Back to Search Start Over

Identification of an epilepsy-linked gut microbiota signature in a pediatric rat model of acquired epilepsy

Authors :
Riva, A
Sahin, E
Volpedo, G
Petretto, A
Lavarello, C
Di Sapia, R
Barbarossa, D
Zaniani, N
Craparotta, I
Barbera, M
Sezerman, U
Vezzani, A
Striano, P
Ravizza, T
Riva A.
Sahin E.
Volpedo G.
Petretto A.
Lavarello C.
Di Sapia R.
Barbarossa D.
Zaniani N. R.
Craparotta I.
Barbera M. C.
Sezerman U.
Vezzani A.
Striano P.
Ravizza T.
Riva, A
Sahin, E
Volpedo, G
Petretto, A
Lavarello, C
Di Sapia, R
Barbarossa, D
Zaniani, N
Craparotta, I
Barbera, M
Sezerman, U
Vezzani, A
Striano, P
Ravizza, T
Riva A.
Sahin E.
Volpedo G.
Petretto A.
Lavarello C.
Di Sapia R.
Barbarossa D.
Zaniani N. R.
Craparotta I.
Barbera M. C.
Sezerman U.
Vezzani A.
Striano P.
Ravizza T.
Publication Year :
2024

Abstract

A dysfunctional gut microbiota-brain axis is emerging as a potential pathogenic mechanism in epilepsy, particularly in pediatric forms of epilepsy. To add new insights into gut -related changes in acquired epilepsy that develops early in life, we used a multi-omics approach in a rat model with a 56% incidence of epilepsy. The presence of spontaneous seizures was assessed in adult rats ( n = 46) 5 months after status epilepticus induced by intra-amygdala kainate at postnatal day 13, by 2 weeks (24/7) ECoG monitoring. Twenty-six rats developed epilepsy (Epi) while the remaining 20 rats (No-Epi) did not show spontaneous seizures. At the end of ECoG monitoring, all rats and their sham controls ( n = 20) were sacrificed for quantitative histopathological and immunohistochemical analyses of the gut structure, glia and macrophages, as well as RTqPCR analysis of inflammation/oxidative stress markers. By comparing Epi, No-Epi rats, and sham controls, we found structural, cellular, and molecular alterations reflecting a dysfunctional gut, which were specifically associated with epilepsy. In particular, the villus height -tocrypt depth ratio and number of Goblet cells were reduced in the duodenum of Epi rats vs both No-Epi rats and sham controls ( p < 0.01). Villus height and crypt depth in the duodenum and jejunum (p < 0.01) were increased in No-Epi vs both Epi and sham controls. We also detected enhanced Iba1-positive macrophages, together with increased IL1b and NFE2L2 transcripts and TNF protein, in the small intestine of Epi vs both No-Epi and sham control rats ( p < 0.01), denoting the presence of inflammation and oxidative stress. Astroglial GFAPimmunostaining was similar in all experimental groups. Metagenomic analysis in the feces collected 5 months after status epilepticus showed that the ratio of two dominant phyla ( Bacteroidota-to-Firmicutes ) was similarly increased in Epi and No-Epi rats vs sham control rats. Notably, the relative abundance of families

Details

Database :
OAIster
Notes :
STAMPA, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1456740718
Document Type :
Electronic Resource