4.6 Article

NMR-Based Identification of Metabolites in Polar and Non-Polar Extracts of Avian Liver

期刊

METABOLITES
卷 7, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/metabo7040061

关键词

NMR spectroscopy; liver tissue; extraction protocol; metabolite identification by NMR; diet, effect of on liver metabolites

资金

  1. National Science Foundation [IOS-1354893]
  2. Biomedical Technology Research, Resources (BTRR) Program of the National Institute of General, Medical Sciences (NIGMS), National Institutes of Health (NIH) [P41GM103399]
  3. National Center for Biomolecular NMR Data Processing and Analysis - NIH (NIGMS) [P41GM111135]
  4. Division Of Integrative Organismal Systems
  5. Direct For Biological Sciences [1354893] Funding Source: National Science Foundation

向作者/读者索取更多资源

Metabolites present in liver provide important clues regarding the physiological state of an organism. The aim of this work was to evaluate a protocol for high-throughput NMR-based analysis of polar and non-polar metabolites from a small quantity of liver tissue. We extracted the tissue with a methanol/chloroform/water mixture and isolated the polar metabolites from the methanol/water layer and the non-polar metabolites from the chloroform layer. Following drying, we re-solubilized the fractions for analysis with a 600 MHz NMR spectrometer equipped with a 1.7 mm cryogenic probe. In order to evaluate the feasibility of this protocol for metabolomics studies, we analyzed the metabolic profile of livers from house sparrow (Passer domesticus) nestlings raised on two different diets: livers from 10 nestlings raised on a high protein diet (HP) for 4 d and livers from 12 nestlings raised on the HP diet for 3 d and then switched to a high carbohydrate diet (HC) for 1 d. The protocol enabled the detection of 52 polar and nine non-polar metabolites in H-1 NMR spectra of the extracts. We analyzed the lipophilic metabolites by one-way ANOVA to assess statistically significant concentration differences between the two groups. The results of our studies demonstrate that the protocol described here can be exploited for high-throughput screening of small quantities of liver tissue (approx. 100 mg wet mass) obtainable from small animals.

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