7,094 research outputs found

    Neuroprotective and anti-inflammatory effects of myricetin 3-glucoside in a rat model of cerebral ischemia

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    Purpose: To investigate the effect of myricetin 3-glucoside (M3GLS) on middle cerebral artery occlusion (MCAO)-induced cerebral ischemia in a rat model, and the mechanism of action involved.Methods: A cerebral ischemia rat model was established using MCAO under 10 % chloral hydrate anesthesia. Neurological severity score was determined by analyzing reflex, motor and sensory functions, as well as balancing potential. Infarction volume was determined using triphenyl tetrazolium chloride dye, while counting of Nissl bodies was done after toluidine blue staining. The protein expression levels of Bax and Bcl-2 were assayed using western blotting, while cytokine levels were determined by enzyme-linked immunosorbent assay (ELISA).Results: Treatment of cerebral ischemia rats with M3GLS effectively reduced infarct volume, when compared to vehicle-treated group (p < 0.05). Moreover, M3GLS treatment significantly increased the population of Nissl bodies and effectively improved neurologic scores (p < 0.05). In M3GLS-pretreated rats, cerebral ischemia-induced elevation of protein expressions of TNF-α, IL-6 and IL-1β were significantly suppressed. M3GL treatment significantly reversed cerebral ischemia-mediated downregulation of Bcl-2 protein level, but markedly reduced cerebral ischemia-induced upregulation of Bax protein level (p < 0.05).Conclusion: M3GLS exerts protective effect against cerebral ischemia-induced brain injury in rats via downregulation of inflammatory cytokines. It reduces infarction volume in the brain of cerebral ischemia rats, and regulates Bcl-2/Bax protein ratio. Thus, M3GLS has a potential for use in the clinical management of cerebral ischemia. Keywords: Myricetin, Neuroprotection, Anti-inflammation, Cerebral ischemia, Cytokines, Infarctio

    Distribution-Based Trajectory Clustering

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    Trajectory clustering enables the discovery of common patterns in trajectory data. Current methods of trajectory clustering rely on a distance measure between two points in order to measure the dissimilarity between two trajectories. The distance measures employed have two challenges: high computational cost and low fidelity. Independent of the distance measure employed, existing clustering algorithms have another challenge: either effectiveness issues or high time complexity. In this paper, we propose to use a recent Isolation Distributional Kernel (IDK) as the main tool to meet all three challenges. The new IDK-based clustering algorithm, called TIDKC, makes full use of the distributional kernel for trajectory similarity measuring and clustering. TIDKC identifies non-linearly separable clusters with irregular shapes and varied densities in linear time. It does not rely on random initialisation and is robust to outliers. An extensive evaluation on 7 large real-world trajectory datasets confirms that IDK is more effective in capturing complex structures in trajectories than traditional and deep learning-based distance measures. Furthermore, the proposed TIDKC has superior clustering performance and efficiency to existing trajectory clustering algorithms
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