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1H NMR-based metabolomic study on resistance to diet-induced obesity in AHNAK knock-out mice
- 1H NMR-based metabolomic study on resistance to diet-induced obesity in AHNAK knock-out mice
- Kim I.Y.; Jung J.; Jang M.; Ahn Y.G.; Shin J.H.; Choi J.W.; Sohn M.R.; Shin S.M.; Kang D.-G.; Lee H.-S.; Bae Y.S.; Ryu D.H.; Seong J.K.; Hwang G.-S.
- Ewha Authors
- SCOPUS Author ID
- Issue Date
- Journal Title
- Biochemical and Biophysical Research Communications
- vol. 403, no. 41337, pp. 428 - 434
- SCI; SCIE; SCOPUS
- AHNAK is a giant protein of approximately 700kDa identified in human neuroblastomas and skin epithelial cells. Recently, we found that AHNAK knock-out (AHNAK-/-) mice have a strong resistance to high-fat diet-induced obesity. In this study, we applied 1H NMR-based metabolomics with multivariate statistical analysis to compare the altered metabolic patterns detected in urine from high-fat diet (HFD) fed wild-type and AHNAK-/- mice and investigate the mechanisms underlying the resistance to high-fat diet-induced obesity in AHNAK-/- mice. In global profiling, principal components analysis showed a clear separation between the chow diet and HFD groups; wild-type and AHNAK-/- mice were more distinctly separated in the HFD group compared to the chow diet group. Based on target profiling, the urinary metabolites of HFD-fed AHNAK-/- mice gave higher levels of methionine, putrescine, tartrate, urocanate, sucrose, glucose, threonine, and 3-hydroxyisovalerate. Furthermore, two-way ANOVAs indicated that diet type, genetic type, and their interaction (gene×diet) affect the metabolite changes differently. Most metabolites were affected by diet type, and putrescine, threonine, urocanate, and tartrate were also affected by genetic type. In addition, cis-aconitate, succinate, glycine, histidine, methylamine (MA), phenylacetylglycine (PAG), methionine, putrescine, uroconate, and tartrate showed interaction effects. Through the pattern changes in urinary metabolites of HFD-fed AHNAK-/- mice, our data suggest that the strong resistance to HFD-induced obesity in AHNAK-/- mice comes from perturbations of amino acids, such as methionine, putrescine, threonine, and histidine, which are related to fat metabolism. The changes in metabolites affected by microflora such as PAG and MA were also observed. In addition, resistance to obesity in HFD-fed AHNAK-/- mice was not related to an activated tricarboxylic acid cycle. These findings demonstrate that 1H NMR-based metabolic profiling of urine is suitable for elucidating possible biological pathways perturbed by functional loss of AHNAK on HFD feeding and could elucidate the mechanism underlying the resistance to high-fat diet-induced obesity in AHNAK-/- mice. © 2010 Elsevier Inc.
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