Ewha Med J.  1995 Sep;18(3):161-167. 10.12771/emj.1995.18.3.161.

Effect of Nifedipine on Induction of Cytochrome P-450 1A1 and 2B1 in Spontaneously Hypertensive Rate

Affiliations
  • 1Department of Biochemistry, Medical College, Ewha Womans University, Korea.
  • 2Department of Pharmacology, Medical College, Ewha Womans University, Korea.
  • 3Laboratory Of Comparative Carcinogenesis NCI-Frederick Cancer Research and Developmental Center, Korea.

Abstract

Cytochrome P-450(CYP) enzymes are important in catalyzing the hiotransffrmation on manyendogeneous compounds and xenobiotics, including drugs and carcinogens. In the presentstudy, effect of nifedipine a voltage dependent calcium channel blocker on the induction ofCYP1A1 and 2B1 was investigated. Change of CYP1A1 and 2B1 activities were measuredby using specific enzyme activities and Western blot analysis. CYP1A1, as quantified by ethoxyresorufin-0-deethylase activity and Western blot with monoclonal antibody 1-7-1, increasedin liver microsome of nifedipine-treated spontaneous hypertensive rat(SHR. 30mg/kg.b.w, twicea day for 3days) but not in kidney microsome. CYP2B1, as quantified by benzyloxyresorufin-O-dealkylase activity and Western blot wit]1 monoclonal antibody 2-66-3, markedly increasedin liver microsome of nifedipine-treated SHR but slightly in kidney microsome. The resultsdemonstrate that nifedipine is a potent inducer of CYP2B1 in SHR.


MeSH Terms

Blotting, Western
Calcium Channels
Carcinogens
Cytochrome P-450 CYP1A1
Cytochrome P-450 CYP2B1
Cytochrome P-450 Enzyme System*
Cytochromes*
Kidney
Microsomes
Microsomes, Liver
Nifedipine*
Xenobiotics
Calcium Channels
Carcinogens
Cytochrome P-450 CYP1A1
Cytochrome P-450 CYP2B1
Cytochrome P-450 Enzyme System
Cytochromes
Nifedipine
Xenobiotics
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