NPY, neuropeptide Y, 4852

N. diseases: 381; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype BEFREE This study aims to investigate the potential effects of anticonvulsant drugs on neuropeptides (galanin and neuropeptide Y) and neurotrophic factors (BDNF and NGF) in pentylenetetrazol (PTZ)-kindled seizures in the rat. 31518546 2020
CUI: C0036572
Disease: Seizures
Seizures
0.400 GeneticVariation phenotype BEFREE We subsequently studied to what extent CPON might affect seizure susceptibility and memory performance, respectively, to address two important questions to evaluate the potential of NPY gene therapy in epilepsy. 30367522 2019
CUI: C0036572
Disease: Seizures
Seizures
0.400 AlteredExpression phenotype BEFREE Viral overexpression of human NPY in the thalamus and somatosensory cortex in GAERS significantly reduced the time spent in seizure activity and number of seizures, whereas seizure duration was only reduced after thalamic NPY overexpression. 29414380 2018
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype BEFREE Neuropeptide Y (NPY) is one of the most abundant protein transmitters in the central nervous system with roles in a variety of biological functions including: food intake, cardiovascular regulation, cognition, seizure activity, circadian rhythms, and neurogenesis. 26620558 2016
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype BEFREE NPY has recently gained much attention as an endogenous antiepileptic and antidepressant agent, as drugs with antiepileptic and/or mood-stabilizing properties may exert their action by increasing NPY concentrations, which in turn can reduce anxiety and depression levels, dampen seizures or increase seizure threshold. 23994577 2013
CUI: C0036572
Disease: Seizures
Seizures
0.400 AlteredExpression phenotype BEFREE Recent findings showed a long-lasting NPY over-expression in the rat hippocampus by local application of recombinant AAV vectors associated with reduced generalization of seizures, delayed kindling epileptogenesis, and strong reduction of chronic spontaneous seizures. 19332323 2009
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype BEFREE Several candidate genes such as neuropeptide Y and galanin have been demonstrated in preclinical studies to have a positive effect on seizure activity. 18717707 2009
CUI: C0036572
Disease: Seizures
Seizures
0.400 AlteredExpression phenotype BEFREE In a subset of APdE9 mice, seizure phenotype was associated with a loss of calbindin-D28k immunoreactivity in dentate granular cells and ectopic expression of neuropeptide Y in mossy fibers. 19295151 2009
CUI: C0036572
Disease: Seizures
Seizures
0.400 Therapeutic phenotype CTD_human Intracerebroventricular (10 nmol/3 microL) and intrahippocampal (20-50 microm) NPY administration increased hippocampal dopamine and attenuated pilocarpine-induced seizures. 18005069 2007
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype CTD_human Intracerebroventricular (10 nmol/3 microL) and intrahippocampal (20-50 microm) NPY administration increased hippocampal dopamine and attenuated pilocarpine-induced seizures. 18005069 2007
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype BEFREE These results establish a proof-of-principle for the applicability of AAV-NPY vectors for the inhibition of seizures in epilepsy. 17196301 2007
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype CTD_human In SS gerbil, NPY immunoreactivity in the hippocampus was lower than that in seizure resistant gerbil. 16194568 2005
CUI: C0036572
Disease: Seizures
Seizures
0.400 Therapeutic phenotype CTD_human In SS gerbil, NPY immunoreactivity in the hippocampus was lower than that in seizure resistant gerbil. 16194568 2005
CUI: C0036572
Disease: Seizures
Seizures
0.400 Therapeutic phenotype CTD_human The present results in amygdala kindling and chemical seizure models suggest that NPY may play a more prominent role in determining seizure thresholds and severity of seizures than in events leading to epileptogenesis. 15451008 2004
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype CTD_human The present results in amygdala kindling and chemical seizure models suggest that NPY may play a more prominent role in determining seizure thresholds and severity of seizures than in events leading to epileptogenesis. 15451008 2004
CUI: C0036572
Disease: Seizures
Seizures
0.400 GeneticVariation phenotype BEFREE This concept is strongly supported by evidence that genetically modified rats overexpressing the NPY gene are less susceptible to seizures while deletion of NPY or Y2 receptor genes results in increased susceptibility to seizures. 15337376 2004
CUI: C0036572
Disease: Seizures
Seizures
0.400 GeneticVariation phenotype BEFREE Our data suggested that a C to T substitution at the 5671 locus of the NPY gene may be associated with seizure during alcohol withdrawal. 11410744 2001
CUI: C0036572
Disease: Seizures
Seizures
0.400 Biomarker phenotype BEFREE The present review is intended to provide an overview of recent work implicating a role for NPY in limbic seizures. 9711903 1998