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Experimental study on the effect of cortisone in mice infected with Toxocara canis: Histopathological findings of granuloma in the liver
Keun-Tae Lee and Hong-Ki Min
Department of Parasitology, College of Medicine, Yonsei University, Korea.
Department of Parasitology, College of Medicine, Ewha Womans University, Korea.
Abstract
The present study was carried out to examine the effect of "Cortisone" on the worm burden migrated in the organs, and granulomatous change in the liver of mice infected with Toxocara canis eggs. Daily does of 0.5 mg "Cortisone" was administrated subcutaneously to Toxocara-infected mice with different schedule.
The results are summarized as follows;
1. More number of Toxocara larvae migrated into the muscle tissue, especially into the carcass through the wall of the large intestine and higher distribution rate and longer persistence of worms were also recognized in the carcass of the experimental group than in the control.
2. Cortisone administration resulted the inhibition of granuloma formation, as well as the resolution of granuloma in the liver. However, the discontinuation of the administration induced the reccurence of heavier grade of inflammation. In non-cortisone treated group (control), cellular infiltration appeared around the worms in the liver on the 10th day of the infection, and typical granulomatosis was followed on the 20th day.
As in above results, it is considered cortisone has remarkable anti-inflammatory and immunosuppressive effects in mice infected with T.canis, but histopathological changes on the granuloma formation might be related closely with the duration of Toxocara infection, dosage, duration and timing of cortisone administration.
Figures
Fig. 1 No inflammatory response around larva in the mouse liver. control, 5th day after infection, × 400
Fig. 2 A typical granuloma. control, 20th day after infection, × 100
Fig. 3 Resolved granuloma with localized cellular response. Group II, Cortisone treatment for 20 days since the day after infection, × 100
Fig. 4 Recurred granuloma. Group II, 5th day after discontinuation of cortisone treatment, × 100
Fig. 5 Confluent granulomas with eosinophilic abscess and extensive cellular infiltration. Group II, 20th day after discontinuation of cortisone treatment, × 100
Fig. 6 Moderately resolved granuloma with central necrosis. Group III, cortisone treatment for 10 days since 11th day after infection, × 400
Fig. 7 Granuloma with central eosinophilic abscess and necrosis. Group III, 15th day after discontinuation of cortisone treatment, × 100
Fig. 8 Resolving granuloma with central necrosis. Group IV, cortisone treatment for 5 days since 21th day after infection, × 100
Tables
Table 1 Distribution rates* of Toxocara canis larvae in the tissues of infected mice at various periods after infection.
References
1.
Ashton N. Larval granulomatosis of the retina due to Toxocara. Br J Ophthalmol 1960;44:129–148.
2.
Beaver PC, Snyder CH, Carrera GM, Dent JH, Lafferty JW. Chronic eosinophilia due to visceral larva migrans; report of three cases. Pediatrics 1952;9(1):7–19.
Beaver PC. The nature of visceral larva migrans. J Parasitol 1969;55(1):3–12.
5.
Behrer M. J Parasit 1951;38:635–640.
6.
Brill R, Churg J, Beaver PC. Allergic granulomatosis associated with visceral larva migrans; case report with autopsy findings on Toxocara infection in a child. Am J Clin Pathol 1953;23(12):1208–1215.
7.
Burren CH. Experimental toxocariasis. I. Some observations on the histopathology of the migration of Toxocara canis larvae in the mouse. Z Parasitenkd 1968;30(2):152–161.
8.
Coker CM. Effects of cortisone on Trichinella spiralis infections in nonimmunized mice. J Parasitol 1955;41(5):498–504.
9.
Cross JH Jr. The natural resistance of the white rat to Nematospiroides dubius and the effect of cortisone on this resistance. J Parasitol 1960;46:175–185.
10.
Dent JH, Nichols RL, Beaver PC, Carrera GM, Staggers RJ. Visceral larva migrans; with a case report. Am J Pathol 1956;32(4):777–803.
11.
Dobson C. Host Endocrine Interactions With Nematode Infections. I. Effects Of Sex, Gonadectomy, And Thyroidectomy On Experimental Infections In Lambs. Exp Parasitol 1964;15:200–212.
12.
Fellers FX. Agglutination studies in visceral larva migrans. AMA Am J Dis Child 1953;86(6):767–771.
13.
Fernando ST. Immunological response of rabbits to Toxocara canis infection. Parasitology 1968;58(1):91–103.
14.
Friedman S, Hervada AR. Severe myocarditis with recovery in a child with visceral larva migrans. J Pediatr 1960;56:91–96.
15.
Hendricks JR. The relationship between precipitin titer and number of Trichinella spiralis in the intestinal tract of mice following test infections. J Immunol 1950;64(3):173–177.
16.
Jung RC, Pacheco G. Use of a hemagglutination test in visceral larva migrans. Am J Trop Med Hyg 1960;9:185–191.
17.
Kass EH, Finland M. Adrenocortical hormones in infection and immunity. Annu Rev Microbiol 1953;7:361–388.
18.
Mathies AW. J Parasit 1961;10:244–248.
19.
Mercer RD, Lund HZ, Bloomfield RA, Caldwell FE. Larval ascariasis as a cause of chronic eosinophilia with visceral manifestations. Am J Dis Child 1950;80(1):46–58.
20.
Miller TA. J Parasit 1966;52:285–290.
21.
Mitchell JR. Detection of Toxacara Canis Antibodies with Fluorescent Antibody Technique. Proc Soc Exp Biol Med 1964;117:267–270.
22.
Oshima T. Standardization of techniques for infecting mice with Toxocara canis and observations on the normal migration routes of the larvae. J Parasitol 1961;47:652–656.
23.
Smith MH, Beaver PC. Persistence and distribution of Toxocara larvae in the tissues of children and mice. Pediatrics 1953;12(5):491–497.
24.
Tiner JD. The migration, distribution in the brain, and growth of ascarid larvae in rodents. J Infect Dis 1953;92(2):105–113.
25.
van Thiel P. Comments on a case of Toxocara infection in the Netherlands. Trop Geogr Med 1960;12:67–70.
26.
Weinstein PP. The effect of cortisone on the immune response of the white rat to Nippostrongylus muris. Am J Trop Med Hyg 1955;4(1):61–74.
27.
Wiseman RA, Woodruff AW. Toxocariasis in Britain as revealed by skin sensitivity tests. Br Med J 1968;1(5593):677–678.
28.
Zuelzer WW, Apt L. Disseminated visceral lesions associated with extreme eosinophilia; pathologic and clinical observations on a syndrome of young children. Am J Dis Child 1949;78(2):153–181.
29.
Zurier RB, Weissman G. Anti-immunologic and anti-inflammatory effects of steroid therapy. Med Clin North Am 1973;57(5):1295–1307.