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Metabolic Profiling for Evaluating the Dipeptidyl Peptidase-IV Inhibitory Potency of Diverse Green Tea Cultivars and Determining Bioactivity-Related Ingredients and Combinations. | LitMetric

AI Article Synopsis

  • - The study investigates the anti-hyperglycemic effects of various Japanese green tea cultivars, focusing on their ability to inhibit the DPP-IV enzyme, which is important for controlling blood sugar levels in diabetes.
  • - Different tea extracts showed varying rates of DPP-IV inhibition, and metabolic profiling revealed distinct compositional differences among the cultivars.
  • - New DPP-IV inhibitors like epigallocatechin-3--(3--methyl)gallate and others were identified, indicating that combining specific compounds can enhance tea extract bioactivity, demonstrating the effectiveness of metabolic profiling in assessing these properties.

Article Abstract

There are numerous cultivars of tea ( L.), but the differences in their anti-hyperglycemic-related effects are largely unknown. The inhibition of the dipeptidyl peptidase (DPP)-IV enzyme plays an essential role in controlling hyperglycemia in diabetes by blocking the degradation of incretin hormones, which is necessary for insulin secretion. In this study, we examined the DPP-IV inhibitory activity of leaf extracts from diverse Japanese green tea cultivars. The inhibitory rates differed among tea extracts. Metabolic profiling (MP), using liquid chromatography-mass spectrometry, of all cultivars revealed compositional differences among cultivars according to their DPP-IV inhibitory capacity. Epigallocatechin-3--(3--methyl)gallate, kaempferol-3--rutinoside, myricetin-3--glucoside/galactoside, and theogallin were newly identified as DPP-IV inhibitors. The bioactivity of a tea extract was potentiated by adding these ingredients in combination. Our results show that MP is a useful approach for evaluating the DPP-IV inhibitory potency of green tea and for determining bioactivity-related ingredients and combinations.

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Source
http://dx.doi.org/10.1021/acs.jafc.2c01693DOI Listing

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