Experimental studies on the endothelium ultrastructure of heart capillaries under moderate (28-30 degrees) and deep (22-24 degrees) hypothermia without perfusion
Gm. Kazanskaya et al., Experimental studies on the endothelium ultrastructure of heart capillaries under moderate (28-30 degrees) and deep (22-24 degrees) hypothermia without perfusion, MICROVASC R, 58(3), 1999, pp. 250-267
Ultrastructural changes in endothelial cells (EC) of myocardial capillaries
were studied in 24 dogs which underwent hypothermia without perfusion. Bio
psy specimens for electron microscopy were taken from the left ventricle of
each dog in the control group, during anesthesia (prior to active cooling)
, and at the end of moderate (28-30 degrees) and deep (22-24 degrees) artif
icial body cooling. The following morphological types of the EC were identi
fied both in the control group and in all test groups: those with moderatel
y dense cytoplasm, light, dark, and irreversibly damaged cells. Dark cells
showed increased numbers of plasmalemmal vesicles and appeared to be more t
ransport-specialized as opposed to other types. In all stages of the experi
ment the amount of dark cells continuously increased (to 23.80, 34.62, and
47.17%, respectively). On cooling to 28-30 degrees, subcellular manifestati
on of reduced synthetic activity of organelles (nucleus; Golgi complex, and
rough endoplasmic reticulum) was observed in all types of the EC. These ch
anges persisted, or even increased, at the end of deep hypothermia. The tra
nsport activity of the EC changed differently in three experimental groups
in all cell types. Micropinocytotic activity increased under spontaneous mi
ld hypothermia (34-35 degrees) during anesthesia and tended to decrease wit
h subsequent artificial lowering of the temperature to 22-24 degrees. These
ultrastructural changes seem to make up an integral part of the process of
capillary endothelium adaptation to body surface cooling, and they might c
ontribute to the development of tolerance to subsequent ischemic exposure d
uring cardiac arrest. (C) 1999 Academic Press.