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脊髓去甲肾上腺素能终末系统介导抗伤害感受。

Spinal noradrenergic terminal system mediates antinociception.

作者信息

Reddy S V, Yaksh T L

出版信息

Brain Res. 1980 May 12;189(2):391-401. doi: 10.1016/0006-8993(80)90099-2.

Abstract

Intrathecal administration of norepinephrine (NE) into the lumbar subarachnoid space of rats and cats implanted with chronic spinal catheters produced a strong, dose-dependent, behaviorally defined analgesia. The effect appeared mediated by an alpha-receptor inasmuch as phenylephrine, but not isoproterenol produced the intrathecal effect. Moreover, the antinociceptive effect of NE was antagonized by the prior systemic or intrathecal administration of phentolamine (an alpha-blocker), but was unaffected by pretreatment with propranolol (a beta-blocker). The effect of intrathecal NE was significantly potentiated by prior administration of Lilly 51641 (a monoamine oxidase inhibitor) and protriptyline (a re-uptake inhibitor), and was not antagonized by the intrathecal administration of a non-specific vasodilator, papaverine. The antinociceptive effect of intrathecal NE showed tachyphylaxis following repeated injections. No cross-tolerance between intrathecal NE and morphine was observed, suggesting that the spinal action of morphine is not mediated by spinal noradrenergic terminals. Importantly, naloxone had no effect on the intrathecal NE effect. The present data provide further evidence for the modulatory role of a spinal noradrenergic system on the spinal processing of nociceptive transmission.

摘要

将去甲肾上腺素(NE)鞘内注射到植入慢性脊髓导管的大鼠和猫的腰段蛛网膜下腔,可产生强烈的、剂量依赖性的、行为学定义的镇痛作用。该效应似乎是由α受体介导的,因为苯肾上腺素可产生鞘内效应,而异丙肾上腺素则不能。此外,NE的抗伤害感受作用可被事先全身或鞘内给予酚妥拉明(一种α受体阻滞剂)所拮抗,但不受普萘洛尔(一种β受体阻滞剂)预处理的影响。事先给予利 Lilly 51641(一种单胺氧化酶抑制剂)和普罗替林(一种再摄取抑制剂)可显著增强鞘内注射NE的效应,且鞘内注射非特异性血管扩张剂罂粟碱不会拮抗该效应。重复注射后,鞘内注射NE的抗伤害感受作用出现快速耐受。未观察到鞘内注射NE与吗啡之间的交叉耐受性,这表明吗啡的脊髓作用不是由脊髓去甲肾上腺素能终末介导的。重要的是,纳洛酮对鞘内注射NE的效应没有影响。目前的数据为脊髓去甲肾上腺素能系统对伤害性信息传递的脊髓处理的调节作用提供了进一步的证据。

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