Xylazine

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  • Xylazine is a veterinary sedative, analgesic, and muscle relaxant that belongs to the class of drugs known as alpha-2 adrenergic receptor agonists. 
  • First synthesized in the early 1960s, it was initially explored for human medical use but was deemed unsafe due to severe side effects, particularly profound hypotension, bradycardia, and respiratory depression. As a result, its approved use is restricted to veterinary medicine, where it is commonly employed to sedate and immobilize animals such as horses, cattle, deer, and other large mammals for surgical procedures, diagnostic tests, or handling. Its effects are rapid and potent, making it a valuable tool for veterinarians managing difficult or dangerous species.
  • Pharmacologically, xylazine works by stimulating alpha-2 adrenergic receptors in the central nervous system, leading to decreased norepinephrine release. This action reduces sympathetic nervous activity, which results in sedation, analgesia, and muscle relaxation. However, this same mechanism also accounts for its dangerous side effects, including low blood pressure, slow heart rate, reduced cardiac output, and depressed breathing. In animals, these effects are typically manageable under veterinary supervision, especially when xylazine is combined with other anesthetics or reversed with specific antagonists such as yohimbine or tolazoline.
  • In recent years, xylazine has become a serious public health concern because it has entered the illicit drug supply, particularly in combination with opioids such as fentanyl and heroin. Sometimes referred to as “tranq” or “tranq dope”, it is used to prolong the euphoric effects of opioids, but it greatly increases the risk of fatal overdose. Unlike opioids, xylazine is not reversed by naloxone, which complicates emergency response. Moreover, chronic use has been linked to severe skin ulcerations, abscesses, and necrotic tissue injuries, sometimes leading to amputations. These wounds are not fully understood but are thought to result from reduced blood circulation and tissue oxygenation caused by the drug’s vasoconstrictive and sedative effects.
  • Legally, xylazine is not classified as a controlled substance in many countries, which has made it relatively accessible compared to strictly regulated opioids. However, growing concerns about its misuse have led to increasing calls for tighter regulation and monitoring. Public health agencies, particularly in the United States, have highlighted xylazine as a major emerging threat in the ongoing opioid crisis, noting its role in escalating overdose deaths and complicating treatment strategies.
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