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1.
Drug Metab Dispos ; 49(8): 694-705, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-34035125

RESUMO

3,3'-Diindolylmethane (DIM), a major phytochemical derived from ingestion of cruciferous vegetables, is also a dietary supplement. In preclinical models, DIM is an effective cancer chemopreventive agent and has been studied in a number of clinical trials. Previous pharmacokinetic studies in preclinical and clinical models have not reported DIM metabolites in plasma or urine after oral dosing, and the pharmacological actions of DIM on target tissues is assumed to be solely via the parent compound. Seven subjects (6 males and 1 female) ranging from 26-65 years of age, on a cruciferous vegetable-restricted diet prior to and during the study, took 2 BioResponse DIM 150-mg capsules (45.3 mg DIM/capsule) every evening for one week with a final dose the morning of the first blood draw. A complete time course was performed with plasma and urine collected over 48 hours and analyzed by UPLC-MS/MS. In addition to parent DIM, two monohydroxylated metabolites and 1 dihydroxylated metabolite, along with their sulfate and glucuronide conjugates, were present in both plasma and urine. Results reported here are indicative of significant phase 1 and phase 2 metabolism and differ from previous pharmacokinetic studies in rodents and humans, which reported only parent DIM present after oral administration. 3-((1H-indole-3-yl)methyl)indolin-2-one, identified as one of the monohydroxylated products, exhibited greater potency and efficacy as an aryl hydrocarbon receptor agonist when tested in a xenobiotic response element-luciferase reporter assay using Hepa1 cells. In addition to competitive phytochemical-drug adverse reactions, additional metabolites may exhibit pharmacological activity highlighting the importance of further characterization of DIM metabolism in humans. SIGNIFICANCE STATEMENT: 3,3'-Diindolylmethane (DIM), derived from indole-3-carbinol in cruciferous vegetables, is an effective cancer chemopreventive agent in preclinical models and a popular dietary supplement currently in clinical trials. Pharmacokinetic studies to date have found little or no metabolites of DIM in plasma or urine. In marked contrast, we demonstrate rapid appearance of mono- and dihydroxylated metabolites in human plasma and urine as well as their sulfate and glucuronide conjugates. The 3-((1H-indole-3-yl)methyl)indolin-2-one metabolite exhibited significant aryl hydrocarbon receptor agonist activity, emphasizing the need for further characterization of the pharmacological properties of DIM metabolites.


Assuntos
Indóis , Administração Oral , Anticarcinógenos/sangue , Anticarcinógenos/farmacocinética , Anticarcinógenos/urina , Cápsulas , Suplementos Nutricionais , Desenvolvimento de Medicamentos , Vias de Eliminação de Fármacos , Feminino , Humanos , Inativação Metabólica/fisiologia , Indóis/sangue , Indóis/farmacocinética , Indóis/urina , Masculino , Pessoa de Meia-Idade , Compostos Fitoquímicos/sangue , Compostos Fitoquímicos/farmacocinética , Compostos Fitoquímicos/urina
2.
Yao Xue Xue Bao ; 48(9): 1471-4, 2013 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-24358783

RESUMO

In order to study the excretion of genistein (GEN) capsule, an estrogen drugs, in human, 30 healthy volunteers were selected and orally administered 50, 100, and 300 mg genistein in an parallel study. Genistein were determined in urine by LC-MS/MS and glucuronidated genistein (GENG) were indirectly determined with enzymatic hydrolysis in urine by LC-MS/MS, and the pharmacokinetic parameters were analyzed by DAS software (ver 2.0). The result showed that the concentrations of genistein in human urine were less than 1% of the GENG, and the cumulative excretion of GEN in 48 h were 0.037, 0.134, and 0.142 mg, separately, and the urinary excretion percentage were only 0.07%, 0.13%, and 0.05%, separately. But the cumulative excretion of GENG in 48 h was 5.3, 13.8, and 15.4 mg, separately, and the urinary excretion percentage were 10.6%, 13.8%, and 5.1%, separately, and the max urinary excretive rate was 0.4, 1.0, and 1.4 mg x h(-1), separately (tmax were 6 h). Studies showed that part of drug excreted through kidney in a form of GENG in human, and the cumulative urinary excretion and the maximum excretion rate of GENG showed a proportional increase conditioned with the dose in the range of 50-100 mg, but showed non-linear increase feature in 300 mg.


