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The Journal of Thoracic and Cardiovascular Surgery, Vol 104, 966-971, Copyright © 1992 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
JD Fonger, XM Yang, RA Cohen, CC Haudenschild and RJ Shemin
Internal mammary artery specimens from 17 patients were each divided into
three separate rings. One ring (control) remained in Krebs solution and the
other two were clamped for 30 minutes with either a soft or hard jaw clamp.
Isometric tensions were measured in an organ chamber by contracting the
rings twice with a thromboxane A2 mimetic, U46619, and relaxing the rings
first with the endothelium-dependent agent acetylcholine followed by the
endothelium-independent agent sodium nitroprusside. Endothelium-dependent
maximal relaxation of the rings was impaired from control after both soft
(20% versus 91%; p < 0.01) and hard (1% versus 91%; p < 0.01) jaw
clamps were used. However, relaxation after use of hard jaw clamps was
significantly less than after use of soft jaw clamps (1% versus 20%; p <
0.05). Endothelium- independent maximal relaxation was not impaired from
control after soft jaw clamps (89% versus 97%) were applied but was
significantly impaired after use of the hard jaw clamps compared with
control (73% versus 97%; p < 0.01) and compared with soft jaw clamps
(73% versus 89%; p < 0.05). Rings of internal mammary artery specimens
from 10 patients from each experimental group were silver stained. The
percentage of intact endothelial cells was significantly greater after soft
jaw clamping than after hard jaw clamping (39% versus 15%; p < 0.02).
These data suggest that soft jaw clamps significantly reduce the degree of
vasoactive dysfunction compared with hard jaw clamps. In addition, soft jaw
clamps produce fewer morphologic changes in the human mammary artery after
temporary occlusion.
ARTICLES
Impaired relaxation of the human mammary artery after temporary clamping
Department of Cardiothoracic Surgery, University Hospital, Boston University School of Medicine, Mass. 02118.
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