Effects of andrographolide on the expression of eosinophil granulocytes and possible mechanisms.
- Author:
Yan-Hua LI
1
;
Mei-Yi WANG
;
Rong JIN
;
Sheng GUO
;
Xiao-Yong FAN
;
Hui MA
;
Liang-Xia WU
;
Jian-Hua ZHANG
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Asthma; drug therapy; Bronchoalveolar Lavage Fluid; cytology; Chemokine CCL11; analysis; genetics; Diterpenes; pharmacology; Eosinophils; drug effects; physiology; Female; Interleukin-5; analysis; genetics; Mice; Mice, Inbred BALB C; RNA, Messenger; analysis
- From: Chinese Journal of Contemporary Pediatrics 2012;14(5):371-374
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVEAndrographolide, the active component in andrographis paniculata, has potent anti-inflammatory actions. This study aimed to evaluate the effects of andrographolide on eosinophil granulocytes (EOS) and the expression of eotaxin and IL-5 in mice with asthma.
METHODSBALB/c mice were randomly assigned into normal control, asthma, budesonide treatment and andrographolide treatment groups (n=8 each). Mice in the latter three groups were sensitized and challenged with ovalbumin (OVA) to induce asthma. ELISA was used to detect the concentrations of eotaxin and IL-5 in bronchoalveolar lavage fluid (BALF) and peripheral blood. The expression of eotaxin mRNA and IL-5 mRNA in lung tissues was detected by real-time quantitative PCR.
RESULTSAndrographolide treatment significantly decreased EOS count in BALF (P<0.05) and the effect of andrographolide was better than the effect of budesonide. Andrographolide treatment significantly down-regulated the expression of eotaxin and IL-5 in BALF, lung eotaxin mRNA expression and blood IL-5 expression (P<0.05), but the effects of andrographolide were poorer than the effects of budesonide. Andrographolide treatment resulted in a decrease in blood eotaxin expression and lung IL-5 mRNA expression and the effects of andrographolide were similar to budesonide.
CONCLUSIONSAndrographolide can down-regulate the expression of IL-5 and eotaxin and thus suppress the inflitration of EOS in a mouse model of asthma.
