# Metabolic Mechanisms in Electroconvulsive Therapy for Schizophrenia: Role, Potential and Future Directions

**Authors:** Wenjing Ding, Tianhao Bao

PMC · DOI: 10.3390/ijms27041749 · 2026-02-11

## TL;DR

This paper explores how metabolism and immune-endocrine interactions during ECT may help treat schizophrenia, offering new biomarkers and treatment insights.

## Contribution

Proposes a novel 'metabolism-immunity-neuroendocrine' hypothesis to explain ECT's antipsychotic effects and compares it with other therapies.

## Key findings

- ECT regulates brain and peripheral metabolism, impacting energy pathways and redox stress.
- Key metabolites in energy and immune pathways show potential as schizophrenia biomarkers.
- Comparative analysis reveals similarities and differences in metabolic regulation across therapies and disorders.

## Abstract

The metabolism of the four major substances—glucose, lipids, amino acids, and nucleotides—constitutes the most prominent metabolic phenotype of schizophrenia. The pathological axis shared by these substances involves energy pathway imbalances, redox stress, immune-inflammatory activation, and abnormalities in neurotransmitter synthesis/degradation. Existing research confirms that key metabolites within these pathways hold potential as biomarkers for diagnosis or progression monitoring. In recent years, electroconvulsive therapy (ECT) has been shown to improve psychotic symptoms while exerting broad regulatory effects on neurogenesis, immune homeostasis, and the hypothalamic–pituitary–target gland axis, though its precise mechanisms remain unclear. Recent studies indicate that ECT treatment can also regulate changes in brain and peripheral metabolism. We propose an integrated “metabolism-immunity-neuroendocrine” hypothesis to systematically elucidate how metabolic reprogramming during ECT treatment cascades sequentially to the immune, neural, and endocrine systems, thereby revealing the molecular basis of its antipsychotic effects. Furthermore, we conduct a comparative analysis of the effects of antipsychotic drugs on the same metabolic network and explore the universality and specificity of metabolic regulation in other physical therapies (such as rTMS, tDCS) and psychiatric disorders like depression and bipolar disorder. This research aims to provide novel biomarkers and intervention targets for the precision diagnosis and treatment of schizophrenia.

## Linked entities

- **Diseases:** schizophrenia (MONDO:0005090), depression (MONDO:0002050), bipolar disorder (MONDO:0004985)

