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Metabolomics Approach After Acute Intake of Grumixama Juice

2016年6月13日 更新者:Luciane de Lira Teixeira、University of Sao Paulo

Metabolomics Approach After Acute Intake of Grumixama Juice (Eugenia Brasiliensis Lam)

Investigate the bioavailability of the main flavonoid, their colonic transformation and untargeted metabolites by an metabolomic approach following acute intake of a grumixama juice by humans.

研究概览

地位

完全的

条件

详细说明

The grumixama is a sweet and little cherry native of the South and Southeast regions of the Atlantic Forest of Brazil rich in phenolic compounds, mainly anthocyanins and ellagitannins. The objective of this study is Investigate the bioavailability of the main flavonoid, their colonic transformation and untargeted metabolites by an metabolomic approach following acute intake of a grumixama juice by humans.

Fifteen healthy subjects consumed grumixama juice at single dose, and urine and plasma samples were collected at different time points over 24 h period. The metabolites were analyzed by LC-ESI-MSn, LC-Q-TOF plasma and urine were also analyzed using untargeted metabolomic approach for amino acids and organic acids by GCMS.

研究类型

介入性

注册 (实际的)

15

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 49年 (成人)

接受健康志愿者

是的

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Not have medical historical of cardiovascular, gastrointestinal, hepatic, renal, thyroid and/or diabetes dysfunction
  • Not be alcohol addicts, not use vitamins and other supplements
  • Not are using any kind of medication which affect the digestion and absorption of food, not be smokers
  • Not are pregnant.

Exclusion Criteria:

  • Have medical historical of cardiovascular, gastrointestinal, hepatic, renal, thyroid and/or diabetes dysfunction
  • Be alcohol addicts, use vitamins and other supplements
  • Are using any kind of medication which affect the digestion and absorption of food, be smokers
  • Are pregnant.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
其他:Grumixama Juice

Juice of grumixama purple fruit (Eugenia brasiliensis Lam.), which is good source of anthocyanins and ellagitannins. It was made with filtered water and sanitized fruits, with a blender. It was administered in single dose of 0.97 mg of anthocyanins and of 4.71 mg of ellagitannins per mL of juice. Which volunteers ingested 10 mL of juice per each Kg body weight.

The metabolomic approach of plasma and urine samples following acute intake of grumixama juice was done by the collection of blood samples and urine, following the intake of grumixama juice.

In the morning of experimental day after 10 h fasting, the volunteers have been collect the first urine in the morning and it was collected the blood before the intake of grumixama juice, after they drink the juice (0 min), it was collected blood at the times: 15 min, 30 min, 60 min,120 min, 240 min and 24 h; and it was also collected urine at the period: 0 -1h, 1 - 2h, 2 - 4h, 4 - 6 h, 6 - 12 h, 12 - 14 h, the first urine in the morning in the second day (24 h). During the period in the first 4 h of experiment the volunteers only intake the juice.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Identification of metabolites in plasma and urine samples of 15 healthy volunteers after intake of grumixama juice by LCMS
大体时间:2 months
The blood and urine samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the anthocyanins and ellagitannins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by LC-ESI-MSn (for phenolic acids and anthocyanins) and LC-Q-TOF (for urolithins), the mass fragments were expressed in m/z.
2 months
Identification of metabolites in plasma and urine samples of 15 healthy volunteers after intake of grumixama juice by GCMS.
大体时间:2 months
The samples were collected as describe in "Arms and Interventions", but for urine samples were used only the samples collected at times 0 (before the juice intake), 0-1h, 1-2h, 2-4h and at 24h after intake. The plasma samples had their proteins precipitated with cold methanol, the metabolites were extracted, concentrated and the amino acids and organic acids were derivatized to became volatile and the samples were analyzed by GCMS. For urine samples the procedures were similar. The mass fragment profile of derivatized compounds were compared to a GCMS library.
2 months

