Effect of all-trans retinoic acid on airway inflammation in asthmatic rats and its mechanism.
- Author:
Hong FANG
1
;
Hongfang JIN
;
Hongwei WANG
Author Information
1. Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Asthma;
metabolism;
pathology;
Bronchoalveolar Lavage Fluid;
cytology;
Dexamethasone;
pharmacology;
I-kappa B Proteins;
biosynthesis;
genetics;
Inflammation;
Intercellular Adhesion Molecule-1;
biosynthesis;
genetics;
Male;
NF-kappa B;
biosynthesis;
genetics;
Random Allocation;
Rats;
Rats, Sprague-Dawley;
Respiratory System;
Tretinoin;
pharmacology
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2004;24(3):229-232
- CountryChina
- Language:English
-
Abstract:
The inhibitive effects of all-trans retinoic acid (ARTA) on airway inflammation in asthmatic rats and its mechanism on the basis of the regulation of nuclear factor kappaB (NF-kappaB) were explored. Thirty-two SD rats were randomly divided into 4 groups: control group, asthma group, dexamethasone treatment group and retinotic acid treatment group. The total and differential cell counts in the collected bronchoalveolar lavage fluid (BALF) were measured. The pathological changes in lung tissues were estimated by scoring. The expression of NF-kappaB inhibitor (IkappaBa), NF-kappaB, intercellular adhering molecule-1 (ICAM-1) in lung tissue was detected by immunohistochemical method. The results showed that in the two treatment groups, the total cell counts and proportion of inflammatory cells in BALF were significantly reduced, but there was no significant difference in differential cell counts in BALF between them. The pathological changes in lung tissues in the treatment groups were significantly attenuated as compared with asthma group. Except the epithelial injury in retinotic acid treatment group was milder than in dexamethasone treatment group, the remaining lesions showed no significant difference between them. In the two treatment groups, the expression of IkappaBa was increased, while the expression of NF-kappaB and ICAM-1 decreased with the difference between the two groups being not significant. It was concluded that the similar anti-inflammatory effects and mechanism of ATRA on airway in asthmatic rats to those of dexamethasone were contributed to the increase of cytoplasmic IkappaBa content and suppression of NF-kappaB activation and expression.
