Neuroprotective effects of atomoxetine against traumatic spinal cord injury in rats

Authors

  • Cui-Jun Jiang Department of Orthopedics, Hospital of Qingdao University, Qingdao, Shandong, 266000, China
  • Li Yu Department of Pharmacy, Qilu Hospital of Shandong University (Qingdao Hospital District),Qingdao, Shandong, 266000, China
  • Qing-Xian Hou Department of Orthopedics, Hospital of Qingdao University, Qingdao, Shandong, 266000, China
  • Shao-Qi Tian Department of Orthopedics, Hospital of Qingdao University, Qingdao, Shandong, 266000, China
  • Wen-Jiu Yang Department of Orthopedics, Hospital of Qingdao University, Qingdao, Shandong, 266000, China
  • Zhi-Jie Wang Department of Orthopedics, Hospital of Qingdao University, Qingdao, Shandong, 266000, China
Abstract:

Objective(s):Spinal cord injury (SCI) often causes serious and irreversible neurological deficit leading to disability or impairment of normal physical activity. Atomoxetine, a selective norepinephrine transporter (NET) inhibitor has gained much attention in the field of the neurodevelopmental disorder, but its effect on SCI has not been evaluated. The present study has been undertaken to investigate the neuroprotective effects of atomoxetine. Materials and Methods: Administration of atomoxetine 20 mg/kg IP was compared with methylprednisolone (MP) 30 mg/kg IP in traumatic spinal cord injured Wistar rats. Tissue samples were evaluated for apoptosis, inflammation, and oxidative stress, along with histopathological examination and neurological evaluation. Results: There was no significant difference in the caspase-3 activity between the control and the sham groups or between the MP and the atomoxetine groups (P=0.811). The administration of atomoxetine significantly reduced tissue tumour necrosis factor alpha (TNF-α), and nitric oxide (NO) levels compared to the trauma group (P

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Journal title

volume 19  issue 3

pages  272- 280

publication date 2016-03-01

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