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1.
Egyptian Journal of Hospital Medicine [The]. 2013; 50: 127-136
in English | IMEMR | ID: emr-170272

ABSTRACT

Xenoestrogens are compounds like estrogens in effect but not in structure which are mimicking the action of endogenous estrogen and activate estrogen receptor. Xenoestrogens are chemically distinct industrial products potentially able to disrupt the endocrine system by mimicking the action of endogenous steroid hormones. Among such compounds, the ubiquitous environmental contaminants bisphenol-A [BPA] may promote adverse effects in humans triggering estrogenic signals in target tissues. Bisphenol- A is widely used in food and drinks packaging. The present study is carrying out to evaluate the effect of bisphenol-A on sexual hormonal pattern in male albino rats. 64 adult male Sprague-Dawley rats [100-120 g] were divided to four groups [16 rats/group].Group [1]: control group without any treatment. Group[2]: positive control group was injected subcutaneously [s.c] with sesame oil daily. Group [3]: received BPA daily with low dose [10 mg/kg/day s.c]. Group [4]: received BPA daily with high dose [30 mg/kg/day s.c]. The experiment durated 30 days, half rats of each group were sacrificed after 15 days of treatment and the other half of groups after 30 days. The blood was collected, serum was separated and used for estimation of [hormonal levels, prolactin, gonadotrophin and testosterone] and some biochemical parameters [liver enzymes, kidney function, protein and lipid profile]. Testis, liver and kidney were taken for the histopathological examination. Biochemical results showed significant elevation in prolactin and FSH levels and significant reduction in LH and testosterone levels in all groups compared to the control group. Increased serum enzymes [ASAT, ALATand ALP] levels with increased concentration of urea and creatinine were detected in all the treated groups compared to the control group. Decline in protein profile and elevation in the concentration of lipid profile, while HDL was decreased in all the treated groups. Histopathological results showed dystrophic changes in the form of congestion in the blood vessels of the testis, liver and kidney of rats with thickening of walls of the blood vessels especially in the testis. In liver, focal inflammatory areas, with dilated and congested central and portal veins were found. Vacuolar degenerative changes in hepatocytes were seen. In the kidney, mild nephritis, sclerotic changes in glomerular tuft, hyaline casts in the lumen of epithelial cells which lining convoluted tubule were noticed. From the previous results we concluded that bisphenol-A has dangerous effects on the testis, liver and kidney tissues. Also it disrupted sexual hormonal pattern and affect biochemical and lipid parameters. So, we recommended minimizing the utililizing of these compound to protect people from its hazardous effects


Subject(s)
Male , Animals, Laboratory , Phenols/adverse effects , Gonadal Steroid Hormones/analysis , Prolactin/blood , Follicle Stimulating Hormone/blood , Testosterone/blood , Testis/pathology , Kidney/pathology , Liver , Histology , Rats
2.
New Egyptian Journal of Medicine [The]. 2010; 43 (1): 46-56
in English | IMEMR | ID: emr-125189

ABSTRACT

Many studies in vitro and in vivo have shown immunomodulating and antiviral activities of Isoprinosine [inosine pranobex]. Chemotherapy means the use of a drug which is most effective at, killing cells that are rapidly dividing. Vinorelbine [Navelbine, 5 oranhydrovinblastine] is a third-generation vinca alkaloid anti-tumor drug. It is widely used in the treatment of cancer such as advanced non-small-cell lung cancer [NSCLC] and advanced breast cancer. The aim of this study was to determine the possible protective effects of Isoprinosine in bacterially infected and non infected mice at a dose level of 8.75 mg/kg/day orally every second day for 15 days under the effect of anticancer Navelbine. Mitochondrial DNA fragmentation, Lipid pereoxidation [MDA], glutathione contents [GSH], phagocytosis test and serum level of immunoglobulin G and M antibodies were evaluated, a significant increase in liver homogenate and mitochondria protein carbonyl levels was observed in Navelbine alone treated mice when compared to control group. DNA fragmentation in homogenate and mitochondria was significantly increased in all test groups when compared to control group except Isoprinosine treated animal group which showed significant decrease in DNA fragmentation. The results of this study proved the immune protective and immunomodulatory effects of Isoprinosine against Navelbine induced toxicity in Pseudomonas aeruginosa infected and non infected mice


Subject(s)
Male , Animals, Laboratory , Vinblastine/analogs & derivatives , Oxidative Stress , Lipid Peroxidation , Glutathione , Protective Agents , Inosine Pranobex , Treatment Outcome
3.
Egyptian Journal of Hospital Medicine [The]. 2006; 25 (December): 630-655
in English | IMEMR | ID: emr-76502

