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Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus

The purpose of this study was to investigate the effects of lotus leaf on hyperglycemia and dyslipidemia in animal model of diabetes. Inhibitory activity of ethanol extract of lotus leaf against yeast α-glucosidase was measured in vitro. The effect of lotus leaf on the postprandial increase in blood...

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Autores principales: Kim, Ah-Rong, Jeong, Soo-Mi, Kang, Min-Jung, Jang, Yang-Hee, Choi, Ha-Neul, Kim, Jung-In
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679324/
https://www.ncbi.nlm.nih.gov/pubmed/23766876
http://dx.doi.org/10.4162/nrp.2013.7.3.166
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author Kim, Ah-Rong
Jeong, Soo-Mi
Kang, Min-Jung
Jang, Yang-Hee
Choi, Ha-Neul
Kim, Jung-In
author_facet Kim, Ah-Rong
Jeong, Soo-Mi
Kang, Min-Jung
Jang, Yang-Hee
Choi, Ha-Neul
Kim, Jung-In
author_sort Kim, Ah-Rong
collection PubMed
description The purpose of this study was to investigate the effects of lotus leaf on hyperglycemia and dyslipidemia in animal model of diabetes. Inhibitory activity of ethanol extract of lotus leaf against yeast α-glucosidase was measured in vitro. The effect of lotus leaf on the postprandial increase in blood glucose levels was assessed in streptozotocin-induced diabetic rats. A starch solution (1 g/kg) with and without lotus leaf extract (500 mg/kg) was administered to the rats after an overnight fast, and postprandial plasma glucose levels were monitored. Four-week-old db/db mice were fed a basal diet or a diet containing 1% lotus leaf extract for 7 weeks after 1 week of acclimation to study the chronic effect of lotus leaf. After sacrifice, plasma glucose, insulin, triglycerides (TG), total cholesterol (CHOL), high-density lipoprotein (HDL)-CHOL, and blood glycated hemoglobin levels were measured. Lotus leaf extract inhibited α-glucosidase activity by 37.9%, which was 1.3 times stronger than inhibition by acarbose at a concentration of 0.5 mg/mL in vitro. Oral administration of lotus leaf extract significantly decreased the area under the glucose response curve by 35.1% compared with that in the control group (P < 0.01). Chronic feeding of lotus leaf extract significantly lowered plasma glucose and blood glycated hemoglobin compared with those in the control group. Lotus leaf extract significantly reduced plasma TG and total CHOL and elevated HDL-CHOL levels compared with those in the control group. Therefore, we conclude that lotus leaf is effective for controlling hyperglycemia and dyslipidemia in an animal model of diabetes mellitus.
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spelling pubmed-36793242013-06-13 Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus Kim, Ah-Rong Jeong, Soo-Mi Kang, Min-Jung Jang, Yang-Hee Choi, Ha-Neul Kim, Jung-In Nutr Res Pract Original Research The purpose of this study was to investigate the effects of lotus leaf on hyperglycemia and dyslipidemia in animal model of diabetes. Inhibitory activity of ethanol extract of lotus leaf against yeast α-glucosidase was measured in vitro. The effect of lotus leaf on the postprandial increase in blood glucose levels was assessed in streptozotocin-induced diabetic rats. A starch solution (1 g/kg) with and without lotus leaf extract (500 mg/kg) was administered to the rats after an overnight fast, and postprandial plasma glucose levels were monitored. Four-week-old db/db mice were fed a basal diet or a diet containing 1% lotus leaf extract for 7 weeks after 1 week of acclimation to study the chronic effect of lotus leaf. After sacrifice, plasma glucose, insulin, triglycerides (TG), total cholesterol (CHOL), high-density lipoprotein (HDL)-CHOL, and blood glycated hemoglobin levels were measured. Lotus leaf extract inhibited α-glucosidase activity by 37.9%, which was 1.3 times stronger than inhibition by acarbose at a concentration of 0.5 mg/mL in vitro. Oral administration of lotus leaf extract significantly decreased the area under the glucose response curve by 35.1% compared with that in the control group (P < 0.01). Chronic feeding of lotus leaf extract significantly lowered plasma glucose and blood glycated hemoglobin compared with those in the control group. Lotus leaf extract significantly reduced plasma TG and total CHOL and elevated HDL-CHOL levels compared with those in the control group. Therefore, we conclude that lotus leaf is effective for controlling hyperglycemia and dyslipidemia in an animal model of diabetes mellitus. The Korean Nutrition Society and the Korean Society of Community Nutrition 2013-06 2013-06-03 /pmc/articles/PMC3679324/ /pubmed/23766876 http://dx.doi.org/10.4162/nrp.2013.7.3.166 Text en ©2013 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Kim, Ah-Rong
Jeong, Soo-Mi
Kang, Min-Jung
Jang, Yang-Hee
Choi, Ha-Neul
Kim, Jung-In
Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus
title Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus
title_full Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus
title_fullStr Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus
title_full_unstemmed Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus
title_short Lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus
title_sort lotus leaf alleviates hyperglycemia and dyslipidemia in animal model of diabetes mellitus
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679324/
https://www.ncbi.nlm.nih.gov/pubmed/23766876
http://dx.doi.org/10.4162/nrp.2013.7.3.166
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