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1.
Eur. j. anat ; 23(3): 201-213, mayo 2019. ilus, graf, tab
Artigo em Inglês | IBECS | ID: ibc-182981

RESUMO

Cisplatin is a potent chemotherapeutic agent used to treat a variety of cancers such as ovarian, uterine, and bladder. The major limiting side effect of cisplatin is its hepatotoxicity. The possible mechanism of cisplatin hepatotoxicity was due to the affection of oxidant-antioxidant system. Platelet-rich plasma (PRP) has a powerful therapeutic option for its ability to deliver a great variety of biologically active GFs to the site of injury. PRP has grown as an attractive biologic instrument in regenerative medicine for its powerful healing properties. It is considered as a source of growth factors that may induce tissue repairing and improve fibrosis. This product has proven its efficacy in multiple studies, but its effect on cisplatin-induced hepatotoxicity has not yet been elucidated. The present study was designed to analyze the therapeutic role of PRP in cisplatin-induced hepatotoxicity. 30 adult male adult male albino rats were used in the present study divided into 3 groups (control group, cisplatin-treated group and PRP-treated group). By the end of the experimental period, blood samples were collected for measurement of serum AST, ALT and ALP enzymes; then the rats were sacrificed by cervical dislocation. Fresh liver parts were used to measure the oxidative markers in liver homogenates, while other parts were processed and subjected for histopathological and histomorphometric and immunohistochemical analyses for VEGF, Caspase 3 expression of the different experimental groups. The statistical study was done for the resultant data. Group II (Cisplatin-treated group) showed marked pathological hepatic changes; loss of architecture, congested dilated sinusoids lined by darkly stained pyknotic Kupffer cells; and hepatocytes nuclei were pyknotic and karyolitic. Dilated congested portal vein, interstitial acidophilic exudate, marked polymorphic cellular infiltration. There were increased collagen fibers deposition, a weak positive PAS reaction, strong positive caspase 3 reactions and strong positive VEGF reaction. Also, there were a marked increase in hepatic enzymes, MDA levels and a marked decrease in GSH level. Treatment with PRP in Group III revealed improvement of the hepatic parenchymal architecture with strong PAS reaction and minimal collagen fibers deposition. Weak positive caspase immunoreaction and strong positive VEGF reaction were noticed. Also, there was a marked improvement in the parameter of hepatic enzymes, MDA and GSH level comparable with the control group. It is concluded that PRP could ameliorate the liver against cisplatin-induced hepatotoxicity


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Assuntos
Animais , Ratos , Terapêutica , Plasma Rico em Plaquetas/química , Cisplatino/toxicidade , Fator Apoptótico 1 Ativador de Proteases/toxicidade , Caspase 3/toxicidade , Fator Apoptótico 1 Ativador de Proteases/efeitos adversos , Plasma Rico em Plaquetas/enzimologia , Imuno-Histoquímica , Receptores de Fatores de Crescimento do Endotélio Vascular/administração & dosagem , Projetos de Pesquisa , Fígado/química , Fígado/enzimologia , Biomarcadores , Análise de Variância
2.
Eur. j. anat ; 23(2): 113-119, mar. 2019. ilus, tab
Artigo em Inglês | IBECS | ID: ibc-182421

RESUMO

Nephrotoxicity is considered the most important side effect which limits cisplatin therapy in various diseases. It is might be due to oxidative stress, decreased renal blood flow and reduction in the glomerular filtration. Sildenafil citrate is used for treatment of erectile dysfunction, but its effect in ameliorating cisplatin nephrotoxicity was not yet clearly studied. So the present work aimed to evaluate the protective role of Sildenafil citrate against cisplatin-induced nephrotoxicity in adult male albino rats. 24 adult male albino rats were divided into 4 groups (6 rats each): Group I, control; Group II, sham control; Group III, Cisplatin-treated group, and Group IV, Sildenafil-and-Cisplatin-treated group. At the end of the experiment, the kidney of each animal was excised, trimmed and prepared for histological, histochemical and immunohistochemical study. Blood samples were obtained to evaluate the kidney functions. Kidney sections of Group III showed marked degenerative changes in the proximal convoluted tubules, vacuolations, exfoliation of the lining epithelium, cast formation and interstitial hemorrhagic exudate. There was marked elevation of serum creatinine and urea with significant increase in nitric oxide (NO) and decrease in glutathione reductase (GSH) concentrations in the kidney tissue and weak periodic acid Schiff (PAS) reaction. Treatment with Sildenafil citrate in Group IV offered marked improvement in the renal structure, kidney function tests and other parameters. The present study concluded that Sildenafil citrate could protect the kidney against Cisplatin-induced nephrotoxicity in adult male albino rat


No disponible


Assuntos
Animais , Ratos , Estresse Oxidativo/efeitos dos fármacos , Citrato de Sildenafila/efeitos adversos , Antineoplásicos/efeitos adversos , Nefropatias/induzido quimicamente , Cisplatino/efeitos adversos , Ratos Sprague-Dawley , Animais de Laboratório/anatomia & histologia
3.
Ann Anat ; 196(5): 336-51, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25048844

RESUMO

BACKGROUND: Age related changes in the lacrimal gland are associated with alterations in the structural organization and functional response in the gland of diverse mammalian species. Dry eye syndrome is one of the most common ocular problems in the world especially in old age. It results when the lacrimal gland fails to secrete proteins and fluid in sufficient quantity or appropriate composition. AIM OF THE WORK: The present study is designed to demonstrate the influence of aging on the structure of the lacrimal gland of albino rat and to provide a morphological basis to explain the pathogenesis of the dry eye syndrome with ageing. It also aims to carry out a comparative analysis of age-dependent changes in male and female rats and to address how the lacrimal gland ages in each sex. MATERIAL AND METHODS: Eighty albino rats were used in this study. The animals were divided into two age groups, young adult and senile. Tear secretion was measured using a modified Schirmer test. Corneal impression cytology of the anesthetized rats was done. The glands were subjected to gross morphologic examination, microscopic examination using H&E, PAS, Masson's trichrome and Giemsa stains. Electron microscopic examination was done in addition to quantitative histomorphometric estimations included acinar density, ductal count and mast cell count. RESULTS: Light microscopic examination of the lacimal glands of the senile rats revealed different pathological changes. These included acinar, ductal as well as stromal changes. Electron microscope examination of the lacrimal gland of the senile group showed a decrease in the electron dense secretory vesicles, mitochondrial swelling and lipofuscin-like inclusions were frequently seen in the cytoplasm of acinar cells in senile rats. CONCLUSION: The structural changes in the lacrimal glands of senile rats were associated with reduction in tear secretion as well as alterations in corneal epithelium. Gender difference in lacrimal gland structure was recorded.


Assuntos
Envelhecimento/fisiologia , Aparelho Lacrimal/crescimento & desenvolvimento , Animais , Contagem de Células , Colágeno/metabolismo , Feminino , Inflamação/patologia , Aparelho Lacrimal/anatomia & histologia , Aparelho Lacrimal/ultraestrutura , Masculino , Microscopia Eletrônica , Ratos , Ratos Wistar , Caracteres Sexuais
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