Ketogenic Diets Alter the Gut Microbiome, Resulting in Decreased Susceptibility to and Cognitive Impairment in Rats with Pilocarpine-Induced Status Epilepticus
A ketogenic diet (KD) is a high-fat, low-carbohydrate, and low-protein diet that exerts antiepileptic effects by attenuating spontaneous recurrent seizures, ameliorating learning and memory impairments, and modulating the gut microbiota composition. However, the role of the gut microbiome in the ant...
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creator | Li, Bianli Ma, Yue Wang, Xuhui Zhao, Di Wang, Ziqin Wang, Guoyang Li, Chunyi Yang, Lin Ji, Hui Liu, Kunmei Chen, Qiuyuan Yang, Yong Ma, Wenqian Du, Jianbin Ma, Lei Zhang, Lianxiang Qiang, Yuanyuan |
description | A ketogenic diet (KD) is a high-fat, low-carbohydrate, and low-protein diet that exerts antiepileptic effects by attenuating spontaneous recurrent seizures, ameliorating learning and memory impairments, and modulating the gut microbiota composition. However, the role of the gut microbiome in the antiepileptic effects of a KD on temporal lobe epilepsy (TLE) induced by lithium-pilocarpine in adult rats is still unknown. Our study provides evidence demonstrating that a KD effectively mitigates seizure behavior and reduces acute-phase epileptic brain activity and that KD treatment alleviates hippocampal neuronal damage and improves cognitive impairment induced by TLE. We also observed that the beneficial effects of a KD are compromised when the gut microbiota is disrupted through antibiotic administration. Analysis of gut microbiota components via 16S rRNA gene sequencing in fecal samples collected from TLE rats fed either a KD or a normal diet. The Chao1 and ACE indices showed decreased species variety in KD-fed rats compared to TLE rats fed a normal diet. A KD increased the levels of
Actinobacteriota, Verrucomicrobiota
and
Proteobacteria
and decreased the level of
Bacteroidetes
. Interestingly, the abundances of
Actinobacteriota
and
Verrucomicrobiota
were positively correlated with learning and memory ability, and the abundance of
Proteobacteria
was positively correlated with seizure susceptibility. In conclusion, our study revealed the significant antiepileptic and neuroprotective effects of a KD on pilocarpine-induced epilepsy in rats, primarily mediated through the modulation of the gut microbiota. However, whether the gut microbiota mediates the antiseizure effects of a KD still needs to be better elucidated. |
doi_str_mv | 10.1007/s11064-024-04168-y |
format | Article |
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Actinobacteriota, Verrucomicrobiota
and
Proteobacteria
and decreased the level of
Bacteroidetes
. Interestingly, the abundances of
Actinobacteriota
and
Verrucomicrobiota
were positively correlated with learning and memory ability, and the abundance of
Proteobacteria
was positively correlated with seizure susceptibility. In conclusion, our study revealed the significant antiepileptic and neuroprotective effects of a KD on pilocarpine-induced epilepsy in rats, primarily mediated through the modulation of the gut microbiota. However, whether the gut microbiota mediates the antiseizure effects of a KD still needs to be better elucidated.</description><identifier>ISSN: 0364-3190</identifier><identifier>ISSN: 1573-6903</identifier><identifier>EISSN: 1573-6903</identifier><identifier>DOI: 10.1007/s11064-024-04168-y</identifier><identifier>PMID: 38935224</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Abundance ; Animals ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Brain damage ; Brain injury ; Carbohydrates ; Cell Biology ; Cognitive ability ; Cognitive Dysfunction - metabolism ; Convulsions & seizures ; Diet ; Diet, Ketogenic ; Epilepsy ; Epilepsy, Temporal Lobe - chemically induced ; Epilepsy, Temporal Lobe - metabolism ; Feces ; Gastrointestinal Microbiome - drug effects ; Gene sequencing ; High carbohydrate diet ; High fat diet ; Hippocampus ; Hippocampus - drug effects ; Hippocampus - metabolism ; Impairment ; Intestinal microflora ; Ketogenesis ; Learning ; Lithium ; Low carbohydrate diet ; Low fat diet ; Low protein diet ; Male ; Memory ; Microbiomes ; Microbiota ; Microorganisms ; Neurochemistry ; Neurology ; Neuromodulation ; Neuroprotection ; Neurosciences ; Nutrient deficiency ; Original Paper ; Pilocarpine ; Protein composition ; Proteobacteria ; Rats ; Rats, Sprague-Dawley ; rRNA 16S ; Seizures ; Status Epilepticus - chemically induced ; Status Epilepticus - diet therapy ; Temporal lobe</subject><ispartof>Neurochemical research, 2024-10, Vol.49 (10), p.2726-2742</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c256t-e0bdf0431cae4ffd19190aecf8506103094236e247555eb733dda79812e9df2c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11064-024-04168-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11064-024-04168-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38935224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Bianli</creatorcontrib><creatorcontrib>Ma, Yue</creatorcontrib><creatorcontrib>Wang, Xuhui</creatorcontrib><creatorcontrib>Zhao, Di</creatorcontrib><creatorcontrib>Wang, Ziqin</creatorcontrib><creatorcontrib>Wang, Guoyang</creatorcontrib><creatorcontrib>Li, Chunyi</creatorcontrib><creatorcontrib>Yang, Lin</creatorcontrib><creatorcontrib>Ji, Hui</creatorcontrib><creatorcontrib>Liu, Kunmei</creatorcontrib><creatorcontrib>Chen, Qiuyuan</creatorcontrib><creatorcontrib>Yang, Yong</creatorcontrib><creatorcontrib>Ma, Wenqian</creatorcontrib><creatorcontrib>Du, Jianbin</creatorcontrib><creatorcontrib>Ma, Lei</creatorcontrib><creatorcontrib>Zhang, Lianxiang</creatorcontrib><creatorcontrib>Qiang, Yuanyuan</creatorcontrib><title>Ketogenic Diets Alter the Gut Microbiome, Resulting in Decreased Susceptibility to and Cognitive Impairment in Rats with Pilocarpine-Induced Status Epilepticus</title><title>Neurochemical research</title><addtitle>Neurochem Res</addtitle><addtitle>Neurochem Res</addtitle><description>A ketogenic diet (KD) is a high-fat, low-carbohydrate, and low-protein diet that exerts antiepileptic effects by attenuating spontaneous recurrent seizures, ameliorating learning and memory impairments, and modulating the gut microbiota composition. However, the role of the gut microbiome in the antiepileptic effects of a KD on temporal lobe epilepsy (TLE) induced by lithium-pilocarpine in adult rats is still unknown. Our study provides evidence demonstrating that a KD effectively mitigates seizure behavior and reduces acute-phase epileptic brain activity and that KD treatment alleviates hippocampal neuronal damage and improves cognitive impairment induced by TLE. We also observed that the beneficial effects of a KD are compromised when the gut microbiota is disrupted through antibiotic administration. Analysis of gut microbiota components via 16S rRNA gene sequencing in fecal samples collected from TLE rats fed either a KD or a normal diet. The Chao1 and ACE indices showed decreased species variety in KD-fed rats compared to TLE rats fed a normal diet. A KD increased the levels of
Actinobacteriota, Verrucomicrobiota
and
Proteobacteria
and decreased the level of
Bacteroidetes
. Interestingly, the abundances of
Actinobacteriota
and
Verrucomicrobiota
were positively correlated with learning and memory ability, and the abundance of
Proteobacteria
was positively correlated with seizure susceptibility. In conclusion, our study revealed the significant antiepileptic and neuroprotective effects of a KD on pilocarpine-induced epilepsy in rats, primarily mediated through the modulation of the gut microbiota. However, whether the gut microbiota mediates the antiseizure effects of a KD still needs to be better elucidated.</description><subject>Abundance</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain damage</subject><subject>Brain injury</subject><subject>Carbohydrates</subject><subject>Cell Biology</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - metabolism</subject><subject>Convulsions & seizures</subject><subject>Diet</subject><subject>Diet, Ketogenic</subject><subject>Epilepsy</subject><subject>Epilepsy, Temporal Lobe - chemically induced</subject><subject>Epilepsy, Temporal Lobe - metabolism</subject><subject>Feces</subject><subject>Gastrointestinal Microbiome - drug effects</subject><subject>Gene sequencing</subject><subject>High carbohydrate diet</subject><subject>High fat diet</subject><subject>Hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Impairment</subject><subject>Intestinal microflora</subject><subject>Ketogenesis</subject><subject>Learning</subject><subject>Lithium</subject><subject>Low carbohydrate diet</subject><subject>Low fat diet</subject><subject>Low protein