Syringic Acid Ameliorates Bleomycin Induced Pulmonary Inflammation and Fibrosis in Rats via Maintenance of Endogenous Antioxidants and Downregulation of Pro-Inflammatory Markers

Background

Chronic administration of Bleomycin (BLM), a chemotherapeutic drug, has been linked to Idiopathic Pulmonary Fibrosis (IPF). It has been observed that syringic acid, a phenolic compound, has antiapoptotic, anti-inflammatory and antioxidant properties.

Objectives

To assess syringic acid's therapeutic potential against lung fibrosis caused by BLM and determine potential mechanism of action.

Materials and Methods

Sprague-Dawley rats were inducted into IPF after receiving 7.5 IU/kg of BLM intratracheally. Syringic acid (50 mg/kg, p.o.) was administered to rats for 14 days, after which different parameters in lung and Bronchoalveolar Lavage Fluid (BALF) were measured.

Results

Altered BALF differential cell counts, elevated lung index, hydroxyproline, NO, MDA levels and reduction in GSH, GPx, SOD and CAT in group receiving BLM were evidence of pulmonary toxicity. Administering 50 mg/kg of syringic acid significantly reduced (p<0.001) the changes brought about by BLM. The expression of TNF-α was greatly reduced by syringic acid when it was stimulated by BLM. The BLM-treated group's histological analysis revealed significant lung damage with alveolar septal thickening, interstitial infiltration, collapsing alveolar gaps and an elevated Szapiel score. Syringic acid lessened these effects. Syringic acid group (p<0.01) markedly reduced Szapiel score, collagen deposition, lung edema and fibrotic alterations. It also inhibited infiltration of myofibroblasts and inflammatory cells, primarily macrophages and lymphocytes. This, in turn, improves control of oxidant and pro-inflammatory markers (TNF-α) to decrease collagen deposition during pulmonary fibrosis.

Conclusion

Finally, it is concluded that Syringic acid can protect the lung against BLM-induced pulmonary oxidative stress, inflammation and fibrosis.