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Hepatic regeneration after partial hepatectomy in mice infected with Schistosoma mansoni, at the acute and chronic phases of the disease

Regeneração hepática após hepatectomia parcial em camundongos infectados com Schistosoma mansoni, nas fases aguda e crônica da doença

Abstracts

Outbred male albino mice normal or infected with 30 cercariae of Schistosoma mansoni (LE strain) were submitted to 65% hepatectomy during the acute (70 days) and chronic phase (160 days) phases of the disease. A group of the infected animals was treated with 400 mg/kg of oxamniquine during the acute phase before hepatectomy. Non-infected, infected and treated but not hepatectomized animals were kept as controls. Hepatic regeneration was evaluated by incorporation of tritiated thymidine, intraperitoneally injected into non-hepatectomized and hepatectomized animals, 24 hours after surgery. The results showed that removal of 65% of the hepatic parenchyma, during the acute phase, led to a statistically significant increase of thymidine incorporation, when compared with the uninfected hepatectomized controls. This phenomenon was not observed at the chronic phase. Treatment with oxamniquine administered during the acute phase led to a decrease in thymidine incorporation rate 160 days after infection (90 days after treatment) and 24 hours after hepatectomy. The data suggest that infection with S. mansoni represents a considerable stimulus for the regenerative capacity of the liver during the acute, but not the chronic phase of disease.

Schistosoma mansoni; Liver regeneration; Hepatectomy; Thymidine incorporation


Camundongos albinos não-isogênicos, normais ou infectados com 30 cercárias de Schistosoma mansoni (cepa LE) foram submetidos a hepatectomia parcial (65%) na fase aguda (70 dias) ou crônica (160 dias) da doença. Um grupo de animais infectados foi tratado, na fase aguda, com 400 mg/kg oxamniquine antes da hepatectomia. Animais não infectados, infectados e tratados mas não hepatectomizados, foram mantidos como controles. A regeneração hepática foi avaliada pela incorporação de timidina tritiada, injetada peritonealmente em animais hepatectomizados ou não, 24 horas após cirurgia. Os resultados mostraram que a remoção de 65% do parênquina hepático, na fase aguda, levou a um aumento estatisticamente significativo da incorporação de timidina, quando comparado com os animais controles (não infectados e hepatectomizados). Este fenômeno não foi observado na fase crônica. O tratamento com oxamniquina, administrado na fase aguda, levou a uma diminuição da taxa de incorporação de timidina, 160 dias após infecção (90 dias após tratamento) e 24 horas após hepatectomia. Os dados obtidos sugerem que a infecção com S. mansoni representa um estímulo considerável para a capacidade regeneradora do fígado na fase aguda, mas não na fase crônica da doença.


Hepatic regeneration after partial hepatectomy in mice infected with Schistosoma mansoni, at the acute and chronic phases of the disease

G. COSTA(1) (1) Department of Surgery, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (2) Department of Pathologic Anatomy, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (3) GEN-CAD Service, Federal University of Minas Gerais, MG, Brazil. (4) Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, MG, Brazil. (5) "Santa Casa de Misericórdia", Belo Horizonte, MG, Brazil. , J.R. CUNHA-MELO(1,3) (1) Department of Surgery, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (2) Department of Pathologic Anatomy, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (3) GEN-CAD Service, Federal University of Minas Gerais, MG, Brazil. (4) Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, MG, Brazil. (5) "Santa Casa de Misericórdia", Belo Horizonte, MG, Brazil. , B.G. AGUIAR(1) (1) Department of Surgery, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (2) Department of Pathologic Anatomy, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (3) GEN-CAD Service, Federal University of Minas Gerais, MG, Brazil. (4) Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, MG, Brazil. (5) "Santa Casa de Misericórdia", Belo Horizonte, MG, Brazil. , S.C. GONÇALVES(1) (1) Department of Surgery, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (2) Department of Pathologic Anatomy, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (3) GEN-CAD Service, Federal University of Minas Gerais, MG, Brazil. (4) Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, MG, Brazil. (5) "Santa Casa de Misericórdia", Belo Horizonte, MG, Brazil. , N.H. TOPPA(2) (1) Department of Surgery, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (2) Department of Pathologic Anatomy, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (3) GEN-CAD Service, Federal University of Minas Gerais, MG, Brazil. (4) Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, MG, Brazil. (5) "Santa Casa de Misericórdia", Belo Horizonte, MG, Brazil. & P.M.Z. COELHO(4,5) (1) Department of Surgery, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (2) Department of Pathologic Anatomy, School of Medicine, Federal University of Minas Gerais, MG, Brazil. (3) GEN-CAD Service, Federal University of Minas Gerais, MG, Brazil. (4) Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, MG, Brazil. (5) "Santa Casa de Misericórdia", Belo Horizonte, MG, Brazil.

