Antimetabolites: Sulfonamides and trimethoprim
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Antimetabolites: Sulfonamides and trimethoprim
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Laboratory value | Result |
Arterial blood gas | |
pH | 7.39 |
PaO2 | 142 mm Hg |
PaCO2 | 34 |
Oxygen saturation | 99% |
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Agranulocytosis p. 591
sulfa drug allergies p. 251
Anemia
sulfa drug allergies as cause p. 251
Chlamydia spp. p. 146
sulfonamides for p. 191
Hemolysis
sulfonamides as cause p. 191
Hemolytic anemia p. 427
sulfa drug allergies p. 251
Hypersensitivity reactions p. 110-111
sulfonamides p. 191
Nephrotoxicity
sulfonamides p. 191
Nocardia spp.
sulfonamides for p. 191
Photosensitivity (cutaneous)
sulfonamides p. 191
Stevens-Johnson syndrome p. 191, 490, 560
sulfa drug allergies p. 251
Sulfa drugs p. 251
acute pancreatitis p. 404
erythema multiforme p. 490
G6PD deficiency from p. 415
megaloblastic p. 249
rash p. 249
Sulfonamides p. 191
acute interstitial nephritis from p. 620
cytochrome P-444 and p. 251
hemolysis in G6PD deficiency p. 249
hypothyroidism p. 248
mechanism p. 184
Nocardia spp. p. 137
photosensitivity p. 249
pregnancy contraindication p. 200
trimethroprim p. 191
vitamin BNaN deficiency p. 66
Thrombocytopenia p. 413
sulfa drug allergies p. 251
Urinary tract infections (UTIs) p. 179, 619
sulfa drugs for p. 251
sulfonamides for p. 191
Urticaria p. 483, 485
sulfa drug allergies p. 251
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Antimetabolites are medications that interfere with the synthesis of DNA.
Some antimetabolites are used in chemotherapy to kill cancer cells, while others are used as antibiotics since they inhibit bacterial folate synthesis.
Folate, or folic acid, also known as vitamin B9, is necessary for the synthesis of nucleic acids, which are the building blocks of DNA and RNA.
Simply put, a lack of folate results in a lack of nucleic acids, which then results in decreased DNA and RNA synthesis, leading to hindered cell division and function.
Now, a key difference between our cells and bacterial cells is that we get all of our folate through our diet, while bacteria can make their own folate from scratch.
Because of this, we can target the bacterial folate synthesis pathway to minimize the damage done to our cells.
So in order to synthesize folate, the bacteria will first use the host’s para-aminobenzoic acid, or pABA, and convert it to dihydropteroic acid via the enzyme dihydropteroate synthetase, or DHPS.
In the second step, dihydropteroic acid is converted into dihydrofolic acid by dihydrofolate synthetase.
The third step is the conversion of dihydrofolic acid into tetrahydrofolic acid via dihydrofolate reductase.
Tetrahydrofolic acid is a folic acid derivative and can be used to synthesize purines like adenine and guanine, which are used to build DNA and RNA, as well as thymidine, which is only used in DNA.
Now, the first group of antimetabolite antibiotics are the sulfonamides, which include sulfamethoxazole, or SMX, sulfisoxazole, and sulfadiazine.
These medications bind to dihydropteroate synthetase, or DHPS, in the first step of folate synthesis and prevents the bacteria from making dihydropteroic acid.
These medications can be given peroral or injected into a vein, but they need to be metabolized by the liver in order to work.
Now, they are broad spectrum and can treat a variety of gram positive and gram negative bacteria, as well as chlamydia and nocardia species.
Next we have trimethoprim, which inhibits the 3rd step of folate synthesis by inhibiting dihydrofolate reductase, or DHFR, preventing the formation of tetrahydrofolic acid.
Sources
- "Katzung & Trevor's Pharmacology Examination and Board Review,12th Edition" McGraw-Hill Education / Medical (2018)
- "Rang and Dale's Pharmacology" Elsevier (2019)
- "Goodman and Gilman's The Pharmacological Basis of Therapeutics, 13th Edition" McGraw-Hill Education / Medical (2017)
- "Methotrexate, and trimethoprim-sulfamethoxazole: toxicity from this combination continues to occur" Can Fam Physician (2014)
- "Prophylactic Trimethoprim-Sulfamethoxazole Does Not Affect Pharmacokinetics or Pharmacodynamics of Methotrexate" Journal of Pediatric Hematology/Oncology (2016)
- "Medication Use and the Risk of Stevens–Johnson Syndrome or Toxic Epidermal Necrolysis" New England Journal of Medicine (1995)