[Influence of sucrose on aspirin ulcer].

K Okuma, A Fujii
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引用次数: 0

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)

[蔗糖对阿司匹林溃疡的影响]。
未标记:在药物相互作用的现阶段,对食物-药物相互作用的研究很少。众所周知,过量摄入蔗糖会导致动脉硬化、肥胖、糖尿病、对血细胞的毒性、龋齿和血液中代谢产物的积累。在这种情况下,口服合成抗炎药等致溃疡药物可能引起严重的胃损害。本实验研究了蔗糖对10%蔗糖溶液维持大鼠阿司匹林致胃损伤(阿司匹林溃疡)的影响。因此,蔗糖对Shay和Sun提出的侵袭性和保护性因子的影响进行了研究。方法:将60只大鼠随意灌饮10%蔗糖溶液4周(10%蔗糖组)。60只大鼠随意给予纯净水作为对照组。大鼠禁食24小时,实验前允许自由饮水,然后进行以下实验:(1)每组20只大鼠制备幽门结扎大鼠。结扎后,每组10只大鼠立即给予1% CMC剂量的阿司匹林(100mg/kg体重)。收集6小时内分泌的胃液,用其上清(1500 x g)测定pH、酸度、酸输出、胃蛋白酶活性和胃蛋白酶输出。用高效液相色谱法测定胃液中阿司匹林和水杨酸的含量。(2)对(1)胃粘膜进行己糖胺分析。未结扎幽门的各组各取20只进行分析。其中,每组10只大鼠给予1% CMC剂量的阿司匹林,剂量为300 mg/kg体重。(3)每组10只大鼠给予剂量为300 mg/kg体重的阿司匹林,给药30 min后取胃(每组10只)进行组织化学研究,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的阿司匹林,剂量为300 mg/kg体重。给药后6 h处死大鼠,取胃,用10%中性福尔马林处理。显微镜下测量病变长度(× 10),计算溃疡指数。(摘要删节为400字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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