“…The α-agonists are commonly used as sedative agents in livestock, but analgesic effects have also been demonstrated, particularly at below-sedative doses. At sedative doses (0.4 mg/kg xylazine in sheep), some of the findings must be interpreted with care: if a reduction in nociceptive response is recorded coincidental with moderate to deep sedation, but not when no or mild sedation is observed [325,374], is this truly evidence of analgesia, or merely evidence that the animal is unable to, or is very slow to, respond to the stimulus? However, at very low doses, reductions in nociceptive threshold (pinprick or electrical stimulus) have been reported [37,227,228,[375][376][377][378][379] when xylazine (0.05 mg/kg), clonidine (0.002-0.005 mg/kg) or detomidine (0.01 mg/kg) have been administered intravenously, intramuscularly, intraperitoneally or epidurally.…”