Assuntos
Anticarcinógenos/farmacocinética , Genisteína/farmacocinética , Fitoestrógenos/farmacocinética , Administração Oral , Adulto , Anticarcinógenos/administração & dosagem , Anticarcinógenos/urina , Cromatografia Líquida , Feminino , Genisteína/administração & dosagem , Genisteína/urina , Glucuronídeos/urina , Voluntários Saudáveis , Humanos , Masculino , Fitoestrógenos/administração & dosagem , Fitoestrógenos/urina , Espectrometria de Massas em Tandem , Adulto Jovem
3.
Nutr Cancer ; 55(1): 53-62, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16965241

RESUMO

Broccoli sprouts are widely consumed in many parts of the world. There have been no reported concerns with respect to their tolerance and safety in humans. A formal phase I study of safety, tolerance, and pharmacokinetics appeared justified because these sprouts are being used as vehicles for the delivery of the glucosinolate glucoraphanin and its cognate isothiocyanate sulforaphane [1-isothiocyanato-(4R)-(methylsulfinyl)butane] in clinical trials. Such trials have been designed to evaluate protective efficacy against development of neoplastic and other diseases. A placebo-controlled, double-blind, randomized clinical study of sprout extracts containing either glucosinolates (principally glucoraphanin, the precursor of sulforaphane) or isothiocyanates (principally sulforaphane) was conducted on healthy volunteers who were in-patients on our clinical research unit. The subjects were studied in three cohorts, each comprising three treated individuals and one placebo recipient. Following a 5-day acclimatization period on a crucifer-free diet, the broccoli sprout extracts were administered orally at 8-h intervals for 7 days (21 doses), and the subjects were monitored during this period and for 3 days after the last treatment. Doses were 25 micromol of glucosinolate (cohort A), 100 micromol of glucosinolate (cohort B), or 25 micromol of isothiocyanate (cohort C). The mean cumulative excretion of dithiocarbamates as a fraction of dose was very similar in cohorts A and B (17.8 +/- 8.6% and 19.6 +/- 11.7% of dose, respectively) and very much higher and more consistent in cohort C (70.6 +/- 2.0% of dose). Thirty-two types of hematology or chemistry tests were done before, during, and after the treatment period. Indicators of liver (transaminases) and thyroid [thyroid-stimulating hormone, total triiodothyronine (T3), and free thyroxine (T4)] function were examined in detail. No significant or consistent subjective or objective abnormal events (toxicities) associated with any of the sprout extract ingestions were observed.


Assuntos
Brassica , Glucosinolatos/metabolismo , Isotiocianatos/metabolismo , Fígado/enzimologia , Extratos Vegetais/metabolismo , Hormônios Tireóideos/sangue , Adulto , Anticarcinógenos/metabolismo , Anticarcinógenos/farmacocinética , Anticarcinógenos/urina , Análise Química do Sangue , Brassica/química , Estudos de Coortes , Qualidade de Produtos para o Consumidor , Dieta , Relação Dose-Resposta a Droga , Método Duplo-Cego , Feminino , Glucosinolatos/farmacocinética , Glucosinolatos/urina , Humanos , Isotiocianatos/farmacocinética , Isotiocianatos/urina , Masculino , Pessoa de Meia-Idade , Neoplasias , Extratos Vegetais/urina
4.
Clin Chim Acta ; 316(1-2): 43-53, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11750273

RESUMO

BACKGROUND: Humans are exposed to substantial quantities of isothiocyanates and glucosinolates from vegetables. Since dietary isothiocyanates are widely regarded as potentially important chemoprotectors against cancer, reliable methods for measuring the plasma and tissue pharmacokinetics of isothiocyanates and their dithiocarbamate metabolites are essential for defining dosing regimens. METHODS: Isothiocyanates (ITC) and dithiocarbamates (DTC) react quantitatively with 1,2-benzenedithiol to produce 1,3-benzodithiole-2-thione that can be quantified spectroscopically. Although this cyclocondensation reaction has been highly useful for analyzing plant material and urine samples, the determination of DTC/ITC (the total quantity of DTC and ITC components in a sample that react in the cyclocondensation reaction) in blood and tissues has been hampered by their low levels and the high concentrations of proteins that interfere with the cyclocondensation reaction. The protein content of blood and tissues was reduced by the precipitation with polyethylene glycol (PEG) or ultrafiltration, and the sensitivity of the method was increased substantially by the solid phase extraction of the cyclocondensation product. RESULTS: Pharmacokinetic measurements were made in four human volunteers who received single doses of about 200 micromol of broccoli sprout isothiocyanates (largely sulforaphane, with lesser amounts of iberin and erucin). Isothiocyanates were absorbed rapidly, reached peak concentrations of 0.943-2.27 micromol/l in plasma, serum and erythrocytes at 1 h after feeding and declined with first-order kinetics (half-life of 1.77+/-0.13 h). The cumulative excretion at 8 h was 58.3+/-2.8% of the dose. Clearance was 369+/-53 ml/min, indicating active renal tubular secretion. CONCLUSION: A sensitive and specific method for quantifying DTC levels in human plasma, serum, and erythrocytes has been devised. Determinations of ITC/DTC levels are important because: (i) dietary isothiocyanates are of potential value in reducing the risk of cancer, and (ii) humans are extensively exposed to DTC as fungicides, insecticides, pesticides and rubber vulcanization accelerators.


