Adaptive mechanisms of intracellular calcium homeostasis in mammalian hibernators
Shi Qiang Wang1,2,*,
Edward G. Lakatta2,
Heping Cheng2 and
Zeng Quan Zhou1
1 National Laboratory of Biomembrane and Membrane Biotechnology, College of
Life Sciences, Peking University, Beijing 100871, China
2 Laboratory of Cardiovascular Sciences, National Institute on Aging, NIH,
Baltimore, MD 21224, USA

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Fig. 1. Low temperature increases intracellular free [Ca2+] markedly in
resting cardiac myocytes from the rat, but not in those from the ground
squirrel. The Ca2+ concentration was measured using the indo-1
fluorescence ratio as described in Wang and Zhou
(1999b ). Values are means
± S.E.M. (N=12 for rat, N=9 for ground squirrel;
P<0.01 at 10°C).
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Fig. 2. General scheme of intracellular Ca2+ cycling. Ca2+
can enter the cell via Ca2+ channels and, in some
situations, via the Na+Ca2+ exchanger
(NCX). Ca2+ can be released from sarcoplasmic/endoplasmic reticulum
(SR/ER) via Ca2+-release channels, including ryanodine
receptors and inositol (1,4,5)-trisphosphate receptors. Ca2+ is
removed from the cytosol by SR/ER Ca2+-ATPase (SERCA), cytolemmal
Ca2+-ATPase, Na+Ca2+ exchange and the
mitochondrial uniportor.
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Fig. 3. A comparison of action potential and contraction between cardiac myocytes
from non-hibernating and hibernating ground squirrels. The arrow indicates the
absence of the action potential plateau phase due to reduced L-type
Ca2+ currents during hibernation. Note the larger contraction
amplitude in the hibernating state (Wang
et al., 1995 ).
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Fig. 4. Cardiac sarcoplasmic reticulum vesicles from winter-hibernating ground
squirrels exhibit faster Ca2+ uptake than those from autumn,
non-hibernating individuals. The graph shows the normalized change in
[Ca2+] in 1 ml of reaction medium after addition of 1 mg SR
protein. The initial uptake rates for non-hibernating and hibernating groups
were 137±13 and 235±17 nmol
Ca2+min-1mg-1 SR protein, respectively
(Tang et al., 1995 ).
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© The Company of Biologists Ltd 2002