Modulation of ionising radiation generated oxidative stress by HI-6 (asoxime) in a laboratory rat model
Language English Country Sweden Media print
Document type Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
21187825
PII: NEL31S210A10
Knihovny.cz E-resources
- MeSH
- Antidotes pharmacology MeSH
- Antioxidants pharmacology MeSH
- Glutathione Reductase metabolism MeSH
- Radiation, Ionizing MeSH
- Liver drug effects metabolism radiation effects MeSH
- Rats MeSH
- Thiobarbituric Acid Reactive Substances metabolism MeSH
- Models, Animal MeSH
- Oxidative Stress drug effects radiation effects MeSH
- Oximes pharmacology MeSH
- Rats, Wistar MeSH
- Pyridinium Compounds pharmacology MeSH
- Spleen drug effects metabolism radiation effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antidotes MeSH
- Antioxidants MeSH
- asoxime chloride MeSH Browser
- Glutathione Reductase MeSH
- Thiobarbituric Acid Reactive Substances MeSH
- Oximes MeSH
- Pyridinium Compounds 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.
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