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Arachidonic acid cascade enzyme

Molecular classification
Enzyme, Oxidoreductase (for some members), Hydrolase (for phospholipases)
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Overview

The term "Arachidonic acid cascade enzymes" refers collectively to the family of enzymes responsible for metabolizing arachidonic acid into bioactive lipid mediators known as eicosanoids. These include key enzyme classes such as phospholipases (notably phospholipase A₂), cyclooxygenases (COX‑1, COX‑2), lipoxygenases (5-lipoxygenase, among others), various synthases downstream from these pathways, and cytochrome P450 monooxygenases. The products generated by these enzymatic reactions—prostaglandins, thromboxanes, leukotrienes—play central roles in regulating inflammation, pain perception, immune responses, vascular tone, platelet function, fever generation, and other physiological processes. Because dysregulation or overactivation of this pathway contributes to numerous diseases—including inflammatory conditions like arthritis or asthma; pain syndromes; cardiovascular disease; certain cancers—the individual component enzymes are major therapeutic targets. Drugs that inhibit one or more steps in this cascade are widely used clinically but can have significant safety concerns depending on their selectivity profile. Note: For structured data purposes it is recommended to refer to specific canonical targets within this group rather than the collective term "Arachidonic acid cascade enzyme."

Other names
Arachidonic acid pathway enzymesEicosanoid biosynthetic enzymesAA cascade enzymes
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Mechanism of action

– Inhibition of prostaglandin synthesis via cyclooxygenase inhibition (e.g., NSAIDs) – Inhibition of leukotriene synthesis via lipoxygenase inhibition – Multi-target inhibition affecting both prostaglandin and leukotriene pathways for improved efficacy and reduced side effects

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Biological functions

Inflammation mediationPain signalingImmune response modulationRegulation of vascular tone and platelet aggregation
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Disease associations

InflammationPain disordersCardiovascular diseaseCancer (certain components such as 5-lipoxygenase)
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Safety considerations

Gastrointestinal toxicity from non-selective COX inhibition (e.g., ulcers with NSAIDs)Increased cardiovascular risk with selective COX‑2 inhibitors like rofecoxib and celecoxib
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Interacting drugs

Non-steroidal anti-inflammatory drugs (NSAIDs) such as aspirin and ibuprofen

2 more in the full profile.

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Biomarkers

Prostaglandins or their metabolites in plasma/urine for inflammation monitoringLeukotrienes in respiratory diseases

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