P. Saitongdee et al., Increased connexin43 gap junction protein in hamster cardiomyocytes duringcold acclimatization and hibernation, CARDIO RES, 47(1), 2000, pp. 108-115
Citations number
43
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective: The physiology of hibernation is characterized by dramatic reduc
tions of heart rate, respiration, metabolism, blood pressure and body tempe
rature and by resistance to ventricular fibrillation. Gap junctions in the
heart provide low resistance pathways, facilitating electrical and metaboli
c coupling between cardiac muscle cells for coordinated action of the heart
and tissue homeostasis. The conductance of these junctions, and therefore
their function, is likely to be affected by the physiological changes that
take place during hibernation. Our objective was to quantitate gap junction
protein levels in cold acclimatization, hibernation and arousal. Methods:
We have used specific antibodies to connexins 43 and 40, in combination wit
h confocal microscopy, to quantitatively analyze the expression of connexin
protein in hamster (Mesocricetus auratus) left ventricles in four animal g
roups: normal controls at euthermy, cold controls (cold-exposed animals tha
t did not undergo hibernation), hibernating animals and animals aroused fro
m hibernation for 2 h. Results: Connexin40 immunostaining was not detected
in ventricular cardiomyocytes in any animal group but connexin43 was found
in all groups. Connexin43 expression was significantly enhanced in hibernat
ion and cold control ventricular cardiomyocytes. Total plaque area, numeric
al density and plaque size were higher in the cold controls and hibernating
hamsters compared to normal controls and animals aroused from hibernation.
Conclusion: It is possible that the increased size and number of connexin4
3 gap junction plaques in the cold controls may represent a compensatory re
sponse in order to maintain sufficient gap junction communication during ph
ysiological conditions that would reduce conductance. These changes may rep
resent a mechanism by which the hamster avoids ventricular fibrillation dur
ing hibernation and arousal. (C) 2000 Elsevier Science B.V. All rights rese
rved.