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Alteration of egg yolk cholesterol content and plasma lipoprotein profiles following administration of a totally synthetic HMG-CoA reductase inhibitor to laying hens
PD 123244-15 [(+/-)-(R*,R*)-3,4-dibromo-beta,delta-dihydroxy-2-(4-fluor ophenyl)-5-(1-methylethyl)-1H-pyrrol-1-heptanoic acid, sodium salt], a totally synthetic HMG-CoA reductase inhibitor, was fed to laying hens at dietary levels of either 0, 0.0091, 0.0273, or 0.0819% for 20 days (experiment 1) or...
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Published in: | Journal of agricultural and food chemistry 1993-07, Vol.41 (7), p.1094-1101 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | PD 123244-15 [(+/-)-(R*,R*)-3,4-dibromo-beta,delta-dihydroxy-2-(4-fluor ophenyl)-5-(1-methylethyl)-1H-pyrrol-1-heptanoic acid, sodium salt], a totally synthetic HMG-CoA reductase inhibitor, was fed to laying hens at dietary levels of either 0, 0.0091, 0.0273, or 0.0819% for 20 days (experiment 1) or 0, 0.0273, 0.0546, or 0.0819% for 42 days (experiment 2). In each experiment, PD 123244-15 generally had little effect on egg or yolk weights, while hens fed 0.0819% PD 123244-15 produced fewer (P 0.05) eggs than the other three groups. Egg cholesterol contents varied inversely with the amount of dietary PD 123244-15, with a maximum reduction of approximately 30% obtained at the highest drug level in both experiments. With the exception of samples from hens fed 0.0091% PD 123244-15, plasma total cholesterol and triglyceride concentrations also varied inversely with the dietary amount of PD 123244-15. Further analysis of the plasma samples by high-performance gel permeation chromatography revealed that the PD 123244-15-mediated lowering of total cholesterol and triglycerides was almost totally accounted for by a reduction in the VLDL fraction. On the basis of reversed-phase HPLC analysis, no drug residues were detected in egg yolk and albumen extracts from hens fed 0.0819% PD 123244-15 |
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ISSN: | 0021-8561 1520-5118 |
DOI: | 10.1021/jf00031a016 |