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. Author manuscript; available in PMC: 2015 Jan 1.
Published in final edited form as: World J Biol Psychiatry. 2013 Sep 12;15(1):2–16. doi: 10.3109/15622975.2013.829585

Table I.

Astrocyte dysfunction in SUDs and depression.*

SUDs Depression
Decreased astrocyte density in PFC and
other brain regions (AUDs)
Decreased astrocyte density in PFC and other brain regions
Altered glutamate transporter expression
e.g., decreased astrocytic EAAT2/
GLT- 1 in DUDs (cocaine, opioids)
Impaired glutamate transport, e.g., decreased expression of
EAAT1/GLAST, EAAT2/GLT-1, EAAT4, and vGluT1
Changes in neurotrophic factors, e.g
GDNF, BDNF, and FGF-2/bFGF
Decreased neurotrophic factor production/secretion, e.g., BDNF
Reactive gliosis (DUDs) Altered glutamate and glutamine levels in several brain
regions
Astrocyte-mediated tolerance in
DUDs (opioids)
Gliotrophic effects of traditional antidepressants, e.g
SSRIs, TCAs
Gliotrophic effects of experimental antidepressants, e.g
riluzole

SUD, substance use disorder; PFC, prefrontal cortex; AUD, alcohol use disorder; EAAT2, excitatory amino acid transporter-2; GLT-1, glial glutamate transporter-1; GDNF, glial derived neurotrophic factor; BDNF, brain derived neurotrophic factor; FGF-2/bFGF, basic fibroblast growth factor-2; DUD, drug use disorder; SSRI, selective serotonin reuptake inhibitor; TCA, tricyclic antidepressant.

*

Italicised text denotes potential convergent mechanisms in SUDs and depressive disorders.