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[麦角苄酯治疗高催乳素血症——5例患者的经验]

[Terguride in hyperprolactinemia--experiences with 5 patients].

作者信息

Wüster C, Scholz A, Schmelzle A, Horowski R, Ziegler R

机构信息

Abteilung Innere Medizin, Medizinische Klinik, Heidelberg.

出版信息

Klin Wochenschr. 1990 Apr 2;68(7):384-7. doi: 10.1007/BF01650889.

DOI:10.1007/BF01650889
PMID:2188044
Abstract

Hyperprolactinemia can successfully be treated by dopaminagonists such as bromocriptin or lisuride. About 10% of patients complain about side effects like orthostatic hypotension, nausea or vomiting, which may lead to discontinuation of treatment. We therefore conducted a study using terguride--a new dopaminagonist--in 5 patients with hyperprolactinemia and intolerable side effects under conventional treatment. Terguride is the transdihydroderivative of lisuride (Dopergin). We treated 5 patients, 2 men with macroprolactinoma and 3 women with microprolactinoma with terguride. The mean duration of treatment was 15.6 months (7-37 months). Patients were treated with up to 5 mg terguride daily. All 5 patients had a marked initial decrease of elevated prolactin levels 8 h after administration of 0.25 mg terguride orally. Three patients became normoprolactinemic after sufficient increase of the dose of terguride, 2 female patients with a microprolactinoma got eumenorrhoeic thereafter. The treatment with terguride was tolerated without side effects by all patients. There were no significant changes of the examined parameters of clinical chemistry nor the other pituitary hormones. Results of cranial computertomography did not change in 4 patients, one patient had tumor progression. Tergurid as a dopaminagonist is an effective inhibitor of prolactin with little side effects and thus a useful drug in the treatment of hyperprolactinemia.

摘要

高催乳素血症可用溴隐亭或利舒脲等多巴胺激动剂成功治疗。约10%的患者抱怨有体位性低血压、恶心或呕吐等副作用,这可能导致治疗中断。因此,我们对5例高催乳素血症且在传统治疗下出现难以耐受副作用的患者使用了一种新的多巴胺激动剂——替古瑞肽进行研究。替古瑞肽是利舒脲(多培那明)的反式二氢衍生物。我们用替古瑞肽治疗了5例患者,其中2例患有大催乳素瘤的男性和3例患有微催乳素瘤的女性。平均治疗时长为15.6个月(7 - 37个月)。患者每日使用替古瑞肽的剂量最高达5毫克。所有5例患者在口服0.25毫克替古瑞肽8小时后,升高的催乳素水平均有明显的初始下降。在充分增加替古瑞肽剂量后,3例患者催乳素水平恢复正常,2例患有微催乳素瘤的女性患者随后月经恢复正常。所有患者对替古瑞肽治疗耐受且无副作用。临床化学检查参数及其他垂体激素均无显著变化。4例患者的头颅计算机断层扫描结果未改变,1例患者出现肿瘤进展。替古瑞肽作为一种多巴胺激动剂,是一种有效的催乳素抑制剂,副作用小,因此是治疗高催乳素血症的一种有用药物。

