Zhang J X, Okamura T, Toda N
Department of Pharmacology, Shiga University of Medical Sciences, Ohtsu, Japan.
Eur J Pharmacol. 1996 Sep 12;311(2-3):169-76. doi: 10.1016/0014-2999(96)00425-6.
Transmural electrical stimulation (5-30 Hz) produced a frequency-dependent increase in the perfusion pressure of isolated, perfused dog mesenteric artery segments, which was suppressed by prazosin and abolished by tetrodotoxin. Treatment with endothelin-1 in low concentrations (10(-10) and 3 x 10(-10) M) inhibited the response to electrical nerve stimulation. The effect was not affected by NG-nitro-L-arginine, indomethacin and removal of the endothelium. The endothelin-1-induced inhibition was antagonized by 10(-7) M BQ123[cyclo(D-Trp-D-Asp-L-Pro-D-Val-L-Leu-)sodium], an endothelin ETA receptor antagonist, but not by 10(-5) M BQ788 [N-cis-2,6-dimethyl-piperidinocarbonyl-L- gamma-methylleucyl-D-1-methoxycarbonyltryptophanyl-D-norleuc ine], an antagonist of endothelin ETB1 and ETB2 receptors. IRL1620 [Suc-[Glu9, Ala11,15]endothelin-1-(8-21)], a selective endothelin ETB1 receptor agonist, did not alter the response to electrical stimulation. However, raising the concentration of endothelin-1 to 10(-9) M or higher potentiated the response. Similar results were also obtained in mesenteric artery strips in response to electrical stimulation. Endothelin-1 at low concentrations did not alter the contraction caused by exogenous norepinephrine in the artery strips, whereas the peptide at high concentrations potentiated the response. 3H-overflow evoked by transmural electrical stimulation from tissues prelabeled with [3H]norepinephrine was decreased by endothelin-1 (3 x 10(-10) M) in the superfused dog mesenteric arteries. It is concluded that endothelin-1 at low concentrations activates prejunctional endothelin ETA receptors and inhibits adrenergic nerve-mediated contractions by an inhibition of amine release, whereas the peptide at high concentrations potentiates the neurally induced contractions by a postjunctional enhancement, via endothelin ETA receptors, of the action of norepinephrine. Low concentrations of endothelin-1 appear to act as a vasodilator in adrenergically innervated mesenteric artery
透壁电刺激(5 - 30赫兹)使离体灌注的犬肠系膜动脉段的灌注压呈频率依赖性升高,此效应被哌唑嗪抑制,被河豚毒素消除。用低浓度(10⁻¹⁰和3×10⁻¹⁰摩尔/升)的内皮素 - 1处理可抑制对电神经刺激的反应。该效应不受NG - 硝基 - L - 精氨酸、吲哚美辛及去除内皮的影响。内皮素 - 1诱导的抑制作用可被10⁻⁷摩尔/升的BQ123[环(D - 色氨酸 - D - 天冬氨酸 - L - 脯氨酸 - D - 缬氨酸 - L - 亮氨酸)钠]拮抗,BQ123是一种内皮素ETA受体拮抗剂,但不被10⁻⁵摩尔/升的BQ788 [N - 顺式 - 2,6 - 二甲基 - 哌啶羰基 - L - γ - 甲基亮氨酰 - D - 1 - 甲氧基羰基色氨酰 - D - 去甲亮氨酸]拮抗,BQ788是内皮素ETB1和ETB2受体的拮抗剂。IRL1620 [琥珀酰 - [Glu9, Ala11,15]内皮素 - 1 - (8 - 21)],一种选择性内皮素ETB1受体激动剂,并未改变对电刺激的反应。然而,将内皮素 - 1的浓度提高到10⁻⁹摩尔/升或更高则增强了该反应。在肠系膜动脉条对电刺激的反应中也获得了类似结果。低浓度的内皮素 - 1不会改变动脉条中外源性去甲肾上腺素引起的收缩,而高浓度的该肽则增强了反应。在灌注的犬肠系膜动脉中,内皮素 - 1(3×10⁻¹⁰摩尔/升)使经[³H]去甲肾上腺素预标记的组织透壁电刺激诱发的³H溢出减少。结论是,低浓度的内皮素 - 1激活节前内皮素ETA受体,并通过抑制胺释放来抑制肾上腺素能神经介导的收缩,而高浓度的该肽则通过节后增强作用,经由内皮素ETA受体增强去甲肾上腺素的作用,从而增强神经诱导的收缩。低浓度的内皮素 - 1在肾上腺素能神经支配的肠系膜动脉中似乎起血管舒张剂的作用