Disposition of glucosinolates and sulforaphane in humans after ingestion of steamed and fresh broccoli
Conaway CC, Getahun SM, Liebes LL, Pusateri DJ, Topham DK, Botero-Omary M, Chung FL
Nutrition and cancer · 222 citas
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Cómo se estudió
- Diseño
- Ensayo controlado aleatorizado (indexado por PubMed)
- Estudiado en
- Personas
- Resultado principal
- Sin resultado de salud
- Consumo medido con
- Comida provista por los investigadores
Quién lo pagó
- Financiación
- Financiación no declarada
Publicación
- Publicado
- 2000-11-01 · Nutr Cancer · vol. 38 · número 2 · págs. 168–178
- Editorial
- Routledge
- Citado
- 345 citas · más que el 89% de estudios similares · 2.4× el promedio de su campo
- Referencias
- 39 trabajos
- Acceso
- De pago
- Áreas de investigación
- Genomics, phytochemicals, and oxidative stress · Phytochemicals and Antioxidant Activities · Nitrogen and Sulfur Effects on Brassica
- Palabras clave
- glucosinolates, sulforaphane, isothiocyanates, broccoli, steaming, urinary excretion, chemoprevention, human dietary exposure
- MeSH
- humans, brassica, oximes, thiocyanates, imidoesters, isothiocyanates, sulfoxides, glycoside hydrolases, glucosinolates, glucose, anticarcinogenic agents, chromatography, high pressure liquid, cross-over studies, biological availability, intestinal absorption, adult, middle aged, male, cooking
7 autores
- C. Clifford Conaway🇺🇸Institute for Cancer Prevention
- Serkadis M. Getahun
- Leonard L. Liebes
- Donald J. Pusateri
- Debra K. W. Topham
- María Botero Omary
- Fung‐Lung Chung
Resumen
El texto original del estudio, en el idioma en que se publicó.
The cancer-chemopreventive effects of broccoli may be attributed, in part, to isothiocyanates (ITCs), hydrolysis products of glucosinolates. Glucosinolates are hydrolyzed to their respective ITCs by the enzyme myrosinase, which is inactivated by heat. In this study, the metabolic fate of glucosinolates after ingestion of steamed and fresh broccoli was compared in 12 male subjects in a crossover design. During each 48-hour baseline period, no foods containing glucosinolates or ITCs were allowed. The subjects then consumed 200 g of fresh or steamed broccoli; all other dietary sources of ITCs were excluded. Blood and urine samples were collected during the 24-hour period after broccoli consumption. Total ITC equivalents in broccoli and total ITC equivalents in plasma and urine were assayed by high-performance liquid chromatography as the cyclocondensation product of 1,2-benzenedithiol. The content of ITCs in fresh and steamed broccoli after myrosinase treatment was found to be virtually identical (1.1 vs. 1.0 micromol/g wet wt). The average 24-hour urinary excretion of ITC equivalents amounted to 32.3 +/- 12.7% and 10.2 +/- 5.9% of the amounts ingested for fresh and steamed broccoli, respectively. Approximately 40% of total ITC equivalents in urine, 25.8 +/- 13.9 and 6.9 +/- 2.5 micromol for fresh and steamed broccoli, respectively, occurred as the N-acetyl-L-cysteine conjugate of sulforaphane (SFN-NAC). Total ITC metabolites in plasma peaked between 0 and 8 hours, whereas urinary excretion of total ITC equivalents and SFN-NAC occurred primarily between 2 and 12 hours. Results of this study indicate that the bioavailability of ITCs from fresh broccoli is approximately three times greater than that from cooked broccoli, in which myrosinase is inactivated. Considering the cancer-chemopreventive potential of ITCs, cooking broccoli may markedly reduce its beneficial effects on health.
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