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In muscle mitochondria of mice infected by Trichinella spiralis larvae and treated by following benzimidazoles: mebendazole (MBZ), oxfendazole (OXF) and thiabendazole (TBZ) their differential influence on uncoupling of host mitochondria was observed. Both MBZ and OXF (in doses of 80 mg/kg of body weight and 60 mg/kg of body weight, respectively) improved the bioenergetic properties of host muscles mitochondria i.e. increase the respiratory control index (RCI) in the muscular phase of this infection. The experiments with the use of OXF in Trichinella pseudospiralis infection have proved that this drug normalizes also in this infection the activity of two mitochondrial inner membrane-located enzymes: mtATPase and SDH in the muscular phase of the infection. A similar effectiveness of OXF in the latter infection was reached using a single and a double dose of the drug (200 mg/kg of body weight, divided into two parts).
Larvae of the parasitic nematode Trichinella spiralis migrate via the bloodstream or the lymphatic system to the skeletal muscle cells where they induce multiple alterations in the intracellular environment leading to the formation of nurse cells. The “nurse cell-T. spiralis larva” complex is composed of a transformed fragment of a skeletal muscle cell and the wall of the larva. The pathological process responsible for the formation of this complex, known as basophilic transformation, is essential for the development of T. spiralis larvae, but it still not known how newborn larvae penetrate the transformed fragment of the muscle cell. In this study, we aimed to characterize the ultrastructure of the region of the nurse cell in direct contact with the larval wall, after one and two weeks of T. spiralis infection in mice. For this purpose, a transmission electron microscope fitted with a goniometer was used to make observations of samples tilted at an angle of ±40° relative to the axis of the electron beam. Examination of electron micrographs revealed the continuity of the nurse cell membrane adjacent to the larval surface and the presence of a large quantity of glycogen particles close to the inner surface of this membrane. Our results showed that death of the T. spiralis larvae was associated with destruction of the contact region between the larval wall and the adjacent surface of the nurse cell. We conclude that the T. spiralis larva does not penetrate the nurse cell, but a morphological “junction” is formed between the larval wall and the cell membrane.
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