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JCR 2016
جستجوی مقالات
سه شنبه 18 آذر 1404
Physiology and Pharmacology
، جلد ۱۵، شماره ۴، صفحات ۴۸۶-۴۹۸
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Effect of glial inhibition in attenuation of neuropathic pain and improvement of morphine analgesic effect in a rat model of neuropathy
چکیده انگلیسی مقاله
Introduction: Pharmacological blockage of glial activity has been proved useful for treatment of neuropathic pain by lowering proinflammatory cytokines. The present study is to confirm the effect of post-injury administration of pentoxifylline on chronic constriction injury (CCI)-induced neuropathic pain symptoms_ and improved the efficacy of morphine anti-nociception. Methods: Male Wistar rats (230-270 g) underwent surgery for induction of CCI model of neuropathy. In the sham group the nerve was exposed but not ligated. In 5 groups (n=8) morphine (2.5, 5, 7.5, 10, 15 mg/kg s.c.) was administered in post-operative days (POD) 0, 6 and 14. To evaluate the analgesic effect of different doses of morphine, Von Frey and Hargreaves tests were performed before and 30 minutes after morphine administration. In different groups, pentoxifylline (8, 15, 30 mg/kg i.p.) or normal saline (vehicle) were administered from POD6 to POD13. Behavioral tests were utilized after last dose of pentoxifylline and also on POD14 again after injection of a single dose of morphine (5 mg/kg, s.c.). Results: The analgesic effect of morphine (5 mg/kg) on POD6 and morphine (5, 7.5, 10, 15 mg/kg) on POD14 was significantly decreased in comparison to POD0. Pentoxifylline effectively attenuated thermal hyperalgesia (at 15 and 30 mg/kg) and mechanical allodynia (at 30 mg/kg) on POD13. However, pentoxifylline (15, 30 mg/kg) improved the antihyperalgesic effect of morphine (5 mg/kg s.c.) on POD14. Conclusion: Analgesic effect of morphine was reduced after nerve injury and it may be due to the activation of glia. Inhibition of glial activity is an effective way to attenuate CCI-induced neuropathic pain and also to improve the antihyperalgesic effect of morphine, without significant effect on its anti-allodynic effect.
کلیدواژههای انگلیسی مقاله
Neuropathic pain, Glia, Morphine, Allodynia, Hyperalgesia
نویسندگان مقاله
صمد ناظمی | samad nazemi
department of physiology shahid beheshti university, m.c., evin st. ,shahid chamran express-way p.o.box 19615-1178, tehran, iran
سازمان اصلی تایید شده
: دانشگاه شهید بهشتی (Shahid beheshti university)
هما مناهجی | homa manaheji
department of physiology shahid beheshti university, m.c., evin st. ,shahid chamran express-way p.o.box 19615-1178, tehran, iran
سازمان اصلی تایید شده
: دانشگاه شهید بهشتی (Shahid beheshti university)
عباس حق پرست | abbas haghparast
neuroscience research center shahid beheshti university, m.c., evin st. ,shahid chamran express-way p.o.box 19615-1178, tehran, iran
سازمان اصلی تایید شده
: دانشگاه شهید بهشتی (Shahid beheshti university)
جلال زرین قلم مقدم | jalal zaringhalam moghadam
department of physiology shahid beheshti university, m.c., evin st. ,shahid chamran express-way p.o.box 19615-1178, tehran, iran
سازمان اصلی تایید شده
: دانشگاه شهید بهشتی (Shahid beheshti university)
مهدی صادقی | mehdi sadegi
department of physiology shahid beheshti university, m.c., evin st. ,shahid chamran express-way p.o.box 19615-1178, tehran, iran
سازمان اصلی تایید شده
: دانشگاه شهید بهشتی (Shahid beheshti university)
نشانی اینترنتی
http://www.phypha.ir/ppj/browse.php?a_code=A-10-578-1&slc_lang=en&sid=en
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کد مقاله (doi)
زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
Pain and addiction
نوع مقاله منتشر شده
Original Research
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