First published online March 14, 2005
Journal of Experimental Biology 208, 1045-1052 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01506
Endothelin-1, superoxide and adeninediphosphate ribose cyclase in shark vascular smooth muscle
Susan K. Fellner1,2,* and
Laurel Parker1
1 Mount Desert Island Biological Laboratory, Salisbury Maine 04672
USA
2 Department of Cell and Molecular Physiology, University of North Carolina
at Chapel Hill, Chapel Hill, NC 27599-7545, USA

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Fig. 1. Representative tracing of cytosolic Ca2+
([Ca2+]i) response of shark anterior mesenteric artery
vascular smooth muscle (VSM) to endothelin-1 (ET-1) in Ca2+-free
shark Ringers followed by the addition of Ca2+ (2.5 mmol
l-1).
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Fig. 2. Effect of inhibitors of ADPR cyclase on endothelin-1 (ET-1)-stimulated
increases in [Ca2+]i in vascular smooth muscle (VSM).
(A) Representative tracing of the [Ca2+]i response to
ET-1 in the presence and absence of nicotinamide. (B) Representative tracing
of the response to ET-1 in the presence and absence of Zn2+. (C)
Summary data of the effects of nicotinamide (N=15) and
Zn2+ (N=11) on the ET-1-induced peak elevation of
[Ca2+]i. *P<0.01 for both
inhibitors vs ET-1 alone.
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Fig. 3. Effect of NAD(P)H oxidase inhibitor (DPI) and superoxide dismutase mimetic
(TEMPOL) on endothelin-1 (ET-1) stimulation of [Ca2+]i
in shark vascular smooth muscle (VSM). (A) Typical tracing of the
[Ca2+]i response to ET-1 in the presence and absence of
DPI. (B) Typical tracing of the ET-1 in the presence and absence of TEMPOL.
(C) Summary data showing the inhibitory effects of DPI (N=19) and
TEMPOL (N=19) on the ET-1 induced elevation of
[Ca2+]i. *P<0.01 for ET-1 plus
DPI or TEMPOL vs ET-1 alone.
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Fig. 4. Effects of combining inhibitors of the IP3 receptor with an
inhibitor of NAD(P)H oxidase (DPI) or a superoxide scavenger (TEMPOL) in
Ca2+-free shark Ringers. In each case, the combination of
antagonists blocked the [Ca2+]i response to endothelin-1
(ET-1) by 83±1%. *P<0.01.
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© The Company of Biologists Ltd 2005