orientin and Reperfusion-Injury

orientin has been researched along with Reperfusion-Injury* in 2 studies

Other Studies

2 other study(ies) available for orientin and Reperfusion-Injury

ArticleYear
Neuroprotective effects of orientin on oxygen-glucose deprivation/reperfusion-induced cell injury in primary culture of rat cortical neurons.
    Experimental biology and medicine (Maywood, N.J.), 2018, Volume: 243, Issue:1

    Topics: Animals; Antioxidants; Cell Survival; Cells, Cultured; Flavonoids; Glucose; Glucosides; Neurons; Neuroprotective Agents; Oxygen; Rats, Sprague-Dawley; Reactive Oxygen Species; Reperfusion Injury

2018
Orientin Attenuates Cerebral Ischemia/Reperfusion Injury in Rat Model through the AQP-4 and TLR4/NF-κB/TNF-α Signaling Pathway.
    Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2017, Volume: 26, Issue:10

    Orientin has been reported to have extensive pharmaceutical effects of antioxidant, anti-inflammatory, antithrombosis, antiapoptosis, and so on. In the present study, we tried to investigate the protective effects of orientin on cerebral ischemia-reperfusion (I/R) injury and explored the possible mechanisms.. Middle cerebral artery occlusion rat model was established and then treated with low, middle, and high concentrations of orientin, respectively, with edaravone as a positive control. The treatment effect of orientin was evaluated by measuring the neurological deficit score, cerebral infarction, brain edema, oxidative stress, excitatory amino acids release, the expression levels of aquaporin-4 (AQP-4), and related inflammatory molecules using different methods including immunohistochemistry, enzyme-linked immunosorbent assay, real-time PCR, and western blot. Moreover, morphological and structural changes were also observed by hematoxylin-eosin staining and transmission electron microscope.. Orientin provided a significant reduction on neurological deficits, cerebral infarction, cerebral edema, oxidative damage, and neurotoxicity of excitatory amino acids compared to model group (P < .05) in a dose-dependent manner. In addition, orientin substantially downregulated AQP-4 and inflammatory factors expression (P < .05) and improved cell morphology and structure in rats following I/R injury.. Orientin was able to mediate noticeable protection against cerebral I/R injury through the attenuation of oxidative stress and neurotoxicity of amino acids and inhibiting the upregulation of AQP-4 and inflammatory cytokines.

    Topics: Animals; Aquaporin 4; Brain; Brain Edema; Brain Ischemia; Disease Models, Animal; Dose-Response Relationship, Drug; Flavonoids; Glucosides; Male; Neuroprotective Agents; NF-kappa B; Oxidative Stress; Rats, Sprague-Dawley; Reperfusion Injury; RNA, Messenger; Signal Transduction; Toll-Like Receptor 4; Tumor Necrosis Factor-alpha

2017