Anti-trypanosomal Activity of Bufonidae (Toad) Venom Crude Extract on Trypanosoma brucei brucei in Swiss Mice

E. J., Pam V. A., Uzoigwe N. R., Omalu I. C. J., O. A, A. O., A. F, T. S., Adejoh V. A., A. S., Ayim J. O., D. S, Aimankhu P. O., Maikenti J. I., Ajah L. J., A. O., A. A, A. A., O. A., Anyebe G. E., Kure M. S.
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Abstract

Trypanosomiasis afflicts about 6 ~ 7 million people globally and to a large extent impedes livestock production in Africa. Naturally, trypanosomal parasites undergo genetic mutation and have developed resistance over a wide range of therapies. The utilization of animals and plants products has presented therapeutic potential for identifying novel anti-trypanosomal drugs. This study evaluated toad venom for anti-trypanosomal potency invivo in Swiss mice. Toads were collected from July to August 2019. The acute oral toxicity and biochemical characterization of the toad venom were determined. The experimental mice were administered various doses (130 mg/kg, 173 mg/kg and 217 mg/kg) of the toad venom crude extract and 0.75 mg/mL of Diamizan Plus standard drug for the treatment of trypanosomiasis, once daily for 3 days. The in-vivo anti-trypanosomal activity was evaluated by a curative test, after infecting the mice with Trypanosoma brucei brucei. The pre-patent period was 72 hours before treatment commenced. The overall results showed that trypanosomal load was highest in the control group while the group treated with Diamizan drug had the least trypanosomal load. As such, the mean trypanosomal load in relation to treatments showed a very high significant difference (P<0.05). Also, the mean trypanosomal load in Swiss mice in relation to the highest dosage of toad venom versus Diamizan drug showed a very high significant difference (P<0.05). The mean change in relation to the haematological parameters across treatments groups varied significantly (P<0.05) with the exception of Hb which showed no significant difference (P>0.05) across treatment groups. The over 50% reduction in the trypanosomal load in the 130 mg/kg group in comparison with the control group brings to bare the anti-trypanosomal potency of the toad venom. The anti-trypanosomal activity demonstrated by the toad venom has provided basis for development of new therapeutic agents from different toad species. The study recommends further studies (both in-vivo and invitro) followed by the characterization of the active compounds present in the toad venom responsible for the anti-tyrpanosomal activity observed alongside the management and conservation of these species.
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蟾毒粗提物对瑞士小鼠布氏锥虫的抗锥虫活性研究
锥虫病折磨着全球约600万至700万人,并在很大程度上阻碍了非洲的畜牧生产。自然地,锥虫体寄生虫经历基因突变,并对广泛的治疗产生耐药性。利用动植物产品鉴定抗锥虫药物具有潜在的治疗潜力。本研究评估了蟾蜍毒液在瑞士小鼠体内抗锥虫体的效力。蟾蜍于2019年7月至8月收集。测定了蟾蜍毒液的急性口服毒性和生化特性。实验小鼠分别给予不同剂量(130 mg/kg、173 mg/kg和217 mg/kg)的蟾蜍毒粗提物和0.75 mg/mL的双咪嗪加治疗锥虫病标准药物,每日1次,连用3 d。用治疗试验评价小鼠感染布鲁氏锥虫后体内抗锥虫活性。专利前期为治疗开始前72小时。总体结果显示,对照组的锥虫病载量最高,而双咪唑组的锥虫病载量最低。因此,各处理组间的平均锥虫体载量有非常高的显著差异(P0.05)。与对照组相比,130 mg/kg组的锥虫病负荷减少了50%以上,显示出蟾蜍毒液的抗锥虫效力。蟾蜍毒液所显示的抗锥虫活性为从不同蟾蜍种中开发新的治疗剂提供了依据。该研究建议进一步研究(体内和体外),然后对蟾蜍毒液中存在的负责抗tyrpanosomal活性的活性化合物进行表征,同时观察到这些物种的管理和保护。
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