Department of Physiology, Faculty of Medical and Health Sciences, The University of Auckland, New Zealand.
Curr Neuropharmacol. 2009 Sep;7(3):246-56. doi: 10.2174/157015909789152155.
Adenosine is a signalling molecule that modulates cellular activity in the central nervous system and peripheral organs via four G protein-coupled receptors designated A(1), A(2A), A(2B), and A(3). This review surveys the literature on the role of adenosine in auditory function, particularly cochlear function and its protection from oxidative stress. The specific tissue distribution of adenosine receptors in the mammalian cochlea implicates adenosine signalling in sensory transduction and auditory neurotransmission although functional studies have demonstrated that adenosine stimulates cochlear blood flow, but does not alter the resting and sound-evoked auditory potentials. An interest in a potential otoprotective role for adenosine has recently evolved, fuelled by the capacity of A(1) adenosine receptors to prevent cochlear injury caused by acoustic trauma and ototoxic drugs. The balance between A(1) and A(2A) receptors is conceived as critical for cochlear response to oxidative stress, which is an underlying mechanism of the most common inner ear pathologies (e.g. noise-induced and age-related hearing loss, drug ototoxicity). Enzymes involved in adenosine metabolism, adenosine kinase and adenosine deaminase, are also emerging as attractive targets for controlling oxidative stress in the cochlea. Other possible targets include ectonucleotidases that generate adenosine from extracellular ATP, and nucleoside transporters, which regulate adenosine concentrations on both sides of the plasma membrane. Developments of selective adenosine receptor agonists and antagonists that can cross the blood-cochlea barrier are bolstering efforts to develop therapeutic interventions aimed at ameliorating cochlear injury. Manipulations of the adenosine signalling system thus hold significant promise in the therapeutic management of oxidative stress in the cochlea.
腺苷是一种信号分子,通过四种 G 蛋白偶联受体(A(1)、A(2A)、A(2B) 和 A(3))调节中枢神经系统和外周器官的细胞活动。本综述调查了腺苷在听觉功能中的作用,特别是耳蜗功能及其免受氧化应激的保护作用。哺乳动物耳蜗中腺苷受体的特定组织分布表明,尽管功能研究表明腺苷刺激耳蜗血流,但不改变静息和声音诱发的听觉电位,腺苷信号参与了感觉转导和听觉神经传递。最近,由于 A(1) 腺苷受体能够预防声创伤和耳毒性药物引起的耳蜗损伤,人们对腺苷的潜在耳保护作用产生了兴趣。A(1) 和 A(2A) 受体之间的平衡被认为对耳蜗对氧化应激的反应至关重要,氧化应激是最常见的内耳病变(例如噪声诱导和年龄相关性听力损失、药物耳毒性)的潜在机制。参与腺苷代谢的酶,如腺苷激酶和腺苷脱氨酶,也被认为是控制耳蜗氧化应激的有吸引力的靶点。其他可能的靶点包括从细胞外 ATP 生成腺苷的外核苷酸酶,以及调节质膜两侧腺苷浓度的核苷转运体。选择性腺苷受体激动剂和拮抗剂的开发能够穿过血耳蜗屏障,这为开发旨在改善耳蜗损伤的治疗干预措施提供了支持。因此,对腺苷信号系统的操纵在耳蜗氧化应激的治疗管理中具有重要意义。