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吲哚美辛对低剂量内皮素和毒蜥毒素所致局部血流动力学反应的影响。

Effects of indomethacin on the regional haemodynamic responses to low doses of endothelins and sarafotoxin.

作者信息

Gardiner S M, Compton A M, Bennett T

机构信息

Department of Physiology & Pharmacology, Medical School, Queen's Medical Centre, Nottingham.

出版信息

Br J Pharmacol. 1990 May;100(1):158-62. doi: 10.1111/j.1476-5381.1990.tb12069.x.

Abstract
  1. Regional haemodynamic responses to i.v. bolus injections of low doses (4 pmol and 40 pmol) of endothelin-1, -2, -3 and sarafotoxin-S6b were assessed in conscious, Long Evans rats in the absence and presence of indomethacin. 2. Both doses of endothelin-3 and sarafotoxin-S6b caused early renal vasodilatations that were not affected by indomethacin. Endothelin-1 caused an initial renal vasodilatation only in the presence of indomethacin, indicating that this peptide produced concurrent release of cyclo-oxygenase products that caused renal vasoconstriction. Neither dose of endothelin-2 produced an increase in renal conductance. 3. The 4 pmol dose of all four peptides caused mesenteric vasoconstrictions only. With the 40 pmol dose of the peptides, none caused early mesenteric vasoconstriction except in the presence of indomethacin. Thus, in this vascular bed the primary vasoconstrictor effects of the peptides (seen with the 4 pmol dose) were offset, following the 40 pmol dose, by release of vasodilator cyclo-oxygenase products. Indomethacin alone caused significant vasoconstriction only in the mesenteric vascular bed, indicating that in this region of the circulation, vasodilator prostanoids might be involved also in the tonic control of vascular conductance. 4. All four peptides at both doses caused early hindquarters vasodilatation. However, only the initial hypotensive and hindquarters vasodilator effects of the 40 pmol dose of sarafotoxin-S6b were attenuated by indomethacin. Under these conditions the hindquarters vasodilator effects of sarafotoxin-S6b were similar to those of the other peptides, indicating that the more marked effects of sarafotoxin-S6b in the absence of indomethacin were contributed to by vasodilator cyclo-oxygenase products in the hindquarters.
摘要
  1. 在清醒的Long Evans大鼠中,在不存在和存在吲哚美辛的情况下,评估了静脉推注低剂量(4皮摩尔和40皮摩尔)内皮素-1、-2、-3和蛙皮毒素-S6b后的局部血流动力学反应。2. 两种剂量的内皮素-3和蛙皮毒素-S6b均引起早期肾血管舒张,且不受吲哚美辛影响。内皮素-1仅在存在吲哚美辛的情况下引起初始肾血管舒张,表明该肽同时释放了导致肾血管收缩的环氧化酶产物。两种剂量的内皮素-2均未引起肾电导增加。3. 所有四种肽的4皮摩尔剂量仅引起肠系膜血管收缩。对于40皮摩尔剂量的肽,除了在存在吲哚美辛的情况下,均未引起早期肠系膜血管收缩。因此,在该血管床中,肽的主要血管收缩作用(在4皮摩尔剂量时可见)在40皮摩尔剂量后被血管舒张性环氧化酶产物的释放所抵消。单独使用吲哚美辛仅在肠系膜血管床引起显著的血管收缩,表明在该循环区域,血管舒张性前列腺素也可能参与血管电导的紧张性控制。4. 两种剂量的所有四种肽均引起早期后肢血管舒张。然而,只有40皮摩尔剂量的蛙皮毒素-S6b的初始降压和后肢血管舒张作用被吲哚美辛减弱。在这些条件下,蛙皮毒素-S6b的后肢血管舒张作用与其他肽相似,表明在不存在吲哚美辛的情况下,蛙皮毒素-S6b更显著的作用是由后肢的血管舒张性环氧化酶产物所致。

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