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. 2021 Nov 25:12:100171.
doi: 10.1016/j.fochx.2021.100171. eCollection 2021 Dec 30.

Orange thyme: Phytochemical profiling, in vitro bioactivities of extracts and potential health benefits

Affiliations

Orange thyme: Phytochemical profiling, in vitro bioactivities of extracts and potential health benefits

Amélia M Silva et al. Food Chem X. .

Abstract

Orange thyme (Thymus fragrantissimus) is becoming widely used in food as a condiment and herbal tea, nevertheless its chemical composition and potential bioactivities are largely unknown. Thus the objective of this work is to obtain a detailed phytochemical profile of T. fragrantissimus by exhaustive ethanolic extraction and by aqueous decoction mimicking its consumption. Extracts showed high content in rosmarinic acid, luteolin-O-hexuronide and eriodictyol-O-hexuronide; these were the main phenolic compounds present in orange thyme accounting for 85% of the total phenolic compounds. Orange thyme extracts presented high scavenging activity against nitric oxide and superoxide radicals. Both extracts presented significant inhibitory effect of tyrosinase activity and moderate anti-acetylcholinesterase activity. Both extracts showed a good in vitro anti-inflammatory activity and a weak anti-proliferative/cytotoxic activity against Caco-2 and HepG2 cell lines supporting its safe use. Orange thyme is a very good source of bioactive compounds with potential use in different food and nutraceutical industries.

Keywords: Anti-inflammatory activity; Anti-proliferative; Antioxidant activity; Apigenin (PubChem CID: 5280443); Aqueous extract; Eriodictyol (Pubchem CID 440735); Hydroethanolic extract; Luteolin (PubChem CID: 5280445); Orange thyme; Phenolic composition; Radical scavenging activities; Rosmarinic acid (PubChem CID: 5281792); Salvianolic acid I (Pubchem CID 10459878); Salvianolic acid K (Pubchem CID 10482829).

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Conflict of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Fig. 1
Fig. 1
Chromatograms of (A) hydroethanolic (HE) and (B) aqueous decoction (AD) extracts obtained from orange thyme (T. fragrantissimus). For peak identification please refer to Table 2.
Fig. 2
Fig. 2
Effect of orange thyme (T. fragrantissimus) aqueous decoction (AD) and hydroethanolic (HE) extracts on Caco-2 (A and B), HepG2 (C and D) and Raw 264.7 (E and F) cells, after 24 h or 48 h exposure, as indicated. (G) Values of IC50 (half maximal inhibitory concentration) obtained for Caco-2, HepG2 and Raw 264.7 cells exposed orange thyme AD and HE extracts, as denoted. Results are expressed as mean ± SD (n = 4). Statistically significant differences (p < 0.05) between the control and sample concentrations at respective incubation time are denoted by an *, and those between exposure times, at the same concentration, are denoted by a #.
Fig. 3
Fig. 3
Anti-inflammatory activity of orange thyme (T. fragrantissimus) extracts. (A) Inhibition of nitric oxide (NO) release by LPS-stimulated RAW 264.7 cells when induced by AD (left bars, white) and by HE (right bars, blue) extracts, expressed as percentage of control (see methods for details). (B) RAW 264.7 cells viability upon exposure to AD (white bars) and HE (blue bars) extracts (see methods for details). Results are expressed as mean ± SD (n = 4 independent assays).

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