» Articles » PMID: 25713723

Mitochondrial Complex I and III Gene MRNA Levels in Schizophrenia, and Their Relationship with Clinical Features

Overview
Publisher Biomed Central
Specialty Psychiatry
Date 2015 Feb 26
PMID 25713723
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The etiology of schizophrenia is not precisely known; however, mitochondrial function and cerebral energy metabolism abnormalities were determined to be possible factors associated with the etiology of schizophrenia. Impaired mitochondrial function negatively affects neuronal plasticity, and can cause cognitive deficits and behavioral abnormalities observed during the clinical course of schizophrenia. The present study aimed to investigate the relationship between the clinical features of schizophrenia, and mitochondrial complex activation, based on measurement of mRNA levels in the NDUFV1, NDUFV2, NDUFS1, and UQCR10 genes involved in the peripheral mitochondrial complex.

Methods: The study included 138 schizophrenia patients and 42 healthy controls. The schizophrenia group was divided into a chronic schizophrenia subgroup (n = 84) and a first-episode schizophrenia subgroup (n = 54). The symptoms profile and severity of disorder were evaluated using the Scale for the Assessment of Negative Symptoms (SANS), Scale for the Assessment of Positive Symptoms (SAPS), and Brief Psychiatric Rating Scale (BPRS).

Results: The level of mRNA expression of NDUFV1, NDUFV2, and NDUFS1 was significantly higher in the schizophrenia group than in the control group. The mRNA level of NDUFV2 was positively correlated with BPRS and SAPS scores in the first-episode schizophrenia subgroup.

Conclusion: The findings showed that there was a positive correlation between gene mRNA levels and psychotic symptomatology, especially positive symptoms. Our results suggest that mRNA levels of the NDUFV1, NUDFV2, and NDUFS1 genes of complex I of the mitochondrial electron transport chain might become a possible peripheral marker for the diagnosis of schizophrenia.

Citing Articles

Circulating Cell-Free Mitochondrial DNA in Plasma of Individuals with Schizophrenia and Cognitive Deficit in Mexican Population.

Garcia-de la Cruz D, Juarez-Rojop I, Tovilla-Zarate C, Nicolini H, Genis-Mendoza A Neuropsychiatr Dis Treat. 2024; 20:1757-1765.

PMID: 39323935 PMC: 11423824. DOI: 10.2147/NDT.S460554.


Acetylome analyses provide novel insights into the effects of chronic intermittent hypoxia on hippocampus-dependent cognitive impairment.

Liu F, Yan W, Chen C, Zeng Y, Kong Y, He X Front Mol Neurosci. 2024; 17:1324458.

PMID: 38455734 PMC: 10917988. DOI: 10.3389/fnmol.2024.1324458.


Transcriptomic analysis reveals mitochondrial pathways associated with distinct adolescent behavioral phenotypes and stress response.

Santos-Silva T, Hazar Ulgen D, Lopes C, Guimaraes F, Alberici L, Sandi C Transl Psychiatry. 2023; 13(1):351.

PMID: 37978166 PMC: 10656500. DOI: 10.1038/s41398-023-02648-3.


The druggable schizophrenia genome: from repurposing opportunities to unexplored drug targets.

Lago S, Bahn S NPJ Genom Med. 2022; 7(1):25.

PMID: 35338153 PMC: 8956592. DOI: 10.1038/s41525-022-00290-4.


The Etiology of Auditory Hallucinations in Schizophrenia: From Multidimensional Levels.

Shao X, Liao Y, Gu L, Chen W, Tang J Front Neurosci. 2021; 15:755870.

PMID: 34858129 PMC: 8632545. DOI: 10.3389/fnins.2021.755870.


References
1.
Ben-Shachar D, Nadri C, Karry R, Agam G . Mitochondrial complex I subunits are altered in rats with neonatal ventral hippocampal damage but not in rats exposed to oxygen restriction at neonatal age. J Mol Neurosci. 2008; 38(2):143-51. DOI: 10.1007/s12031-008-9144-9. View

2.
Taurines R, Thome J, Duvigneau J, Forbes-Robertson S, Yang L, Klampfl K . Expression analyses of the mitochondrial complex I 75-kDa subunit in early onset schizophrenia and autism spectrum disorder: increased levels as a potential biomarker for early onset schizophrenia. Eur Child Adolesc Psychiatry. 2009; 19(5):441-8. DOI: 10.1007/s00787-009-0074-z. View

3.
Barrientos A, Marin C, Miro O, Casademont J, Gomez M, Nunes V . Biochemical and molecular effects of chronic haloperidol administration on brain and muscle mitochondria of rats. J Neurosci Res. 1998; 53(4):475-81. DOI: 10.1002/(SICI)1097-4547(19980815)53:4<475::AID-JNR9>3.0.CO;2-3. View

4.
Buchsbaum M, Buchsbaum B, Hazlett E, Haznedar M, Newmark R, Tang C . Relative glucose metabolic rate higher in white matter in patients with schizophrenia. Am J Psychiatry. 2007; 164(7):1072-81. DOI: 10.1176/ajp.2007.164.7.1072. View

5.
Ben-Shachar D, Laifenfeld D . Mitochondria, synaptic plasticity, and schizophrenia. Int Rev Neurobiol. 2004; 59:273-96. DOI: 10.1016/S0074-7742(04)59011-6. View