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Elevated inflammation in the midbrain of ~ 45% of people with schizophrenia may relate to altered trophic support for neurons in schizophrenia. Dopamine neurons require trophic support from Brain-Derived Neurotrophic Factor (BDNF), that signals via the full-length Tropomyosin kinase B receptor (TrkBTK+). The truncated BDNF receptor (TrkBTK−) may perpetuate neuroinflammation and the apoptosis-related p75 receptor may counteract the effects of BDNF. We hypothesised that transcriptional changes in either BDNF, and/or a transcription factor critical for the maintenance of dopamine neurons (Nuclear Receptor Related-1 protein; NURR1), and/or BDNF receptors – TrkB (TK + or TK-) and p75, would be found in the post-mortem schizophrenia midbrain, particularly in high inflammation cases. Using RT-qPCR, mRNA levels of NURR1, BDNF, TrkB and p75 were quantified from schizophrenia (n = 65) and control (n = 64) ventral mesencephalon. We found significant decreases in BDNF IV, TrkBTK+ and NURR1 (14–18%) and increases in TrkBTK− and p75 (18–35%) mRNA levels in schizophrenia compared to controls (all p < 0.05), with exacerbation in high inflammation schizophrenia. To determine whether these changes result from chronic antipsychotic treatment, we treated healthy adult rats with antipsychotics and found all corresponding trophic mRNAs to be unaltered. SnRNAseq of human midbrain showed that p75 receptor mRNA is primarily localised in oligodendrocytes and pan-TrkB mRNA is distributed to both neurons and astrocytes. We confirmed that p75 was localised to oligodendrocyte-like cells by immunohistochemistry. Altogether, we find transcriptional evidence of reduced levels of trophic support in the midbrain in schizophrenia and suggest that this may directly impact dopamine neuron health, particularly in neuroinflammatory conditions.
Elevated inflammation in the midbrain of ~ 45% of people with schizophrenia may relate to altered trophic support for neurons in schizophrenia. Dopamine neurons require trophic support from Brain-Derived Neurotrophic Factor (BDNF), that signals via the full-length Tropomyosin kinase B receptor (TrkBTK+). The truncated BDNF receptor (TrkBTK−) may perpetuate neuroinflammation and the apoptosis-related p75 receptor may counteract the effects of BDNF. We hypothesised that transcriptional changes in either BDNF, and/or a transcription factor critical for the maintenance of dopamine neurons (Nuclear Receptor Related-1 protein; NURR1), and/or BDNF receptors – TrkB (TK + or TK-) and p75, would be found in the post-mortem schizophrenia midbrain, particularly in high inflammation cases. Using RT-qPCR, mRNA levels of NURR1, BDNF, TrkB and p75 were quantified from schizophrenia (n = 65) and control (n = 64) ventral mesencephalon. We found significant decreases in BDNF IV, TrkBTK+ and NURR1 (14–18%) and increases in TrkBTK− and p75 (18–35%) mRNA levels in schizophrenia compared to controls (all p < 0.05), with exacerbation in high inflammation schizophrenia. To determine whether these changes result from chronic antipsychotic treatment, we treated healthy adult rats with antipsychotics and found all corresponding trophic mRNAs to be unaltered. SnRNAseq of human midbrain showed that p75 receptor mRNA is primarily localised in oligodendrocytes and pan-TrkB mRNA is distributed to both neurons and astrocytes. We confirmed that p75 was localised to oligodendrocyte-like cells by immunohistochemistry. Altogether, we find transcriptional evidence of reduced levels of trophic support in the midbrain in schizophrenia and suggest that this may directly impact dopamine neuron health, particularly in neuroinflammatory conditions.
Schizophrenia is a frequently debilitating and complex mental disorder affecting approximately 1% of the global population, characterized by symptoms such as hallucinations, delusions, disorganized thoughts and behaviors, cognitive dysfunction, and negative symptoms. Traditional treatment has centered on postsynaptic dopamine antagonists, commonly known as antipsychotic drugs, which aim to alleviate symptoms and improve functioning and the quality of life. Despite the availability of these medications, significant challenges remain in schizophrenia therapeutics, including incomplete symptom relief, treatment resistance, and medication side effects. This opinion article explores advancements in schizophrenia treatment, emphasizing molecular mechanisms, novel drug targets, and innovative delivery methods. One promising approach is novel strategies that target neural networks and circuits rather than single neurotransmitters, acknowledging the complexity of brain region interconnections involved in schizophrenia. Another promising approach is the development of biased agonists, which selectively activate specific signaling pathways downstream of receptors, offering potential for more precise pharmacological interventions with fewer side effects. The concept of molecular polypharmacy, where a single drug targets multiple molecular pathways, is exemplified by KarXT, a novel drug combining xanomeline and trospium to address both psychosis and cognitive dysfunction. This approach represents a comprehensive strategy for schizophrenia treatment, potentially improving outcomes for patients. In conclusion, advancing the molecular understanding of schizophrenia and exploring innovative therapeutic strategies hold promise for addressing the unmet needs in schizophrenia treatment, aiming for more effective and tailored interventions. Future research should focus on these novel approaches to achieve better clinical outcomes and improve the functional level and quality of life for individuals with schizophrenia.
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