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[蔗糖对阿司匹林溃疡的影响]

[Influence of sucrose on aspirin ulcer].

作者信息

Okuma K, Fujii A

出版信息

Nichidai Koko Kagaku. 1989 Dec;15(4):409-22.

PMID:2489809
Abstract

UNLABELLED

At the present stage of drug interactions, little has been studied on food-drug interactions. Excess intake of sucrose is well known to cause arteriosclerosis, obesity, diabetes mellitus, toxicity to blood cells, dental caries, and accumulations of metabolic products in blood. Under the such conditions, it is possible that the ulcerogenic drugs, such as synthetic anti-inflammatory drugs, may cause severe gastric lesions by oral administration. The present investigation was undertaken to study the influences of sucrose on the gastric lesions induced by aspirin (aspirin ulcer) in rats maintained with 10% sucrose solution. Thus, the effect of sucrose on aggressive and protective factors, proposed by Shay and Sun, was studied.

METHOD

Sixty rats were maintained with 10% sucrose solution ad libitum as drinking solution for 4 weeks (10% sucrose group). As control, purified water was given ad libitum to 60 rats (control group). Rats were starved for 24 hours, but allowed free access of water before the experiment, and then were subjected to the following experiments: (1) Twenty rats from each group were treated to prepare pylorus-ligated rats. Aspirin in 1% CMC (100mg/kg body-weight) was given in 10 rats from each group immediately after the ligation. Gastric juice excreted during 6 hours was collected and its supernatant (1,500 x g) was used for determinations of pH, acidity, acid output, pepsin activity, and pepsin output. Aspirin and salicylic acid contents in gastric juice were also determined by HPLC. (2) The mucosa of the stomach of (1) were subjected to the analysis of hexosamine. Twenty rats from each group without pylorus-ligation were also used for the analysis. Among them, 10 rats from each group were given aspirin in 1% CMC with the dose of 300 mg/kg body-weight. (3) Ten rats from each group were given aspirin with the dose of 300 mg/kg body-weight and the stomach (n = 10 for each group) was extracted 30 minutes after the aspirin administration for histochemical study to obtain covering mucus index, epitherial mucus index, total mucus index, and rate of mucous injury. (4) Aspirin in 1% CMC was given to 10 rats of each group with the dose of 300 mg/kg body-weight. Rats were sacrificed 6 hours after the administration of aspirin, and then stomachs were extracted and treated with 10% neutral formalin. The length of lesions was measured under a microscope (x 10), and then Ulcer Index was obtained.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

未标注

在药物相互作用的现阶段,关于食物 - 药物相互作用的研究较少。众所周知,过量摄入蔗糖会导致动脉硬化、肥胖、糖尿病、血细胞毒性、龋齿以及血液中代谢产物的积累。在这种情况下,致溃疡药物,如合成抗炎药,口服时可能会导致严重的胃部损伤。本研究旨在探讨蔗糖对以10%蔗糖溶液喂养的大鼠阿司匹林诱导的胃部损伤(阿司匹林溃疡)的影响。因此,研究了蔗糖对Shay和Sun提出的攻击和保护因素的影响。

方法

60只大鼠以10%蔗糖溶液作为自由饮用的溶液饲养4周(10%蔗糖组)。作为对照,60只大鼠自由饮用纯净水(对照组)。实验前大鼠禁食24小时,但可自由饮水,然后进行以下实验:(1)每组20只大鼠用于制备幽门结扎大鼠。每组10只大鼠在结扎后立即给予1%羧甲基纤维素(CMC)中的阿司匹林(100mg/kg体重)。收集6小时内分泌的胃液,其上清液(1500×g)用于测定pH值、酸度、酸分泌量、胃蛋白酶活性和胃蛋白酶分泌量。胃液中的阿司匹林和水杨酸含量也通过高效液相色谱法测定。(2)对(1)中大鼠的胃黏膜进行氨基己糖分析。每组20只未进行幽门结扎的大鼠也用于分析。其中,每组10只大鼠给予1% CMC中的阿司匹林,剂量为300mg/kg体重。(3)每组10只大鼠给予剂量为300mg/kg体重的阿司匹林,给药30分钟后取出胃(每组n = 10)进行组织化学研究,以获得覆盖黏液指数、上皮黏液指数、总黏液指数和黏液损伤率。(4)每组10只大鼠给予1% CMC中的阿司匹林,剂量为300mg/kg体重。给药6小时后处死大鼠,然后取出胃并用10%中性福尔马林处理。在显微镜下(×10)测量损伤长度,然后获得溃疡指数。(摘要截断于400字)

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