Allicin up-regulates cellular glutathione level in vascular endothelial cells.

BACKGROUND: Allicin in garlic is the primary active compound known to rapidly interact with free thiols. AIMS OF THE STUDY: To examine the effect of allicin on gene expression and glutathione cellular level in vascular endothelial cells. METHODS: Cultured endothelial cells were exposed to allicin; m...

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Publicado en:European Journal of Nutrition Vol. 48; no. 2; pp. 67 - 75
Autores principales: Horev-Azaria L, Eliav S, Izigov N, Pri-Chen S, Mirelman D, Miron T, Rabinkov A, Wilchek M, Jacob-Hirsch J, Amariglio N, Savion N
Formato: research tables/charts Journal Article
Publicado: Springer Nature Mar2009
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Mar2009
      vid: 48
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00394-008-0762-3
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        atl: Allicin up-regulates cellular glutathione level in vascular endothelial cells.
      aug:
        au:
          Horev-Azaria L
          Eliav S
          Izigov N
          Pri-Chen S
          Mirelman D
          Miron T
          Rabinkov A
          Wilchek M
          Jacob-Hirsch J
          Amariglio N
          Savion N
        affil: Goldschleger Eye Research Institute, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
      sug:
        subj:
          Endothelium
          Garlic
          Gene Expression
          Glutathione
          Analysis of Variance
          Enzymes
          Polymerase Chain Reaction
          RNA
          T-Tests
          Human
      ab: BACKGROUND: Allicin in garlic is the primary active compound known to rapidly interact with free thiols. AIMS OF THE STUDY: To examine the effect of allicin on gene expression and glutathione cellular level in vascular endothelial cells. METHODS: Cultured endothelial cells were exposed to allicin; mRNA was prepared and subjected to Micro-array and Real-Time PCR. Glutathione cellular level was determined on cell lysates. RESULTS: Micro-array analysis demonstrated allicin-induced up- and down-regulation of 116 and 100 genes, respectively. Up-regulated genes included the phase II detoxifying enzymes thioredoxin reductase 1 and 2, heme oxygenase-1 and glutamate cysteine lygaze modifier subunit, the rate limiting enzyme in glutathione biosynthesis. Endothelial cells exposed to allicin and its derivatives containing glutathione or cysteine residues increased cellular glutathione. Allicin increased the glutathione level in a concentration and time-dependent manner up to 8-fold at a concentration of 10-20 microM after 28 h exposure. Furthermore, allicin derivative-treated cultures demonstrated a 50% decrease in tBuOOH cytotoxicity. CONCLUSIONS: These results may suggest a putative role for allicin and its derivatives in preventing reactive oxygen species damage by up-regulating the phase II detoxifying enzymes and increasing the cellular glutathione level.
      pubtype: Academic Journal
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        research
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      ougenre: Article
    language: English
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