Influence of melatonin pretreatment and preconditioning by hypobaric hypoxia on the development of cortical photothrombotic ischemic lesion
Language English Country Czech Republic Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
17298202
DOI
10.33549/physiolres.931143
PII: 1143
Knihovny.cz E-resources
- MeSH
- Antioxidants administration & dosage metabolism MeSH
- Atmospheric Pressure MeSH
- Rose Bengal radiation effects MeSH
- Endothelial Cells metabolism pathology radiation effects MeSH
- Hypoxia metabolism MeSH
- Intracranial Thrombosis etiology metabolism pathology MeSH
- Brain Ischemia complications prevention & control MeSH
- Rats MeSH
- Melatonin administration & dosage metabolism MeSH
- Cerebral Cortex metabolism pathology MeSH
- Neuroprotective Agents administration & dosage metabolism MeSH
- Rats, Wistar MeSH
- Ischemic Preconditioning methods MeSH
- Severity of Illness Index MeSH
- Light MeSH
- Free Radicals adverse effects metabolism radiation effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Antioxidants MeSH
- Rose Bengal MeSH
- Melatonin MeSH
- Neuroprotective Agents MeSH
- Free Radicals MeSH
Photothrombotic model of ischemia (PT) is based on free radical-mediated endothelial dysfunction followed by thrombosis. Free radicals are also involved in hypoxic preconditioning. We tested the sensitivity of PT to preconditioning with hypobaric hypoxia and to pretreatment with melatonin. In adult Wistar rats, after intravenous application of Rose Bengal, a stereo-tactically defined spot on the denuded skull was irradiated by a laser for 9 min. The first experimental group underwent hypobaric hypoxia three days before irradiation. In the second experimental group, melatonin was applied intraperitoneally one hour before irradiation. Three days after irradiation, animals were sacrificed, the brains perfused, and stained with TTC. Ischemic lesions were divided into grades (I, II, III). In the control group (where no manipulation preceded photothrombosis), most animals displayed deep damage involving the striatum (grade III). The group pre-exposed to hypoxia showed similar results. Only 28.57 % of the melatonin pretreated animals exhibited grade III lesions, and in 57.14 % no signs of lesions were detected. Pre-exposure to hypoxia was not protective in our model. Pretreatment with melatonin lead to a significant reduction of the number of large ischemic lesions. This result is probably caused by protection of endothelial cells by melatonin.
References provided by Crossref.org
Perinatal hypoxic-ischemic damage: review of the current treatment possibilities