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Hypoxia/Ischemia a Key Player in Early Post Stroke Seizures: Modulation by Opioidergic and Nitrergic Systems Publisher Pubmed



Gooshe M1, 2, 3 ; Abdolghaffari AH4, 5 ; Aleyasin AR1, 2, 3 ; Chabouk L3 ; Tofigh S3 ; Hassanzadeh GR6 ; Payandemehr B3 ; Partoazar A3 ; Azizi Y7 ; Dehpour AR1, 3
Authors
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Authors Affiliations
  1. 1. Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Students Scientific Research Center (SSRC), Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Pharmacology and Applied Medicine, Department of Medicinal Plants Research Center, Institute of Medicinal Plants, Karaj, Iran
  5. 5. International Campus, ICTUMS, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Department of Physiology, School of Medicine, Tehran University of Medical Science, Tehran, Iran

Source: European Journal of Pharmacology Published:2015


Abstract

Stroke is a leading cause of death, disability, and socioeconomic loss worldwide. All attempts at pharmacological reduction of the complications of stroke (e.g. post-stroke seizure, and brains vulnerability to hypoxic/ischemic injury) have failed. Endogenous opioids and nitric oxide (NO) overproduction has been documented in brain hypoxia/ischemia (H/I), which can exert pro-convulsive effects. In this study, we aimed to examine the possible involvement of opioidergic and nitrergic pathways in the pathogenesis of post-stroke seizure. H/I was induced by right common carotid ligation and sham-operated mice served as controls. We demonstrated that right common carotid ligation decreases the threshold for clonic seizures induced by pentylenetetrazole (PTZ), a GABA antagonist. Furthermore, pro-convulsive effect of H/I following right common carotid ligation was blocked by naltrexone (NTX) (3 mg/kg), NG-Nitro-l-arginine methyl ester (l-NAME) (10 mg/kg), and aminoguanidine (AG) (100 mg/kg) administration (P<0.001). Interestingly, co-administration of non-effective doses of NTX and l-NAME (1 and 0.5 mg/kg, respectively) reverses epileptogenesis of H/I (P<0.001). In the same way, co-administration of non-effective doses of NTX and AG (1 and 5 mg/kg, respectively), reverses epileptogenesis of H/I (P<0.001). Indeed, the histological studies performed on mice exposed to H/I confirmed our previous data. These findings suggest hyper-susceptibility to PTZ induced seizure following H/I is mediated by interaction of opioidergic, and iNOS/NO pathways. Therefore, our results identify new pharmacological targets and provide the rationale for a novel strategy to promote recovery after stroke and possibly other brain injuries. © 2014 Elsevier B.V. All rights reserved.
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