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Antiepileptogenic effects of borneol in pentylenetetrazole-induced kindling in mice
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  • 作者:Rufi Tambe ; Pankaj Jain ; Sachin Patil…
  • 关键词:Kindling ; Borneol ; Pentylenetetrazole ; Oxidative Stress ; Glial fibrillary acidic protein
  • 刊名:Naunyn-Schmiedeberg's Archives of Pharmacology
  • 出版年:2016
  • 出版时间:May 2016
  • 年:2016
  • 卷:389
  • 期:5
  • 页码:467-475
  • 全文大小:750 KB
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  • 作者单位:Rufi Tambe (1)
    Pankaj Jain (1)
    Sachin Patil (1)
    Priya Ghumatkar (1)
    Sadhana Sathaye (1)

    1. Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Nathalal Parekh Marg, Matunga, Mumbai-19, Maharashtra, India
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Pharmacology and Toxicology
    Neurosciences
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-1912
文摘
Borneol, a bicyclic monoterpene, can easily cross the blood brain barrier and was found to possess gamma amino butyric acid (GABA) modulatory effect. The present study was aimed at investigating the antiepileptogenic effect of borneol in the pentylenetetrazole (PTZ)-induced kindling besides its ability to suppress oxidative stress and neuroinflammatory marker, glial fibrillary acidic protein (GFAP). Repeated administration of a subconvulsive dose of PTZ (35 mg/kg, i.p.) on every alternate day for 4 weeks produced kindling in mice. Borneol (5, 10, and 25 mg/kg, i.p.) and diazepam (1 mg/kg, i.p.) were given as a pretreatment prior to each PTZ injection during the progression of kindling. Oxidative stress parameters such as superoxide dismutase (SOD), reduced glutathione (GSH), catalase (CAT), and lipid peroxidation (LPO) were assessed at the end of the study. Neuronal damage was assessed by hematoxylin and eosin staining technique. GFAP was also evaluated in the hippocampus region of the brain by using immunohistochemistry. Borneol significantly suppressed the process of epileptogenesis in PTZ-kindled mice. The biochemical alterations induced by PTZ kindling were ameliorated in borneol-treated animals which was indicated by decreased LPO and increased SOD, GSH, CAT levels. The distinct neuronal damage observed in the kindled group was counteracted by borneol. Furthermore, it decreased the levels of GFAP which was manifested by reduced immunostaining. The above results are suggestive of the antiepileptogenic potential of borneol in the PTZ-induced kindling model of epilepsy, and thus, it could be a prospective molecule in the treatment of epilepsy.

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