Hypoglycaemic activity of Bauhinia holophylla through GSK3-β inhibition and glycogenesis activation.


Journal

Pharmaceutical biology
ISSN: 1744-5116
Titre abrégé: Pharm Biol
Pays: England
ID NLM: 9812552

Informations de publication

Date de publication:
Dec 2019
Historique:
entrez: 23 4 2019
pubmed: 23 4 2019
medline: 31 12 2019
Statut: ppublish

Résumé

Bauhinia L. species, including Bauhinia holophylla (Bong.) Steud. (Fabaceae), have traditionally been used to treat diabetes. Bauhinia is a complex botanical genus, and the indiscriminate use of the diverse Bauhinia species is reflected in the experimental divergence of their medicinal potential. The hypoglycaemic and hypolipidaemic effects, molecular mechanism of action and phytochemical properties of an authentic extract of B. holophylla leaves were evaluated. A phytochemical study of a 70% EtOH extract was performed using FIA-ESI-IT-MS/MS HPLC-PAD-ESI-IT-MS analysis identified flavonoid derivatives of quercetin, myricetin, luteolin and kaempferol. Treatment with 400 mg/kg of the extract reduced blood glucose (269.0 ± 32.4 mg/dL vs. 468.0 ± 32.2 mg/dL for diabetic animals), improved glucose tolerance, decreased cholesterol and triglyceride levels, and increased the mRNA expression of proteins involved in glucogenesis in the liver and muscle, such as PI3-K/Akt, GS, GSK3-β (ser-9), AMPK and Glut4. The activity of intestinal maltase was inhibited in vitro (IC Treatment with B. holophylla was associated with a marked hypoglycaemic effect through the stimulation of glycogenesis and inhibition of gluconeogenesis and intestinal glucose absorption, without increasing basal insulinaemia.

Identifiants

pubmed: 31007116
doi: 10.1080/13880209.2019.1599962
pmc: PMC6493280
doi:

Substances chimiques

Blood Glucose 0
Hypoglycemic Agents 0
Plant Extracts 0
Streptozocin 5W494URQ81
Glycogen Synthase Kinase 3 beta EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

269-279

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Auteurs

Nathalia Ap De Paula Camaforte (NAP)

a Institute of Biosciences, São Paulo State University , Botucatu , São Paulo, Brazil.

Luiz Leonardo Saldanha (LL)

a Institute of Biosciences, São Paulo State University , Botucatu , São Paulo, Brazil.

Priscilla Maria Ponce Vareda (PMP)

a Institute of Biosciences, São Paulo State University , Botucatu , São Paulo, Brazil.

João M Rezende-Neto (JM)

b Laboratory of Experimental and Computational Biochemistry of Drugs , Oswaldo Cruz Institute (FIOCRUZ) , Rio de Janeiro , Brazil.

Mario R Senger (MR)

b Laboratory of Experimental and Computational Biochemistry of Drugs , Oswaldo Cruz Institute (FIOCRUZ) , Rio de Janeiro , Brazil.

Aislan Q Delgado (AQ)

a Institute of Biosciences, São Paulo State University , Botucatu , São Paulo, Brazil.

Henrique J N Morgan (HJN)

c Department of Biological Sciences , São Paulo State University , Bauru , São Paulo, Brazil.

Natalia Moretti Violato (NM)

a Institute of Biosciences, São Paulo State University , Botucatu , São Paulo, Brazil.

Laís Goyos Pieroni (LG)

a Institute of Biosciences, São Paulo State University , Botucatu , São Paulo, Brazil.

Anne Lígia Dokkedal (AL)

c Department of Biological Sciences , São Paulo State University , Bauru , São Paulo, Brazil.

Floriano P Silva-Júnior (FP)

b Laboratory of Experimental and Computational Biochemistry of Drugs , Oswaldo Cruz Institute (FIOCRUZ) , Rio de Janeiro , Brazil.

José Roberto Bosqueiro (JR)

d Department of Physical Education , São Paulo State University , Bauru , São Paulo, Brazil.

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Classifications MeSH