Literature DB >> 2661183

Zinc compounds, a new treatment in peptic ulcer.

G Escolar1, O Bulbena.   

Abstract

Effects of zinc in gastric ulcer have been reviewed through investigations carried out on zinc acexamate (ZAC). ZAC is an organic compound that has been shown to possess an experimental antiulcer effect and a wide therapeutic index, making it a useful drug in the treatment of peptic ulcer disease. ZAC protects from ulceration in several experimental models such as pylorus occlusion, reserpine-induced ulcer, necrotizing agents, PAF-induced ulcer and cold-restraint stress. ZAC first reduces the gastric acid output by inhibiting the mast cell degranulation, an action likely to be mediated through a membrane stabilizing action. Secondly, it enhances the mucosal protection factors by increasing mucus secretion, inhibiting the H+ retrodiffusion and improving microcirculation. ZAC is also effective in acetic acid-induced chronic ulcer, restoring the continuity of the damaged mucosa. Several clinical trials have shown the usefulness of ZAC in acute and maintenance treatment of both gastric and duodenal ulcers. Endoscopic studies showed that ZAC reduced the inflammatory processes (gastritis and duodenitis) associated with ulcer healing. This reduction was statistically significant and not observed with other comparative treatments (H2-antagonists). The observed side-effects were minimal and affected less than 2% of treated patients. The pharmacological profile, clinical effectiveness and good tolerance of ZAC suggest this compound as an interesting option in the treatment of peptic disease.

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Year:  1989        PMID: 2661183

Source DB:  PubMed          Journal:  Drugs Exp Clin Res        ISSN: 0378-6501


  9 in total

1.  Concentrations of metals in gastric juice in health and peptic ulcer disease.

Authors:  J J Powell; S M Greenfield; R P Thompson
Journal:  Gut       Date:  1992-12       Impact factor: 23.059

2.  Pharmacokinetic study of orally administered zinc in humans: evidence for an enteral recirculation.

Authors:  J Nève; M Hanocq; A Peretz; F Abi Khalil; F Pelen; J P Famaey; J Fontaine
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1991 Oct-Dec       Impact factor: 2.441

3.  Inhibition of endogenous CO by ZnPP protects against stress-induced gastric lesion in adult male albino rats.

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Journal:  J Physiol Biochem       Date:  2012-01-13       Impact factor: 4.158

Review 4.  Zinc and gastrointestinal disease.

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Journal:  World J Gastrointest Pathophysiol       Date:  2014-11-15

5.  Secretagogue-dependent and -independent transport of zinc hydration forms in rat parietal cells.

Authors:  Florentina Sophie Ferstl; Alice Miriam Kitay; Rebecca Marion Trattnig; Abrar Alsaihati; John Peter Geibel
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6.  Absorption and metabolism of oral zinc gluconate in humans in fasting state, during, and after a meal.

Authors:  J Nève; M Hanocq; A Peretz; F A Khalil; F Pelen
Journal:  Biol Trace Elem Res       Date:  1992 Jan-Mar       Impact factor: 3.738

7.  The role of zinc sulfate and metallothionein in protection against ethanol-induced gastric damage in rats.

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8.  Development and Validation of a Liquid Chromatography-Tandem Mass Spectrometry Method for the Determination of ε-Acetamidocaproic Acid in Rat Plasma.

Authors:  Tae Hyun Kim; Yong Seok Choi; Young Hee Choi; Yoon Gyoon Kim
Journal:  Toxicol Res       Date:  2013-09

Review 9.  Zinc and gut microbiota in health and gastrointestinal disease under the COVID-19 suggestion.

Authors:  Emidio Scarpellini; Lukas M Balsiger; Valentina Maurizi; Emanuele Rinninella; Antonio Gasbarrini; Nena Giostra; Pierangelo Santori; Ludovico Abenavoli; Carlo Rasetti
Journal:  Biofactors       Date:  2022-02-26       Impact factor: 6.438

  9 in total

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