1. The role of astrocytes in depression, its prevention, and treatment by targeting astroglial gliotransmitter release.
- Author
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Duarte Y, Quintana-Donoso D, Moraga-Amaro R, Dinamarca I, Lemunao Y, Cárdenas K, Bahamonde T, Barrientos T, Olivares P, Navas C, Carvajal FJ, Santibánez Y, Castro-Lazo R, Paz Meza M, Jorquera R, Gómez GI, Henke M, Alarcón R, Gabriel LA, Schiffmann S, Cerpa W, Retamal MA, Simon F, Linsambarth S, Gonzalez-Nilo F, and Stehberg J
- Subjects
- Animals, Rats, Male, Glutamic Acid metabolism, Receptors, N-Methyl-D-Aspartate metabolism, Rats, Sprague-Dawley, Stress, Psychological metabolism, Serine metabolism, Neurotransmitter Agents metabolism, Antidepressive Agents pharmacology, Astrocytes metabolism, Astrocytes drug effects, Connexin 43 metabolism, Depression metabolism, Depression drug therapy, Hippocampus metabolism
- Abstract
The role of ventral hippocampus (vHipp) astroglial gliotransmission in depression was studied using chronic restraint stress (CRS) and chronic unpredictable mild stress (CUMS) rodent models. CRS increased Cx43 hemichannel activity and extracellular glutamate levels in the vHipp and blocking astroglial Cx43 hemichannel-dependent gliotransmission during CRS prevented the development of depression and glutamate buildup. Moreover, the acute blockade of Cx43 hemichannels induced antidepressant effects in rats previously subjected to CRS or CUMS. This antidepressant effect was prevented by coinjection of glutamate and D-serine. Furthermore, Cx43 hemichannel blockade decreased postsynaptic NMDAR currents in vHipp slices in a glutamate and D-serine-dependent manner. Notably, chronic microinfusion of glutamate and D-serine, L-serine, or the NMDAR agonist NMDA, into the vHipp induced depressive-like symptoms in nonstressed rats. We also identified a small molecule, cacotheline, which blocks Cx43 hemichannels and its systemic administration induced rapid antidepressant effects, preventing stress-induced increases in astroglial Cx43 hemichannel activity and extracellular glutamate in the vHipp, without sedative or locomotor side effects. In conclusion, chronic stress increases Cx43 hemichannel-dependent release of glutamate and D-/L-serine from astrocytes in the vHipp, overactivating postsynaptic NMDARs and triggering depressive-like symptoms. This study highlights the critical role of astroglial gliotransmitter release in chronic stress-induced depression and suggests it can be used as a target for the prevention and treatment of depression., Competing Interests: Competing interests statement:M.A.R., D.G.-N., and J.S. authored a Patent application filed in 2013-05-31 (WO 2013/179264), which was granted in the US (US-9879058-B2) on the date 2018/01/30, entitled “Use of compounds that selectively modulate astrocytic release of substances through hemichannels of connexins and pannexins, without influencing gap junctions, for the treatment of psychiatric disorders,” which included cacotheline as an example. All other authors report no conflicts of interest.
- Published
- 2024
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