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Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs.

Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs. Research Abstract Details 

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  • Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs. Abstract Text:

    raymond k kudejRaymond K Kudej,you-tang shenYou-Tang Shen,athanasios p peppasAthanasios P Peppas,cheng-hsiung huangCheng-Hsiung Huang,wei chenWei Chen,lin yanLin Yan,dorothy e vatnerDorothy E Vatner,stephen f vatnerStephen F Vatner,

    We tested the hypothesis that cardiac nerves may mediate ischemic preconditioning. Pigs were chronically instrumented to measure aortic, left atrial and left ventricular pressures, and regional myocardial function (wall thickening). Hemodynamic variables, area at risk, and tissue blood flows (radioactive microspheres) were similar among groups. Myocardial infarct size following 60 minutes coronary artery occlusion and 4 days reperfusion, expressed as a fraction of the area at risk, was 42+/-4.0%, in innervated pigs and similar in pigs with regional cardiac denervation (CD, 41+/-2.5%). Infarct size in innervated pigs during the first window of preconditioning (first window) was markedly reduced (6+/-1.8%, P<0.01), as it was in the second window of preconditioning (second window) (16+/-3.3%, P<0.01). Although infarct size was still reduced in pigs with CD and first window preconditioning (9+/-1.8%, P<0.01), the protective effects of second window were abrogated in pigs with CD resulting in an infarct size of 38+/-5.6%. In another group of innervated pigs during pharmacological alpha(1)-adrenergic receptor (AR) blockade, infarct size was also not reduced during the second window (48+/-3.2%). Additionally, Western blot analysis of inducible nitric oxide synthase and cyclooxygenase-2 proteins demonstrated significant (P<0.05) upregulation following the second window in innervated pigs, but not in pigs with CD or alpha(1)-AR blockade. Thus, the mechanism of protection during the second window, but not the first window, appears to be dependent on cardiac nerves and alpha(1)-AR stimulation.

    Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs. Publishing Authors By Initials

    rk kudejRK Kudej,yt shenYT Shen,ap peppasAP Peppas,ch huangCH Huang,w chenW Chen,l yanL Yan,de vatnerDE Vatner,sf vatnerSF Vatner,

    For similar animals: chordata: vertebrates: mammals: artiodactyla: swine research abstracts see: animals: chordata: vertebrates: mammals: artiodactyla: swine research

    PUBMED ID PMID:

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    Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Circulation research

    VOLUME: 99

    Page Numbers: 1270-6

    Journal Abbreviation: Circ. Res.

    ISSN: 1524-4571

    DAY: 26

    MONTH: 10

    YEAR: 2006

    Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 47103

    Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs. Keywords Mesh Terms:

    KEYWORDS: Swine

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs. Information

    Substance Name: Cyclooxygenase 2

    Registry Number: EC 1.14.99.1

    Grant and Affiliation Information for Obligatory role of cardiac nerves and alpha1-adrenergic receptors for the second window of ischemic preconditioning in conscious pigs.

    AFFILIATION: Cardiovascular Research Institute, Department of Cell Biology and Molecular Medicine, UMDNJ-New Jersey Medical School, Newark 07103, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: HL59139

    ACRONYM: HL

    MEDLINETA: Circ Res

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