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鞘内注射和全身应用R-苯异丙基腺苷可减少大鼠单神经病模型中的搔抓行为。

Intrathecal and systemic R-phenylisopropyl-adenosine reduces scratching behaviour in a rat mononeuropathy model.

作者信息

Sjölund K F, Sollevi A, Segerdahl M, Hansson P, Lundeberg T

机构信息

Department of Anaesthesiology and Intensive Care, Karolinska Institutet/ Hospital, Stockholm, Sweden.

出版信息

Neuroreport. 1996 Jul 29;7(11):1856-60. doi: 10.1097/00001756-199607290-00034.

DOI:10.1097/00001756-199607290-00034
PMID:8905680
Abstract

The aim of the present study was to investigate the effect of intravenous or intrathecal (i.t.) administration of R-phenylisopropyladenosine (R-PIA), a selective A1 adenosine receptor agonist, on spontaneous scratching behaviour, a phenomenon presumably related to pain in a mononeuropathy model (sciatic nerve ligation) in rats. The acute effect of daily i.t. R-PIA injections was studied up to 21 days following nerve ligation. The results demonstrate that both i.v. (30 nmol) and i.t. (3 nmol) R-PIA, in doses not producing any motor impairment, significantly reduces scratching behaviour in this animal model. The mechanism of action for this presumed antinociceptive effect is suggested to occur at the spinal cord level.

摘要

本研究的目的是探讨静脉内或鞘内注射选择性A1腺苷受体激动剂R-苯异丙基腺苷(R-PIA)对大鼠单神经病变模型(坐骨神经结扎)中自发搔抓行为的影响,该现象可能与疼痛有关。在神经结扎后长达21天的时间里研究了每日鞘内注射R-PIA的急性效应。结果表明,静脉注射(30 nmol)和鞘内注射(3 nmol)R-PIA,在不产生任何运动障碍的剂量下,均可显著减少该动物模型中的搔抓行为。这种推测的抗伤害感受作用的作用机制被认为发生在脊髓水平。

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Intrathecal and systemic R-phenylisopropyl-adenosine reduces scratching behaviour in a rat mononeuropathy model.鞘内注射和全身应用R-苯异丙基腺苷可减少大鼠单神经病模型中的搔抓行为。
Neuroreport. 1996 Jul 29;7(11):1856-60. doi: 10.1097/00001756-199607290-00034.
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Intrathecal administration of the adenosine A1 receptor agonist R-phenylisopropyl adenosine reduces presumed pain behaviour in a rat model of central pain.鞘内注射腺苷A1受体激动剂R-苯异丙基腺苷可减轻中枢性疼痛大鼠模型中的假定疼痛行为。
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Marked enhancement of anti-allodynic effect by combined intrathecal administration of the adenosine A1-receptor agonist R-phenylisopropyladenosine and morphine in a rat model of central pain.在大鼠中枢性疼痛模型中,鞘内联合给予腺苷A1受体激动剂R-苯异丙基腺苷和吗啡可显著增强抗痛觉过敏作用。
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Adenosine receptor activation suppresses tactile hypersensitivity and potentiates spinal cord stimulation in mononeuropathic rats.腺苷受体激活可抑制单神经病大鼠的触觉超敏反应并增强脊髓刺激。
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Pharmacology of the spinal adenosine receptor which mediates the antiallodynic action of intrathecal adenosine agonists.介导鞘内腺苷激动剂抗痛觉过敏作用的脊髓腺苷受体药理学。
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Adenosine A1 but not A2a receptor agonist reduces hyperalgesia caused by a surgical incision in rats: a pertussis toxin-sensitive G protein-dependent process.腺苷A1受体激动剂而非A2a受体激动剂可减轻大鼠手术切口所致的痛觉过敏:这是一个百日咳毒素敏感的G蛋白依赖性过程。
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Effects of intrathecal morphine, baclofen, clonidine and R-PIA on the acute allodynia-like behaviours after spinal cord ischaemia in rats.鞘内注射吗啡、巴氯芬、可乐定和R-苯异丙腺苷对大鼠脊髓缺血后急性痛觉过敏样行为的影响。
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Intrathecal adenosine does not relieve allodynia-like behavior in spinally injured rats.鞘内注射腺苷不能缓解脊髓损伤大鼠的痛觉过敏样行为。
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Intrathecal adenosine analog administration reduces substance P in cerebrospinal fluid along with behavioral effects that suggest antinociception in rats.鞘内注射腺苷类似物可降低大鼠脑脊液中P物质水平,并产生提示抗伤害感受的行为效应。
Anesth Analg. 1997 Sep;85(3):627-32. doi: 10.1097/00000539-199709000-00025.

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