Abnormal myocardial contraction in α1A- and α 1B-adrenoceptor double-knockout mice

Diana T. mccloskey, Lynne Turnbull, Philip Swigart, Timothy D. O'Connell, Paul C. Simpson, Anthony J. Baker

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36 Scopus citations


We used double-knockout mice (ABKO) lacking both predominant myocardial α1-adrenergic receptor (AR) subtypes (α1A and α1B) to determine if α1-ARs are required for normal myocardial contraction. Langendorff-perfused ABKO hearts had higher developed pressure than wild type (WT) hearts (123 ± 3 mmHg n = 22 vs. 103 ± 3 mmHg, n = 38, P < 0.001). Acutely inhibiting α 1-ARs in WT hearts with prazosin did not increase pressure, suggesting that the increased pressure of ABKO hearts was mediated by long-term trophic effects on contraction rather than direct regulatory effects of α1-AR removal. Similar to perfused hearts, ABKO ventricular trabeculae had higher submaximal force at 2 mM extracellular [Ca2+] than WT (11.4 ± 1.7 vs. 6.9 ± 0.6 mN/mm2, n = 8, P < 0.05); however, the peaks of fura-2 Ca2+ transients were not different (0.79 ± 0.11 vs. 0.75 ± 0.16 μM, n = 10-12, P > 0.05), suggesting ABKO myocardium had increased myofilament Ca 2+-sensitivity. This conclusion was supported by measuring the Ca2+-force relationship using tetanization. Increased myofilament Ca2+-sensitivity was not explained by intracellular pH, which did not differ between ABKO and WT (7.41 ± 0.01 vs. 7.39 ± 0.02, n = 4-6, P > 0.05; from BCECF fluorescence). However, ABKO displayed impaired troponin I phosphorylation, which may have played a role. In contrast to increased submaximal force, ABKO trabeculae had lower maximal force than WT at high extracellular [Ca2+] (29.6 ± 1.9 vs. 37.6 ± 1.4 mN/mm2, n = 7, P < 0.01). However, peak cytosolic [Ca 2+] was not different (1.13 ± 0.15 vs. 1.19 ± 0.04 μM, n = 6-7, P > 0.05), suggesting ABKO myocardium had impaired myofilament function. Finally, ABKO myocardium had decreased responsiveness to β-AR stimulation. We conclude: α1-ARs are required for normal myocardial contraction; α1-ARs mediate long-term trophic effects on contraction; loss of α1-AR function causes some of the functional abnormalities that are also found in heart failure.

Original languageEnglish (US)
Pages (from-to)1207-1216
Number of pages10
JournalJournal of Molecular and Cellular Cardiology
Issue number10
StatePublished - Oct 1 2003

Bibliographical note

Funding Information:
This work was supported by NIH grants HL 56257 and P01 HL68738 – project 3 (A.J.B.), HL 54890 and HL 31113 (P.C.S.); and a postdoctoral fellowship HL10422 (D.T.M.); and by a Grant-in-Aid from the American Heart Association, Western States Affiliate (A.J.B.). A.J. Baker is an Established Investigator of the American Heart Association. Some of these data were published in abstract form: Biophys J 2002;82:190a.


  • ABKO
  • Ca
  • Langendorff
  • Myofilament Ca-sensitivity
  • PH
  • Trabeculae
  • α-adrenergic receptor
  • β-adrenergic receptor


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