diet</subject><subject>Male</subject><subject>Memory</subject><subject>Microbiomes</subject><subject>Microbiota</subject><subject>Microorganisms</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>Neuromodulation</subject><subject>Neuroprotection</subject><subject>Neurosciences</subject><subject>Nutrient deficiency</subject><subject>Original Paper</subject><subject>Pilocarpine</subject><subject>Protein composition</subject><subject>Proteobacteria</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>rRNA 16S</subject><subject>Seizures</subject><subject>Status Epilepticus - chemically induced</subject><subject>Status Epilepticus - diet therapy</subject><subject>Temporal lobe</subject><issn>0364-3190</issn><issn>1573-6903</issn><issn>1573-6903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhi0EokvhD3BAlrhwIHRsx_k4VttSVrQCFThbjjPZukqc4A_Q_hr-Kt5uCxIHDqM5zPO-4_FLyEsG7xhAfRIYg6osgOcqWdUUu0dkxWQtiqoF8ZisQOSxYC0ckWch3AJkGWdPyZFoWiE5L1fk10eM8xadNfTMYgz0dIzoabxBepEivbLGz52dJ3xLrzGkMVq3pdbRMzQedcCefknB4BJtZ0cbdzTOVLueruets9H-QLqZFm39hC7uddc67_hp4w39bMfZaL9Yh8XG9cnsvaKOKdDzxY57S5PCc_Jk0GPAF_f9mHx7f_51_aG4_HSxWZ9eFobLKhYIXT9AKZjRWA5Dz9p8tUYzNBIqBgLakosKeVlLKbGrheh7XbcN49j2AzfimLw5-C5-_p4wRDXZfNc4aodzCkpAzRsmZQ0Zff0Pejsn7_LrMtW2HHjViEzxA5U_MASPg1q8nbTfKQZqH586xKdyfOouPrXLolf31qmbsP8jecgrA-IAhDxyW_R_d__H9jeUb6gS</recordid><startdate>20241001</startdate><enddate>20241001</enddate><creator>Li, Bianli</creator><creator>Ma, Yue</creator><creator>Wang, Xuhui</creator><creator>Zhao, Di</creator><creator>Wang, Ziqin</creator><creator>Wang, Guoyang</creator><creator>Li, Chunyi</creator><creator>Yang, Lin</creator><creator>Ji, Hui</creator><creator>Liu, Kunmei</creator><creator>Chen, Qiuyuan</creator><creator>Yang, Yong</creator><creator>Ma, Wenqian</creator><creator>Du, Jianbin</creator><creator>Ma, Lei</creator><creator>Zhang, Lianxiang</creator><creator>Qiang, Yuanyuan</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20241001</creationdate><title>Ketogenic Diets Alter the Gut Microbiome, Resulting in Decreased Susceptibility to and Cognitive Impairment in Rats with Pilocarpine-Induced Status Epilepticus</title><author>Li, Bianli ; Ma, Yue ; Wang, Xuhui ; Zhao, Di ; Wang, Ziqin ; Wang, Guoyang ; Li, Chunyi ; Yang, Lin ; Ji, Hui ; Liu, Kunmei ; Chen, Qiuyuan ; Yang, Yong ; Ma, Wenqian ; Du, Jianbin ; Ma, Lei ; Zhang, Lianxiang ; Qiang, Yuanyuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c256t-e0bdf0431cae4ffd19190aecf8506103094236e247555eb733dda79812e9df2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Abundance</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain damage</topic><topic>Brain injury</topic><topic>Carbohydrates</topic><topic>Cell Biology</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction - metabolism</topic><topic>Convulsions & seizures</topic><topic>Diet</topic><topic>Diet, Ketogenic</topic><topic>Epilepsy</topic><topic>Epilepsy, Temporal Lobe - chemically induced</topic><topic>Epilepsy, Temporal Lobe - metabolism</topic><topic>Feces</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>Gene sequencing</topic><topic>High carbohydrate diet</topic><topic>High fat diet</topic><topic>Hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Impairment</topic><topic>Intestinal microflora</topic><topic>Ketogenesis</topic><topic>Learning</topic><topic>Lithium</topic><topic>Low carbohydrate diet</topic><topic>Low fat diet</topic><topic>Low protein diet</topic><topic>Male</topic><topic>Memory</topic><topic>Microbiomes</topic><topic>Microbiota</topic><topic>Microorganisms</topic><topic>Neurochemistry</topic><topic>Neurology</topic><topic>Neuromodulation</topic><topic>Neuroprotection</topic><topic>Neurosciences</topic><topic>Nutrient deficiency</topic><topic>Original Paper</topic><topic>Pilocarpine</topic><topic>Protein composition</topic><topic>Proteobacteria</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>rRNA 16S</topic><topic>Seizures</topic><topic>Status Epilepticus - chemically induced</topic><topic>Status Epilepticus - diet therapy</topic><topic>Temporal