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μνλΉμ μΈλμν¬μλ―Ό μμΉΌλ‘μ΄λμ΄μ νΉμ΄μ μν2-μλλ λ λ¦° μμ©μ²΄ κΈΈνμ μ λλ€. μμνμμλ μ£Όλ‘ μν2 μμ©μ (νΉν μμΌλΌμ§)μ μ§μ λ° μ¬νκ΄κ³ ν¨κ³Όλ₯Ό μμ μν€λ λ° μ¬μ©λ©λλ€. λν μλ―ΈνΈλΌμ¦ μ€λ μ ν¨κ³Όμ μΈ ν΄λ μ μ΄λ©° μλ°© λͺ©μ μΌλ‘λ μ¬μ©λ μ μμ΅λλ€. νλ μμμμ λ±μ€λ©λ°ν λ―Έλμ μμ μλ μ£Όλ‘ μν°νλ©μ‘Έμ΄ μ¬μ©λμ§λ§, μνλΉμ μ¬μ ν μ€μν μκΈ λ° μμ μ λ‘ λ¨μ μμ΅λλ€.
μμ© κΈ°μ : Yohimbine competitively blocks central and peripheral **presynaptic alpha-2 adrenergic receptors**. - **Mechanism:** By blocking these autoreceptors, yohimbine prevents the negative feedback loop that normally inhibits neurotransmitter release β **increases synaptic norepinephrine** release β enhances sympathetic outflow. - **Systemic Effects:** This surge in sympathetic tone results in increased heart rate, elevated blood pressure, CNS stimulation, and antidiuresis, effectively counteracting the profound sedation, bradycardia, and hypotension induced by alpha-2 agonists.
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- Xylazine reversal (Llamas/Camelids) Β· 0.25 mg/kg IV or IM Β· IV/IM Β· once Β· Dosing specifically reported for Llamas.
- Xylazine reversal Β· 0.125 mg/kg IV Β· IV Β· once
- Xylazine reversal (Routine/Emergency) Β· IM administration preferred for routine; 0.1 mg/kg IV for emergency Β· IM/IV Β· once Β· IM preferred to decrease CNS/CV risks. Wait 30-45 min post-IM or 15-30 min post-IV xylazine to allow ketamine/Telazol to resolve before reversing.
- Xylazine reversal Β· 0.075 mg/kg IV Β· IV Β· once Β· ARCI UCGFS Class 2 Drug.
- Alpha2-adrenergic agonist reversal (e.g., xylazine) Β· 0.1 mg/kg IV Β· IV Β· once
- Xylazine reversal (Rabbits) Β· 0.2 mg/kg IV Β· IV Β· as needed Β· Also partially antagonizes ketamine and acepromazine.
- Xylazine reversal (Mice/Rats) Β· 0.2 mg/kg IP Β· IP Β· as needed Β· Also partially antagonizes ketamine and acepromazine.
- Xylazine reversal Β· 0.11 mg/kg IV slowly OR 0.1 mg/kg IV Β· IV Β· once
- Medetomidine reversal Β· 0.11 mg/kg IV Β· IV Β· once
- Amitraz toxicity reversal (centrally mediated bradycardia/hypotension) Β· 0.1 mg/kg IV Β· IV Β· repeat as necessary
- Amitraz toxicity (demodicosis treatment) Β· 0.11 mg/kg IV or 0.25 mg/kg IM (with atipamezole 50 mcg/kg IM) Β· IV/IM Β· once Β· Used to treat or prevent acute toxicity episodes.
- Prevention of side effects from amitraz dips Β· 0.1 mg/kg IV Β· IV Β· once Β· May give prior to, or after bathing.
- Antiemetic Β· 0.25-0.5 mg/kg SC or IM Β· SC/IM Β· q12h
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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κΈκΈ°
- Hypersensitivity to yohimbine
- Renal disease (extrapolated from human medicine)
- Patients with active seizure disorders
μ΄μλ°μ
- Transient apprehension or anxiety
- CNS excitement
- Muscle tremors
- Hypersalivation
- Increased respiratory rate (panting)
- Hyperemic (red) mucous membranes
- Tachycardia
μ½λ¬Ό μνΈμμ©
- Tricyclic Antidepressants Β· May cause severe hypertension; concurrent use is not recommended.
- Other Alpha-2 Antagonists Β· Additive antagonistic effects; use with caution.
- CNS Stimulants Β· Additive CNS stimulation and increased risk of seizures or severe agitation.
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- CNS status (arousal level, signs of excitement or apprehension)
- Cardiac rate and rhythm
- Blood pressure (if indicated and practical)
- Respiratory rate and effort
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Overdoses can cause significant CNS and cardiovascular overstimulation. - **Experimental Data:** Dogs receiving 0.55 mg/kg (5 times the recommended dose) exhibited clinical signs of transient seizures and muscle tremors. - **Clinical Reports (APCC):** Reported findings in dogs include diarrhea, disorientation, hyperactivity, panting, tachycardia, and hypersalivation. - **Treatment:** Primarily supportive and symptomatic. Avoid further CNS stimulation and manage seizures if they occur.
VetSheet μ½λ¬Ό λ νΌλ°μ€λ λ©΄ν μμ μ λ¬Έκ°λ₯Ό μν μμ μμ¬κ²°μ 보쑰 λꡬμ΄λ©°, μ λ¬Έμ νλ¨μ΄λ μ μ‘°μ¬μ μ΅μ λΌλ²¨μ λμ νμ§ μμ΅λλ€.