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Targeted gut microbiota manipulation attenuates seizures in a model of infantile spasms syndrome
Chunlong Mu, Naghmeh Nikpoor, Thomas A. Tompkins, Anamika Choudhary, Melinda Wang, Wendie N. Marks, Jong M. Rho, Morris H. Scantlebury, Jane Shearer
Chunlong Mu, Naghmeh Nikpoor, Thomas A. Tompkins, Anamika Choudhary, Melinda Wang, Wendie N. Marks, Jong M. Rho, Morris H. Scantlebury, Jane Shearer
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Research Article Metabolism

Targeted gut microbiota manipulation attenuates seizures in a model of infantile spasms syndrome

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Abstract

Infantile spasms syndrome (IS) is a devastating early-onset epileptic encephalopathy associated with poor neurodevelopmental outcomes. When first-line treatment options, including adrenocorticotropic hormone and vigabatrin, are ineffective, the ketogenic diet (KD) is often employed to control seizures. Since the therapeutic impact of the KD is influenced by the gut microbiota, we examined whether targeted microbiota manipulation, mimicking changes induced by the KD, would be valuable in mitigating seizures. Employing a rodent model of symptomatic IS, we show that both the KD and antibiotic administration reduce spasm frequency and are associated with improved developmental outcomes. Spasm reductions were accompanied by specific gut microbial alterations, including increases in Streptococcus thermophilus and Lactococcus lactis. Mimicking the fecal microbial alterations in a targeted probiotic, we administered these species in a 5:1 ratio. Targeted probiotic administration reduced seizures and improved locomotor activities in control diet–fed animals, similar to KD-fed animals, while a negative control (Ligilactobacillus salivarius) had no impact. Probiotic administration also increased antioxidant status and decreased proinflammatory cytokines. Results suggest that a targeted probiotic reduces seizure frequency, improves locomotor activity in a rodent model of IS, and provides insights into microbiota manipulation as a potential therapeutic avenue for pediatric epileptic encephalopathies.

Authors

Chunlong Mu, Naghmeh Nikpoor, Thomas A. Tompkins, Anamika Choudhary, Melinda Wang, Wendie N. Marks, Jong M. Rho, Morris H. Scantlebury, Jane Shearer

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Figure 5

Effects of targeted and negative control probiotic administration on seizures and behaviors.

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Effects of targeted and negative control probiotic administration on sei...
(A) Targeted probiotics (Pro) were administered after epilepsy induction following the timeline shown (left panel); effects of targeted probiotic treatment on seizure frequency (right). (n = 16, 14, 9, 12, and 7 for CDE, CDE + Pro, KDE, KDE + Pro, and CDE + Lsa, respectively). (B) Body weight gain (n = 10, 13, 9, 12, and 7 for CDE, CDE + Pro, KDE, KDE + Pro, and CDE + Lsa, respectively). Two-way ANOVA with repeated-measure analysis was applied to compare the effects of age or treatment on the body weight gain. (C) Blood ketone concentration (n = 18, 15, 18, 10, and 7 for CDE, CDE + Pro, KDE, KDE + Pro, and CDE + Lsa, respectively). (D) Blood glucose concentration (n = 16, 13, 12, 10, and 7 for CDE, CDE + Pro, KDE, KDE + Pro, and CDE + Lsa, respectively). (E) Surface righting time (n = 12, 14, 8, 14, and 7 for CDE, CDE + Pro, KDE, KDE + Pro, and CDE + Lsa, respectively). (F) Negative geotaxis (n = 6, 13, 6, 10, and 7 for CDE, CDE + Pro, KDE, KDE + Pro, and CDE + Lsa, respectively). (G) Open field activities (n = 10, 11, 8, 10, and 7 for CDE, CDE + Pro, KDE, KDE + Pro, and CDE + Lsa, respectively). The data were analyzed using 1-way ANOVA with Tukey’s post hoc (A and C–G). Values are mean ± SEM. *P < 0.05, **P < 0.01, ****P < 0.0001. CDE, control diet, epilepsy induction; CDE + Pro, CDE with probiotics; KDE, ketogenic diet, epilepsy induction; KDE + Pro, KDE + probiotics; Lsa, L. salivarius negative control.

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