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. 2020 Dec 30;22(1):339. doi: 10.3390/ijms22010339

Table 5.

Summary of the effects of first-line mood stabilisers and other anticonvulsants on the expression and function of Cx43.

Agent Model (Region) Treatment
(Dose, Duration)
Effect
(Hemichannel)
Reference
Carbamazepine rat cortical astrocyte in vitro
(40–400 µM for 24 h)
no effect (protein) [110]
rat cortical astrocyte in vitro
(100 µM for 7 days)
no effect (protein)
(no effect)
[2]
Lacosamide rat cortical astrocyte in vitro
(30–100 µM for 7 days)
no effect (protein)
(inhibition)
[2]
Zonisamide rat cortical astrocyte in vitro
(30 µM for 7 days)
decrease (protein)
(inhibition)
[2]
Valproate Rat (frontal) in vivo
(300 mg/kg for 21 days)
no effect (protein) [76]
rat cortical astrocyte in vitro
(350–1400 µM for 24 h)
no effect (protein) [110]
rat cortical astrocyte in vitro
(1000–3000 µM for 7 days)
increase (protein)
(activation)
[3]
Gabapentin rat cortical astrocyte in vitro
(60–600 µM for 24 h)
no effect (protein) [110]
Phenytoin rat cortical astrocyte in vitro
(40–400 µM for 24 h)
no effect (protein) [110]
Diazepam rat cortical astrocyte in vitro
(25 µM for 48 h)
no effect (protein) [77]

We searched MEDLINE using the keywords “(((connexin) OR (hemichannel) OR (gap junction)) AND ((anticonvulsant) OR (psychotropic drugs)))” for papers published by 1 November 2020. Relevant articles were obtained in full and assessed for inclusion independently by reviewers. Disagreements among reviewers were resolved via discussion to reach a consensus.