lobe</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Bianli</creatorcontrib><creatorcontrib>Ma, Yue</creatorcontrib><creatorcontrib>Wang, Xuhui</creatorcontrib><creatorcontrib>Zhao, Di</creatorcontrib><creatorcontrib>Wang, Ziqin</creatorcontrib><creatorcontrib>Wang, Guoyang</creatorcontrib><creatorcontrib>Li, Chunyi</creatorcontrib><creatorcontrib>Yang, Lin</creatorcontrib><creatorcontrib>Ji, Hui</creatorcontrib><creatorcontrib>Liu, Kunmei</creatorcontrib><creatorcontrib>Chen, Qiuyuan</creatorcontrib><creatorcontrib>Yang, Yong</creatorcontrib><creatorcontrib>Ma, Wenqian</creatorcontrib><creatorcontrib>Du, Jianbin</creatorcontrib><creatorcontrib>Ma, Lei</creatorcontrib><creatorcontrib>Zhang, Lianxiang</creatorcontrib><creatorcontrib>Qiang, Yuanyuan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurochemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Bianli</au><au>Ma, Yue</au><au>Wang, Xuhui</au><au>Zhao, Di</au><au>Wang, Ziqin</au><au>Wang, Guoyang</au><au>Li, Chunyi</au><au>Yang, Lin</au><au>Ji, Hui</au><au>Liu, Kunmei</au><au>Chen, Qiuyuan</au><au>Yang, Yong</au><au>Ma, Wenqian</au><au>Du, Jianbin</au><au>Ma, Lei</au><au>Zhang, Lianxiang</au><au>Qiang, Yuanyuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ketogenic Diets Alter the Gut Microbiome, Resulting in Decreased Susceptibility to and Cognitive Impairment in Rats with Pilocarpine-Induced Status Epilepticus</atitle><jtitle>Neurochemical research</jtitle><stitle>Neurochem Res</stitle><addtitle>Neurochem Res</addtitle><date>2024-10-01</date><risdate>2024</risdate><volume>49</volume><issue>10</issue><spage>2726</spage><epage>2742</epage><pages>2726-2742</pages><issn>0364-3190</issn><issn>1573-6903</issn><eissn>1573-6903</eissn><abstract>A ketogenic diet (KD) is a high-fat, low-carbohydrate, and low-protein diet that exerts antiepileptic effects by attenuating spontaneous recurrent seizures, ameliorating learning and memory impairments, and modulating the gut microbiota composition. However, the role of the gut microbiome in the antiepileptic effects of a KD on temporal lobe epilepsy (TLE) induced by lithium-pilocarpine in adult rats is still unknown. Our study provides evidence demonstrating that a KD effectively mitigates seizure behavior and reduces acute-phase epileptic brain activity and that KD treatment alleviates hippocampal neuronal damage and improves cognitive impairment induced by TLE. We also observed that the beneficial effects of a KD are compromised when the gut microbiota is disrupted through antibiotic administration. Analysis of gut microbiota components via 16S rRNA gene sequencing in fecal samples collected from TLE rats fed either a KD or a normal diet. The Chao1 and ACE indices showed decreased species variety in KD-fed rats compared to TLE rats fed a normal diet. A KD increased the levels of
Actinobacteriota, Verrucomicrobiota
and
Proteobacteria
and decreased the level of
Bacteroidetes
. Interestingly, the abundances of
Actinobacteriota
and
Verrucomicrobiota
were positively correlated with learning and memory ability, and the abundance of
Proteobacteria
was positively correlated with seizure susceptibility. In conclusion, our study revealed the significant antiepileptic and neuroprotective effects of a KD on pilocarpine-induced epilepsy in rats, primarily mediated through the modulation of the gut microbiota. However, whether the gut microbiota mediates the antiseizure effects of a KD still needs to be better elucidated.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>38935224</pmid><doi>10.1007/s11064-024-04168-y</doi><tpages>17</tpages></addata></record> |
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subjects | Abundance Animals Biochemistry Biomedical and Life Sciences Biomedicine Brain damage Brain injury Carbohydrates Cell Biology Cognitive ability Cognitive Dysfunction - metabolism Convulsions & seizures Diet Diet, Ketogenic Epilepsy Epilepsy, Temporal Lobe - chemically induced Epilepsy, Temporal Lobe - metabolism Feces Gastrointestinal Microbiome - drug effects Gene sequencing High carbohydrate diet High fat diet Hippocampus Hippocampus - drug effects Hippocampus - metabolism Impairment Intestinal microflora Ketogenesis Learning Lithium Low carbohydrate diet Low fat diet Low protein diet Male Memory Microbiomes Microbiota Microorganisms Neurochemistry Neurology Neuromodulation Neuroprotection Neurosciences Nutrient deficiency Original Paper Pilocarpine Protein composition Proteobacteria Rats Rats, Sprague-Dawley rRNA 16S Seizures Status Epilepticus - chemically induced Status Epilepticus - diet therapy Temporal lobe |
title | Ketogenic Diets Alter the Gut Microbiome, Resulting in Decreased Susceptibility to and Cognitive Impairment in Rats with Pilocarpine-Induced Status Epilepticus |
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