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Therapeutic Effects of Azithromycin on Spinal Cord Injury in Male Wistar Rats: A Role for Inflammatory Pathways.
Rismanbaf, Ali; Afshari, Khashayar; Ghasemi, Mehdi; Badripour, Abolfazl; Haj-Mirzaian, Arvin; Dehpour, Ahmad Reza; Shafaroodi, Hamed.
Afiliación
  • Rismanbaf A; Department of Pharmacology and Toxicology, Islamic Azad University Tehran Medical Sciences, School of Pharmacy, Tehran, Iran (the Islamic Republic of).
  • Afshari K; Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran (the Islamic Republic of).
  • Ghasemi M; Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran (the Islamic Republic of).
  • Badripour A; Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts, United States.
  • Haj-Mirzaian A; Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran (the Islamic Republic of).
  • Dehpour AR; Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran (the Islamic Republic of).
  • Shafaroodi H; Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran (the Islamic Republic of).
J Neurol Surg A Cent Eur Neurosurg ; 83(5): 411-419, 2022 Sep.
Article en En | MEDLINE | ID: mdl-34781403
ABSTRACT

BACKGROUND:

Inflammatory responses, including macrophages/microglia imbalance, are associated with spinal cord injury (SCI) complications. Accumulating evidence also suggests an anti-inflammatory property of azithromycin (AZM). MATERIAL AND

METHODS:

Male Wistar rats were subjected to T9 vertebra laminectomy. SCI was induced by spinal cord compression at this level with an aneurysmal clip for 60 seconds. They were divided into three groups the sham-operated group and two SCI treatment (normal saline as a vehicle control vs. AZM at 180 mg/kg/d intraperitoneally for 3 days postsurgery; first dose 30 minutes after surgery) groups. Locomotor scaling and behavioral tests for neuropathic pain were evaluated and compared through a 28-day period. At the end of the study, tissue samples were taken to assess neuroinflammatory changes and neural demyelination using ELISA and histopathologic examinations, respectively. In addition, the proportion of M1/M2 macrophage polarization was assessed by using flow cytometry.

RESULTS:

Post-SCI AZM treatment (180 mg/kg/d for 3 days) significantly improved locomotion (p < 0.01) and decreased sensitivity to mechanical (p < 0.01) and thermal allodynia (p < 0.001). Moreover, there was a significant tumor necrosis factor-α (TNF-α) decline (p < 0.01) and interleukin-10 (IL-10) elevation (p < 0.01) in the spinal cord tissue of the AZM-treated group compared with the control groups 28 days post-SCI. AZM significantly improved neuroinflammation as evidenced by reduction of the M1 expression, elevation of M2 macrophages, and reduction of the M1/M2 ratio in both the dorsal root ganglion and the spinal cord tissue after SCI compared with controls (p < 0.01).

CONCLUSION:

AZM treatment can be considered a therapeutic agent for SCI, as it could reduce neuroinflammation and SCI sensory/locomotor complications.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Traumatismos de la Médula Espinal / Azitromicina Límite: Animals Idioma: En Revista: J Neurol Surg A Cent Eur Neurosurg Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Traumatismos de la Médula Espinal / Azitromicina Límite: Animals Idioma: En Revista: J Neurol Surg A Cent Eur Neurosurg Año: 2022 Tipo del documento: Article