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**νλ‘λ² λ€μλ(Probenecid)**λ μ£Όλ‘ **μμ° λ°°μ€ μ΄μ§μ ** λ° **μ μΈλ¨κ΄ λΆλΉ μ΅μ μ **λ‘ μ¬μ©λλ μ€ν°μλ§μ΄λ μ λ체μ λλ€. * **μμνμ μ©λ**: μν ν¬μ λ₯μμμ μμμ μ¬μ©μ μ νμ μ΄μ§λ§, **νμΆ©λ₯**μ ν΅ν(κ³ μμ°νμ¦) κ΄λ¦¬μ νΉν μ μ©ν©λλ€. * **μ½λ¦¬νμ μ μ©μ±**: μμ¬μ , μ½λ¦¬νμ μΌλ‘ νλ‘λ² λ€μλλ μ½ν μ κΈ°μ°, νΉν **λ² νλ½νκ³ νμμ **(νλμ€λ¦° λ° μΈνλ‘μ€ν¬λ¦°)μ μ μ₯ λ°°μ€μ μ΅μ νλ λ₯λ ₯μΌλ‘ μ λͺ ν©λλ€. μ΄λ₯Ό ν΅ν΄ μ΄λ¬ν μ½λ¬Όμ λ°κ°κΈ°λ₯Ό ν¬κ² μ°μ₯νκ³ νμ² λλλ₯Ό λμ λλ€. * **μμ μμ **: κ°μμ νλ‘λ² λ€μλλ μ¬λ(6.5μκ°)μ λΉν΄ λ§€μ° κΈ΄ μ κ±° λ°κ°κΈ°(μ½ 18μκ°)λ₯Ό κ°μ§λ©°, μ΄λ μ΄λ‘ μ μΌλ‘ κ³ κ°μ΄κ±°λ λΉ λ₯΄κ² μ κ±°λλ μ½λ¬Όμ ν¬μ¬ κ°κ²©μ μ°μ₯νλ λ° μ 리ν μ μμΌλ, κ°μ λν κ°λ ₯ν μμ μνμ μμ§ λΆμ‘±ν©λλ€.
μμ© κΈ°μ : Probenecid exerts its effects via competitive inhibition at the proximal renal tubules: * **Uricosuric Effect**: Competitively inhibits the **Urate Transporter 1 (URAT1)** on the apical membrane of the proximal tubule β prevents the reabsorption of uric acid from the urine back into the blood β enhances uric acid excretion and lowers serum urate levels. * **Secretion Inhibition**: Competitively inhibits **Organic Anion Transporters (OAT1, OAT3)** on the basolateral membrane β prevents the active tubular secretion of weak organic acids (e.g., penicillins, cephalosporins, NSAIDs) from the blood into the urine β prolongs the systemic half-life of these drugs.
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- Gout Β· 250 mg PO q12h; can be increased as needed. Β· PO Β· q12h Β· Suggested dosage based upon human data as dose is not established for reptiles.
- Gout Β· 40 mg/kg PO q12h Β· PO Β· q12h
- Gout Β· 250 mg (total dose) PO twice daily; may increase as needed. Β· PO Β· twice daily
μ©λμ λ©΄ν μμ μ λ¬Έκ°λ₯Ό μν μμ μ°Έκ³ μλ£μ λλ€. νμ μ΅μ λΌλ²¨κ³Ό κ°λ³ νμμ λν΄ νμΈνμμμ€.
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- Patients with or susceptible to uric acid renal or bladder calculus formation
- Urate nephropathy (e.g., cancer chemotherapy with rapidly cytolytic agents)
- Severe renal impairment (creatinine clearance < 30 mL/min)
- Gout in birds (can exacerbate the condition)
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- Headache (humans)
- Inappetence
- Nausea
- Mild vomiting
- Rashes
- Increased rate of gouty attacks initially (if no prophylaxis)
- Hypersensitivity (rare)
- Bone marrow suppression (rare)
- Hepatotoxicity (rare)
- Nephrotic syndrome (rare)
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- Acyclovir Β· Increased acyclovir serum concentrations; probenecid can decrease renal excretion
- Antineoplastics (rapidly cytolytic) Β· Increased chance of uric acid nephropathy
- Aspirin (and other salicylates) Β· Salicylates antagonize the uricosuric effects of probenecid
- Benzodiazepines (lorazepam, oxazepam) Β· Probenecid may prolong action or reduce time for onset of action
- Beta-lactam antibiotics Β· Probenecid may increase serum concentrations by reducing renal excretion
- Beta-lactamase inhibitors (sulbactam, tazobactam) Β· Probenecid may increase serum concentrations by reducing renal excretion (does not affect clavulanic acid)
- Chlorpropamide Β· Probenecid decreases elimination; hypoglycemia is possible
- Ciprofloxacin/Enrofloxacin Β· Probenecid reduces renal tubular secretion of ciprofloxacin by about 50%. Significantly reduces renal excretion of enrofloxacin in goats.
- Dapsone Β· Possible accumulation of dapsone or its active metabolites
- Furosemide Β· Increased serum furosemide levels
- Heparin Β· Probenecid may increase and prolong heparin's effects
- Methotrexate Β· Probenecid may increase levels; increased risks for toxicity
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- Serum uric acid
- Urine uric acid
- Acid-base balance (if concomitant urine alkalinization is used)
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Limited information is available in veterinary species. * **Human Data**: One massive (>45 g) overdose caused CNS stimulation, seizures, protracted vomiting, and respiratory failure. * **Management**: Handle initially using standardized protocols for removal of drug from the gut and preventing absorption. Treat supportively. Use caution co-administrating drugs that may compete with probenecid for tubular secretion. Consider contacting an animal poison control center for guidance.
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