Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1993 Mar;24(2):305-10.
doi: 10.1016/0306-3623(93)90307-j.

The negative inotropic effects of amiodarone on isolated guinea pig heart: a possible role of Na(+)-Ca2+ exchange

Affiliations

The negative inotropic effects of amiodarone on isolated guinea pig heart: a possible role of Na(+)-Ca2+ exchange

M Aomine et al. Gen Pharmacol. 1993 Mar.

Abstract

1. The negative inotropic effects of amiodarone (AM) were studied in isolated, isometrically contracting ventricular papillary muscles from guinea pigs. 2. AM, 4.4 x 10(-5) M, significantly decreased ouabain (10(-6) M)-induced increase in the developed tension. 3. Manganese (10(-2) M), a partial blocker of Na(+)-Ca2+ exchange, attenuated the AM's negative inotropy. 4. Theophylline (1.5 x 10(-2) M), an inhibitor of phosphodiesterase, produced a marked increase in the tension (about twice compared to the ouabain effect). 5. However, the magnitude of decrease by AM in the tension in the presence of theophylline was similar to that in the case of ouabain. 6. Tetrodotoxin (TTX) decreased the contraction by about a half, and then subsequent addition of AM in the presence of TTX led to a further decrease in the tension. 7. Eventually co-existence of TTX and AM led to a decrease in tension of same degree, compared to the decrease in tension by AM alone. 8. The results suggest that a large portion of negative inotropic action of AM may, at least, reflect interference with the Na(+)-Ca2+ exchange mechanism. 9. This interference with the Na(+)-Ca2+ exchange mechanism may exert a strong negative inotropic effect of the drug, in combination with a decrease in Ca2+ influx via Ca2+ channels and/or an impairment of Ca(2+)-sequestration.

PubMed Disclaimer

LinkOut - more resources