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Modulatory Effect of an Urera Aurantiaca Extract on Immune and Tumoral Cells During Inflammation
Author(s) -
Marrassini Carla,
Anesini Claudia
Publication year - 2017
Publication title -
phytotherapy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 129
eISSN - 1099-1573
pISSN - 0951-418X
DOI - 10.1002/ptr.5743
Subject(s) - lipopolysaccharide , nitric oxide , cell growth , inflammation , prostaglandin e2 , pharmacology , mapk/erk pathway , immune system , chemistry , cancer research , biology , immunology , biochemistry , kinase , endocrinology
There is a well known link between inflammation and cancer during initiation, propagation and metastasis. Urera aurantiaca (UA) Wedd. (Urticaceae) is a medicinal plant used in traditional medicine to treat inflammatory processes with proven in vivo antiinflammatory and antinociceptive effects. The effects of a methanolic extract (UA) and a purified fraction (PF) on the proliferation of normal and tumoral lymphocytes under the effect of prostaglandin E 2 (PGE 2 ) and on nitric oxide production by lipopolysaccharide‐stimulated macrophages was evaluated. Both UA and PF stimulated normal lymphocytes but, in presence of PGE 2, a modulatory effect was observed. The normal lymphocyte proliferation induced by PGE 2 was driven by pathways involving both PKC and H 2 O 2 . In macrophages, UA and PF did not modify cell viability and abrogated the synthesis of nitric oxide induced by lipopolysaccharide. In tumoral lymphocytes, the UA exerted a biphasic effect: at low concentrations it increased cell proliferation, while at high concentrations, it displayed an antiproliferative effect. UA and PF were capable of reverting the proliferative action of PGE 2 . The tumoral cell proliferation induced by PGE 2 is related to PKC, ERK 1/2 and MAP Kinase P38 pathways. The observed effects could be attributed to polyphenols, flavonoids and tannins. This work demonstrates the modulatory effects of the UA on different cell types during inflammatory conditions, which reinforces its antiinflammatory action. Copyright © 2016 John Wiley & Sons, Ltd.