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1.
Journal of Veterinary Science ; : 251-254, 2005.
Article in English | WPRIM | ID: wpr-213962

ABSTRACT

Akabane, Aino and Chuzan virus are arthropod-borne (arbo)viruses mainly associated with reproductive failures in cattle. We investigated apoptosis in Vero cells (C-1586) infected with Akabane, Aino and Chuzan virus. The fragmentation of chromosomal DNA was simultaneously detected with the progress of cytopathic effect from 48 hr to 72 hr post infection, depending on viruses. Although the treatment of cycloheximide blocked apoptosis in Vero cells infected with three viruses, actinomycin D did not prevent DNA oligomerization, thus indicating that de novo viral protein synthesis is critical for viral apoptosis. In addition, the activation of caspase-3 was also detected in Vero cells by indirect fluorescent assay. From the present results, it is of future interest whether apoptotic characteristics of these viruses are related to pathogenecity in vivo.


Subject(s)
Animals , Apoptosis/physiology , Bunyaviridae/physiology , Caspase 3 , Caspases/metabolism , Chlorocebus aethiops , Cytopathogenic Effect, Viral/physiology , DNA Fragmentation/physiology , Dactinomycin , Enzyme Activation , Orbivirus/physiology , Vero Cells
2.
Journal of Veterinary Science ; : 11-18, 2004.
Article in English | WPRIM | ID: wpr-178957

ABSTRACT

Accurate estimation of the exposure-response relationship between ambient urban particulate matters (PM) and public health is important for regulatory perspective of ambient urban particulate matters (PM). Ambient PM contains various transition metals and organic compounds. PM10 (aerodynamic diameter less than 10 microgram) is known to induce diverse diseases such as chronic cough, bronchitis, chest illness, etc. However, recent evaluation of PM2.5 (aerodynamic diameter less than 2.5 microgram) against health outcomes has suggested that the fine particles may be more closely associated with adverse respiratory health effects than particles of larger size. This study was performed to evaluate PM2.5-induced oxidative stress in rat lung epithelial cell in order to provide basic data for the risk assessment of PM2.5. PM2.5 showed higher cytotoxicity than PM10. Also, PM 2.5 induced more malondialdehyde (MDA) formation than PM10. In Hoechst 33258 dye staining and DNA fragmentation assay, apopotic changes were clearly detected in PM2.5 treated cells in compared to PM10. Expression of catalase mRNA was increased by PM2.5 rather than PM10. PM2.5 induced higher Mth1 mRNA than PM10. In pBR322 DNA treated with PM2.5, production of single strand breakage of DNA was higher than that of PM10. In Western blot analysis, PM2.5 induced more Nrf-2 protein, associated with diverse transcriptional and anti-oxidative stress enzymes, compared to PM10. Our data suggest that PM2.5 rather than PM10 may be responsible for PM-induced toxicity. Additional efforts are needed to establish the environmental standard of PM2.5.


Subject(s)
Animals , Rats , Air Pollutants/chemistry , Apoptosis/physiology , Benzimidazoles/metabolism , Blotting, Western , Cell Line , Cell Survival/physiology , DNA Fragmentation/physiology , DNA Repair Enzymes/genetics , DNA-Binding Proteins/metabolism , Epithelial Cells/drug effects , Formazans/metabolism , GA-Binding Protein Transcription Factor , Lipid Peroxides/metabolism , Lung Diseases/chemically induced , Oxidative Stress/physiology , RNA, Messenger/chemistry , Reverse Transcriptase Polymerase Chain Reaction , Tetrazolium Salts/metabolism , Transcription Factors/metabolism
3.
Biocell ; 27(2): 213-224, Aug. 2003.
Article in English | LILACS | ID: lil-384241

ABSTRACT

CG 10-248 (3,4-dihydro-2,2-dimethyl-9-chloro-2H-naphtho[1,2b]pyran-5,6-dione; CG-NQ), a beta-lapachone analogue, modified the ultrastructure of rat hepatocytes, as demonstrated by light and electron microscopy. After 4 h incubation with 100 microM CG-NQ, the following effects were observed: (a) nuclear chromatin condensation; (b) chromatin fragmentation; (c) displacement of mitochondria, concentrated around the nucleus; (d) disruption or expansion of mitochondrial outer or inner membranes, respectively; (e) displacement and alteration of endoplasmic reticulum (rough and smooth); (f) decrease of microvilli; (g) blebbing of plasma membrane and production of apoptotic bodies formed by folding of plasma membrane fragments around mitochondria or peroxysomes; and (h) production of hydrogen peroxide. Expression of such effects varied according to hepatocyte samples and taken together strongly support an apoptotic action of CG-NQ dependent on reactive oxygen species.


