Seizures
|
0.360 |
AlteredExpression
|
phenotype |
BEFREE |
In sharp contrast, layer 5 PNs and somatostatin-expressing INs were gradually and asynchronously recruited into the ictal activity during the course of seizures.
|
31657482 |
2020 |
Seizures
|
0.360 |
AlteredExpression
|
phenotype |
BEFREE |
We have shown that sustained vector-mediated hippocampal somatostatin (SST) expression can both block epileptogenesis and reverse seizure susceptibility in fully kindled rats.
|
30735971 |
2019 |
Seizures
|
0.360 |
Biomarker
|
phenotype |
BEFREE |
Regional and temporal regulation and role of somatostatin receptor subtypes in the mouse brain following systemic kainate-induced acute seizures.
|
30685491 |
2019 |
Seizures
|
0.360 |
AlteredExpression
|
phenotype |
BEFREE |
Somatostatin is expressed widely in the hippocampus and notably in hilar GABAergic neurons that are vulnerable to seizure neuropathology in chronic temporal lobe epilepsy.
|
28167431 |
2017 |
Seizures
|
0.360 |
Biomarker
|
phenotype |
BEFREE |
We report a girl with congenital hyperinsulinism due to novel homozygous mutation (c.2041-25 G>A; aberrant splicing mutation) in the ABCC8 gene encoding SUR1 and during somatostatin analog (octreotide) discontinuation developed by nonhypoglycemic seizures.
|
22876555 |
2012 |
Seizures
|
0.360 |
Therapeutic
|
phenotype |
CTD_human |
SRA880 did not affect seizure severity and did not reverse the anticonvulsive action of SRIF-14 (1 microM) against pilocarpine-induced seizures, suggesting that hippocampal sst(1) receptors are not involved in the anticonvulsive effects of SRIF-14.
|
20134357 |
2010 |
Seizures
|
0.360 |
Biomarker
|
phenotype |
CTD_human |
SRA880 did not affect seizure severity and did not reverse the anticonvulsive action of SRIF-14 (1 microM) against pilocarpine-induced seizures, suggesting that hippocampal sst(1) receptors are not involved in the anticonvulsive effects of SRIF-14.
|
20134357 |
2010 |
Seizures
|
0.360 |
Biomarker
|
phenotype |
CTD_human |
Our study suggests that the ability of Ang IV to inhibit pilocarpine-induced convulsions is dependent on somatostatin receptor-2 activation, and is possibly mediated via the inhibition of IRAP resulting in an elevated concentration of somatostatin-14 in the brain.
|
16771832 |
2006 |
Seizures
|
0.360 |
Therapeutic
|
phenotype |
CTD_human |
Our study suggests that the ability of Ang IV to inhibit pilocarpine-induced convulsions is dependent on somatostatin receptor-2 activation, and is possibly mediated via the inhibition of IRAP resulting in an elevated concentration of somatostatin-14 in the brain.
|
16771832 |
2006 |
Seizures
|
0.360 |
Biomarker
|
phenotype |
BEFREE |
Pharmacological studies show that somatostatin affects electrophysiological properties of neurons, modulates classical neurotransmission and has anticonvulsant properties in experimental models of seizures.
|
10583466 |
1999 |
Seizures
|
0.360 |
Therapeutic
|
phenotype |
CTD_human |
[Effect of intracerebral injections of somatostatin and neurotensin on motor functions in seizure].
|
7913897 |
1994 |
Seizures
|
0.360 |
Biomarker
|
phenotype |
CTD_human |
[Effect of intracerebral injections of somatostatin and neurotensin on motor functions in seizure].
|
7913897 |
1994 |