Overview of the nature of vasoconstriction in arterial grafts for coronary operations

Guo Wei He, Cheng Qin Yang, Albert Starr

Research output: Contribution to journalArticle

99 Citations (Scopus)

Abstract

Many vasoconstrictors (spasmogens) may cause arterial graft spasm; however, there is lack of an overview of the nature of vasoconstriction in grafts. This study was designed to investigate the response of three major arterial grafts currently used for coronary artery bypass grafting to various vasoconstrictor substances. Segments of three arterial grafts (gastroepiploic [GEA], n = 28; internal mammary [IMA], n = 213; inferior epigastric [IEA], n = 24) taken from patients undergoing coronary artery bypass grafting were studied in organ baths under a physiologic pressure. Cumulative concentration-contraction curves were established for the following vasoconstrictor substances: endothelin-1, U46619, prostaglandin F, norepinephrine, methoxamine, phenylephrine, 5-hydroxytryptamine, and potassium chloride (K+). In IMA, the highest contraction force was induced by U46619 (5.69 ± 0.48 g), endothelin-1 (4.43 ± 0.4 g), PGF (6.29 ± 1.42 g), and K+ (4.58 ± 0.5 g). Internal mammary artery is highly sensitive to endothelin-1 (EC50, -8.13 ± 0.08 log M) and U46619 (EC50, -8.21 ± 0.21 log M) (lower than any other vasoconstrictors, p <0.001). Next sensitive vasoconstrictors were PGF and norepinephrine. 5-Hydroxytryptamine induced significantly higher contraction force in the IMA without endothelium (2.8 ± 0.64 g versus 1.4 ± 0.23 g, p <0.05). In GEA and IEA, endothelin-1 and U46619 were more potent vasoconstrictors (EC50 for endothelin-1: -8.06 ± 0.02 log M in GEA and -8.22 ± 0.04 in IEA; for U46619: -8.49 ± 0.24 log M in GEA and -8.25 ± 0.09 in IEA) than that for norepinephrine (-6.86 ± 0.11 log M for GEA and -6.59 ± 0.18 log M for IEA, p <0.0001), although all of them (and K+) evoked a strong contraction. In summary, the present study reveals that there are basically two types of vasoconstrictors that are important spasmogens in arterial grafts. Type I (endothelin, prostaglandins (thromboxane A2 and prostaglandin F), and α1-adrenoceptor agonists) are the most potent vasoconstrictors and they strongly contract arterial grafts even when endothelium is intact. Type II vasoconstrictors (such as 5-HT) only induce a weak vasoconstriction when endothelium is intact. However, those vasoconstrictors probably play an important role in the spasm of arterial grafts if endothelium is lost by surgical handling.

Original languageEnglish (US)
Pages (from-to)676-683
Number of pages8
JournalThe Annals of Thoracic Surgery
Volume59
Issue number3
DOIs
StatePublished - 1995
Externally publishedYes

Fingerprint

Vasoconstrictor Agents
Vasoconstriction
Transplants
15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid
Endothelin-1
Dinoprost
Endothelium
Serotonin
Norepinephrine
Breast
Spasm
Coronary Artery Bypass
Methoxamine
Thromboxane A2
Mammary Arteries
Potassium Chloride
Endothelins
Phenylephrine
Baths
Adrenergic Receptors

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Pulmonary and Respiratory Medicine
  • Surgery

Cite this

Overview of the nature of vasoconstriction in arterial grafts for coronary operations. / He, Guo Wei; Yang, Cheng Qin; Starr, Albert.

In: The Annals of Thoracic Surgery, Vol. 59, No. 3, 1995, p. 676-683.

Research output: Contribution to journalArticle

He, Guo Wei ; Yang, Cheng Qin ; Starr, Albert. / Overview of the nature of vasoconstriction in arterial grafts for coronary operations. In: The Annals of Thoracic Surgery. 1995 ; Vol. 59, No. 3. pp. 676-683.
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N2 - Many vasoconstrictors (spasmogens) may cause arterial graft spasm; however, there is lack of an overview of the nature of vasoconstriction in grafts. This study was designed to investigate the response of three major arterial grafts currently used for coronary artery bypass grafting to various vasoconstrictor substances. Segments of three arterial grafts (gastroepiploic [GEA], n = 28; internal mammary [IMA], n = 213; inferior epigastric [IEA], n = 24) taken from patients undergoing coronary artery bypass grafting were studied in organ baths under a physiologic pressure. Cumulative concentration-contraction curves were established for the following vasoconstrictor substances: endothelin-1, U46619, prostaglandin F2α, norepinephrine, methoxamine, phenylephrine, 5-hydroxytryptamine, and potassium chloride (K+). In IMA, the highest contraction force was induced by U46619 (5.69 ± 0.48 g), endothelin-1 (4.43 ± 0.4 g), PGF2α (6.29 ± 1.42 g), and K+ (4.58 ± 0.5 g). Internal mammary artery is highly sensitive to endothelin-1 (EC50, -8.13 ± 0.08 log M) and U46619 (EC50, -8.21 ± 0.21 log M) (lower than any other vasoconstrictors, p <0.001). Next sensitive vasoconstrictors were PGF2α and norepinephrine. 5-Hydroxytryptamine induced significantly higher contraction force in the IMA without endothelium (2.8 ± 0.64 g versus 1.4 ± 0.23 g, p <0.05). In GEA and IEA, endothelin-1 and U46619 were more potent vasoconstrictors (EC50 for endothelin-1: -8.06 ± 0.02 log M in GEA and -8.22 ± 0.04 in IEA; for U46619: -8.49 ± 0.24 log M in GEA and -8.25 ± 0.09 in IEA) than that for norepinephrine (-6.86 ± 0.11 log M for GEA and -6.59 ± 0.18 log M for IEA, p <0.0001), although all of them (and K+) evoked a strong contraction. In summary, the present study reveals that there are basically two types of vasoconstrictors that are important spasmogens in arterial grafts. Type I (endothelin, prostaglandins (thromboxane A2 and prostaglandin F2α), and α1-adrenoceptor agonists) are the most potent vasoconstrictors and they strongly contract arterial grafts even when endothelium is intact. Type II vasoconstrictors (such as 5-HT) only induce a weak vasoconstriction when endothelium is intact. However, those vasoconstrictors probably play an important role in the spasm of arterial grafts if endothelium is lost by surgical handling.

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