TY - JOUR
T1 - Aspirin and indomethacin, nonsteroidal antiinflammatory agents alter the responses to microvascular injury in brain and mesentery
AU - Rosenblum, William I.
AU - El-Sabban, F.
AU - Ellis, E. F.
PY - 1980
Y1 - 1980
N2 - We can produce platelet aggregation in the pial or mesentric microcirculation by illuminating a microscopic field containing such vessels with an appropriately filtered mercury lamp in the presence of intravascular sodium fluorescein (4, 5). This phenomenon appears to be a result of endothelial damage produced by the light in the prescence of the dye (5). Pretreatment of the animal with either aspirin or indomethacin inhibits the aggregation in the pial arterioles (5), but enhances aggregation in the mesenteric arterioles (6). During the course of our published studies concerning aggregation we observed arteriolar constriction in the mesentery and dilation in the pia, the latter being augmented and the former being reduced by aspirin and indomethacin. These observations are the subject of this brief report.
AB - We can produce platelet aggregation in the pial or mesentric microcirculation by illuminating a microscopic field containing such vessels with an appropriately filtered mercury lamp in the presence of intravascular sodium fluorescein (4, 5). This phenomenon appears to be a result of endothelial damage produced by the light in the prescence of the dye (5). Pretreatment of the animal with either aspirin or indomethacin inhibits the aggregation in the pial arterioles (5), but enhances aggregation in the mesenteric arterioles (6). During the course of our published studies concerning aggregation we observed arteriolar constriction in the mesentery and dilation in the pia, the latter being augmented and the former being reduced by aspirin and indomethacin. These observations are the subject of this brief report.
UR - https://www.scopus.com/pages/publications/0019300235
U2 - 10.1016/0026-2862(80)90066-7
DO - 10.1016/0026-2862(80)90066-7
M3 - Article
C2 - 7207229
AN - SCOPUS:0019300235
SN - 0026-2862
VL - 20
SP - 374
EP - 378
JO - Microvascular Research
JF - Microvascular Research
IS - 3
ER -