Histological demonstration of apoptosis activation in the liver fluke (Fasciola hepatica) following Closantel treatment of experimentally-infected sheep

SOLANA M.V.; LOMBARDO D.; SCARCELLA S.; SOLANA H.; BIANCO F.

Mar del PLata

Congreso; XXI Reunion anual de la Sociedad Argentina de Protozoologia; 2019

The apoptosis can be by DNA damage, cytokine expression, etc. The study of apoptosis has application for the understanding of biological events, such as the tumorogenesis,the action mechanism to drugs, etc. For the apoptosis detection in differentcell lines and tissues there are methods such as TdT-mediated dUDP nick endlabelling (TUNEL) or directly the immunolocalization of Caspase-3. Closantel is an antiparasitic halogenated salicilanilide for the treatment of Fasciola hepatica infestation in farm animals. Its action mechanism is not fully known. It´s known decouple the oxidative phosphorylation but the probable degree of contribution of apoptosis. In this work, were used the Caspase-3 detection and TUNEL techniques to assess the probable involvement of the closantel in the generation of apoptosis in Fasciola hepatica. Fourteen lambs were infected orally with 200 metacercariae of Fasciola hepatica. At 16 weeks post-infection, 10 lambs were treated orally with closantel (10mg/kg.). Adult flukes were recovered from the liver of individual lambs at 0h (notreated n:4), 24h (n:5) and 36h (n:5) post treatment. The flukes were processed for usual histological analysis. There were no injuries at the controls. The F. hepatica at 24 h PT showed minor damage to the posterior end of syncytium. Those of 36 h PT lost large areas of the syncytium in the posterior and dorsal end with cell depletion in testis and vitelline follicles and the oocytes appear rounded with condensed cytoplasm, indicating apoptosis. In testis, ovary and vitelline follicles, defects in closantel-treated trematodes were aligned with failure inthe energy-demanding processes of mitosis and differentiation. These changes could be attributed to anthelmintic-induced blockage of intermediary metabolismand neuromuscular paralysis. This work confirm that closantel activates apoptosis being too this phenomenon its mechanism of action.