2019
DOI: 10.1007/s13760-019-01240-1
|View full text |Cite
|
Sign up to set email alerts
|

Effects of anterior thalamic nuclei stimulation on gene expression in a rat model of temporal lobe epilepsy

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 7 publications
(2 citation statements)
references
References 36 publications
0
2
0
Order By: Relevance
“…Their results showed that this microRNA plays a role in the development of epilepsy by regulating the inflammation or apoptosis [15]. Consistently, the downregulation of miR-15a-5p expression levels in serum have been reported in children with TLE by [44]. They also investigated the effect of the over-expression of this microRNA on the cell viability and apoptosis of hippocampal cells and their results proved that high levels of miR-15a-5p caused the inhibition of apoptosis and enhanced the cell viability.…”
Section: Discussionmentioning
confidence: 60%
“…Their results showed that this microRNA plays a role in the development of epilepsy by regulating the inflammation or apoptosis [15]. Consistently, the downregulation of miR-15a-5p expression levels in serum have been reported in children with TLE by [44]. They also investigated the effect of the over-expression of this microRNA on the cell viability and apoptosis of hippocampal cells and their results proved that high levels of miR-15a-5p caused the inhibition of apoptosis and enhanced the cell viability.…”
Section: Discussionmentioning
confidence: 60%
“…Although high frequency stimulation of the ANT has been widely used to treat partial seizures [7] there are few studies on ANT DBSrelated mechanisms of action. The variety of possible mechanisms that culminate with seizure reduction include reduction of cell death [46], mossy fiber sprouting [47], apoptosis and inflammation [29,48], altered gene expression in calcium signaling pathways and glutamatergic synapses [49], enhancement of local nonselective norepinephrine and serotonin release [50,51], local decreased glutamate and aspartate release with concomitant increase of GABA [52], and increased levels of adenosine in the hippocampus [22,28]. In line with those mechanisms, our current results demonstrate that ANT-DBS resulted in hippocampal neuroprotection and reduced expression of ADK.…”
Section: Discussionmentioning
confidence: 99%