Dehydration is known to significantly reduce both the time required for the
first platelet aggregate and the time to full occlusion in photochemically
-induced thrombosis, in vivo. Ultrastructural changes that contribute to su
ch events remain unknown. Therefore, the effect of water deprivation for 24
hr, las a model for dehydration) on the ultrastructure of mouse pial micro
vessels was investigated. The possible beneficial effect of garlic in preve
nting such ultrastructural changes was also investigated. Four groups of TO
strain: control, control-garlic treated, dehydrated, and dehydrated-garlic
treated male mice, 10/group, were used. Dehydration was induced by water d
eprivation for 24 hr. Garlic solution was i.p. injected at 0.1 ml/10g body
weight. In urethane-anesthetized (2 mg/g, i.p.) mice, topical and transvess
el bimodal fixation of pial microvessels was done with a phosphate buffered
mixture of glutaraldehyde and paraformaldehyde, followed by a conventional
electron microscopy procedure. Examination of control cerebral pial microv
essels showed no evidence of cellular damage. Membranes of endothelial cell
s were intact. Within pial microvessels there was no evidence of platelet a
ggregation. Garlic treatments did not cause any ultrastructure abnormalitie
s in control mice. Compared with control, dehydration caused the appearance
of thrombi that consisted of platelet aggregates. Discoid platelets contai
ning granules, spheroid degranulated platelets, and those with large pseudo
podia were present in 80% of dehydrated mice. The venular endothelial surfa
ce of dehydrated mice revealed dilated profiles of endoplasmic reticulum an
d variously shaped vacuoles, Swelling of nuclear envelopes and mitochondria
l distension were also present in dehydrated mice. Concomitant garlic treat
ment prevented most of these ultrastructural changes. These findings demons
trated the extent of damage to the pial microvessels in response to water d
eprivation and demonstrated the beneficial effect of garlic as a possible m
ean of protection against oncoming vascular pathology. Anat Rec 263:85-90,
2001. (C) 2001 Wiley-Liss, Inc.