Medical Journals

Direct Effects of Hydrogen Peroxide on Airway Smooth Muscle Tone: Roles of Ca2+ Influx and Rho-kinase.

Authors:
  • Kojima Katsuyuki
  • Kume Hiroaki
  • Ito Satoru
  • Oguma Tetsuya
  • Shiraki Akira
  • Kondo Masashi
  • Ito Yasushi
  • Shimokata Kaoru

From: Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

European journal of pharmacology

  • Publish Date: Feb 2007
  • ISSN: 0014-2999
  • Volume: 556
  • Issue: 1-3
  • Pages: 151-6
  • Medium: Print
  • Language: English
  • Citation (JAMA): Kojima Katsuyuki, Kume Hiroaki, Ito Satoru, et al. Direct Effects of Hydrogen Peroxide on Airway Smooth Muscle Tone: Roles of Ca2+ Influx and Rho-kinase.. Eur. J. Pharmacol. Feb 2007;556:151-6

Abstract

Reactive oxidant species are implicated in the chronic airway inflammation related to asthma and chronic obstructive pulmonary disease. This study was designed to determine mechanisms underlying contraction induced by hydrogen peroxide (H(2)O(2)), a clinical marker of oxidative stress, in airway smooth muscle. Isometric tension and fluorescent intensities of fura-2, an index of intracellular Ca(2+) concentrations ([Ca(2+)](i)), were measured in epithelium-denuded tracheal smooth muscle tissues isolated from guinea pigs. H(2)O(2) (0.01-1 mM) caused contraction with an augmentation of [Ca(2+)](i) in a concentration-dependent manner in the normal physiological solution containing 2.4 mM of extracellular Ca(2+) concentrations. The contractile force and [Ca(2+)](i) by H(2)O(2) (1 mM) were approximately half of those in response to 1 microM methacholine. However, contraction by H(2)O(2) was not generated under the condition that extracellular Ca(2+) concentrations were less than 0.15 mM. Verapamil (10 microM), an inhibitor of voltage-operated Ca(2+) channels, partially but significantly inhibited the H(2)O(2)-induced contraction. In contrast, SKF-96365 (1-{beta-[3-(4-methoxyphenyl)propoxy]-4-methoxyphenethyl}-1H-imidazole hydrochloride) (100 microM), a non-selective inhibitor of Ca(2+) channels, completely abolished both the contraction and the increase in [Ca(2+)](i) elicited by H(2)O(2). Moreover, Y-27632 ((R)-(+)-trans-N-(4-Pyridyl)-4-(1-aminoethyl)-cyclohexanecarboxamide) (0.03-10 microM), an inhibitor of Rho-kinase, caused a concentration-dependent inhibition of the H(2)O(2)-induced contraction. In conclusion, both the Ca(2+) influx from the extracellular side and the Ca(2+) sensitization by Rho-kinase are involved in the regulation of airway smooth muscle tone induced by H(2)O(2). An inhibition of the Rho/Rho-kinase pathway may be beneficial for the treatment of airflow limitation mediated by oxidative stress.

Mesh Headings (Keywords): Amides, Animals, Bronchoconstrictor Agents, Calcium, Calcium Channel Blockers, Epithelium, Guinea Pigs, Hydrogen Peroxide, Imidazoles, Intracellular Signaling Peptides and Proteins, Isometric Contraction, Male, Methacholine Chloride, Muscle Tonus, Muscle, Smooth, Oxidative Stress, Protein-Serine-Threonine Kinases, Pyridines, Signal Transduction, Trachea, Verapamil, rho-Associated Kinases


Check for Full Text / PubMed Unique Identifier (PMID): 17157292


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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