Assuntos
Eritrócitos/química , Plasma/química , Tiocarbamatos/farmacocinética , Urina/química , Anticarcinógenos/sangue , Anticarcinógenos/farmacocinética , Anticarcinógenos/urina , Brassica/química , Cromatografia Líquida de Alta Pressão , Testes de Química Clínica/métodos , Testes de Química Clínica/normas , Humanos , Indicadores e Reagentes , Isotiocianatos/sangue , Isotiocianatos/farmacocinética , Isotiocianatos/urina , Extratos Vegetais/administração & dosagem , Extratos Vegetais/química , Extratos Vegetais/farmacocinética , Sensibilidade e Especificidade , Compostos de Sulfidrila , Tiocarbamatos/sangue , Tiocarbamatos/urina , Tionas
5.
J Chromatogr B Biomed Sci Appl ; 764(1-2): 3-25, 2001 Nov 25.
Artigo em Inglês | MEDLINE | ID: mdl-11817034

RESUMO

Although a great number of papers demonstrate an association between high intake of fruits and vegetables and reduced risk of certain types of cancer, the epidemiological evidence is not conclusive. The identification and quantification of specific dietary anticancer compounds in plasma, urine and tissues is an important aspect of this research. We surveyed the recent literature for original papers which involved the use of separation techniques for the detection and quantification in biological fluids and tissues of putative anticancer compounds which are present in the diet. The compounds included in this review are flavonoids, phytoestrogens, carotenoids, retinoids, vitamin E and ascorbic acid. The review covers papers published in the last 3 years. For each class of compounds we discuss the sample preparation, chromatographic conditions, and validation of the methods used, in order to identify current trends in the bioanalysis of each class of these substances.


Assuntos
Anticarcinógenos/metabolismo , Líquidos Corporais/metabolismo , Dieta , Isoflavonas , Anticarcinógenos/sangue , Anticarcinógenos/urina , Ácido Ascórbico/sangue , Ácido Ascórbico/metabolismo , Ácido Ascórbico/urina , Carotenoides/sangue , Carotenoides/metabolismo , Carotenoides/urina , Estrogênios não Esteroides/sangue , Estrogênios não Esteroides/metabolismo , Estrogênios não Esteroides/urina , Flavonoides/sangue , Flavonoides/metabolismo , Flavonoides/urina , Fitoestrógenos , Preparações de Plantas , Retinoides/sangue , Retinoides/metabolismo , Retinoides/urina , Vitamina E/sangue , Vitamina E/metabolismo , Vitamina E/urina
6.
Cancer Epidemiol Biomarkers Prev ; 9(8): 773-9, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10952093

RESUMO

Previous studies suggest that the estrogen metabolite 16alpha-hydroxyestrone acts as a breast tumor promoter. The alternative product of estrogen metabolism, 2-hydroxyestrone, does not exhibit estrogenic properties in breast tissue, and lower values of the ratio 2-hydroxyestrone:16alpha-hydroxyestrone (2:16) in urine may be an endocrine biomarker for greater breast cancer risk. Vegetables of the Brassica genus, such as broccoli, contain a phytochemical, which may shift estrogen metabolism and increase the 2:16 ratio. Adding 500 g/day of broccoli to a standard diet shifts 2:16 values upward in humans; however, it is unknown as to whether healthy women are able to consume a sufficient quantity of Brassica to affect breast cancer risk through this mechanism. In this study, 34 healthy postmenopausal women participated in an intensive intervention designed to facilitate the addition of Brassica to the daily diet. The diet was measured by repeated 24-h recall, and estrogen metabolites were measured by enzyme immunoassay in 24-h urine samples. In a crude analysis, there was a nonsignificant increase in the urinary 2:16 ratio associated with greater Brassica consumption. With adjustment for other dietary parameters, Brassica vegetable consumption was associated with a statistically significant increase in 2:16 values, such that for each 10-g/day increase in Brassica consumption, there was an increase in the 2:16 ratio of 0.08 (95% confidence interval, 0.02-0.15). To the extent that the 2:16 ratio, as measured in urine, is associated with breast cancer risk, future research should consider Brassica vegetable consumption as a potentially effective and acceptable dietary strategy to prevent breast cancer.


