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isoproterenol and Asymmetric Septal Hypertrophy, Familial

isoproterenol has been researched along with Asymmetric Septal Hypertrophy, Familial in 8 studies

Isoproterenol: Isopropyl analog of EPINEPHRINE; beta-sympathomimetic that acts on the heart, bronchi, skeletal muscle, alimentary tract, etc. It is used mainly as bronchodilator and heart stimulant.
isoprenaline : A secondary amino compound that is noradrenaline in which one of the hydrogens attached to the nitrogen is replaced by an isopropyl group. A sympathomimetic acting almost exclusively on beta-adrenergic receptors, it is used (mainly as the hydrochloride salt) as a bronghodilator and heart stimulant for the management of a variety of cardiac disorders.

Research Excerpts

ExcerptRelevanceReference
"Arrhythmias were attenuated with the β-blocker atenolol and protein kinase A inhibitor PKI."1.91Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy. ( Barratt Ross, S; Cserne Szappanos, H; Dixon, RE; Hill, A; Holliday, M; Hool, LC; Ito, DW; Lim, S; Mangala, M; Semsarian, C; Viola, HM, 2023)
"Troponin T (TnT) mutations that cause familial hypertrophic cardiomyopathy (FHC) and sudden cardiac death frequently increase myofilament Ca2+ sensitivity, suggesting that their Ca2+-sensitizing effect contributes importantly to the FHC pathogenesis."1.33Differential effect of troponin T mutations on the inotropic responsiveness of mouse hearts--role of myofilament Ca2+ sensitivity increase. ( Knollmann, BC; Potter, JD; Sirenko, SG, 2006)
"Sudden cardiac death is related to adrenergic stress and is independent of the development of fibrosis but occurred only in male mice."1.32Hypertrophy, fibrosis, and sudden cardiac death in response to pathological stimuli in mice with mutations in cardiac troponin T. ( Ikeda, K; Leinwand, LA; Maass, AH; Maier, SK; Oberdorf-Maass, S, 2004)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19901 (12.50)18.7374
1990's0 (0.00)18.2507
2000's5 (62.50)29.6817
2010's1 (12.50)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Cserne Szappanos, H1
Viola, HM1
Ito, DW1
Lim, S1
Mangala, M1
Holliday, M1
Barratt Ross, S1
Semsarian, C1
Hill, A1
Dixon, RE1
Hool, LC1
Peña, JR1
Szkudlarek, AC1
Warren, CM1
Heinrich, LS1
Gaffin, RD1
Jagatheesan, G2
del Monte, F1
Hajjar, RJ1
Goldspink, PH1
Solaro, RJ2
Wieczorek, DF3
Wolska, BM1
Knollmann, BC2
Kirchhof, P1
Sirenko, SG2
Degen, H1
Greene, AE1
Schober, T1
Mackow, JC1
Fabritz, L1
Potter, JD2
Morad, M1
WHALEN, RE1
COHEN, AI1
SUMNER, RG1
McINTOSH, HD1
Prabhakar, R1
Petrashevskaya, N2
Schwartz, A2
Aronow, B1
Boivin, GP1
Molkentin, JD1
Maass, AH1
Ikeda, K1
Oberdorf-Maass, S1
Maier, SK1
Leinwand, LA1
Rajan, S1
Boivin, G1
Arteaga, GM1
Liggett, SB1

Other Studies

8 other studies available for isoproterenol and Asymmetric Septal Hypertrophy, Familial

ArticleYear
Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy.
    Scientific reports, 2023, 07-12, Volume: 13, Issue:1

    Topics: Animals; Arrhythmias, Cardiac; Cardiomyopathy, Hypertrophic; Cardiomyopathy, Hypertrophic, Familial;

2023
Neonatal gene transfer of Serca2a delays onset of hypertrophic remodeling and improves function in familial hypertrophic cardiomyopathy.
    Journal of molecular and cellular cardiology, 2010, Volume: 49, Issue:6

    Topics: Actin Cytoskeleton; Adenoviridae; Animals; Animals, Newborn; Atrial Natriuretic Factor; Calcium-Bind

2010
Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling.
    Circulation research, 2003, Mar-07, Volume: 92, Issue:4

    Topics: Action Potentials; Anesthesia; Animals; Blood Pressure; Calcium; Cardiomyopathy, Hypertrophic, Famil

2003
Demonstration of the dynamic nature of idiopathic hypertrophic subaortic stenosis.
    The American journal of cardiology, 1963, Volume: 11

    Topics: Aortic Valve Stenosis; Cardiomyopathy, Hypertrophic; Cardiomyopathy, Hypertrophic, Familial; Constri

1963
A mouse model of familial hypertrophic cardiomyopathy caused by a alpha-tropomyosin mutation.
    Molecular and cellular biochemistry, 2003, Volume: 251, Issue:1-2

    Topics: Amino Acid Sequence; Animals; Binding Sites; Body Weight; Cardiomyopathy, Hypertrophic, Familial; Ca

2003
Hypertrophy, fibrosis, and sudden cardiac death in response to pathological stimuli in mice with mutations in cardiac troponin T.
    Circulation, 2004, Oct-12, Volume: 110, Issue:15

    Topics: Adrenergic alpha-Agonists; Adrenergic beta-Agonists; Amino Acid Substitution; Angiotensin II; Animal

2004
Differential effect of troponin T mutations on the inotropic responsiveness of mouse hearts--role of myofilament Ca2+ sensitivity increase.
    The Journal of physiology, 2006, Aug-15, Volume: 575, Issue:Pt 1

    Topics: Actin Cytoskeleton; Adrenergic beta-Antagonists; Animals; Calcium; Cardiomyopathy, Hypertrophic, Fam

2006
Rescue of tropomyosin-induced familial hypertrophic cardiomyopathy mice by transgenesis.
    American journal of physiology. Heart and circulatory physiology, 2007, Volume: 293, Issue:2

    Topics: Actin Cytoskeleton; Adrenergic beta-Agonists; Animals; Calcium; Cardiomyopathy, Hypertrophic, Famili

2007