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腺苷 A1 受体在外源性酮补充剂诱发的抗癫痫作用中的推测作用。

Putative Role of Adenosine A1 Receptors in Exogenous Ketone Supplements-Evoked Anti-Epileptic Effect.

机构信息

Department of Biology, BDTTC, ELTE Eötvös Loránd University, Károlyi Gáspár tér 4., 9700 Szombathely, Hungary.

Institute of Biology, University of Pécs, Ifjúság Str. 6, 7624 Pécs, Hungary.

出版信息

Int J Mol Sci. 2024 Sep 12;25(18):9869. doi: 10.3390/ijms25189869.

Abstract

Approximately 30% of patients with epilepsy are drug-refractory. There is an urgent need to elucidate the exact pathophysiology of different types of epilepsies and the mechanisms of action of both antiseizure medication and metabolic therapies to treat patients more effectively and safely. For example, it has been demonstrated that exogenous ketone supplement (EKS)-generated therapeutic ketosis, as a metabolic therapy, may decrease epileptic activity in both animal models and humans, but its exact mechanism of action is unknown. However, it was demonstrated that therapeutic ketosis, among others, can increase adenosine level, which may enhance activity of A1 adenosine receptors (ARs) in the brain. It has also been demonstrated previously that adenosine has anti-epileptic effect through ARs in different models of epilepsies. Thus, it is possible that (i) therapeutic ketosis generated by the administration of EKSs may exert its anti-epileptic effect through, among other mechanisms, increased adenosine level and AR activity and that (ii) the enhanced activity of ARs may be a necessary anti-epileptic mechanism evoked by EKS administration-generated ketosis. Moreover, EKSs can evoke and maintain ketosis without severe side effects. These results also suggest that the therapeutic application of EKS-generated ketosis may be a promising opportunity to treat different types of epilepsies. In this literature review, we specifically focus on the putative role of ARs in the anti-epileptic effect of EKS-induced ketosis.

摘要

大约 30%的癫痫患者对药物没有反应。迫切需要阐明不同类型癫痫的精确病理生理学以及抗癫痫药物和代谢疗法的作用机制,以便更有效地、更安全地治疗患者。例如,已经证明外源性酮补充剂 (EKS) 产生的治疗性酮症作为一种代谢疗法,可能会降低动物模型和人类的癫痫活动,但确切的作用机制尚不清楚。然而,已经证明治疗性酮症可以增加大脑中的腺苷水平,从而增强 A1 腺苷受体 (AR) 的活性。先前也已经证明,在不同类型的癫痫模型中,腺苷通过 AR 具有抗癫痫作用。因此,(i)EKS 给药产生的治疗性酮症可能通过增加腺苷水平和 AR 活性等机制发挥其抗癫痫作用,(ii)AR 活性增强可能是 EKS 给药产生的酮症诱发的必要抗癫痫机制。此外,EKS 可以引发并维持酮症而没有严重的副作用。这些结果还表明,EKS 产生的酮症的治疗应用可能是治疗不同类型癫痫的有前途的机会。在这篇文献综述中,我们特别关注 AR 在 EKS 诱导的酮症的抗癫痫作用中的假定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a29e/11432942/f9a288d6c7d6/ijms-25-09869-g001.jpg

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