Circulation, Vol 80, 401-409, Copyright © 1989 by American Heart Association
K Komori, H Shimokawa and PM Vanhoutte
The present study examined the protective role of the venous endothelium
against aggregating platelets and its modulation by diet. Yorkshire pigs
were fed a regular chow (control pigs), 2% high- cholesterol diet (for 10
weeks, cholesterol-fed pigs), and regular chow plus cod-liver oil (30
ml/day for 4 weeks, oil-fed pigs). Endothelium- dependent responses were
examined in vitro in rings of femoral veins in the presence of the
inhibitor of cyclooxygenase indomethacin. In control pigs, aggregating
platelets, serotonin, and ADP caused endothelium-dependent relaxations. The
platelet-induced relaxations were attenuated by methiothepin (a combined
5-HT1 and 5-HT2 serotonergic blocker) or apyrase (an ADPase and ATPase) and
were abolished by the combination of the two agents. In quiescent rings,
platelets caused contractions, which were reduced in the presence of
endothelium; the contractions were prevented by ketanserin (a 5-HT2
serotonergic blocker) or methiothepin but not by R 68 070 (a thromboxane A2
receptor blocker) or dazoxiben (a thromboxane-synthetase blocker). In
cholesterol-fed pigs, the platelet-induced relaxations were not altered,
whereas in oil-fed pigs, the endothelium-dependent relaxations to
platelets, serotonin, and ADP were augmented. Platelet- induced
contractions were significantly reduced in rings with endothelium from
oil-fed pigs, whereas the contractions were comparable in rings without
endothelium among the three groups. Endothelium- dependent relaxations in
response to the calcium ionophore A23187, direct relaxations in response to
sodium nitroprusside, and direct contractions in response to potassium
chloride were comparable among the three groups.(ABSTRACT TRUNCATED AT 250
WORDS)
ARTICLES
Endothelium-dependent relaxation in response to aggregating platelets in porcine femoral veins and its modulation by diet
Department of Physiology and Biophysics, Mayo Clinic, Rochester, MN 55905.
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