Exploring bioactivity potential of polyphenolic water-soluble lignin derivative.
5): lignin
Dendritic cells [maturation]
IC50
Polyphenols
Tritium labeling
Journal
Environmental research
ISSN: 1096-0953
Titre abrégé: Environ Res
Pays: Netherlands
ID NLM: 0147621
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
15
05
2020
revised:
06
08
2020
accepted:
07
08
2020
pubmed:
15
9
2020
medline:
12
1
2021
entrez:
14
9
2020
Statut:
ppublish
Résumé
Many natural substances exhibit anti-inflammatory activity and considerable potential in prophylaxis and treatment of allergies. Knowing exact molecular targets, which is required for developing these as medicinal products, is often challenging for multicomponent compositions. In the present study we examined novel polyphenolic substance, a water-soluble fraction of wood lignin (laboratory code BP-Cx-1). In our previous study, a number of polyphenolic components of BP-Cx-1 (flavonoids, sapogenins, phenanthrenes etc.) were identified as the major carriers of biological activity of BP-Cx drug family, and several molecular targets involved in cancer and/or inflammation signaling pathways were proposed based on the results of the in vitro and in silico screening studies. In the present study, half maximal inhibitory concentration (IC50) of BP-Cx-1 was established with a radioligand method and a range of IC50 values between 22.8 and 40.3 μg/ml were obtained for adenosine receptors A1, A2A and prostaglandin receptors EP2, IP (PGI2). IC50 for serotonin 5-HT1 and for glucocorticoid GR receptors were 3.0 μg/ml and 12.6 μg/ml, respectively, both being within the range of BP-Cx-1 concentrations achievable in in vivo models. Further, distribution of [
Identifiants
pubmed: 32926891
pii: S0013-9351(20)30946-4
doi: 10.1016/j.envres.2020.110049
pii:
doi:
Substances chimiques
Cytokines
0
Water
059QF0KO0R
Lignin
9005-53-2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
110049Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.