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Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism

BACKGROUND: To elucidate whether rice protein can possess a vital function in improving lipids level and adiposity, the effects of rice proteins extracted by alkaline (RP-A) and α-amylase (RP-E) on triglyceride metabolism were investigated in 7-week-old male Wistar rats fed cholesterol-enriched diet...

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Autores principales: Yang, Lin, Chen, Jia-Hou, Lv, Jie, Wu, Qiong, Xu, Tong, Zhang, Hua, Liu, Qiao-Hong, Yang, Hong-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311603/
https://www.ncbi.nlm.nih.gov/pubmed/22330327
http://dx.doi.org/10.1186/1476-511X-11-24
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author Yang, Lin
Chen, Jia-Hou
Lv, Jie
Wu, Qiong
Xu, Tong
Zhang, Hua
Liu, Qiao-Hong
Yang, Hong-Kun
author_facet Yang, Lin
Chen, Jia-Hou
Lv, Jie
Wu, Qiong
Xu, Tong
Zhang, Hua
Liu, Qiao-Hong
Yang, Hong-Kun
author_sort Yang, Lin
collection PubMed
description BACKGROUND: To elucidate whether rice protein can possess a vital function in improving lipids level and adiposity, the effects of rice proteins extracted by alkaline (RP-A) and α-amylase (RP-E) on triglyceride metabolism were investigated in 7-week-old male Wistar rats fed cholesterol-enriched diets for 2 weeks, as compared with casein (CAS). RESULTS: Compared with CAS, plasma concentrations of glucose and lipids were significantly reduced by RP-feeding (P < 0.05), as well as hepatic accumulation of lipids (P < 0.05). RP-A and RP-E significantly depressed the hepatic activities of fatty acid synthase (FAS), glucose 6-phosphate dehydrogenase (G6PD) and malate dehydrogenase (MDH) (P < 0.05), whereas the activities of lipoprotein lipase (PL) and hepatic lipase (HL) were significantly stimulated (P < 0.05), as compared to CAS. Neither lipids level nor activities of enzymes were different between RP-A and RP-E (P > 0.05). There was a significant positive correlation between protein digestibility and deposit fat (r = 0.8567, P < 0.05), as well as the plasma TG concentration (r = 0.8627, P < 0.05). CONCLUSIONS: The present study demonstrates that rice protein can modify triglyceride metabolism, leading to an improvement of body weight and adiposity. Results suggest that the triglyceride-lowering action as well as the potential of anti-adiposity induced by rice protein is attributed to upregulation of lipolysis and downregulation of lipogenesis, and the lower digestibility of rice protein may be the main modulator responsible for the lipid-lowering action.
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spelling pubmed-33116032012-03-24 Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism Yang, Lin Chen, Jia-Hou Lv, Jie Wu, Qiong Xu, Tong Zhang, Hua Liu, Qiao-Hong Yang, Hong-Kun Lipids Health Dis Research BACKGROUND: To elucidate whether rice protein can possess a vital function in improving lipids level and adiposity, the effects of rice proteins extracted by alkaline (RP-A) and α-amylase (RP-E) on triglyceride metabolism were investigated in 7-week-old male Wistar rats fed cholesterol-enriched diets for 2 weeks, as compared with casein (CAS). RESULTS: Compared with CAS, plasma concentrations of glucose and lipids were significantly reduced by RP-feeding (P < 0.05), as well as hepatic accumulation of lipids (P < 0.05). RP-A and RP-E significantly depressed the hepatic activities of fatty acid synthase (FAS), glucose 6-phosphate dehydrogenase (G6PD) and malate dehydrogenase (MDH) (P < 0.05), whereas the activities of lipoprotein lipase (PL) and hepatic lipase (HL) were significantly stimulated (P < 0.05), as compared to CAS. Neither lipids level nor activities of enzymes were different between RP-A and RP-E (P > 0.05). There was a significant positive correlation between protein digestibility and deposit fat (r = 0.8567, P < 0.05), as well as the plasma TG concentration (r = 0.8627, P < 0.05). CONCLUSIONS: The present study demonstrates that rice protein can modify triglyceride metabolism, leading to an improvement of body weight and adiposity. Results suggest that the triglyceride-lowering action as well as the potential of anti-adiposity induced by rice protein is attributed to upregulation of lipolysis and downregulation of lipogenesis, and the lower digestibility of rice protein may be the main modulator responsible for the lipid-lowering action. BioMed Central 2012-02-13 /pmc/articles/PMC3311603/ /pubmed/22330327 http://dx.doi.org/10.1186/1476-511X-11-24 Text en Copyright ©2012 Yang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Yang, Lin
Chen, Jia-Hou
Lv, Jie
Wu, Qiong
Xu, Tong
Zhang, Hua
Liu, Qiao-Hong
Yang, Hong-Kun
Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism
title Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism
title_full Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism
title_fullStr Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism
title_full_unstemmed Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism
title_short Rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism
title_sort rice protein improves adiposity, body weight and reduces lipids level in rats through modification of triglyceride metabolism
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3311603/
https://www.ncbi.nlm.nih.gov/pubmed/22330327
http://dx.doi.org/10.1186/1476-511X-11-24
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