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肝素对兔肠系膜动脉中鱼精蛋白血管舒张作用的影响。

Effects of heparin on the vasodilator action of protamine in the rabbit mesenteric artery.

作者信息

Akata T, Kodama K, Takahashi S

机构信息

Department of Anaesthesiology and Critical Care Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Br J Pharmacol. 1993 Aug;109(4):1247-53. doi: 10.1111/j.1476-5381.1993.tb13756.x.

Abstract
  1. The effects of protamine on the rabbit isolated small mesenteric artery were investigated both in the presence and in the absence of heparin, by the isometric tension-recording method. 2. The dissociation constant for the binding of heparin to protamine has never been previously reported, so in order to minimize the effects of protamine, known to have a vasodilator action, and to examine only the effects of a heparin-protamine complex, the experiments with heparin were performed in the presence of high concentrations of heparin (21-700 u ml-1), concentrations at which heparin itself does not affect the vascular tone. 3. Protamine (15-500 micrograms ml-1), in the absence of heparin, was found to inhibit (P < 0.05) noradrenaline (1 microM)-induced contractions both in endothelium-intact and in endothelium-denuded tissues. 4. Such vasodilator action of protamine in either endothelium-intact or -denuded tissues continued, even in the presence of excess heparin at a heparin/protamine (H/P) ratio of 1.4 u micrograms -1, but was almost completely blocked in the presence of a much greater excess of heparin (H/P ratio > or = 4.7 u micrograms -1): heparin was present both before and during the application of protamine. 5. The vasodilator action of protamine in the absence of heparin was prolonged both in the endothelium-intact and -denuded tissues after protamine had been washed out from the bath with Krebs solution. Although this washing out with a Krebs solution containing excess heparin (4.7 u ml-1) readily reversed such prolonged vasodilator action of protamine both in the endothelium-denuded strips and in the endothelium-intact strips which had been pretreated with inhibitors of the endothelium-derived relaxing factor (EDRF) pathway, it did not affect the prolonged vasodilator action of protamine in the endothelium-intact strips which received no pharmacological intervention.6. These results suggest that: (1) only protamine, not a heparin-protamine complex, exerts vasodilator action in vitro; (2) the vasodilator action of protamine presumably has an EDRF-mediated component;and (3) protamine probably exerts its direct vasodilator action without entering the smooth muscle cell.
摘要
  1. 采用等长张力记录法,研究了在有肝素和无肝素情况下鱼精蛋白对兔离体小肠系膜动脉的作用。2. 肝素与鱼精蛋白结合的解离常数此前从未有过报道,因此,为了将已知具有血管舒张作用的鱼精蛋白的影响降至最低,并仅研究肝素 - 鱼精蛋白复合物的作用,在高浓度肝素(21 - 700 U/ml)存在的情况下进行了肝素实验,该浓度下肝素本身不影响血管张力。3. 发现在无肝素情况下,鱼精蛋白(15 - 500 μg/ml)在完整内皮组织和去内皮组织中均能抑制(P < 0.05)去甲肾上腺素(1 μM)诱导的收缩。4. 即使在肝素/鱼精蛋白(H/P)比为1.4 U/μg的过量肝素存在的情况下,鱼精蛋白在完整内皮组织或去内皮组织中的这种血管舒张作用仍持续存在,但在过量得多的肝素(H/P比≥4.7 U/μg)存在时几乎完全被阻断:在应用鱼精蛋白之前和期间均存在肝素。5. 在用克雷布斯溶液将鱼精蛋白从浴槽中冲洗掉后,鱼精蛋白在无肝素情况下的血管舒张作用在完整内皮组织和去内皮组织中均持续存在。尽管用含有过量肝素(4.7 U/ml)的克雷布斯溶液冲洗能迅速逆转鱼精蛋白在去内皮条带和用内皮源性舒张因子(EDRF)途径抑制剂预处理的完整内皮条带中的这种延长的血管舒张作用,但它并不影响未接受药理学干预的完整内皮条带中鱼精蛋白延长的血管舒张作用。6. 这些结果表明:(1)在体外发挥血管舒张作用的是鱼精蛋白本身,而非肝素 - 鱼精蛋白复合物;(2)鱼精蛋白的血管舒张作用可能有EDRF介导的成分;(3)鱼精蛋白可能在不进入平滑肌细胞的情况下发挥其直接的血管舒张作用。

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本文引用的文献

1
Effect of protamine on heparin-antithrombin III complexes. In vitro studies.
Thromb Res. 1980;17(3-4):367-74. doi: 10.1016/0049-3848(80)90071-7.
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Protamine: a review of its toxicity.
Anesth Analg. 1985 Mar;64(3):348-61.

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