Effect of phenyl vinyl sulphone cysteine protease inhibitor on Schistosoma mansoni: in vitro and in vivo experimental studies

• Published in: Journal of parasitic diseases Vol. 41; no. 4; pp. 1049 - 1058
• Main Authors: Mahmoud, Manal Salah El-Din, Ibrahim, Ayman Nabil, Badawy, Abeer Fathy, Abdelmoniem, Nourhan Mohamed
• Format: Journal Article
• Language: English
• Published: New Delhi Springer India 01.12.2017; Springer Nature B.V
• Subjects: Cell culture; Cysteine proteinase; Granuloma; Health Promotion and Disease Prevention; Hemoglobin; Infections; Infectious Diseases; Intestine; Liver; Medicine; Medicine & Public Health; Mortality; Original; Original Article; Ova; Schistosoma mansoni; Phenyl vinyl sulphone; In vivo; Cysteine protease inhibitor; Cysteine protease; Praziquantel; In vitro; Schistosoma mansoni
• ISSN: 0971-7196; 0975-0703
• DOI: 10.1007/s12639-017-0933-3

The present work aimed to study the effect of phenyl vinyl sulphone (PVS), a CPI, on different stages of Schistosoma (S.) mansoni in an in vitro culture study and in experimentally infected mice, compared to PZQ. As regards the in vitro study, different concentrations of PVS (1, 2, 4, 6, 8 and 10 µg/ml) and PZQ (1 µg/ml) were assessed by % worm mortality for schistosomula and adults, and hemoglobin degradation by schistosomula. In vivo study included 8 groups of mice. Intraperitoneal PVS, subgroup (a), and oral PZQ, subgroup (b), were assessed at different durations post infection (pi); at 1, 3, 5 and 7 weeks pi (groups I, II, III and IV, respectively). Infection, PVS, PZQ, and normal control groups (groups V–VIII) were included. The anti-schistosomal effects of PVS were assessed by parasitological, histopathological and haematological parameters. In in vitro study, PVS had a schistosomicidal effect in a concentration and time dependent manner, PVS showed 100% schistosomula mortality at day 2 and 92% adult worm mortality at day 5. Furthermore, PVS decreased hemoglobin degradation by schistosomula. In in vivo study, PVS showed a decrease in total worm burden and tissue egg load in intestine and liver with an increase in number of dead ova in intestine of mice. Furthermore, PVS resulted in a decrease in number, size and cellularity of hepatic granulomas and an increase in hemoglobin concentration.PVS was better than PZQ in reducing each of tissue egg count in intestine at 5 and 7 weeks pi, and hepatic granuloma size at 3, 5 and 7 weeks pi. These results suggest that PVS can be a promising chemotherapeutic agent in Schistosoma mansoni infection.