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首页> 外文期刊>Brain research >Anti-hyperalgesic effects of intrathecally administered neuropeptide W-23, and neuropeptide B, in tests of inflammatory pain in rats.
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Anti-hyperalgesic effects of intrathecally administered neuropeptide W-23, and neuropeptide B, in tests of inflammatory pain in rats.

机译:鞘内注射神经肽W-23和神经肽B的抗痛觉过敏作用,用于测试大鼠的炎性疼痛。

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摘要

Neuropeptide W-23 (NPW23) is an endogenous ligand of both GPR7 and GPR8, and neuropeptide B (NPB) is an endogenous ligand of GPR7. GPR7 mRNA has been detected in regions of the cortex, the hippocampus, the hypothalamus, and the spinal cord in the rat, but GPR8 has not been found in rodents. GPR7 and GPR8 receptors have structural features in common with both opioid and somatostatin receptors. The effects of intrathecal (i.t.) application of NPW23 and NPB were tested in two inflammatory pain models (plantar injection of formalin or carrageenan) and two thermal nociceptive tests (52.5 degrees C and 50.5 degrees C hot plates) and one mechanical nociceptive test in the rat. I.t. injection of either NPW23 or NPB decreased the number of agitation behaviors induced by paw formalin injection and attenuated the level of mechanical allodynia, but not the level of thermal hyperalgesia, induced by paw carrageenan injection in a dose-dependent manner at a dose between 0.1 and 10 mug, significantly. The effects of either 10 mug of NPW23 or 10 mug of NPB were not antagonized by 10 mug of naloxone. I.t. injection of either NPW23 or NPB had no effect in both the 52.5 degrees C hot plate test or in the 50.5 degrees C hot plate tests at a dose between 1 and 100 mug. I.t. injection of either 10 mug of NPW23 or 10 mug of NPB had no effect in the mechanical nociceptive test. I.t. injection of either 10 mug of NPW23 or 10 mug of NPB significantly suppressed the expression of Fos-like immunoreactivity of the L4-5 spinal dorsal horn induced by paw formalin injection. These data suggest that both spinally-applied NPW23 and NPB suppressed the input of nociceptive information to the spinal dorsal horn, produced an analgesic effect in the formalin test, and attenuated the level of mechanical allodynia in the carrageenan test, and that either spinally applied NPW23 or spinally applied NPB had no effect in the physiological condition.
机译:神经肽W-23(NPW23)是GPR7和GPR8的内源性配体,而神经肽B(NPB)是GPR7的内源性配体。在大鼠的皮质,海马,下丘脑和脊髓区域均检测到GPR7 mRNA,但在啮齿动物中未发现GPR8。 GPR7和GPR8受体具有与阿片类和生长抑素受体相同的结构特征。在两个炎症性疼痛模型(足底注射福尔马林或角叉菜胶)和两个热伤害性试验(52.5摄氏度和50.5摄氏度热板)和一个机械伤害性试验中,对鞘内施用NPW23和NPB的效果进行了测试。鼠。它。 NPW23或NPB的注射减少了爪福尔马林注射引起的躁动行为的数量,并且减弱了爪角叉菜胶注射以0.1至0.1之间的剂量依赖性诱导的机械性异常性疼痛的水平,但没有减弱热痛觉过敏的水平。 10杯,明显。 10杯纳洛酮不能对抗10杯NPW23或10杯NPB的作用。它。在52.5摄氏度的热板测试或50.5摄氏度的热板测试中,以1至100杯的剂量注射NPW23或NPB均无效。它。注射10杯NPW23或10杯NPB不会对机械伤害感受产生影响。它。注射10杯NPW23或10杯NPB可以显着抑制爪福尔马林注射诱导的L4-5脊髓背角Fos样免疫反应性的表达。这些数据表明,脊柱施加的NPW23和NPB均抑制了对脊髓背角的伤害性信息输入,在福尔马林试验中产生了止痛作用,并且在角叉菜胶试验中减弱了机械性异常性疼痛的水平,并且两种脊柱施加的NPW23或NPB脊髓施用对生理状况没有影响。

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