Literature DB >> 2818447

Removal of endothelial function in coronary resistance vessels by saponin.

E Wiest1, V Trach, J Dämmgen.   

Abstract

Studies of the role of the endothelium in coronary resistance vessels are limited to investigations of endothelium-derived relaxing factor mediated effects using various blocking agents. Endothelium removal as an alternative approach, is restricted to larger epicardial vessels. This study demonstrates the effect of endothelial damage by saponin on coronary resistance vessels remaining intact within the heart. In an isolated perfused guinea pig heart a saponin-containing solution (50 micrograms/ml) was infused over 2 min to damage specifically the endothelium. Increases of coronary flow in response to carbachol, histamine, and serotonin were completely blocked and reversed to decreases. Angiotensin-I-induced vasoconstriction was attenuated, whereas angiotensin-II-induced vasoconstriction remained unchanged. Vasodilatory response to sodium-nitroprusside was not attenuated by saponin-treatment. In contrast inhibition of endothelium derived relaxing factor by gossypol inhibited carbachol-induced vasodilation but did not result in vasoconstriction. Electron microscopic examination ensured that while the endothelium was destroyed by saponin-treatment the vascular smooth muscle was left intact. Our data indicate a regulating influence of the vascular endothelium on coronary resistance vessels which can be totally eliminated by saponin-treatment.

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Year:  1989        PMID: 2818447     DOI: 10.1007/BF01908199

Source DB:  PubMed          Journal:  Basic Res Cardiol        ISSN: 0300-8428            Impact factor:   17.165


  24 in total

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Journal:  J Cardiovasc Pharmacol       Date:  1986 Mar-Apr       Impact factor: 3.105

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Journal:  Eur J Pharmacol       Date:  1987-04-14       Impact factor: 4.432

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Journal:  Basic Res Cardiol       Date:  1985 Sep-Oct       Impact factor: 17.165

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Authors:  L Kaiser; H V Sparks
Journal:  Arch Intern Med       Date:  1987-03

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Authors:  R F Furchgott
Journal:  Annu Rev Pharmacol Toxicol       Date:  1984       Impact factor: 13.820

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Journal:  J Physiol       Date:  1981-07       Impact factor: 5.182

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Journal:  Blood Vessels       Date:  1987

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Authors:  T M Griffith; D H Edwards; M J Lewis; A C Newby; A H Henderson
Journal:  Nature       Date:  1984 Apr 12-18       Impact factor: 49.962

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Authors:  T M Griffith; A H Henderson; D H Edwards; M J Lewis
Journal:  J Physiol       Date:  1984-06       Impact factor: 5.182

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Authors:  U Förstermann; M Goppelt-Strübe; J C Frölich; R Busse
Journal:  J Pharmacol Exp Ther       Date:  1986-07       Impact factor: 4.030

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  5 in total

1.  Mechanism of 5-hydroxytryptamine-induced coronary vasodilation assessed by direct detection of nitric oxide production in guinea-pig isolated heart.

Authors:  A J Ellwood; M J Curtis
Journal:  Br J Pharmacol       Date:  1996-10       Impact factor: 8.739

2.  Acetylcholine-induced vasoconstrictor response of coronary vessels in rats: a possible contribution of M2 muscarinic receptor activation.

Authors:  Y Nasa; H Kume; S Takeo
Journal:  Heart Vessels       Date:  1997       Impact factor: 2.037

3.  Alteration of vascular endothelium and endothelium smooth muscle interaction after carbogen gas perfusion of isolated rat and guinea pig heart.

Authors:  H Mertens; T Ballhausen; H G Hollweg; J C Kirkpatrick; H Kammermeier
Journal:  Basic Res Cardiol       Date:  1994 Jul-Aug       Impact factor: 17.165

4.  Indomethacin reduces acute baroreceptor resetting in the dog.

Authors:  W Wang; M Brändle; I H Zucker
Journal:  J Physiol       Date:  1993-09       Impact factor: 5.182

5.  Endothelium-dependent modulation of resistance vessel contraction: studies with NG-nitro-L-arginine methyl ester and NG-nitro-L-arginine.

Authors:  M A Bennett; P A Watt; H Thurston
Journal:  Br J Pharmacol       Date:  1992-10       Impact factor: 8.739

  5 in total

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