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受体特异性P物质激动剂的行为效应。

Behavioural effects of receptor-specific substance P agonists.

作者信息

Papir-Kricheli Dalia, Frey Joseph, Laufer Ralph, Gilon Chaim, Chorev Michael, Selinger Zvi, Devor Marshall

机构信息

Life Sciences Institute, Hebrew University of Jerusalem, Jerusalem 91904 Israel Institute of Chemistry, Hebrew University of Jerusalem, Jerusalem 91904 Israel School of Pharmacy, Hebrew University of Jerusalem, Jerusalem 91904 Israel.

出版信息

Pain. 1987 Nov;31(2):263-276. doi: 10.1016/0304-3959(87)90041-8.

DOI:10.1016/0304-3959(87)90041-8
PMID:2448728
Abstract

Septide and senktide are synthetic substance P (SP) agonists with extremely high selectivity for 1 of the 3 known SP receptor subtypes. When injected intrathecally, they produced dramatically different behavioural effects. Septide, the selective SP-P receptor agonist, evoked intense, compulsive scratching, biting and licking of the hind limb, with no sign of motor flaccidity, and without measurable effect on responses to noxious thermal or mechanical stimulation of the foot or tail. In contrast, senktide, the selective SP-N receptor agonist, produced profound, but transient, motor flaccidity, reduced response to noxious stimuli and, at low doses, 'wet-dog shakes.' These various symptoms, all previously associated with SP and/or synthetic SP analogues, appear therefore to derive from activation of distinct SP receptor subtypes.

摘要

Septide和senktide是对3种已知P物质(SP)受体亚型中的1种具有极高选择性的合成SP激动剂。鞘内注射时,它们产生了截然不同的行为效应。选择性SP-P受体激动剂Septide引起后肢强烈、强迫性的抓挠、啃咬和舔舐,没有运动弛缓的迹象,并且对足部或尾部的有害热刺激或机械刺激反应没有可测量的影响。相比之下,选择性SP-N受体激动剂senktide产生了深刻但短暂的运动弛缓,对有害刺激的反应降低,并且在低剂量时会出现“湿狗样抖动”。因此,所有这些先前与SP和/或合成SP类似物相关的各种症状似乎都源于不同SP受体亚型的激活。

相似文献

1
Behavioural effects of receptor-specific substance P agonists.受体特异性P物质激动剂的行为效应。
Pain. 1987 Nov;31(2):263-276. doi: 10.1016/0304-3959(87)90041-8.
2
Neurochemical mediators of the behavioural effects of receptor-selective substance P agonists administered intrathecally in the rat.鞘内注射受体选择性P物质激动剂对大鼠行为影响的神经化学介质
Neuropharmacology. 1990 Nov;29(11):1055-65. doi: 10.1016/0028-3908(90)90112-5.
3
Differential effects of substance P analogs on neurokinin 1 receptor agonists in the mouse spinal cord.P物质类似物对小鼠脊髓中神经激肽1受体激动剂的不同作用。
J Pharmacol Exp Ther. 1991 Oct;259(1):205-10.
4
Comparative behavioural profile of centrally administered tachykinin NK1, NK2 and NK3 receptor agonists in the guinea-pig.豚鼠中枢给予速激肽NK1、NK2和NK3受体激动剂的比较行为特征
Br J Pharmacol. 1995 Nov;116(5):2496-502. doi: 10.1111/j.1476-5381.1995.tb15101.x.
5
N-terminal substance P fragments inhibit the spinally induced, NK 1 receptor mediated behavioural responses in mice.P物质N端片段可抑制小鼠脊髓诱导的、NK1受体介导的行为反应。
Life Sci. 1990;47(20):PL109-13. doi: 10.1016/0024-3205(90)90291-x.
6
Substance P analogues containing D-histidine antagonize the behavioural effects of intrathecally co-administered substance P in mice.含有D-组氨酸的P物质类似物可拮抗小鼠鞘内共同给予P物质的行为效应。
Eur J Pharmacol. 1989 Dec 19;174(2-3):153-60. doi: 10.1016/0014-2999(89)90307-5.
7
Behavioural effects of tachykinins and related peptides.速激肽及相关肽的行为效应。
Brain Res. 1986 Aug 27;381(1):68-76. doi: 10.1016/0006-8993(86)90691-8.
8
Receptors mediating tachykinin-evoked depolarisations of neurons in the neonatal rat spinal cord.介导新生大鼠脊髓中速激肽诱发神经元去极化的受体。
Acta Biol Hung. 1996;47(1-4):129-44.
9
Cardiovascular and behavioural effects of intracerebroventricularly administered tachykinin NK3 receptor antagonists in the conscious rat.脑室内注射速激肽NK3受体拮抗剂对清醒大鼠心血管及行为的影响
Br J Pharmacol. 1997 Oct;122(4):643-54. doi: 10.1038/sj.bjp.0701435.
10
Demonstration of a 'septide-sensitive' inflammatory response in rat skin.大鼠皮肤中“septide敏感”炎症反应的证明。
Br J Pharmacol. 1995 Oct;116(4):2170-4. doi: 10.1111/j.1476-5381.1995.tb15050.x.

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