Street Sarah E, Sowa Nathaniel A
Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA,
Subcell Biochem. 2015;76:283-305. doi: 10.1007/978-94-017-7197-9_13.
Chronic pain is one of the most debilitating and expensive diseases, yet current therapies are often insufficient in bringing about long-term relief. Further, many treatments for chronic pain also carry significant side effects. The molecule adenosine has long been identified as a potent inhibitor of nociceptive circuits in the spinal cord; however, the widespread expression of adenosine receptors in many organ systems has limited its use as an analgesic. Recently several 5' ectonucleotidases, including tissue non-specific alkaline phosphatase (TNAP), have been characterized for their ability to generate endogenous adenosine in nociceptive circuitry of the dorsal spinal cord. These ectonucleotidases have the ability to hydrolyze the endogenous pronociceptive nucleotides like adenosine triphosphate (ATP) into the antinociceptive nucleoside adenosine. This chapter discusses the role of TNAP and other ectonucleotidases in nociceptive circuits, and their potential as future targets of new therapeutics to treat chronic pain.
慢性疼痛是最使人衰弱且花费高昂的疾病之一,然而目前的治疗方法往往不足以带来长期缓解。此外,许多慢性疼痛的治疗方法也有显著的副作用。长期以来,分子腺苷一直被认为是脊髓中伤害性感受回路的有效抑制剂;然而,腺苷受体在许多器官系统中的广泛表达限制了其作为镇痛药的应用。最近,包括组织非特异性碱性磷酸酶(TNAP)在内的几种5'外切核苷酸酶,因其在脊髓背角伤害性感受回路中产生内源性腺苷的能力而得到表征。这些外切核苷酸酶能够将内源性促伤害性核苷酸如三磷酸腺苷(ATP)水解为抗伤害性核苷腺苷。本章讨论了TNAP和其他外切核苷酸酶在伤害性感受回路中的作用,以及它们作为治疗慢性疼痛新疗法未来靶点的潜力。