Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 1995;77:80-87

This Article
Right arrow Full Text
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kihara, Y.
Right arrow Articles by Sasayama, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kihara, Y.
Right arrow Articles by Sasayama, S.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*(L)-METHIONINE
*CALCIUM COMPOUNDS
*CALCIUM, ELEMENTAL
(Circulation Research. 1995;77:80-87.)
© 1995 American Heart Association, Inc.


Articles

L-Methionine Augments Mammalian Myocardial Contraction by Sensitizing the Myofilament to Ca2+

Yasuki Kihara, Moriaki Inoko, Shigetake Sasayama

From the Second Department of Internal Medicine, Toyama (Japan) Medical and Pharmaceutical University School of Medicine (Y.K., M.I.), and the Third Division, Department of Internal Medicine, Kyoto (Japan) University Faculty of Medicine (S.S.).

Correspondence to Yasuki Kihara, MD, PhD, Third Division, Department of Internal Medicine, Kyoto University Faculty of Medicine, 54 Shogoin Kawaharacho, Sakyo, Kyoto 606, Japan.

Abstract L-Methionine is an essential amino acid that has been reported to have a potent positive inotropic effect on the mammalian myocardium. We studied the mechanisms of the inotropic effect in ventricular myocardium from the rabbit. In the isolated coronary-perfused whole heart, L-methionine in a millimolar range exerted concentration-dependent positive inotropic effects on the isovolumic left ventricle, which were associated with negative lusitropic effects (prolonged time course of relaxation). The chronotropic state and the coronary perfusion pressure were not affected. These complex effects on the isolated whole heart were not blocked by pretreatment with (µmol/L) propranolol 1, prazosin 1, carbachol 3, staurosporine 1, or [Ser1,Ile8]angiotensin II 0.1. To further study the subcellular mechanisms, isolated ventricular papillary muscles from the same species were loaded with a bioluminescent indicator, aequorin, to monitor [Ca2+]i. In the presence of 3 mmol/L L-methionine, the isometric tension showed a similar combination of the positive inotropic and negative lusitropic effects as observed in the whole heart. In contrast, the simultaneously recorded intracellular Ca2+ signals did not increase in amplitude but instead decreased. The [Ca2+]i-tension relation shifted to the left compared with that obtained in response to [Ca2+]o. In saponin (250 µg/mL)–treated skinned preparations, 3 mmol/L L-methionine also shifted the force-pCa curve to the left by 0.16 pCa units. This is the first demonstration that an essential amino acid directly acts on the myofilaments and modulates their responsiveness to Ca2+, thereby producing a positive inotropic effect.


Key Words: essential amino acids • inotropic effects • Ca2+ • aequorin • rabbits




This article has been cited by other articles:


Home page
Physiol. Rev.Home page
A. Takahashi, P. Camacho, J. D. Lechleiter, and B. Herman
Measurement of Intracellular Calcium
Physiol Rev, October 1, 1999; 79(4): 1089 - 1125.
[Abstract] [Full Text] [PDF]