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Harnessing the bioactive potential of Limonium spathulatum (Desf.) Kuntze: insights into enzyme inhibition and phytochemical profile

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Abstract(s)

This study assessed the halophyte species <i>Limonium spathulatum</i> (Desf.) as a possible source of natural ingredients with the capacity to inhibit enzymes related to relevant human health disorders and food browning. Extracts using food-grade solvents such as water and ethanol were prepared by maceration from dried <i>L. spathulatum</i> leaves. They were evaluated for in vitro inhibition activity of enzymes such as acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), α-glucosidase, tyrosinase and lipase, related to Alzheimer’s disease, type-2-diabetes mellitus, skin hyperpigmentation, and obesity, respectively. These extracts were also appraised for in vitro acute toxicity on tumoral and non-tumoral cell lines and their chemical composition by high-performance liquid chromatography coupled with electrospray ionization mass spectrometry (HPLC-ESI-MS/MS). The extracts were more effective towards BChE than AChE. The best results were obtained with the hydroethanolic and water extracts, with IC<sub>50</sub> values of 0.03 mg/mL and 0.06 mg/mL, respectively. The hydroethanolic extract had the highest capacity to inhibit α-glucosidase (IC<sub>50</sub>: 0.04 mg/mL), higher than the positive control used (acarbose, IC<sub>50</sub> = 3.14 mg/mL). The ethanol extract displayed the best inhibitory activity against tyrosinase (IC<sub>50</sub> = 0.34 mg/mL). The tested samples did not inhibit lipase and exhibited low to moderate cytotoxic activity against the tested cell lines. The hydroethanolic extract had a higher diversity of compounds, followed by the ethanol and water samples. Similar molecules were identified in all the extracts and were mainly hydroxybenzoic acids, hydroxycinnamic acids, and flavonoids. Taken together, these results suggest that <i>L. spathulatum</i> should be further explored as a source of bioactive ingredients for the food, cosmetic, and pharmaceutical industries.

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Keywords

Sea lavender Enzyme inhibitors Phenolic compounds Cytotoxicity

Citation

Plants 12 (19): 3391 (2023)

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