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Brazilein-induced contraction of rat arterial smooth muscle involves activation of Ca(2+) entry and ROK, ERK pathways.

Brazilein-induced contraction of rat arterial smooth muscle involves activation of Ca(2+) entry and ROK, ERK pathways. Research Abstract Details 

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  • Brazilein-induced contraction of rat arterial smooth muscle involves activation of Ca(2+) entry and ROK, ERK pathways. Abstract Text:

    jia shenJia Shen,siewting yipSiewting Yip,zhixing wangZhixing Wang,wei wangWei Wang,dongming xingDongming Xing,lijun duLijun Du,

    Brazilein (6a,7-dihydro-3,6a,10-trihydroxy-benz[b]indeno[1,2-d]pyran-9(6H)-one) is a compound isolated from Caesalpinia sappan. The vasoactivities of brazilein were evaluated in isolated rat thoracic aorta. The results showed that brazilein can dose-dependently induce contraction of rat thoracic aorta in the resting and phenylephrine pre-evoked state. The average response to 100 muM of brazilein was 30% of the 50 mM KCl contraction, 26% of the 10 muM phenylephrine and 116% of the 20 mM caffeine contraction in comparison. The effects of vasocontraction were proved not to be endothelial dependent and could not be inhibited by alpha-adrenergic receptor blocker phentolamine, beta-adrenergic receptor blocker propranolol, M-adrenaline receptor blocker atropine, angiotensin II receptor blocker losartan or the non-selective nitric oxide synthase (NOS) inhibitor NG-Nitro-l-Arginine Methyl Ester (l-NAME). However the influx of extracellular calcium seemed to be required for this action, because depletion of extracellular calcium and the addition of L-type calcium ion channel antagonist (nimodipine and diltiazem), calcium ion channel activator (BAY-K8644) and potassium ion channel opener (pinacidil) could significantly affect the contraction induced by brazilein. We also investigated the possible signal mechanisms underlying brazilein-induced contraction using selective inhibitors. The inhibitors of myosin light chain kinase (MLCK), Rho-kinase (ROK) and extracellular signal regulated kinase (ERK) can suppress the effect of brazilein respectively, whereas inhibitors of other signaling or receptor molecules such as protein kinase C (PKC) and inositol 1,4,5-triphosphate (IP(3)) receptor had no effect. All these results demonstrated that brazilein can induce contraction of rat aorta, that the Ca(2+) influx, ROK and ERK signal pathways and MLCK activation must be involved in the contractile processes.

    Brazilein-induced contraction of rat arterial smooth muscle involves activation of Ca(2+) entry and ROK, ERK pathways. Publishing Authors By Initials

    j shenJ Shen,s yipS Yip,z wangZ Wang,w wangW Wang,d xingD Xing,l duL Du,

    For similar abstracts research abstracts see: abstracts research

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    Brazilein-induced contraction of rat arterial smooth muscle involves activation of Ca(2+) entry and ROK, ERK pathways. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: European journal of pharmacology

    VOLUME: 580

    Page Numbers: 366-71

    Journal Abbreviation: Eur. J. Pharmacol.

    ISSN: 0014-2999

    DAY: 17

    MONTH: 11

    YEAR: 2007

    Brazilein-induced contraction of rat arterial smooth muscle involves activation of Ca(2+) entry and ROK, ERK pathways. Information

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    LANGUAGE: eng

    NlmUniqueID: 1254354

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    Grant and Affiliation Information for Brazilein-induced contraction of rat arterial smooth muscle involves activation of Ca(2+) entry and ROK, ERK pathways.

    AFFILIATION: Protein Science Laboratory of the Ministry of Education, Laboratory of Pharmaceutical Sciences, Department of Biological Sciences and Biotechnology, Tsinghua University, Beijing 100084, China.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: Eur J Pharmacol

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