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1.
J Neurosci Methods ; 156(1-2): 154-60, 2006 Sep 30.
Article in English | MEDLINE | ID: mdl-16621014

ABSTRACT

Immunohistochemistry is an important tool that is often used for the diagnosis of pathologies; however, the length of time required to process the tissue is relatively long. Furthermore, the quality and sensitivity of immunohistochemical staining is affected by formalin fixation which results in variable loss of antigenicity, known as masking effect. Here we assess the effect of microwave irradiation on the incubation time required to obtain high quality immunohistochemical staining for cox-2 using archival formalin-fixed, paraffin-embedded human oligodendrogliomas and astrocytomas. The results show that intermittent microwave irradiation during the incubation with the primary antibody reduced the time requirement to 5 min while the staining quality was indistinguishable from 1 or 24 h long incubations. Thus, the use of this procedure results in a significant saving of time which is important for a timely diagnosis of pathological conditions that await treatment.


Subject(s)
Antigens, Neoplasm/isolation & purification , Astrocytoma/immunology , Brain Neoplasms/immunology , Cyclooxygenase 2/immunology , Oligodendroglioma/immunology , Calibration , Fixatives , Formaldehyde , Humans , Immunohistochemistry , Microwaves , Paraffin Embedding
2.
Acta Histochem ; 107(6): 421-34, 2006.
Article in English | MEDLINE | ID: mdl-16256175

ABSTRACT

In this study, we aimed to investigate the effect of vitamin A on the transformation of the Ito cells to fibrogenic form and suppression of the development of fibrosis. Carbon tetrachloride intoxication was performed on rats for 2, 8, 12 or 20 weeks and 5x10(4) IU vitamin A (as retinol palmitate) was injected subcutaneously once every 4 weeks. Ito cells were detected by gold chloride impregnation, as well as desmin and alpha-smooth muscle actin (alpha-SMA) immunohistochemistry. Additionally, all groups were examined ultrastructurally. The number of Ito cells that were labelled positively with gold impregnation decreased in the fibrotic groups; however, alpha-SMA and desmin immunopositive Ito cells increased. The samples from animals that were treated with vitamin A showed an increase in labelling with gold impregnation but a decrease in alpha-SMA immunopositivity. The data showed that vitamin A can prevent hepatic injury, by suppressing the transformation of Ito cells to fibrogenic form. We conclude that vitamin A has potential for the treatment of hepatic fibrotic diseases. Alpha-SMA immunohistochemistry was found to be more informative than desmin immunohistochemistry for monitoring liver fibrosis.


Subject(s)
Hepatocytes/drug effects , Liver Cirrhosis/prevention & control , Vitamin A/therapeutic use , Actins/analysis , Animals , Antioxidants/pharmacology , Antioxidants/therapeutic use , Carbon Tetrachloride , Cell Proliferation/drug effects , Desmin/analysis , Gold Compounds/analysis , Hepatocytes/chemistry , Hepatocytes/pathology , Hepatocytes/ultrastructure , Histocytochemistry , Immunohistochemistry , Liver Cirrhosis/chemically induced , Liver Cirrhosis/drug therapy , Liver Cirrhosis/pathology , Male , Microscopy, Electron , Rats , Rats, Wistar , Vitamin A/pharmacology
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