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高血压患者静脉注射肼屈嗪反应的决定因素

Determinants of response to intravenous hydralazine in hypertension.

作者信息

Shepherd A, Lin M S, McNay J, Ludden T, Musgrave G

出版信息

Clin Pharmacol Ther. 1981 Dec;30(6):773-81. doi: 10.1038/clpt.1981.237.

DOI:10.1038/clpt.1981.237
PMID:7307426
Abstract

There is marked interindividual variation in hypotensive response to intravenous hydralazine (H). We examined the determinants of response in patients with hypertension. After a single intravenous dose of 0.3 mg/kg H, response was correlated independently (r = 0.8364) with both predrug blood pressure and acetylator index (AI). Intravenous dose ranging studies showed that response also depended on the amount of H in the systemic circulation. Although plasma H levels depend on AI after oral doses, this is not so after intravenous administration. AI must therefore affect response to H by an alternative, presumably nonmetabolic mechanism which, not related to AI, perhaps indicating specificity of this effect for H. These data reinforce the potential usefulness of determining AI before giving H to a patient.

摘要

静脉注射肼屈嗪(H)后,个体间的降压反应存在显著差异。我们研究了高血压患者反应的决定因素。单次静脉注射0.3mg/kg H后,反应与用药前血压和乙酰化指数(AI)均独立相关(r = 0.8364)。静脉剂量范围研究表明,反应还取决于体循环中H的量。虽然口服给药后血浆H水平取决于AI,但静脉给药后并非如此。因此,AI必须通过一种替代机制影响对H的反应,推测该机制可能是非代谢性的,与AI无关,这可能表明这种效应对H具有特异性。这些数据强化了在给患者使用H之前测定AI的潜在实用性。

相似文献

1
Determinants of response to intravenous hydralazine in hypertension.高血压患者静脉注射肼屈嗪反应的决定因素
Clin Pharmacol Ther. 1981 Dec;30(6):773-81. doi: 10.1038/clpt.1981.237.
2
Should the acetylator phenotype be determined when prescribing hydralazine for hypertension?在为高血压患者开肼屈嗪处方时,是否应该确定乙酰化代谢表型?
Eur J Clin Pharmacol. 1984;26(1):39-42. doi: 10.1007/BF00546706.
3
Effect of oral dose size on hydralazine kinetics and vasodepressor response.口服剂量大小对肼屈嗪动力学和血管减压反应的影响。
Clin Pharmacol Ther. 1984 Nov;36(5):595-600. doi: 10.1038/clpt.1984.227.
4
Plasma concentration and acetylator phenotype determine response to oral hydralazine.
Hypertension. 1981 Sep-Oct;3(5):580-5. doi: 10.1161/01.hyp.3.5.580.
5
Hydralazine kinetics after single and repeated oral doses.
Clin Pharmacol Ther. 1980 Dec;28(6):804-11. doi: 10.1038/clpt.1980.238.
6
Acetylation status using hydralazine in African hypertensives at Kenyatta National Hospital.肯尼亚肯雅塔国家医院使用肼苯哒嗪治疗非洲高血压患者的乙酰化状态。
East Afr Med J. 1992 Jul;69(7):406-8.
7
Haemodynamic response to intravenous hydralazine in patients with pulmonary hypertension.肺动脉高压患者对静脉注射肼屈嗪的血流动力学反应。
Br Heart J. 1983 Dec;50(6):579-85. doi: 10.1136/hrt.50.6.579.
8
Effect of dose on acetylator phenotype distribution of hydralazine.
Clin Pharmacol Ther. 1981 Mar;29(3):337-43. doi: 10.1038/clpt.1981.46.
9
Hemodynamic effects of intravenous hydralazine in pregnant women with severe hypertension.静脉注射肼屈嗪对重度高血压孕妇的血流动力学影响。
Obstet Gynecol. 1985 Oct;66(4):453-8.
10
The hypotensive response to hydralazine, in triple therapy, is not related to acetylator phenotype.三联疗法中,肼屈嗪引起的降压反应与乙酰化代谢表型无关。
Br J Clin Pharmacol. 1982 May;13(5):747-50. doi: 10.1111/j.1365-2125.1982.tb01452.x.

引用本文的文献

1
Genotype-Guided Hydralazine Therapy.基因型指导下的肼屈嗪治疗。
Am J Nephrol. 2020;51(10):764-776. doi: 10.1159/000510433. Epub 2020 Sep 14.
2
Genetically determined variability in acetylation and oxidation. Therapeutic implications.乙酰化和氧化的基因决定变异性。治疗意义。
Drugs. 1985 Apr;29(4):342-75. doi: 10.2165/00003495-198529040-00003.
3
Drug interactions in hypertensive patients. Pharmacokinetic, pharmacodynamic and genetic considerations.高血压患者的药物相互作用。药代动力学、药效学及遗传学考量
Clin Pharmacokinet. 1990 Apr;18(4):295-317. doi: 10.2165/00003088-199018040-00003.