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Protective and therapeutic effects of molsidomine on radiation induced neural injury in rats.
- Source :
-
Biotechnic & histochemistry : official publication of the Biological Stain Commission [Biotech Histochem] 2017; Vol. 92 (1), pp. 68-77. Date of Electronic Publication: 2017 Feb 06. - Publication Year :
- 2017
-
Abstract
- We investigated the protective and therapeutic effects of molsidomine (MOL) in a rat model of whole brain radiotherapy (RT). Forty female rats were divided into five groups of eight: group 1, control; group 2, 15 Gy single dose RT (RT); group 3, 4 mg/kg MOL treated for 5 days (MOL); group 4, 4 mg/kg MOL for 5 days, 10 days after RT treatment (RT + MOL); group 5, 4 mg/kg MOL treatment for 5 days before RT treatment and for 5 days after RT treatment (MOL + RT). All rats were sacrificed on day 16. Neurodegenerative changes in the brain and tissue levels of oxidants and antioxidants were evaluated. The oxidative parameters were increased and antioxidant status was decreased in group RT compared to groups MOL + RT and RT + MOL. Histopathological examination showed that treatment with MOL after RT application and treatment with MOL before RT treatment decreased neuronal degeneration. No difference in neuronal appearance was found between groups RT + MOL and MOL + RT. MOL treatment protected the nervous system of rats and may be a treatment option for preventing RT induced neural injury.
- Subjects :
- Animals
Brain metabolism
Female
Glutathione
Malondialdehyde
Molsidomine administration & dosage
Radiation, Ionizing
Radiation-Protective Agents administration & dosage
Radiation-Protective Agents therapeutic use
Rats
Superoxide Dismutase
Brain radiation effects
Molsidomine therapeutic use
Radiation Injuries, Experimental prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 1473-7760
- Volume :
- 92
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biotechnic & histochemistry : official publication of the Biological Stain Commission
- Publication Type :
- Academic Journal
- Accession number :
- 28166419
- Full Text :
- https://doi.org/10.1080/10520295.2016.1271454