Target intelligence / Profile preview

Superoxide dismutase enzyme (SOD)

Target
SOD
Molecular classification
Enzyme, Antioxidant enzyme family, Metalloprotein
01

Overview

Superoxide dismutase enzyme refers to a family of metalloenzymes present in nearly all aerobic organisms that catalyze the conversion ("dismutation") of the highly reactive superoxide anion radical into molecular oxygen and hydrogen peroxide—a critical antioxidant defense mechanism protecting cells from oxidative damage caused by normal metabolism or environmental stresses. In humans, there are several isoforms including cytosolic Cu/Zn-SOD (SOD1), mitochondrial Mn-SOD (SOD2), and extracellular forms. Deficiency or mutation—especially in SOD1—is linked to neurodegenerative disorders such as familial amyotrophic lateral sclerosis. The enzymes play dual roles both limiting ROS toxicity and regulating redox-sensitive cellular signaling pathways involved in apoptosis, inflammation, aging-related diseases, cancer progression/inhibition, cardiovascular health, among others.

Other names
Superoxide dismutaseSODCu/Zn superoxide dismutase (for the cytosolic form, SOD1)Manganese superoxide dismutase (MnSOD, for mitochondrial form, SOD2)Orgotein (pharmaceutical preparation)PaloseinMetalloprotein
02

Mechanism of action

Drugs or supplements containing superoxide dismutase act by catalyzing the conversion of harmful superoxide radicals into molecular oxygen and hydrogen peroxide, thereby reducing oxidative stress in tissues. This mechanism underlies their proposed anti-inflammatory effects in diseases like osteoarthritis and rheumatoid arthritis.

03

Biological functions

Destruction of free superoxide radicals (antioxidant defense)Regulation of reactive oxygen species (ROS) and reactive nitrogen species levelsProtection against oxidative stress-induced cell damageModulation of apoptosis and cell signaling pathways
04

Disease associations

Neurodegenerative disease (e.g., amyotrophic lateral sclerosis, Parkinson's disease)Inflammation (e.g., rheumatoid arthritis, osteoarthritis)Cardiovascular diseaseCancer (investigational/experimental roles)
05

Safety considerations

Oral supplementation is limited by poor bioavailability due to degradation by gastric acidNewer formulations attempt to address bioavailability issuesInjectable forms may cause pain/irritation at injection sitesLimited evidence regarding long-term safetyGenerally regarded as nontoxic but data on new formulations are lackingUse during pregnancy/lactation is not recommended due to insufficient safety data
06

Interacting drugs

Bovine or plant-derived SOD (in pharmaceutical preparations/supplements)

2 more in the full profile.

07

Biomarkers

Superoxide dismutase activity levels in blood or tissues (for oxidative stress status)Mutations in the SOD1 gene (for familial amyotrophic lateral sclerosis)

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