SUMMARY

Outbred male albino mice normal or infected with 30 cercariae of Schistosoma mansoni (LE strain) were submitted to 65% hepatectomy during the acute (70 days) and chronic phase (160 days) phases of the disease. A group of the infected animals was treated with 400 mg/kg of oxamniquine during the acute phase before hepatectomy. Non-infected, infected and treated but not hepatectomized animals were kept as controls.

Hepatic regeneration was evaluated by incorporation of tritiated thymidine, intraperitoneally injected into non-hepatectomized and hepatectomized animals, 24 hours after surgery. The results showed that removal of 65% of the hepatic parenchyma, during the acute phase, led to a statistically significant increase of thymidine incorporation, when compared with the uninfected hepatectomized controls. This phenomenon was not observed at the chronic phase. Treatment with oxamniquine administered during the acute phase led to a decrease in thymidine incorporation rate 160 days after infection (90 days after treatment) and 24 hours after hepatectomy.

The data suggest that infection with S. mansoni represents a considerable stimulus for the regenerative capacity of the liver during the acute, but not the chronic phase of disease.

KEYWORDS: Schistosoma mansoni; Liver regeneration; Hepatectomy; Thymidine incorporation.

INTRODUCTION

Schistosoma mansoni is a parasite that infects millions of individuals in various regions of the world. The eggs that are laid in tissues are fundamental elements in the pathogeny of the disease, being the liver the most affected organ.

Hepatic regeneration in murine schistosomiasis was studied after partial hepatectomy (30%)26 but only during the acute phase of the disease, and with removal of a small amount of parenchyma, that was not able to promote an adequate regenerative stimulus. Regeneration of the normal liver takes place in an accelerated manner, when 60% of the parenchyma is removed3,14,28. Insufficient removal of the hepatic parenchyma (up to 30%), in chronic murine schistosomiasis, showed that the numbers of labelled hepatocytes in the animals bearing schistosomotic fibrosis were lower than in controls at 24, 48 and 72 hours after hepatectomy29 as demonstrated by autoradiography. There are few published papers dealing with hepatic regeneration in experimental schistosomiasis in spite of the importance of this disease. The aim of the present investigation was to study the effect of partial hepatectomy (65% of parenchyma) on the hepatic regeneration of mice infected with S. mansoni during the acute (70 days) and chronic (160 days) phases of the disease, and the effect of treatment with oxamniquine at the acute phase on liver regeneration.

MATERIAL AND METHODS

Animals – A total of 102 outbred male albino mice, weighing about 25 g at the beginning of the experiment, were used.

S. mansoni – The LE strain of S. mansoni, isolated from faeces of a patient living in Belo Horizonte, MG, Brazil, and maintained under laboratory conditions for more than 30 years, was used in the experiments.

Infection of animals – Mice were infected with 30 cercariae, by subcutaneous injection.

Chemotherapeutic treatment – The animals were treated with a single dose of 400 mg/kg oxamniquine (Mansil, Pfizer Laboratory), by the oral route (n=16) at 70 days post-infection (acute phase of the disease), according to COELHO & TAVARES, 19916.

Assessment of worm burden and efficacy of chemotherapeutic treatment – Five infected and untreated animals, and five oxamniquine-treated animals were sacrificed by cervical fracture and submitted to perfusion for worm recovery21 30 days after treatment. The control group showed a mean worm recovery of 15 worms/animal. In the treated group no worm was recovered.

Surgical procedures – Hepatectomy was performed on days 70 and 160 after infection and 90 days after oxamniquine treatment according to a previously described technique14. The animals were submitted to inhalatory anesthesia with enflurane. Antisepsis of the abdominal skin was disinfected with povidone-iodine and a 3.0 cm median laparotomy was performed. The abdominal cavity was exposed and the falciform and hepatogastric ligaments were cut. The median and left lateral lobes were extirpated after individual ligature of their basis with 000 silk thread. Laparorrhaphy was carried out on a single layer, by means of continuous suture with 000 poliglycolic acid thread. The animals were maintained in a heated room until total recovery from anesthesia.

Injection of tritiated thymidine – Twenty-four hours after hepatectomy, the animals were inoculated intraperitoneally with tritiated thymidine (Methyl-3H, 20.00 Ci/mMol, Du Pont), at the dose of 0.5 mCi/g body weight.

Recovery of the livers – Twenty-four hours after inoculation with thymidine, the animals were sacrificed by inhalation of sulfuric ether and the livers removed, weighed and kept at –20 ºC.

