Assessing the In Vitro Inhibitory Effects on Key Enzymes Linked to Type-2 Diabetes and Obesity and Protein Glycation by Phenolic Compounds of Lauraceae Plant Species Endemic to the Laurisilva Forest

Molecules. 2021 Apr 1;26(7):2023. doi: 10.3390/molecules26072023.

Abstract

Methanolic leaf extracts of four Lauraceae species endemic to Laurisilva forest (Apollonias barbujana, Laurus novocanariensis, Ocotea foetens and Persea indica) were investigated for the first time for their potential to inhibit key enzymes linked to type-2 diabetes (α-amylase, α-glucosidase, aldose reductase) and obesity (pancreatic lipase), and protein glycation. Lauraceae extracts revealed significant inhibitory activities in all assays, altough with different ability between species. In general, P. indica showed the most promissing results. In the protein glycation assay, all analysed extracts displayed a stronger effect than a reference compound: aminoguanidine (AMG). The in vitro anti-diabetic, anti-obesity and anti-glycation activities of analysed extracts showed correlation with their flavonols and flavan-3-ols (in particular, proanthocyanins) contents. These Lauraceae species have the capacity to assist in adjuvant therapy of type-2 diabetes and associated complications, through modulation of the activity of key metabolic enzymes and prevention of advanced glycation end-products (AGEs) formation.

Keywords: Lauraceae; aldose reductase inhibition; digestive enzymes inhibition; polyphenols; protein glycation inhibition; type-2 diabetes.

MeSH terms

  • Aldehyde Reductase / antagonists & inhibitors
  • Aldehyde Reductase / chemistry
  • Animals
  • Biomarkers*
  • Diabetes Mellitus, Type 2 / enzymology
  • Diabetes Mellitus, Type 2 / etiology
  • Diabetes Mellitus, Type 2 / metabolism*
  • Forests
  • Glycoproteins / metabolism*
  • Glycosylation
  • Hypoglycemic Agents / chemistry
  • Hypoglycemic Agents / pharmacology*
  • Lauraceae / chemistry*
  • Metabolic Networks and Pathways
  • Molecular Structure
  • Obesity / enzymology
  • Obesity / etiology
  • Obesity / metabolism*
  • Phenols / chemistry
  • Phenols / pharmacology*
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Rats

Substances

  • Biomarkers
  • Glycoproteins
  • Hypoglycemic Agents
  • Phenols
  • Plant Extracts
  • Aldehyde Reductase