ABSTRACT

The present study is an attempt to evaluate the protective effect of schistosomula antigen and the current antischistosomal drug praziquantel [PZQ] as a reference drug on mice infected with S. mansoni. Mice were vaccinated by irradiated or non-irradiated schistosomula antigen, both at a dose of 100 ug protein/mice once weekly for 3 weeks, before infection with a live cercariae and compared with the treatment with i.m. injection of praziquantel at a dose, of 40 mg/kg b.wt. 4 times once weekly for 4 weeks after infection. The degree of resistance or protection induced by immunization and chemotherapy was assessed 45 days post-infection and evaluated by physiological, parasitological, immunological as well as histological parameters. The results indicated that immunization with lambda irradiated antigen at 20 Krad or the treatment with PZQ resulted in significant reduction in ova count in liver and intestine tissues more than those vaccinated with non-irradiated antigen compared with infected group. Immunized group with irradiated antigen and the group treated with PZQ showed a significant decrease in liver enzymes activity [ALT, AST and lambda -GT], while in immunized group with non-irradiated antigen, there was a significant increase in AST and lambda -GT as compared to infected group. The level of alkaline phosphatase enzyme was significantly increased in all investigated groups compared to infected one. Treatment with PZQ or immunization with irradiated or non-irradiated schistosomula antigen induced amelioration in serum IL-10 and TNF-alpha. Scanning electron microscope demonstrated normal mature worms in infected group after 45 days from infection. In contrast, many changes were detected in the rest groups as alterations in the tegument, implosion of tubercles which appeared pealed and sloughed off and most of the spines were detached and separated. Histological examination of liver sections of infected mice revealed lobular cellular infiltration and cloudy swelling in hepatocytes with occurrence of necrotic foci. Also, granuloma of infiltrating cells was noticed around the portal structures and inbetween the degenerated cells. Congested portal vein could be seen lodged with adult worms and the portal tracts showed fibrous thickening. Whereas, the lung revealed destructed bronchioles which appeared surrounded by intense inflammatory foci. Thickened interalveolar septae were also marked, however many alveoli appeared with shed destroyed epithelium. Moreover, peribronchiolar and perivascular fibrosis was quite prominent. Gross pathological alterations were observed in both liver and lung of immunized groups with non-irradiated antigen. In controversy, immunization with irradiated antigen can reduce the granulomatous reaction and collagen deposition. There are also little inflammation and less congestion, however the hepatic and pulmonary architectures appeared otherwise normal. The present histological findings proved that PZQ has a valuable schistosomicidal effect but some pathological changes are still detectable. On the whole, it could be concluded that irradiated antigen produced marked protection against S.mansoni infection and this may reflect its possible beneficial effect on the diseased liver and lung


Subject(s)
Animals, Laboratory , Animals , Protective Agents , Antigens/immunology , Immunization , Praziquantel/drug therapy , Liver Function Tests , Liver/pathology , Histology , Lung/pathology , Microscopy, Electron, Scanning , Mice
4.
Journal of the Egyptian Society of Toxicology. 2004; 30: 117-129
in English | IMEMR | ID: emr-66689

ABSTRACT

The present study investigates the interaction of Dexamethasone with acute inflammation induced by Carrageenan [CGN] in the presence of the synthetic insecticide pyrethroid. Sixty adult male Sprague Dawly rats were utilized to study the immunological, histological and ultrastructure of the spleen, thymus gland and skeletal muscles. The animals were divided into six groups: Control group, carrageenan-treated group, carrageenan-dexamathasone-treated group, and three insecticide exposed groups, one of them was exposed to insecticidal preparation only whereas the two other groups were treated with either CGN or CGN with dexamethasone. Microscopic examination of spleen and thymus gland parraffin sections of the CGN animals showed distortion of their normal architecture, degenerative changes and dilated and congested blood capillaries. Moreover, hyaline appearance, hemorrhage, cellular debris and necrosis could be observed. Extensive changes in the skeletal muscles were observed, while electron microscopic examination revealed irregular shaped nuclei and mitochondria. In addition insecticide-exposed CGN treated groups have shown microscopic degenerative changes both in spleen and thymus. These degenerative changes disappeared when treated with dexamethasone. Ultrastructure examination showed highly disintegrated myofilaments and completely degenerated mitochondria of the skeletal muscle. This study included also the determination of serum total protein, albumin, globulin and total immunoglobulin G, which recorded a disturbance in the immunoresponse, especially in the carrageenan and dexamethasone, pyrethroids-exposed groups


Subject(s)
Animals, Laboratory , Dexamethasone , Drug Interactions , Rats , Male , Spleen/ultrastructure , Thymus Gland/ultrastructure , Immunohistochemistry , Microscopy, Electron , Immunoglobulin G/blood , Pyrethrins
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