Laboratório de Neurobiologia e Metabolismo (NeuroMet), Departamento de Fisiologia, Instituto de Ciências Básicas da Saúde (ICBS), Universidade Federal do Rio Grande do Sul (UFRGS), Rua Ramiro Barcelos, 2600, lab. 660, Porto Alegre, Brazil; Programa de Pós-Graduação em Ciências Biológicas: Fisiologia, Instituto de Ciências Básicas da Saúde (ICBS), Universidade Federal do Rio Grande do Sul (UFRGS), Rua Ramiro Barcelos, 2600, Porto Alegre, Brazil; Centro de Pesquisa Experimental, Hospital de Clínicas de Porto Alegre (HCPA), Rua Ramiro Barcelos, 2350, Porto Alegre, Brazil.
Laboratório de Endocrinologia Experimental (LABENEX), Departamento de Fisiologia, Instituto de Ciências Básicas da Saúde (ICBS), Universidade Federal do Rio Grande do Sul (UFRGS), Rua Ramiro Barcelos, 2600, lab. 660, Porto Alegre, Brazil; Programa de Pós-Graduação em Ciências Biológicas: Fisiologia, Instituto de Ciências Básicas da Saúde (ICBS), Universidade Federal do Rio Grande do Sul (UFRGS), Rua Ramiro Barcelos, 2600, Porto Alegre, Brazil.
Neuroscience. 2023 Aug 21;526:144-163. doi: 10.1016/j.neuroscience.2023.06.022. Epub 2023 Jun 29.
GPR81 is a G-protein coupled receptor (GPCR) discovered in 2001, but deorphanized only 7 years later, when its affinity for lactate as an endogenous ligand was demonstrated. More recently, GPR81 expression and distribution in the brain were also confirmed and the function of lactate as a volume transmitter has been suggested since then. These findings shed light on a new function of lactate acting as a signaling molecule in the central nervous system, in addition to its well-known role as a metabolic fuel for neurons. GPR81 seems to act as a metabolic sensor, coupling energy metabolism, synaptic activity, and blood flow. Activation of this receptor leads to G-mediated downregulation of adenylyl cyclase and subsequent reduction in cAMP levels, regulating several downstream pathways. Recent studies have also suggested the potential role of lactate as a neuroprotective agent, mainly under brain ischemic conditions. This effect is usually attributed to the metabolic role of lactate, but the underlying mechanisms need further investigation and could be related to lactate signaling via GPR81. The activation of GPR81 showed promising results for neuroprotection: it modulates many processes involved in the pathophysiology of ischemia. In this review, we summarize the history of GPR81, starting with its deorphanization; then, we discuss GPR81 expression and distribution, signaling transduction cascades, and neuroprotective roles. Lastly, we propose GPR81 as a potential target for the treatment of cerebral ischemia.
GPR81 是一种于 2001 年发现的 G 蛋白偶联受体(GPCR),但直到 7 年后才被确定为孤儿受体,当时证明了其对乳酸作为内源性配体的亲和力。最近,GPR81 在大脑中的表达和分布也得到了证实,此后,乳酸作为容积递质的功能也被提出。这些发现揭示了乳酸作为中枢神经系统信号分子的新功能,除了作为神经元代谢燃料的已知作用。GPR81 似乎作为代谢传感器起作用,将能量代谢、突触活动和血流联系起来。该受体的激活导致 G 介导的腺苷酸环化酶下调和随后 cAMP 水平降低,调节几种下游途径。最近的研究还表明,乳酸作为神经保护剂的潜在作用,主要在脑缺血条件下。这种作用通常归因于乳酸的代谢作用,但潜在的机制需要进一步研究,可能与通过 GPR81 的乳酸信号有关。GPR81 的激活显示出对神经保护的有希望的结果:它调节了缺血病理生理学涉及的许多过程。在这篇综述中,我们从 GPR81 的去孤儿化开始,总结了 GPR81 的历史;然后,我们讨论了 GPR81 的表达和分布、信号转导级联和神经保护作用。最后,我们提出 GPR81 作为治疗脑缺血的潜在靶点。