Omeprazole ameliorates aspirin-induced gastroduodenal injury.

Author: BehlerE M, EltaG H, LoefflerK M, ScheimanJ M

Paper Details 
Original Abstract of the Article :
Aspirin and nonsteroidal antiinflammatory drugs (NSAIDs) damage the gastroduodenal epithelium by two mechanisms: direct toxic effects and effects related to the depletion of endogenous prostaglandins. The prostaglandin-depleted mucosa has increased susceptibility to luminal aggressive factors, yet t...See full text at original site
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引用元:
https://doi.org/10.1007/BF02090067

データ提供:米国国立医学図書館(NLM)

Omeprazole: A Protective Shield Against Aspirin-Induced Gastroduodenal Injury

Aspirin, a common pain reliever, can cause damage to the stomach lining, a condition known as gastroduodenal injury. It's like a scorching desert sun that can burn and irritate the delicate skin of a traveler. This study explores the protective effects of omeprazole, a proton pump inhibitor, against aspirin-induced injury.

The researchers conducted a double-blind, placebo-controlled, crossover study involving healthy volunteers. They found that omeprazole significantly reduced aspirin-induced gastric mucosal injury, protecting the stomach lining from damage. This is like providing a caravan with a protective shield against the harsh desert sun, ensuring their safety and well-being.

Protecting the Digestive System: A Vital Role for Omeprazole

This study highlights the importance of omeprazole in preventing aspirin-induced gastroduodenal injury. It suggests that omeprazole could be a valuable tool for protecting the digestive system, especially in individuals who need to take aspirin for medical reasons.

Dr. Camel's Conclusion

This study is like a camel caravan discovering a hidden oasis of protection in the desert of aspirin-induced gastroduodenal injury. It reveals the potential of omeprazole to shield the digestive system from damage, offering a safe passage through the harsh terrain of aspirin use.

Date :
  1. Date Completed 1994-02-17
  2. Date Revised 2022-04-09
Further Info :

Pubmed ID

8281875

DOI: Digital Object Identifier

10.1007/BF02090067

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PICO Info
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Languages

English

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