Assuntos
Anticarcinógenos/urina , Brassica/uso terapêutico , Neoplasias da Mama/prevenção & controle , Estrogênios/metabolismo , Fitoterapia , Pós-Menopausa/metabolismo , Idoso , Análise de Variância , Brassica/metabolismo , Neoplasias da Mama/urina , Estrogênios/urina , Feminino , Humanos , Hidroxiestronas/urina , Análise dos Mínimos Quadrados , Pessoa de Meia-Idade , Pós-Menopausa/urina
7.
Cancer Epidemiol Biomarkers Prev ; 9(8): 781-6, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10952094

RESUMO

Isoflavones are soy phytoestrogens that have been suggested to be anticarcinogenic. Our previous study in premenopausal women suggested that the mechanisms by which isoflavones exert cancer-preventive effects may involve modulation of estrogen metabolism away from production of potentially carcinogenic metabolites [16alpha-(OH) estrone, 4-(OH) estrone, and 4-(OH) estradiol] (X. Xu et al., Cancer Epidemiol. Biomark. Prev., 7: 1101-1108, 1998). To further evaluate this hypothesis, a randomized, cross-over soy isoflavone feeding study was performed in 18 healthy postmenopausal women. The study consisted of three diet periods, each separated by a washout of approximately 3 weeks. Each diet period lasted for 93 days, during which subjects consumed their habitual diets supplemented with soy protein isolate providing 0.1 (control), 1, or 2 mg isoflavones/kg body weight/day (7.1 +/- 1.1, 65 +/- 11, or 132 +/- 22 mg/day). A 72-h urine sample was collected 3 days before the study (baseline) and days 91-93 of each diet period. Urine samples were analyzed for 10 phytoestrogens and 15 endogenous estrogens and their metabolites by a capillary gas chromatography-mass spectrometry method. Compared with the soy-free baseline and very low isoflavone control diet, consumption of 65 mg isoflavones increased the urinary 2/16alpha-(OH) estrone ratio, and consumption of 65 or 132 mg isoflavones decreased excretion of 4-(OH) estrone. When compared with baseline values, consumption of all three soy diets increased the ratio of 2/4-(OH) estrogens and decreased the ratio of genotoxic: total estrogens. These data suggest that both isoflavones and other soy constituents may exert cancer-preventive effects in postmenopausal women by altering estrogen metabolism away from genotoxic metabolites toward inactive metabolites.


Assuntos
Anticarcinógenos/uso terapêutico , Neoplasias da Mama/prevenção & controle , Estrogênios/metabolismo , Isoflavonas/uso terapêutico , Pós-Menopausa/metabolismo , Proteínas de Soja/uso terapêutico , Análise de Variância , Anticarcinógenos/urina , Estudos Cross-Over , Estrogênios/urina , Estrogênios não Esteroides/urina , Feminino , Humanos , Isoflavonas/urina , Análise dos Mínimos Quadrados , Pessoa de Meia-Idade , Fitoestrógenos , Preparações de Plantas , Pós-Menopausa/urina , Proteínas de Soja/urina
8.
J Epidemiol ; 10(2): 127-35, 2000 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10778038

RESUMO

Biological effects of dietary isoflavones, such as daidzein and genistein are of interest in preventive medicine. We estimated the dietary intake of isoflavones from dietary records and compared the values with the plasma concentrations and urinary excretions in Japanese middle-aged women. The dietary intake of daidzein and genistein was 64.6 and 111.6 mumol /day/capita (16.4 and 30.1 mg/day/capita), respectively. The isoflavones intake was mostly attributable to tofu, natto and miso. The median of plasma daidzein and genistein concentration was 72.46 and 206.09 nmol/L, respectively. The median of urinary excretion was 20.54 mumol /day for daidzein, 10.79 for genistein, 15.74 for equol and 1.64 for O-desmethylangolensin (O-DMA). Equol and O-DMA were excreted by 50% and 84% of all participants, respectively. Equol metabolizers were significantly lower the plasma and urinary daidzein and urinary O-DMA. The dietary intake of daidzein and genistein after the adjustment for total energy intake was significantly correlated with the urinary excretion (r = 0.365 for daidzein and r = 0.346 for genistein) and plasma concentration (r = 0.335 for daidzein and r = 0.429 for genistein). The plasma concentration of isoflavones was also significantly correlated with the urinary excretion. We conclude that in epidemiological studies measurements of plasma concentration or urinary excretion of these isoflavones are useful biomarkers of dietary intake and important for studies on their relation to human health.


