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溴隐亭对甲基多巴治疗的高血压的影响。

The effects of bromocriptine in methyldopa treated hypertension.

作者信息

Lewis M J, Henderson A H

出版信息

Br J Clin Pharmacol. 1980 Jan;9(1):57-60. doi: 10.1111/j.1365-2125.1980.tb04797.x.

Abstract
  1. The effects of treatment with the dopaminergic agonist bromocriptine were studied in nine patients with essential hypertension receiving methyldopa as sole therapy. 2. In Phase 1 of the study, the addition of bromocriptine on a single-blind basis caused a significant fall in lying and standing blood pressures. Plasma prolactin fell significantly but there was no significant change in the other biochemical parameters measured. All patients volunteered that they felt a sense of well-being after starting bromocriptine treatment. 3. In Phase 2 of the study the substitution of placebo for bromocriptine in a randomized double-blind trial significantly increased lying and standing blood pressures and plasma prolactin. No consistent or significant changes were observed in methyldopa-induced side-effects following the substitution of placebo for bromocriptine. 4. In Phase 3 of the study, a gradual increase in blood pressure was observed in all patients over a few months after stopping bromocriptine therapy. 5. The significance of these findings in relation to the role played by plasma prolactin and central dopaminergic activity in blood pressure regulation is discussed.
摘要
  1. 对9例仅接受甲基多巴治疗的原发性高血压患者,研究了多巴胺能激动剂溴隐亭的治疗效果。2. 在研究的第一阶段,单盲添加溴隐亭导致卧位和立位血压显著下降。血浆催乳素显著降低,但所测的其他生化参数无显著变化。所有患者均表示开始溴隐亭治疗后感觉良好。3. 在研究的第二阶段,在随机双盲试验中用安慰剂替代溴隐亭,显著升高了卧位和立位血压及血浆催乳素。用安慰剂替代溴隐亭后,甲基多巴引起的副作用未观察到一致或显著的变化。4. 在研究的第三阶段,停止溴隐亭治疗后的几个月内,所有患者的血压均逐渐升高。5. 讨论了这些发现与血浆催乳素和中枢多巴胺能活性在血压调节中所起作用的相关性。

相似文献

1
The effects of bromocriptine in methyldopa treated hypertension.溴隐亭对甲基多巴治疗的高血压的影响。
Br J Clin Pharmacol. 1980 Jan;9(1):57-60. doi: 10.1111/j.1365-2125.1980.tb04797.x.
2
Bromocriptine in the treatment of hypertension.溴隐亭治疗高血压
Eur J Clin Pharmacol. 1986;30(2):141-4. doi: 10.1007/BF00614291.
6
Comparison of trimazosin and methyldopa in hypertension.
Clin Pharmacol Ther. 1977 Oct;22(4):425-9. doi: 10.1002/cpt1977224425.

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