Abstract

Background: Terpenoid compounds, despite their established antioxidant ability, are neglected as potential glycation regulators. Methods: In-vitro model systems of lysine (0.1 M) with glucose (0.1 M and 1 M) were incubated at 80 °C and 100 °C for 3 h in the presence of aniseed oil, thymol and linalool (2–8 μΜ). Color development, absorbance at UV-Vis (280 nm, 360 nm, 420 nm), fluorescence intensity (λexc = 370 nm, λemm = 440 nm) and lysine depletion (HPLC-FL) were measured to monitor the progress of the Maillard reaction. Response Surface Methodology was used to analyze the impact of the five experimental conditions on the glycation indices. Results: All terpenoid compounds promoted color development and did not affect lysine depletion. The choice of terpenoid compound impacted glycation at 280 nm, 360 nm and 420 nm (p < 0.02). The effect was stronger at lower temperatures (p < 0.002) and 0.1 M glucose concentrations (p < 0.001). Terpenoid concentration was important only at 360 nm and 420 nm (p < 0.01). No impact was seen for fluorescence intensity from the choice of terpenoid compounds and their dose (p = 0.08 and p = 0.44 respectively). Conclusion: Terpenoid compounds show both anti- and proglycative activity based on the incubation conditions. Thymol showed the largest antiglycative capacity, followed by aniseed oil and linalool. Maximal antiglycative capacity was seen at 0.1 M glucose, 2 μΜ terpenoid concentration, 80 °C and 1 h incubation.

Highlights

  • Essential oils (EOs) constitute a large class of secondary plant metabolites with important defensive and attractive role between plants and their environment [1]

  • The addition oftoterpenoid during the treatment of the glucose/lysine associated with greater color development at all time‐points

  • The study highlighted a general promotion of glycation by terpenoid compounds as measured by color development and lysine depletion

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Summary

Introduction

Essential oils (EOs) constitute a large class of secondary plant metabolites with important defensive and attractive role between plants and their environment [1]. Their volatile fraction is composed principally by mono-, sesqui- and di-terpenes alongside some volatile phenolic substances like phenylpropanoids [2] Their ability to act as hydrogen donators or radical scavengers has been linked with inhibition of lipid peroxidation [3]. This ability to terminate the lipid peroxidation chain reaction is the main application of EOs as natural food antioxidants and it is linked to their terpenoid content [4] Among terpenoids, those with phenolic ring like thymol and carvacrol possess the highest antioxidant activity followed by the monoterpene hydrocarbons with strongly activated methylene group like terpinolene, α-terpinene and γ-terpinene. A tertiary allylic alcohol, shows a pro-oxidant effect while benzene derivatives (other than thymol and carvacrol) like estragol, a phenylopropanoid, are more efficient in preventing the formation of primary lipid oxidation products [5]

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