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Apinhasmit W, Sobhon P. Opisthorchis viverrini: Effect of praziquantel on the adult tegument. Southeast Asian J Trop Med Public Health 1996;27:304-11. |
Ultrastructural
changes of the tegument of adult liver flukes, Opisthorchis viverrini, after
in vitro incubation in Minimal Essential Medium containing 0, 0.1, 1.0 and
10.0 ( g/ml of anthelminthic praziquantel for 5, 15, 30, 45 and 60 minutes
were investigated by scanning (SEM) and transmission (TEM) electron microscopy.
SEM observations showed that the surface damage was composed of blebbing
due to the swelling of microvilli, followed later by the disruption of these
structures to form lesions that caused the erosion and desquamation of the
surface. Sensory papillae, by contrast, appeared relatively unaffected.
The surface changes could be observed at all doses but the extent of damage
increased with increasing duration of incubation and concentration of the
drug. The ventral as well as the dorsal surfaces exhibited similar change,
whereas the anterior part tended to be damaged less than the posterior part.
Under TEM observations, the earliest sign of changes was the depolymerization
of the microtrabecular network in scattered foci, which resulted in the
formation of non-membrane-bound vacuoles under microvilli. The basal infoldings
also became dilated, and some turned into membrane-bound vacuoles in the
basal zone. Subsequently, microvilli became enlarged, and eventually formed
blebs that later rupture to form lesion spots as observed in the SEM. Finally,
the microtrabecular network in all regions broke down, creating vacuoles
of various sizes throughout the tegument, leading to its total disintegration
and detachment. The sequence of morphological changes was generally similar
at all doses; however, the changes occurred faster at the higher doses and
the longer incubation times. In addition, at the longer durations myofilaments
in most muscle cells also became depolymerized, while microtubules were
unchanged by the drug. Therefore, it is possible that praziquantel, through
its induction of Ca2+ influx, causes depolymerization of the microtrabecular
network that leads to the vacuolization, swelling, blebbing, and eventually
the disruption and detachment of the tegument, and the breakdown of myofilaments
in the muscle cells.
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