Document details

Assessing the intestinal permeability and anti-inflammatory potential of sesquiterpene lactones from chicory

Author(s): Matos, Melanie S. ; Anastácio, José D. ; Allwood, J. William ; Carregosa, Diogo ; Marques, Daniela ; Sungurtas, Julie ; McDougall, Gordon J. ; Menezes, Regina ; Matias, Ana A. ; Stewart, Derek ; Dos Santos, Cláudia Nunes

Date: 2020

Persistent ID: http://hdl.handle.net/10362/109482

Origin: Repositório Institucional da UNL

Subject(s): 11β,13-dihydrolactucin; 11β,13-dihydrolactucopicrin; Calcineurin; Lactucin; Lactucopicrin; NFAT; Food Science; Nutrition and Dietetics; SDG 3 - Good Health and Well-being


Description

Funding: This research and the article processing cost were funded by EU Horizon 2020 research & innovation programme under grant agreement N. 760891 project CHIC. M.S.M. also acknowledges the financial support from Fundação para a Ciência e Tecnologia for her PhD scholarship (SFRD/BD/145551/2019).

Cichorium intybus L. has recently gained major attention due to large quantities of health-promoting compounds in its roots, such as inulin and sesquiterpene lactones (SLs). Chicory is the main dietary source of SLs, which have underexplored bioactive potential. In this study, we assessed the capacity of SLs to permeate the intestinal barrier to become physiologically available, using in silico predictions and in vitro studies with the well-established cell model of the human intestinal mucosa (differentiated Caco-2 cells). The potential of SLs to modulate inflammatory responses through modulation of the nuclear factor of activated T-cells (NFAT) pathway was also evaluated, using a yeast reporter system. Lactucopicrin was revealed as the most permeable chicory SL in the intestinal barrier model, but it had low anti-inflammatory potential. The SL with the highest anti-inflammatory potential was 11β,13-dihydrolactucin, which inhibited up to 54% of Calcineurin-responsive zinc finger (Crz1) activation, concomitantly with the impairment of the nuclear accumulation of Crz1, the yeast orthologue of human NFAT.

Document Type Journal article
Language English
Contributor(s) Centro de Estudos de Doenças Crónicas (CEDOC); NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM); RUN
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