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1.
J Parasit Dis ; 42(2): 277-286, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29844633

ABSTRACT

Some reports have shown that mesenchymal stem cells (MSCs) therapy could ameliorate chemically-induced hepatic fibrosis. This research assesses the therapeutic action of bone marrow mesenchymal stem cells (BM-MSCs) on chronic diseased liver in Schistosoma mansoni infected mice. All infected female mice divided into three groups, one group (15 mice) treated with oral praziquantel (PZQ), second group (15 mice) received intravenous injection of BM-MSCs and third group (15 mice) treated with both MSCs + PZQ. Two control groups (15 mice each) subdivided into one infected and second healthy one. BM-MSCs were obtained from bones of both femur and tibia of male mice (30 mice), then cultured and characterized morphologically by detection of CD105 by flow cytometer. Liver tissues for all groups were examined histopathologically. Measuring of the collagen 1 gene expression was done by real-time PCR and immunohistochemical study to detect stem cells differentiation for detection of MSCs engraftments in liver tissue. MSCs treatment caused marked improvement and regression of fibrosis, and prevents deposition of collagen and reduced the expression of collagen 1 gene in infected mice on their liver tissues, especially when used with PZQ in mice treatment. It can be concluded that, MSCs is a good therapeutic method for liver fibrosis caused by S. mansoni infection.

2.
J Egypt Soc Parasitol ; 47(1): 81-92, 2017 Apr.
Article in English | MEDLINE | ID: mdl-30157335

ABSTRACT

Histopathological diagnosis was used to understand the pathological events associated with Heterophyes heterophyes (H. heterophyes) infection. CD3 and CD79α antibodies had been used as markers for both T and. B lymphocytes respectively. Immunohistochemical techniques had several advantages as remarkable sensitivity and specificity. This study aims to evaluate the roles-of praziquantel (PZQ) and aminoguanidine (AG) treatment in H heterophyes infected dogs pathologically and immunohisto-chemically. Study design included experimental infection of dogs with encysted metacercariae of H heterophyes followed by treatment with PZQ and AG. Tissue samples were taken from small intestinal, liver, heart and lung of all groups for histopathological and immunohistochemical studies. Pathological changes were detected in infected tissues by histopathological examination. There was different degree of CD79α+B lymphocytic & CD3+T lymphocytic infiltration detected in immuno-histochemical stained tissues. PZQ caused improvement of pathological changes in the small intestine. However the cellular inflammatory infiltration increased. There was reduction in inflammatory infiltration after intake of AG. Both PZQ and AG improved the pathological changes in the.liver, heart and lung, while the cellular inflammatory infiltration increased after PZQ and reduced by AG. Moreover in the lung AG improves pulmonary congestion and alveolar wall thickness.


Subject(s)
Anthelmintics/therapeutic use , Guanidines/therapeutic use , Heterophyidae , Nitric Oxide Synthase/antagonists & inhibitors , Praziquantel/therapeutic use , Trematode Infections/drug therapy , Animals , Anthelmintics/pharmacology , Antibodies, Helminth/immunology , CD3 Complex/immunology , CD79 Antigens/immunology , Case-Control Studies , Dogs , Enzyme Inhibitors/pharmacology , Enzyme Inhibitors/therapeutic use , Guanidines/pharmacology , Heterophyidae/drug effects , Immunohistochemistry , Intestine, Small/immunology , Intestine, Small/parasitology , Intestine, Small/pathology , Liver/immunology , Liver/parasitology , Liver/pathology , Lung/immunology , Lung/parasitology , Lung/pathology , Male , Myocardium/immunology , Myocardium/pathology , Praziquantel/pharmacology , Trematode Infections/pathology
3.
J Egypt Soc Parasitol ; 39(3): 907-16, 2009 Dec.
Article in English | MEDLINE | ID: mdl-20120754

ABSTRACT

Forty of eighty mice (10 each group) were infected with S. mansoni cercariae and sacrificed at 3 weeks (G-A), 6 weeks (G-B), 12 weeks (G-C) and 16 weeks (G-D) post infection (P.I). The other forty mice were used as control groups of ten mice each. There were highly significant difference between egg counts after 12 weeks & 16 weeks of infection compared to 6 weeks P.I. The maximum egg count and mature eggs were in 6th week P.I while dead eggs reached the peak at 16th weeks P.I. Liver egg counts showed maximum followed by intestinal and then, stool egg counts. A highly significant differences in hydroxyproline, TGF-Bland IL-4 of infected than in controls and their peak at 16 weeks P.I. A significant difference in the IFN-gamma in the infected than in controls with peak occurred at 6 weeks P.I. and declined after that reaching a low level at 16 weeks P.I. A highly significant positive correlation was between TGF-Bland IL4 and significant negative correlation between IFN-gamma and both IL4 & TGF-B1. A highly significant and significant negative correlation between TGF-B1 and egg count at 12 & 16 weeks P.I respectively. Negative correlation was between IL-4 and egg count at 16 weeks P.I. But, significant positive correlation was between IFN-gamma with the egg count at 16 weeks P.I. A significant negative correlation was between TGF-B1 and oogram at 6 & 16 weeks P.I, but highly significant positivity was between IFN-gamma and oogram at 16 weeks P.I. A significant negative correlation was between IL-4 and oogram at 16 weeks P.I. A significant positive correlation was between levels of hydroxyproline and TGF-B1 at 12 & 16 weeks P.I. Highly significant negative correlation between hydroxyproline and IFN-gamma was at 12 weeks P.I with significant and highly significant positive correlation between hydroxyproline and IL4 at 12 & 16 weeks P.I.


Subject(s)
Cytokines/blood , Liver Cirrhosis, Experimental/immunology , Schistosomiasis mansoni/immunology , Animals , Hydroxyproline/blood , Interferon-gamma/blood , Interleukin-4/blood , Liver Cirrhosis, Experimental/blood , Liver Cirrhosis, Experimental/parasitology , Mice , Parasite Egg Count , Random Allocation , Schistosoma mansoni/immunology , Schistosomiasis mansoni/blood , Time Factors , Transforming Growth Factor beta1/blood
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