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Experimentally induced gastric ulcer in the rat MUDr. Michal Jurajda.

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Presentation on theme: "Experimentally induced gastric ulcer in the rat MUDr. Michal Jurajda."— Presentation transcript:

1 Experimentally induced gastric ulcer in the rat MUDr. Michal Jurajda

2 Objective n To study the influence of H2-receptor antagonist on the development of the peptic ulcers of the stomach in the rats.The peptic ulcers will be induced experimentally by NSAID (cyclo- oxygenase inhibitor).

3 Physiology n Motor functions of the stomach n Gastric secretion

4 Physiology n Motor functions of the stomach –storage: reduction of the tone in the muscular wall –mixing and propulsion: constrictor ring leading to the retropulsion –emptying

5 Physiology n Secretions –parietal cells - HCl, intrinsic factor –chief cells – enzymes (pepsinogen, gastric lipase) –surface cells - mucous, sodium bicarbonate

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10 Mucous neck cell Parietal cell Chief cell

11 Gastric mucosa surface cells neck cells parietal and chief cells

12 Hydrochloric acid secretion

13 Regulation of HCl secretion

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15 Pathology n Gastritis –Acute - stress (Cushing’s ulcer), infection, radiation, corrosives –Chronic A type – autoimmune destruction of the parietal cells, B type – inflammation of the antral mucosa caused by H. pylori

16 Gastritis - acute

17 Chronic gastritis A

18 Chronic gastritis B

19 Helicobacter pylori

20 Peptic ulcer n Mucosal defect reaching deeper than muscularis mucosae layer, localized in areas exposed to acid-pepsin secretions.

21 Pathological anatomy

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23 RTG with barium contrast Gastric ulcer

24 Duodenal peptic ulcer

25 Complications of peptic ulcer n Bleeding n Perforation n Penetration n Pyloric channel narrowing

26 Peptic ulcer ulcer

27 Bleeding

28 Perforation and penetration

29 Perforation – free intraperitoneal air

30 Ulcerogenic factors n NSAID n Stress n Chronic gastritis type B n A habitual increase of oxyntic glands secretion (increased number, increased sensitivity to k histamine or gastrin. n Zollinger-Ellison syndrom

31 Pharmacotherapy

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33 H2 receptor antagonists n block histamine receptors 2 type udecrease HCl secretion in the gastric glands

34 Cyclooxygenase inhibitors n decrease synthesis of prostaglandins uanti-inflammatory effect uanalgetic effect uanti-trombotic effect uThe adverse side effect - the gastric ulcer


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