## Full-text entities

- **Genes:** TMEM108 (transmembrane protein 108) [NCBI Gene 66000] {aka CT124, RTLN}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, ABCA13 (ATP binding cassette subfamily A member 13) [NCBI Gene 154664], ENO1 (enolase 1) [NCBI Gene 2023] {aka ENO1-IT1, ENO1L1, HEL-S-17, MPB1, NNE, PPH}, SLC2A1 (solute carrier family 2 member 1) [NCBI Gene 6513] {aka CSE, DYT17, DYT18, DYT9, EIG12, GLUT}, ATP1A3 (ATPase Na+/K+ transporting subunit alpha 3) [NCBI Gene 478] {aka AHC2, CAPOS, DEE99, DYT12, RDP}, CNR1 (cannabinoid receptor 1) [NCBI Gene 1268] {aka CANN6, CB-R, CB1, CB1A, CB1K5, CB1R}, GRIN2B (glutamate ionotropic receptor NMDA type subunit 2B) [NCBI Gene 2904] {aka DEE27, EIEE27, GluN2B, MRD6, NMDAR2B, NR2B}, SREBF2 (sterol regulatory element binding transcription factor 2) [NCBI Gene 6721] {aka SREBP-2, SREBP2, bHLHd2}, DAOA (D-amino acid oxidase activator) [NCBI Gene 267012] {aka LG72, SG72}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, SLC39A8 (solute carrier family 39 member 8) [NCBI Gene 64116] {aka BIGM103, CDG2N, LZT-Hs6, PP3105, ZIP8}, SLC6A9 (solute carrier family 6 member 9) [NCBI Gene 6536] {aka GCENSG, GLYT1, IS6}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539] {aka CNSHA1, G6PD1}, ALDOC (aldolase, fructose-bisphosphate C) [NCBI Gene 230] {aka ALDC}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, PDP1 (pyruvate dehydrogenase phosphatase catalytic subunit 1) [NCBI Gene 54704] {aka PDH, PDP, PDPC, PDPC 1, PPM2A, PPM2C}, GLUL (glutamate-ammonia ligase) [NCBI Gene 2752] {aka DEE116, GLNS, GS, PIG43, PIG59}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, SLC16A1 (solute carrier family 16 member 1) [NCBI Gene 6566] {aka HHF7, MCT, MCT1, MCT1D}, ACACA (acetyl-CoA carboxylase alpha) [NCBI Gene 31] {aka ACAC, ACACAD, ACACalpha, ACC, ACC1, ACCA}, GRM3 (glutamate metabotropic receptor 3) [NCBI Gene 2913] {aka GLUR3, GPRC1C, MGLUR3, mGlu3}, ADAMTS9 (ADAM metallopeptidase with thrombospondin type 1 motif 9) [NCBI Gene 56999], SLC6A1 (solute carrier family 6 member 1) [NCBI Gene 6529] {aka GABATHG, GABATR, GAT1, MAE, hGAT-1}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}, SLC3A2 (solute carrier family 3 member 2) [NCBI Gene 6520] {aka 4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1}, GNAQ (G protein subunit alpha q) [NCBI Gene 2776] {aka CMAL, G-ALPHA-q, GAQ, SWS}, DISC1 (DISC1 scaffold protein) [NCBI Gene 27185] {aka C1orf136, SCZD9}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, DRD2 (dopamine receptor D2) [NCBI Gene 1813] {aka D2DR, D2R}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, SLC2A3 (solute carrier family 2 member 3) [NCBI Gene 6515] {aka GLUT3}, F11R (F11 receptor) [NCBI Gene 50848] {aka CD321, JAM, JAM1, JAMA, JCAM, KAT}, MPO (myeloperoxidase) [NCBI Gene 4353], GPX3 (glutathione peroxidase 3) [NCBI Gene 2878] {aka GPx-P, GSHPx-3, GSHPx-P}, CAT (catalase) [NCBI Gene 847], DGKZ (diacylglycerol kinase zeta) [NCBI Gene 8525] {aka DAGK5, DAGK6, DGK-ZETA, hDGKzeta}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], TRPA1 (transient receptor potential cation channel subfamily A member 1) [NCBI Gene 8989] {aka ANKTM1, FEPS, FEPS1, p120}, KMO (kynurenine 3-monooxygenase) [NCBI Gene 8564] {aka dJ317G22.1}, GAD1 (glutamate decarboxylase 1) [NCBI Gene 2571] {aka CPSQ1, DEE89, GAD, GAD-67, SCP}, ME2 (malic enzyme 2) [NCBI Gene 4200] {aka ODS1}, DDO (D-aspartate oxidase) [NCBI Gene 8528] {aka DASOX, DASPO, DDO-1, DDO-2}, NTF3 (neurotrophin 3) [NCBI Gene 4908] {aka HDNF, NGF-2, NGF2, NT-3, NT3}, GLO1 (glyoxalase I) [NCBI Gene 2739] {aka GLOD1, GLYI, HEL-S-74}, SLC1A2 (solute carrier family 1 member 2) [NCBI Gene 6506] {aka DEE41, EAAT2, EIEE41, GLT-1, GLT1, HBGT}, GRIN2A (glutamate ionotropic receptor NMDA type subunit 2A) [NCBI Gene 2903] {aka EPND, FESD, GluN2A, LKS, NMDAR2A, NR2A}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, PDHB (pyruvate dehydrogenase E1 subunit beta) [NCBI Gene 5162] {aka E1beta, PDHBD, PDHE1-B, PDHE1B, PHE1B}, PLA2G1B (phospholipase A2 group IB) [NCBI Gene 5319] {aka PLA2, PLA2A, PPLA2}, S100a6 (S100 calcium binding protein A6 (calcyclin)) [NCBI Gene 20200] {aka 2A9, 5B10, CALCYCLIN, Cacy, PRA}, SREBF1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 6720] {aka HMD, IFAP2, SREBP1, bHLHd1}, Itgam (integrin alpha M) [NCBI Gene 16409] {aka CD11b/CD18, CR3, CR3A, Cd11b, F730045J24Rik, Ly-40}, GRIA1 (glutamate ionotropic receptor AMPA type subunit 1) [NCBI Gene 2890] {aka GLUH1, GLUR1, GLURA, GluA1, HBGR1, MRD67}, HACE1 (HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1) [NCBI Gene 57531] {aka SPPRS}, GCLC (glutamate-cysteine ligase catalytic subunit) [NCBI Gene 2729] {aka CNSHA7, GCL, GCS, GLCL, GLCLC}
