2007
DOI: 10.1002/jbt.20194
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Modulation of indomethacin‐induced gastric injury by spermine and taurine in rats

Abstract: This study investigated the involvement of neutrophil infiltration, nitric oxide (NO) generation, and oxidative stress in indomethacin-induced ulcer and the possible gastroprotective potentials of spermine and taurine, known for their tissue regenerating and antioxidant effects, respectively. Male Wistar albino rats (180-220 g) were allocated into a normal control group, ulcer control group (received a single dose of indomethacin 40 mg-kg p.o.), and two ulcer groups pretreated with spermine (150 mg-kg p.o. 1 h… Show more

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Cited by 57 publications
(45 citation statements)
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References 51 publications
(62 reference statements)
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“…Taurine (2-amino ethanesulfonic acid) is an amino acid conferred significant gastroprotection against indomethacin-induced gastric injury by preventing glutathione depletion and maintaining glutathione reductase and superoxide dismutase activity (Motawi et al, 2007). Taurine also exerted a prophylactic effect against induction of gastric mucosal lesions by water immersion restraint stress, suggesting taurine may have a potential clinical benefit for preventing stress-associated gastritis (Ma et al, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…Taurine (2-amino ethanesulfonic acid) is an amino acid conferred significant gastroprotection against indomethacin-induced gastric injury by preventing glutathione depletion and maintaining glutathione reductase and superoxide dismutase activity (Motawi et al, 2007). Taurine also exerted a prophylactic effect against induction of gastric mucosal lesions by water immersion restraint stress, suggesting taurine may have a potential clinical benefit for preventing stress-associated gastritis (Ma et al, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…The solvent was evaporated and the product was purified by column chromatography on silica gel (petroleum ether/ethyl acetate/methanol, 3:1:0.2); to give 6 as white needles (yield: 91%); m.p. : 160-162 °C; 1 (3R,4R)-1-Allyl-3,4-dihydroxy-2-((2-methyl-1-H-benzimidazol-1-yl)…”
Section: (3r4r)-1-allyl-34-dihydroxy-5-((2-methyl-1-h-benzimidazol-mentioning
confidence: 99%
“…A stirred solution of 1-hydroxymethyl-2-methylbenzimidazole (0.81 g, 5.0 mmol) in dry dichloromethane (20 mL) and trichloroacetonitrile (5 mL, 50 mmol) was treated with DBU (71 L) at room temperature and then left for 10 h. The solvent was evaporated and the product was purified by column chromatography (5% triethylamine in toluene) to give 3 as pale yellow oil (yield: 1.14 g, 75%); 1 …”
Section: -Methyl N-(trichloroacetamidomethyl)benzimidazolementioning
confidence: 99%
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