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Accumulation of phenolic compounds in in vitro cultures and wild plants of Lavandula viridis L’Hér and their antioxidant and anti-cholinesterase potential
Institution:1. Dipartimento di Fisica, Università degli Studi di Trento, Via Sommarive 14 Povo, Trento, 38123 Italy;2. Trento Institute for Fundamental Physics and Applications (INFN-TIFPA), Via Sommarive 14 Povo, Trento, 38123 Italy;3. European Centre for Theoretical Studies in Nuclear Physics and Related Areas (ECT*-FBK), via Sommarive 18, I-38123 Trento, Italy
Abstract:In this study, we evaluated the phenolic profile, antioxidant and anti-cholinesterase potential of different extracts from wild plants and in vitro cultures of Lavandula viridis L’Hér. The HPLC–DAD analysis allowed the identification and quantification of 3-O-caffeoylquinic, 4-O-caffeoylquinic, 5-O-caffeoylquinic and rosmarinic acids, and luteolin and pinocembrin. Water/ethanol extract from in vitro cultures contained the highest amount of the identified phenolic compounds (51652.92 mg/kg). To investigate the antioxidant activity we used Trolox equivalent antioxidant capacity, oxygen radical absorbance capacity, Fe2+ chelation activity and the inhibition of Fe2+-induced lipid peroxidation in mouse brain homogenates (in vitro). Overall, all the extracts from both wild plants and in vitro cultures exhibited ability to scavenge free radicals, to chelate Fe2+ and to protect against lipid peroxidation. In addition, the extracts from L. viridis were active in inhibiting both acetylcholinesterase and butyrylcholinesterase (Ellman’s method). Our findings suggest that L. viridis in vitro cultures represent a promising alternative for the production of active metabolites with antioxidant and anti-cholinesterase activity.
Keywords:Wild plants  Phenolic compounds  Rosmarinic acid  Free radical scavenging  Anti-cholinesterase activity
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