Neurobehavioral Differences of Valproate and Risperidone on MK-801 Inducing Acute Hyperlocomotion in Mice [PDF]
Objective. The glutamate system plays a major role in the development of neuropsychiatric disorders such as addiction, epilepsy, dementia, and psychosis.
Po-An Chen +4 more
doaj +2 more sources
Effects of haloperidol inhalation on MK-801- and memantine-induced locomotion in mice [PDF]
The administration of therapeutic agents is difficult in many patients, such as patients with post-operative delirium or dementia or patients with schizophrenia, who are upset in an emergency room.
Hiroshi Ueno +8 more
doaj +2 more sources
Effect of MK-801, an antagonist of NMDA receptor in the pedunculopontine tegmental nucleus, on cardiovascular parameters in normotensive and hydralazine hypotensive rats [PDF]
Objective(s): In the present study, the cardiovascular effects of glutamate NMDA receptor of the pedunculopontine tegmental nucleus (PPT) in normotensive and hydralazine (HLZ) hypotensive rats were evaluated.
Mohammad Reza Hosseiniravesh +5 more
doaj +2 more sources
Effect of MK-801 and clozapine on the proteome of cultured human oligodendrocytes [PDF]
Separate lines of evidence have demonstrated the involvement of NMDA receptor and oligodendrocyte dysfunctions in schizophrenia. Here we have carried out shotgun mass spectrometry proteome analysis of oligodendrocytes treated with the NMDA receptor ...
Juliana Silva Cassoli +8 more
doaj +3 more sources
Cortico-Striatal-Midbrain Circuit Dysregulation Underlying MK-801 Induced Impulsivity and the Ameliorative Effects of SEP. [PDF]
Impulsivity is a symptom across multiple psychiatric disorders, yet its neural basis remains elusive. This study shows that the NMDAR antagonist MK‐801 elevates dopamine release and disrupts neuronal selectivity in the nucleus accumbens, leading to impulsive behavior.
Wang X +6 more
europepmc +2 more sources
α2 Adrenergic Agonists Prevent MK-801 Neurotoxicity [PDF]
Antagonists of the N-methyl-D-aspartate (NMDA) subtype of glutamate receptor are of considerable interest for various neurotherapeutic purposes, including preventing neuronal degeneration in stroke and CNS trauma, suppressing neuropathic pain and preventing the development of tolerance to opiate analgesics.
N B, Farber +3 more
openaire +3 more sources
Effect of the glucocorticoid receptor antagonist RU486 on MK-801 induced behavioural sensitisation. [PDF]
Stress is known to modulate sensitisation to repeated psychostimulant exposure. However, there is no direct evidence linking glucocorticoids and sensitisation achieved by repeated administration of the NMDA receptor antagonist MK-801.
Emilia M Lefevre +5 more
doaj +1 more source
Antidepressant Effects of (+)-MK-801 and (-)-MK-801 in the Social Defeat Stress Model [PDF]
Current data on antidepressant action of the N-methyl-D-aspartate receptor antagonist, (+)-MK-801, is inconsistent. This study was conducted to examine the effects of (+)-MK-801 and its less potent stereoisomer, (-)-MK-801, in the social defeat stress model of depression.The antidepressant effects of (+)-MK-801 (0.1mg/kg) and (-)-MK-801 (0.1mg/kg) in ...
Yang, Bangkun +4 more
openaire +2 more sources
Dizocilpine (MK-801), a non-competitive N-methyl-D-aspartic acid receptor (NMDA-R) antagonist, can induce schizophrenia-like symptoms in healthy individuals, implicating NMDA-R hypofunction in disease pathogenesis. Brain-derived neurotrophic factor (BDNF)
Wenjuan Yu +8 more
doaj +1 more source
BackgroundIn neonatal rats, MK-801 treatment generates schizophrenia-like symptoms. Resveratrol (RSV) is a phenolic compound and a potent neuroprotective agent.
Juan Niu, Yuquan Cao, Yongjuan Ji
doaj +1 more source

