Pathological quantification of experimental gastric ulcer in mice

AIM: To develop a method of quantifying the pathological changes gastric ulcer in the experimental mice. METHODS: The experimental mice were fed with alcohol to establish the model of gastric ulcer. The area of the ulcer was quantified by weight and picture integration. Then the ratio of ulcer area to total stomach area (ulcer area ratio, UAR) was calculated to assess the degrees of the ulcers on the stomach wall. Furthermore, the methods of weighing, picture integration, marking, and grading were compared. RESULTS: The mark indexes and the UAR by weight and picture integration were significantly different between different grading groups (Grade 4 vs Grade 2 vs Grade 1: 84.0 27.8 vs 19.6 8.1 vs 4.0 1.0, P 0.05). Except in one mouse, the differences of UAR between by weight and picture integration in other five mice were 0.69, 4.89, 7.41, 1.26 and 2.76 respectively, which showed UAR had no marked difference between the two methods. In comparison of model I with model II, there were no obvious differences in the mark indexes, grading indexes and the numbers of petechiae while the UARs between by weight and picture integration were significantly different (6.14 0.08% vs 27.64 0.31%, P<0.05; 6.56 0.07% vs 21.22 0.21%, P<0.05). CONCLUSION: The degrees of the gastric ulcer can be accessed by weight, picture integration, marking and grading. Weighing is better for measuring the ulcer over the fourth grade while picture integration can be used in all the degrees. The sensitivity and accuracy of picture integration and weighing are higher than those of traditional marking and grading.

[1]  C. Pan,et al.  Protective role of metallothionein in stress-induced gastric ulcer in rats. , 2005, World journal of gastroenterology.

[2]  P. Deng,et al.  The protective effects of rutaecarpine on gastric mucosa injury in rats. , 2005, Planta medica.

[3]  M. Arbid,et al.  Evaluation of the anti-inflammatory, anti-nociceptive and gastric effects of Ginkgo biloba in the rat. , 2004, Pharmacological research.

[4]  G. Schmeda-Hirschmann,et al.  Oleanolic acid promotes healing of acetic acid-induced chronic gastric lesions in rats. , 2003, Pharmacological research.

[5]  J. Xing,et al.  Effects of sea buckthorn (Hippophaë rhamnoides L.) seed and pulp oils on experimental models of gastric ulcer in rats. , 2002, Fitoterapia.

[6]  Chang-dong Yan,et al.  Neuroregulative mechanism of hypothalamic paraventricular nucleus on gastric ischemia-reperfusion injury in rats. , 2002, Life sciences.

[7]  Chang-dong Yan,et al.  [Protective effects of paraventricular nucleus stimulation and vasopressin on gastric ischemia-reperfusion injury in rats]. , 2002, Sheng li xue bao : [Acta physiologica Sinica].

[8]  J. Grover,et al.  Extracts of Benincasa hispida prevent development of experimental ulcers. , 2001, Journal of ethnopharmacology.

[9]  V. Motilva,et al.  Effects of food intake and oxidative stress on intestinal lesions caused by meloxicam and piroxicam in rats. , 2001, European journal of pharmacology.

[10]  T. Dimo,et al.  Effects of methanol, cyclohexane and methylene chloride extracts of Bidens pilosa on various gastric ulcer models in rats. , 2000, Journal of ethnopharmacology.

[11]  E. Yeşilada,et al.  Anti-ulcerogenic effects of Spartium junceum flowers on in vivo test models in rats. , 2000, Journal of ethnopharmacology.

[12]  M. Uchida,et al.  A novel method to produce extensive gastric antral ulcer in rats: Pharmacological factors involved in the etiology of antral ulceration , 1999, Journal of Physiology-Paris.

[13]  D. Martins,et al.  Gastroprotective effect from Calophyllum brasiliense Camb. bark on experimental gastric lesions in rats and mice. , 1999, Journal of ethnopharmacology.

[14]  E. Silveira,et al.  Gastroprotective effect of Copaifera langsdorffii oleo-resin on experimental gastric ulcer models in rats. , 1998, Journal of ethnopharmacology.

[15]  P. Chiu,et al.  Effects of a gastric antisecretory-cytoprotectant 2-methyl-8-(phenylmethoxy)imidazo[1,2-a]pyridine-3-acetonitrile (Sch 28 080) on cysteamine, reserpine and stress ulcers in rats. , 1984, Arzneimittel-Forschung.

[16]  J. Davis,et al.  Mild irritants prevent gastric necrosis through "adaptive cytoprotection" mediated by prostaglandins. , 1983, The American journal of physiology.