The Influence of Chemical Precision on Neuroscience Discovery

Research Article
Open access

The Influence of Chemical Precision on Neuroscience Discovery

Mingyuan Zhou 1*
  • 1 Sichuan University    
  • *corresponding author zhoumingyuan@stu.scu.edu.cn
Published on 27 August 2025 | https://doi.org/10.54254/2753-8818/2025.SH26242
TNS Vol.131
ISSN (Print): 2753-8818
ISSN (Online): 2753-8826
ISBN (Print): 978-1-80590-291-1
ISBN (Online): 978-1-80590-292-8

Abstract

This paper explains the importance of chemical precision in neuroscience research and details the selection and optimization of research methodologies. By reviewing and analyzing related papers, this paper firstly explains the importance of chemical precision in neuroscience research and describes in detail the selection and optimization of research methodologies. The importance of chemical precision in neuroscience research is first explained, and the selection and optimization of the research method are described in detail. The study demonstrates that improved chemical precision significantly enhances both the effectiveness and the reliability of neuroscience research, thereby increasing the reproducibility of experimental data and facilitating new scientific discoveries. The paper concludes by summarizing the main contributions of the study while proposing a new approach to neuroscience alongside directions for future research and policy recommendations.

Keywords:

Chemical Precision, Neuroscience, Research Method, Data Reliability, New Findings

Zhou,M. (2025). The Influence of Chemical Precision on Neuroscience Discovery. Theoretical and Natural Science,131,67-73.
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1. Introduction

With the advancement of technology and the deepening of scientific research, chemical precision has become a critical driving force in the development of neuroscience. In this field, precision not only affects the accuracy of experimental data but also determines the reliability, reproducibility, and interpretability of research outcomes. From improved analytical techniques to emerging tools such as high-resolution imaging and single-cell sequencing, advances in chemical methodologies have significantly enhanced our understanding of brain mechanisms and facilitated the development of new therapies for neurodegenerative diseases. Furthermore, the growing demand for precise experimental design, particularly in areas such as cellular signal transduction and brain functional imaging, highlights the increasing relevance of chemical accuracy in neuroscience. As interdisciplinary research becomes more prevalent, the role of chemical precision extends beyond chemistry, offering methodological insights and practical value to neuroscience and related fields. This review aims to explore how advancements in chemical precision contribute to neuroscientific discovery, emphasizing their impact on experimental reliability, biomarker identification, and translational potential. By clarifying these relationships, the paper seeks to provide a theoretical foundation and practical guidance for future interdisciplinary research in neuroscience.

2. The theoretical basis and the innovation of legal theory

2.1. The importance of research

Chemical precision plays a vital role in the advancement of neuroscience research. It not only affects the accuracy and reliability of experimental data but also directly influences the quality, depth, and reproducibility of scientific discoveries [1]. In recent years, with rapid technological progress and increasing methodological diversity, improving chemical precision has become a central focus for scientists in this field [2].

As scientific research continues to evolve, the enhancement of chemical precision has emerged as a key driver of breakthroughs in neuroscience [1]. Technological advances in areas such as fractionation, cell biology, and chemical analysis have enabled researchers to explore the structure and function of the brain with unprecedented clarity and depth [3,4]. These improvements not only strengthen the precision of data but also deepen our understanding of the complexity of the nervous system. However, despite these advancements, neuroscience research continues to face significant challenges, including the intricacies of experimental design, the accuracy of data collection, and the interpretation of complex and often heterogeneous results [5,6]. These issues can compromise the reliability of findings and hinder progress in subsequent studies. Therefore, improving chemical precision is not only essential for producing more accurate and reproducible results but also serves as a catalyst for the development of innovative methodologies and technologies. This, in turn, promotes the overall advancement of neuroscience as a discipline [7,8].

2.2. Research on the classification and selection of method

This part will discuss how different research methods affect the influence of chemical precision on neuroscience research. B.S. Somashekar et al. developed a simple pulse-acquired nuclear magnetic resonance (NMR) method to accurately quantify the calcium, magnesium, and sodium in the -like, which improves the accuracy and precision of the method [9]. On this basis, Holmes Elaine et al. combined 1H NMR spectroscopy with computerized pattern recognition analysis to investigate the cerebrospinal fluid metabolic profiles of the first-episode paranoid schizophrenia patients and healthy controls who were not treated or slightly treated with drugs [10]. The results showed that early pre-treatment may affect disease progression and outcome. In addition, Benjamin Albrecht et al. proposed the -effect protocol for an NMR metabolomics study of cerebrospinal fluid samples, aiming to improve the repeatability of the experiment through standardized operation procedures, and discussed the optimal conditions for sample preparation and pH control [6]. In summary, these research methods not only improve the chemical precision, but also provide reliable data for the discovery of neuroscience, which promotes the development of this field.

