Dergiler / Turkish Journal of Veterinary and Animal Sciences / 2011 / Cilt: 35 - Sayı: 4

Pathological and immunohistochemical evaluation of the effects of interferon gamma (IFN-γ) and aminoguanidine in rats experimentally infected with Fasciola hepatica

Sayfa
243–253
Yayın Tarihi
2011-04-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Given the low numbers of parasites and the limited repair in the liver of the animals administered IFN-g and the severity of the lesions in the livers of the animals administered AG, it was concluded that IFN-g positively affected the immune system and that AG blocked NO production in the animals.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:The present study was aimed at pathologically and immunohistochemically evaluating the effects of interferon gamma (IFN-g) and aminoguanidine (AG) in rats experimentally infected with Fasciola hepatica.
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Temel Bulgular & Veri:A total of 44 Wistar rats were divided into 4 groups.
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Sonuç & Katkı:Given the low numbers of parasites and the limited repair in the liver of the animals administered IFN-g and the severity of the lesions in the livers of the animals administered AG, it was concluded that IFN-g positively affected the immune system and that AG blocked NO production in the animals.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Key words: Aminoguanidine · fasciolosis · immunohistochemistry

Özet

The present study was aimed at pathologically and immunohistochemically evaluating the effects of interferon gamma (IFN-g) and aminoguanidine (AG) in rats experimentally infected with Fasciola hepatica. A total of 44 Wistar rats were divided into 4 groups. With the exception of the controls (fourth group), the remaining rats were infected orally with 25 metacerceria of F. hepatica. The first group was administered 0.2% AG in drinking water daily, in order to block nitric oxide (NO) production. The second group was administered 250 units of IFN-g daily, in order to stimulate NO synthesis. The third group was administered a placebo only. At the end of the 2 month experimentation period all the rats were killed under ether anesthesia and necropsied. Migrating tracts, necrosis, and enlargement of the main bile duct were the predominant lesions in infected livers. The parasite burden was lower in the IFN-g-treated rats than rats in the other groups. Acute migrating tracts were occluded with numerous erythrocytes, necrotic hepatocytes, and neutrophils and surrounded by mononuclear cell infiltration interspersed with eosinophils. Chronic migrating tracts were generally repaired with fibrous connective tissue and surrounded by chronic inflammatory infiltrate. Immunohistochemistry detected CD3+ T and CD79acy + B lymphocyte infiltration, l IgG + plasmocytes and PCNA-positive cells in the infected livers, hepatic and mesenterial lymph nodes, and Peyer's patches. Given the low numbers of parasites and the limited repair in the liver of the animals administered IFN-g and the severity of the lesions in the livers of the animals administered AG, it was concluded that IFN-g positively affected the immune system and that AG blocked NO production in the animals.

Abstract

The present study was aimed at pathologically and immunohistochemically evaluating the effects of interferon gamma (IFN-g) and aminoguanidine (AG) in rats experimentally infected with Fasciola hepatica. A total of 44 Wistar rats were divided into 4 groups. With the exception of the controls (fourth group), the remaining rats were infected orally with 25 metacerceria of F. hepatica. The first group was administered 0.2% AG in drinking water daily, in order to block nitric oxide (NO) production. The second group was administered 250 units of IFN-g daily, in order to stimulate NO synthesis. The third group was administered a placebo only. At the end of the 2 month experimentation period all the rats were killed under ether anesthesia and necropsied. Migrating tracts, necrosis, and enlargement of the main bile duct were the predominant lesions in infected livers. The parasite burden was lower in the IFN-g-treated rats than rats in the other groups. Acute migrating tracts were occluded with numerous erythrocytes, necrotic hepatocytes, and neutrophils and surrounded by mononuclear cell infiltration interspersed with eosinophils. Chronic migrating tracts were generally repaired with fibrous connective tissue and surrounded by chronic inflammatory infiltrate. Immunohistochemistry detected CD3+ T and CD79acy + B lymphocyte infiltration, l IgG + plasmocytes and PCNA-positive cells in the infected livers, hepatic and mesenterial lymph nodes, and Peyer's patches. Given the low numbers of parasites and the limited repair in the liver of the animals administered IFN-g and the severity of the lesions in the livers of the animals administered AG, it was concluded that IFN-g positively affected the immune system and that AG blocked NO production in the animals.

