In vitro effects of some drugs on catalase purified from human skin

J Enzyme Inhib Med Chem. 2006 Apr;21(2):231-4. doi: 10.1080/14756360500483453.

Abstract

Catalase enzyme (H202: oxidoreductase; E.C. 1.11.1.6) was purified from human skin homogenate using ammonium sulfate precipitation and DEAE-Sephadex A50 ion exchange chromatography at 4 degrees C and some characteristics of the enzyme were investigated. The human skin enzyme, having a specific activity of 1354.5 EU/mg proteins was purified with a yield of 43.13% and 1110-fold. Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) showed a single band for the enzyme. Inhibition by piroxicam, ketoprofen, diclofenac sodium, sulfamethoxazole and nidazole occurred with I50 values of 0.414, 1.29, 1.8, 3.83, and 8.64 mM, respectively.

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / metabolism
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Catalase / isolation & purification
  • Catalase / metabolism*
  • Diclofenac / pharmacology
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • In Vitro Techniques
  • Inhibitory Concentration 50
  • Ketoprofen / pharmacology
  • Piroxicam / pharmacology
  • Skin / cytology
  • Skin / enzymology*
  • Sulfamethoxazole / pharmacology

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Enzyme Inhibitors
  • Piroxicam
  • Diclofenac
  • Ketoprofen
  • Catalase
  • Sulfamethoxazole