次要结果测量

结果测量
措施说明
大体时间
Urinary creatinine values of 15 healthy volunteers for data normalization
大体时间:15 days
The creatinine was measured in the 15 volunteers by using a commercial kit, the results obtained in mg/dL, and these values were transformed in mol/L. The values of creatinine were used to normalize the quantification data.
15 days
Cycle cell analysis in breast cancer cells treated with metabolites extracted from plasma and urine of 10 healthy volunteers after grumixama juice intake
大体时间:2 days

Plasma and urine preparations were obtained by SPE extraction were dried and tested against breast cancer cells (MDA-MB 231) MDA-MB 231 cells were cultured in monolayer on Dulbecco Eagle modified culture medium supplemented with 10% fetal bovine serum, it was used 5x10-4 cells per well. The cells were incubated in a humidified chamber including 5% CO2 at 37ºC into a confluence of approximately 80%. Cells were further exposed to 200 mg/mL of urine and plasma extract preparations and phenolic compound standards (PCA, VA, HA, C3G) at 0.25 and 25 mg/mL, and maintained at 37ºC, under an atmosphere of 5% CO2 for 48 hours. Negative control was supplied with growth media and DMSO, and blank wells containing growth media only.

The cells were lysed, the RNA were degraded and the DNA were marked with propidium iodide (1mg/mL) and the fluorescence was measure by flow cytometer and the cell cycle analysis were done by FlowJo. The results were expressed in % of cell for each cell cycle phase.

