Does exogenous melatonin influence the free radicals metabolism and pain sensation in rat?
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
11829321
Knihovny.cz E-zdroje
- MeSH
- bolest farmakoterapie metabolismus MeSH
- fyzické omezení MeSH
- fyzikální stimulace MeSH
- fyziologický stres farmakoterapie metabolismus MeSH
- hyperalgezie farmakoterapie metabolismus MeSH
- krysa rodu Rattus MeSH
- látky reagující s kyselinou thiobarbiturovou metabolismus MeSH
- melatonin farmakologie MeSH
- měření bolesti účinky léků MeSH
- oxidační stres účinky léků MeSH
- potkani Wistar MeSH
- scavengery volných radikálů farmakologie MeSH
- volné radikály metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- látky reagující s kyselinou thiobarbiturovou MeSH
- melatonin MeSH
- scavengery volných radikálů MeSH
- volné radikály MeSH
Melatonin has been shown to play a role in antioxidative defence. We therefore studied its effect on oxidative damage to the rat cerebral cortex evoked by painful stimulation and immobilization-induced stress. Moreover, the effect of melatonin on chronic pain perception was examined. Rats were injected with either a high dose of melatonin (100 mg/kg i.p.) or a vehicle for five days and were subjected to painful stimulation or immobilization stress 30 min after the treatment. To determine the degree of oxidative stress, the levels of free radicals, thiobarbituric acid reactive substances (TBARS) as indicators of lipid peroxidation and glutathione peroxidase (GSHPx) were estimated in somatosensory cortex. Pain perception was measured by the tail-flick and plantar test. Melatonin reduced the level of TBARS previously increased by painful stimulation. Melatonin also exhibited a slight analgesic effect in those animals exposed to painful stimulation but its role in free radical scavenging did not contribute to this effect.
Assessment of biochemical markers in patients with pain of vascular origin