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脊髓α2肾上腺素能受体在麻醉兔急性伤害性刺激后后肢退缩反射的长期调节中的作用。

Involvement of spinal α2 -adrenoceptors in prolonged modulation of hind limb withdrawal reflexes following acute noxious stimulation in the anaesthetized rabbit.

作者信息

Harris John

机构信息

School of Biosciences, University of Nottingham, Sutton Bonington Campus, Loughborough, LE12 5RD, UK.

出版信息

Eur J Neurosci. 2016 Mar;43(6):834-45. doi: 10.1111/ejn.13185. Epub 2016 Feb 28.

DOI:10.1111/ejn.13185
PMID:26804327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4949523/
Abstract

The role of spinal α2 -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.

摘要

在戊巴比妥麻醉的兔子中,研究了脊髓α2-肾上腺素能受体在介导急性有害化学刺激远处异位和局部同位部位后后肢退缩反射的持久调节中的作用。通过电刺激同侧足跟在踝伸肌内侧腓肠肌(MG)中诱发的反射,以及通过刺激同侧脚趾基部在踝屈肌胫骨前肌和膝屈肌半腱肌中诱发的反射,在将芥子油(20%)应用于口鼻部或对侧MG后可被抑制超过1小时。在同侧足的跖趾关节处涂抹芥子油后,足跟-MG反应也受到抑制,而这种同位刺激促进了两种屈肌反应。芥子油应用于三个测试部位中的任何一个时也会引起显著的升压作用。选择性α2-肾上腺素能受体拮抗剂RX 821002(100-300μg,鞘内注射)对反射本身没有影响,但确实导致平均动脉血压下降。在存在α2-阻滞剂的情况下,芥子油对反射的抑制和促进作用完全被消除。这些数据表明,急性有害刺激远处部位后脊髓反射的持久抑制涉及脊髓上的去甲肾上腺素能通路的激活,其作用依赖于脊髓水平完整的α2-肾上腺素能受体系统。这些通路和受体似乎也参与了对同一肢体施加有害刺激后反射的促进(敏化)以及抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/09896fb04591/EJN-43-834-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/ed4f06e76de2/EJN-43-834-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/9a83b2512d4c/EJN-43-834-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/31532f736b60/EJN-43-834-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/7d6480a42524/EJN-43-834-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/d16be937a5fd/EJN-43-834-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/09896fb04591/EJN-43-834-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/ed4f06e76de2/EJN-43-834-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/9a83b2512d4c/EJN-43-834-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/31532f736b60/EJN-43-834-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/7d6480a42524/EJN-43-834-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/d16be937a5fd/EJN-43-834-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ae/4949523/09896fb04591/EJN-43-834-g006.jpg

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