Diterpene quinone tanshinone IIA selectively inhibits mouse and human cytochrome P4501A2

Yune Fang Ueng, Ya Hui Kuo, Hsiao Chi Peng, Ta Liang Chen, Woan Ching Jan, F. Peter Guengerich, Yun Lian Lin

研究成果: 雜誌貢獻文章

45 引文 (Scopus)

摘要

1. Tanshinone IIA is the main active diterpene quinone in the herbal medicine Salvia miltiorrhiza. In untreated mouse liver microsomes, tanshinone IIA selectively inhibited 7-ethoxyresorufin O-deethylation (EROD) and 7-methoxyresorufin O-demethylation (MROD) activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, N-nitrosodimethylamine and nifedipine. Tanshinone IIA was a competitive inhibitor of MROD activity with a Ki of 7.2 ± 0.7 nM. 2. In 3-methylcholanthrene-treated mouse liver microsomes, tanshinone IIA and two minor tanshinones, tanshinone I and cryptotanshinone, inhibited liver microsomal MROD activity without affecting EROD and benzo(a)pyrene hydroxylation activities at the concentrations up to 1 μM. Tanshinone IIA induced a type I binding spectrum with a spectral dissociation constant Ks of 2.3 ± 0.8 μM without cooperativity. 3. In human liver microsomes, tanshinone IIA decreased EROD and MROD activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, chtorzoxazone and nifedipine. 4. In Escherichia coli membranes expressing bicistronic human CYP1A enzymes, tanshinone IIA inhibited EROD activity of CYP1A1 with an IC50 48 times higher than that for CYP1A2. Tanshinone I and cryptotanshinone had the same IC50 ratio (1A1/1A2) of 4. 5. The results indicate that tanshinone represents a new group of CYP1A inhibitors, and tanshinone IIA had the highest selectivity in inhibition of CYP1A2.

原文英語
頁(從 - 到)603-613
頁數11
期刊Xenobiotica
33
發行號6
DOIs
出版狀態已發佈 - 六月 1 2003
對外發佈Yes

指紋

Diterpenes
Cytochromes
Liver
Benzo(a)pyrene
Liver Microsomes
Cytochrome P-450 CYP1A2
Tolbutamide
Nifedipine
Inhibitory Concentration 50
benzoquinone
tanshinone
Salvia miltiorrhiza
Dimethylnitrosamine
Oxidation
Hydroxylation
Cytochrome P-450 CYP1A1
Methylcholanthrene
Herbal Medicine
Escherichia coli

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry
  • Pharmacology
  • Toxicology
  • Health, Toxicology and Mutagenesis

引用此文

Ueng, Y. F., Kuo, Y. H., Peng, H. C., Chen, T. L., Jan, W. C., Guengerich, F. P., & Lin, Y. L. (2003). Diterpene quinone tanshinone IIA selectively inhibits mouse and human cytochrome P4501A2. Xenobiotica, 33(6), 603-613. https://doi.org/10.1080/0049825031000105769

Diterpene quinone tanshinone IIA selectively inhibits mouse and human cytochrome P4501A2. / Ueng, Yune Fang; Kuo, Ya Hui; Peng, Hsiao Chi; Chen, Ta Liang; Jan, Woan Ching; Guengerich, F. Peter; Lin, Yun Lian.

於: Xenobiotica, 卷 33, 編號 6, 01.06.2003, p. 603-613.

