First published online February 15, 2008
Journal of Experimental Biology 211, 661-670 (2008)
Published by The Company of Biologists 2008
doi: 10.1242/jeb.011478
Modulatory effects of adenosine and adenine nucleotides on different heart preparations of the American lobster, Homarus americanus
Gereon Maurer1,*,
Jerrel L. Wilkens2 and
Manfred K. Grieshaber1
1 Institut für Zoophysiologie, Heinrich-Heine-Universität,
Universitätsstraße 1, 40225 Düsseldorf, Germany
2 Department of Biological Science, University of Calgary, Calgary, Alberta T2N
1N4, Canada

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Fig. 1. Comparison of (A) heart rate (beats min–1), (B) cardiac
output (ml min–1), (C) ventricular pressure (kPa) and (D)
stroke volume (ml beat–1) in semi-isolated hearts of the
American lobster, Homarus americanus, before
(t0–t5), during
(t6–t7) and after
(t8–t25) the perfusion of 2.5
mmol l–1 solutions of adenosine or adenine nucleotides. The
vertical dashed lines indicate the infusion period. Data are presented as
means ± s.d. (N is given in the respective graphs). An
asterisk denotes a value significantly different from the control value
(P 0.05).
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Fig. 2. Comparison of heart rate (beats min–1) in intact (A) and
cardioregulatory-denervated (B) Homarus americanus before
(t0–t10), during
(t11–t20) and after
(t21–t60) the perfusion of a
solution of 2.4 nmol min–1 g–1 body mass of
adenosine or adenine nucleotides. The vertical dashed lines indicate the
infusion period. Data are presented as means ± s.d. (N is
given in the respective graphs). All values under the lines with asterisks at
each end are significantly different from the control value
(P 0.05).
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Fig. 3. Comparison of heart rate in intact (black bars) and
cardioregulatory-denervated (grey bars) Homarus americanus. Values
are the differences between the mean value of the control period and the value
at t20 during the perfusion of a solution of 2.4 nmol
min–1 g–1 body mass of adenosine or adenine
nucleotides. t20 corresponds with the end of the infusion.
Data are presented as means ± s.d. An asterisk denotes a value
significantly different from the control value (P 0.05).
[N=9 (intact) and 10 (cardioregulatory denervated) for adenosine; 7
and 5 for AMP; 6 and 0 for ADP, and 6 and 9 for ATP.]
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Fig. 4. Heart rate (beats min–1) of sham operated lobsters before
(t0–t10), during
(t11–t20) and after
(t21–t60) the perfusion of a solution of
2.4 nmol min–1 g–1 body mass of adenosine.
The vertical dashed lines indicate the infusion period. Data are presented as
means ± s.d. All values under the line with asterisks at each end are
significantly different from the control value (P 0.05)
(N is given in the respective graphs).
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Fig. 5. Comparison of heart rate (beats min–1) and haemolymph
velocity, vHL (mm s–1) in the posterior
aorta, the sternal artery and the left lateral artery in intact (A) and
cardioregulatory-denervated (B) Homarus americanus before
(t0–t10), during
(t11–t20) and after
(t21–t60) the perfusion of
Ringer solution (pH 8.0). The vertical dashed lines indicate the infusion
period. Data are presented as means ± s.d. (N is given in the
respective graphs).
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Fig. 6. Comparison of haemolymph velocity, vHL (mm
s–1) in the posterior aorta in intact (A) and
cardioregulatory-denervated (B) Homarus americanus before
(t0–t10), during
(t11–t20) and after
(t21–t60) the perfusion of a
solution of 2.4 nmol min–1 g–1 body mass of
adenosine or adenine nucleotides. The vertical dashed lines indicate the
infusion period. Data are presented as means ± s.d. (N is
given in the respective graphs). All values under the lines with asterisks at
each end are significantly different from the control value
(P 0.05).
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Fig. 7. Comparison of haemolymph velocity, vHL (mm
s–1) in the sternal artery in intact (A) and
cardioregulatory-denervated (B) Homarus americanus before
(t0–t10), during
(t11–t20) and after
(t21–t60) the perfusion of a
solution of 2.4 nmol min–1 g–1 body mass of
adenosine or adenine nucleotides. The vertical dashed lines indicate the
infusion period. Data are presented as means ± s.d. (N is
given in the respective graphs). All values under the line with asterisks at
each end are significantly different from the control value
(P 0.05).
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Fig. 8. Comparison of haemolymph velocity, vHL (mm
s–1) in the left lateral artery in intact (A) and
cardioregulatory-denervated (B) Homarus americanus before
(t0–t10), during
(t11–t20) and after
(t21–t60) the perfusion of a
solution of 2.4 nmol min–1 g–1 body mass of
adenosine or adenine nucleotides. The vertical dashed lines indicate the
infusion period. Data are presented as means ± s.d. (N is
given in the respective graph). All values under the line with asterisks at
each end are significantly different from the control value
(P 0.05).
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Fig. 9. Haemolymph concentration of dopamine (A), serotonin (B) and octopamine (C)
before (t0), during
(t2.5–t10) and after
(t12.5–t30) the perfusion of a
solution of 2.4 nmol min–1 g–1 body mass of
adenosine. The vertical dotted lines indicate the infusion period. Data are
presented as means ± s.d. (N=5).
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© The Company of Biologists Ltd 2008