TY - JOUR
T1 - Effects of OR-1896, an active metabolite of levosimendan, on contractile force and aequorin light transients in intact rabbit ventricular myocardium
AU - Takahashi, Reiko
AU - Hassan Talukder, M. A.
AU - Endoh, Masao
PY - 2000
Y1 - 2000
N2 - We performed experiments in rabbit ventricular papillary muscles loaded with aequorin to elucidate the mechanism of positive inotropic effect (PIE) of OR-1896, an active metabolite of levosimendan. The concentration-response curve (CRC) for OR-1896 was biphasic: PIE of OR-1896 reached a plateau at 10-5> M (first phase), and the CRC became steeper at 10-3> M and higher (second phase). Maximal response of the first phase was 11% of the maximal response to isoproterenol (ISO(max)) and associated with an increase in Ca2+ transients of 5% of ISO(max). For a given degree of PIE, the increase in Ca2+ transients by OR-1896 was lower than that induced by elevation of [Ca2+](o). The PIE of OR-1896 was not associated with impairment of relaxation, and it was abolished by carbachol. In conclusion, OR-1896 has a PIE partly due to an increase in myofibrillar Ca2+ sensitivity that is exerted through crosstalk with signal transduction mediated by cyclic adenosine monophosphate (cAMP).
AB - We performed experiments in rabbit ventricular papillary muscles loaded with aequorin to elucidate the mechanism of positive inotropic effect (PIE) of OR-1896, an active metabolite of levosimendan. The concentration-response curve (CRC) for OR-1896 was biphasic: PIE of OR-1896 reached a plateau at 10-5> M (first phase), and the CRC became steeper at 10-3> M and higher (second phase). Maximal response of the first phase was 11% of the maximal response to isoproterenol (ISO(max)) and associated with an increase in Ca2+ transients of 5% of ISO(max). For a given degree of PIE, the increase in Ca2+ transients by OR-1896 was lower than that induced by elevation of [Ca2+](o). The PIE of OR-1896 was not associated with impairment of relaxation, and it was abolished by carbachol. In conclusion, OR-1896 has a PIE partly due to an increase in myofibrillar Ca2+ sensitivity that is exerted through crosstalk with signal transduction mediated by cyclic adenosine monophosphate (cAMP).
UR - http://www.scopus.com/inward/record.url?scp=12944316443&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=12944316443&partnerID=8YFLogxK
U2 - 10.1097/00005344-200007000-00016
DO - 10.1097/00005344-200007000-00016
M3 - Article
C2 - 10892669
AN - SCOPUS:12944316443
SN - 0160-2446
VL - 36
SP - 118
EP - 125
JO - Journal of Cardiovascular Pharmacology
JF - Journal of Cardiovascular Pharmacology
IS - 1
ER -