Inhibitory effect of tramadol on vasorelaxation mediated by ATP-sensitive K+ channels in rat aorta-Reference-Cited by-同舟云学术

Inhibitory effect of tramadol on vasorelaxation mediated by ATP-sensitive K+ channels in rat aorta

Published:2007-06 Issue:6 Volume:54 Page:453-460
ISSN:0832-610X
Container-title:Canadian Journal of Anesthesia/Journal canadien d'anesthésie
language:en
Short-container-title:Can J Anesth/J Can Anesth

Author:

Cho Hyoung-Chan,Sohn Ju-Tae,Park Kyeong-Eon,Shin Il-Woo,Chang Ki Churl,Lee Jae-Wan,Lee Heon-Keun,Chung Young-Kyun

Publisher

Springer Science and Business Media LLC

Subject

Anesthesiology and Pain Medicine,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03022031.pdf

Reference24 articles.

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2. Cavero I, Mondot S, Mestre M. Vasorelaxant effects of cromakalim in rats are mediated by glibenclamide-sensitive potassium channels. J Pharmacol Exp Ther 1989; 248: 1261–8.

3. Quast U. Do the K+ channel openers relax smooth muscle by opening K+ channels? Trends Pharmacol Sci 1993; 14: 332–7.

4. Raffa RB. A novel approach to the pharmacology of analgesics. Am J Med 1996; 101(1A): 40S-6S.

5. Guven M, Mert T, Gunay I. Effects of tramadol on nerve action potentials in rat: comparisons with ben-zocaine and lidocaine. Intern J Neurosci 2005; 115: 339–49.

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