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通过生酮饮食诱导的代谢途径调节来控制癫痫发作。

Control of seizures by ketogenic diet-induced modulation of metabolic pathways.

作者信息

Clanton Ryan M, Wu Guoyao, Akabani Gamal, Aramayo Rodolfo

机构信息

Department of Nuclear Engineering, Texas A&M University, College Station, TX, 77843, USA.

Systems Radiobiology Laboratory, Texas A&M Institute for Preclinical Studies, Texas A&M University, 800 Raymond Stotzer Parkway, College Station, TX, 77843, USA.

出版信息

Amino Acids. 2017 Jan;49(1):1-20. doi: 10.1007/s00726-016-2336-7. Epub 2016 Sep 28.

Abstract

Epilepsy is too complex to be considered as a disease; it is more of a syndrome, characterized by seizures, which can be caused by a diverse array of afflictions. As such, drug interventions that target a single biological pathway will only help the specific individuals where that drug's mechanism of action is relevant to their disorder. Most likely, this will not alleviate all forms of epilepsy nor the potential biological pathways causing the seizures, such as glucose/amino acid transport, mitochondrial dysfunction, or neuronal myelination. Considering our current inability to test every individual effectively for the true causes of their epilepsy and the alarming number of misdiagnoses observed, we propose the use of the ketogenic diet (KD) as an effective and efficient preliminary/long-term treatment. The KD mimics fasting by altering substrate metabolism from carbohydrates to fatty acids and ketone bodies (KBs). Here, we underscore the need to understand the underlying cellular mechanisms governing the KD's modulation of various forms of epilepsy and how a diverse array of metabolites including soluble fibers, specific fatty acids, and functional amino acids (e.g., leucine, D-serine, glycine, arginine metabolites, and N-acetyl-cysteine) may potentially enhance the KD's ability to treat and reverse, not mask, these neurological disorders that lead to epilepsy.

摘要

癫痫过于复杂,不能被视为一种单一疾病;它更像是一种综合征,其特征为癫痫发作,可由各种各样的疾病引发。因此,针对单一生物途径的药物干预仅对那些药物作用机制与自身病症相关的特定个体有帮助。很可能,这无法缓解所有形式的癫痫,也无法消除引发癫痫发作的潜在生物途径,比如葡萄糖/氨基酸转运、线粒体功能障碍或神经元髓鞘形成。鉴于我们目前无法有效地针对每个个体检测其癫痫的真正病因,且误诊数量惊人,我们提议将生酮饮食(KD)作为一种有效且高效的初步/长期治疗方法。生酮饮食通过将底物代谢从碳水化合物转变为脂肪酸和酮体(KBs)来模拟禁食状态。在此,我们强调有必要了解生酮饮食调节各种癫痫形式的潜在细胞机制,以及包括可溶性纤维、特定脂肪酸和功能性氨基酸(如亮氨酸、D-丝氨酸、甘氨酸、精氨酸代谢物和N-乙酰半胱氨酸)在内的各种代谢物如何可能增强生酮饮食治疗和逆转而非掩盖这些导致癫痫的神经系统疾病的能力。

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