Therapeutic Effect of Bilsaan, Sambucus nigra Stem Exudate, on the OVA-Induced Allergic Asthma in Mice.
Faris A AlrumaihiAhmad A AlmatroudiKhaled S AllemailemArshad Husain RahmaniArif KhanMasood Alam KhanPublished in: Oxidative medicine and cellular longevity (2020)
Asthma is characterized by the elevated level of Th2 immune responses, oxidative stress, and airway inflammation. Bilsaan, an exudate from the stem of Sambucus nigra, has been traditionally used in the treatment of various ailments in Saudi Arabia. Here, we investigated the therapeutic potential of Bilsaan against ovalbumin- (OVA-) induced allergic asthma in a mouse model. In order to induce allergic asthma, mice were intraperitoneally injected with alum-emulsified-OVA (20 μg/mouse) on days 0, 14, and 21 that is followed by an intranasal OVA exposure from days 22 to 30. During this time, mice were orally administered with Bilsaan at the doses of 5, 10, and 25 mg/kg. The numbers of total and differential inflammatory cells and the levels of Th2 cytokines (IL-4, IL-5, and IL-13) and IgE were determined in bronchoalveolar lavage fluid (BALF). Moreover, the therapeutic effect of Bilsaan was also assessed to analyze the oxidative stress and inflammatory changes in the lung tissues. The results demonstrated that Bilsaan treatment significantly reduced the total and differential inflammatory cell count in the BALF. The BALF from the mice treated with Bilsaan showed significantly lower levels of IL-4, IL-5, IL-13, and IgE. Interestingly, a similar pattern was observed in IL-4, IL-5, and IL-13 secreted by OVA-sensitized splenocytes from the mice of various groups. Bilsaan treatment alleviated the status of oxidative stress by modulating malondialdehyde (MDA), superoxide dismutase (SOD), and catalase levels in the lung. Moreover, Bilsaan treatment reduced the infiltration of inflammatory cells, thickening of alveolar wall, and congestion in the lung tissues. The findings of the present study demonstrated an antiasthmatic effect of Bilsaan through the modulation of Th2 immune responses, inflammation, and the oxidative stress.
Keyphrases
- oxidative stress
- induced apoptosis
- diabetic rats
- immune response
- chronic obstructive pulmonary disease
- mouse model
- dna damage
- ischemia reperfusion injury
- lung function
- high fat diet induced
- gene expression
- endoplasmic reticulum stress
- cell cycle arrest
- high glucose
- combination therapy
- cell death
- signaling pathway
- single cell
- mesenchymal stem cells
- adipose tissue
- toll like receptor
- skeletal muscle
- cell proliferation
- dendritic cells
- metabolic syndrome
- high resolution
- atomic force microscopy
- bone marrow
- heat stress