Literature DB >> 2207498

The influence of the initial stretch and the agonist-induced tone on the effect of basal and stimulated release of EDRF.

I A Dainty1, J C McGrath, M Spedding, A G Templeton.   

Abstract

1. The effects of initial stretch and degree of agonist-induced tone on acetylcholine-induced relaxations were examined in rings of rat isolated aorta. The relaxation to acetylcholine was antagonized by atropine and almost completely abolished by haemoglobin. Relaxation to sodium nitroprusside was similar in rings with an intact or disrupted endothelium but that to isoprenaline was greater in intact preparations. 2. In preparations with either an intact or disrupted endothelium there was a similar length-dependent increase in the resting tension of the aortic rings. The size of the contractile response to phenylephrine (1 microM) was dependent on the initial length (and hence degree of stretch) of the preparation in both rubbed and unrubbed tissues. The absolute difference in contractile response between rubbed and unrubbed was greatest at 1.8 mm and less at the other lengths tested, including the optimum degree of stretch for contraction i.e. 2.4 mm. 3. The absolute acetylcholine-induced relaxation (only seen in rings with an intact endothelium) was dependent on the initial length (and hence degree of stretch) of the preparation and was maximum at 2.4 mm. The proportionate relaxation (i.e. expressed as a percentage of induced tone) was also length-dependent being optimal at 1.5 mm. 4. The sensitivity of the vessels to acetylcholine varied depending on the level of agonist-induced tone. When tone was low, acetylcholine sensitivity was high (at [NA] 0.03 microM: pIC50 = 7.36 +/- 0.07), when the concentration of noradrenaline was increased the tone increased and the acetylcholine sensitivity was low (at [NA] 0.3 microM: pIC50 = 6.57 +/- 0.07). 5. The absolute sensitivities and maximum relaxations induced by acetylcholine are discussed in relation to the initial degree of stretch (and hence length of the preparation) or the degree of agonist-induced tone.

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Year:  1990        PMID: 2207498      PMCID: PMC1917605          DOI: 10.1111/j.1476-5381.1990.tb14090.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  12 in total

1.  Differences in basal endothelium-derived relaxing factor activity in different artery types.

Authors:  P Collins; S P Chappell; T M Griffith; M J Lewis; A H Henderson
Journal:  J Cardiovasc Pharmacol       Date:  1986 Nov-Dec       Impact factor: 3.105

2.  Contractile properties of small arterial resistance vessels in spontaneously hypertensive and normotensive rats.

Authors:  M J Mulvany; W Halpern
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3.  Alpha 2-adrenoceptors and endothelium-dependent relaxation in canine large arteries.

Authors:  J A Angus; T M Cocks; K Satoh
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4.  Vascular physiology: the end of the quest?

Authors:  P M Vanhoutte
Journal:  Nature       Date:  1987 Jun 11-17       Impact factor: 49.962

Review 5.  Role of endothelium in responses of vascular smooth muscle.

Authors:  R F Furchgott
Journal:  Circ Res       Date:  1983-11       Impact factor: 17.367

6.  Distension-dependent changes in noradrenaline sensitivity in small arteries from the rat.

Authors:  H Nilsson; N Sjöblom
Journal:  Acta Physiol Scand       Date:  1985-11

7.  Influence of the vascular endothelium on agonist-induced contractions and relaxations in rat aorta.

Authors:  G R Bullock; S G Taylor; A H Weston
Journal:  Br J Pharmacol       Date:  1986-12       Impact factor: 8.739

8.  Depression of contractile responses in rat aorta by spontaneously released endothelium-derived relaxing factor.

Authors:  W Martin; R F Furchgott; G M Villani; D Jothianandan
Journal:  J Pharmacol Exp Ther       Date:  1986-05       Impact factor: 4.030

9.  The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine.

Authors:  R F Furchgott; J V Zawadzki
Journal:  Nature       Date:  1980-11-27       Impact factor: 49.962

10.  Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor.

Authors:  R M Palmer; A G Ferrige; S Moncada
Journal:  Nature       Date:  1987 Jun 11-17       Impact factor: 49.962

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  12 in total

1.  Mechanical stretch reveals different components of endothelial-mediated vascular tone in rat aortic strips.

Authors:  S Franchi-Micheli; P Failli; L Mazzetti; D Bani; M Ciuffi; L Zilletti
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2.  Regulation of vascular nitric oxide in vitro and in vivo; a new role for endogenous hydrogen sulphide?

Authors:  M Y Ali; C Y Ping; Y-Yp Mok; L Ling; M Whiteman; M Bhatia; P K Moore
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4.  A new experimental approach in endothelium-dependent pharmacological investigations on isolated porcine coronary arteries mounted for impedance planimetry.

Authors:  L B Tankó; E O Mikkelsen; U Simonsen
Journal:  Br J Pharmacol       Date:  1999-09       Impact factor: 8.739

5.  Chronic social isolation in the prairie vole induces endothelial dysfunction: implications for depression and cardiovascular disease.

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6.  Arterial contractions induced by cumulative addition of calcium in hypertensive and normotensive rats: influence of endothelium.

Authors:  M Kähönen; P Arvola; X Wu; I Pörsti
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1994-06       Impact factor: 3.000

7.  Novel signal transduction pathway mediating endothelium-dependent beta-adrenoceptor vasorelaxation in rat thoracic aorta.

Authors:  D W Gray; I Marshall
Journal:  Br J Pharmacol       Date:  1992-11       Impact factor: 8.739

8.  Stretch revealed three components in the hyperpolarization of guinea-pig coronary artery in response to acetylcholine.

Authors:  H C Parkington; M Tare; M A Tonta; H A Coleman
Journal:  J Physiol       Date:  1993-06       Impact factor: 5.182

9.  Impaired cyclic nucleotide-mediated vasorelaxation may contribute to closure of the human umbilical artery after birth.

Authors:  S Renowden; D H Edwards; T M Griffith
Journal:  Br J Pharmacol       Date:  1992-06       Impact factor: 8.739

10.  Relaxation of rat thoracic aorta induced by the Ca(2+)-ATPase inhibitor, cyclopiazonic acid, possibly through nitric oxide formation.

Authors:  H Moritoki; T Hisayama; S Takeuchi; W Kondoh; M Imagawa
Journal:  Br J Pharmacol       Date:  1994-03       Impact factor: 8.739

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