Evaluation of tritiated thymidine incorporation rate – The livers were thawed and transferred to test tubes containing 5 ml of distilled water and sonicated with supersonic sound waves until the total desintegration of the cells. Small amounts of distilled water to a final dilution of 1:10 (m/v) were added and 0.4 ml were transferred to a different test tube. A volume of 2 ml of NCS tissue solubilizer was added and the test tubes were kept at room temperature until total solubilization of the homogenate. A sample of 0.5 ml of this solution was transferred to a 4 ml vial and 3 ml of Bray’s scintillation solution for the determination of CPM (countings per minute). The 24 h-period for evaluation of thymidine incorporation was based on published methods4.

Statistical analysis – Data were analyzed by one-way analysis of variance with p<0.05 being considered significant.

RESULTS

Table 1 shows that 65% hepatectomy induces an increase in thymidine incorporation in normal mice, when compared to normal intact mice (p<0.042). The acute phase of schistosomiasis led to a significant increase of thymidine incorporation when compared with the respective infected control groups (p<0.0003). The presence of S. mansoni, by itself, during the acute phase increased significantly the incorporation rate, when compared with the uninfected intact animals (p<0.0000086).

Table 1

Rate of tritiated thymidine incorporation by the hepatic parenchyma in hepatectomized mice, at 70 days after infection with Schistosoma mansoni

* p < 0.042; ** p < 0.0000086, when compared with normal animals;

# p < 0.0003, when compared with infected animals.

During the chronic phase of the disease (160 days after infection), 65% hepatectomy led to an increase of thymidine incorporation in both infected and uninfected animals (Table 2). During that phase of the disease, no statistically significant differences were detected between infected and non-hepatectomized normal. In the oxamniquine-treated animals (400 mg/kg), no statistically significant differences between hepatectomized and normal animals were detected during the acute phase (70 days). However, this last group showed a marked decrease of thymidine incorporation (p<0.0002), when compared with the untreated normal group – hepatectomized or not, and infected group, hepatectomized or not.

Group Scintillations per minute Normal (n=12) 765 ± 91 Normal hepatectomized (n=11) 837 ± 64 * Infected (n=8) 697 ± 96 · Infected hepatectomized (n=5) 846 ± 128 ** Treated (n=10) 540 ± 132 # Treated hepatectomized (n=6) 535 ± 99 ##

Table 2

Rate of tritiated thymidine incorporation by the hepatic parenchyma in hepatectomized mice, at 160 days after infection with Schistosoma mansoni, and at 90 days after treatment administered at the acute phase

* p < 0.042; ** p < 0.03; # p < 0.00013; ## p < 0.00016; · p < 0.12, when compared with normal animals.

The perfusion of 5 mice submitted to treatment with 400 mg/kg oxamniquine, 30 days after drug administration, did not detect surviving worms. The mortality rate after surgery was very low in all the animal groups studied.

DISCUSSION

The phenomenon of hepatic regeneration was described a long time ago. Grecian mythology includes the legend of Prometheus, whose liver was partially eaten by an eagle, that returned everyday and repeated the torture after regeneration of the organ.

The mechanisms related to hepatic regeneration show a complex interaction among biochemical, genetic, physical and environmental processes. The regeneration varies according to the studied species, age of the animal, diet, amount of removed hepatic portion, diurnal luminosity and hepatic diseases18. A number of gene induce the production of several growth factors, such as hepatocyte growth factor (HGF), epidermal growth factor (EGF), transforming growth factor-µ (TGF-µ ), interleukin-6, tumor necrosis factor (TNF), insuline, and norepinephrine among the most important18,25.

An experimental model, consisting of rats submitted to simple 60%, was the basis for the technique14. The removal of specific hepatic lobes induced an accelerate hepatic regeneration, with the recovery of the original hepatic biomass, 5-7 days after surgery. In this experiment, we used mice since the acute and chronic phases, and the lesions caused by granulomatous reactions around the eggs in tissues, in this model are very similar to the ones detected in human disease9,17,27.

There are few reports in the literature concerning the phenomenon of hepatic regeneration in experimental schistosomiasis following partial hepatectomy in mice26, or rats1,12, which are considered inadequate hosts for S. mansoni19,22.

