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GABAergic modulation of descending inhibitory systems from the rostral ventromedial medulla (RVM). Dose-response analysis of nociception and neurological deficits.

机译:GABA能性调节来自延髓腹侧延髓(RVM)的递减抑制系统。伤害感受和神经功能缺损的剂量反应分析。

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We have examined the effects of muscimol and bicuculline microinjected in the rostral ventromedial medulla (RVM) on motor function and on nociception in three pain tests. In Exp. 1 microinjection of muscimol (6.25-400 ng in 1 microl) in the RVM dose-dependently decreased pain threshold of rats and the ED(50) for muscimol was the same in both the hot plate and tail immersion pain tests. In the hot plate test, but not in the tail immersion test, paw withdrawal latencies increased again with high doses of muscimol (75-400 ng). High doses also produced catalepsy. Exp. 2 examined the effects of muscimol (50 ng) and bicuculline (50 ng) over a range of formalin concentrations (0.25-4%) in the formalin test. Muscimol increased responsiveness to formalin and reduced the slope of the formalin dose-response relation. Bicuculline decreased responses to formalin and reduced the slope of the formalin dose-response relation. It is suggested that RVM cells with inhibitory projections to the dorsal horn are not subject to strong GABAergic influence under mild noxious stimulation. RVM cells are thus active, and spinal dorsal horn relay neurons are inhibited. On the other hand, intense noxious peripheral stimulation may stimulate the release of GABA onto RVM cells, which in turn shuts off descending inhibitory fibers to allow transmission of nociceptor input through the dorsal horn.
机译:我们在三个疼痛测试中检查了在腹侧延髓延髓(RVM)中微注射的麝香酚和双瓜氨酸对运动功能和伤害感受的影响。在实验中在热板法和尾部浸入式疼痛试验中,在RVM中1次微量注射麝香酚(1微升中的6.25-400 ng)可剂量依赖性地降低大鼠的疼痛阈值,而麝香酚的ED(50)相同。在热板试验中,但在尾部浸没试验中没有,大剂量的麝香酚(75-400 ng)会使爪子退缩潜伏期再次增加。高剂量也会导致僵直。经验2研究人员在福尔马林试验中,在一定的福尔马林浓度(0.25-4%)范围内,研究了麝香酚(50 ng)和双瓜氨酸(50 ng)的作用。 Muscimol可增加对福尔马林的反应性,并降低福尔马林剂量反应关系的斜率。 Bicuculline降低了对福尔马林的反应,并降低了福尔马林剂量反应关系的斜率。提示对背角具有抑制性投射的RVM细胞在轻度有害刺激下不受强GABA能的影响。因此,RVM细胞是活跃的,并且脊髓背角中继神经元受到抑制。另一方面,强烈的有害周围刺激可能会刺激GABA释放到RVM细胞上,从而关闭下降的抑制性纤维,从而允许伤害感受器输入通过背角传递。

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