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J Thorac Cardiovasc Surg 1994;107:647-0647
© 1994 Mosby, Inc.
Letters to the Editor |
Erasme Hospital
808, Route de Lennik
B-1070 Brussels, Belgium
Institut de Pharmacie
Université Libre de Bruxelles
Boulevard du Triomphe
B-1050 Brussels, Belgium
To the Editor:
We read with interest the article by Dignan and colleagues
1 in the January 1992 issue of the JOURNAL, reporting that gastroepiploic artery (GEA) segments had a stronger contraction in response to potassium chloride, norepinephrine, and serotonin than did the internal mammary artery (IMA). They suggested that prevention of platelet-, adrenergic-, or potassium-induced contraction may be more important for GEA as an alternate coronary bypass conduit. To assess the role of the endothelium and to evaluate the response to endothelin-1, we also conducted a study on the GEA and IMA.
2 The vessels were obtained from 11 patients undergoing gastrectomy or duodenopancreatectomy and from 16 patients during coronary artery bypass operations. The rings were suspended in organ chambers to record isometric tension. The experiments were performed in the presence of phentolamine (1 µmol/L), propranolol (1 µmol/L), and indomethacin (10 µmol/L). The relaxations in response to acetylcholine on vessels precontracted with prostaglandin F2
were similar in both vessels. The maximal contractions to serotonin, normalized as a percent of potassium chlorideinduced contraction (90 mmol/L) were 46% ± 15% for IMA and 18% ± 5% for GEA. Endothelium removal equally potentiated the responses to serotonin in both preparations. The maximal contractions to endothelin-1 were also higher in the IMA: 166% ± 19% versus 102% ± 6% of potassium chloride (p < 0.05) but were not affected by endothelium removal. However, the capacity to contract, expressed in tension developed, was higher in the GEA: the potassium chlorideinduced (90 mmol/L) contraction was 2.6 ± 0.3 g in the IMA versus 7.9 ± 0.9 g in the GEA (p < 0.001). A histologic examination of the vessels tested showed similar wall thickness and paucity of atherosclerosis, but the media was mainly elastic in the IMA and muscular in the GEA, consistent with the results reported by Van Son and associates.
3
Our results thus extend those of Dignan and colleagues
1; namely, a greater responsiveness of IMA, not only to potassium chloride and serotonin (when normalized as a percent of potassium chlorideinduced contraction) but also to endothelin-1, a potent endogenous vasoconstrictor, and nevertheless a greater contractile capacity of GEA, which may be a disadvantage in terms of graft patency despite similar endothelial function.
References
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