Table 1.
In Vitro Model | Study |
SH-SY5Y cell line | Study of molecular mechanisms and study of transmission in signaling pathways [150] |
Multipotent stem cells | Gene expression studies and pathway dysfunctions associated with mitochondrial metabolism and oxidative stress [151] Analysis of gene and receptor expression, study of neurodevelopmental pathways [152] |
Pluripotent stem cells | |
HT-22 cell line | Study of biochemical basis of cellular function and disease processes and neurodevelopmental pathways [153] |
Three-dimensional culture systems (3D) | Toxicity studies and determination of the biological or biochemical activity of the compounds [154] |
In Vivo Model | Study/Effect |
Amphetamine model Phencyclidine model |
Locomotor sensitization; increased mesolimbic dopamine response; persistent deficit in prepulse inhibition (PPI); cognitive impairments [77,155] Enhanced mesolimbic dopamine response; no sustained deficit in PPI; reduced social interaction [90,112] |
MAM model Neonatal ventral hippocampal lesion model |
Spontaneous hyperactivity; amphetamine- and NMDA antagonist-induced hyperactivity; deficits in PPI; cognitive impairment; reduced social interaction [143,156] Amphetamine- and NMDA antagonist-induced locomotor hyperactivity; cognitive impairments; deficits in PPI and social interaction [149,157] |
DISC-1 knock-out Neuregulin1 and ErbB4 knock-out |
Increased sensitivity to psychostimulants; cognitive deficits; reduced social interaction; depressive-like behavior; deficits in PPI in some mutants [120,125,158] Spontaneous locomotor hyperactivity; social interaction impairment; PPI deficits in Neuregulin1 but not ErbB4 mutants [130,159] |