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高选择性μ和δ阿片类药物在大鼠脊髓水平的体内相互作用。

Interaction between highly selective mu and delta opioids in vivo at the rat spinal cord.

作者信息

Russell R D, Leslie J B, Su Y F, Watkins W D, Chang K J

机构信息

Department of Anesthesiology, Duke University Medical Center, Durham, N.C. 27710.

出版信息

NIDA Res Monogr. 1986;75:97-100.

PMID:2829017
Abstract

Possible interactions between mu- and delta-receptors in the rat spinal cord were studied using the radiant-heat-induced tail flick response and the highly selective mu- or delta-ligands: [NMePhe3,D-Pro4] morphiceptin(PL-17) and cyclic[D-Pen2,D-Pen5]enkephalin(DPDPE). Intrathecal infusions of PL-17 (0.5 microgram/hr) for 5 days caused 61- and 6-fold shifts to the right of the dose-response curves for PL-17 and DPDPE, respectively. Since PL-17 and DPDPE are highly selective agonists for mu- and delta-receptors, the partial cross-tolerance to the delta-agonist induced by PL-17 is probably not resultant from a cross-reactivity between these ligands. These data suggest that there may be an interaction between mu- and delta-receptors in the rat spinal cord.

摘要

利用辐射热诱导的甩尾反应以及高选择性的μ或δ配体:[NMePhe3,D-Pro4]吗啡肽(PL-17)和环[D-Pen2,D-Pen5]脑啡肽(DPDPE),研究了大鼠脊髓中μ受体和δ受体之间可能的相互作用。鞘内注射PL-17(0.5微克/小时),持续5天,分别使PL-17和DPDPE的剂量反应曲线向右移动了61倍和6倍。由于PL-17和DPDPE分别是μ受体和δ受体的高选择性激动剂,PL-17诱导的对δ激动剂的部分交叉耐受性可能并非源于这些配体之间的交叉反应性。这些数据表明,大鼠脊髓中μ受体和δ受体之间可能存在相互作用。

相似文献

1
Interaction between highly selective mu and delta opioids in vivo at the rat spinal cord.高选择性μ和δ阿片类药物在大鼠脊髓水平的体内相互作用。
NIDA Res Monogr. 1986;75:97-100.
2
Continuous intrathecal opioid analgesia: tolerance and cross-tolerance of mu and delta spinal opioid receptors.鞘内持续给予阿片类药物镇痛:μ和δ脊髓阿片受体的耐受性及交叉耐受性
J Pharmacol Exp Ther. 1987 Jan;240(1):150-8.
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Delta opioid receptor enhancement of mu opioid receptor-induced antinociception in spinal cord.脊髓中δ阿片受体对μ阿片受体诱导的抗伤害感受的增强作用。
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Spinal opioid receptors and adenosine release: neurochemical and behavioral characterization of opioid subtypes.脊髓阿片受体与腺苷释放:阿片类亚型的神经化学和行为学特征
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Role of mu and delta receptors in the supraspinal and spinal analgesic effects of [D-Pen2, D-Pen5]enkephalin in the mouse.μ和δ受体在小鼠中[D-青霉胺2,D-青霉胺5]脑啡肽的脊髓上和脊髓镇痛作用中的作用
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Evidence for delta opioid receptor subtypes in rat spinal cord: studies with intrathecal naltriben, cyclic[D-Pen2, D-Pen5] enkephalin and [D-Ala2, Glu4]deltorphin.大鼠脊髓中δ阿片受体亚型的证据:鞘内注射纳曲苄、环[D-青霉胺2,D-青霉胺5]脑啡肽和[D-丙氨酸2,谷氨酸4]强啡肽的研究
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Mu opioid antagonist properties of a cyclic somatostatin octapeptide in vivo: identification of mu receptor-related functions.一种环状生长抑素八肽在体内的μ阿片受体拮抗剂特性:μ受体相关功能的鉴定
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Mu and delta opioid receptor desensitization in undifferentiated human neuroblastoma SHSY5Y cells.未分化人神经母细胞瘤SHSY5Y细胞中μ和δ阿片受体脱敏
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The role of mu- and delta- opioid receptors on the intestinal propulsion in rats.μ和δ阿片受体在大鼠肠道推进中的作用。
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Differential effects of intrathecally administered delta and mu opioid receptor agonists on formalin-evoked nociception and on the expression of Fos-like immunoreactivity in the spinal cord of the rat.鞘内注射δ和μ阿片受体激动剂对福尔马林诱发的伤害感受及大鼠脊髓中Fos样免疫反应表达的不同影响。
J Pharmacol Exp Ther. 1998 Jan;284(1):378-87.

引用本文的文献

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In vivo activation of a mutant mu-opioid receptor by naltrexone produces a potent analgesic effect but no tolerance: role of mu-receptor activation and delta-receptor blockade in morphine tolerance.纳曲酮在体内激活突变型μ-阿片受体可产生强效镇痛作用但无耐受性:μ-受体激活和δ-受体阻断在吗啡耐受性中的作用
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Development of delta opioid peptides as nonaddicting analgesics.δ阿片肽作为非成瘾性镇痛药的研发。
Pharm Res. 1991 Jan;8(1):1-8. doi: 10.1023/a:1015809702296.