Gastric antisecretory and antiulcer activity of bovine hemoglobin

被引:6
作者
Al Asmari, Abdulrahman K. [1 ]
Al Omani, Saud [2 ]
Elfaki, Ibrahim [1 ]
Tariq, Mohammad [1 ]
Al Malki, Ahmed [3 ]
Al Asmary, Saeed [4 ]
机构
[1] Prince Sultan Mil Med City, Res Ctr, Riyadh 11159, Saudi Arabia
[2] Prince Sultan Mil Med City, Dept Surg, Riyadh 11159, Saudi Arabia
[3] Prince Sultan Mil Med City, Dept Gastroenterol, Riyadh 11159, Saudi Arabia
[4] Prince Sultan Mil Med City, Riyadh 11159, Saudi Arabia
关键词
Bovine hemoglobin; Gastric ulcers; Indomethacin; Ethanol; Ischemic injury; Rats; UPPER GASTROINTESTINAL HEMORRHAGE; REDUCES INFARCT SIZE; MUCOSAL BLOOD-FLOW; OXYGEN CARRIER; ANTIINFLAMMATORY DRUGS; INHIBITORY POLYPEPTIDE; MICROVASCULAR INJURY; LIPID-PEROXIDATION; REPERFUSION INJURY; OXIDATIVE STRESS;
D O I
10.3748/wjg.v19.i21.3291
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate gastric antisecretory and gastro-protective activity of bovine hemoglobin (B-Hb) in rats. METHODS: Adult Albino-Wistar rats were divided into groups of 6 animals each. B-Hb in doses of 100, 300 and 900 mg/kg body weight was tested for gastric acid secretion and antiulcer activity. Gastric secretions were measured 6 h after pylorus ligation in rats pretreated with B-Hb. The acidity was measured by titrating gastric contents against 0.01 mol/L NaOH to pH 7. Indomethacin ulcers were produced by oral administration of 30 mg/kg bw in the rats pretreated with B-Hb one hour before indomethacin. Six hours after indomethacin stomach removed and ulcer index was recorded. Ethanol ulcer were produced by 1 mL of ethanol in the rats pretreated with B-Hb 30 min before the ethanol. One hour after ethanol stomach were cut open to score ulcers. Histological examination and analysis of gastric wall mucus, non-protein sulfhydryl groups (NP-SH), and myeloperoxidase (MPO) were carried in gastric tissue following ethanol administration. RESULTS: In control rats pylorus ligation for 6 h resulted in the accumulation of 8.1 +/- 0.61 mL of gastric secretion. The treatment of the rats with 100, 300 and 900 mg/kg of B-Hb produced a significant decrease in the volume of gastric secretion 5.6 +/- 0.63, 5.5 +/- 0.75 and 4.7 +/- 0.58 mL respectively as compared to the control group [analysis of variance (ANOVA) F = 4.77, P < 0.05]. The lesion area in the control group was found to be 22.4 +/- 3.2 mm(2) six hours after the administration of indomethacin. Treatment of rats with B-Hb at doses of 100 mg/kg (24.3 +/- 3.29 mm2), 300 mg/kg (16.2 +/- 1.45 mm2) and 900 mg/kg (12.6 +/- 1.85 mm2) produced a dose dependent decreased the lesion scores (ANOVA F = 4.50, P < 0.05). The ulcer index following one hour after 1 mL ethanol was 7.1 +/- 0.31. Pretreatment of rats with B-Hb at the doses of 100 mg/kg (2.5 +/- 0.42), 300 mg/kg (2.1 +/- 0.4) and 900 mg/kg (0.7 +/- 0.21) significantly inhibited the formation of gastric lesions (ANOVA F = 63.26, P < 0.0001). Histological examination of gastric mucosa following ethanol showed significant lesions in the form of gastric pits with detachment of the surface epithelium; vacuolation of epithelial cells and elongation of microvessels. The changes were dose-dependently attenuated by B-Hb. The treatment of rats with ethanol significantly decreased the Alcian blue binding capacity of gastric wall mucus (480 +/- 25.6 mu g Alcian blue/g of tissue) as compared to control rats (667 +/- 25.8 mu g). Pretreatment of rats with B-Hb at the doses of 100 mg/kg (516 +/- 31.6 mu g/g), 300 mg/kg (558 +/- 28.8 mu g/g) and 900 mg/kg (654 +/- 33.8 mu g/g) significantly attenuated ethanol induced depletion of gastric wall mucus (ANOVA F = 8.05, P < 0.005). A significant and dose dependent increase of gastric mucosal NP-SH (ANOVA F = 19.62, P < 0.001) and decrease in MPO activity (ANOVA F = 3.1, P < 0.05) was observed in B-Hb treated rats. CONCLUSION: B-Hb possesses significant gastric antisecretory and gastroprotective activity against experimentally induced gastric lesion. The gastroprotective effects of B-Hb are accompanied by inhibition of neutrophils activity, reduction of oxidative stress and maintenance of mucosal integrity. (C) 2013 Baishideng. All rights reserved.
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页码:3291 / 3299
页数:9
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