Ruskin David N, Kawamura Masahito, Masino Susan A
Department of Psychology, Neuroscience Program, Trinity College, Hartford, Connecticut, USA.
Department of Pharmacology, Jikei University School of Medicine, Minato-ku, Tokyo, Japan.
J Caffeine Adenosine Res. 2020 Sep 1;10(3):104-109. doi: 10.1089/caff.2020.0011. Epub 2020 Sep 16.
It is well known that the neuromodulator adenosine, acting through the adenosine A receptor subtype, can limit or stop seizures. In 2008, adenosine was proposed as a key component of the anticonvulsant mechanism of the ketogenic diet (KD), a very low carbohydrate diet that can be highly effective in drug-refractory epilepsy. In this study, we review the accumulated data on the intersection among adenosine, ketosis, and anticonvulsant/antiepileptogenic effects. In several rodent models of epilepsy and seizures, antiseizure effects of ketogenic treatments (the KD itself, exogenous ketone bodies, medium-chain triglycerides or fatty acids) are reversed by administration of an adenosine A receptor antagonist. In addition, KD treatment elevates extracellular adenosine and tissue adenosine content in brain. Efforts to maintain or mimic a ketogenic milieu in brain slices reveal a state of reduced excitability produced by pre- and postsynaptic adenosine A receptor-based effects. Long-lasting seizure reduction may be due to adenosine-based epigenetic effects. In conclusion, there is accumulating evidence for an adenosinergic anticonvulsant action in the ketogenic state. In some cases, the main trigger is mildly but consistently lowered glucose in the brain. More research is needed to investigate the importance of adenosine in the antiepileptogenic and neuroprotective effects of these treatments. Future research may begin to investigate alternative adenosine-promoting strategies to enhance the KD or to find use as treatments themselves.
众所周知,神经调质腺苷通过腺苷A受体亚型发挥作用,可限制或阻止癫痫发作。2008年,腺苷被认为是生酮饮食(KD)抗惊厥机制的关键组成部分,生酮饮食是一种碳水化合物含量极低的饮食,对药物难治性癫痫可能非常有效。在本研究中,我们回顾了关于腺苷、酮症和抗惊厥/抗癫痫发生作用之间交集的累积数据。在几种癫痫和癫痫发作的啮齿动物模型中,生酮治疗(KD本身、外源性酮体、中链甘油三酯或脂肪酸)的抗癫痫作用可通过给予腺苷A受体拮抗剂而逆转。此外,KD治疗可提高大脑中的细胞外腺苷和组织腺苷含量。在脑片中维持或模拟生酮环境的研究表明,由基于突触前和突触后腺苷A受体的作用产生了兴奋性降低的状态。长期癫痫发作减少可能归因于基于腺苷的表观遗传效应。总之,越来越多的证据表明生酮状态下存在腺苷能抗惊厥作用。在某些情况下,主要触发因素是大脑中葡萄糖轻度但持续降低。需要更多研究来调查腺苷在这些治疗的抗癫痫发生和神经保护作用中的重要性。未来的研究可能开始探索促进腺苷生成的替代策略,以增强KD或本身用作治疗方法。