The anti-diabetic effect of eight Lagerstroemia speciosa leaf extracts based on the contents of ellagitannins and ellagic acid derivatives.


Journal

Food & function
ISSN: 2042-650X
Titre abrégé: Food Funct
Pays: England
ID NLM: 101549033

Informations de publication

Date de publication:
26 Feb 2020
Historique:
pubmed: 1 2 2020
medline: 21 10 2020
entrez: 1 2 2020
Statut: ppublish

Résumé

Previously, we have reported the opposite effects of compounds isolated from Lagerstroemia speciosa leaves on a glucose transport (GLUT4) assay. Ellagitannins from L. speciosa activated GLUT4, while ellagic acid derivatives showed an inhibitory effect. As part of our continuing research on anti-diabetic nutritional supplements, we herein compared the anti-diabetic effects of several extracts (LE1-8) from leaves of L. speciosa using different manufacturing processes based on the contents of ellagitannins and ellagic acid derivatives. Their anti-diabetic effects were evaluated through glucose uptake and adipocyte differentiation in 3T3-L1 cells in vitro as well as alloxan induced diabetic mice in vivo. These extracts were given to mice by gavage at doses of 0.25, 1.0, and 4.0 g per kg body weight once a day for 21 consecutive days. Results showed that LE1 (1.0 g kg-1), LE3 (1.0 or 4.0 g kg-1), LE4 (1.0 or 4.0 g kg-1), LE5 (0.25 or 1.0 or 4.0 g kg-1) and LE7 (1.0 or 4.0 g kg-1) showed significant anti-diabetic effects in alloxan-induced diabetic mice as indicated by the decreased levels of fasting blood glucose, body weight, serum biomarkers, tissue weight and body fat, and increased final insulin levels. LE8 (1.0 g kg-1) showed a moderate anti-diabetic effect as illustrated by the reduced fasting blood glucose level while LE2 and LE6 showed slight effects in alloxan-induced diabetic mice. The potential correlation of the content of ellagitannins, ellagic acid derivatives, and corosolic acid with the anti-diabetic activity was discussed.

Identifiants

pubmed: 32003379
doi: 10.1039/c9fo03091c
doi:

Substances chimiques

Blood Glucose 0
Hydrolyzable Tannins 0
Hypoglycemic Agents 0
Plant Extracts 0
Ellagic Acid 19YRN3ZS9P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1560-1571

Auteurs

Sen Guo (S)

College of Food Science and Technology, Northwest University, 229 Taibai North Road, Xi'an, Shaanxi 710069, China. nsbai@nwu.edu.cn and College of Chemical Engineering, Department of Pharmaceutical Engineering, Northwest University, 229 Taibai North Road, Xi'an, Shaanxi 710069, China.

Xiameng Ren (X)

College of Food Science and Technology, Northwest University, 229 Taibai North Road, Xi'an, Shaanxi 710069, China. nsbai@nwu.edu.cn.

Kan He (K)

Herbalife International of America, 950 W. 190th Street, Torrance, CA 90502, USA.

Xiaozhuo Chen (X)

Department of Biomedical Sciences and Edison Biotechnology Institute, Ohio University, Athens, OH 45701, USA.

Shanshan Zhang (S)

College of Chemical Engineering, Department of Pharmaceutical Engineering, Northwest University, 229 Taibai North Road, Xi'an, Shaanxi 710069, China.

Marc Roller (M)

Naturex SA, Site d'Agroparc BP 1218, 84911 Avignon Cedex 9, France.

Bolin Zheng (B)

Naturex Inc., 375 Huyler Street, South Hackensack, NJ 07606, USA.

Qunyi Zheng (Q)

Herbalife International of America, 950 W. 190th Street, Torrance, CA 90502, USA.

Chi-Tang Ho (CT)

Department of Food Science, Rutgers University, 65 Dudley Road, New Brunswick, NJ 08901, USA.

Naisheng Bai (N)

College of Food Science and Technology, Northwest University, 229 Taibai North Road, Xi'an, Shaanxi 710069, China. nsbai@nwu.edu.cn.

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Classifications MeSH