Gibuła-Tarłowska Ewa, Wiszniewska Anna, Turyk Magdalena, Szymczyk Paulina, Kotlińska Jolanta H, Kędzierska Ewa
Department of Pharmacology and Pharmacodynamics, Faculty of Pharmacy, Medical University of Lublin, 20-093 Lublin, Poland.
Student Scientific Club "Synapse", Department of Pharmacology and Pharmacodynamics, Faculty of Pharmacy, Medical University of Lublin, 20-093 Lublin, Poland.
Molecules. 2025 Jun 30;30(13):2824. doi: 10.3390/molecules30132824.
Ketamine, originally developed as an anesthetic, is gaining increasing attention due to its multifaceted pharmacological properties. In addition to its use in anesthesia, ketamine exerts potent analgesic effects via N-methyl-D-aspartate (NMDA) receptor antagonism, modulating pain perception and reducing central sensitization, particularly in chronic and neuropathic pain conditions. Emerging evidence also supports ketamine's potential in the treatment of substance use disorder, where it may disrupt maladaptive reward-related memories and promote neuroplasticity which facilitates behavioral change. Moreover, in recent years, S-ketamine has shown rapid and potent antidepressant effects, especially in treatment-resistant depression (TRD), probably due to increased glutamatergic signaling, synaptic plasticity and the release of neurotrophic factors. This heterogeneous therapeutic profile positions ketamine as a unique agent at the interface of anesthesia, pain management, addiction medicine and psychiatry, warranting further exploration into its mechanism and long-term effectiveness.
氯胺酮最初是作为一种麻醉剂开发的,由于其多方面的药理特性而受到越来越多的关注。除了用于麻醉外,氯胺酮通过拮抗N-甲基-D-天冬氨酸(NMDA)受体发挥强大的镇痛作用,调节疼痛感知并减少中枢敏化,特别是在慢性和神经性疼痛情况下。新出现的证据还支持氯胺酮在治疗物质使用障碍方面的潜力,它可能会破坏与适应不良奖励相关的记忆,并促进神经可塑性,从而有助于行为改变。此外,近年来,S-氯胺酮已显示出快速而强大的抗抑郁作用,尤其是在难治性抑郁症(TRD)中,这可能是由于谷氨酸能信号增强、突触可塑性和神经营养因子的释放。这种异质性的治疗特性使氯胺酮成为麻醉、疼痛管理、成瘾医学和精神病学领域的一种独特药物,值得进一步探索其作用机制和长期有效性。