spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Summary Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wang, S. Q.
Right arrow Articles by Zhou, Z. Q.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, S. Q.
Right arrow Articles by Zhou, Z. Q.

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



View larger version (12K):

[in a new window]
 
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 (1999bGo). Values are means ± S.E.M. (N=12 for rat, N=9 for ground squirrel; P<0.01 at 10°C).

 


View larger version (22K):

[in a new window]
 
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.

 


View larger version (10K):

[in a new window]
 
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., 1995Go).

 


View larger version (17K):

[in a new window]
 
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., 1995Go).

 





© The Company of Biologists Ltd 2002