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Antibiotics With Therapeutic Effects on Spinal Cord Injury: A Review Publisher Pubmed



Afshari K1, 2, 3 ; Momeni Roudsari N4 ; Lashgari NA4 ; Haddadi NS1, 2, 3 ; Hajmirzaian A2 ; Hassan Nejad M5 ; Shafaroodi H2 ; Ghasemi M6 ; Dehpour AR1, 2 ; Abdolghaffari AH4, 7, 8
Authors
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Authors Affiliations
  1. 1. Brain and Spinal Cord Injury Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, 1419733141, Iran
  2. 2. Experimental Medicine Research Center, Tehran University of Medical Sciences, P.O. Box 13145-784, Tehran, Iran
  3. 3. Department of Dermatology, University of Massachusetts Medical School, Worcester, 01655, MA, United States
  4. 4. Department of Toxicology & Pharmacology, Faculty of Pharmacy, Tehran Medical Sciences, Islamic Azad University, No. 99, Yakhchal, Gholhak, Shariati St., Tehran, P. O. Box: 19419-33111, Iran
  5. 5. Department of Infectious Diseases, Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran, 1419733141, Iran
  6. 6. Department of Neurology, University of Massachusetts School of Medicine, Worcester, 01655, MA, United States
  7. 7. Medicinal Plants Research Center, Institute of Medicinal Plants, ACECR, Karaj, 31375-1369, Iran
  8. 8. Gastrointestinal Pharmacology Interest Group (GPIG), Universal Scientific Education and Research Network (USERN), Tehran, 1419733151, Iran

Source: Fundamental and Clinical Pharmacology Published:2021


Abstract

Accumulating evidence indicates that a considerable number of antibiotics exert anti-inflammatory and neuroprotective effects in different central and peripheral nervous system diseases including spinal cord injury (SCI). Both clinical and preclinical studies on SCI have found therapeutic effects of antibiotics from different families on SCI. These include macrolides, minocycline, β-lactams, and dapsone, all of which have been found to improve SCI sequels and complications. These antibiotics may target similar signaling pathways such as reducing inflammatory microglial activity, promoting autophagy, inhibiting neuronal apoptosis, and modulating the SCI-related mitochondrial dysfunction. In this review paper, we will discuss the mechanisms underlying therapeutic effects of these antibiotics on SCI, which not only could supply vital information for investigators but also guide clinicians to consider administering these antibiotics as part of a multimodal therapeutic approach for management of SCI and its complications. © 2020 Societe Francaise de Pharmacologie et de Therapeutique
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