[Influence of peroxisome proliferator-activated receptor gamma on airway inflammation of guinea pigs with asthma]

Zhonghua Jie He He Hu Xi Za Zhi. 2004 Mar;27(3):169-73.
[Article in Chinese]

Abstract

Objective: To investigate the influence and mechanism of peroxisome proliferator-activated receptor gamma (PPAR-gamma) and its ligand agonist rosiglitazone on airway inflammation of guinea pigs with asthma.

Methods: 35 guinea pigs were divided into 5 groups by random number meter: a control group (A group), an asthma group (B group), a dexamethasone (DXM) group (C group), a rosiglitazone group (D group), and a rosiglitazone + 1/2 DXM group (E group), with 7 guinea pigs in each. Bronchoalveolar lavage (BAL) cell count and differential was studied, and the pathologic alteration of the bronchi and the lung tissue was observed. The expression of PPAR-gamma, COX-2 was measured by RT-PCR.

Results: BAL eosinophil count was 0.050 +/- 0.020 in D group, 0.110 +/- 0.020 in B group, the difference being significantly (t = 5.61, P < 0.001). The total cell number and neutrophils were (15.5 +/- 3.9) x 10(8)/L and 0.069 +/- 0.020 in D group, and (19.9 +/- 4.3) x 10(8)/L and 0.076 +/- 0.020 in B group, the difference being not significant (t = 2.02, 0.66, P > 0.05 respectively). The thickness of airway wall of D group was (22.0 +/- 5.0) micro m, and in B group it was (28.0 +/- 5.0) micro m, the difference being significant (t = 2.61, P < 0.05), but the thickness of mucosa and submucosa of D group (12.2 +/- 2.9) micro m was not different as compared with B group (14.9 +/- 3.3) micro m (t = 1.63, P > 0.05). Expression of PPAR-gamma mRNA of D group 19.5 +/- 3.0 was not different compared with B group 18.1 +/- 3.1 and A group 15.6 +/- 2.9 respectively (t = 0.92, 0.49, P > 0.05, respectively). When the expression of COX-2 mRNA of B group 49 +/- 7 was compared with D group 39 +/- 6, the difference was significant (t = 2.77, P < 0.05).

Conclusions: Rosiglitazone decreases airway eosinophils and the thickness of airway wall in guinea pigs with asthma, via suppression of COX-2 mRNA expression by activating PPAR-gamma. The anti-inflammatory effect of PPAR-gamma may be associated with the use of ligand agonist and(or) glucocorticoids.

MeSH terms

  • Animals
  • Asthma / chemically induced
  • Asthma / metabolism*
  • Asthma / pathology
  • Bronchi / metabolism*
  • Bronchi / pathology
  • Bronchoalveolar Lavage Fluid / cytology
  • Cyclooxygenase 2
  • Eosinophils / cytology
  • Female
  • Guinea Pigs
  • Inflammation / metabolism
  • Inflammation / pathology
  • Isoenzymes / biosynthesis*
  • Isoenzymes / genetics
  • Lung / metabolism
  • Lung / pathology
  • Male
  • Prostaglandin-Endoperoxide Synthases / biosynthesis*
  • Prostaglandin-Endoperoxide Synthases / genetics
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptors, Cytoplasmic and Nuclear / biosynthesis*
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Rosiglitazone
  • Thiazolidinediones / pharmacology*
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics

Substances

  • Isoenzymes
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Thiazolidinediones
  • Transcription Factors
  • Rosiglitazone
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases