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ABSTRACT: Background
Retinal inflammation is a devastating pathological process in ocular diseases. Functional impairment of retinal pigment epithelium (RPE) is associated with inflammatory retinal diseases. Enhancing the protective axis namely ACE2/Ang-(1-7)/Mas by activation of ACE2 presents anti-inflammatory properties. We investigated whether diminazene aceturate (DIZE), an angiotensin-converting enzyme 2 (ACE2) activator, prevented lipopolysaccharide (LPS)-induced inflammatory response by activating the protective axis and whether the effect was mediated by inhibiting the mitogen-activated protein kinase (MAPK) and the nuclear factor-κB (NF-κB) pathways.Methods
Cell counting kit-8 (CCK-8) assay and real-time PCR were used to determine the optimum concentration and incubation tim
SUBMITTER: Tao L
PROVIDER: S-EPMC4748536 | biostudies-literature | 2016 Feb
REPOSITORIES: biostudies-literature