兔主动脉中缓激肽的受体 - Suppr

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Receptors for bradykinin in rabbit aortae.

作者信息

Regoli D, Barabé J, Park W K

出版信息

Can J Physiol Pharmacol. 1977 Aug;55(4):855-67. doi: 10.1139/y77-115.

DOI:10.1139/y77-115

PMID:902160

Abstract

摘要

相似文献

Receptors for bradykinin in rabbit aortae.兔主动脉中缓激肽的受体

Can J Physiol Pharmacol. 1977 Aug;55(4):855-67. doi: 10.1139/y77-115.

Non-selectivity of new bradykinin antagonists for B1 receptors.

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Bradykinin B1 receptors in the rabbit urinary bladder: induction of responses, smooth muscle contraction, and phosphatidylinositol hydrolysis.兔膀胱中的缓激肽B1受体：反应诱导、平滑肌收缩及磷脂酰肌醇水解

Br J Pharmacol. 1995 Feb;114(3):612-7. doi: 10.1111/j.1476-5381.1995.tb17183.x.

Competitive antagonists of bradykinin: in vitro (jugular vein) and in vivo (blood pressure response) studies.缓激肽竞争性拮抗剂：体外（颈静脉）和体内（血压反应）研究

Adv Exp Med Biol. 1989;247B:407-9. doi: 10.1007/978-1-4615-9546-5_67.

Development of bradykinin antagonists: structure-activity relationships for new categories of antagonist sequences.缓激肽拮抗剂的研发：新型拮抗剂序列的构效关系

Adv Exp Med Biol. 1989;247B:395-400. doi: 10.1007/978-1-4615-9546-5_65.

Bradykinin interaction with 5-hydroxytryptamine, norepinephrine, and potassium chloride in rabbit aorta.缓激肽与兔主动脉中5-羟色胺、去甲肾上腺素及氯化钾的相互作用

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Structure-activity relationships of bradykinin potentiating peptides.缓激肽增强肽的构效关系。

Eur J Pharmacol. 1978 Jul 15;50(2):119-22. doi: 10.1016/0014-2999(78)90006-7.

DesArg10[Hoe 140] is a potent B1 bradykinin antagonist.

Agents Actions Suppl. 1992;38 ( Pt 2):406-13.

Response of rabbit detrusor muscle to bradykinin.兔逼尿肌对缓激肽的反应。

Life Sci. 1981 Feb 9;28(6):603-8. doi: 10.1016/0024-3205(81)90123-5.

Characterization of smooth muscle receptors for angiotensin: studies with an antagonist.

Am J Physiol. 1974 Jan;226(1):185-90. doi: 10.1152/ajplegacy.1974.226.1.185.

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Bradykinin increases BP in endotoxemic rat: functional and biochemical evidence of angiotensin II AT /bradykinin B receptor heterodimerization.内毒素血症大鼠的缓激肽增加血压：血管紧张素 II AT/缓激肽 B 受体异二聚体的功能和生化证据。

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A specific inhibitor of mammalian kallikrein, Phe-Phe-Arg-chloromethyl ketone, inhibits the production of vasoactive substances from trout plasma by kallikrein and blocks endogenous kallikrein-like activity in trout gills.一种哺乳动物激肽释放酶的特异性抑制剂，苯丙氨酰-苯丙氨酰-精氨酸-氯甲基酮，可抑制激肽酶从鳟鱼血浆中产生血管活性物质，并阻断鳟鱼鳃中的内源性激肽酶样活性。

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