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Potentiative effects of sulfhydryl compounds on carrageenin-induced oedema in rats and relationship to their potencies as inhibitors of angiostin-coverting enzyme in vivo.

作者信息

Iso T, Yamauchi H, Suda H, Nakajima N, Nishimura K, Iwao J

出版信息

Experientia. 1978 Sep 15;34(9):1202-3. doi: 10.1007/BF01922957.

DOI:10.1007/BF01922957
PMID:214334
Abstract

Carrageenin-induced oedema in rats was potentiated by oral administration of (4R)-3-[(2S)-3-mercapto-2-methylpropanoyl]-4-thiazolidinecarboxylic acid (SA291) and related sulfhydryl compounds, and the effect was closely correlated with their potencies as inhibitors of angiotensin-converting enzyme in vivo.

摘要

相似文献

1
Potentiative effects of sulfhydryl compounds on carrageenin-induced oedema in rats and relationship to their potencies as inhibitors of angiostin-coverting enzyme in vivo.
Experientia. 1978 Sep 15;34(9):1202-3. doi: 10.1007/BF01922957.
2
[Potentiative effects of angiotensin converting enzyme inhibitors on carrageenan-induced edema in rats].
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3
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4
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Potentiating mechanism of bradykinin action on smooth muscle by sulfhydryl compounds.巯基化合物对缓激肽作用于平滑肌的增强机制。
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Effects of YS-980, an orally active converting enzyme inhibitor, on blood pressure in normotensive and hypertensive rats.口服活性转化酶抑制剂YS - 980对正常血压和高血压大鼠血压的影响。
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Clin Exp Hypertens (1978). 1981;3(1):121-40. doi: 10.3109/10641968109037172.
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Inhibition of angiotensin converting enzyme by SQ 14,225 in conscious rabbits.
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引用本文的文献

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Potentiation of the pro-inflammatory effects of bradykinin by inhibition of angiotensin-converting enzyme and aminopeptidase P in rat paws.通过抑制大鼠爪中的血管紧张素转换酶和氨肽酶P增强缓激肽的促炎作用
Naunyn Schmiedebergs Arch Pharmacol. 1996 Nov;354(5):670-6. doi: 10.1007/BF00170844.
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Some pharmacological properties of tiopronin.硫普罗宁的一些药理特性。
Agents Actions. 1981 Dec;11(6-7):741-5. doi: 10.1007/BF01978799.
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Effect of angiotensin-converting enzyme inhibitor YS980 on prostaglandin synthesis in rabbit kidney medulla slices.

本文引用的文献

1
Inhibition by various substances of oedema formation in the bind-paw of the rat induced by 5-hydroxytryptamine, histamine, dextran, egg-white and compound 48/80.各种物质对5-羟色胺、组胺、右旋糖酐、蛋清和48/80化合物诱导的大鼠足趾水肿形成的抑制作用。
Br J Pharmacol Chemother. 1958 Mar;13(1):65-70. doi: 10.1111/j.1476-5381.1958.tb00192.x.
2
Proceedings: the concomitant release of bradykinin and prostaglandin in the inflammatory response to carrageenin.论文集：角叉菜胶炎症反应中缓激肽与前列腺素的协同释放
Br J Pharmacol. 1974 Sep;52(1):108P-109P.
3
Studies on the mediators of the acute inflammatory response induced in rats in different sites by carrageenan and turpentine.
血管紧张素转换酶抑制剂YS980对兔肾髓质切片中前列腺素合成的影响。
Br J Pharmacol. 1987 Nov;92(3):479-81. doi: 10.1111/j.1476-5381.1987.tb11346.x.
对角叉菜胶和松节油在大鼠不同部位诱导的急性炎症反应介质的研究。
J Pathol. 1971 May;104(1):15-29. doi: 10.1002/path.1711040103.
4
Characterization of a dipeptide hydrolase (kininase II: angiotensin I converting enzyme).一种二肽水解酶（激肽酶II：血管紧张素I转换酶）的特性描述
J Pharmacol Exp Ther. 1971 Apr;177(1):291-300.
5
Enhancement of carrageenin foot oedema by 1,10 -phenanthroline and evidence for the bradykinin as endogenous mediator.
Agents Actions. 1975 Oct;5(4):359-63. doi: 10.1007/BF02205243.
6
New sulfhydryl compounds with potent antihypertensive activities.具有强效降压活性的新型巯基化合物。
Chem Pharm Bull (Tokyo). 1978 Apr;26(4):1333-5. doi: 10.1248/cpb.26.1333.
7
Design of potent competitive inhibitors of angiotensin-converting enzyme. Carboxyalkanoyl and mercaptoalkanoyl amino acids.血管紧张素转换酶强效竞争性抑制剂的设计。羧基烷酰基和巯基烷酰基氨基酸。
Biochemistry. 1977 Dec 13;16(25):5484-91. doi: 10.1021/bi00644a014.
8
Design of specific inhibitors of angiotensin-converting enzyme: new class of orally active antihypertensive agents.血管紧张素转换酶特异性抑制剂的设计：新型口服活性抗高血压药物
Science. 1977 Apr 22;196(4288):441-4. doi: 10.1126/science.191908.
9
The kinins. A status report.激肽。一份现状报告。
Biochem Pharmacol. 1976 Jul 15;25(14):1563-9. doi: 10.1016/0006-2952(76)90465-2.