Modulation of ionising radiation generated oxidative stress by HI-6 (asoxime) in a laboratory rat model
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem
PubMed
21187825
PII: NEL31S210A10
Knihovny.cz E-zdroje
- MeSH
- antidota farmakologie MeSH
- antioxidancia farmakologie MeSH
- glutathionreduktasa metabolismus MeSH
- ionizující záření MeSH
- játra účinky léků metabolismus účinky záření MeSH
- krysa rodu Rattus MeSH
- látky reagující s kyselinou thiobarbiturovou metabolismus MeSH
- modely u zvířat MeSH
- oxidační stres účinky léků účinky záření MeSH
- oximy farmakologie MeSH
- potkani Wistar MeSH
- pyridinové sloučeniny farmakologie MeSH
- slezina účinky léků metabolismus účinky záření MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antidota MeSH
- antioxidancia MeSH
- asoxime chloride MeSH Prohlížeč
- glutathionreduktasa MeSH
- látky reagující s kyselinou thiobarbiturovou MeSH
- oximy MeSH
- pyridinové sloučeniny MeSH
OBJECTIVES: HI-6 is an antidotum suitable for treatment of intoxication by nerve agents. The recent investigation appointed its modulation of inflammatory response as well as vegetative nervous system activity. However, the present experiments were carried out in order to assess the antioxidant effect of HI-6 in irradiated animals. METHODS: male Wistar rats were irradiated by ionizing radiation (7.5 Gy, LD50/30). Animals were divided into four groups: i.e. controls (A), irradiated (B), treated with HI-6 (C), and both irradiated and treated with HI-6 (D). Ferric reducing antioxidant power (FRAP), thiobarbituric acid reactive substances (TBARS) and glutathione reductase activity were assayed in liver, spleen, plasma, and whole blood. Clinical biochemistry markers were determined in plasma samples. RESULTS: We found significantly increased FRAP levels in liver, while its levels decreased in the spleen of B group animals. Ionising radiation (B group) also significantly elevated TBARS values in spleen. HI-6 reversed FRAP and TBARS values to control levels. Glutathione reductase activity was significantly elevated in spleen and liver of animals exposed to HI-6 (C and D groups). Clinical biochemistry markers were shifted only slightly. The in vitro test confirmed the inhibitory effect of HI-6 towards acetylcholinesterase. CONCLUSIONS: In conclusion, HI-6 is potent in suppressing oxidative stress and might be a promising drug in the field of radiation protection.
Alpha7 nicotinic acetylcholine receptor is a target in pharmacology and toxicology