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"Inflammatory enzymes" collectively refer to various enzymes that play key roles in initiating, propagating, regulating, or resolving inflammatory responses within tissues and organs.[3] These include but are not limited to proteases such as serine proteases and matrix metalloproteinases; oxidoreductases like cyclooxygenases; hydrolases including phospholipase A2; caspases involved in cell death pathways; deubiquitinylating enzymes modulating immune signaling cascades; among others.[2][7] They act through diverse mechanisms—such as activating pro-inflammatory cytokines,[1] degrading extracellular matrix components during tissue injury,[4] generating lipid mediators,[4] or controlling immune cell migration—and their dysregulation contributes significantly to acute and chronic inflammatory diseases.[2][4] For research or clinical purposes requiring structured information about drug targets, it is necessary to specify *which* particular inflammatory mediator/enzyme you mean—such as “cyclooxygenase‑2,” “matrix metalloproteinase‑9,” etc.—rather than using the generic category “inflammatory enzyme.”
Varies depending on the enzyme: Inhibition of prostaglandin synthesis via COX inhibition reduces inflammation. Protease inhibitors block tissue-degrading proteolytic activity. Modulation/inhibition of cytokine processing or release.
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