TY - JOUR
T1 - Different ketogenesis strategies lead to disparate seizure outcomes
AU - Dolce, Alison
AU - Santos, Polan
AU - Chen, Weiran
AU - Hoke, Ahmet
AU - Hartman, Adam L.
N1 - Funding Information:
This study was supported by K08NS070931 (ALH) and NCRR 1S10RR026630-01 (AH). For assistance with kainic acid statistical analyses (linear regression), we thank Carol B. Thompson (Johns Hopkins Bloomberg School of Public Health Biostatistics Center), supported by the National Center for Research Resources and the National Center for Advancing Translational Sciences of the National Institutes of Health grant 1 UL1TR001079 . The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of Neurological Disorders and Stroke, National Center for Research Resources, National Center for Advancing Translational Sciences, or the National Institutes of Health. This work was performed while ALH was a full-time employee of Johns Hopkins University. The funding source did not have a role in study design; in the collection, analysis and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.
Publisher Copyright:
© 2018
PY - 2018/7
Y1 - 2018/7
N2 - Background: Despite the introduction of new medicines to treat epilepsy over the last 50 years, the number of patients with poorly-controlled seizures remains unchanged. Metabolism-based therapies are an underutilized treatment option for this population. We hypothesized that two different means of systemic ketosis, the ketogenic diet and intermittent fasting, would differ in their acute seizure test profiles and mitochondrial respiration. Methods: Male NIH Swiss mice (aged 3–4 weeks) were fed for 12–13 days using one of four diet regimens: ketogenic diet (KD), control diet matched to KD for protein content and micronutrients (CD), or CD with intermittent fasting (24 h feed/24 h fast) (CD-IF), tested post-feed or post-fast. Mice were subject to the 6 Hz threshold test or, in separate cohorts, after injection of kainic acid in doses based on their weight (Cohort I) or a uniform dose regardless of weight (Cohort II). Mitochondrial respiration was tested in brain tissue isolated from similarly-fed seizure-naïve mice. Results: KD mice were protected against 6 Hz-induced seizures but had more severe seizure scores in the kainic acid test (Cohorts I & II), the opposite of CD-IF mice. No differences were noted in mitochondrial respiration between diet regimens. Interpretation: KD and CD-IF do not share identical antiseizure mechanisms. These differences were not explained by differences in mitochondrial respiration. Nevertheless, both KD and CD-IF regimens protected against different types of seizures, suggesting that mechanisms underlying CD-IF seizure protection should be explored further.
AB - Background: Despite the introduction of new medicines to treat epilepsy over the last 50 years, the number of patients with poorly-controlled seizures remains unchanged. Metabolism-based therapies are an underutilized treatment option for this population. We hypothesized that two different means of systemic ketosis, the ketogenic diet and intermittent fasting, would differ in their acute seizure test profiles and mitochondrial respiration. Methods: Male NIH Swiss mice (aged 3–4 weeks) were fed for 12–13 days using one of four diet regimens: ketogenic diet (KD), control diet matched to KD for protein content and micronutrients (CD), or CD with intermittent fasting (24 h feed/24 h fast) (CD-IF), tested post-feed or post-fast. Mice were subject to the 6 Hz threshold test or, in separate cohorts, after injection of kainic acid in doses based on their weight (Cohort I) or a uniform dose regardless of weight (Cohort II). Mitochondrial respiration was tested in brain tissue isolated from similarly-fed seizure-naïve mice. Results: KD mice were protected against 6 Hz-induced seizures but had more severe seizure scores in the kainic acid test (Cohorts I & II), the opposite of CD-IF mice. No differences were noted in mitochondrial respiration between diet regimens. Interpretation: KD and CD-IF do not share identical antiseizure mechanisms. These differences were not explained by differences in mitochondrial respiration. Nevertheless, both KD and CD-IF regimens protected against different types of seizures, suggesting that mechanisms underlying CD-IF seizure protection should be explored further.
KW - 6 Hz test
KW - Beta-hydroxybutyrate
KW - Kainic acid
KW - Mitochondria
UR - http://www.scopus.com/inward/record.url?scp=85046354475&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85046354475&partnerID=8YFLogxK
U2 - 10.1016/j.eplepsyres.2018.04.011
DO - 10.1016/j.eplepsyres.2018.04.011
M3 - Article
C2 - 29723773
AN - SCOPUS:85046354475
SN - 0920-1211
VL - 143
SP - 90
EP - 97
JO - Journal of Epilepsy
JF - Journal of Epilepsy
ER -