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Effects of phenacetin, paracetamol and caffeine on the erosive activity of acetylsalicylic acid in the rat stomach: dose-response relationships, time course of erosion development and effects on acid secretion
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- A J M Seegers
- National Institute of Public Health , P.O. Box 1, 3720 BA Bilthoven,
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- L P Jager
- Department of Pharmacology, Subfaculty of Pharmacy, State University of Utrecht ,
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- J van Noordwijk
- National Institute of Public Health , P.O. Box 1, 3720 BA Bilthoven,
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Description
<jats:title>Abstract</jats:title><jats:p>Adult male and female Wistar rats were equally susceptible to gastric injury induced with acetylsalicylic acid (aspirin). Both in male and in female rats simultaneous administration of caffeine and aspirin caused significantly more gastric erosions than the same dose of aspirin alone; likewise addition of paracetamol to aspirin decreased the incidence of gastric lesions in either sex, and addition of phenacetin to aspirin had no effect. The potentiation by caffeine and the inhibition by paracetamol were both dose-dependent and only markedly influenced the development of erosions after 3–4 h. Pretreatment with phenacetin or paracetamol 1 h before administration of aspirin did not affect its erosive activity. Administration of benorylate caused no more gastric erosions than the vehicle or than equivalent mixtures of aspirin and paracetamol. The histamine-stimulated acid output of the stomach during gastric perfusion with aspirin was rapidly diminished. Neither paracetamol nor caffeine initially affected this decrease in acid output. However, 30 min after perfusion with aspirin and caffeine, acid secretion increased approximately as strongly as after caffeine alone. Caffeine potentiates aspirin-induced erosions by its stimulatory effect on acid secretion whereas paracetamol inhibits these erosions by preventing their growth.</jats:p>
Journal
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- Journal of Pharmacy and Pharmacology
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Journal of Pharmacy and Pharmacology 31 (1), 840-848, 1979-09-01
Oxford University Press (OUP)
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Details 詳細情報について
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- CRID
- 1360011143853943040
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- ISSN
- 20427158
- 00223573
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- Data Source
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- Crossref