维生素A和青蒿琥酯对疟疾感染的白化小鼠的影响

Onyemeh L. O., Freitas A. A., Olaide Z., Okoye A. C., Faloye D. A., Muoneke J. N.
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引用次数: 0

摘要

疟疾是一种潜在的致命疾病,由寄生原生动物感染引起,这种疾病通过已经感染寄生虫的蚊子叮咬传播给人类。本研究探讨了同时给予维生素A和青蒿琥酯对伯氏疟原虫感染的白化小鼠的影响。一组16只白化小鼠,平均体重28g,性别不确定,接种柏氏单胞菌。老鼠被分成四组,每组4只。A组服用青蒿琥酯,B组服用蒸馏水,C组接受维生素A形式的抗氧化治疗,D组接受青蒿琥酯和维生素A的联合治疗。研究监测了寄生虫血症水平、红细胞压积(PVC)、死亡率百分比以及在给予各种治疗后的体重变化,包括抗疟药(青蒿琥酯)、蒸馏水、维生素A、以及青蒿琥酯和维生素a的联合治疗。维生素a和青蒿琥酯的联合施用可能会降低青蒿琥酯治疗疟疾感染的有效性。这项研究阐明了感染疟疾的小鼠体内青蒿琥酯和抗氧化剂(维生素A)之间的复杂关系。青蒿琥酯清除寄生虫的效果表现为:第5天的+2(++)降至第7天的+3(+++),第9天降至+2(++),第10天降至+1(+)。维生素A和青蒿琥酯的联合施用导致后者治疗疟疾的效力下降,特别是在寄生虫水平在第5、第7和第11天为+3(+++)和第9天为+2(++)的情况下。这一过程表明维生素A可以作为青蒿琥酯抗疟疾作用的拮抗剂。此外,死亡率为50%,与a组相比,PCV减少了。青蒿琥酯是一种促氧化剂,可产生自由基,对寄生虫起作用。然而,维生素A等抗氧化剂的存在可能抵消了促氧化剂的作用,表明存在某种形式的药理拮抗作用。研究结果表明,维生素A和青蒿琥酯合用可能会降低治疗效果。建议实施临床干预措施,以规范青蒿琥酯和维生素A的同时施用,因为这可能影响疟疾治疗的治疗目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Co-administration of Vitamin A and Artesunate in Malaria-Infected Albino Mice
Malaria is a potentially fatal illness that results from infection by parasitic protozoa, which spread to humans via the bites of mosquitoes that have already been infected with the parasite. This research examines the impact of the simultaneous administration of Vitamin A and Artesunate on Plasmodium berghei-infected albino mice. A cohort of sixteen (16) albino mice, with a mean weight of 28g and indeterminate gender, were subjected to P. berghei inoculation. The mice were separated into four groups, each consisting of four animals. Artesunate was administered to Group A, distilled water was administered to Group B, Group C received antioxidant treatment in the form of vitamin A, and Group D was subjected to a combination treatment of Artesunate and Vitamin A. The study monitored the parasitemia level, hematocrit (PVC), percentage mortality rate, and change in body weight following the administration of various treatments, including an antimalarial drug (Artesunate), distilled water, Vitamin A, and a combination therapy of both Artesunate and Vitamin A. The co-administration of vitamin A and Artesunate may decrease the effectiveness of Artesunate in treating malaria infection. The research illustrates the intricate relationship between Artesunate and antioxidant (vitamin A) in mice infected with malaria. The efficacy of Artesunate in clearing the parasite was demonstrated by the reduction of Parasitaemia levels from +2(++) on the 5th day to +3 (+++) on the 7th day, followed by a decrease to +2(++) on the 9th day, and ultimately to +1(+) Parasitaemia on the 10th day. The co-administration of Vitamin A and Artesunate resulted in a reduction of the latter's efficacy in treating malaria, particularly in cases where the parasitemia level was at +3(+++) on the 5th, seventh, and 11th days and +2(++) on the ninth day. This procedure suggests that Vitamin A acted as an antagonist to the antimalarial effects of Artesunate. Furthermore, the mortality rate was 50%, and the PCV was reduced compared to Group A. Artesunate, a pro-oxidant that generates free oxygen radicals that act against the parasite. However, the presence of antioxidants like Vitamin A potentially counteracted the effects of pro-oxidants, indicating some form of pharmacological antagonism. The research findings indicate that the co-administration of vitamin A and Artesunate may reduce therapeutic effectiveness. Clinical interventions are recommended to be implemented to regulate the simultaneous administration of Artesunate and Vitamin A, as this may impact the therapeutic objective of malaria treatment.
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