Effect of Cyclocarya Paliurus on Hypoglycemic Effect in Type 2 Diabetic Mice.


Journal

Medical science monitor : international medical journal of experimental and clinical research
ISSN: 1643-3750
Titre abrégé: Med Sci Monit
Pays: United States
ID NLM: 9609063

Informations de publication

Date de publication:
23 Apr 2019
Historique:
entrez: 24 4 2019
pubmed: 24 4 2019
medline: 12 9 2019
Statut: epublish

Résumé

BACKGROUND The aim of this study was to assess the hypoglycemic effect of Cyclocarya paliurus extract (CPE) on diabetes mellitus (DM) mice. MATERIAL AND METHODS A DM mouse model was established to test FBG, TC, and TG. The DM mice were divided into 3 groups: a DM group, a DM+CPE (0.5 g/Kg) group, and a DM+CPE (1.0 g/Kg) group. The FBG and body weight were measured. The glucose tolerance ability was determined by OGTT test. FINS was measured to calculate ISI and IRI. Serum MDA, SOD, and GSH-Px levels were detected. NIT-1 cells were cultured in vitro and divided into 4 groups: a control group, a STZ group, a STZ+CPE (80 μg/mL) group, and a STZ+CPE (160 μg/mL) group. Cell apoptosis and ROS content were assessed by flow cytometry. Cell proliferation was detected by EdU staining. RESULTS Compared with the control group, FBG, TC, and TG were significantly increased in the DM group. CPE gavage obviously reduced FBG level, increased body weight, enhanced glucose tolerance, elevated FINS level and ISI, and reduced IRI, all in a dose-dependent manner. CPE gavage reduced serum MDA content and increased SOD and GSH-Px enzyme activities in DM mice. STZ markedly enhanced ROS production, induced apoptosis, and inhibited proliferation in NIT-1 cells. CPE treatment clearly reduced ROS production and apoptosis, enhanced cell proliferation, and alleviated STZ damage to NIT-1 cells. CONCLUSIONS CPE has the effects of decreasing blood glucose and insulin resistance, and enhancing glucose tolerance in DM mice, which may be related to its effects of reducing oxidation and reduced apoptosis, and relieving STZ in pancreatic beta cell injury.

Identifiants

pubmed: 31011149
pii: 913368
doi: 10.12659/MSM.913368
pmc: PMC6492607
doi:

Substances chimiques

Antioxidants 0
Blood Glucose 0
Hypoglycemic Agents 0
Insulin 0
Plant Extracts 0
Triglycerides 0
Cholesterol 97C5T2UQ7J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2976-2983

Références

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Auteurs

Lichun Zhao (L)

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).

Xue Wang (X)

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).

Junxiu Li (J)

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).

Xiaoming Tan (X)

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).

Lanlan Fan (L)

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).

Zhenwei Zhang (Z)

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).

Jing Leng (J)

College of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).

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Classifications MeSH