2.3. The innovation and challenge of legal theory

2.3.1. The innovative formula of the theory of law

This part will discuss how the innovation in the theory of law can improve the chemical precision and affect the discovery of neuroscience research. Crews Bridgit et al. revealed the statistical significance of changes in mass spectrometry-based metabolomics data by analyzing the variability of plasma and cerebrospinal fluid, indicating the importance of precise control of sample processing conditions. On this basis, Benjamin Albrecht et al. proposed a protocol for the preparation of cerebrospinal fluid samples, which was based on nuclear magnetic resonance (NMR)-based metabolomics research, and evaluated the effects of pH control and temperature dependence on sample stability during sample preservation. The impact of this has achieved a more significant improvement in spectral data and overall sample stability. In addition, Williams Michael emphasized the importance of verification reagents for improving the repeatability of the experiment, pointing out that the lack of verification reagents will negatively affect the reproducibility of the experimental results. In summary, these studies highlight the importance of methodological innovations for improving chemical precision and neuroscientific findings, and emphasize the importance of standardized operating procedures and experimental reagent verification in ensuring the reliability and repeatability of experimental results.

2.3.2. Challenges ahead

This part will explore the influence of chemical precision on neuroscience research, especially the challenges of reliability and experimental transparency. Lindsley Craig W proposes in his chapter criteria for improving the findings of studies published in the journal ACS Chemical Neuroscience, including new criteria to enhance reproducibility, experimental transparency, reliability, and the value of negative data. This shows the importance of chemical precision in neuroscience research. In addition, Zewen Zhang et al. discussed the cross-talk between immunology and neuroscience in the tumor microenvironment. Although this is mainly focused on the field of biology, it also emphasizes the importance of interdisciplinary cooperation in solving complex disease mechanisms, in which chemical precision is an indispensable tool. In summary, chemical precision is of great significance for the discovery of the field of neuroscience, especially in improving the reliability of research results and experimental transparency. It is necessary to strengthen interdisciplinary cooperation and standardized processes.

2.3.3. Selection and optimization of legal theory

This section will discuss the importance of selecting and optimizing the method theory in neuroscience research to improve the accuracy and repeatability of experimental results. Holmes Elaine et al. studied 152 cerebrospinal fluid samples by 1H nuclear magnetic resonance spectroscopy combined with computerized pattern recognition analysis, and found that early treatment may affect the progression and outcome of schizophrenia, which indicates that early treatment is important for improving the prognosis of psychiatric patients. In addition, Victoria G. Dunne et al. used multivariate statistics and 1H nuclear magnetic resonance spectroscopy to study the metabolites in the cerebrospinal fluid of patients with subarachnoid hemorrhage, successfully predicted the clinical results of patients, and revealed the potential of metabolomics in the diagnosis of neurological diseases. Furthermore, Crews Bridgit et al. used the global liquid chromatography/mass spectrometry metabolomics strategy to evaluate the analysis and variability of in the slurry and cerebrospinal fl. This paper explains the importance of chemical precision in neuroscience research and details the selection and optimization of research methodologies, and found that the metabolomics platform had good reproducibility, which provided a solid foundation for the discovery of markers. Finally, Benjamin Albrecht et al. proposed a new NMR generation. The protocol for the preparation of cerebrospinal fluid samples emphasizes the importance of standardized operation procedures to achieve the consistency and stability of sample processing.

3.  Analysis of research results

3.1. Comprehensive review of the research results

This part will comprehensively review the influence of chemical precision on neuroscience research. First, Cloarec Olivier et al. proposed the statistical total correlation spectroscopy (STOCSY) [11], which is based on the 1H NMR data set of metabolomics to identify the potential biomarkers. By combining supervised pattern recognition and orthogonal partial least squares discriminant analysis (O-PLS-DA), this method provides a strong framework for metabolomics data analysis. In addition, Victoria G. Dunne et al. used 1H NMR spectroscopy and multivariate statistical analysis to study the relationship between metabolites in cerebrospinal fluid and clinical results in patients with subarachnoid hemorrhage [12]. The results showed that the method could predict the clinical results of patients and confirm the existence of subarachnoid hemorrhage. Furthermore, Benjamin Albrecht et al. proposed a protocol to address the heterogeneity of sample preparation in NMR metabolomics studies [6], aiming to solve the problem of sample degradation and improve the repeatability of experiments. By monitoring the sample degradation process, they identified some metabolic candidates that may be affected by sample storage. In summary, these studies highlight the importance of chemical precision in neuroscience research, especially in the identification of biomarkers and experimental repeatability, and emphasize the importance of developing a unified standard operating procedure to facilitate inter-laboratory data comparison and sharing.

