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Role of endothelium in responses of vascular smooth muscle.内皮细胞在血管平滑肌反应中的作用。
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The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine.内皮细胞在乙酰胆碱介导的动脉平滑肌舒张中所起的不可或缺的作用。
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Influence of the vascular endothelium on agonist-induced contractions and relaxations in rat aorta.血管内皮对大鼠主动脉中激动剂诱导的收缩和舒张的影响。
Br J Pharmacol. 1986 Dec;89(4):819-30. doi: 10.1111/j.1476-5381.1986.tb11187.x.
7
Depression of contractile responses in rat aorta by spontaneously released endothelium-derived relaxing factor.自发性释放的内皮源性舒张因子对大鼠主动脉收缩反应的抑制作用。
J Pharmacol Exp Ther. 1986 May;237(2):529-38.
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Precontraction-induced contractile response of isolated canine portal vein to alpha-2 adrenoceptor agonists.
Naunyn Schmiedebergs Arch Pharmacol. 1988 May;337(5):525-30. doi: 10.1007/BF00182726.
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Evidence for prazosin-resistant, rauwolscine-sensitive alpha-adrenoceptors mediating contractions in the isolated vascular bed of the rat tail.哌唑嗪耐药、育亨宾敏感的α-肾上腺素能受体介导大鼠尾部离体血管床收缩的证据。
Br J Pharmacol. 1989 Jun;97(2):563-71. doi: 10.1111/j.1476-5381.1989.tb11986.x.
10
Differences in basal endothelium-derived relaxing factor activity in different artery types.不同动脉类型中基础内皮衍生舒张因子活性的差异。
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初始拉伸和激动剂诱导的张力对内皮舒张因子基础释放和刺激释放效应的影响。

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

作者信息

Dainty I A, McGrath J C, Spedding M, Templeton A G

机构信息

Institute of Physiology, University of Glasgow.

出版信息

Br J Pharmacol. 1990 Aug;100(4):767-73. doi: 10.1111/j.1476-5381.1990.tb14090.x.

DOI:10.1111/j.1476-5381.1990.tb14090.x
PMID:2207498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917605/
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.
摘要
  1. 在大鼠离体主动脉环中研究了初始拉伸和激动剂诱导张力程度对乙酰胆碱诱导舒张的影响。乙酰胆碱诱导的舒张可被阿托品拮抗,且几乎完全被血红蛋白消除。完整或受损内皮的血管环对硝普钠的舒张反应相似,但完整制剂对异丙肾上腺素的舒张反应更大。2. 在完整或受损内皮的制剂中,主动脉环的静息张力均有类似的长度依赖性增加。苯肾上腺素(1 microM)引起的收缩反应大小取决于制剂的初始长度(以及拉伸程度),在摩擦和未摩擦组织中均如此。摩擦和未摩擦组织收缩反应的绝对差异在1.8 mm时最大,在其他测试长度时较小,包括收缩的最佳拉伸程度即2.4 mm。3. 乙酰胆碱诱导的绝对舒张(仅在完整内皮的血管环中可见)取决于制剂的初始长度(以及拉伸程度),在2.4 mm时最大。比例舒张(即表示为诱导张力的百分比)也呈长度依赖性,在1.5 mm时最佳。4. 血管对乙酰胆碱的敏感性因激动剂诱导张力水平而异。当张力较低时,乙酰胆碱敏感性较高(在[去甲肾上腺素]0.03 microM时:pIC50 = 7.36 +/- 0.07),当去甲肾上腺素浓度增加时,张力增加,乙酰胆碱敏感性降低(在[去甲肾上腺素]0.3 microM时:pIC50 = 6.57 +/- 0.07)。5. 讨论了乙酰胆碱诱导的绝对敏感性和最大舒张与初始拉伸程度(以及制剂长度)或激动剂诱导张力程度的关系。