Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Assiut University, Assiut, Egypt.
Hoba Therapeutics ApS, Copenhagen, Denmark.
Biochem Pharmacol. 2024 Apr;222:116091. doi: 10.1016/j.bcp.2024.116091. Epub 2024 Feb 25.
Despite the worldwide prevalence and huge burden of pain, pain is an undertreated phenomenon. Currently used analgesics have several limitations regarding their efficacy and safety. The discovery of analgesics possessing a novel mechanism of action has faced multiple challenges, including a limited understanding of biological processes underpinning pain and analgesia and poor animal-to-human translation. Computational pharmacology is currently employed to face these challenges. In this review, we discuss the theory, methods, and applications of computational pharmacology in pain research. Computational pharmacology encompasses a wide variety of theoretical concepts and practical methodological approaches, with the overall aim of gaining biological insight through data acquisition and analysis. Data are acquired from patients or animal models with pain or analgesic treatment, at different levels of biological organization (molecular, cellular, physiological, and behavioral). Distinct methodological algorithms can then be used to analyze and integrate data. This helps to facilitate the identification of biological molecules and processes associated with pain phenotype, build quantitative models of pain signaling, and extract translatable features between humans and animals. However, computational pharmacology has several limitations, and its predictions can provide false positive and negative findings. Therefore, computational predictions are required to be validated experimentally before drawing solid conclusions. In this review, we discuss several case study examples of combining and integrating computational tools with experimental pain research tools to meet drug discovery challenges.
尽管疼痛在全球范围内普遍存在且负担巨大,但疼痛仍是一种治疗不足的现象。目前使用的镇痛药在疗效和安全性方面存在一些局限性。具有新型作用机制的镇痛药的发现面临着多重挑战,包括对疼痛和镇痛的生物学过程的理解有限以及动物到人类的转化效果不佳。目前正在使用计算药理学来应对这些挑战。在这篇综述中,我们讨论了计算药理学在疼痛研究中的理论、方法和应用。计算药理学涵盖了广泛的理论概念和实用方法学方法,其总体目标是通过数据采集和分析来获得生物学见解。数据来自有疼痛或接受镇痛治疗的患者或动物模型,涵盖不同的生物学组织水平(分子、细胞、生理和行为)。然后可以使用不同的方法学算法来分析和整合数据。这有助于确定与疼痛表型相关的生物分子和过程,建立疼痛信号的定量模型,并提取人类和动物之间可转化的特征。然而,计算药理学存在一些局限性,其预测可能会提供假阳性和假阴性结果。因此,在得出可靠结论之前,需要通过实验验证计算预测。在这篇综述中,我们讨论了将计算工具与实验疼痛研究工具相结合和整合的几个案例研究示例,以应对药物发现的挑战。