Subject(s)
Humans , Male , Apoptosis/drug effects , Hepatocytes/drug effects , Naphthoquinones/pharmacology , Naphthoquinones/toxicity , Apoptosis/physiology , Cells, Cultured , Chromatin/drug effects , Chromatin/pathology , Cell Surface Extensions/drug effects , Cell Surface Extensions/pathology , Cell Surface Extensions/ultrastructure , DNA Fragmentation/drug effects , DNA Fragmentation/physiology , Hepatocytes/metabolism , Hepatocytes/ultrastructure , Microscopy, Electron , Intracellular Membranes/drug effects , Intracellular Membranes/pathology , Intracellular Membranes/ultrastructure , Microvilli/drug effects , Microvilli/pathology , Microvilli/ultrastructure , Mitochondria/drug effects , Mitochondria/pathology , Mitochondria/ultrastructure , Hydrogen Peroxide/metabolism , Rats , Rats, Wistar , Endoplasmic Reticulum/drug effects , Endoplasmic Reticulum/pathology , Endoplasmic Reticulum/ultrastructure
4.
Journal of Veterinary Science ; : 279-283, 2002.
Article in English | WPRIM | ID: wpr-148812

ABSTRACT

We examined the localization of the anti-apoptotic molecule Bcl-2 in the spinal cords of Lewis rats with experimental autoimmune encephalomyelitis (EAE). Western blot analysis showed that Bcl-2 was constitutively expressed in normal spinal cords, and weakly increased in response to complete Freund's adjuvant(CFA) immunization. In EAE, with infiltration of inflammatory cells into spinal cords, Bcl-2 declined during the peak stage and further decreased during the recovery stage. Immunohistochemically, some neurons and glial cells constitutively expressed Bcl-2 in normal rat spinal cords. In the spinal cords of rats with EAE, Bcl-2 was also immunoreacted in some perivascular inflammatory cells while some brain cells, such as neurons and GFAP (+) astrocytes showed less Bcl-2 immunoreaction.These findings suggest that in EAE, Bcl-2 expression in the CNS host cells decreases with CNS inflammation, possibly progressing to cell death in some cases, while the survival of host cells, including neurons, astrocytes, and some inflammatory cells, is associated with activation of the anti-apoptotic molecule Bcl-2. Taking all into considerations, its is postulated that Bcl-2 either beneficially or detrimentally functions in some host cells depending on the activation stage of each cell type.


Subject(s)
Animals , Female , Male , Rats , Blotting, Western , DNA Fragmentation/physiology , Encephalomyelitis, Autoimmune, Experimental/metabolism , Immunohistochemistry , In Situ Nick-End Labeling , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats, Inbred Lew , Spinal Cord/metabolism
5.
São Paulo; s.n; 2001. 106 p. ilus, tab, graf.
Thesis in Portuguese | LILACS | ID: lil-313760

ABSTRACT

Investigou-se o efeito do colesterol em enterócitos fetais e na linhagem IEC-6. Para isso, analisou-se a composição dos ácidos graxos, a atividade da citrato sintase e a proliferação dessas células na presença de colesterol. A expressão da HMG-CoA redutase nos intestinos fetais, células IEC-6 e em quatro segmentos intestinais de ratos adultos: duodeno, jejuno, íleo e instestino grosso foi determinada por RT-PCR. Estudou-se a indução da fragmentação do DNA e condensação da cromatina na linhagem IEC-6 pelo colesterol, através de citometria de fluxo e microscopia de fluorescência utilizandoo Hoescht 33342. Avaliou-se o efeito do colesterol na expressão da HMG-CoA redutase e PPAR . Também, o efeito de drogas...


Subject(s)
Animals , Rats , Cholesterol , Enterocytes , DNA Fragmentation/physiology , Intestines , Cell Line , Cell Count/methods , Flow Cytometry , Microscopy, Fluorescence/methods , Microscopy, Fluorescence , Reverse Transcriptase Polymerase Chain Reaction
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