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Azathioprine as a Neuroprotective Agent in Experimental Traumatic Spinal Cord Injury
- Publication Year :
- 2021
- Publisher :
- TURKISH NEUROSURGICAL SOC, 2021.
-
Abstract
- WOS:000631709500009 PMID: 33372253 AIM: To evaluate the protective effects of azathioprine, a macrophage-inhibiting agent, on secondary injury in spinal cord trauma. MATERIAL and METHODS: A total of 40 Wistar rats were randomly divided into 4 groups. All the animals had undergone T8-10 laminectomy. Except in group I (control), all the animals were exposed to spinal cord trauma at the T9 level. Animals in group II (trauma) received no treatment following trauma. Animals in group 3 (treatment) and group IV (vehicle) were given intraperitoneal azathioprine 4 mg/kg and saline 2 ml, respectively, 30 minutes after the trauma. Half of the animals in each group were sacrificed 24 hours after injury and specimens were used for biochemical and immunohistochemical evaluations. The rest of the animals were followed-up for 4 weeks in terms of neurological functions and were also sacrificed to perform the histopathological analysis. RESULTS: Significant decrease in apoptotic cells and improved neurological function were observed in the animals treated with azathioprine. Biological and immunohistochemical analysis also showed less oxidative stress in this group compared to those without treatment. CONCLUSION: Azathioprine, a potent macrophage-inhibiting agent, has been shown to decrease the extent of secondary injury following spinal cord trauma.
- Subjects :
- Male
Traumatic spinal cord injury
medicine.medical_treatment
Azathioprine
Spinal cord injury
medicine.disease_cause
Neuroprotection
Trauma
Thoracic Vertebrae
Random Allocation
medicine
Animals
Rats, Wistar
Saline
Spinal Cord Injuries
business.industry
Laminectomy
Secondary injury
Rats
Oxidative Stress
Neuroprotective Agents
Apoptosis
Anesthesia
Immunohistochemistry
Rat
Surgery
Neurology (clinical)
business
Oxidative stress
Immunosuppressive Agents
medicine.drug
Subjects
Details
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....f83b85efc591671f72443d8b863cd1ca