2000
DOI: 10.1016/s0021-9150(00)80593-6
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Dose-dependent cholesterol-lowering effects of D-003 on normocholesterolemic rabbits

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Cited by 11 publications
(9 citation statements)
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“…The presence of a homologous series of very long chain fatty acids in the material used in this study, i.e., cane wax from Egypt, contrasts with the absence of similar compounds documented by previous studies (Delange et al, 2002;Gamez et al, 2000). It is difficult to say whether this striking difference is caused by differences in the geographical origin of the analyzed cane (Egyptian cane in our case, Cuban cane in the case of Gonzales et al, 2002), or if it can be ascribed to different instrumentation and methodology.…”
Section: Resultscontrasting
confidence: 99%
See 1 more Smart Citation
“…The presence of a homologous series of very long chain fatty acids in the material used in this study, i.e., cane wax from Egypt, contrasts with the absence of similar compounds documented by previous studies (Delange et al, 2002;Gamez et al, 2000). It is difficult to say whether this striking difference is caused by differences in the geographical origin of the analyzed cane (Egyptian cane in our case, Cuban cane in the case of Gonzales et al, 2002), or if it can be ascribed to different instrumentation and methodology.…”
Section: Resultscontrasting
confidence: 99%
“…A natural mixture of higher primary aliphatic acids (24:0 to 36:0) was obtained from sugar cane (Saccharum officinarum L.) wax (Gonzales et al, 2002). This product was found to be responsible for some biological properties related to health, such as antioxidant and cholesterol-lowering effects, determined in both in vivo and in vitro models (Gamez et al, 2000;Rodriguez et al, 2004), beneficial effects on platelet aggregation in healthy volunteers (Arruzazabala et al, 2005), as well as antiplatelet and antithrombotic activities (Molina et al, 2000;Mas, 2004). The nutritional significance and metabolism of very long chain fatty alcohols and acids from sugar cane has recently been reviewed (Hargrove et al, 2004).…”
Section: Introductionmentioning
confidence: 99%
“…In an experiment on normocholesterolemic rabbits, D-003 (5 to 200 mg/kg/day) for 30 days showed a reversible and dose-dependent decrease in circulating concentrations of TC and LDL-C [20]. Additionally, HDL-C concentrations were increased, but not in a dose-dependent manner.…”
Section: Evidence From Animal Studiesmentioning
confidence: 95%
“…[6][7][8][9] Also, D-003 administered from 5 to 50 mg/day has shown cholesterol-lowering effects in healthy volunteers and patients with Type II hypercholesterolemia causing reduction of serum LDL-C and TC, while markedly raising HDL-C. [10][11][12] On the other hand, D-003 orally administered also induces anti-platelet effects in animal models and human beings, [12][13][14][15][16][17] which appears to be mediated through reduced thromboxane A 2 levels and increased prostacyclin values. 15,16 Thus, D-003 shows a pharmacological profile suggesting that it could be a promising agent for treating atherothrombotic diseases, as expected from its cholesterol-lowering and anti-platelet effects.…”
Section: Introductionmentioning
confidence: 99%