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首页> 外文期刊>Journal of Bangladesh Society of Physiologist >Status of Gastric Mucosa and Liver in Mice upon Treatment with Diclofenac Sodium
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Status of Gastric Mucosa and Liver in Mice upon Treatment with Diclofenac Sodium

机译:双氯芬酸钠治疗小鼠胃黏膜和肝脏的状况

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Diclofenac sodium is a non-steroidal anti-inflammatory drug with reportedly undesirable harmful side effects including blood disorders, abdominal pain, ulceration and bleeding of the stomach or intestine. Objective:The present study was conducted to investigate the effect of diclofenac sodium on erythropoiesis, on stomach and liver under different conditions. Method: This experimental study on animal model was conducted in the Department of Physiology, Bangladesh Agricultural University, Mymensingh, between July and August 2007. A total of 45 Swiss Albino mice were randomly assigned into five equal groups (n=9) and they all were fed with standard broiler pellet (25 gm/mice/day) throughout the experimental period of 40 days. Keeping 1 group as control(groupA), 4 groups were treated with diclofenac sodium @ 3 mg/kg body weight (bwt) orally in empty (group B)or full stomach with (group c) or without vitamin B12 (group D) @ 10 μg/Kg body weight through intramuscular route. Total erythrocyte count (TEC) and Hb% was determined to assess erythropoiesis. Macroscopic and microscopic changes of liver and stomach were studied by standard laboratory method. Data were analyzed statistically by ANOVA and un paired t test. Result: Oral administration of this drug significantly (p<0.01) decreased Total Erythrocyte Count(TEC) and Hb in the animals treated with diclofenac sodium in empty stomach and in the animals treated with diclofenac sodium plus vitamin B12 in empty stomach. All the treated mice showed slight to moderate congestion of the gastric mucosa and liver. Conclusion: Intake of diclofenac sodium in empty stomach may produce harmful side effect on stomach and liver. Key words: Stomach; Mice; Diclofenac sodium. DOI: 10.3329/jbsp.v5i2.6783J Bangladesh Soc Physiol. 2010 December; 5(2): 89-93
机译:双氯芬酸钠是一种非甾体抗炎药,据报道具有不良的不良副作用,包括血液疾病,腹痛,溃疡和胃或肠出血。目的:研究双氯芬酸钠在不同条件下对红细胞生成,胃和肝脏的影响。方法:该动物模型实验研究于2007年7月至8月在孟加拉国农业大学Mymensingh生理学系进行。总共将45只瑞士白化病小鼠随机分为5组,每组9只,每组9只。在整个40天的实验期内,向其饲喂标准的肉鸡颗粒(25 gm /小鼠/天)。保留一组作为对照组(A组),四组分别以空腹(B组)或全胃(C组)或不添加维生素B12(D组)口服双氯芬酸钠3 mg / kg体重(bwt)。通过肌内途径达到10μg/ Kg体重。确定总红细胞计数(TEC)和Hb%来评估红细胞生成。通过标准实验室方法研究了肝和胃的宏观和微观变化。数据通过方差分析和非配对t检验进行统计分析。结果:口服该药可显着(p <0.01)降低空腹双氯芬酸钠治疗的动物和空肠双氯芬酸钠加维生素B12治疗的动物的总红细胞计数(TEC)和血红蛋白。所有治疗的小鼠均显示出胃粘膜和肝脏的轻度至中度充血。结论:空腹服用双氯芬酸钠可能对胃和肝产生有害的副作用。关键字:胃;老鼠;双氯芬酸钠。 DOI:10.3329 / jbsp.v5i2.6783J孟加拉国Soc Physiol。 2010年12月; 5(2):89-93

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