研究成果: 雜誌貢獻文章

Ueng, YF, Kuo, YH, Peng, HC, Chen, TL, Jan, WC, Guengerich, FP & Lin, YL 2003, 'Diterpene quinone tanshinone IIA selectively inhibits mouse and human cytochrome P4501A2', Xenobiotica, 卷 33, 編號 6, 頁 603-613. https://doi.org/10.1080/0049825031000105769
Ueng, Yune Fang ; Kuo, Ya Hui ; Peng, Hsiao Chi ; Chen, Ta Liang ; Jan, Woan Ching ; Guengerich, F. Peter ; Lin, Yun Lian. / Diterpene quinone tanshinone IIA selectively inhibits mouse and human cytochrome P4501A2. 於: Xenobiotica. 2003 ; 卷 33, 編號 6. 頁 603-613.
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abstract = "1. Tanshinone IIA is the main active diterpene quinone in the herbal medicine Salvia miltiorrhiza. In untreated mouse liver microsomes, tanshinone IIA selectively inhibited 7-ethoxyresorufin O-deethylation (EROD) and 7-methoxyresorufin O-demethylation (MROD) activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, N-nitrosodimethylamine and nifedipine. Tanshinone IIA was a competitive inhibitor of MROD activity with a Ki of 7.2 ± 0.7 nM. 2. In 3-methylcholanthrene-treated mouse liver microsomes, tanshinone IIA and two minor tanshinones, tanshinone I and cryptotanshinone, inhibited liver microsomal MROD activity without affecting EROD and benzo(a)pyrene hydroxylation activities at the concentrations up to 1 μM. Tanshinone IIA induced a type I binding spectrum with a spectral dissociation constant Ks of 2.3 ± 0.8 μM without cooperativity. 3. In human liver microsomes, tanshinone IIA decreased EROD and MROD activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, chtorzoxazone and nifedipine. 4. In Escherichia coli membranes expressing bicistronic human CYP1A enzymes, tanshinone IIA inhibited EROD activity of CYP1A1 with an IC50 48 times higher than that for CYP1A2. Tanshinone I and cryptotanshinone had the same IC50 ratio (1A1/1A2) of 4. 5. The results indicate that tanshinone represents a new group of CYP1A inhibitors, and tanshinone IIA had the highest selectivity in inhibition of CYP1A2.",
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AU - Ueng, Yune Fang

AU - Kuo, Ya Hui

AU - Peng, Hsiao Chi

AU - Chen, Ta Liang

AU - Jan, Woan Ching

AU - Guengerich, F. Peter

AU - Lin, Yun Lian

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N2 - 1. Tanshinone IIA is the main active diterpene quinone in the herbal medicine Salvia miltiorrhiza. In untreated mouse liver microsomes, tanshinone IIA selectively inhibited 7-ethoxyresorufin O-deethylation (EROD) and 7-methoxyresorufin O-demethylation (MROD) activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, N-nitrosodimethylamine and nifedipine. Tanshinone IIA was a competitive inhibitor of MROD activity with a Ki of 7.2 ± 0.7 nM. 2. In 3-methylcholanthrene-treated mouse liver microsomes, tanshinone IIA and two minor tanshinones, tanshinone I and cryptotanshinone, inhibited liver microsomal MROD activity without affecting EROD and benzo(a)pyrene hydroxylation activities at the concentrations up to 1 μM. Tanshinone IIA induced a type I binding spectrum with a spectral dissociation constant Ks of 2.3 ± 0.8 μM without cooperativity. 3. In human liver microsomes, tanshinone IIA decreased EROD and MROD activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, chtorzoxazone and nifedipine. 4. In Escherichia coli membranes expressing bicistronic human CYP1A enzymes, tanshinone IIA inhibited EROD activity of CYP1A1 with an IC50 48 times higher than that for CYP1A2. Tanshinone I and cryptotanshinone had the same IC50 ratio (1A1/1A2) of 4. 5. The results indicate that tanshinone represents a new group of CYP1A inhibitors, and tanshinone IIA had the highest selectivity in inhibition of CYP1A2.

AB - 1. Tanshinone IIA is the main active diterpene quinone in the herbal medicine Salvia miltiorrhiza. In untreated mouse liver microsomes, tanshinone IIA selectively inhibited 7-ethoxyresorufin O-deethylation (EROD) and 7-methoxyresorufin O-demethylation (MROD) activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, N-nitrosodimethylamine and nifedipine. Tanshinone IIA was a competitive inhibitor of MROD activity with a Ki of 7.2 ± 0.7 nM. 2. In 3-methylcholanthrene-treated mouse liver microsomes, tanshinone IIA and two minor tanshinones, tanshinone I and cryptotanshinone, inhibited liver microsomal MROD activity without affecting EROD and benzo(a)pyrene hydroxylation activities at the concentrations up to 1 μM. Tanshinone IIA induced a type I binding spectrum with a spectral dissociation constant Ks of 2.3 ± 0.8 μM without cooperativity. 3. In human liver microsomes, tanshinone IIA decreased EROD and MROD activities without affecting the oxidation of benzo(a)pyrene, tolbutamide, chtorzoxazone and nifedipine. 4. In Escherichia coli membranes expressing bicistronic human CYP1A enzymes, tanshinone IIA inhibited EROD activity of CYP1A1 with an IC50 48 times higher than that for CYP1A2. Tanshinone I and cryptotanshinone had the same IC50 ratio (1A1/1A2) of 4. 5. The results indicate that tanshinone represents a new group of CYP1A inhibitors, and tanshinone IIA had the highest selectivity in inhibition of CYP1A2.

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