Abstract

Type 2 diabetes mellitus is increasing worldwide, and the United Arab Emirates is presenting one of the world's highest prevalence rates. Dietary polyphenols exert an antidiabetic effect by modulating carbohydrates digestion and cellular glucose uptake. Due to their particularly high content in polyphenols, date seeds represent a potential antidiabetic agent. This study aims to determine if date seed polyphenols inhibit the activity of the enzymes (α-amylase and α-glucosidase), responsible for the digestion of carbohydrates and modulating the glucose uptake by human liver cells. In vitro activity of the intestinal α-glucosidase, pancreatic α-amylase, the glucose uptake by HepG2 cells, and the expression of GLUT4 and AMPK analyzed by western blotting (with and without date seeds extract). Our result showed that the maximum enzymes inhibition was obtained with 400 μg/mL and 900 μg/mL DSE for α-amylase and α-glucosidase, respectively. The HepG2 cell viability significantly decreased up to 80% at 4000 μg/mL DSE. The expression of GLUT4 was higher at 100 μg/mL DSE (with insulin and without insulin). However, the expressions of P-AMPK and AMPK were increased by DSE, mainly in a non-insulin-dependent manner. Therefore, DSE, by inhibiting carbohydrate digestion and stimulating glucose uptake by HepG2, can potentially demonstrate the therapeutic potential for diabetes management.

Highlights

  • Type 2 diabetes mellitus (T2DM) is a complex metabolic disorder characterized by hyperglycemia resulting from abnormal glucose metabolism

  • Our data showed that date seeds extract (DSE) inhibited α-amylase and α-glucosidase and increased the expression of GLUT4, AMPactivated protein kinase (AMPK), and P-AMPK. ese results support a potential role of DSE in the regulation of glucose homeostasis. ese beneficial effects of DSE may be related to its high polyphenolic contents, especially the abundance of phenolics and flavan-3-ols for which antidiabetic properties have already been reported [25]

  • Our data highlighted the inhibitory effect of DSE on the activity of α-amylase and α-glucosidase, both human digestive enzymes responsible for the breakdown of dietary carbohydrates

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Summary

Introduction

Type 2 diabetes mellitus (T2DM) is a complex metabolic disorder characterized by hyperglycemia resulting from abnormal glucose metabolism. It is associated with many complications, including hypertension, retinopathy, nephropathy, and neuropathy [1]. T2DM is among the top ten causes of death in the world [2]. It is continuously increasing despite significant therapeutic advancement. In the United Arab Emirates (UAE), the prevalence of T2DM is 18.7%, one of the greatest in the world and expected to reach 21.4% by 2030 [3]. It is urgent to identify new strategies to stop this progression

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