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Vol. 290, Issue 3, 1006-1012, September 1999
Meiji Institute of Health Science, Meiji Milk Products Co., Ltd.,
Odawara, Kanagawa, Japan
The effects of natural cyclodepsipeptides (CDPs) on isolated rat
cardiac tissue preparations were examined in vitro. Destruxin A,
destruxin B (DB), roseotoxin B (RB), and roseocardin (RC), a novel CDP,
each caused a concentration-dependent increase in the contraction force
of the right atrium and the papillary and trabecular muscles of the
right ventricle at 0.6 to 600 µM. RB, destruxin A, and DB did not
affect the half-decay time of relaxation of the papillary muscles, but
RC slightly prolonged it, although to a much lesser extent than BA
41899, a calcium sensitizer. This inotropic effect is accompanied by a
prolongation of the automatic atrial contraction intervals. The
RB-induced increase in the contraction force of papillary muscle was
not affected by phentolamine, propranolol, pyrilamine, or cimetidine.
RB- and RC-induced increases in the contraction force of papillary
muscles were not affected by 3-isobutyl-1-methylxanthine or carbachol.
Neither peptide changed the cyclic AMP levels in trabecular muscles.
Neither RB nor RC affected the activity of Na+,K+-ATPase from rat kidney. Neither RB, RC,
nor DB affected the resting membrane potential or the apparent input
resistance of papillary muscles. These results suggest that these CDPs
produce both non-cyclic AMP-dependent positive inotropic and negative
chronotropic effects.