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通过微透析对小鼠皮肤内源性一氧化氮进行体内定量测定。

Quantitative determination of endogenous nitric oxide in the mouse skin in vivo by microdialysis.

作者信息

Andoh T, Kuraishi Y

机构信息

Department of Applied Pharmacology, Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Japan.

出版信息

Eur J Pharmacol. 1997 Aug 13;332(3):279-82. doi: 10.1016/s0014-2999(97)01114-x.

Abstract

We have developed a subcutaneous microdialysis system for the determination of nitric oxide (NO) concentration in the skin. The skin was microdialyzed using a degassed solution containing 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide and the perfusate was reacted on-line with Griess' reagent. This method could reveal NO production following intradermal injection of bradykinin (10-100 nmol/site) in mice. The increase in cutaneous NO after bradykinin (100 nmol/site) was dose dependently suppressed by the NO synthase inhibitor. NG-nitro-L-arginine methyl ester, and the bradykinin B, receptor antagonist, D-Arg-[Hyp3, Thi5.8, D-Phe7]-bradykinin. This system may be useful for pharmacological and physiological experiments on the role of NO in the skin.

摘要

我们开发了一种用于测定皮肤中一氧化氮(NO)浓度的皮下微透析系统。使用含有2-(4-羧基苯基)-4,4,5,5-四甲基咪唑啉-1-氧基3-氧化物的脱气溶液对皮肤进行微透析,灌注液与格里斯试剂在线反应。该方法可揭示小鼠皮内注射缓激肽(10 - 100 nmol/部位)后NO的产生情况。缓激肽(100 nmol/部位)引起的皮肤NO增加被NO合酶抑制剂NG-硝基-L-精氨酸甲酯和缓激肽B2受体拮抗剂D-Arg-[Hyp3, Thi5.8, D-Phe7]-缓激肽剂量依赖性地抑制。该系统可能有助于进行关于NO在皮肤中作用的药理和生理实验。

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