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[乙酰水杨酸诱导的上消化道损伤的昼夜节律特点及雷尼替丁的保护作用]

[Circadian aspects of acetylsalicylic acid induced injury and protective effect of ranitidine on the the upper gastrointestinal tract].

作者信息

Müller P, Arce L, Jackisch P, Simon B

机构信息

Krankenhaus Salem, Heidelberg.

出版信息

Arzneimittelforschung. 1994 Aug;44(8):962-5.

PMID:7945542
Abstract

Circadian Aspects of Acetylsalicylic Acid Induced Injury and Protective Effect of Ranitidine on the Upper Gastrointestinal Tract. In a randomised parallel double-blind study the gastric and duodenal effects of 300 mg acetylsalicylic acid (ASA, CAS 50-78-2) daily in the presence and absence of 150 mg ranitidine (Zantic, CAS 66357-35-5) daily was evaluated in 32 healthy volunteers undergoing upper gastrointestinal endoscopy. Drugs were taken over a period of 7 days either at 8 a.m. (n = 16) or at 8 p.m. (n = 16). Endoscopic controls were performed at entry and repeated after 7 days of treatment. At entry both groups showed comparable mucosal damages: 8 a.m. group: ASA/placebo 0.8 +/- 0.1 (stomach) and 0.1 +/- 0.1 (duodenum): ASA/ranitidine 1.0 +/- 0.0 (stomach) and 0.07 +/- 0.06 (duodenum). 8 p.m. group: ASA/placebo 0.9 +/- 0.06 (stomach) and 0.1 +/- 0.09 (duodenum). ASA/ranitidine 0.8 +/- 0.08 (stomach) and 0.07 +/- 0.06 (duodenum). After 7 days of treatment the lesions score increased in the ASA/Placebo group in the 8 a.m. group to 9.1 +/- 1.1 (stomach) and 2.7 +/- 1.0 (duodenum), and in the 8 p.m. group to 10.9 +/- 1.1 (stomach) and to 3.9 +/- 0.9 duodenum). The corresponding values in the ASA/ranitidine group were 2.6 +/- 0.8 (stomach) and 0.2 +/- 0.08 (duodenum) (8 a.m.) and 4.8 +/- 0.8 (stomach) and 0.3 +/- 0.1 (duodenum) (8 p.m.). There was no statistical difference between the morning- and the evening dose of ASA. In addition, ranitidine protection was also time-independent.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

乙酰水杨酸诱导的损伤的昼夜节律方面以及雷尼替丁对上消化道的保护作用。在一项随机平行双盲研究中,对32名接受上消化道内镜检查的健康志愿者评估了每日300毫克乙酰水杨酸(ASA,CAS 50 - 78 - 2)在有和没有每日150毫克雷尼替丁(善胃得,Zantic,CAS 66357 - 35 - 5)情况下对胃和十二指肠的影响。药物服用7天,分别于上午8点(n = 16)或晚上8点(n = 16)服用。在研究开始时及治疗7天后进行内镜检查。研究开始时两组黏膜损伤情况相当:上午8点组:ASA/安慰剂组,胃为0.8±0.1,十二指肠为0.1±0.1;ASA/雷尼替丁组,胃为1.0±0.0,十二指肠为0.07±0.06。晚上8点组:ASA/安慰剂组,胃为0.9±0.06,十二指肠为0.1±0.09;ASA/雷尼替丁组,胃为0.8±0.08,十二指肠为0.07±0.06。治疗7天后,上午8点的ASA/安慰剂组病变评分增加到胃9.1±1.1,十二指肠2.7±1.0;晚上8点组增加到胃10.9±1.1,十二指肠3.9±0.9。ASA/雷尼替丁组相应值为上午8点时胃2.6±0.8,十二指肠0.2±0.08;晚上8点时胃4.8±0.8,十二指肠0.3±0.1。ASA早晚剂量之间无统计学差异。此外,雷尼替丁的保护作用也与时间无关。(摘要截短至250字)

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