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Antagonists of substance P.

作者信息

Caranikas S, Mizrahi J, D'Orléans-Juste P, Regoli D

出版信息

Eur J Pharmacol. 1982 Jan 22;77(2-3):205-6. doi: 10.1016/0014-2999(82)90023-1.

DOI:10.1016/0014-2999(82)90023-1
PMID:6174355
Abstract
摘要

相似文献

1
Antagonists of substance P.P物质拮抗剂
Eur J Pharmacol. 1982 Jan 22;77(2-3):205-6. doi: 10.1016/0014-2999(82)90023-1.
2
Synthesis of substance P antagonists: [D-Pro4, D-Trp7,9,Nle11]-substance P(4-11).
Pharmazie. 1984 Jan;39(1):65-7.
3
Partial agonists and antagonists for substance P.P物质的部分激动剂和拮抗剂。
Eur J Pharmacol. 1983 Jul 15;91(1):139-40. doi: 10.1016/0014-2999(83)90376-x.
4
Synthesis and biological activities of substance P antagonists.P物质拮抗剂的合成与生物活性
J Med Chem. 1982 Nov;25(11):1313-6. doi: 10.1021/jm00353a008.
5
A specific substance P antagonist blocks smooth muscle contractions induced by non-cholinergic, non-adrenergic nerve stimulation.一种特异性P物质拮抗剂可阻断由非胆碱能、非肾上腺素能神经刺激所引起的平滑肌收缩。
Nature. 1981 Dec 3;294(5840):467-9. doi: 10.1038/294467a0.
6
Mini review: smooth muscle pharmacology of substance P.迷你综述：P物质的平滑肌药理学
Pharmacology. 1982;24(1):1-25. doi: 10.1159/000137572.
7
Inhibition of smooth muscle contractions induced by capsaicin and electrical transmural stimulation by a substance P antagonist.P物质拮抗剂对辣椒素和电透壁刺激诱导的平滑肌收缩的抑制作用。
Acta Physiol Scand Suppl. 1983;515:11-6.
8
Novel substance P analogues inhibit circular muscle contraction of guinea pig ileum and depolarization of new born rat spinal cord induced by substance P.新型P物质类似物可抑制豚鼠回肠的环形肌收缩以及P物质诱导的新生大鼠脊髓去极化。
Regul Pept. 1993 Jul 2;46(1-2):321-5. doi: 10.1016/0167-0115(93)90073-h.
9
N-acylated pentapeptides antagonists of substance P on guinea-pig ileum.
Biochem Biophys Res Commun. 1988 Oct 14;156(1):323-7. doi: 10.1016/s0006-291x(88)80843-x.
10
[Role of tachykinins in non-muscarinic contraction of the isolated guinea-pig colon].
Nihon Heikatsukin Gakkai Zasshi. 1989 Oct;25(5):222-4.

引用本文的文献

1
A study of [D-Pro2, D-Phe7, D-Trp9]-substance P and [D-Trp7,9]-substance P as tachykinin partial agonists in the rat colon.[D-脯氨酸2，D-苯丙氨酸7，D-色氨酸9]-P物质和[D-色氨酸7,9]-P物质作为速激肽部分激动剂在大鼠结肠中的研究
Br J Pharmacol. 1984 Jun;82(2):441-51. doi: 10.1111/j.1476-5381.1984.tb10779.x.
2
Development of a new tachykinin antagonist.一种新型速激肽拮抗剂的研发。
Experientia. 1984 Jan 15;40(1):86-8. doi: 10.1007/BF01959116.
3
Study of the contractile effect of 5-hydroxytryptamine (5-HT) in the isolated longitudinal muscle strip from guinea-pig ileum. Evidence for two distinct release mechanisms.
豚鼠回肠离体纵行肌条中5-羟色胺（5-HT）收缩效应的研究。两种不同释放机制的证据。
Naunyn Schmiedebergs Arch Pharmacol. 1985 Mar;329(1):36-41. doi: 10.1007/BF00695189.
4
Immunohistochemical and behavioral analysis of spinal lesions induced by a substance P antagonist and protection by thyrotropin releasing hormone.P物质拮抗剂诱导的脊髓损伤的免疫组织化学和行为分析以及促甲状腺激素释放激素的保护作用
Exp Brain Res. 1989;74(2):279-92. doi: 10.1007/BF00248861.
5
Effect of the tachykinin antagonist, [D-Pro4, D-Trp7,9,10] substance P-(4-11), on tachykinin- and histamine-induced inositol phosphate generation in intestinal smooth muscle.速激肽拮抗剂[D-脯氨酸4，D-色氨酸7,9,10]P物质-(4-11)对速激肽和组胺诱导的肠平滑肌肌醇磷酸生成的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1987 Mar;335(3):296-300. doi: 10.1007/BF00172800.
6
Tachykinins and bombesin excite non-pyramidal neurones in rat hippocampus.速激肽和蛙皮素可兴奋大鼠海马中的非锥体神经元。
J Physiol. 1986 Oct;379:417-28. doi: 10.1113/jphysiol.1986.sp016261.
7
An examination of the pharmacology of two substance P antagonists and the evidence for tachykinin receptor subtypes.两种P物质拮抗剂的药理学研究及速激肽受体亚型的证据
Br J Pharmacol. 1986 Jan;87(1):79-85. doi: 10.1111/j.1476-5381.1986.tb10159.x.
8
Naloxone-reversible effect of spantide on the spinally mediated behavioural response induced by neurokinin-2 and -3 receptor agonists.
Naunyn Schmiedebergs Arch Pharmacol. 1992 Jul;346(1):69-75. doi: 10.1007/BF00167573.