2 days
Multivariate data analysis of metabolites identified in plasma and urine of 15 healthy volunteers after intake of grumixama juice by GCMS
大体时间:2 months
The peak intensity of each compound identified by GCMS were normalized by using a internal standards (D4-alanine). For urine these data also were normalized by creatinine values to normalize sample volume. Multivariate data analysis were done observe changes in these metabolites (amino acids and organic acids) during the 24h after grumixama juice intake. The data were analyzed by MetaboAnalyst 3.0 (http://www.metaboanalyst.ca/).
2 months
Pathway analysis of metabolites identified by GCMS
大体时间:1 month
The samples were collected as describe in "Arms and Interventions", but for urine samples were used only the samples collected at times 0 (before the juice intake), 0-1h, 1-2h, 2-4h and at 24h after intake. The plasma samples had their proteins precipitated with cold methanol, the metabolites were extracted, concentrated and the amino acids and organic acids were derivatized to became volatile and the samples were analyzed by GCMS. For urine samples the procedures were similar. The mass fragment profile of derivatized compounds were compared to a GCMS library.
1 month
Identification of anthocyanins in urine samples of 10 healthy volunteers by LCMS.
大体时间:2 months
The blood and urine samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the anthocyanins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by LC-ESI-MSn (for phenolic acids and anthocyanins) the mass fragments were expressed in m/z.
2 months
Identification of phenolic acids in plasma and urine samples of 10 healthy volunteers by LCMS
大体时间:2 months
The blood and urine samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the anthocyanins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by LC-ESI-MSn (for phenolic acids and anthocyanins) the mass fragments were expressed in m/z.
2 months
Identification of urolithins in urine samples of 10 healthy volunteers by LCMS
大体时间:2 months
The urine samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the ellagitannins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by LC-Q-TOF (for urolithins), the mass fragments were expressed in m/z.
2 months
Quantification of anthocyanins in urine samples of 10 healthy volunteers by HPLC
大体时间:2 months
The urine samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the anthocyanins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by HPLC, the results were expressed nmol/mol of creatinine for urine samples. It was made to each volunteer, in each point of collection sample.
2 months
Quantification of urolithins in urine samples of 10 healthy volunteers by HPLC
大体时间:2 months
The urine samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the ellagitannins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by HPLC, the results were expressed in mmol/mol of creatinine. It was made to each volunteer, in each point of collection sample.
2 months
Antiproliferative activity of metabolites extracted from plasma of 10 healthy volunteers after grumixama juice intake
大体时间:2 days
Plasma preparations were obtained by SPE extraction were dried and tested against breast cancer cells (MDA-MB 231) MDA-MB 231 cells were cultured in monolayer on Dulbecco Eagle modified culture medium supplemented with 10% fetal bovine serum, it was used 5x10-4 cells per well. The cells were incubated in a humidified chamber including 5% CO2 at 37ºC into a confluence of approximately 80%. Cells were further exposed to 200 mg/mL of plasma extract preparations and phenolic compound standards (PCA, VA, HA, C3G) at 0.25 and 25 mg/mL, and maintained at 37ºC, under an atmosphere of 5% CO2 for 48 hours. Negative control was supplied with growth media and DMSO, and blank wells containing growth media only. Cells were marked with CFSE, and fluorescence was measured by flow cytometer. The results were expressed as % of proliferation inhibition.
2 days
Antiproliferative activity of metabolites extracted from urine of 10 healthy volunteers after grumixama juice intake
大体时间:2 days
Urine preparations were obtained by SPE extraction were dried and tested against breast cancer cells (MDA-MB 231) MDA-MB 231 cells were cultured in monolayer on Dulbecco Eagle modified culture medium supplemented with 10% fetal bovine serum, it was used 5x10-4 cells per well. The cells were incubated in a humidified chamber including 5% CO2 at 37ºC into a confluence of approximately 80%. Cells were further exposed to 200 mg/mL of urine extract preparations and phenolic compound standards (PCA, VA, HA, C3G) at 0.25 and 25 mg/mL, and maintained at 37ºC, under an atmosphere of 5% CO2 for 48 hours. Negative control was supplied with growth media and DMSO, and blank wells containing growth media only. Cells were marked with CFSE, and fluorescence was measured by flow cytometer. The results were expressed as % of proliferation inhibition
2 days
Quantification of amino acids identified by GCMS
大体时间:1 month
Standards curves of the amino acids that changed significantly after grumixama juice intake were made by GCMS. Through these standards curves the amino acids and organic acids were quantified and the results were expressed in mmol/μmol of creatinine for urine samples and mmol/mL of plasma.
1 month
Quantification of organic acids identified by GCMS
大体时间:1 month
Standards curves of organic acids that changed significantly after grumixama juice intake were made by GCMS. Through these standards curves the organic acids were quantified and the results were expressed in mmol/μmol of creatinine for urine samples and mmol/mL of plasma.
1 month
Quantification of phenolic acids in plasma samples of 10 healthy volunteers by HPLC
大体时间:2 months
The blood samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the anthocyanins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by HPLC, the results were expressed in μmol/mL of plasma. It was made to each volunteer, in each point of collection sample.
2 months
Quantification of phenolic acids in urine samples of 10 healthy volunteers by HPLC
大体时间:2 months
The urine samples were collected in the times describe in "Arms and Interventions". The samples were acidified and the anthocyanins metabolites were extracted by SPE column, these metabolites extracted were concentrated and analyzed by HPLC, the results were expressed in mmol/mol of creatinine for urine samples. It was made to each volunteer, in each point of collection sample.
2 months
Pharmacokinetic parameters (AUC) of anthocyanins in urine of 10 healthy volunteers after intake of grumixama juice
大体时间:1 month
Using the quantification results for each collection time was calculated the area under curve (AUC) of anthocyanins in urine (expressed in μmol/h).
1 month
Pharmacokinetic parameters (AUC) of phenolic acids in urine of 10 healthy volunteers after intake of grumixama juice
大体时间:1 month
Using the quantification results for each collection time was calculated the area under curve (AUC) of phenolic acids in urine (expressed in mmol/h).
1 month
Pharmacokinetic parameters (AUC) of urolithins in urine of 10 healthy volunteers after intake of grumixama juice
大体时间:1 month
Using the quantification results for each collection time was calculated the area under curve (AUC) of urolithins in urine (expressed in mmol/h).
1 month
Urine volume
大体时间:1 day
The volume of each urine sample was measured in mL.
1 day
The total elimination of anthocyanins in urine of 10 healthy volunteers after intake of grumixama juice
大体时间:1 month
The total elimination amount of anthocyanins was calculated using the urine volume and it was expressed in nmol.
1 month
The total elimination of phenolic acids in urine of 10 healthy volunteers after intake of grumixama juice
大体时间:1 month
The total elimination amount of phenolic acids was calculated using the urine volume and it was expressed in µmol.
1 month
The total elimination of urolithins in urine of 10 healthy volunteers after intake of grumixama juice
大体时间:1 month
The total elimination amount of urolithins was calculated using the urine volume and it was expressed in µmol.
1 month

