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. 2021 Jan 6;8(1):ENEURO.0108-20.2020. doi: 10.1523/ENEURO.0108-20.2020

Table 4.

Overview of studies in which pharmacological agents were administered intracranially with the aim of inducing reactivation-dependent amnesia for contextual fear memories in rodents, as identified by the systematic review

Target/function Drug Subjects Administration
route
Dose Amnesic effect
obtained?
Protein synthesis inhibitors
 DNA and protein synthesis interference Anisomycin Mice ACC 50 μg -
Mice BLA 62.5 μg/side +
Mice CA1 60 μg/side +/−3
Mice CA1 62.5 μg/side + and +/−2, 3
Mice dHipp 62.5 μg/side +
Mice dHipp 75 μg +/−2
Mice mPFC 62.5 μg/side -
Mice i.c.v. 0.1 mg +/−3
Rats ACC 62.5 μg/side +
Rats BLA 62.5 μg/side +
Rats CA1 80 μg/side *
Rats CA1 250 μg/side +
Rats MC 62.5 μg/side -
 RNA Polymerase II DRB Rats CA1 10 ng/side +
Receptor antagonists
 CB1-R (inverse agonist) AM251 Rats amygdala 280 pg + and -
 NMDA-R D-AP5 Rats dHipp 5 μg/side +
 β-Adrenergic receptor Propranolol Rats BLA 1.25 μg/side +
 5-HT6-R SB-271046 Rats CA1 10 μg/side -
 5-HT5A-R SB699551 Rats CA1 10 μg/side +/−
 mAch-R Scopolamine Rats amygdala 50 μg -
 Histamine H3-R
(inverse agonist)
Thioperamide Rats amygdala 44 pg -
Receptor agonists
 GABAa-R Muscimol Rats IL 4 nmol/side -
Rats PL 4 nmol/side +
 5-HT7-R AS-19 Rats CA1 5 μg/side -
 5-HT6-R WAY-208466 Rats CA1 0.04 μg/side +/−
Cannabinoids
 CB1 and CB2-R agonist Anandamide Rats CA1 0.17 ng/side +
 CP55,940 Rats CA1 2.5 μg/side +
Rats IL 2.5 μg/side +
Rats RSC 2.5 μg/side +
Intracellular molecule inhibitors
 PARP-1 3-aminobenzamide Mice dHipp 18 μg/side +
Mice mPFC 18 μg/side -
PJ34 Mice dHipp 0.2 mM/side +
 LIM kinase BMS-5 Rats CA1 200 μm/side +
 PKC Chelerythrine Rats PL 3 nmol/side +/−
 PKMζ ZIP Rats PL 10 nmol/side +/−
 MEK U0126 Rats dHipp 2/4 μg/side -
 IKK Sulfasalazine Rats dHipp 2 μg/side + and -
Rats i.c.v. 5/10 mM +/−4
 Proteasome β-lac Rats dHipp 32 ng/side -
 Calpain ALLN Mice CA1 1 μg/side +
PD150606 Rats CA1 0.153 ng/side +
 Rac NSC23766 Rats BLA 5 μg/side -
Rats CeA 5 μg/side -
Rats CA1 5 μg/side +
 mTOR Rapamycin Rats dHipp 5 μg/side +
 N-glycosylation inhibition Swainsonine Mice dHipp 0.5 μg/side +
1-deoxynojirimycin Mice dHipp 16 μg/side +
Tunicamycin Mice dHipp 0.5 μg/side +
Other
 Glutamatergic system blocker Riluzole Rats dHipp 2 μm/side +
 Sodium channel blocker Tetrodotoxin Rats Ent 5 ng/side +
Rats amygdala 5 ng/side +
 Hormone Angiotensin II Rats CA1 0.5 nmol/side *
 Peptide Nociceptin Mice i.c.v 1/3 nmol +/−4
 Cytokine IL-1β Rats CA1 5 ng/side +

Additional details for each study, including PubMed ID, strain, duration of the reactivation session (ranging from 1 to 10 min), time of drug administration, and time between training and reactivation session (ranging from 1 to 36 d), are available at https://osf.io/x2pkq/. ACC = anterior cingulate cortex; ALLN = N-Acetyl-Leu-Leu-norleucinal; BLA = basolateral amygdala; CeA = Central amygdala; dHipp = dorsal hippocampus; D-AP5 = D-2-amino-5-phosphonovaleric acid; DRB = 5,6-dichloro-1-b-dribofuranosylbenzimidazole; Ent = entorhinal cortex; IL = infralimbic cortex; i.c.v. = intracerebroventricular; MC = motor cortex; mPFC = medial prefrontal cortex; PL = prelimbic cortex; RSC = retrosplenial cortex; + = at least one study reported a statistically significant amnestic effect; * = amnestic effect was found to be transient; - = at least one study reported a non-significant effect; +/− = at least one study observed that the amnestic effect occurred under some conditions (superscripts see Table 3).