| Literature DB >> 33477841 |
Györgyi Horváth1, Eszter Csikós1, Eichertné Violetta Andres1, Tímea Bencsik1, Anikó Takátsy2, Gergely Gulyás-Fekete2, Erika Turcsi2, József Deli1,2, Éva Szőke3, Ágnes Kemény3,4,5, Maja Payrits3,5, Lajos Szente6, Marianna Kocsis7, Péter Molnár1, Zsuzsanna Helyes3,5.
Abstract
Melilotus officinalis is known to contain several types of secondary metabolites. In contrast, the carotenoid composition of this medicinal plant has not been investigated, although it may also contribute to the biological activities of the drug, such as anti-inflammatory effects. Therefore, this study focuses on the isolation and identification of carotenoids from Meliloti herba and on the effect of isolated (all-E)-lutein 5,6-epoxide on primary sensory neurons and macrophages involved in nociception, as well as neurogenic and non-neurogenic inflammatory processes. The composition of the plant extracts was analyzed by high performance liquid chromatography (HPLC). The main carotenoid was isolated by column liquid chromatography (CLC) and identified by MS and NMR. The effect of water-soluble lutein 5,6-epoxide-RAMEB (randomly methylated-β-cyclodextrin) was investigated on Ca2+-influx in rat primary sensory neurons induced by the activation of the transient receptor potential ankyrin 1 receptor agonist to mustard-oil and on endotoxin-induced IL-1β release from isolated mouse peritoneal macrophages. (all-E)-Lutein 5,6-epoxide significantly decreased the percent of responsive primary sensory neurons compared to the vehicle-treated stimulated control. Furthermore, endotoxin-evoked IL-1β release from macrophages was significantly decreased by 100 µM lutein 5,6-epoxide compared to the vehicle-treated control. The water-soluble form of lutein 5,6-epoxide-RAMEB decreases the activation of primary sensory neurons and macrophages, which opens perspectives for its analgesic and anti-inflammatory applications.Entities:
Keywords: (all-E)-lutein-5,6-epoxide-RAMEB complex; Fabaceae; Melilotus officinalis (L.) Pall.; anti-inflammatory; carotenoid
Year: 2021 PMID: 33477841 PMCID: PMC7832904 DOI: 10.3390/molecules26020503
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411