Title of article :
Tanshinone IIA attenuates ovalbumin-induced airway inflammation and hyperresponsiveness in a murine model of asthma
Author/Authors :
Guo, Xiao-Feng Department of Pediatric - Fujian Provincial Meternity and Children’s Hospital of Fujian Medical University - Fuzhou - Fujian 350001, China , Wang, Shi-Biao Department of Pediatric - Fujian Provincial Meternity and Children’s Hospital of Fujian Medical University - Fuzhou - Fujian 350001, China , Wengj, Bin Department of Pediatric - Fujian Provincial Meternity and Children’s Hospital of Fujian Medical University - Fuzhou - Fujian 350001, China , Zhang, Hui-Jie Department of Pediatric - Fujian Provincial Meternity and Children’s Hospital of Fujian Medical University - Fuzhou - Fujian 350001, China , Tang, Su-Ping Department of Allergy - Fuzhou Children’s Hospital - Teaching Hospital of Fujian Medical University - Fuzhou - Fujian 350005, China
Abstract :
Tanshinone IIA (T. IIA), one of the most pharmacologically active components extracted
from Salviae miltiorrhiza, has anti-inflammatory and antioxidant features. The aim of the present
study is to investigate the benefit of T. IIA on asthma using a murine model of asthma induced by
ovalbumin (OVA).
Materials and Methods: Male BALB/c mice were used in the present study. The mice were sensitized by
OVA intraperitoneal injection on days 0 and 14, and received aerosolized OVA challenge for 30 min daily on
days 21-23. T. IIA (10 mg/kg twice daily) intraperitoneal injection was performed on days 18-23.
Results: Treatment of T. IIA reduced the levels of interleukin (IL)-4, IL-5, and IL-13 in bronchoalveolar
lavage fluid (BALF) (P<0.05 for all cases). The OVA-induced elevation of total white blood cells as
well as differential white blood cells in BALF and blood were inhibited by T. IIA (P<0.05 for all cases).
Moreover, airway hyperresponsiveness was dampened in T. IIA-treated group (P<0.05). T. IIA inhibited
the activation of nuclear factor-κB in asthmatic mice (P<0.05). The activity of nuclear factor erythroid-
2-related factor 2 was enhanced in T. IIA-treated group (P<0.05). T. IIA elevated the activities of heme
oxygenase-1, glutathione peroxidase, and superoxide dismutase (P<0.05 for all cases).
Conclusion: T. IIA inhibits OVA-induced airway inflammation and hyperresponsiveness. T. IIA is a
potential therapeutic agent for asthma.
Keywords :
Tanshinone IIA , Asthma , Inflammation , Nuclear factor-κB , Oxidative stress
Journal title :
Astroparticle Physics