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      •   صفحهٔ اصلی
      • نشریات انگلیسی
      • Iranian Journal of Pharmaceutical Research
      • Volume 16, Issue 2
      • مشاهده مورد
      •   صفحهٔ اصلی
      • نشریات انگلیسی
      • Iranian Journal of Pharmaceutical Research
      • Volume 16, Issue 2
      • مشاهده مورد
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      How Nitric Oxide increases in diabetic morphine tolerated male rats

      (ندگان)پدیدآور
      Mortada, YassarJoharchi, KhojastehZarei, MalekMansouri, ArdalanJorjani, Masoumeh
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      نوع مدرک
      Text
      Research article
      زبان مدرک
      English
      نمایش کامل رکورد
      چکیده
      Neuropathic pain is a complication of inflammation, infection or some diseases such as diabetes. Opioids are used as a salvage therapy for neuropathic pain but tolerance restricts their use. In our previous study we have observed an increase of Nitric Oxide in diabetes and in morphine tolerance. This study was performed to clarify the role of inducible nitric oxide synthase, iNOS, and cationic amino acid transporter, CAT-2, in these conditions. Thus male rats were divided into four groups: control, diabetic, morphine tolerated and diabetic morphine tolerated. For evaluating tolerance Hot-Plate test was achieved. Molecular study was performed by real time PCR and Western blotting techniques to compare gene and protein expression. Our findings showed that in diabetic animals, morphine tolerance occurred prior to non-diabetic rats. In molecular study, the expression of iNOS was increased in the spinal cord whereas the CAT-2 did not change in diabetic morphine tolerated rats. It seems that the nitric oxide elevation in diabetic morphine tolerated state is mostly due to the increase of iNOS in male rats.
      کلید واژگان
      Diabetes
      Morphine tolerance
      Nitric Oxide Synthase
      Cationic Amino Acid Transporter-2
      Male Rat
      toxicology and Pharmacology

      شماره نشریه
      2
      تاریخ نشر
      2017-06-01
      1396-03-11
      ناشر
      School of Pharmacy, Shahid Beheshti University of Medical Sciences
      سازمان پدید آورنده
      Department of Pharmacology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
      Shahid Beheshti University of Medical Sciences, Tehran, Iran
      Department of Pharmacology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
      Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
      Department of Pharmacology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran

      شاپا
      1735-0328
      1726-6890
      URI
      https://dx.doi.org/10.22037/ijpr.2017.2056
      http://ijpr.sbmu.ac.ir/article_2056.html
      https://iranjournals.nlai.ir/handle/123456789/312922

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