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中缝大核诱导的脊髓伤害性神经元下行抑制是通过猫的对侧脊髓通路介导的。

Raphe magnus-induced descending inhibition of spinal nociceptive neurons is mediated through contralateral spinal pathways in the cat.

作者信息

Sandkühler J, Maisch B, Zimmermann M

出版信息

Neurosci Lett. 1987 May 6;76(2):168-72. doi: 10.1016/0304-3940(87)90710-5.

DOI:10.1016/0304-3940(87)90710-5
PMID:3587751
Abstract

In anesthetized cats, extracellular recordings were made from lumbar spinal dorsal horn neurons, driven by noxious radiant skin heating. Heat-evoked responses were inhibited during electrical stimulation in the medullary nucleus raphe magnus (NRM). To identify the spinal pathways mediating this descending inhibition, reversible blocks in the spinal cord white matter were produced by microinjection of the local anesthetic lidocaine. Descending inhibition from the NRM was significantly reduced during blocks in the dorsal and medial, but not ventral parts of the contralateral lateral funiculus (LF). Blocks at any site in the ipsilateral LF failed to affect NRM-induced descending inhibition. These results indicate that NRM-induced inhibition of nociceptive dorsal horn neurons is conveyed primarily in fibers descending in the contralateral spinal white matter.

摘要

在麻醉猫中,对由伤害性皮肤辐射热刺激驱动的腰段脊髓背角神经元进行细胞外记录。在延髓中缝大核(NRM)进行电刺激期间,热诱发反应受到抑制。为了确定介导这种下行抑制的脊髓通路,通过微量注射局部麻醉药利多卡因在脊髓白质中产生可逆性阻断。在对侧外侧索(LF)的背侧和内侧部分而非腹侧部分进行阻断期间,来自NRM的下行抑制显著降低。同侧LF中任何部位的阻断均未影响NRM诱导的下行抑制。这些结果表明,NRM诱导的对伤害性背角神经元的抑制主要通过对侧脊髓白质中下行的纤维进行传递。

相似文献

1
Raphe magnus-induced descending inhibition of spinal nociceptive neurons is mediated through contralateral spinal pathways in the cat.中缝大核诱导的脊髓伤害性神经元下行抑制是通过猫的对侧脊髓通路介导的。
Neurosci Lett. 1987 May 6;76(2):168-72. doi: 10.1016/0304-3940(87)90710-5.
2
Spinal pathways mediating tonic or stimulation-produced descending inhibition from the periaqueductal gray or nucleus raphe magnus are separate in the cat.在猫中,介导来自中脑导水管周围灰质或中缝大核的紧张性或刺激产生的下行抑制的脊髓通路是分开的。
J Neurophysiol. 1987 Aug;58(2):327-41. doi: 10.1152/jn.1987.58.2.327.
3
Spinal pathways mediating tonic, coeruleospinal, and raphe-spinal descending inhibition in the rat.介导大鼠紧张性、蓝斑脊髓和中缝脊髓下行抑制的脊髓通路。
J Neurophysiol. 1987 Jul;58(1):138-59. doi: 10.1152/jn.1987.58.1.138.
4
Quantitative comparison of inhibition in spinal cord of nociceptive information by stimulation in periaqueductal gray or nucleus raphe magnus of the cat.猫中脑导水管周围灰质或中缝大核刺激对脊髓伤害性信息抑制作用的定量比较
J Neurophysiol. 1983 Dec;50(6):1433-45. doi: 10.1152/jn.1983.50.6.1433.
5
Inhibition of spinal nociceptive information by stimulation in midbrain of the cat is blocked by lidocaine microinjected in nucleus raphe magnus and medullary reticular formation.猫中脑刺激对脊髓伤害性信息的抑制作用,可被微量注射于中缝大核和延髓网状结构的利多卡因阻断。
J Neurophysiol. 1983 Dec;50(6):1446-59. doi: 10.1152/jn.1983.50.6.1446.
6
Inhibition of the responses of cat dorsal horn neurons to noxious skin heating by stimulation in medial or lateral medullary reticular formation.通过刺激延髓内侧或外侧网状结构抑制猫脊髓背角神经元对皮肤有害热刺激的反应。
Exp Brain Res. 1988;72(1):51-62. doi: 10.1007/BF00248500.
7
Relative contributions of the nucleus raphe magnus and adjacent medullary reticular formation to the inhibition by stimulation in the periaqueductal gray of a spinal nociceptive reflex in the pentobarbital-anesthetized rat.中缝大核及相邻延髓网状结构对戊巴比妥麻醉大鼠中脑导水管周围灰质刺激抑制脊髓伤害性反射的相对贡献。
Brain Res. 1984 Jul 2;305(1):77-87. doi: 10.1016/0006-8993(84)91121-1.
8
Differential inhibitory effects of medial and lateral midbrain stimulation on spinal neuronal discharges to noxious skin heating in the cat.中脑内侧和外侧刺激对猫脊髓神经元对皮肤有害热刺激放电的不同抑制作用。
J Neurophysiol. 1980 Feb;43(2):332-42. doi: 10.1152/jn.1980.43.2.332.
9
Inhibition of spinal nociceptive neurons by excitation of cell bodies or fibers of passage at various brainstem sites in the cat.通过刺激猫的不同脑干部位的细胞体或传导通路纤维来抑制脊髓伤害性神经元。
Neurosci Lett. 1988 Oct 31;93(1):67-72. doi: 10.1016/0304-3940(88)90014-6.
10
Inhibition of spinal nociceptive neurons by microinjections of somatostatin into the nucleus raphe magnus and the midbrain periaqueductal gray of the anesthetized cat.通过向麻醉猫的中缝大核和中脑导水管周围灰质微量注射生长抑素对脊髓伤害性神经元的抑制作用
Neurosci Lett. 1995 Mar 3;187(2):137-41. doi: 10.1016/0304-3940(95)11345-2.

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