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Comparative effects of parenteral antimalarials in Swiss albino mice after chronic exposure to Plasmodium berghei

机译:慢性暴露于伯氏疟原虫后瑞士白化病小鼠肠胃外抗疟药的比较作用

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摘要

Mice are considered to be a similar model to humans in the pathogenesis of malaria. This study evaluates the effect of parenteral antimalarials on the spleen and liver of Swiss albino mice after chronic exposure to Plasmodium berghei. After chronic exposure to P.  berghei NK65 strain, the level of parasitemia was assessed. The mice were treated for 3 days using chloroquine (5 mg/kg), quinine (10 mg/kg), and artemether (2 mg/kg). The effect of chronic exposure and the pattern of recovery were evaluated. There was significant decrease in total body weight after chronic exposure to P. berghei (P < 0.05). An increase in total weight recovery was seen after day 15 of treatment with the antimalarials; this was more pronounced with artemether. A significant increase in liver and spleen weights due to P. berghei infection was seen. There was a recovery pattern due to decrease in liver and spleen weights following antimalarial administration, which was greatest with artemether (P < 0.05). Significant changes were more in parasitized, quinine and artemether groups (P < 0.05). There was a significant decrease in total spleen protein due to chloroquine but a decrease due to quinine and artemether (P < 0.05). No significant changes in liver and spleen albumin were observed after treatment. The highest parasite clearance was observed with artemether, followed by quinine. Five mice died after chronic exposure in all the groups prior to treatment. There was significant enlargement and discoloration of spleen and liver after chronic exposure. This study showed that artemether aided recovery of the liver and spleen better than quinine and chloroquine in albino mice after chronic exposure to P. berghei. This suggests there is potential for improvement in antimalarial therapy.
机译:在疟疾的发病机理中,小鼠被认为是与人类相似的模型。这项研究评估了慢性暴露于伯氏疟原虫后,胃肠外抗疟药对瑞士白化病小鼠的脾脏和肝脏的影响。长期暴露于伯氏疟原虫NK65菌株后,评估了寄生虫血症的水平。用氯喹(5 mg / kg),奎宁(10 mg / kg)和蒿甲醚(2 mg / kg)治疗小鼠3天。评估了慢性暴露的影响和恢复方式。长期暴露于伯氏疟原虫后,总体重显着下降(P <0.05)。用抗疟药治疗第15天后,总体重的恢复增加。 Artemether更明显。观察到由于伯氏疟原虫感染导致肝脏和脾脏重量显着增加。抗疟疾治疗后由于肝脏和脾脏重量的减少而出现了恢复模式,其中蒿甲醚的恢复模式最大(P <0.05)。寄生虫,奎宁和蒿甲醚组的显着变化更大(P <0.05)。氯喹使脾脏总蛋白显着下降,但奎宁和蒿甲醚使脾脏总蛋白下降(P <0.05)。治疗后未观察到肝和脾白蛋白的显着变化。用蒿甲醚观察到最高的寄生虫清除率,其次是奎宁。在治疗前所有组中的慢性暴露后有五只小鼠死亡。慢性暴露后,脾脏和肝脏明显肿大和变色。这项研究表明,长期暴露于伯氏疟原虫后,蒿甲醚对白化病小鼠肝脏和脾脏的恢复优于奎宁和氯喹。这表明抗疟疾治疗有改善的潜力。

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