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Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats
OBJECTIVE: Cinnamon is a cooking spice and a medicinal herb. It is increasingly used as a health supplement due to its perceived benefit to prevent and or manage type 2 diabetes and metabolic disorders. However, it is unclear if regular consumption of this medicinal plant will interfere with normal...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272659/ https://www.ncbi.nlm.nih.gov/pubmed/34306160 http://dx.doi.org/10.1155/2021/9892088 |
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author | Huang, Xiaomin Cai, Haiyang Li, Han Su, Yixun Li, Hui Li, Weihong Yi, Chenju Oliver, Brian G. Chen, Hui |
author_facet | Huang, Xiaomin Cai, Haiyang Li, Han Su, Yixun Li, Hui Li, Weihong Yi, Chenju Oliver, Brian G. Chen, Hui |
author_sort | Huang, Xiaomin |
collection | PubMed |
description | OBJECTIVE: Cinnamon is a cooking spice and a medicinal herb. It is increasingly used as a health supplement due to its perceived benefit to prevent and or manage type 2 diabetes and metabolic disorders. However, it is unclear if regular consumption of this medicinal plant will interfere with normal physiological functions. Therefore, this study investigated the impact of daily cinnamon supplements on glucose and lipid metabolic profiles in healthy rats. METHODS: Male rats (Sprague Dawley, 8 weeks) were supplied with cinnamon in their diet (equivalent to ∼1 g/day in humans) for two weeks. Blood glucose and lipid levels, as well as metabolic markers in both liver and abdominal white adipose tissue, were measured. RESULTS: Cinnamon significantly increased fat mass and blood cholesterol and low-density lipoprotein (LDL) levels, but reduced fasting blood glucose level by 12%. Liver functional enzymes were normal in rats consuming cinnamon. However, several lipid metabolic markers were impaired which may contribute to dyslipidemia, including two main switches for energy metabolism (sirtuin 1 and peroxisome proliferator-activated receptor-gamma coactivator-1α) and the LDL receptor. However, de novo lipid synthesis enzymes and inflammatory markers were also reduced in the liver by cinnamon treatment, which may potentially prevent the development of steatosis. Markers for lipid oxidation were downregulated in fat tissue in cinnamon-treated rats, contributing to increased fat accumulation. CONCLUSION: Daily low-dose cinnamon supplementation seems to promote abdominal adipose tissue accumulation and disturb lipid homeostasis in healthy rats, raising the concerns regarding daily use in healthy people. |
format | Online Article Text |
id | pubmed-8272659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-82726592021-07-22 Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats Huang, Xiaomin Cai, Haiyang Li, Han Su, Yixun Li, Hui Li, Weihong Yi, Chenju Oliver, Brian G. Chen, Hui Evid Based Complement Alternat Med Research Article OBJECTIVE: Cinnamon is a cooking spice and a medicinal herb. It is increasingly used as a health supplement due to its perceived benefit to prevent and or manage type 2 diabetes and metabolic disorders. However, it is unclear if regular consumption of this medicinal plant will interfere with normal physiological functions. Therefore, this study investigated the impact of daily cinnamon supplements on glucose and lipid metabolic profiles in healthy rats. METHODS: Male rats (Sprague Dawley, 8 weeks) were supplied with cinnamon in their diet (equivalent to ∼1 g/day in humans) for two weeks. Blood glucose and lipid levels, as well as metabolic markers in both liver and abdominal white adipose tissue, were measured. RESULTS: Cinnamon significantly increased fat mass and blood cholesterol and low-density lipoprotein (LDL) levels, but reduced fasting blood glucose level by 12%. Liver functional enzymes were normal in rats consuming cinnamon. However, several lipid metabolic markers were impaired which may contribute to dyslipidemia, including two main switches for energy metabolism (sirtuin 1 and peroxisome proliferator-activated receptor-gamma coactivator-1α) and the LDL receptor. However, de novo lipid synthesis enzymes and inflammatory markers were also reduced in the liver by cinnamon treatment, which may potentially prevent the development of steatosis. Markers for lipid oxidation were downregulated in fat tissue in cinnamon-treated rats, contributing to increased fat accumulation. CONCLUSION: Daily low-dose cinnamon supplementation seems to promote abdominal adipose tissue accumulation and disturb lipid homeostasis in healthy rats, raising the concerns regarding daily use in healthy people. Hindawi 2021-07-02 /pmc/articles/PMC8272659/ /pubmed/34306160 http://dx.doi.org/10.1155/2021/9892088 Text en Copyright © 2021 Xiaomin Huang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Huang, Xiaomin Cai, Haiyang Li, Han Su, Yixun Li, Hui Li, Weihong Yi, Chenju Oliver, Brian G. Chen, Hui Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats |
title | Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats |
title_full | Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats |
title_fullStr | Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats |
title_full_unstemmed | Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats |
title_short | Cinnamon as Dietary Supplement Caused Hyperlipidemia in Healthy Rats |
title_sort | cinnamon as dietary supplement caused hyperlipidemia in healthy rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272659/ https://www.ncbi.nlm.nih.gov/pubmed/34306160 http://dx.doi.org/10.1155/2021/9892088 |
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