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IUPHAR review: Navigating the role of preclinical models in pain research
被引:4
|作者:
Karimi, Seyed Asaad
[1
]
Zahra, Fatama Tuz
[2
]
Martin, Loren J.
[1
,2
,3
]
机构:
[1] Univ Toronto Mississauga, Dept Psychol, Mississauga, ON L5L 1C6, Canada
[2] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON M5S 3G5, Canada
[3] Univ Toronto Mississauga, Dept Psychol, 3359 Mississauga Rd, Mississauga, ON L5L 1C6, Canada
基金:
加拿大自然科学与工程研究理事会;
加拿大健康研究院;
关键词:
Pain;
Preclinical;
Translational;
Drug discovery;
Mouse;
Rat;
NERVE GROWTH-FACTOR;
GENE-RELATED PEPTIDE;
HINDPAW WITHDRAWAL LATENCY;
CALCIUM-CHANNEL BLOCKERS;
MU-OPIOID RECEPTOR;
DERMAL BLOOD-FLOW;
NEUROPATHIC PAIN;
DOUBLE-BLIND;
ANIMAL-MODELS;
MONOCLONAL-ANTIBODY;
D O I:
10.1016/j.phrs.2024.107073
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Chronic pain is a complex and challenging medical condition that affects millions of people worldwide. Understanding the underlying mechanisms of chronic pain is a key goal of preclinical pain research so that more effective treatment strategies can be developed. In this review, we explore nociception, pain, and the multifaceted factors that lead to chronic pain by focusing on preclinical models. We provide a detailed look into inflammatory and neuropathic pain models and discuss the most used animal models for studying the mechanisms behind these conditions. Additionally, we emphasize the vital role of these preclinical models in developing new pain -relief drugs, focusing on biologics and the therapeutic potential of NMDA and cannabinoid receptor antagonists. We also discuss the challenges of TRPV1 modulation for pain treatment, the clinical failures of neurokinin (NK)- 1 receptor antagonists, and the partial success story of Ziconotide to provide valuable lessons for preclinical pain models. Finally, we highlight the overall success and limitations of current treatments for chronic pain while providing critical insights into the development of more effective therapies to alleviate the burden of chronic pain.
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页数:19
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