  • Cytokines
  • Enzymes
  • Inflammation Mediators
  • Membrane Proteins
  • Plant Extracts
  • Ceruletide
  • Heme Oxygenase-1
  • Hmox1 protein, mouse