Suppressive effects of nitric oxide-releasing prednisolone NCX-1015 on the allergic pleural eosinophil recruitment in rats

Clin Exp Allergy. 2008 Nov;38(11):1830-7. doi: 10.1111/j.1365-2222.2008.03083.x. Epub 2008 Aug 3.

Abstract

Background: The addition of a nitric oxide (NO)-releasing moiety to prednisolone was shown to enhance the anti-inflammatory activity of this glucocorticoid in some experimental conditions, but its effectiveness in the context of eosinophilic inflammation remains to be elucidated.

Objective: This study compared the anti-inflammatory effect of prednisolone to a NO-releasing derivative of prednisolone, NCX-1015, using a model of allergen-evoked eosinophil recruitment in rats. The efficacy of a NO-donor compound, DETA-NONOate, was also assessed for comparison.

Methods: Wistar rats were actively sensitized with Al(OH)(3) plus ovalbumin and 14 days later challenged with antigen intrapleurally. Treatments were performed locally 1 h before challenge. Cysteinyl-leucotrienes (Cys-LT) and eotaxin were measured by ELISA.

Results: Antigen challenge induced an eosinophil infiltration at 12 h, maximal at 24 h. It also caused an increase in the levels of Cys-LTs in the pleural exudate and in the expression of 5-lipoxygenase (5-LO) in infiltrated leucocytes at 6 h, peaking at 12 h and persisting for at least 24 h. Treatment with equimolar doses of prednisolone and NCX-1015 inhibited the late eosinophil infiltration, although the dose required to produce maximal inhibition was about one-tenth that of prednisolone. Cys-LT generation and 5-LO expression were inhibited by NCX-1015 but not by prednisolone. Treatment with prednisolone combined with the NO-donor DETA-NONOate led to a greater inhibition of the eosinophilia and Cys-LT generation as compared with either drug alone. Administration of the steroid receptor antagonist RU 486, 1 h before prednisolone and NCX-1015, abolished the inhibitory effect of the former, under conditions where it only partially affected the latter.

Conclusions: Our findings indicate that NCX-1015 provided a greater anti-inflammatory effect than prednisolone on the allergic eosinophil recruitment in rats, suggesting that NO-releasing steroids can be considered as a promising therapeutic approach to allergic diseases.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / therapeutic use
  • Arachidonate 5-Lipoxygenase / metabolism
  • Chemokine CCL11 / metabolism
  • Cysteine / metabolism
  • Disease Models, Animal
  • Drug Therapy, Combination
  • Eosinophilia / etiology
  • Eosinophilia / pathology
  • Eosinophilia / prevention & control*
  • Eosinophils / cytology
  • Hypersensitivity / complications*
  • Hypersensitivity / drug therapy
  • Leukocytes / cytology
  • Leukocytes / metabolism
  • Leukocytes, Mononuclear / cytology
  • Leukotrienes / metabolism
  • Male
  • Mifepristone / pharmacology
  • Neutrophils / cytology
  • Nitric Oxide Donors / therapeutic use*
  • Nitroso Compounds / therapeutic use
  • Ovalbumin / immunology
  • Pleural Cavity / metabolism
  • Pleural Cavity / pathology
  • Pleurisy / etiology
  • Pleurisy / pathology
  • Pleurisy / prevention & control*
  • Prednisolone / analogs & derivatives*
  • Prednisolone / therapeutic use
  • Rats
  • Rats, Wistar
  • Receptors, Glucocorticoid / antagonists & inhibitors

Substances

  • Anti-Inflammatory Agents
  • Ccl11 protein, mouse
  • Chemokine CCL11
  • Leukotrienes
  • Nitric Oxide Donors
  • Nitroso Compounds
  • Receptors, Glucocorticoid
  • cysteinyl-leukotriene
  • prednisolone 21-((4'-nitrooxymethyl)benzoate)
  • 2,2'-(hydroxynitrosohydrazono)bis-ethanamine
  • Mifepristone
  • Ovalbumin
  • Prednisolone
  • Arachidonate 5-Lipoxygenase
  • Cysteine