3.2. Significance of the findings

This part will discuss the influence of chemical precision on the results of neuroscience research. Through systematic review and meta-analysis, Steen R Grant et al. evaluated the application of 1H magnetic resonance spectroscopy in patients with schizophrenia and found that N-acyl γ-glutamic acid was generally reduced in the brain of patients with schizophrenia[13], indicating that the chemical measurement of γ-glutamic acid accuracy is of great significance for understanding mental illness. In addition, Victoria G. Dunne et al. studied the metabolites of cerebrospinal fluid in patients with subarachnoid hemorrhage by 1H nuclear magnetic resonance spectroscopy and multivariate statistical analysis, revealed the correlation between metabolite concentration and clinical results, and further demonstrated the value of precise chemical measurement in predicting the prognosis of patients [11]. Furthermore, Shayne Mason et al. identified the drug components in the cerebrospinal fluid of meningitis cases by 1H nuclear magnetic resonance spectroscopy, and demonstrated the potential of precise chemical measurement in neurological diagnosis. In summary, chemical precision plays an important role in neuroscience research. It not only contributes to the early diagnosis of diseases, but also improves the reliability and repeatability of research results, and promotes the progress of neuroscience.

3.3. Embodiment of research contributions

This chapter focuses on how chemical precision affects discoveries in the field of neuroscience, especially the importance of repeatability, reliability, and transparency of studies. Lindsley Craig W. proposed new standards to improve the standards of chemical neuroscience discovery [14], enhance the repeatability, transparency, and reliability of experiments, and increase the value of negative data. These criteria are of great significance for research in the field of neuroscience, because they are directly related to the quality and verifiability of the research results. In addition, Elena Voronina et al. did not provide research on the direct effect of chemical precision on neuroscience, but their work emphasized the importance of experimental preparation, especially the processing of CSF samples in NMR metabolomics [6], which is important to ensure the data Ω and stability. Kuo Chang Hung et al. focused on macrophage polarization as a biomarker of the severity of asthma in children [15]. Although this is not directly related to chemical precision, it emphasizes the importance of accurate experimental design and manipulation in obtaining reliable data. In summary, chemical precision plays a key role in ensuring the quality and repeatability of neuroscience research. Through the new standard proposed by Lindsley Craig W., researchers were encouraged to adopt a more rigorous and standardized experimental design and data analysis method, which doubted the reliability and value of neuroscience findings. Therefore, chemical precision is a factor that cannot be ignored to promote the development of neuroscience.

3.4. Research innovations

This chapter reviews the application of chemical precision in neuroscience research and its influence on the discovery of new biomarkers. Crews et al. adopted. In addition, the study of Kuo et al. focused on the changes of macrophage polarization state by flow cytometry in the study of childhood asthma, which may be used as biomarkers to measure the severity of asthma. This indicates the importance of chemical precision in the accurate measurement. Finally, Lindsley Craig W emphasized the importance of improving the repeatability, transparency, and reliability of experiments in chemical neuroscience research [7], which also includes the precision requirements for chemical experiments. These studies have shown that chemical precision not only affects the accuracy of a single experiment, but also plays an important role in the development of the whole research field and the newly discovered push.

4. Conclusion

In this paper, by reviewing recent advancements and representative studies, we conclude that chemical precision significantly enhances the accuracy, reproducibility, and interpretability of neuroscience research. Improved chemical analysis allows for more detailed exploration of interactions between neurotransmitters, neuroactive compounds, and their receptors, which is essential for understanding neural mechanisms. Moreover, the integration of chemical precision with disciplines such as biology and informatics has enriched both experimental approaches and data interpretation models.

Despite this progress, challenges remain. These include the technical complexity and high cost of precision instruments, limited accessibility across research settings, and insufficient standardization of experimental protocols. Future research should focus on developing low-cost, user-friendly chemical analysis technologies and advancing their integration with other scientific tools. Additionally, in the era of big data, there is a pressing need to link chemical analysis results with bioinformatics and computational models to facilitate systems-level understanding. Investment in methodological innovation and interdisciplinary collaboration will be key to further accelerating discoveries in neuroscience.

