2007
DOI: 10.1111/j.1478-3231.2007.01460.x
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A novel therapeutic drug (copper nicotinic acid complex) for non‐alcoholic fatty liver

Abstract: The Cu complex may serve as a novel chemical restoring agent in fatty degenerated liver cells and for renewal of their structure and functions. However, clinical trials are required for more evaluation of the Cu complex in humans.

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Cited by 30 publications
(31 citation statements)
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“…This, in turn, results in lower levels of ferroportin in copper deficient rats; coincidentally, NAFLD patients show less ferroportin expression than controls (93). Copper supplementation has been suggested as a therapy for NAFLD based on study in which a diet-induced (high carbohydrate fat-free diet) NAFLD in rats was improved by treatment with a Cu(I)-nicotinate complex (95).…”
Section: Copper and Nafldmentioning
confidence: 99%
“…This, in turn, results in lower levels of ferroportin in copper deficient rats; coincidentally, NAFLD patients show less ferroportin expression than controls (93). Copper supplementation has been suggested as a therapy for NAFLD based on study in which a diet-induced (high carbohydrate fat-free diet) NAFLD in rats was improved by treatment with a Cu(I)-nicotinate complex (95).…”
Section: Copper and Nafldmentioning
confidence: 99%
“…In addition, these cellular improving characters were microscopically obvious by utilization of the copper complex under consideration as a protective agent. This improvement was predicted since this complex has been confirmed previously as a therapeutic agent against induced non-alcoholic fatty liver in experimental animals [20].…”
Section: Discussionmentioning
confidence: 56%
“…Reduction of accumulated levels NO and lipid peroxides in hepatic tissue by BHT and the copper complex cotreatment that was regulated and promoted by elevation of antioxidant cellular chemicals such as GSH and total thiols [39], this could be attributed frankly to the antioxidant effect of BHT [20,40] and the cellular protective antioxidant Cu(I)-nicotinate complex [41]. Since, induction of protective GST has been posited possible chemoprotective mechanism by BHT and other phenolic antioxidant as enzyme promoters has been confirmed before by Hayes et al, (1996) [42].…”
Section: Discussionmentioning
confidence: 99%
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“…Liver weight, liver trans aminases and alkaline phosphates were decreased and nitric oxides, super oxides; lipid peroxides were changed to normal level. Cu complex was important for renewal of structure and functions [15].…”
Section: Metal Complexes Of Nicotinic Acid and Imidazole:-cu +2 Complmentioning
confidence: 99%