Aripiprazole Improves Spinal Cord Injury in Rats: Involvement of Inflammatory Pathways

Ali Rismanbaf; Khashayar Afshari; Nazgol-Sadat Haddadi; Ahmad Reza Dehpour; Hamed Shafaroodi

doi:10.18502/acta.v60i9.11100

Ali Rismanbaf Department of Pharmacology and Toxicology, School of Pharmacy, Tehran Azad University of Medical Sciences, Tehran, Iran
Khashayar Afshari Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran
Nazgol-Sadat Haddadi Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran
Ahmad Reza Dehpour Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran
Hamed Shafaroodi Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran

DOI: https://doi.org/10.18502/acta.v60i9.11100

Keywords: Aripiprazole; Spinal cord injury; Neuropathy; Neuroinflammation; Microglia; Macrophages

Abstract

Macrophages and glial activation contribute to the pathophysiology of spinal cord injury (SCI). Some preclinical studies have shown the anti-inflammatory effects of aripiprazole (ARP). In the current study, we evaluated the anti-inflammatory effects of ARP in a rat SCI model. Forty male Wistar rats underwent either T9 vertebra laminectomy or were used as a sham-operated group without laminectomy. There were four major groups in this study: a sham-operated, three treatments (normal saline [vehicle] control versus ARP 10 and 20 mg/kg/day for three days after surgery, first dose 30 minutes post-surgery) SCI groups. We evaluated locomotor scaling and neuropathic pain behavioral tests over 28 days. On Day 28, tissue samples were investigated for neuroinﬂammatory and histopathology changes through flow cytometry and ELISA. ARP (10 and 20 mg/kg/day, 3 days) treatment significantly reduced locomotors disability (P<0.01) and mechanical (P<0.01) and thermal allodynia (P<0.001) scores. Additionally, Levels of tumor necrosis factor (TNF)-α level and interleukin (IL)-10 were significantly altered in ARP-treated spinal cord tissues 28 days after SCI (P<0.01). Moreover, spinal cord tissue expression of M1 and M2 macrophages, as well as M1/M2 ratio, were reduced in ARP-treated SCI animals, concurrent with decreased M1 and increased M2 and M1/M2 in dorsal root ganglion (P<0.001). Our study indicates that ARP has therapeutic effects on SCI via the reduction of neuroinflammation and SCI sensory and locomotor abnormalities.