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依前列醇(前列环素,PGI2)可增加人体肝脏的表观血流量。

Epoprostenol (prostacyclin,PGI2) increases apparent liver blood flow in man.

作者信息

Hassan S, Pickles H

出版信息

Prostaglandins Leukot Med. 1983 Apr;10(4):449-54. doi: 10.1016/0262-1746(83)90057-4.

DOI:10.1016/0262-1746(83)90057-4
PMID:6344102
Abstract

When epoprostenol (prostacyclin, PGI2) is given by infusion to man, cardiac output is increased, and it appears that the gastrointestinal tract may receive a disproportionate share of this. We have used the clearance of indocyanine green dye to estimate liver blood flow in 8 healthy subjects. During an infusion of PGI2 at a dose of 5 ng/kg/min, apparent liver blood flow increased from 925 +/- 220 ml/min (Mean +/- s.d) to 1320 +/- 453 ml/min, an average increase of 41.1%. Significant changes in heart rate, headache, facial flushing, systolic blood pressure, and pulse pressure were noticed. We suggest that endogenous epoprostenol (PGI2) may be of importance in the physiological regulation of liver blood flow in man. As this dose of epoprostenol could be tolerated readily, epoprostenol therapy could prove a therapeutic advance in some liver disorders, particularly liver transplantation, and possibly in the therapy of certain drug overdoses.

摘要

当向人体输注依前列醇(前列环素,PGI2)时,心输出量增加,而且胃肠道似乎获得了不成比例的血流量。我们利用吲哚菁绿染料清除率来估计8名健康受试者的肝血流量。在以5 ng/kg/min的剂量输注PGI2期间,表观肝血流量从925±220 ml/min(平均值±标准差)增加至1320±453 ml/min,平均增加41.1%。注意到心率、头痛、面部潮红、收缩压和脉压有显著变化。我们认为内源性依前列醇(PGI2)可能在人体肝血流量的生理调节中起重要作用。由于该剂量的依前列醇易于耐受,依前列醇疗法可能在某些肝脏疾病,特别是肝移植中,以及可能在某些药物过量的治疗中成为一种治疗进展。

相似文献

1
Epoprostenol (prostacyclin,PGI2) increases apparent liver blood flow in man.依前列醇(前列环素,PGI2)可增加人体肝脏的表观血流量。
Prostaglandins Leukot Med. 1983 Apr;10(4):449-54. doi: 10.1016/0262-1746(83)90057-4.
2
Noninvasive assessment of the cardiovascular effects of prostacyclin (PGI2) in man.前列环素(PGI2)对人体心血管作用的无创评估。
Eur J Cardiol. 1980;12(2):73-80.
3
Effect of epoprostenol (prostacyclin, PGI2) on cerebral blood flow in man.依前列醇(前列环素,PGI2)对人体脑血流量的影响。
J Neurol Neurosurg Psychiatry. 1982 Nov;45(11):1033-6. doi: 10.1136/jnnp.45.11.1033.
4
The cardiovascular and platelet effects of epoprostenol (prostacyclin, PGI2) are unaffected by beta-adrenoceptor blockade in man.依前列醇(前列环素,PGI2)对人体心血管及血小板的作用不受β-肾上腺素受体阻断的影响。
Br J Clin Pharmacol. 1982 Sep;14(3):369-77. doi: 10.1111/j.1365-2125.1982.tb01993.x.
5
Effects of intravenous epoprostenol on platelets and the cardiovascular system are not potentiated by dipyridamole.双嘧达莫不会增强静脉注射依前列醇对血小板和心血管系统的作用。
Clin Pharmacol Ther. 1983 Feb;33(2):178-82. doi: 10.1038/clpt.1983.27.
6
Effects of prostacyclin on hepatic vasculature and metabolism of renin in conscious dogs.
Am J Physiol. 1982 Oct;243(4):H584-9. doi: 10.1152/ajpheart.1982.243.4.H584.
7
The effect of intravenous epoprostenol (prostacyclin, PGI2) on cerebral blood flow and cardiac output in man.静脉注射依前列醇(前列环素,PGI2)对人体脑血流量和心输出量的影响。
Br J Clin Pharmacol. 1983 Dec;16(6):707-11. doi: 10.1111/j.1365-2125.1983.tb02245.x.
8
Prostacyclin (PGI2) induces coronary vasodilatation in anaesthetised dogs.前列环素(PGI2)可使麻醉犬的冠状动脉扩张。
Cardiovasc Res. 1978 Dec;12(12):720-30.
9
Prostacyclin, indomethacin and the cerebral circulation.前列环素、吲哚美辛与脑循环
Brain Res. 1980 Sep 22;197(2):425-31. doi: 10.1016/0006-8993(80)91127-0.
10
Effects of prostacyclin on renal haemodynamics, renal tubular function and vasoactive hormones in healthy humans. A placebo-controlled dose-response study.前列环素对健康人肾血流动力学、肾小管功能及血管活性激素的影响。一项安慰剂对照剂量反应研究。
Br J Clin Pharmacol. 1997 Nov;44(5):471-6. doi: 10.1046/j.1365-2125.1997.t01-1-00608.x.

引用本文的文献

1
The effects of prostacyclin on gastric intramucosal pH in patients with septic shock.前列环素对感染性休克患者胃黏膜内pH值的影响。
Intensive Care Med. 1995 May;21(5):414-21. doi: 10.1007/BF01707410.
2
Drug interactions with thrombolytic agents. Current perspectives.与溶栓药物的药物相互作用。当前观点
Clin Pharmacokinet. 1995 Apr;28(4):315-26. doi: 10.2165/00003088-199528040-00004.
3
Effect of indomethacin on cerebral blood flow, carbon dioxide reactivity and the response to epoprostenol (prostacyclin) infusion in man.
消炎痛对人体脑血流量、二氧化碳反应性及依前列醇(前列环素)输注反应的影响。
J Neurol Neurosurg Psychiatry. 1984 Jan;47(1):51-5. doi: 10.1136/jnnp.47.1.51.