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miR143-3p–Mediated NRG-1–Dependent Mitochondrial Dysfunction Contributes to Olanzapine Resistance in Refractory Schizophrenia.

Authors :
Sun, Jing
Zhang, Xiaoya
Cong, Qijie
Chen, Dong
Yi, Zhenghui
Huang, Hailiang
Wang, Cong
Li, Mo
Zeng, Rongsen
Liu, Yunxi
Huai, Cong
Chen, Luan
Liu, Chuanxin
Zhang, Yan
Xu, Yong
Fan, Lingzi
Wang, Guoqiang
Song, Chuanfu
Wei, Muyun
Du, Huihui
Source :
Biological Psychiatry. Sep2022, Vol. 92 Issue 5, p419-433. 15p.
Publication Year :
2022

Abstract

Olanzapine is an effective antipsychotic medication for treatment-resistant schizophrenia (TRS); however, the therapeutic effectiveness of olanzapine has been found to vary in individual patients. It is imperative to unravel its resistance mechanisms and find reliable targets to develop novel precise therapeutic strategies. Unbiased RNA sequencing analysis was performed using homogeneous populations of neural stem cells derived from induced pluripotent stem cells in 3 olanzapine responder (reduction of Positive and Negative Syndrome Scale score ≥25%) and 4 nonresponder (reduction of Positive and Negative Syndrome Scale score <25%) inpatients with TRS. We also used a genotyping study from patients with TRS to assess the candidate genes associated with the olanzapine response. CRISPR (clustered regularly interspaced short palindromic repeats)/Cas9-mediated genome editing, neurologic behavioral tests, RNA silencing, and microRNA sequencing were used to investigate the phenotypic mechanisms of an olanzapine resistance gene in patients with TRS. Neuregulin-1 (NRG-1) deficiency–induced mitochondrial dysfunction is associated with olanzapine treatment outcomes in TRS. NRG-1 knockout mice showed schizophrenia-relevant behavioral deficits and yielded olanzapine resistance. Notably, miR143-3p is a critical NRG-1 target related to mitochondrial dysfunction, and miR143-3p levels in neural stem cells associate with severity to olanzapine resistance in TRS. Meanwhile, olanzapine resistance in NRG-1 knockout mice could be rescued by treatment with miR143-3p agomir via intracerebral injection. Our findings provide direct evidence of olanzapine resistance resulting from NRG-1 deficiency–induced mitochondrial dysfunction, and they link olanzapine resistance and NRG-1 deficiency–induced mitochondrial dysfunction to an NRG-1/miR143-3p axis, which constitutes a novel biomarker and target for TRS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00063223
Volume :
92
Issue :
5
Database :
Academic Search Index
Journal :
Biological Psychiatry
Publication Type :
Academic Journal
Accession number :
158309217
Full Text :
https://doi.org/10.1016/j.biopsych.2022.03.012