شماره ركورد :
416844
عنوان مقاله :
اثر تزريق زيرجلدي مورفين بر فعاليت نورونهاي هسته ميخي شكل موش بزرگ آزمايشگاهي
عنوان به زبان ديگر :
Effect of Subcutaneous Morphine Injection on Neuronal Activity in the Nucleus Cuneiformis of Rat
پديد آورندگان :
حق پرست، عباس نويسنده مركز تحقيقات علوم اعصاب-دانشگاه علوم پزشكي و خدمات بهداشتي درماني شهيد بهشتي HAGHPARAST, A. , علي زاده، اميرمحمد نويسنده مركز تحقيقات علوم اعصاب، دانشگاه علوم پزشكي و خدمات بهداشتي درماني شهيد بهشتي ALIZADEH, A.M. , معتمدي، فرشته نويسنده مركز تحقيقات علوم اعصاب، دانشگاه علوم پزشكي شهيد بهشتي MOTAMEDI, F.
رتبه نشريه :
-
تعداد صفحه :
11
از صفحه :
253
تا صفحه :
263
كليدواژه :
نورونهاي هسته , موش بزرگ آزمايشگاهي , مورفين , Morphine , Neural activity , Single unit recording , تزريق زيرجلدي , Nucleus Cuneiformis
چكيده لاتين :
Background: The similarities between periaqueductal gray matter and the nucleus cuneiformis in both ultrastructural and functional levels suggest that this nucleus may play an important role in the morphine-induced analgesia. This study was designed to determine neuronal activity and responsiveness to peripheral morphine administration in the nucleus coneiformis of rat. Materials and Methods: In this study, neural activity of cuneiform neurons in response to peripheral administration of morphine was recorded by extracellular single unit recording technique. Firing rate of neurons was recorded in four groups: intact group (n=19) to determine the spontaneous (baseline) activity, saline group (n=20), morphine group (n=39) and morphine + naloxone group (n=12), before and after drug administration. Results: Our findings showed that the firing rate in majority of cuneiform neurons decreased after morphine (3.8 mg/kg; SC) administration. Activity of neurons (n=39) in the cuneiform neurons was reduced significantly (P<0.01) after morphine injection (6.66±0.67 spike/sec) in comparison with pre-injection time (12.47±1.84 spike/sec) and the saline group (11.6±1.58 spike/sec). The firing rate and response pattern of many of neurons in response to peripheral application of morphine were reversed after naloxone injection (2 mg/kg; SC) in this nucleus. Conclusion: Based on the above findings, we suggest that the changes of activity pattern in spontaneous activity of cuneiform neurons in response to peripheral administration of morphine maybe resulted from direct action of morphine on opioid receptors in the nucleus cuneiformis. Nevertheless, the role of pain transmission and modulation pathways are still important in the antinociceptive effect of morphine as well.
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