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SQ22536和W-7可抑制福斯高林诱导的新生羊肺静脉中环磷酸腺苷(cAMP)升高,但不抑制其舒张。

SQ22536 and W-7 inhibit forskolin-induced cAMP elevation but not relaxation in newborn ovine pulmonary veins.

作者信息

Gao Y, Raj J U

机构信息

Department of Pediatrics, Harbor-UCLA Medical Center, University of California, Los Angeles, School of Medicine, Torrance, CA 90509, USA.

出版信息

Eur J Pharmacol. 2001 Apr 20;418(1-2):111-6. doi: 10.1016/s0014-2999(01)00929-3.

Abstract

The role of cAMP in forskolin-induced relaxation was studied in isolated pulmonary veins of newborn lambs (7-12 days). In vessels preconstricted with endothelin-1, forskolin at concentrations < or =10(-7) M had no effect on cAMP content and adenylyl cyclase activity but caused up to 50% relaxation. At higher concentrations, forskolin markedly elevated cAMP content and adenylyl cyclase activity and caused a further relaxation. SQ22536 [9-(tetrahydro-2-furanyl)-9H-purin-6-amine; an adenylyl cyclase inhibitor] and W-7 [N-(6-aminohexyl)-5-chloro-1-naphthalensulfonamide; a calmodulin-dependent adenylyl cyclase inhibitor] had no significant effect on forskolin-induced relaxation but markedly inhibited the elevation of cAMP content and adenylyl cyclase activity caused by forskolin. Rp-8-CPT-cAMPS [8-(4-chlorophenylthio)-adenosine-3',5'-cyclic monophosphorothioate; an inhibitor of cAMP-dependent protein kinases] and Rp-8-Br-PET-cGMPS (beta-phenyl-1, N(2)-etheno-8-bromoguanosine-3',5'-cyclic monophosphorothioate; an inhibitor of cGMP-dependent protein kinases) attenuated the relaxation caused by a cAMP analog but not that caused by forskolin. These results suggest that cAMP may not play a major role in forskolin-induced relaxation of pulmonary veins of newborn lambs.

摘要

在新生羔羊(7 - 12日龄)的离体肺静脉中研究了环磷酸腺苷(cAMP)在福司可林诱导的舒张中的作用。在内皮素 - 1预收缩的血管中,浓度≤10⁻⁷ M的福司可林对cAMP含量和腺苷酸环化酶活性无影响,但可引起高达50%的舒张。在较高浓度下,福司可林显著提高cAMP含量和腺苷酸环化酶活性,并引起进一步舒张。SQ22536 [9 - (四氢 - 2 - 呋喃基) - 9H - 嘌呤 - 6 - 胺;一种腺苷酸环化酶抑制剂]和W - 7 [N - (6 - 氨基己基) - 5 - 氯 - 1 - 萘磺酰胺;一种钙调蛋白依赖性腺苷酸环化酶抑制剂]对福司可林诱导的舒张无显著影响,但显著抑制福司可林引起的cAMP含量升高和腺苷酸环化酶活性升高。Rp - 8 - CPT - cAMPS [8 - (4 - 氯苯基硫代) - 腺苷 - 3',5' - 环一磷酸硫酯;一种cAMP依赖性蛋白激酶抑制剂]和Rp - 8 - Br - PET - cGMPS(β - 苯基 - 1,N(2) - 乙烯基 - 8 - 溴鸟苷 - 3',5' - 环一磷酸硫酯;一种cGMP依赖性蛋白激酶抑制剂)减弱了cAMP类似物引起的舒张,但未减弱福司可林引起的舒张。这些结果表明,cAMP在福司可林诱导的新生羔羊肺静脉舒张中可能不发挥主要作用。

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