相似文献

1
[Terguride in hyperprolactinemia--experiences with 5 patients].[麦角苄酯治疗高催乳素血症——5例患者的经验]
Klin Wochenschr. 1990 Apr 2;68(7):384-7. doi: 10.1007/BF01650889.
2
Chronic treatment of pathological hyperprolactinemia and acromegaly with the new ergot derivative terguride.新型麦角衍生物泰舒达对病理性高催乳素血症和肢端肥大症的长期治疗
J Clin Endocrinol Metab. 1986 Oct;63(4):1002-7. doi: 10.1210/jcem-63-4-1002.
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Terguride as a new anti-hyperprolactinemic agent: characterization in rats and dogs in comparison with bromocriptine.
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4
Effect of terguride on prolactin levels in normal, puerperal and hyperprolactinaemic women.泰舒达对正常、产后及高催乳素血症女性催乳素水平的影响。
Eur J Clin Pharmacol. 1986;30(2):195-7. doi: 10.1007/BF00614302.
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Pharmacokinetics of oral terguride in patients with a prolactinoma.口服泰舒达在泌乳素瘤患者中的药代动力学
Eur J Clin Pharmacol. 1986;30(3):363-5. doi: 10.1007/BF00541546.
6
Terguride in the treatment of hyperprolactinemia.泰舒达治疗高泌乳素血症
Acta Univ Palacki Olomuc Fac Med. 1990;125:155-60.
7
[Pharmacokinetic/pharmacodynamic analysis of anti-hyperprolactinemic effect of terguride based on dopamine D2 receptor occupancy].基于多巴胺D2受体占有率的泰舒达抗高泌乳素血症作用的药代动力学/药效学分析
Yakugaku Zasshi. 2003 Apr;123(4):255-60. doi: 10.1248/yakushi.123.255.
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Terguride--a new dopamine agonist drug: a comparison of its neuroendocrine and side effect profile with bromocriptine.
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Gender differences in the prevalence, clinical features and response to cabergoline in hyperprolactinemia.高泌乳素血症在患病率、临床特征及对卡麦角林反应方面的性别差异。
Eur J Endocrinol. 2003 Mar;148(3):325-31. doi: 10.1530/eje.0.1480325.
10
Cabergoline in the long-term therapy of hyperprolactinemic disorders.卡麦角林用于高催乳素血症疾病的长期治疗
Acta Endocrinol (Copenh). 1992 Jun;126(6):489-94. doi: 10.1530/acta.0.1260489.

本文引用的文献

1
Dual action on central dopamine function of transdihydrolisuride, a 9, 10-dihydrogenated analogue of the ergot dopamine agonist lisuride.反式二氢麦角酰二乙胺(一种麦角多巴胺激动剂麦角酰二乙胺的9,10-二氢化类似物)对中枢多巴胺功能的双重作用。
Life Sci. 1983 Jan 24;32(4):421-32. doi: 10.1016/0024-3205(83)90089-9.
2
Effect of the new ergot derivative terguride on plasma PRL and GH levels in patients with pathological hyperprolactinemia or acromegaly.新型麦角衍生物泰舒达对病理性高催乳素血症或肢端肥大症患者血浆催乳素(PRL)和生长激素(GH)水平的影响。
J Endocrinol Invest. 1985 Apr;8(2):147-51. doi: 10.1007/BF03350671.
3
Long term suppression of prolactin concentrations after bromocriptine induced regression of pituitary prolactinomas.
溴隐亭诱导垂体泌乳素瘤消退后泌乳素浓度的长期抑制。
Br Med J (Clin Res Ed). 1985 Jan 12;290(6462):117-8. doi: 10.1136/bmj.290.6462.117-a.
4
Bromocriptine as primary therapy for prolactin-secreting macroadenomas: results of a prospective multicenter study.溴隐亭作为分泌催乳素大腺瘤的一线治疗:一项前瞻性多中心研究结果
J Clin Endocrinol Metab. 1985 Apr;60(4):698-705. doi: 10.1210/jcem-60-4-698.
5
Chronic treatment of pathological hyperprolactinemia and acromegaly with the new ergot derivative terguride.新型麦角衍生物泰舒达对病理性高催乳素血症和肢端肥大症的长期治疗
J Clin Endocrinol Metab. 1986 Oct;63(4):1002-7. doi: 10.1210/jcem-63-4-1002.
6
Terguride--a new dopamine agonist drug: a comparison of its neuroendocrine and side effect profile with bromocriptine.
Fertil Steril. 1988 Apr;49(4):589-94. doi: 10.1016/s0015-0282(16)59823-9.
7
Rapid regression of macroprolactinomas by the new dopamine partial agonist terguride.新型多巴胺部分激动剂替古瑞肽使大泌乳素瘤迅速消退
Acta Endocrinol (Copenh). 1986 Apr;111(4):460-6. doi: 10.1530/acta.0.1110460.
8
Suppression of puerperal lactation by terguride. A double-blind study.
Gynecol Obstet Invest. 1988;26(1):33-8. doi: 10.1159/000293669.