Haemanthus coccineus extract and its main bioactive component narciclasine display profound anti-inflammatory activities in vitro and in vivo

التفاصيل البيبلوغرافية
العنوان: Haemanthus coccineus extract and its main bioactive component narciclasine display profound anti-inflammatory activities in vitro and in vivo
المؤلفون: Clemens A. J. Erdelmeier, Egon Koch, Robert Fürst, Liliana Schaefer, S Fuchs, Louise T. Hsieh, Thomas A. Wichelhaus, Werner Saarberg
المصدر: Journal of Cellular and Molecular Medicine
بيانات النشر: BlackWell Publishing Ltd, 2015.
سنة النشر: 2015
مصطلحات موضوعية: Male, Croton Oil, Anti-Inflammatory Agents, Pharmacology, chemistry.chemical_compound, isocarbostyril alkaloid, Leukocytes, Edema, Croton oil, adhesion molecules, Haemanthus coccineus extract, Cells, Cultured, Chemokine CCL2, Arachidonic Acid, Cell adhesion molecule, NF-kappa B, Bioactive compound, Phenanthridines, Biochemistry, Neutrophil Infiltration, Molecular Medicine, medicine.symptom, Signal Transduction, leucocyte-endothelial cell interactions, endothelium, medicine.drug_class, Narciclasine, Blotting, Western, Inflammation, Mice, Inbred Strains, Biology, Anti-inflammatory, In vivo, Cell Line, Tumor, medicine, Cell Adhesion, Liliaceae, Animals, Humans, Plant Extracts, Macrophages, Endothelial Cells, Cell Biology, Original Articles, In vitro, Mice, Inbred C57BL, chemistry, Microscopy, Fluorescence, inflammation, Amaryllidaceae Alkaloids, sense organs, Cell Adhesion Molecules, narciclasine, NFκB
الوصف: Haemanthus coccineus extracts (HCE) have traditionally been used to treat a variety of diseases, like febrile colds or asthma. Since new therapeutic options against inflammatory processes are still urgently needed, we aimed to pharmacologically characterise the anti-inflammatory potential of HCEin vitro and in vivo and to identify the underlying bioactive component(s). The action of HCE on oedema formation and leucocyte infiltration were analysed in two murine models of inflammation (dermal oedema induced by arachidonic acid and croton oil; kidney injury caused by unilateral ureteral obstruction). The interaction of leucocytes with endothelial cells (ECs) as well as the activation parameters of these two cell types were analysed. Moreover, the nuclear factor κB (NFκB) pathway was investigated in detail in ECs. Using different fractions of HCE, the bioactive principle was identified. In vivo, HCE (450 mg/kg orally or 2 mg/kg intraperitoneally) inhibited oedema formation, leucocyte infiltration and cytokine synthesis. In vitro, HCE (100–300 ng/ml) blocked leucocyte-EC interaction as well as the activation of isolated leucocytes (cytokine synthesis and proliferation) and of primary ECs (adhesion molecule expression). HCE suppressed NFκB-dependent gene transcription in the endothelium, but did not interfere with the NFκB activation cascade (IκB degradation, p65 nuclear translocation and NFκB DNA-binding activity). The alkaloid narciclasine was elucidated as the bioactive compound responsible for the anti-inflammatory action of HCE. Our study highlights HCE and its main alkaloid narciclasine as novel interesting approach for the treatment of inflammation-related disorders.
اللغة: English
تدمد: 1582-4934
1582-1838
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4fa5738bca71a622e493cb32150c51
http://europepmc.org/articles/PMC4420604
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....3c4fa5738bca71a622e493cb32150c51
قاعدة البيانات: OpenAIRE