Bovine lung tissue was hydrolyzed using three different proteases, papain, pepsin, or Alcalase, to generate hydrolysates. Hydrolysates showed little antioxidant activity in noncellular or cellular assays. The antiâinflammatory activity of hydrolysates was assessed in RAW264.7 macrophages and Jurkat T cells. Treatment with the Alcalase hydrolysate significantly decreased the production of the proâinflammatory cytokines interleukin (IL)â6 and ILâ1ÎČ in a dose dependent manner in RAW264.7 cells. Nitric oxide production also significantly decreased following treatment with this hydrolysate. The papain hydrolysate decreased ILâ6, ILâ1ÎČ, and NO production in RAW264.7 cells and ILâ2 production in Jurkat T cells. However, the decrease was likely due to cytotoxicity of this hydrolysate toward these cell lines. The pepsin hydrolysate had no effect on cytokine production in RAW264.7 cells and only slightly decreased ILâ2 production in Jurkat T cells.
Practical applications
Meat production generates large amounts of protein rich coâproducts, which are often discarded as waste or sold as low value animal feeds. The enzymatic hydrolysis of these protein coâproducts may produce hydrolysates that are capable of reducing oxidation or inflammation. Novel hydrolysates were generated from the hydrolysis of bovine lung and results from this study indicate that the hydrolysis of bovine lung using the commercially available protease Alcalase may have potential as an antiâinflammatory agent.