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1.
J Helminthol ; 97: e95, 2023 Dec 06.
Article in English | MEDLINE | ID: mdl-38053397

ABSTRACT

Schistosomiasis is a serious tropical disease. Despite extensive research into the etiology of liver fibrosis, effective therapeutic options remain limited. This study aims to assess the effectiveness of auranofin in treating hepatic granuloma and fibrogenesis produced by Schistosoma (S.) mansoni eggs. Auranofin is a gold complex that contains thioglucose tetraacetate and triethylphosphine. Eighty BALB/c male mice were divided into four groups (n=20/group): negative control (GI), positive control (GII), and early (GIII) and late (GIV) treatment groups with oral auranofin according to beginning of treatment 4th week and 6th week post-infection. Mice were infected subcutaneously in a dose of 60±10 cercariae/mouse. Worm counts, egg loads, and oogram patterns were determined. Biochemical, histological, and immunostaining of interleukin-1ß (IL-1ß), Sirtuin 3 (SIRT3), and smooth muscle actin (SMA) were assessed. GIII showed a significant decrease in the total S. mansoni worm burden and ova/gram in liver tissue (with reduction percent of 63.07% and 78.26%, respectively). Schistosomal oogram patterns, immature and mature ova, also showed a significant decrease. The reduction in granuloma number and size was 40.63% and 48.66%, respectively, in GIII, whereas in GIV, the reduction percent was 76.63% and 67.08%. In addition, the degree of fibrosis was significantly diminished in both treated groups. GIV showed significant reduction in IL-1ß and SMA expression and increase in SIRT3 expression. These findings reveal how auranofin suppresses the development of liver fibrosis. Therefore, it is crucial to take another look at auranofin as a prospective medication for the treatment of S. mansoni egg-induced hepatic granuloma and consequent fibrosis.


Subject(s)
Schistosomiasis mansoni , Sirtuin 3 , Male , Animals , Mice , Schistosoma mansoni , Schistosomiasis mansoni/drug therapy , Schistosomiasis mansoni/pathology , Auranofin/pharmacology , Auranofin/therapeutic use , Prospective Studies , Sirtuin 3/pharmacology , Sirtuin 3/therapeutic use , Ovum/pathology , Liver/pathology , Liver Cirrhosis/drug therapy , Liver Cirrhosis/pathology , Granuloma/drug therapy , Granuloma/pathology
2.
Arch Razi Inst ; 76(4): 781-793, 2021 10.
Article in English | MEDLINE | ID: mdl-35096314

ABSTRACT

The biosynthesis of silver nanoparticles (AgNPs) is a new approach in nanotechnology which was optimistically implemented in medicine, food control, and pharmacology. The present study aimed to investigate the antioxidant and cytotoxicity effects of AgNPs produced by Lactobacillus gasseri filtrate. Also, changing color from yellow to brown confirmed the production of AgNPs. AgNPs were characterized using ultraviolet-visible spectroscopy, FE-SEM, and Fourier Transform Infrared Spectroscopy (FTIR). The antioxidant activity of AgNPs was tested using the DPPH assay. The scavenging test for DPPH showed 19.3%, 32.6%, 47.6%, 72%, 85.3% at concentrations (6.25, 12.5, 25, 52, 100) µg/ml, respectively, which proved that the scavenging percentage increased with increasing concentration. The effect of AgNPs on the chromosomal pattern was also studied. The results of the experiment of AgNPs against SK-GT-4 cancer cells showed the toxic activity of the used particles against the strains of these human esophageal cancer cells and failed to affect normal cells.


Subject(s)
Lactobacillus gasseri , Metal Nanoparticles , Animals , Anti-Bacterial Agents/pharmacology , Antioxidants , Metal Nanoparticles/toxicity , Plant Extracts/chemistry , Silver/chemistry , Silver/toxicity
3.
Br J Oral Maxillofac Surg ; 25(5): 410-4, 1987 Oct.
Article in English | MEDLINE | ID: mdl-3478086

ABSTRACT

Burkitt's lymphoma is a tumour that most often affects the jaws, especially in endemic areas of Africa. In non-endemic areas, the jaws are affected in about 15-18% of cases. A case is presented which demonstrates the significance of jaw lesions in the disease. The history and pathogenesis of the disease also are discussed.


Subject(s)
Burkitt Lymphoma/complications , Gingival Hyperplasia/etiology , Mandibular Neoplasms/complications , Burkitt Lymphoma/pathology , Child , Humans , Male , Mandibular Neoplasms/pathology , Tooth Mobility/etiology
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