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Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice

This study was conducted to evaluate whether Allium hookeri can control diabetic symptoms. Aqueous extract (AE1: 100 mg/kg BW, AE2: 200 mg/kg BW) and ethanol extract (EE1: 100 mg/kg BW, EE2: 200 mg/kg BW) of A. hookeri were orally administrated to diabetic mice (C57BL/J-db/db) for 8 weeks. The negat...

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Autores principales: Choi, Ji-Hye, Kim, Si-Hyun, Lee, Eun-Byeol, Kim, Ji-Su, Jung, Ji-Eeun, Jeong, Un-Yul, Kim, Ju-Hui, Jang, Hwan-Hee, Park, Shin-Young, Kim, Gi-Chang, Lim, Jung-Hyun, Lee, Sung-Hyen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024442/
https://www.ncbi.nlm.nih.gov/pubmed/35455483
http://dx.doi.org/10.3390/ph15040486
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author Choi, Ji-Hye
Kim, Si-Hyun
Lee, Eun-Byeol
Kim, Ji-Su
Jung, Ji-Eeun
Jeong, Un-Yul
Kim, Ju-Hui
Jang, Hwan-Hee
Park, Shin-Young
Kim, Gi-Chang
Lim, Jung-Hyun
Lee, Sung-Hyen
author_facet Choi, Ji-Hye
Kim, Si-Hyun
Lee, Eun-Byeol
Kim, Ji-Su
Jung, Ji-Eeun
Jeong, Un-Yul
Kim, Ju-Hui
Jang, Hwan-Hee
Park, Shin-Young
Kim, Gi-Chang
Lim, Jung-Hyun
Lee, Sung-Hyen
author_sort Choi, Ji-Hye
collection PubMed
description This study was conducted to evaluate whether Allium hookeri can control diabetic symptoms. Aqueous extract (AE1: 100 mg/kg BW, AE2: 200 mg/kg BW) and ethanol extract (EE1: 100 mg/kg BW, EE2: 200 mg/kg BW) of A. hookeri were orally administrated to diabetic mice (C57BL/J-db/db) for 8 weeks. The negative (NC) and the positive (PC) control groups were treated with 0.9% saline and metformin (150 mg/kg BW), respectively. Glucose and lipid profile (triglyceride, total cholesterol (TC), LDL-C, and HDL-C) as biochemical parameters, toxicological factors such as liver/kidney functional parameters (ALT, AST, BUN, and Cr), and NK cell activity in blood were measured. Oral glucose tolerance test (OGTT) and histopathological examination were also conducted. Compared with the NC group, AE and EE decreased blood glucose, HbA1c, area under the curve (AUC) during OGTT, and leptin levels while increasing adiponectin levels. Serum lipid profiles and toxicological factors levels were reduced by the A. hookeri extract. Interestingly, HDL-C, glomerular mesangial expansion score in the kidney, and NK cell activity were effectively controlled in EE groups. Based on the results, EE is considered to be more effective in reducing high blood glucose, lipid profile, and related factor levels than AE, and is comparable to metformin in some biomarkers. It can be presumed that EE can more effectively control the major anomalies in the diabetic model than AE, and it may be used to prevent diabetic symptoms without toxicity in the Type 2 diabetic model.
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spelling pubmed-90244422022-04-23 Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice Choi, Ji-Hye Kim, Si-Hyun Lee, Eun-Byeol Kim, Ji-Su Jung, Ji-Eeun Jeong, Un-Yul Kim, Ju-Hui Jang, Hwan-Hee Park, Shin-Young Kim, Gi-Chang Lim, Jung-Hyun Lee, Sung-Hyen Pharmaceuticals (Basel) Article This study was conducted to evaluate whether Allium hookeri can control diabetic symptoms. Aqueous extract (AE1: 100 mg/kg BW, AE2: 200 mg/kg BW) and ethanol extract (EE1: 100 mg/kg BW, EE2: 200 mg/kg BW) of A. hookeri were orally administrated to diabetic mice (C57BL/J-db/db) for 8 weeks. The negative (NC) and the positive (PC) control groups were treated with 0.9% saline and metformin (150 mg/kg BW), respectively. Glucose and lipid profile (triglyceride, total cholesterol (TC), LDL-C, and HDL-C) as biochemical parameters, toxicological factors such as liver/kidney functional parameters (ALT, AST, BUN, and Cr), and NK cell activity in blood were measured. Oral glucose tolerance test (OGTT) and histopathological examination were also conducted. Compared with the NC group, AE and EE decreased blood glucose, HbA1c, area under the curve (AUC) during OGTT, and leptin levels while increasing adiponectin levels. Serum lipid profiles and toxicological factors levels were reduced by the A. hookeri extract. Interestingly, HDL-C, glomerular mesangial expansion score in the kidney, and NK cell activity were effectively controlled in EE groups. Based on the results, EE is considered to be more effective in reducing high blood glucose, lipid profile, and related factor levels than AE, and is comparable to metformin in some biomarkers. It can be presumed that EE can more effectively control the major anomalies in the diabetic model than AE, and it may be used to prevent diabetic symptoms without toxicity in the Type 2 diabetic model. MDPI 2022-04-17 /pmc/articles/PMC9024442/ /pubmed/35455483 http://dx.doi.org/10.3390/ph15040486 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Choi, Ji-Hye
Kim, Si-Hyun
Lee, Eun-Byeol
Kim, Ji-Su
Jung, Ji-Eeun
Jeong, Un-Yul
Kim, Ju-Hui
Jang, Hwan-Hee
Park, Shin-Young
Kim, Gi-Chang
Lim, Jung-Hyun
Lee, Sung-Hyen
Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice
title Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice
title_full Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice
title_fullStr Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice
title_full_unstemmed Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice
title_short Anti-Diabetic Effects of Allium hookeri Extracts Prepared by Different Methods in Type 2 C57BL/J-db/db Mice
title_sort anti-diabetic effects of allium hookeri extracts prepared by different methods in type 2 c57bl/j-db/db mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024442/
https://www.ncbi.nlm.nih.gov/pubmed/35455483
http://dx.doi.org/10.3390/ph15040486
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