Effects of cyclosporin A on the morphology and tegumentary ultrastructure of Hymenolepis microstoma in vivo

Cyclosporin A (CsA) induced significant changes in parasite morphology when administered to mice infected with Hymenolepis microstoma. Gross morphological damage consisted of proglottis swelling and the formation of protuberances from the worm surface, visible with a low-power dissecting microscope, occurring most frequently in the posterior third of the strobila. Gross morphology and ultrastructure were examined further using scanning and transmission electron microscopy. Swollen proglottides exhibited areas covered in small pits and fissures (diameter approximately 1–2 μm) but it was not possible to establish the significance of this damage. The brush-border and distal cytoplasm appeared largely intact although some evidence of swelling of the basal membrane invaginations and possible fluid accumulation was seen in drug-treated TEM sections. The apparent oedematous condition of many of the proglottides from drug-treated mice may indicate that CsA treatment mediates permeability changes in the worm surface membrane but the mechanisms by which this may occur remain to be elucidated. The effects of CsA on the morphology of H. microstoma correlate with the previously described anthelmintic activity of the drug against this parasite where CsA treatment dramatically reduces worm growth, retards migration into the bile duct and limits parasite survival.

[1]  A. Thomson,et al.  The larvicidal activity of cyclosporin A against Schistosoma mansoni in mice , 1991, Parasitology.

[2]  J. Wastling,et al.  Action of cyclosporin A on the tapeworm Hymenolepis diminuta in mice , 1990, Parasitology.

[3]  D. McLaren,et al.  Schistosoma mansoni: morphology and ultrastructure of adult worms recovered from cyclosporin A-treated mice , 1990, Parasitology.

[4]  J. Wastling,et al.  Action of cyclosporin A on the tapeworms Hymenolepis microstoma, H. diminuta and Mesocestoides corti in vivo , 1989, Parasitology.

[5]  P. Truffa-bachi,et al.  Influence of CsA on humoral immunity and on B lymphocyte activation , 1989 .

[6]  J. Kay Inhibitory effects of cyclosporin A on lymphocyte activation , 1989 .

[7]  A. Thomson Cyclosporin : mode of action and clinical applications , 1989 .

[8]  T. Aw,et al.  Studies on the action of cyclosporine A against Schistosoma mansoni and other parasitic infections. , 1988 .

[9]  R. Grencis,et al.  Cyclosporin A and Trichinella spiralis; anthelminthic effects in immunosuppressed mice , 1988, Parasite immunology.

[10]  L. Chappell,et al.  The interactions between drugs and the parasite surface , 1988, Parasitology.

[11]  K. Richards,et al.  Echinococcus granulosus: in vitro effect of monensin on the tegument of the protoscolex , 1986, Parasitology.

[12]  M. Belosevic,et al.  The effects of cyclosporin A on the course of infection with Giardia muris in mice. , 1986, The American journal of tropical medicine and hygiene.

[13]  J. Remington,et al.  In vivo and in vitro effects of cyclosporin A on Trypanosoma cruzi. , 1985, The American journal of tropical medicine and hygiene.

[14]  A. Capron,et al.  Filaricidal effects of cyclosporin-A against Dipetalonema viteae in Mastomys natalensis. , 1984, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[15]  J. Fierer,et al.  Cyclosporin A inhibits Coccidioides immitis in vitro and in vivo , 1983, Antimicrobial Agents and Chemotherapy.

[16]  C. Gottlieb,et al.  Exacerbation of Trypanosoma cruzi infection in mice treated with the immunoregulatory agent cyclosporin A. , 1983, Tropenmedizin und Parasitologie.

[17]  W. Hughes,et al.  Provocation of infection due to Pneumocystis carinii by cyclosporin A. , 1982, The Journal of infectious diseases.

[18]  R. Prichard,et al.  The effect of praziquantel on calcium in Hymenolepis diminuta. , 1982, Molecular and biochemical parasitology.