Targeting sensory neuron GPCRs for peripheral neuropathic pain

被引:6
|
作者
Uniyal, Ankit [1 ]
Tiwari, Vinod [2 ]
Tsukamoto, Takashi [3 ,4 ]
Dong, Xinzhong [5 ]
Guan, Yun [1 ,6 ]
Raja, Srinivasa N. [1 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Dept Anesthesiol & Crit Care Med, Div Pain Med, Baltimore, MD 21205 USA
[2] Indian Inst Technol BHU, Dept Pharmaceut Engn & Technol, Neurosci & Pain Res Lab, Varanasi, India
[3] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Johns Hopkins Drug Discovery, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Dept Neurosci, Baltimore, MD USA
[6] Johns Hopkins Univ, Dept Neurol Surg, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
DELTA-OPIOID RECEPTORS; THERAPEUTIC TARGET; OXYTOCIN RECEPTOR; MECHANISM; HYPERSENSITIVITY; ANTINOCICEPTION; CANNABINOIDS; ACTIVATION; EXPRESSION; STRATEGIES;
D O I
10.1016/j.tips.2023.10.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the high prevalence of peripheral neuropathic pain (NP) conditions and significant progress in understanding its underlying mechanisms, the management of peripheral NP remains inadequate. Existing pharmacotherapies for NP act primarily on the central nervous system (CNS) and are often associated with CNS-related adverse effects, limiting their clinical effectiveness. Mounting preclinical evidence indicates that reducing the heightened activity in primary sensory neurons by targeting G-protein-coupled receptors (GPCRs), without activating these receptors in the CNS, relieves pain without central adverse effects. In this review, we focus on recent advancements in GPCR-mediated peripheral pain relief and discuss strategies to advance the development of more effective and safer therapies for peripheral NP by shifting from traditional CNS modulatory approaches toward selective targeting of GPCRs on primary sensory neurons.
引用
收藏
页码:1009 / 1027
页数:19
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