Assuntos
Dieta , Estrogênios não Esteroides/administração & dosagem , Isoflavonas/administração & dosagem , Plantas , Adulto , Idoso , Anticarcinógenos/administração & dosagem , Anticarcinógenos/sangue , Anticarcinógenos/urina , Biomarcadores/sangue , Biomarcadores/urina , Cromanos/sangue , Cromanos/urina , Registros de Dieta , Ingestão de Energia , Equol , Feminino , Genisteína/administração & dosagem , Genisteína/sangue , Genisteína/urina , Humanos , Isoflavonas/sangue , Isoflavonas/urina , Pessoa de Meia-Idade , Inibidores da Monoaminoxidase/sangue , Inibidores da Monoaminoxidase/urina , Fitoestrógenos , Preparações de Plantas , Análise de Regressão , Glycine max
9.
Nutr Cancer ; 37(2): 145-54, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11142086

RESUMO

The primary objective of this study was to assess the accuracy of a modified Block food frequency questionnaire (FFQ) with respect to its ability to assess usual dietary intakes of daidzein and genistein. Participants were a convenience sample of 51 Japanese and 18 Caucasian women. All interviews were conducted between February 1997 and October 1997. At each of the four study visits, participants provided a 24-hour urine specimen and a 48-hour dietary recall. At the first visit, participants also completed an interviewer-administered modified Block FFQ. The daidzein and genistein intakes estimated using the FFQ were moderately correlated with the mean estimates of daidzein and genistein intake calculated from four 48-hour dietary recalls (correlation for daidzein = 0.49-0.58 and correlation for genistein = 0.45-0.54) and estimates of urinary concentrations of these compounds calculated from four collections (correlations for daidzein and genistein = 0.49 and 0.30, respectively). The accuracy of the modified Block FFQ for assessment of usual daidzein and genistein intakes is supported by this study. These results support the use of this instrument in epidemiological studies as an easy and low-cost method to assess the usual dietary daidzein or genistein intake.


Assuntos
Anticarcinógenos/administração & dosagem , Estrogênios não Esteroides/administração & dosagem , Genisteína/administração & dosagem , Isoflavonas/administração & dosagem , Inquéritos e Questionários , Anticarcinógenos/urina , Asiático , Registros de Dieta , Estrogênios não Esteroides/urina , Feminino , Genisteína/urina , Humanos , Entrevistas como Assunto , Isoflavonas/urina , Rememoração Mental , Fitoestrógenos , Preparações de Plantas , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Urinálise , População Branca
10.
J Chromatogr B Biomed Sci Appl ; 713(2): 379-86, 1998 Aug 25.
Artigo em Inglês | MEDLINE | ID: mdl-9746253

RESUMO

A high-performance liquid chromatographic (HPLC) method is described for the determination of apigenin and the 4'-methylated derivative acacetin in human urine using column-switching and ultraviolet (UV) absorbance detection. Urine samples were enzymatically hydrolysed and solid-phase extracted prior to injection onto the HPLC system. Prior to elution of apigenin and the internal standard, 5,7,8-trihydroxyflavone, from the first column used for sample clean-up, the six-port valve was switched to the second column for analysis with UV detection. Detection of apigenin was precise and reproducible, with a limit of quantification of 10 ng ml(-1) urine. Detection and quantification of acacetin was linear down to 70 ng ml(-1) urine. The method has been successfully applied to determine the level of apigenin in 100 human urine samples from an intervention study with parsley.


Assuntos
Anticarcinógenos/urina , Flavonas , Flavonoides/análise , Flavonoides/urina , Óleos Voláteis/análise , Apiaceae/química , Arilsulfatases , Camomila , Cromatografia Líquida de Alta Pressão , Flavonoides/química , Glucuronidase , Humanos , Hidrólise , Klebsiella pneumoniae/enzimologia , Óleos Voláteis/química , Plantas Medicinais , Sensibilidade e Especificidade , Espectrofotometria Ultravioleta
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