Conde Silvia V, Monteiro Emilia C, Sacramento Joana F
Centro de Estudos de Doenças Crónicas, NOVA Medical School - Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisboa, Portugal.
Front Pharmacol. 2017 Dec 12;8:913. doi: 10.3389/fphar.2017.00913. eCollection 2017.
It is known that adenosine and adenosine-5'-triphosphate (ATP) are excitatory mediators involved in carotid body (CB) hypoxic signaling. The CBs are peripheral chemoreceptors classically defined by O, CO, and pH sensors. When hypoxia activates the CB, it induces the release of neurotransmitters from chemoreceptor cells leading to an increase in the action potentials frequency at the carotid sinus nerve (CSN). This increase in the firing frequency of the CSN is integrated in the brainstem to induce cardiorespiratory compensatory responses. In the last decade several pathologies, as, hypertension, diabetes, obstructive sleep apnea and heart failure have been associated with CB overactivation. In the first section of the present manuscript we review in a concise manner fundamental aspects of purine metabolism. The second section is devoted to the role of purines on the hypoxic response of the CB, providing the state-of-the art for the presence of adenosine and ATP receptors in the CB; for the role of purines at presynaptic level in CB chemoreceptor cells, as well as, its metabolism and regulation; at postsynaptic level in the CSN activity; and on the ventilatory responses to hypoxia. Recently, we have showed that adenosine is involved in CB hypersensitization during chronic intermittent hypoxia (CIH), which mimics obstructive sleep apnea, since caffeine, a non-selective adenosine receptor antagonist that inhibits A and A adenosine receptors, decreased CSN chemosensory activity in animals subjected to CIH. Apart from this involvement of adenosine in CB sensitization in sleep apnea, it was recently found that P2X3 ATP receptor in the CB contributes to increased chemoreflex hypersensitivity and hypertension in spontaneously hypertension rats. Therefore the last section of this manuscript is devoted to review the recent findings on the role of purines in CB-mediated pathologies as hypertension, diabetes and sleep apnea emphasizing the potential clinical importance of modulating purines levels and action to treat pathologies associated with CB dysfunction.
已知腺苷和腺苷 - 5'-三磷酸(ATP)是参与颈动脉体(CB)缺氧信号传导的兴奋性介质。颈动脉体是经典地由氧、二氧化碳和pH传感器定义的外周化学感受器。当缺氧激活颈动脉体时,它会诱导化学感受器细胞释放神经递质,导致颈动脉窦神经(CSN)动作电位频率增加。CSN放电频率的这种增加在脑干中整合,以诱导心肺代偿反应。在过去十年中,几种疾病,如高血压、糖尿病、阻塞性睡眠呼吸暂停和心力衰竭,都与颈动脉体过度激活有关。在本手稿的第一部分,我们简要回顾嘌呤代谢的基本方面。第二部分致力于嘌呤在颈动脉体缺氧反应中的作用,介绍颈动脉体中腺苷和ATP受体的存在情况;嘌呤在颈动脉体化学感受器细胞突触前水平的作用,以及其代谢和调节;在突触后水平对CSN活动的作用;以及对缺氧的通气反应。最近,我们发现腺苷参与慢性间歇性缺氧(CIH,模拟阻塞性睡眠呼吸暂停)期间的颈动脉体超敏反应,因为咖啡因作为一种抑制A1和A2腺苷受体的非选择性腺苷受体拮抗剂,可降低接受CIH的动物的CSN化学感受活性。除了腺苷在睡眠呼吸暂停中颈动脉体致敏中的这种作用外,最近还发现颈动脉体中的P2X3 ATP受体促成自发性高血压大鼠化学反射超敏反应增加和高血压。因此,本手稿的最后一部分致力于回顾嘌呤在CB介导的疾病如高血压、糖尿病和睡眠呼吸暂停中的作用的最新发现,强调调节嘌呤水平和作用以治疗与CB功能障碍相关疾病的潜在临床重要性。