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Research ArticleExperimental Studies

Comparative Anti-inflammatory Activities of Curcumin and Tetrahydrocurcumin Based on the Phenolic O-H Bond Dissociation Enthalpy, Ionization Potential and Quantum Chemical Descriptor

YUKIO MURAKAMI, HIROAKI ISHII, NAOKI TAKADA, SHOJI TANAKA, MAMORU MACHINO, SHIGERU ITO and SEIICHIRO FUJISAWA
Anticancer Research March 2008, 28 (2A) 699-707;
YUKIO MURAKAMI
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  • For correspondence: ymura@dent.meikai.ac.jp
HIROAKI ISHII
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NAOKI TAKADA
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SHOJI TANAKA
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MAMORU MACHINO
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SHIGERU ITO
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SEIICHIRO FUJISAWA
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Abstract

Curcumin and its reduced derivative tetrahydrocurcumin have been shown to exhibit chemopreventive activity. Cyclooxygenase-2 (COX-2) inhibition in lipopolysaccharide (LPS)- or Porphyromonas gingivalis fimbria-stimulated RAW 264.7 cells was investigated using Northern blot analysis. The fimbria-stimulated expression of the COX-2 gene was inhibited by curcumin but not by tetrahydrocurcumin. LPS-stimulated COX-2 gene expression was completely inhibited by curcumin, but an increase in the concentration of tetrahydrocurcumin did not cause complete inhibition of COX-2 expression. The inhibitory effect of curcumin on nuclear factor kappa B (NF-κB) activation in the cells was clearly observed, but that of tetrahydrocurcumin was incomplete even at a concentration of 20 μM. To explain the difference in effect between the two compounds, analysis of the frontier orbital was performed using ab initio 6-31G* wave function. The calculated chemical hardness (η) for curcumin was clearly smaller, whereas its electronegativity (χ) and electrophilicity (ω) were clearly greater than the corresponding values for the curcumin-related compounds tetrahydrocurcumin, isoeugenol and eugenol. This suggested that the anti-inflammatory activities of curcumin may be related to η-, χ- and/or ω-controlled enzymes. In addition, the bond dissociation enthalpy (BDE) of the phenolic OH was calculated using the density function theory (DFT)/B3LY. The total BDE values of curcumin and tetrahydrocurcumin were almost identical, but the BDE of one-electron oxidation and ionization potential (IP) for curcumin were lower than those for tetrahydrocurcumin, suggesting the highly pro-oxidative activity of curcumin. Curcumin has both oxidant and antioxidant properties. A causal link between the anti-inflammatory activities and molecular properties of phenolic antioxidants is suggested.

  • Curcumin
  • tetrahydrocurcumin
  • COX-2
  • NF-κB
  • chemical descriptors
  • lipopolysaccharide
  • Porphyromonas gingivalis fimbriae
  • Received November 20, 2007.
  • Revision received January 18, 2008.
  • Accepted February 15, 2008.
  • Copyright© 2008 International Institute of Anticaner Research (Dr. John G. Delinassios), All rights reserved
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Anticancer Research: 28 (2A)
Anticancer Research
Vol. 28, Issue 2A
March-April 2008
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Comparative Anti-inflammatory Activities of Curcumin and Tetrahydrocurcumin Based on the Phenolic O-H Bond Dissociation Enthalpy, Ionization Potential and Quantum Chemical Descriptor
YUKIO MURAKAMI, HIROAKI ISHII, NAOKI TAKADA, SHOJI TANAKA, MAMORU MACHINO, SHIGERU ITO, SEIICHIRO FUJISAWA
Anticancer Research Mar 2008, 28 (2A) 699-707;

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Comparative Anti-inflammatory Activities of Curcumin and Tetrahydrocurcumin Based on the Phenolic O-H Bond Dissociation Enthalpy, Ionization Potential and Quantum Chemical Descriptor
YUKIO MURAKAMI, HIROAKI ISHII, NAOKI TAKADA, SHOJI TANAKA, MAMORU MACHINO, SHIGERU ITO, SEIICHIRO FUJISAWA
Anticancer Research Mar 2008, 28 (2A) 699-707;
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