In rats fed a KD, Ziegler et al (2003) found an increase in antioxidant activity using a luminol oxidation assay in the hippocampus, and a four-fold increase in glutathione peroxidase activity. Consistent with these findings, Jarrett et al (2008) recently reported an up-regulation of GSH biosynthesis in adolescent rats fed a KD. Furthermore, these investigators observed improved mitochondrial antioxidant status, and proposed that these changes were responsible for preventing mitochondrial DNA from oxidant-induced damage. Collectively, these studies suggest that the KD may indeed exert neuroprotective activity.

While the effects of leptin on seizure susceptibility and its relationship to KD-induced weight loss are intriguing, there are as yet no direct data supporting leptin as an anticonvulsant mediator of the KD. Certainly, the clinical implications of the study by Xu et al. (2008) are intriguing, namely, that intranasal administration of leptin might be efficacious in aborting acute seizure activity. And if the clinical effects of the KD are due in part to increased leptin levels, then accelerated development and validation of leptin as a novel anticonvulsant medication would be warranted.
Saya tidak berpikir beberapa hal lain yang Anda bicarakan dalam acara ini karena mari kita perjelas jika Anda terjatuh dan Anda memiliki roti kecil dengan burger itu dan Anda mengambil karbohidrat, pada dasarnya Anda sekarang menggunakan diet tinggi kalori, tinggi lemak, yang merupakan kebalikan dari apa yang Anda inginkan pada steak sedikit, sedikit kesalahan untuk membuat masalah besar terjadi pada tubuh Anda. Jadi, bisakah Anda benar-benar ketat tentang rencana makan diet ketogenik ini .
Given these findings, it is not surprising that investigators have studied the effects of dietary supplementation with PUFAs alone, to determine whether these substrates can render an anticonvulsant effect. Early case reports suggested that seizures might be better controlled with this approach (Schlanger et al., 2002). However, a recent randomized trial in adult patients with epilepsy failed to demonstrate superiority of a PUFA supplement (EPA) plus DHA, 2.2 mg/day in a 3:2 ratio) over placebo (Bromfield et al., 2008). Thus, the jury is still out as to whether PUFAs alone can mirror the clinical effects of the KD.

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