2008
DOI: 10.20538/1682-0363-2008-1-51-55
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Нepatoprotective properties of polyphenolic complexes from woodand cellular culture of maackia amurensis

Abstract: Annot For finding-out of a role of separate groups of polyphenols in realization hepatoprotective properties of maksar we investigate activity of polyphenolic complexes (PPC) from duramen and cellular culture of maakia amur. Experiments are carried out on 40 not purebred white rats with an experimental СCl4-hepatites. Therapeutic efficiency of researched objects estimated on their influence on survival rate of animals, morphological and biochemical parameters of a liver and wheys of blood. In rat's CCl4-hepati… Show more

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Cited by 2 publications
(6 citation statements)
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“…Repeated column chromatography using Toyopearl HW-50F and Toyopearl HW-40F columns and preparative HPLC chromatography of the cell culture extract followed by recrystallization yielded 20 isoflavonoids, 6 of which were identified as free isoflavones ( 9 1 and 2). The physical, spectroscopic, and 1 H and 13 C NMR data for the isolated compounds showed identity with the following previously identified isoflavones: daidzein (9), calycosin (10), genistein (12), formononetin (13), pseudobaptigenin (14), and derrone (15); their β-glucosides and malonylglucosides, 4′-O-β-D-glucopyranosyldaidzin (1), 4′-O-β-D-glucopyranosylgenistin (2), daidzin (3), 3′-methoxydaidzin (4), 7-O-β-D-glucopyranosylcalycosin ( 5), genistin ( 6), 6′′-O-malonylgenistin (7), ononin (8), 6′′-O-malonylononin (11); and pterocarpans and their malonyl glucosides, (6aR,11aR)maackiain ( 19), (6aR,11aR)-medicarpin ( 20), (6aR,11aR)-6′-Omalonyl-3-O-β-D-glucopyranosylmaackiain ( 17), (6aR,11aR)-6′-O-malonyl-3-O-β-D-glucopyranosylmedicarpin (18). Only a few authors have provided full NMR spectral assignments for the glucosidic component of the conjugated forms of isoflavonoids.…”
Section: Resultsmentioning
confidence: 51%
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“…Repeated column chromatography using Toyopearl HW-50F and Toyopearl HW-40F columns and preparative HPLC chromatography of the cell culture extract followed by recrystallization yielded 20 isoflavonoids, 6 of which were identified as free isoflavones ( 9 1 and 2). The physical, spectroscopic, and 1 H and 13 C NMR data for the isolated compounds showed identity with the following previously identified isoflavones: daidzein (9), calycosin (10), genistein (12), formononetin (13), pseudobaptigenin (14), and derrone (15); their β-glucosides and malonylglucosides, 4′-O-β-D-glucopyranosyldaidzin (1), 4′-O-β-D-glucopyranosylgenistin (2), daidzin (3), 3′-methoxydaidzin (4), 7-O-β-D-glucopyranosylcalycosin ( 5), genistin ( 6), 6′′-O-malonylgenistin (7), ononin (8), 6′′-O-malonylononin (11); and pterocarpans and their malonyl glucosides, (6aR,11aR)maackiain ( 19), (6aR,11aR)-medicarpin ( 20), (6aR,11aR)-6′-Omalonyl-3-O-β-D-glucopyranosylmaackiain ( 17), (6aR,11aR)-6′-O-malonyl-3-O-β-D-glucopyranosylmedicarpin (18). Only a few authors have provided full NMR spectral assignments for the glucosidic component of the conjugated forms of isoflavonoids.…”
Section: Resultsmentioning
confidence: 51%
“…Polyphenolic compounds extracted from both core wood and callus cultures of M. amurensis decreased the acute toxicity of tetratrachloromethane on liver with similar efficacy, showing a prominent favorable effect on animal survival (14). This effect resulted from the suppression of dystrophy and hepatocyte necrosis, normalization of aminotransferase and γ-glutamyltransferase activities in the blood, and stimulation of bilirubin conjugation (14). Thus, the possibility of creating a renewable source of Maackia isoflavonoids has been demonstrated.…”
Section: Introductionmentioning
confidence: 99%
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“…In addition to possessing hepatoprotective properties, Maksar ® also reduced the total lipid content in blood [ 4 , 5 ]. It prevented the increase in the total serum lipid content and the development of hyperlipoproteinemia in experimental animals [ 6 ] and in clinical trials [ 7 ].…”
Section: Introductionmentioning
confidence: 99%