单用吲哚美辛及利尿剂或肾上腺素受体阻断治疗对高血压患者血压和肾素系统的影响。

J A Lopez-Ovejero, M A Weber, J I Drayer, J E Sealey, J H Laragh
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引用次数: 86

摘要

1. 对三组无钠饮食的原发性高血压患者单独或联合利尿剂或心得安治疗吲哚美辛。2. 在未接受治疗的无并发症高血压患者中,给予吲哚美辛可使肾素分泌减少约30%,在持续利尿剂或β -肾上腺素受体阻断治疗刺激或抑制肾素分泌的患者中,给予吲哚美辛可使肾素分泌减少约75%。3.吲哚美辛给药对未治疗的无并发症高血压患者的血压没有净影响,但它减弱或逆转了利尿剂或心得安治疗的降压作用。4. 在利尿剂或心得安治疗期间,盐和水潴留可能是消炎痛使血压升高的一个重要因素。此外,前列腺素合成可能在抵消α -肾上腺素能张力升高中起重要作用,而α -肾上腺素能张力升高可能限制β -肾上腺素受体阻断的降血压作用。5. 由于这些相互作用及其潜在的加压作用,当与利尿剂或-肾上腺素受体阻滞剂联合使用时,应谨慎使用吲哚美辛。
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Effects of indomethacin alone and during diuretic or beta-adrenoreceptor-blockade therapy on blood pressure and the renin system in essential hypertension.

1. Indomethacin was administered alone or in addition to either diuretic or propranolol therapy to three groups of patients with essential hypertension on a free sodium diet. 2. Indomethacin administration reduced renin secretion by about 30% in untreated uncomplicated hypertensive patients and by about 75% in those whose renin secretion had either been stimulated or suppressed by maintained diuretic or beta-adrenoreceptor-blockade therapy. 3. Indomethacin administration produced no net effect on blood pressure in untreated patients with uncomplicated hypertension but it blunted or reversed the antihypertensive effect of either diuretic or propranolol therapy. 4. Salt and water retention may be an important factor in the blood pressure-raising effect of indomethacin during diuretic or propranolol therapy: In addition, prostaglandin synthesis may be important in counteracting increased alpha-adrenergic tone, which may limit the blood pressure-lowering effect of beta-adrenoreceptor-blockade. 5. Because of these interactions and their pressor potential indomethacin should be used with caution when combined with either diuretics or beta-adrenoreceptor blockers.

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Proceedings of the Fifth Meeting of the International Society of Hypertension, Paris, 12-14 June 1978. Brain catecholamines and catecholamine-synthesizing enzymes in renovascular hypertension in the rat. Enhanced hypothalamic noradrenaline biosynthesis in Goldblatt I renovascular hypertension. Definitive evidence for renin in rat brain by affinity chromatographic separation from protease. Renal release of active and inactive renin in essential and renovascular hypertension.
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