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三环类抗抑郁药治疗消化性溃疡病

Tricyclic antidepressant therapy for peptic ulcer disease.

作者信息

Ries R K, Gilbert D A, Katon W

出版信息

Arch Intern Med. 1984 Mar;144(3):566-9.

PMID:6367680
Abstract

The role of tricyclic antidepressants (TCAs) as agents for treatment of peptic ulcer disease is of growing interest. In both placebo-controlled clinical trials and comparative studies with cimetidine, TCAs have proved effective and safe as ulcer-healing agents. The mechanism of action by which TCAs produce healing has not been fully elucidated. In vivo studies in man have generally shown that TCAs decrease gastric acid secretion. In addition to their well-known anticholinergic properties, in vitro studies have indicated potent H1- and H2-receptor blocking activities for these agents. Separate from these effects on acid output, the antipain/depression effect of TCAs may be of benefit in certain patients with ulcers. Other advantages of these agents include their long half-lives, low cost, and readily available serum monitoring. Further clinical studies with detailed physiologic and psychologic observations and serum monitoring using TCAs in patients with peptic ulcer disease are needed.

摘要

三环类抗抑郁药(TCAs)作为治疗消化性溃疡疾病的药物,其作用正日益受到关注。在安慰剂对照临床试验以及与西咪替丁的对比研究中,三环类抗抑郁药已被证明作为溃疡愈合药物是有效且安全的。三环类抗抑郁药产生愈合作用的作用机制尚未完全阐明。人体的体内研究普遍表明,三环类抗抑郁药可减少胃酸分泌。除了其众所周知的抗胆碱能特性外,体外研究表明这些药物具有强大的H1和H2受体阻断活性。除了对胃酸分泌的这些影响外,三环类抗抑郁药的止痛/抗抑郁作用可能对某些溃疡患者有益。这些药物的其他优点包括半衰期长、成本低以及血清监测易于进行。需要对消化性溃疡疾病患者使用三环类抗抑郁药进行更详细的生理和心理观察以及血清监测的进一步临床研究。

相似文献

1
Tricyclic antidepressant therapy for peptic ulcer disease.三环类抗抑郁药治疗消化性溃疡病
Arch Intern Med. 1984 Mar;144(3):566-9.
2
Agents with tricyclic structures for treating peptic ulcer disease.具有三环结构的用于治疗消化性溃疡疾病的药物。
Clin Pharm. 1983 Sep-Oct;2(5):425-31.
3
Trimipramine and duodenal ulcer.三甲丙咪嗪与十二指肠溃疡
Scand J Gastroenterol Suppl. 1980;58:71-8.
4
Comparative study of cimetidine and trimipramine in the short-term treatment of duodenal and gastric ulcer.西咪替丁与曲米帕明短期治疗十二指肠溃疡和胃溃疡的对比研究
Scand J Gastroenterol. 1983 Jan;18(1):33-8. doi: 10.3109/00365528309181555.
5
Relapse prevention of duodenal ulcers with trimipramine, cimetidine, or placebo. A double-blind comparison.用三甲丙咪嗪、西咪替丁或安慰剂预防十二指肠溃疡复发。一项双盲对照研究。
Scand J Gastroenterol. 1984 May;19(3):405-10.
6
Tricyclic antidepressant therapy in duodenal ulcer.三环类抗抑郁药治疗十二指肠溃疡
J Indian Med Assoc. 1987 Sep;85(9):265-7.
7
Treatment of duodenal ulcer with antacids in combination with trimipramine or cimetidine.用抗酸剂联合曲米帕明或西咪替丁治疗十二指肠溃疡。
Scand J Gastroenterol Suppl. 1980;58:46-52.
8
Doxepin therapy for duodenal ulcer: a controlled trial in patients who failed to respond to cimetidine.多塞平治疗十二指肠溃疡:一项针对西咪替丁治疗无效患者的对照试验。
Clin Ther. 1985;7(3):319-26.
9
Doxepin and cimetidine in the treatment of duodenal ulcer: an open clinical and endoscopic study.多塞平和西咪替丁治疗十二指肠溃疡:一项开放性临床及内镜研究。
J Clin Psychiatry. 1982 Aug;43(8 Pt 2):56-60.
10
An experimental assessment of actions of cimetidine and tricyclic anti-depressants in peptic ulcer.西咪替丁和三环类抗抑郁药在消化性溃疡中作用的实验评估。
J Assoc Physicians India. 1986 Feb;34(2):133-5.

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J Taibah Univ Med Sci. 2018 May 31;13(5):422-431. doi: 10.1016/j.jtumed.2018.04.010. eCollection 2018 Oct.
2
EMOTIONAL FACTORS IN DUODENAL ULCER.十二指肠溃疡中的情感因素
Med J Armed Forces India. 1994 Jan;50(1):34-36. doi: 10.1016/S0377-1237(17)31035-3. Epub 2017 Jun 27.
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Interactions of recombinant human histamine H₁R, H₂R, H₃R, and H₄R receptors with 34 antidepressants and antipsychotics.
重组人源组胺 H₁R、H₂R、H₃R 和 H₄R 受体与 34 种抗抑郁药和抗精神病药的相互作用。
Naunyn Schmiedebergs Arch Pharmacol. 2012 Feb;385(2):145-70. doi: 10.1007/s00210-011-0704-0. Epub 2011 Oct 28.
4
Antiulcer activity of fluvoxamine in rats and its effect on oxidant and antioxidant parameters in stomach tissue.氟伏沙明在大鼠中的抗溃疡活性及其对胃组织氧化和抗氧化参数的影响。
BMC Gastroenterol. 2009 May 20;9:36. doi: 10.1186/1471-230X-9-36.
5
Cost, benefits and unintended gastrointestinal side effects of pharmaceutical therapy.药物治疗的成本、益处及意外的胃肠道副作用。
Pharmacoeconomics. 1992 Mar;1(3):175-81. doi: 10.2165/00019053-199201030-00004.
6
Neurobiology of brain-gut interactions. Implications for ulcer disease.脑-肠相互作用的神经生物学。对溃疡病的影响。
Dig Dis Sci. 1989 Dec;34(12):1809-16. doi: 10.1007/BF01536696.