Table 2.
Drug | Drug profile responsible for anticraving properties | Representing human anticraving studies | Other medical use besides anticraving therapy |
---|---|---|---|
Naltrexonea | A glutamate agonist, is derived from amino acid, taurine | Weinstein et al (2003)5 | |
Naltrexonea | A main μ and δ (lesser extent) opioid receptor antagonist |
Volpicelli et al (1992)11 O'Malley et al (1992)12 |
Opioid overdose |
GHBb | A precursor to GABA, glutamate, and glycine | Addolorato et al (1996)14 | Narcolepsy |
Nalmefeneb | A μ‐opioid receptor antagonist & κ‐opioid partial agonist |
Gual et al (2013)19 van den Brink et al (2014)20 |
|
Topiramate | An antagonist for kainate/AMPA, a subtype of the glutamate |
Johnson et al (2003)22 Johnson et al (2004)23 Johnson et al (2007)24 |
Epilepsy Migraine Lennox‐Gastaut syndrome |
Gabapentin | A drug to facilitate GABA transmission |
Furieri & Nakamura‐Palacio (2007)27 Mason et al (2014)28 |
Epilepsy Nerve pain |
Ondansetron | A 5‐HT3 reuptake inhibitor | Johnson et al (2000)29 | Antiemetic for cancer patients receiving chemotherapy |
Ifenprodil | A GIRK channel inhibitor | Sagaya et al (2018)35 | Dizziness in poststroke patients |
The Arab numbers in superscripts denote the reference entries cited in the article.
AMPA receptors, α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptors; GABA, gamma‐aminobutyric acid; GHB, gamma‐hydroxybutyate; GIRK channel, G protein‐activated inwardly rectifying potassium channel.
Approved by US Food and Drug Administration for anticraving indication in patients with alcohol use disorder.
Approved by European Medicines Agency for anticraving indication in patients with alcohol use disorder.