NPC 15669, an inhibitor of neutrophil recruitment, is efficacious in acetic acid-induced colitis in rats

Gastroenterology. 1993 Apr;104(4):1021-9. doi: 10.1016/0016-5085(93)90269-i.

Abstract

Background: The efficacy of the leukocyte recruitment inhibitor, N-[9H-2,7-dimethylfluoren-9-ylmethoxy)carbonyl]-L-leucine (NPC 15669) was compared with drugs used to treat inflammatory bowel diseases in a rat model, acetic acid-induced colitis.

Methods: Colonic damage assessed by visual inspection, histological quantitation of tissue injury, vascular permeability, myeloperoxidase (MPO) accumulation, and synthesis of inflammatory mediators were measured.

Results: Intrarectal pretreatment with NPC 15669 results in a significant reduction of all measured indices of inflammation. The median effective dose (ED50) of NPC 15669 for inhibition of MPO accumulation and vascular permeability is 13.2 mg/kg and 31 mg/kg, respectively. The active moiety of sulfasalazine, 5-aminosalicylic acid (5-ASA), the antioxidant/5-lipoxygenase inhibitor, nordihydroguaiaretic acid (NDGA) and the corticosteroids dexamethasone and hydrocortisone, yielded ED50 values (MPO accumulation) of 68 mg/kg, 95 mg/kg, 0.7 mg/kg, and 13 mg/kg, respectively. When formulated suspensions of NPC 15669, 5-ASA, or dexamethasone were used, potency was increased 10-40-fold. Furthermore, NPC 15669 (10 mg/kg) administered 7 hours after acetic acid and evaluated 24 hours after acetic acid administration significantly attenuated neutrophil influx (70% inhibition of MPO accumulation), whereas 5-ASA (100 mg/kg) displayed no therapeutic effects.

Conclusions: NPC 15669 may be useful in the treatment of inflammatory disorders.

MeSH terms

  • Acetates
  • Acetic Acid
  • Aminosalicylic Acids / pharmacology
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Capillary Permeability / drug effects
  • Colitis / drug therapy
  • Colitis / pathology
  • Colitis / physiopathology*
  • Colon / drug effects
  • Colon / pathology
  • Colon / physiopathology*
  • Dexamethasone / pharmacology
  • Fluorenes / pharmacology
  • Glycine / analogs & derivatives
  • Glycine / pharmacology
  • Hydrocortisone / pharmacology
  • Leucine / analogs & derivatives*
  • Leucine / pharmacology
  • Leucine / therapeutic use
  • Leukotriene B4 / analysis
  • Leukotriene B4 / metabolism
  • Male
  • Masoprocol / pharmacology
  • Mesalamine
  • Neutrophils / drug effects
  • Neutrophils / physiology*
  • Peroxidase / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Thromboxane B2 / analysis
  • Thromboxane B2 / metabolism

Substances

  • Acetates
  • Aminosalicylic Acids
  • Anti-Inflammatory Agents, Non-Steroidal
  • Fluorenes
  • N-(9H-(2,7-dimethylfluoren-9-ylmethoxy)carbonyl)leucine
  • Leukotriene B4
  • N-(9H-(fluoren-9-ylmethoxy)carbonyl)glycine
  • Mesalamine
  • Thromboxane B2
  • Masoprocol
  • Dexamethasone
  • Peroxidase
  • Leucine
  • Acetic Acid
  • Glycine
  • Hydrocortisone