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Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice

Obesity is a medical condition in which excess body fat has accumulated to a serious extent. It is a chronic disease that can lead to dyslipidemia, insulin resistance, and type 2 diabetes. In the present study, we investigated the anti-obesity effects of Sicyos angulatus (SA) extract on a high-fat d...

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Autores principales: Choi, Ji Hyun, Noh, Jung-Ran, Kim, Yong-Hoon, Kim, Jae-Hoon, Kang, Eun-Jung, Choi, Dong-Hee, Choi, Jung Hyeon, An, Jin-Pyo, Oh, Won-Keun, Lee, Chul-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085266/
https://www.ncbi.nlm.nih.gov/pubmed/32218700
http://dx.doi.org/10.7150/ijms.42247
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author Choi, Ji Hyun
Noh, Jung-Ran
Kim, Yong-Hoon
Kim, Jae-Hoon
Kang, Eun-Jung
Choi, Dong-Hee
Choi, Jung Hyeon
An, Jin-Pyo
Oh, Won-Keun
Lee, Chul-Ho
author_facet Choi, Ji Hyun
Noh, Jung-Ran
Kim, Yong-Hoon
Kim, Jae-Hoon
Kang, Eun-Jung
Choi, Dong-Hee
Choi, Jung Hyeon
An, Jin-Pyo
Oh, Won-Keun
Lee, Chul-Ho
author_sort Choi, Ji Hyun
collection PubMed
description Obesity is a medical condition in which excess body fat has accumulated to a serious extent. It is a chronic disease that can lead to dyslipidemia, insulin resistance, and type 2 diabetes. In the present study, we investigated the anti-obesity effects of Sicyos angulatus (SA) extract on a high-fat diet (HFD)-induced C57BL/6J obese mice. The mice were divided into vehicle and three SA groups (25, 50, and 100 mg/kg body weight). The mice were fed a HFD with or without SA for 12 weeks. The oral administration of SA reduced body and adipose tissue weight in HFD-fed mice compared to those in the vehicle group (p<0.05). Adipocyte size and inflammation significantly decreased in the SA-administered groups in a dose-dependent manner. In particular, adipocytes larger than 5000 µm(2) were remarkably reduced by around 50% in the SA-treated groups (p<0.05). In addition, SA contributes towards reducing insulin resistance (measured as the HOMA-IR index) and glucose intolerance in HFD-induced obese mice (p<0.05; Vehicle 21.5±3.1 vs. SA100 4.7±0.4). These beneficial effects of SA on obesity may be linked to the suppression of lipogenesis and stimulating energy metabolism in white adipose tissue and muscle. In white adipose tissue and muscle, the administration of SA activated AMPK pathway, leading to the inhibition of the development of pathophysiological conditions associated with obesity, including lipogenesis and inflammation. These findings suggest that SA may prevent obesity through inhibiting fat accumulation in HFD-induced obese mice. Therefore, SA is able to exert metabolic benefits in the prevention of obesity and insulin resistance.
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spelling pubmed-70852662020-03-26 Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice Choi, Ji Hyun Noh, Jung-Ran Kim, Yong-Hoon Kim, Jae-Hoon Kang, Eun-Jung Choi, Dong-Hee Choi, Jung Hyeon An, Jin-Pyo Oh, Won-Keun Lee, Chul-Ho Int J Med Sci Research Paper Obesity is a medical condition in which excess body fat has accumulated to a serious extent. It is a chronic disease that can lead to dyslipidemia, insulin resistance, and type 2 diabetes. In the present study, we investigated the anti-obesity effects of Sicyos angulatus (SA) extract on a high-fat diet (HFD)-induced C57BL/6J obese mice. The mice were divided into vehicle and three SA groups (25, 50, and 100 mg/kg body weight). The mice were fed a HFD with or without SA for 12 weeks. The oral administration of SA reduced body and adipose tissue weight in HFD-fed mice compared to those in the vehicle group (p<0.05). Adipocyte size and inflammation significantly decreased in the SA-administered groups in a dose-dependent manner. In particular, adipocytes larger than 5000 µm(2) were remarkably reduced by around 50% in the SA-treated groups (p<0.05). In addition, SA contributes towards reducing insulin resistance (measured as the HOMA-IR index) and glucose intolerance in HFD-induced obese mice (p<0.05; Vehicle 21.5±3.1 vs. SA100 4.7±0.4). These beneficial effects of SA on obesity may be linked to the suppression of lipogenesis and stimulating energy metabolism in white adipose tissue and muscle. In white adipose tissue and muscle, the administration of SA activated AMPK pathway, leading to the inhibition of the development of pathophysiological conditions associated with obesity, including lipogenesis and inflammation. These findings suggest that SA may prevent obesity through inhibiting fat accumulation in HFD-induced obese mice. Therefore, SA is able to exert metabolic benefits in the prevention of obesity and insulin resistance. Ivyspring International Publisher 2020-03-05 /pmc/articles/PMC7085266/ /pubmed/32218700 http://dx.doi.org/10.7150/ijms.42247 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Choi, Ji Hyun
Noh, Jung-Ran
Kim, Yong-Hoon
Kim, Jae-Hoon
Kang, Eun-Jung
Choi, Dong-Hee
Choi, Jung Hyeon
An, Jin-Pyo
Oh, Won-Keun
Lee, Chul-Ho
Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice
title Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice
title_full Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice
title_fullStr Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice
title_full_unstemmed Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice
title_short Sicyos angulatus Prevents High-Fat Diet-Induced Obesity and Insulin Resistance in Mice
title_sort sicyos angulatus prevents high-fat diet-induced obesity and insulin resistance in mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085266/
https://www.ncbi.nlm.nih.gov/pubmed/32218700
http://dx.doi.org/10.7150/ijms.42247
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