Table 2.
Model | Major Problems | References | ||
---|---|---|---|---|
Type | Name/Implicated Molecule | |||
Genetic models | KO | OTR | soc. | [57] |
CNTNAP2 | soc., com. | [128] | ||
MAGEL2 | soc. | [129] | ||
OPRM1 | soc. | [130,131] | ||
Klf7 | soc., rep. | [132] | ||
Fragile X | FMR1 | soc., rep., motor problem, mood | [40] | |
Rett syndrome | MECP2 | soc., com. | [133] | |
Tuberous sclerosis | TSC1, TSC2 | soc., rep.; cerebellum; V2 antagonist | [134] | |
Indirect evidence | NLGN mutations | soc., rest., com. | [103,135] | |
TSHZ3 KO | soc., rep., narrowness of the field of interest | [68,105] | ||
GLUT3 KO | soc., rep., com., memory problems | [111,112] | ||
parvalbumin KO | soc., rep., com. | [136,137] | ||
GAP43 | soc., resistance to change | [138,139] | ||
SERT variants | soc., rep. | [140,141,142,143] | ||
Environmental models | Drugs | VPA | soc., rep., com. | [144,145] |
Maternal infection and inflammation | poly I:C | soc., rep. | [146,147] | |
LPS | soc. | [148,149] | ||
MIA | soc. | [147] |
Abbreviations: CNTNAP2: Contactin Associated Protein 2; Com: communication problems; Fragile Mental Retardation 1 locus (FMR1); GAP43: synaptic growth-associated protein-43; GLUT3: neuronal glucose transporter isoform 3; klf7: Krüppel-like factor 7; KO: knockout; LPS: lipopolysaccharide; MAGEL2: Melanoma Antigen Gene Family Member L2; MIA: maternal immune activation; methyl-CpG binding protein 2 (MECP2), NLGN: neuroligin; rep: repetitive behavior; poly I:C: polyriboinosinic: polyribocytidylic acid; OPRM1: μ opioid receptor; soc: social problems; TSC: tuberous sclerosis complex; TSHZ3: a zinc-finger transcription factor; VPA: valproate [59].