» Articles » PMID: 33396966

Astroglial Connexin43 As a Potential Target for a Mood Stabiliser

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2021 Jan 5
PMID 33396966
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Mood disorders remain a major public health concern worldwide. Monoaminergic hypotheses of pathophysiology of bipolar and major depressive disorders have led to the development of monoamine transporter-inhibiting antidepressants for the treatment of major depression and have contributed to the expanded indications of atypical antipsychotics for the treatment of bipolar disorders. In spite of psychopharmacological progress, current pharmacotherapy according to the monoaminergic hypothesis alone is insufficient to improve or prevent mood disorders. Recent approval of esketamine for treatment of treatment-resistant depression has attracted attention in psychopharmacology as a glutamatergic hypothesis of the pathophysiology of mood disorders. On the other hand, in the last decade, accumulated findings regarding the pathomechanisms of mood disorders emphasised that functional abnormalities of tripartite synaptic transmission play important roles in the pathophysiology of mood disorders. At first glance, the enhancement of astroglial connexin seems to contribute to antidepressant and mood-stabilising effects, but in reality, antidepressive and mood-stabilising actions are mediated by more complicated interactions associated with the astroglial gap junction and hemichannel. Indeed, several depressive mood-inducing stress stimulations suppress connexin43 expression and astroglial gap junction function, but enhance astroglial hemichannel activity. On the other hand, monoamine transporter-inhibiting antidepressants suppress astroglial hemichannel activity and enhance astroglial gap junction function, whereas several non-antidepressant mood stabilisers activate astroglial hemichannel activity. Based on preclinical findings, in this review, we summarise the effects of antidepressants, mood-stabilising antipsychotics, and anticonvulsants on astroglial connexin, and then, to establish a novel strategy for treatment of mood disorders, we reveal the current progress in psychopharmacology, changing the question from "what has been revealed?" to "what should be clarified?".

Citing Articles

Ginsenoside Rg1: A Neuroprotective Natural Dammarane-Type Triterpenoid Saponin With Anti-Depressive Properties.

Han D, Zhao Z, Mao T, Gao M, Yang X, Gao Y CNS Neurosci Ther. 2024; 30(12):e70150.

PMID: 39639753 PMC: 11621566. DOI: 10.1111/cns.70150.


The Janus face of antipsychotics in glial cells: Focus on glioprotection.

Schmitz I, da Silva A, Bobermin L, Goncalves C, Steiner J, Quincozes-Santos A Exp Biol Med (Maywood). 2024; 248(22):2120-2130.

PMID: 38230521 PMC: 10800129. DOI: 10.1177/15353702231222027.


Staphylococcus warneri strain XSB102 exacerbates psoriasis and promotes keratinocyte proliferation in imiquimod-induced psoriasis-like dermatitis mice.

Si W, Li M, Wang K, Li J, Xu M, Zhou X Arch Microbiol. 2023; 206(1):3.

PMID: 37991548 DOI: 10.1007/s00203-023-03726-2.


Astroglial Connexin 43-Mediated Gap Junctions and Hemichannels: Potential Antidepressant Mechanisms and the Link to Neuroinflammation.

Lei L, Wang Y, Hu D, Gai C, Zhang Y Cell Mol Neurobiol. 2023; 43(8):4023-4040.

PMID: 37875763 PMC: 11407732. DOI: 10.1007/s10571-023-01426-5.


A Novel Gliotransmitter, L-β-Aminoisobutyric Acid, Contributes to Pathophysiology of Clinical Efficacies and Adverse Reactions of Clozapine.

Fukuyama K, Motomura E, Okada M Biomolecules. 2023; 13(9).

PMID: 37759688 PMC: 10526296. DOI: 10.3390/biom13091288.


References
1.
Einoch R, Weinreb O, Mandiuk N, Youdim M, Bilker W, Silver H . The involvement of BDNF-CREB signaling pathways in the pharmacological mechanism of combined SSRI- antipsychotic treatment in schizophrenia. Eur Neuropsychopharmacol. 2017; 27(5):470-483. DOI: 10.1016/j.euroneuro.2017.03.005. View

2.
Willner P, Scheel-Kruger J, Belzung C . The neurobiology of depression and antidepressant action. Neurosci Biobehav Rev. 2012; 37(10 Pt 1):2331-71. DOI: 10.1016/j.neubiorev.2012.12.007. View

3.
Fornaro M, Carvalho A, Fusco A, Anastasia A, Solmi M, Berk M . The concept and management of acute episodes of treatment-resistant bipolar disorder: a systematic review and exploratory meta-analysis of randomized controlled trials. J Affect Disord. 2020; 276:970-983. DOI: 10.1016/j.jad.2020.07.109. View

4.
Bahji A, Ermacora D, Stephenson C, Hawken E, Vazquez G . Comparative efficacy and tolerability of pharmacological treatments for the treatment of acute bipolar depression: A systematic review and network meta-analysis. J Affect Disord. 2020; 269:154-184. DOI: 10.1016/j.jad.2020.03.030. View

5.
Quesseveur G, Portal B, Basile J, Ezan P, Mathou A, Halley H . Attenuated Levels of Hippocampal Connexin 43 and its Phosphorylation Correlate with Antidepressant- and Anxiolytic-Like Activities in Mice. Front Cell Neurosci. 2016; 9:490. PMC: 4686612. DOI: 10.3389/fncel.2015.00490. View