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In JoVE (1)
- भ्रूणीय ventral midbrain के Organotypic स्लाइस संस्कृति: एक डोपामिनर्जिक neuronal विकास अध्ययन प्रणाली इन विट्रो में
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Articles by Gabriela Oana Bodea in JoVE
भ्रूणीय ventral midbrain के Organotypic स्लाइस संस्कृति: एक डोपामिनर्जिक neuronal विकास अध्ययन प्रणाली इन विट्रो में
Gabriela Oana Bodea, Sandra Blaess
Institute of Reconstructive Neurobiology, University of Bonn
E12.5 murine भ्रूण midbrain से organotypic स्लाइस उत्पन्न विधि वर्णित है. organotypic टुकड़ा संस्कृतियों डोपामिनर्जिक न्यूरॉन्स या अन्य वेंट्रल मध्यमस्तिष्क न्यूरॉन्स के व्यवहार का निरीक्षण करने के लिए इस्तेमाल किया जा सकता है.
Other articles by Gabriela Oana Bodea on PubMed
Adapted Response of the Antioxidant Defense System to Oxidative Stress Induced by Deoxynivalenol in Hek-293 Cells
Toxicon : Official Journal of the International Society on Toxinology. Jun, 2011 | Pubmed ID: 21549142
The mycotoxin deoxynivalenol (DON), a contaminant of certain foods and feeds, is cytotoxic and genotoxic to mammalians cells. Exposure of human embryonic kidney (Hek-293) cells to DON led to a dose- and time-dependent decrease in cell viability, with an IC(50) about 7.6 μM. The DON effects on Hek-293 morphology, reactive oxygen species, lipid peroxidation and antioxidative system and caspase 3 and bcl-2 expression were studied. Cells became round and in some are progressive loss of cell attachment appeared. These biochemical parameters were assessed after 6, 12 and 24 h of treatment with 2.5 and 5 μM DON. An increase in superoxide dismutase activity within the interval 6-12 h and almost complete recovery by the end of experiment for both concentrations was observed, whereas the profile of catalase activity was the same with the superoxide dismutase one for 2.5 μM and decreased in a time-dependent manner for 5 μM. A temporary activation of glutathione peroxidase and glutathione reductase was recorded at 12 h post-exposure, while the glutathione-S-transferase activity was unchanged for both concentrations. The NADP(+)-dependent isocitrate dehydrogenase activity showed a transient increase at the 12 h post-exposure. The caspase 3 expression remained unchanged and the bcl-2 one decreased after 24 h of exposure for the two concentrations. Our results showed the dose- and time specific changes in the antioxidants system of Hek-293 cells, which could not counteract efficiently the effects DON exposure. The different types of cell death which could be activated by this DON induced changes are mentioned.