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| ===Histamine 2 receptor antagonists=== | | ===Histamine 2 receptor antagonists=== |
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− | Parietal cells secrete HCl upon stimulation of histamine, acetylcholine or gastrin receptors.(EGUC) Competitive H2 receptor antagonists have successfully elevated gastric pH and treated gastric ulcers in mature horses and foals.(44,85,97 in Sachez) | + | Parietal cells secrete HCl upon stimulation of histamine, acetylcholine or gastrin receptors.(EGUC) Competitive H2 receptor antagonists have successfully elevated gastric pH and treated gastric ulcers in mature horses and foals.(44,85,97 in Sachez) There appears to be a great variability among horses in their dose requirements for H2 antagonists which may be explained by individual bioavilability for these compounds.(EGUC) Currently recommended doses proposed to be effective in the majority of horses(Sanchez) are: |
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− | Currently recommended doses proposed to be effective in the majority of horses(Sanchez) are: | |
| *'''Cimetidine''' 20-30mg/kg PO every 8 hours or 6.6mg/kg IV every 6 hours | | *'''Cimetidine''' 20-30mg/kg PO every 8 hours or 6.6mg/kg IV every 6 hours |
| *'''Ranitidine''' 6.6mg/kg PO every 8 hours or 1.5-2mg/kg IV every 6 hours | | *'''Ranitidine''' 6.6mg/kg PO every 8 hours or 1.5-2mg/kg IV every 6 hours |
| *'''Famotidine''' 10-15mg/kg PO every 24 hours | | *'''Famotidine''' 10-15mg/kg PO every 24 hours |
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− | The proton-pump inhibitors constitute a new treatment approach that blocks acid production within the cell. This modality is receptor-independent and therefore more effective.(EGUC)
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− | Cimetidine has been shown to affect hepatic disposition of some drugs.
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− | The problem with treatment of gastric ulcers in horses is that individuals have different dose requirements for effective treatment. This probably relates to varying bioavailability of the drug in individual horses. The wide variability among horses in acid suppression achieved with H2 antagonists
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| ===Proton-pump inhibitors=== | | ===Proton-pump inhibitors=== |