Yohimbine is an alpha2-adrenergic antagonist used principally to reverse xylazine-induced sedation and associated physiologic effects. Its veterinary history predates more selective antagonists. Applications extend to selected other alpha2 agonists and amitraz intoxication, although the degree of reversal depends on the agonist, species and clinical context.
Yohimbine antagonizes alpha2-adrenoceptors and reduces the receptor-mediated inhibition of norepinephrine release caused by alpha2 agonists. Restoration of central noradrenergic activity promotes arousal and reverses part of the sedative and autonomic response. Peripheral receptor antagonism contributes to cardiovascular and metabolic reversal. Amitraz-associated effects may improve because its active compounds also stimulate alpha2 pathways.
Monitor heart rate and rhythm. A full dose may be unnecessary after sedative clearance: reported recommends one-third initially, followed if needed by equal increments every 5-10 minutes.
After ketamine or tiletamine-zolazepam combinations, allow dissociative effects to diminish before reversal to reduce rough recovery. IV reversal can wear off before IM xylazine, causing resedation. Amitraz combination report includes yohimbine 0.11 mg/kg IV or 0.25 mg/kg IM with atipamezole 50 mcg/kg IM; do not treat the combination as automatic routine reversal.
Veterinary use
For veterinary reference. Confirm the indication, dose, route, interval, product strength and any applicable withdrawal period before administration.