2009
DOI: 10.17221/1745-cjas
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Effects of indole-3-carbinol on metabolic parameters and on lipogenesis and lipolysis in adipocytes 182

Abstract: : Indole-3-carbinol (I3C) was found to have possible anticarcinogenic, antioxidant and anti-atherogenic effects on the organism. So far, its influence on metabolic pathways has been unknown. This work was the first attempt to determine the carbohydrate and lipid metabolism changes <I>in vivo</I> after administration of 150 mg/kg b.wt./day I3C to male rats. Additionally, the aim of this trial was to evaluate the direct effect of I3C on basal and hormone-induced lipogenesis and lipolysis in isolated … Show more

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Cited by 5 publications
(3 citation statements)
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“…The glucose levels in our radish sprout-treated flies were significantly lower than those in control flies ( Figure 4 a). This finding is consistent with results obtained by Okulicz and co-workers [ 19 ], who observed that I3C, a breakdown product also present in radish sprouts, affects glucose uptake in adipocytes under basal as well as under insulin-stimulated conditions.…”
Section: Resultssupporting
confidence: 93%
“…The glucose levels in our radish sprout-treated flies were significantly lower than those in control flies ( Figure 4 a). This finding is consistent with results obtained by Okulicz and co-workers [ 19 ], who observed that I3C, a breakdown product also present in radish sprouts, affects glucose uptake in adipocytes under basal as well as under insulin-stimulated conditions.…”
Section: Resultssupporting
confidence: 93%
“…Apart from its antioxidant activities, it has anticancer properties by interrupting cancer cell cycles, promoting cell apoptosis, controlling cell division and angiogenesis deregulation of cancer cells [24]. Recent studies showed that I3C has beneficial effects on lipid metabolism that could be of great value for prevention of DOX-induced cardiotoxicity [25,26]. Previous studies have reported the toxicity profile and protective efficacy of natural compound indole-3-carbinol (I3C) against doxorubicin (DOX)-induced genotoxicity and cardiotoxicity in normal mice [27].…”
Section: Introductionmentioning
confidence: 99%
“…Additionally, (1H-indol-3-yl)methanols have been used as key precursors for the construction of complex indole derivatives that would be useful in pharmaceuticals as drugs and agrochemicals [2][3][4][5][6][7][8][9][10][11][12][13][14]. The simple (1H-indol-3-yl)methanol, a break-down product of glucobrassicin, which can be found in cruciferous vegetables [15], has a wide range of biomedical applications as an anticancer [16], antioxidant, and antiatherogenic agent [17].…”
Section: Introductionmentioning
confidence: 99%