| Literature DB >> 25931161 |
Camilo Ríos1, Sandra Orozco-Suarez, Hermelinda Salgado-Ceballos, Marisela Mendez-Armenta, Concepción Nava-Ruiz, Iván Santander, Veronica Barón-Flores, Nadia Caram-Salas, Araceli Diaz-Ruiz.
Abstract
Spinal cord injury (SCI) is a condition producing irreversible damage to the neurological function. Among the leading mechanisms associated to cell death after SCI, excitotoxicity, oxidative stress, inflammatory response and apoptosis are considered potential targets to prevent tissue damage. We recently reported that dapsone an anti-inflammatory drug, decreases the activity of myeloperoxidase, lipid peroxidation, improve neurological function and increase the amount of spared tissue after SCI in rats. In this study, we characterized the anti-apoptotic effect of dapsone administered at 12.5 mg/kg/24 h dose, starting at 3 and 5 h after SCI. We monitored the activity of caspases-8, 9, and 3 and quantitated Annexin V and TUNEL positive cells in the core of the lesion. Results showed increased activities of caspase-8, 9 and 3 at 72 h by SCI to reach increments of 69, 143 and 293 %, respectively, as compared to sham group. Meanwhile, dapsone, administered at 3 and 5 after SCI, reduced caspase-8 activity by 36 and 44 % respectively, whereas the activity of caspase-9 was diminished by 37 %. Likewise, the activity of caspase-3 showed a decrease of 38 %. Finally, both Annexin V and TUNEL-positive cells were significantly reduced by DDS as compared to untreated SCI animals. Results showed that dapsone exerted anti-apoptotic effect after SCI.Entities:
Mesh：
Substances：
Year: 2015 PMID： 25931161 DOI： 10.1007/s11064-015-1588-z
Source DB: PubMed Journal: Neurochem Res ISSN： 0364-3190 Impact factor: 3.996