首页> 外文期刊>European Journal of Pharmacology: An International Journal >Effects of nefopam on the spinal nociceptive processes: a c-Fos protein study in the rat.
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Effects of nefopam on the spinal nociceptive processes: a c-Fos protein study in the rat.

机译:奈福m对脊髓伤害感受过程的影响:一项在大鼠中进行的c-Fos蛋白研究。

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We have evaluated the effects of nefopam on the spinal c-Fos protein expression in the model of acute (noxious heat) and persistent (intraplantar injection of formalin) nociception in the rat. One and two hours after i.pl. formalin injection, c-Fos immunoreactive (c-Fos-IR) nuclei were preferentially located in the superficial (I-II) and deep (V-VI) laminae of the spinal dorsal horn of segments L4-L5, i.e. spinal areas containing numerous neurons responding exclusively, or not, to peripheral nociceptive stimuli. The doses of 15 and 30 mg/kg (s.c.) of nefopam had significant reducing effects on the formalin-evoked spinal c-Fos protein expression (36+/-14% and 47+/-9% reduction of the total number of c-Fos-IR nuclei per section, respectively, P<0.05 for both). These reducing effects of nefopam were not detectable 2 h after formalin. These results provide evidence that the significant effects of nefopam are time-limited in the formalin model of persistent nociception. One hour after noxious heat stimulation (52 degrees C for 15 s), c-Fos-IR nuclei were principally located in the superficial laminae I-II of the spinal dorsal horn (about 90% of the total number of c-Fos-IR nuclei per section). Nefopam (15 mg/kg s.c.) significantly reduced the noxious heat-evoked spinal c-Fos protein expression (33+/-3% reduction of the total number of c-Fos-IR nuclei, P<0.0001). The present results provide first evidence for the reducing effects of nefopam on the noxiously evoked spinal c-Fos protein expression, principally in acute nociceptive processes. These results suggest that nefopam may produce antinociceptive effects mainly in acute pain states.
机译:我们已经评估了奈福opa对大鼠急性(有毒热)和持续性(足底注射福尔马林)伤害感受模型中脊髓c-Fos蛋白表达的影响。 i.pl之后一两个小时。注射福尔马林后,c-Fos免疫反应性(c-Fos-IR)核优先位于L4-L5段的脊髓背角的浅层(I-II)和深层(V-VI)椎板,即包含大量脊髓的区域神经元对周围伤害性刺激的反应是否唯一。 15和30 mg / kg(sc)的奈福opa剂量对福尔马林诱发的脊髓c-Fos蛋白表达具有显着的降低作用(总c减少36 +/- 14%和47 +/- 9%每段分别为-Fos-IR核,两者均P <0.05)。福尔马林注射后2小时,未检测到奈福opa的这些降低作用。这些结果提供了证据表明,在持续伤害感受的福尔马林模型中,奈福opa的显着作用是有时间限制的。有害热刺激(52摄氏度,持续15 s)一小时后,c-Fos-IR核主要位于脊髓背角的浅层I-II(约占c-Fos-IR总数的90%)每节的原子核)。奈福opa(15 mg / kg s.c.)显着降低了有害的热诱发脊髓c-Fos蛋白表达(c-Fos-IR核总数减少了33 +/- 3%,P <0.0001)。目前的结果提供了主要在急性伤害过程中奈福opa对有害诱发的脊髓c-Fos蛋白表达的降低作用的初步证据。这些结果表明,奈福opa可能主要在急性疼痛状态下产生抗伤害作用。

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