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Bu Makaleye Atıf Yap

BEYTUT, E., AKÇA, A., GÖKÇE, H. İ. (2011). Pathological and immunohistochemical evaluation of the effects of interferon gamma (IFN-γ) and aminoguanidine in rats experimentally infected with Fasciola hepatica. Turkish Journal of Veterinary and Animal Sciences, Cilt: 35 - Sayı: 4, 243–253. https://ajindex.com/articles/122033

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Kaynakça (13)

  1. Coleman, J.W.: Nitric oxide in immunity and infl ammation. Int. Immunopharmacol, 2001; 1: 1397-1406.
  2. James, S.L.: Role of nitric oxide in parasitic infections. Microbiol. Rev., 1995; 59: 533-57.
  3. Tariq, M., Khan, H.A., Al Deeb, S., Al Moutaery, K.: Nitric oxide synthase inhibitor aminoguanidine potentiates iminodipropionitrile-induced neurotoxicity in rats. Neurosci. Lett., 1999; 276: 49-52.
  4. Koide, N., Sugiyama, T., Mu M.M., Mori, I., Yoshida, T., Hamano, T., Yokochi, T.: Gamma inteferon-induced nitric oxide production in mouse CD5 + B1-like cell line and its association with apoptotic cell death. Microbiol. Immunol., 2003; 47: 669-679.
  5. Harris, N., Mark, R., Bulle, L., Karupiah, G.: Gamma interferon induced, nitric oxide-mediated inhibition of vaccinia virus replication. J. Virol., 1995; 69: 910-915.
  6. Misko, T.P., Moore, W.M., Kasten, T.P., Nickols, G.A., Corbett, J.A. Tilton, R.G., Mcdaniel, M.L., Williamson, J.R., Currie, M.G.: Selective inhibition of the inducible nitric oxide synthase by aminoguanidine. Eur. J. Pharmacol., 1993; 233: 119-125.
  7. Cervi, L., Rossi, G., Cejas, H., Masih, D.T.: Fasciola hepatica induced immune suppression of spleen mononuclear cell proliferation: role of nitric oxide. Clin. Immunol. Immunop., 1998; 87: 145-154.
  8. Piedrafi ta, D., Parsons, J.C., Sandeman, R.M., Wood, P.R., Estuningsih, S.E., Partoutomo, S., Spithill, T.W.: Antibody- dependent cell-mediated cytotoxicity to newly excysted juvenile Fasciola hepatica in vitro is mediated by reactive nitrogen intermediates. Parasite Immunol., 2001; 23: 473-482.
  9. Sibille, P., Tliba, O., Boulard, C.: Early and transient cytotoxic response of peritoneal cells from Fasciola hepatica-infected rats. Vet. Res., 2004; 35: 573-584.
  10. Hsu, S., Raine, L., Fanger, H.: Use of avidin-biotin peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. J. Histoch. Cytochem., 1981; 29: 577-580.
  11. Poitou, I., Baeza, E., Boulard, C.: Humoral and cellular immune responses in rats during a primary infestation with Fasciola hepatica. Vet. Parasitol., 1992; 45: 59-71.
  12. Meeusen, E., Lee, C.S., Rickard, M.D., Brandon, M.R.: Cellular responses during liver fl uke infection in sheep and its evasion by the parasite. Parasite Immunol., 1995; 17: 37-45.
  13. Sadeghi-Hashjin, G., Naem, S.: Parasiticidal eff ects of peroxynitrite on ovine liver fl ukes in vitro. J. Helminthol., 2001; 75: 73-76. Pérez, J., Ortega, J., Moreno, T., Morrondo, P., López-Sández, C., Martín