Department of Psychiatry, University of Texas Southwestern Medical Center and Dallas VA Medical Center, Dallas, Texas 75390, USA.
J Clin Invest. 2011 Jul;121(7):2548-50. doi: 10.1172/JCI58391. Epub 2011 Jun 23.
Many individuals with epilepsy benefit from consuming a ketogenic diet, which is similar to the more commonly known Atkins diet. The underlying molecular reason for this has not been determined. However, in this issue of the JCI, Masino et al. have elucidated the mechanism responsible for the antiepileptic effects of the ketogenic diet in mice. The diet is shown to decrease expression of the enzyme adenosine kinase (Adk), which is responsible for clearing the endogenous antiepileptic agent adenosine (Ado) from the extracellular CNS space. Decreased expression of Adk results in increased extracellular Ado, activation of inhibitory Ado A1 receptors, and decreased seizure generation, the desired therapeutic effect. The authors' work serves to emphasize the importance of controlling Adk expression, not only as the mechanism of action of the ketogenic diet, but also as a potential target of future therapies.
许多癫痫患者从生酮饮食中受益,这种饮食类似于更为人熟知的阿特金斯饮食。其潜在的分子机制尚未确定。然而,在本期 JCI 中,Masino 等人阐明了生酮饮食在小鼠中抗癫痫作用的机制。研究表明,该饮食可降低腺苷激酶(Adk)的表达,Adk 负责清除细胞外 CNS 空间中的内源性抗癫痫药物腺苷(Ado)。Adk 表达降低导致细胞外 Ado 增加,抑制性 Ado A1 受体激活,以及癫痫发作减少,从而达到理想的治疗效果。作者的工作强调了控制 Adk 表达的重要性,不仅作为生酮饮食的作用机制,而且作为未来治疗的潜在靶点。