Js. Danetz et al., Age-related effects of St Thomas' Hospital cardioplegic solution on isolated cardiomyocyte cell volume, J THOR SURG, 118(3), 1999, pp. 467-476
Citations number
29
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objectives: We tested the hypothesis that neonatal cells are more sensitive
to cardioplegia-induced cell swelling than more mature cells and spontaneo
us swelling in the absence of ischemia can be prevented by cardioplegia wit
h a physiologic KCl product. Methods: Cell volumes of isolated ventricular
myocytes from neonatal (3-5 days), intermediate (10-13 days), and adult (>6
weeks) rabbits were measured by digital video microscopy. After equilibrat
ion in 37 degrees C physiologic solution, cells were suprafused with 37 deg
rees C or 9 degrees C St Thomas' Hospital solution (standard or low Cl-) or
9 degrees C physiologic solution followed by reperfusion with 37 degrees C
physiologic solution. Results: Neonatal cells swelled 16.2% +/- 1.8% (P <
.01) in 37 degrees C St Thomas' Hospital solution and recovered during repe
rfusion, whereas more mature cells maintained constant volume, In contrast,
9 degrees C St Thomas' Hospital solution caused significant age-dependent
swelling (neonatal, 16.8% +/- 1.5%; intermediate, 8.6% +/- 2.1%; adult, 5.6
% +/- 1.1%). In contrast to more mature cells, neonatal cells remained sign
ificantly edematous throughout reperfusion (8.1% +/- 1.5%). Swelling was no
t due to hypothermia because 9 degrees C physiologic solution did not affec
t volume, Lowering the KCl product of St Thomas' Hospital solution by parti
ally replacing Cl- with an impermeant anion prevented cellular edema in all
groups, Conclusion: In the absence of ischemia, neonatal cells were more s
ensitive to cardioplegia-induced cellular edema than more mature cells, and
edema observed in all groups was avoided by decreasing the KCl product of
St Thomas' Hospital solution to the physiologic range. Differences in cell
volume regulation may explain the sensitivity of neonatal hearts to hyperka
lemic cardioplegic arrest and suggest novel approaches to improving myocard
ial protection.