First published online December 1, 2006
Journal of Experimental Biology 209, 4966-4973 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02595
Beta3-Adrenoceptor in the eel (Anguilla anguilla) heart: negative inotropy and NO-cGMP-dependent mechanism
S. Imbrogno1,2,
T. Angelone1,2,
C. Adamo2,
E. Pulerà2,
B. Tota2,* and
M. C. Cerra1,2
1 Departments of Pharmaco-Biology, University of Calabria, 87030, Arcavacata
di Rende, CS, Italy
2 Departments of Cell Biology, University of Calabria, 87030, Arcavacata di
Rende, CS, Italy

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Fig. 1. Cumulative dose-response curve for BRL37344 on stroke volume
(VS) and stroke work (WS) in isolated
and perfused paced eel hearts. Percentage changes were evaluated as means
± s.e.m. (N=9). Significance of differences from control
values (one-way ANOVA test) **P<0.01.
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Fig. 2. Effects of BRL37344 (10 nmol l-1) before and after
treatment with nadolol (10 µmol l-1) on stroke volume
(VS) and stroke work (WS) in isolated
and perfused paced eel hearts. Percentage changes were evaluated as means
± s.e.m. (N=6). One-way ANOVA was used for comparisons within
groups; significance of differences from control values
*P<0.05. Comparison between groups (two-way ANOVA,
Duncan's test); P<0.05.
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Fig. 3. The sigmoid concentration-response curves of BRL37344-mediated
inhibition on VS of BRL37344 alone (0.1-100
nmol l-1) and of BRL 37344 plus a single concentration
of SR59230 (10 nmol l-1) on the isolated and perfused
working eel heart preparation. Inhibition of contractility is expressed as a
percentage of VS [baseline=0%, peak inhibition by
BRL37344 and BRL37344 plus SR59230= -100%].
The EC50 values (in log mol l-1) of BRL37344
alone was -7.68±0,12 (r2=0.98), of BRL
37344 plus SR59230 (10 nmol l-1) was
-6.6±0.55 (r2=0.96). Comparison between groups
(two-way ANOVA, Duncan's test); P<0.05
(N=8).
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Fig. 4. Effects of isoproterenol (ISO; 100 nmol l-1) before and after
treatment with SR59230 (10 nmol l-1) on stroke volume
(VS) and stroke work (WS) in isolated
and perfused paced eel hearts. Percentage changes were evaluated as means
± s.e.m. (N=7). One-way ANOVA was used for comparisons within
groups; significance of differences from control values
*P<0.05. Comparison between groups (two-way ANOVA,
Duncan's test) P<0.05.
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Fig. 5. Effects of BRL37344 (10 nmol l-1) before and after
treatment with pertussis toxin (PTx; 0.01 nmol l-1) on stroke
volume (VS) and stroke work (WS) in
isolated and perfused paced eel hearts. Percentage changes were evaluated as
means ± s.e.m. (N=6). One-way ANOVA was used for comparisons
within groups; significance of differences from control values
*P<0.05. Comparison between groups (two-way ANOVA,
Duncan's test); P<0.05.
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Fig. 6. Effects of BRL37344 (10 nmol l-1) before and after
treatment with L-N5-(1-iminoethyl)ornitine (L-NIO; 10 µmol
l-1), haemoglobin (Hb; 1 µmol l-1),
1H-(1,2,4)oxadiazolo-(4,3-a)quinoxalin-1-one (ODQ; 10 µmol l-1)
and KT5823 (100 nmol l-1) on stroke volume
(VS) and stroke work (WS) in isolated
and perfused paced eel hearts. Percentage changes were evaluated as means
± s.e.m. (N=7-8 experiments for each drug). One-way ANOVA was
used for comparisons within groups; significance of differences from control
values *P<0.05. Comparison between groups (two-way
ANOVA, Duncan's test) P<0.05.
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© The Company of Biologists Ltd 2006