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Dietary cholesterol feeding suppresses human cholesterol synthesis measured by deuterium incorporation and urinary mevalonic acid levels

Jones PJ, Pappu AS, Hatcher L, Li ZC, Illingworth DR, Connor WE

Arteriosclerosis, thrombosis, and vascular biology · 56 citas

Etiquetas de revisión

Alimentación controladaSolo mecanismos

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Solo mecanismos
Consumo medido con
Comida provista por los investigadores

Quién lo pagó

Financiación
Financiación independiente
Gobierno
National Center for Research Resources
Gobierno
NCRR NIH HHS
Subvenciones
National Center for Research Resources (M01RR00334)

Según 2 financiadores declarados.

Publicación

Publicado
1996-10-01 · Arterioscler Thromb Vasc Biol · vol. 16 · número 10 · págs. 1222–1228
Editorial
Lippincott Williams & Wilkins
Citado
93 citas · más que el 95% de estudios similares · 4.6× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
46 trabajos
Acceso
De pago
Áreas de investigación
Cholesterol and Lipid Metabolism · Lipoproteins and Cardiovascular Health · Cancer, Lipids, and Metabolism
Palabras clave
dietary cholesterol, cholesterol biosynthesis, cholesterogenesis, deuterium incorporation, erythrocyte cholesterol, serum cholesterol, cholesterol intake
MeSH
humans, body weight, deuterium, mevalonic acid, cholesterol, cholesterol, dietary, adult, middle aged, female, male

6 autores

  • Peter J.H. Jones🇺🇸🇨🇦Oregon Health & Science University; McGill University
  • Anuradha S. Pappu🇺🇸🇨🇦Oregon Health & Science University; McGill University
  • Lauren F Hatcher🇺🇸🇨🇦Oregon Health & Science University; McGill University
  • Zi-Chi Li🇺🇸🇨🇦Oregon Health & Science University; McGill University
  • D. Roger Illingworth🇺🇸🇨🇦Oregon Health & Science University; McGill University
  • William E. Connor🇺🇸🇨🇦Oregon Health & Science University; McGill University

Resumen

El texto original del estudio, en el idioma en que se publicó.

The objective of this study was to measure the response of cholesterol biosynthesis in subjects to three different amounts of dietary cholesterol: 50 (low), 350 (medium), and 650 (high) mg cholesterol per 2800 kcal. Individuals with low (n = 7), normal (n = 12), and elevated (n = 11) plasma cholesterol concentrations consumed in random order solid-food test diets (15%, 55%, and 30% of energy as protein, carbohydrate, and fat, respectively) at each dietary cholesterol level. The three diets were consumed for 4 weeks each, and each dietary phase was separated by a 4-week washout period. During the final week of each diet, 0.7 g D2O was given per kilogram of body water and deuterium incorporation into the erythrocyte cholesterol pool was measured for 24 hours. Urinary mevalonate levels were also determined in samples obtained during two consecutive 24-hour periods. Both techniques provided measurements of whole-body cholesterol biosynthesis. In all subjects the cholesterol synthesis rate as measured by deuterium incorporation was significantly lower (P < .05) after the transition from low- to medium- and low- to high-cholesterol diets. Urinary mevalonate excretion decreased after the change from the medium- to high- (P < .05) and low- to high- (P < .01) cholesterol diets. Although correspondence between the two methods was poor, they both indicated some suppression of cholesterol synthesis by dietary cholesterol. The response of cholesterogenesis to different amounts of dietary cholesterol was related to the rate of synthesis under depressed conditions of the low-cholesterol diet. These findings indicate modest downregulation of synthesis in response to dietary cholesterol in humans, independent of plasma cholesterol levels.

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