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Virus-inhibiting activity of dihydroquercetin, a flavonoid from Larix sibirica, against coxsackievirus B4 in a model of viral pancreatitis

机译:西伯利亚落叶松中的类黄酮二氢槲皮素在病毒性胰腺炎模型中对柯萨奇B4病毒的抑制活性

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Members of the family Picornaviridae, in particular, enteroviruses, represent a serious threat to human health. They are responsible for numerous pathologies ranging from mild disease to fatal outcome. Due to the limited number of safe and effective antivirals against enteroviruses, there is a need for search and development of novel drugs with various mechanisms of activity against enteroviruses-induced pathologies. We studied the effect of dihydroquercetin (DHQ), a flavonoid from larch wood, on the course of pancreatitis of white mice caused by coxsackievirus B4 (CVB4). DHQ was applied intraperitoneally at doses of 75 or 150 mg/kg/day once a day for 5 days postinfection (p.i.) starting on day 1 p.i., and its effect was compared to that of the reference compound ribavirin. The application of DHQ resulted in a dose-dependent decrease in the virus titer in pancreatic tissue, reaching, at the highest dose, 2.4 logs on day 5 p.i. Also, the application of DHQ led to restoration of antioxidant activity of pancreatic tissue that was impaired in the course of pancreatitis. Morphologically, pancreatic tissue of DHQ-treated animals demonstrated less infiltration with inflammatory cells and no signs of tissue destruction compared to placebo-treated mice. Both ribavirin- and DHQ-treated animals developed fewer foci of pancreatic inflammation per mouse, and these foci contained fewer infiltrating cells than those in placebo-treated mice. The effect of DHQ was comparable to or exceeded that of ribavirin. Taken together, our results suggest high antiviral activity of DHQ and its promising potential in complex treatment of viral pancreatitis.
机译:Picornaviridae家族的成员,特别是肠病毒,对人类健康构成了严重威胁。他们负责从轻度疾病到致命结果的多种病理。由于针对肠病毒的安全有效抗病毒剂的数量有限,因此需要寻找和开发具有针对肠病毒引起的病理的各种活性机制的新药。我们研究了落叶松木材中的类黄酮二氢槲皮素(DHQ)对由柯萨奇病毒B4(CVB4)引起的白色小鼠胰腺炎过程的影响。从感染后第1天(p.i.)开始,每天一次以75或150 mg / kg /天的剂量腹膜内施用DHQ,持续5天,并将其作用与参考化合物利巴韦林进行比较。 DHQ的使用导致胰腺组织中病毒滴度的剂量依赖性降低,最高剂量在p.i第5天达到2.4 log。而且,DHQ的应用导致胰腺组织抗氧化活性的恢复,这在胰腺炎的过程中受损。在形态上,与安慰剂治疗的小鼠相比,DHQ治疗的动物的胰腺组织表现出更少的炎性细胞浸润,并且没有组织破坏的迹象。利巴韦林和DHQ处理的动物每只小鼠的胰腺炎症灶都更少,并且与安慰剂治疗的小鼠相比,这些灶包含的浸润细胞更少。 DHQ的作用与利巴韦林相当或超过。两者合计,我们的结果表明DHQ的高抗病毒活性及其在病毒性胰腺炎的综合治疗中的潜在潜力。

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