Opposing manner of miR‐455‐3p against NR2B‐PSD‐95‐nNOS complex in the cortex and hippocampus of depressive rats under simulated complex space environment. Issue 3 (1st February 2023)

• Record Type: Journal Article
• Authors: Rasheed, Madiha; Wang, Han; Wang, Chaolei; Sun, Jingyan; Chen, Zixuan; Deng, Yulin
• Is Part Of: Journal of neurochemistry. Volume 165:Issue 3(2023)
• Page Start: 391
• Page End: 412
• Publication Date: 2023-02-01
• Subjects: depression -- microgravity -- miRNA‐455‐3p -- neuroprotection -- NR2B‐PSD‐95‐nNOS complex -- simulated space complex environment; Neurochemistry -- Periodicals; 616.8042
• DOI: 10.1111/jnc.15766
• Languages: English
• ISSNs: 0022-3042

Abstract

Abstract: Depression in astronauts is one of the consequences of space flight effects, negatively impacting their work performances. Unfortunately, the underlying molecular mechanisms in space flight‐induced depression are still unknown; however, various neuropsychiatric disorders reported that overexpressed NR2B‐PSD‐95‐nNOS complex in the brain triggers various pathological pathways, and inhibiting NR2B‐PSD‐95‐nNOS complex asserts antidepressant effects. Through our in silico analysis, we found that epigenetic regulator miR‐445‐3p targets PSD‐95 and is hypothesized to down‐regulate NR2B‐PSD‐95‐nNOS complex to prevent neuronal damage associated with depression. Therefore, the present study is aimed to determine the novel insight of the miR‐455‐3p against the NR2B‐PSD‐95‐nNOS complex in the neurobiology of space flight‐induced depressive behavior. Using a simulated space environment complex model (SCSE) for 21 days, we induced depressive behavior in rats to analyze miR‐455‐3p expression and NR2B‐PSD‐95‐nNOS complex in the cortex and hippocampus of the SCSE depressed rats through qRT‐PCR and western blot analysis. Further, an in vitro microgravity model using rat hippocampus cell lines (RHNC) was utilized to identify the independent role of miR‐455‐3p on (1) NR2B‐PSD‐95‐nNOS complex and TrKB–BDNF proteins, (2) oxidative stress, (3) nitric oxide level, (4) inflammatory cytokines, (5) mitochondrial biogenesis/ dynamics, and (6) cell survival. Our results showed that miR‐455‐3p regulates NR2B‐PSD‐95‐nNOS complex in the SCSE depressed rats in opposite ways, with the cortex revealing a higher level of miR‐455‐3p and low‐level NR2B‐PSD‐95‐nNOS complex and the hippocampus showing down‐regulated miR‐455‐3p and up‐regulated NR2B‐PSD‐95‐nNOS complex, indicating a region‐specific change in the miR‐455‐3p and NR2B‐PSD‐95‐nNOS complex in the SCSE depressed rats. Further RHNC results also confirmed down‐regulated miR‐455‐3p and up‐regulated NR2B‐PSD‐95‐nNOS complex expression, similar to the findings in the hippocampus of SCSE rats, suggesting that microgravity influences miR‐455‐3p and associated changes. Additional investigations revealed that miR‐455‐3p targets PSD‐95 and co‐regulates NR2B‐PSD‐95‐nNOS complex along with TrkB–BDNF signaling and exert protective effects against NR2B‐PSD‐95‐nNOS complex, oxidative stress, nitric oxide, inflammatory cytokines, and mitochondrial defects, suggesting a valuable biomarker for devising depressive disorders. Abstract : This study identified that simulated complex space environment causes abnormal expression of miR‐455‐3p in the cortex and hippocampus of the depressed rats, which disturbed NR2B‐PSD95‐nNOS complex function of the cortex and hippocampus and triggered various neuronal pathological events, such as oxidative stress, neuroinflammation, nitric oxide, and mitochondrial biogenesis/dynamics. This resulted in the behavioral abnormalities and depression as a phenotype. Overall, we speculated that miR‐455‐3p might be useful as a biomarker for depressive disorders.