The Protective Effects of 2,3,5,4'-Tetrahydroxystilbene-2- O -β-d-Glucoside in the OVA-Induced Asthma Mice Model

• Published in: International journal of molecular sciences Vol. 19; no. 12; p. 4013
• Main Authors: Hwang, Yun-Ho, Kim, Su-Jin, Kim, Hangun, Yee, Sung-Tae
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 12.12.2018; MDPI
• Subjects: 2,3,5,4′-tetrahydroxystilbene-2-O-β- d -glucoside (TSG); airway hyperresponsiveness (AHR); Airway management; Animal models; Asthma; Blood; Bronchus; Clinical trials; Cytokines; Cytotoxicity; Glucosides; Health services; Helper cells; Immune response; Immunoglobulin E; Immunoglobulin G; Immunoglobulins; inflammation; Inflammatory diseases; Interleukin 4; Interleukin 5; Liver; Lungs; Lymphocytes T; Natural products; Osteoporosis; Oxidation; Respiratory tract; Respiratory tract diseases; Side effects; Steroids; γ-Interferon; asthma; airway hyperresponsiveness (AHR); inflammation; 2,3,5,4′-tetrahydroxystilbene-2-O-β-d-glucoside (TSG)
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms19124013

Asthma is an inflammatory disease caused by an imbalance of Th1 and Th2 cells. In general, asthma is characterized by a stronger Th2 response. Most conventional asthma treatment focuses on improving airway flow or suppression of airway inflammation. To reduce the side effects of currently used asthma medicines, we have conducted studies on natural products that have no side effects. 2,3,5,4'-tetrahydroxystilbene-2-O-β-d-glucoside (TSG), the main compound of (PM), has various biological activities, including anti-inflammation and anti-oxidation activities. However, the effect of TSG on asthma has not been studied yet. We examined the effects of TSG on Th2 immune responses using an OVA-induced asthma animal model. OVA-sensitized mice were treated with TSG. 24 h after the last intranasal challenge, airway hyperresponsiveness (AHR) was measured or serum and bronchoalveolar lavage fluid (BALF) were harvested. We measured typical Th1 and Th2 cytokines in serum and BALF. As a result, TSG suppressed Th2 responses, as shown by the lower levels of IL-4, IL-5, total IgE, OVA-specific IgE, and OVA-specific IgG1. On the other hand, TSG increased Th1 responses, as shown by the levels of IFN-gamma. Collectively, these results confirm the potential of TSG for asthma treatment through modulation of inflammatory responses. Considering that the cytotoxic effect of PM extract is due to the cis isomer of TSG, if the effect of TSG on asthma treatment is found to be non-toxic in clinical trials, it would be more effective to use it as a purified component than PM extract as an asthma treatment agent.