- **Diseases:** thyroid hormone (MESH:D018382), Depression (MESH:D003866), OCD (MESH:D009771), Negative symptoms (MESH:D064726), Proinflammatory cytokines (MESH:D000080424), neuronal degeneration (MESH:D009410), type 2 diabetes (MESH:D003924), inhibition (MESH:C565433), constipation (MESH:D003248), amino acid metabolism abnormalities (MESH:D000592), Hyperhomocysteinemia (MESH:D020138), BD (MESH:D001714), cerebral lipid abnormalities (MESH:D011017), impaired glucose tolerance (MESH:D018149), chronic (MESH:D002908), memory impairment (MESH:D008569), cognitive deficits (MESH:D003072), Nervous System (MESH:D009422), ATP deficiency (MESH:C566310), neurotransmitter abnormalities (MESH:D000014), Impaired lipid metabolism (MESH:D052439), xc- system dysfunction (MESH:D007154), psychotic (MESH:D011618), Neuroactive steroids (MESH:D016114), hypoglycemia (MESH:D007003), 22q11.2 deletion (MESH:D004062), Lactic acid abnormalities (MESH:C565446), insulin resistance (MESH:D007333), synthetic (OMIM:146820), neurotransmitter receptor dysfunction (MESH:D006938), toxicity (MESH:D064420), HPA axis (MESH:D007029), oligodendrocyte injury (MESH:D056784), congenital n-glycosylation abnormalities (MESH:D018981), energy deficiency (MESH:D011502), overweight (MESH:D050177), psychotic conversion (MESH:D003291), cognitive and psychotic symptoms (MESH:D019954), hyperactivity (MESH:D006948), neurological alterations (MESH:D009461), MDD (MESH:D003865), convulsive (MESH:D012640), energy metabolism disorders (MESH:D008659), hypoxia (MESH:D000860), dopamine dysfunction (MESH:C567730), metabolic syndrome (MESH:D024821), hyperglycemia (MESH:D006943), injury to (MESH:D014947), inflammation (MESH:D007249), fatty acid (MESH:D008067), Mitochondrial dysfunction (MESH:D028361), schizophrenia spectrum disorder (MESH:D019967), anhedonia (MESH:D059445), dyslipidemia (MESH:D050171), folate insufficiency (MESH:D000309), cancer (MESH:D009369), NMDARs (MESH:D060426), Alzheimer's disease (MESH:D000544), impaired (MESH:D060825), Psychiatric Disorders (MESH:D001523)
- **Chemicals:** citrate (MESH:D019343), GSH (MESH:D005978), N-acyl phosphatidylethanolamine (MESH:C000609813), Gln (MESH:D005973), ATP (MESH:D000255), MG (MESH:D011765), endocannabinoid (MESH:D063388), vitamin B12 (MESH:D014805), pentosidine (MESH:C062187), LY2140023 (MESH:C534551), pyridoxal (MESH:D011730), Lipid (MESH:D008055), cysteine (MESH:D003545), D-Asp (MESH:D026603), alcohols (MESH:D000438), membrane lipid (MESH:D008563), TRP (MESH:D014364), N-acetylcysteine (MESH:D000111), pyridoxal phosphate (MESH:D011732), DA (MESH:D004298), sphingolipid (MESH:D013107), LPC (MESH:D008244), cannabinoid (MESH:D002186), N-acetyl serotonin (MESH:C006389), SCFA (MESH:D005232), sphingosine (MESH:D013110), ROS (MESH:D017382), folate (MESH:D005492), Glucose (MESH:D005947), manganese (MESH:D008345), quetiapine (MESH:D000069348), ornithine (MESH:D009952), 5-HIAA (MESH:D006897), SM (MESH:D013109), NO (MESH:D009614), PE (MESH:C483858), 2-AG (MESH:C094503), D-alanine (-), MK-801 (MESH:D016291), ethanolamine (MESH:D019856), paliperidone (MESH:D000068882), cystine (MESH:D003553), n-acylethanolamine (MESH:C022203), olanzapine (MESH:D000077152), betaine (MESH:D001622), PUFAs (MESH:D005231), alpha-ketoglutarate (MESH:D007656), nitrite (MESH:D009573), N-acetyl aspartate (MESH:C000179), AAs (MESH:D000596), Hcy (MESH:D006710), Cr (MESH:D002857), thiol (MESH:D013438), creatine (MESH:D003401), PS (MESH:D010718), PCr (MESH:D010725), MUFAs (MESH:D005229), sulfatides (MESH:D013433), PC (MESH:D010713), MDA (MESH:D008315)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** rs6298, Ser704Cys, phenylalanine to tyrosine, A 7 T, Gln/Glu, Glu in ACC, A391T, glutamate-glutamine, Val66Met, R30, 677C/T, rs12294045, K62E

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12940327/full.md

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Source: https://tomesphere.com/paper/PMC12940327