其他结果措施

结果测量
措施说明
大体时间
Normal blood glycemia values of 15 volunteers before juice intake
大体时间:1 day
The glycemia was measured in 15 volunteers to evaluate if the glycemia values were acceptable. The values were expressed in mg/dL.
1 day
Normal total cholesterol values of 15 volunteers before juice intake
大体时间:1 day
The total cholesterol was measured in 15 volunteers to evaluate if the cholesterol values were acceptable. The values were expressed in mg/dL.
1 day
Normal triglycerides values of 15 volunteers before juice intake
大体时间:1 day
The triglycerides were measured in 15 volunteers to evaluate if the triglycerides values were acceptable. The values were expressed in mg/dL.
1 day
Normal HDL values of 15 volunteers before juice intake
大体时间:1 day
The HDL values were measured in 15 volunteers to evaluate if the HDL and LDL values were acceptable. The values were expressed in mg/dL.
1 day
Similar weight of 15 volunteers before juice intake
大体时间:1 day
The weight was measured in 15 volunteers to calculate the dose of juice to be give to the volunteers and also to calculate the BMI. The results were expressed in Kg of body mass.
1 day
Similar height of 15 volunteers before juice intake
大体时间:1 day
The height was measured in 15 volunteers to calculate the body index mass (BMI). The results were expressed in meters (m).
1 day
Similar BMI of 15 volunteers before juice intake
大体时间:1 day
The height was measured in 15 volunteers to calculate the body index mass (BMI). The results were expressed in Kg/m2. This assessment was made to check if the volunteers had a similar BMI.
1 day
Normal LDL values of 15 volunteers before juice intake
大体时间:1 day
The LDL values were measured in 15 volunteers to evaluate if the HDL and LDL values were acceptable. The values were expressed in mg/dL.
1 day
Normal serum creatinine of 15 volunteers before juice intake
大体时间:1 day
The serum creatinine values were measured in 15 volunteers to evaluate if the values were acceptable. The values were expressed in mg/dL.
1 day
Alanine aminotransferase measures in serum samples of 15 volunteers before juice intake
大体时间:1 day
The alanine aminotransferase was measured in the serum of 15 volunteers to evaluate if the values were acceptable. The values were expressed in U/L.
1 day
The aspartate transaminase measures in serum samples of 15 volunteers before juice intake
大体时间:1 day
The aspartate transaminase was measured in the serum of 15 volunteers to evaluate if the values were acceptable. The values were expressed in U/L.
1 day

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Luciane L. Teixeira, MS、University of Sao Paulo
  • 学习椅:Neuza M. Aymoto Hassimotto, PhD、University of Sao Paulo
  • 学习椅:Franco M. Lajolo, PhD、University of Sao Paulo

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2014年3月1日

初级完成 (实际的)

2014年8月1日

研究完成 (实际的)

2016年3月1日

研究注册日期

首次提交

2016年4月2日

首先提交符合 QC 标准的

2016年5月30日

首次发布 (估计)

2016年6月6日

研究记录更新

最后更新发布 (估计)

2016年6月14日

上次提交的符合 QC 标准的更新

2016年6月13日

最后验证

2016年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • 17449613.8.0000.0067

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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