Portulaca oleracea L. extract reduces hyperglycemia via PI3k/Akt and AMPK pathways in the skeletal muscles of C57BL/Ksj-db/db mice.


Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
05 Oct 2020
Historique:
received: 19 09 2019
revised: 08 05 2020
accepted: 09 05 2020
pubmed: 18 5 2020
medline: 26 2 2021
entrez: 17 5 2020
Statut: ppublish

Résumé

Portulaca oleracea L. is a succulent annual herb, which has various pharmacological effects including antidiabetic property. However, in vivo the reducing effect of P. oleracea on hyperglycemia and its mechanism of action have not been clarified in a mouse model of type 2 diabetes. The effects of Portulaca oleracea L. extract (POE) on hyperglycemia were investigated in an animal model of type 2 diabetes. C57BL/Ksj-db/db mice were randomly divided into three groups: db/db-control group was fed a standard semi-synthetic diet (AIN-93 G), db/db-RG group was fed AIN-93 G supplemented with rosiglitazone (RG) (0.005%, w/w), and db/db-POE group was fed AIN-93 G supplemented with POE (0.4%, w/w) for 6 weeks. Diabetes-related physical and biochemical indicators and the phosphorylation of components of PI3k/Akt and AMPK pathways were measured. The blood glucose and the glycosylated hemoglobin levels (HbA1c) in db/db-POE group were significantly lower than those in db/db-control group. In db/db-POE group, The homeostatic index of insulin resistance (HOMA-IR) decreased significantly, whereas the quantitative insulin sensitivity check index (QUICKI) was higher than those in db/db-control group. POE significantly elicited the phosphorylation of IRS-1 These results indicate that POE reduces hyperglycemia by improving insulin resistance through the PI3k/Akt and AMPK pathways in the skeletal muscle of C57BL/Ksj-db/db mice.

Identifiants

pubmed: 32416244
pii: S0378-8741(19)33722-5
doi: 10.1016/j.jep.2020.112973
pii:
doi:

Substances chimiques

Biomarkers 0
Blood Glucose 0
Glucose Transporter Type 4 0
Glycated Hemoglobin A 0
HbA(1c) protein, mouse 0
Hypoglycemic Agents 0
Plant Extracts 0
Slc2a4 protein, mouse 0
Phosphatidylinositol 3-Kinase EC 2.7.1.137
Proto-Oncogene Proteins c-akt EC 2.7.11.1
AMP-Activated Protein Kinases EC 2.7.11.31

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

112973

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Ji Hyun Lee (JH)

Department of Food Science and Nutrition, Pusan National University, Busan, 46241, South Korea. Electronic address: ljlj9595@naver.com.

Jae Eun Park (JE)

Department of Food Science and Nutrition, Pusan National University, Busan, 46241, South Korea. Electronic address: jaeeun5609@naver.com.

Ji Sook Han (JS)

Department of Food Science and Nutrition, Pusan National University, Busan, 46241, South Korea. Electronic address: hanjs@pusan.ac.kr.

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Classifications MeSH