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Martina’s newest cookbook is not just a comprehensive guide to eating for the ketogenic diet, it is also gorgeous eye candy! It is sheer pleasure just to browse through her gorgeous photographs, wile you drool over the delicious recipes. I love Martina’s recipes especially because they are made with wholesome, real food ingredients, and she is very knowledgeable on how to best source ingredients so they are both tasty and health building. Every recipe is explained clearly and well organized, so you can always get great results when making them at home. If you are following a keto or low-carb lifestyle this book is a must have!
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Martina's popular KetoDiet blog has been a wonderful resource for those following a healthy paleo/primal low carb diet. Not only does she provide a wealth of information for successfully implementing a ketogenic diet, but also shares many of her own delicious low carb recipes. Her recipes have become staples for those seeking low carb alternatives for their favorite foods. This cookbook with 150 new keto diet recipes is a must for any low carb cook's collection.
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Martina is an incredibly talented and innovative food blogger whose low-carb creations taste as spectacular as they look. She's also dedicated to providing accurate, reliable information to people interested in following a healthy, carbohydrate-restricted lifestyle. I'm eagerly awaiting the publication of this book and know that her many fans feel the same way.
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While the relationships between seizure activity, oxidative stress and neuronal injury have yet to be clarified, previous studies have indicated that defects in antioxidant systems may contribute to seizure genesis and epileptogenesis (Cock, 2002; Patel, 2004; Liang & Patel, 2006; Shin et al, 2008). Earlier, the effects of a KD on mitochondrial ROS generation were discussed. Are there other mechanisms through which oxidative stress can be attenuated in epileptic brain?
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In support of this, Yudkoff and colleagues have published widely on the impact of ketone bodies on brain glutamate and GABA metabolism (Yudkoff et al., 2007). In one study, the addition of either acetoacetate or β-hydroxybutyrate was associated with diminished consumption of glutamate via transamination to aspartate and increased formation of labeled GABA (Daikhin et al., 1998). Ketone bodies had earlier been shown by the same group to enhance synthesis of GABA in synaptosomes prepared from rodent forebrain (Erecinska et al, 1996).
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The relevance of leptin to seizure susceptibility was recently highlighted by Erbayat-Altay and colleagues (2008) who demonstrated a significantly decreased threshold in leptin-deficient ob/ob mice to pentylenetetrazol-induced seizures. Indeed, leptin itself inhibits seizures induced by 4-aminopyridine and pentyelenetrazole-induced, possibly through blockade of AMPA receptor-mediated synaptic transmission (Xu et al., 2008). If the limiting of AMPA receptor-mediated transmission is a critical factor, it should be recalled this can also be accomplished by topiramate. With respect to the KD, the leptin signaling system is believed to contribute to slow weight gain associated with chronic treatment in both rodents and humans (Thio et al., 2006). KD-fed juvenile rodents had higher serum leptin levels and lower insulin levels than control rats fed a standard diet.
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The scientific rationale for elucidating mechanisms of disease pathogenesis or of therapeutic interventions has been traditionally based upon the lofty goal of discovering novel treatments, ones that would be more efficacious than existing options and also be devoid of side-effects altogether. Moreover, in epilepsy research, disease prevention or modification has become the “holy grail”, such that we are no longer complacent with symptomatic treatment and increasing attention is being given to understanding the processes of anti-epileptogenesis itself. Researchers in the field of the ketogenic diet (KD) have also embraced these tenets and recently embarked on that all-too-familiar Quixotic journey, with the ultimate aim of reducing the “difficult” KD regimen to a simple pill. If achieved, this result would represent an ironic recapitulation of the early history of the KD in the United States. Although the KD experienced an initial surge of interest following its introduction in the early 1920’s, it was relegated to near obscurity by the emergence of a familiar drug known as phenytoin. Henceforth, until the mid 1990’s, clinicians – for obvious practical reasons – found it simpler to prescribe a pill rather than an exacting diet.