Capsaicin, a Vanilloid Derivative, Modulates Arginine Kinase mRNA Expression in Trypanosoma evansi
摘要
Trypanosoma evansi, the causative agent of Surra, is a significant emerging zoonotic kinetoplastid protozoan parasite with wide host range and limited chemotherapeutic options. Arginine kinase is mainly responsible for providing metabolic plasticity and maintaining cellular homeostasis of trypanosome under adverse conditions.
MethodsThis study investigated the in vitro anti-trypanosomal activity of Vanilloid derivative, Capsaicin against T. evansi and its effect on mRNA expression of arginine kinase enzyme in T. evansi. Herein, we determined the anti-trypanosomal activity of Capsaicin against T. evansi and its safety towards mammalian cells by estimating the selectivity index. From the dataset generated during the experiments, the IC50 values of capsaicin was determined as 115 µM, respectively.
ResultsCytotoxicity assays showed that Capsaicin exhibited moderate cytotoxicity against equine PBMC and Vero cells line with CC50 value of 309.8 µM and 308.3 µM, respectively giving a selectivity index of around 2.68 at the therapeutic dose against T. evansi. Real-time PCR analysis revealed that Capsaicin showed significant alteration of mRNA expression of arginine kinase 1 gene at 24 and 48 h of exposure with IC50 of drug.
ConclusionThe study suggests that Capsaicin may be a potential approach for treating T. evansi infections, warranting further in vivo investigations.