Volume6,Issue2

1. Effect of Ranitidine and Omeprazole on Serum and Gastrc Leptin in Rats with Normal or Ethanol-Injured Gastric Mucosa
Shomali T., Fazeli M., Forghanifard Z., Keshavarzi H., Jalaei J.
Abstract
Stomach is the major source of leptin in the gastrointestinal tract and the leptin has a positive role on gastric ulcer healing. Objective: The present study investigates the effect of ranitidine and omeprazole on gastric and serum leptin in rats with normal or ethanol-injured gastric mucosa. Material and methods: Six equal groups of rats were treated as: control [normal saline]; ranitidine, 50 mg.kg-1 SC; omeprazole, 10 mg.kg-1 orally; ethanol 75%, 4 ml.kg-1 orally; ranitidine+Ethanol 75% and omeprazole+Ethanol 75%. After 3 h, number of lesions was counted in stomachs and lesion area was assessed by planimetry. Gastric and serum leptin was determined by ELISA method. Results: Rats of groups 4, 5 and 6 demonstrated obvious ulcers. Pretreatment only with omeprazole significantly reduced both number of lesions and lesion area as compared to group 4. Serum leptin remained statistically the same among different groups. Gastric leptin in rats treated with ethanol increased significantly as compared to control. Pretreatment with ranitidine and omeprazole decreased gastric leptin appreciably in comparison with group 4. Conclusion: Ranitidine and omeprazole do not affect serum leptin in normal condition while they significantly decrease gastric leptin in rats with acute ethanol-induced gastric damage which may not be desirable with regard to the positive role of leptin on ulcer healing.

2. Anti-inflammatory, Antinociceptive, Antipyretic and Gastroprotective Effects of Calligonum comosum in Rats and Mice.
Abdallah H.M.I., Asaad G.F, Arbid M.S., Abdel-Sattar E.A.
Abstract
Recent ongoing research is directed to find natural products that possess therapeutic effects and devoid of side effects. Inflammation, analgesia, pyrexia and gastric disturbances are associated with several pathological conditions. The present study aimed to investigate the anti-inflammatory, antinociceptive, antipyretic and gastroprotective effects of one promising herb; Calligonum comosum. The methanol extract (100%) of Calligonum comosum was administered in the current study at two dose levels, 250 & 500mg/kg, p.o. The anti-inflammatory activity was tested in carrageenan-induced paw edema model of inflammation in rats. Analgesic profile was ascertained in acetic acid- induced writhing and hot plate models in mice. The antipyretic activity was assessed using yeast-induced hyperthermia in rats. Ethanol-induced gastric ulcer model was used to determine the gastroprotective activity of the extract. The methanolic extract of C.comosum (500mg/kg) inhibited carrageenan-induced edema in rat paw. The extract at both doses (250 & 500mg/kg) also produced analgesic activity in acetic acid-induced abdominal constriction response in mice. In hot-plate test, C.comosum at both doses did not show any significant effect against thermal nociception in mice. Treatment with C.comosum extract showed a dose-dependent reduction in pyrexia in rats and suppressed the ethanol-induced gastric lesions. The present results suggest that C. comosum possessed anti-inflammatory, anti-nociceptive, and antipyretic activities. Besides, the herb showed protective effect against ethanol-induced gastric lesions probably through increasing antioxidant defense