2010
DOI: 10.1517/14656566.2010.515978
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Ketamine for the treatment of chronic non-cancer pain

Abstract: There is now evidence form a limited number of studies that pain relief lasting for months is observed after long-term intravenous ketamine infusion, suggesting a modulatory effect of ketamine in the process of chronic pain, possibly via blockade of upregulated NMDAR.

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Cited by 104 publications
(86 citation statements)
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“…First introduced as an anesthetic in 1964, it has since evolved for use as a veterinary anesthetic, a recreational drug (Special K) sought out for its hallucinatory and dissociative effects, and an analgesic frequently used in the postoperative setting as well as in the management of pain syndromes (1)(2)(3)(4). Ketamine has also become a popular choice for mild sedation when airway reflexes and hemodynamic stability must be maintained.…”
Section: Introductionmentioning
confidence: 99%
“…First introduced as an anesthetic in 1964, it has since evolved for use as a veterinary anesthetic, a recreational drug (Special K) sought out for its hallucinatory and dissociative effects, and an analgesic frequently used in the postoperative setting as well as in the management of pain syndromes (1)(2)(3)(4). Ketamine has also become a popular choice for mild sedation when airway reflexes and hemodynamic stability must be maintained.…”
Section: Introductionmentioning
confidence: 99%
“…Its chiral center on the C 2 atom of the ketamine cyclohexane ring gives rise to two enantiomers of ketamine (S(+)− and R(−)−). [56] It binds to the phencyclidinic site on postsynaptic channels and reduces the frequency and opening time of ion channels. [7] This blockade by ketamine at the NMDA receptors is dose-dependent in that the rate of onset and the recovery from blockade are increased by applying NMDA agonists.…”
Section: Pharmacological Propertiesmentioning
confidence: 99%
“…As a result, antagonists such as ketamine have been seen to stop afferent nociceptive transmission to the brain. [69] Ketamine also maintains blood pressure and preserves spontaneous breathing and laryngeal reflexes. [10] The S(+) isomer increases anesthetic potency two-fold over the racemic mixture while decreasing the psychotomimetic side effects.…”
Section: Pharmacological Propertiesmentioning
confidence: 99%
“…An important culprit in perpetuation of chronic pain is believed to be activation of the NMDA receptor. Drugs with NMDA receptor blocking activity include ketamine, dextromethorphan, amantadine, memantine and methadone [Noppers et al 2010;Shah and Diwan, 2010;Kleinbohl et al 2006]. An ideal pain modulator for chronic pain would be a molecule with the ability to block this receptor, but to date there have been no studies testing any of these agents in patients with rheumatic pain.…”
Section: Nontraditional Analgesic Agentsmentioning
confidence: 99%