首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Involvement of spinal α2‐adrenoceptors in prolonged modulation of hind limb withdrawal reflexes following acute noxious stimulation in the anaesthetized rabbit
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Involvement of spinal α2‐adrenoceptors in prolonged modulation of hind limb withdrawal reflexes following acute noxious stimulation in the anaesthetized rabbit

机译:麻醉兔急性毒性刺激后脊髓α2-肾上腺素能受体参与后肢退缩反射的长期调节

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摘要

The role of spinal >α 2‐adrenoceptors in mediating long‐lasting modulation of hind limb withdrawal reflexes following acute noxious chemical stimulation of distant heterotopic and local homotopic locations has been investigated in pentobarbitone‐anaesthetized rabbits. Reflexes evoked in the ankle extensor muscle medial gastrocnemius (MG) by electrical stimulation of the ipsilateral heel, and reflexes elicited in the ankle flexor tibialis anterior and the knee flexor semitendinosus by stimulation at the base of the ipsilateral toes, could be inhibited for over 1 h after mustard oil (20%) was applied to either the snout or into the contralateral MG. The heel–MG response was also inhibited after applying mustard oil across the plantar metatarsophalangeal joints of the ipsilateral foot, whereas this homotopic stimulus facilitated both flexor responses. Mustard oil also caused a significant pressor effect when applied to any of the three test sites. The selective α2‐adrenoceptor antagonist, RX 821002 (100–300 μg, intrathecally), had no effect on reflexes per se, but did cause a decrease in mean arterial blood pressure. In the presence of the α2‐blocker, inhibitory and facilitatory effects of mustard oil on reflexes were completely abolished. These data imply that long‐lasting inhibition of spinal reflexes following acute noxious stimulation of distant locations involves activation of supraspinal noradrenergic pathways, the effects of which are dependent on an intact α2‐adrenoceptor system at the spinal level. These pathways and receptors also appear to be involved in facilitation (sensitization) as well as inhibition of reflexes following a noxious stimulus applied to the same limb.
机译:在戊巴比妥麻醉的兔子中,研究了脊髓>α 2肾上腺素能受体在介导对远处异位和局部同位异位的急性有害化学刺激后介导的后肢退缩反射的持久调节中的作用。通过电刺激同侧脚后跟引起的反射在踝伸肌内侧腓肠肌(MG)中,并且通过在同侧脚趾基部的刺激在踝屈肌胫骨前和膝屈肌腱引起的反射可以被抑制超过1将芥末油(20%)涂在口鼻部或对侧MG中后h。在芥菜油跨过同侧脚的meta趾指关节后,脚跟-MG反应也被抑制,而这种同位刺激促进了两种屈肌反应。当将芥末油应用于三个测试地点中的任何一个时,也会引起明显的升压效果。选择性α2-肾上腺素受体拮抗剂RX 821002(鞘内100–300μg)本身对反射没有影响,但确实导致平均动脉血压降低。在存在α2受体阻滞剂的情况下,芥子油对反射的抑制作用和促进作用被完全消除。这些数据表明,对远处的急性有害刺激后对脊髓反射的长期抑制涉及激活脊髓上去甲肾上腺素能途径,其作用取决于在脊髓水平上完整的α2-肾上腺素能受体系统。这些途径和受体似乎也参与了对同一肢体的有害刺激后的促进作用(敏化)以及反射抑制。

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