Difference between revisions of "Trimethoprim - Dihydrofolate Reductase Inhibitors"

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[[Image: Trimethoprim.png|thumb|right|250px|Trimethoprim]]
 
[[Image: Trimethoprim.png|thumb|right|250px|Trimethoprim]]
 
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'''Trimethoprim''' is the only dihydrofolate reductase inhibitor currently in veterinary use. It is chemically related to the antimalarial drug pyrimethamine.
  
  
 
==Mechanism of Action==
 
==Mechanism of Action==
  
Sulphonamides act by competing with an essential precursor in folic acid synthesis in bacteria. Bacteria need to synthesise folic acid in order to grow as they are unable to obtain it from their 'diet' like mammals can. Since the bacteria is unable to synthesise RNA or DNA, due to it's lack of folic acid, it's growth is inhibited. As such sulphonamides are '''bacteriostatic'''.
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Trimethoprim works as an antagonist inhibiting the dihydrofolate reductase enzyme. This means that the bacteria is unable to grow as it is denied it's folic acid source. This means that trimethoprim is a bacteriostatic drug.
 
 
  
  
 
==Spectrum of Activity==
 
==Spectrum of Activity==
  
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* It is a broad spectrum antibiotic active against aerobic gram positives and negatives.
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* It isn't active against anaerobes and ''Pseudomonas''.
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* As with [[sulphonamides]] it is inhibited by necrotic tissue as this provides an alternative source of growth products for the bacteria. This bypasses the folic acid use and so the effects of the trimethoprim become obselete.
  
  
 
==Pharmacokinetic Considerations==
 
==Pharmacokinetic Considerations==
Dihydrofolate reductase inhibitors: Lipophilic weak bases. 
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• Orally active.
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It is a lipophilic weak base, that is orally active and fully absorbed by the gastrointestinal tract. It widely distributes throughout the body, reaching quite high concentrations in the kidney, lung, and CSF. It will become ion-trapped in acidic fluid. It is rapidly metabolised by the liver but the rate varies with each species. It's elimination by the kidney will increase with acidic urine due to the basic nature of the drug.
• Widely distributed throughout the body, ion trapped in acidic fluids.
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• Cleared by hepatic metabolism – rate varies with species and individual drug (trimethoprim rapidly metabolised by most veterinary species).
 
  
 
==Side Effects and Contraindications==
 
==Side Effects and Contraindications==
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It is a fairly non-toxic drug. It can cause folic acid deficiency if given at high and extended doses. It is less safe in cats as excessive salivation can occur.

Latest revision as of 13:03, 24 October 2008


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Trimethoprim

Trimethoprim is the only dihydrofolate reductase inhibitor currently in veterinary use. It is chemically related to the antimalarial drug pyrimethamine.


Mechanism of Action

Trimethoprim works as an antagonist inhibiting the dihydrofolate reductase enzyme. This means that the bacteria is unable to grow as it is denied it's folic acid source. This means that trimethoprim is a bacteriostatic drug.


Spectrum of Activity

  • It is a broad spectrum antibiotic active against aerobic gram positives and negatives.
  • It isn't active against anaerobes and Pseudomonas.
  • As with sulphonamides it is inhibited by necrotic tissue as this provides an alternative source of growth products for the bacteria. This bypasses the folic acid use and so the effects of the trimethoprim become obselete.


Pharmacokinetic Considerations

It is a lipophilic weak base, that is orally active and fully absorbed by the gastrointestinal tract. It widely distributes throughout the body, reaching quite high concentrations in the kidney, lung, and CSF. It will become ion-trapped in acidic fluid. It is rapidly metabolised by the liver but the rate varies with each species. It's elimination by the kidney will increase with acidic urine due to the basic nature of the drug.


Side Effects and Contraindications

It is a fairly non-toxic drug. It can cause folic acid deficiency if given at high and extended doses. It is less safe in cats as excessive salivation can occur.