Removal of up to 30% of the hepatic parenchyma at the acute phase of schistosomiasis resulted in a weak regenerative stimulus similar to what was observed in normal animals26 in agreement with previous data for normal animals4,10,28. The differences detected between previously published results26 and the present data, which show significant thymidine incorporation in the animals hepatectomized during the acute phase, were certainly due to the removal of about 65% of the hepatic parenchyma4,14. Care must be taken before considering the result of thymidine incorporation in the liver of animals as the sole cause of the phenomenon of hepatic regeneration considering that mitoses, which occur in the inflammatory process, could be responsible for the consumption of thymidine in the synthesis of deoxyribonucleic acid20,26. S. mansoni eggs are also able to incorporate radioactive thymidine24. The present data showed a markedly higher thymidine incorporation in hepatetomized animals, only during the acute phase. Considering that there are eggs in tissues during both the acute and chronic phases, the inflammatory response induced by the presence of eggs cannot explain the increase of thymidine incorporation. Nevertheless, the inflammatory reactions and the cellular infiltrate in granulomas are more pronounced in the acute phase. Despite these considerations we believe that the exacerbated inflammatory reaction per se would not be sufficient to explain the very high rates of thymidine incorporation, that were detected in the infected-hepatectomized group during the acute phase (Table 1).

The different lymphokines produced during the acute and chronic phases could play a significant role in the liver regenerative kinetics. Production of IL-2, gamma interferon and TNF, produced by TH1 of CD4+ cells during the acute phase of schistosomiasis, have been described. TNF activates transcription factors at the beginning of hepatic regeneration11, and this could left, at least in part, the marked thymidine incorporation detected, during the acute phase in the present study. Conversely, during the chronic phase of schistosomiasis, the TH2 subpopulation of CD4+ cells predominates, with production of IL4 and IL5, besides the appearance of IL10, the latter being an important factor responsible for the transition from the acute to the chronic phase2,5,16,23.

The drug treatment of experimental schistosomiasis enables the animals to modulate the granulomatous response up to 200 days after cure. When reinfected these animals can reduce the intensity of the inflammatory response to egg antigens, as well as avoid a new acute phase7,8. The present study showed that a decrease in the regenerative capacity of treated animals (90 days after treatment), might be due to the absence of living parasite stimuli, as well as to a remaining immunomodulatory capacity that impairs the production of lymphokines seen at the acute phase.

Finally, it is interesting to note that although of hepatic regeneration phenomena in schistosomiasis are accepted as a fascinating subject, they have not been extensively studied and constitute a broad research field to be explored.

RESUMO

Regeneração hepática após hepatectomia parcial em camundongos infectados com Schistosoma mansoni, nas fases aguda e crônica da doença

Camundongos albinos não-isogênicos, normais ou infectados com 30 cercárias de Schistosoma mansoni (cepa LE) foram submetidos a hepatectomia parcial (65%) na fase aguda (70 dias) ou crônica (160 dias) da doença. Um grupo de animais infectados foi tratado, na fase aguda, com 400 mg/kg oxamniquine antes da hepatectomia. Animais não infectados, infectados e tratados mas não hepatectomizados, foram mantidos como controles.

A regeneração hepática foi avaliada pela incorporação de timidina tritiada, injetada peritonealmente em animais hepatectomizados ou não, 24 horas após cirurgia. Os resultados mostraram que a remoção de 65% do parênquina hepático, na fase aguda, levou a um aumento estatisticamente significativo da incorporação de timidina, quando comparado com os animais controles (não infectados e hepatectomizados). Este fenômeno não foi observado na fase crônica. O tratamento com oxamniquina, administrado na fase aguda, levou a uma diminuição da taxa de incorporação de timidina, 160 dias após infecção (90 dias após tratamento) e 24 horas após hepatectomia. Os dados obtidos sugerem que a infecção com S. mansoni representa um estímulo considerável para a capacidade regeneradora do fígado na fase aguda, mas não na fase crônica da doença.

ACKNOWLEDGEMENTS

This work was supported in part by CNPq-PRONEX, FINEP and FAPEMIG, Brazil.

Correspondence to: Prof. Paulo Marcos Zech Coelho, GIDE – ICB/UFMG, Caixa Postal 486, 30l6l-970 Belo Horizonte, MG, Brazil.

Received: 04 February 1999

Accepted: 16 April 1999

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  • (1)
    Department of Surgery, School of Medicine, Federal University of Minas Gerais, MG, Brazil.
    (2)
    Department of Pathologic Anatomy, School of Medicine, Federal University of Minas Gerais, MG, Brazil.
    (3)
    GEN-CAD Service, Federal University of Minas Gerais, MG, Brazil.
    (4)
    Department of Parasitology, Institute of Biological Sciences, Federal University of Minas Gerais, MG, Brazil.
    (5)
    "Santa Casa de Misericórdia", Belo Horizonte, MG, Brazil.
  • Publication Dates

    • Publication in this collection
      09 Nov 1999
    • Date of issue
      July 1999

    History

    • Accepted
      16 Apr 1999
    • Received
      04 Feb 1999
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