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      •   صفحهٔ اصلی
      • نشریات انگلیسی
      • Iranian Journal of Pharmaceutical Research
      • Volume 17, Issue 3
      • مشاهده مورد
      •   صفحهٔ اصلی
      • نشریات انگلیسی
      • Iranian Journal of Pharmaceutical Research
      • Volume 17, Issue 3
      • مشاهده مورد
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      Effect of vitamins B1, B6 and B12 (Neurobion) on diisopropylfluorophosphate–induced delayed neuropathy in mice

      (ندگان)پدیدآور
      Ebrahimi, MohsenKhoshnood, Mohammad JavadZia-Behbahani, Majid
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      نوع مدرک
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      Research article
      زبان مدرک
      English
      نمایش کامل رکورد
      چکیده
      Certain organophosphorus esters such as diisopropylfluorophosphate (DFP) cause delayed neuropathy by inhibition of neuropathy target esterase (NTE) keeping neuron in normal function. In this study, effects of neurobion alone and in combination with dexamethasone on DFP–induced delayed neuropathy were evaluated. Thirty-five mice were divided to five groups that each group consists 7 mice. Except group1 (Normalgroup), group2 received normal saline and 1h later, 1 mg/kg DFP, groupe3,4 and 5 received 150 mg/kg neurobion, 2mg/kg dexamethasone and 150mg/kg neurobion plus 2mg/kg dexamethasone, respectively and 1h later 1mg/kg DFP. Twenty one days after last injection, mice were killed by decapitation under deep anesthesia. NTE level was determined in brain and though there was no significant difference between groups, neurobion and neurobion plus dexamethasone partly - not significantly (p > 0.05) - were be able to prevent reduction of NTE in brain caused by DFP. Histopathological evaluation of sciatic nerves belonged to groups, showed that neurobion and neurobion plus dexamethasone significantly suppressed harmful effect of DFP e.g. demyelination and micro-cavitation in nerve. We also evaluated activity of acetylcholine esterase (AChE), concentration of glutathione (GSH) and malondialdehyde (MDA) levels in serum. Results showed dexamethasone (p 0.05) - were be able to prevent reduction of NTE in brain caused by DFP. Histopathological evaluation of sciatic nerves belonged to groups, showed that neurobion and neurobion plus dexamethasone significantly suppressed harmful effect of DFP e.g. demyelination and micro-cavitation in nerve. We also evaluated activity of acetylcholine esterase (AChE), concentration of glutathione (GSH) and malondialdehyde (MDA) levels in serum. Results showed dexamethasone (p
      کلید واژگان
      Organophosphorus compound
      DFP
      delayed neuropathy
      neuropathy target esterase
      neurobion
      toxicology and Pharmacology

      شماره نشریه
      3
      تاریخ نشر
      2018-07-01
      1397-04-10
      ناشر
      School of Pharmacy, Shahid Beheshti University of Medical Sciences
      سازمان پدید آورنده
      Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran
      Department of Pharmacology and Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran
      Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran.|Department of Pharmacology and Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran. |Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.

      شاپا
      1735-0328
      1726-6890
      URI
      https://dx.doi.org/10.22037/ijpr.2018.2256
      http://ijpr.sbmu.ac.ir/article_2256.html
      https://iranjournals.nlai.ir/handle/123456789/313290

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