Hydromethanolic Extracts from Adansonia digitata L. Edible Parts Positively Modulate Pathophysiological Mechanisms Related to the Metabolic Syndrome

Molecules. 2020 Jun 21;25(12):2858. doi: 10.3390/molecules25122858.

Abstract

Metabolic syndrome includes a cluster of risk factors for many pathological conditions, including hyperglycemia, abdominal obesity, hyperlipidemia, and hypertension. Adansonia digitata L. (also known as baobab) is used in traditional African Medicine and recent studies showed that it improves the metabolism of carbohydrates and lipids. The aim of this study is to investigate the mechanisms of action associated with the beneficial effects of extracts from the edible parts of baobab (fruit pulp, leaves, raw and toasted seeds), evaluating their inhibitory activity against: alpha-amylase, alpha-glucosidase, angiotensin-converting enzyme, 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase, and pancreatic lipase. Baobab fruit pulp and leaf extracts resulted to be the most active ones and were then tested on the differentiation process of SW-872 human liposarcoma cells to mature adipocytes. The addition of these latter extracts did not affect triglyceride accumulation, indicating a neutral impact on this parameter. The findings here reported help to explain the growing amount of evidence on the biological properties of baobab and provide suggestions about their use in food and nutraceutical fields.

Keywords: ACE inhibition; Adansonia digitata L.; HMG-CoA reductase inhibition; SW-872 preadipocytes; baobab edible parts; digestive enzyme inhibition.

MeSH terms

  • Adansonia / chemistry*
  • Adipocytes / drug effects
  • Angiotensin-Converting Enzyme Inhibitors / pharmacology
  • Cell Differentiation / drug effects*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Fruit / chemistry
  • Glycoside Hydrolase Inhibitors / pharmacology
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Kaempferols / chemistry
  • Kaempferols / pharmacology
  • Lipase / antagonists & inhibitors
  • Metabolic Syndrome / drug therapy*
  • Metabolic Syndrome / enzymology
  • Molecular Docking Simulation
  • Plant Extracts / chemistry*
  • Plant Extracts / pharmacology*
  • Plant Leaves / chemistry
  • Quercetin / analogs & derivatives
  • Quercetin / chemistry
  • Quercetin / pharmacology
  • Rutin / chemistry
  • Rutin / pharmacology
  • Seeds / chemistry
  • alpha-Amylases / antagonists & inhibitors

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Glycoside Hydrolase Inhibitors
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Kaempferols
  • Plant Extracts
  • quercitrin
  • Rutin
  • kaempferol
  • Quercetin
  • Lipase
  • PNLIP protein, human
  • alpha-Amylases