Overall, this paper concludes that chemical precision plays a vital role in advancing neuroscience by enhancing experimental accuracy, reproducibility, and translational value. However, there are still some limitations in this review. First, the discussion is primarily based on a qualitative synthesis of existing literature, lacking a quantitative meta-analysis to systematically evaluate the strength of evidence across studies. Second, although the paper highlights several methodological advances, it does not delve deeply into the limitations of current chemical technologies when applied to diverse neural systems or pathological conditions. Third, the interdisciplinary implications—particularly in the context of bioinformatics and systems neuroscience—are proposed conceptually but not substantiated with concrete case studies or comparative evaluations.

In the future, this study will aim to address these limitations by incorporating more quantitative data, conducting case-based analyses, and exploring the practical applications of chemical precision tools in specific neuroscience subfields such as neuroimmunology, neurodegeneration, and neural circuit mapping. Moreover, future research should investigate how chemical precision can be standardized across laboratories to enhance cross-study comparability. Strengthening the integration of chemical methods with computational models and AI-based analysis may also serve as a promising direction for translating chemical precision into clinically meaningful outcomes.


References

[1]. Alayli, A. E., Numan, L., Chen, Y., et al. (2023). Sa1407 Procalcitonin as a biomarker for severity of pancreatitis: A systematic review and meta-analysis. Gastroenterology, 164(6), S-384. https: //doi.org/10.1016/S0016-5085(23)01893-0

[2]. Dujmovic, I., & Deisenhammer, F. (2010). Stability of cerebrospinal fluid/serum glucose ratio and cerebrospinal fluid lactate concentrations over 24 h: Analysis of repeated measurements. Clinical Chemistry and Laboratory Medicine, 48(2), 209–212. https: //doi.org/10.1515/CCLM.2010.040

[3]. Floare, C. G., Bogdan, M., Tomoaia-Cotişel, M., et al. (2022). 1H NMR spectroscopic characterization of inclusion complex of desferrioxamine B chelator and β-cyclodextrin. Journal of Molecular Structure, 1248, 131477. https: //doi.org/10.1016/j.molstruc.2021.131477

[4]. Metabolic profiling of CSF: Evidence that early intervention may impact on disease progression and outcome in schizophrenia. (2006). PLoS Medicine, 3(8). Retrieved July 30, 2025, from https: //kns.cnki.net/kcms2/article/abstract?v=tMRSZR5ycIsmHc-Ndz6WgSdBcGK_hW_5Wf9xT9-ga3ILrzOAwVCyG_y7zWW1U0WuEpCBOQxn_kgR3dKlaYV-wIbELzpmZsNT6gp-LKtzDHOXA2TSXFJQFElmMjINZDbO34gB1bVzk5jdb2tE867IhHlULeQGBJAYCA-VxY3PkG3ubbOLazUYZomYOv85RUOfUs8AO0CKerRznWIxSVpwCRAF_8SjMixL

[5]. Jukarainen, N. M., Korhonen, S. P., Laakso, M. P., et al. (2008). Quantification of 1H NMR spectra of human cerebrospinal fluid: A protocol based on constrained total-line-shape analysis. Metabolomics, 4(2), 150-160. https: //doi.org/10.1007/s11306-008-0106-6

[6]. Kuo, C. H., Tsai, M. L., Li, C. H., et al. (2021). Altered pattern of macrophage polarization as a biomarker for severity of childhood asthma. Journal of Inflammation Research, 14, 6011-6023. https: //doi.org/10.2147/JIR.S319754

[7]. Crews, B., Wikoff, W. R., Patti, G. J., et al. (2009). Variability analysis of human plasma and cerebral spinal fluid reveals statistical significance of changes in mass spectrometry-based metabolomics data. Analytical Chemistry, 81(20), 8538–8544. https: //doi.org/10.1021/ac9014947

[8]. Lee, H., Hedtmann, G., Schwab, S., et al. (2021). Effects of a 4-step standard operating procedure for the treatment of fever in patients with acute stroke. Frontiers in Neurology, 12, 614266. https: //doi.org/10.3389/fneur.2021.614266

[9]. Albrecht, B., Voronina, E., Schipke, C., et al. (2020). Pursuing experimental reproducibility: An efficient protocol for the preparation of cerebrospinal fluid samples for NMR-based metabolomics and analysis of sample degradation. Metabolites, 10(6), 251. https: //doi.org/10.3390/metabo10060251

[10]. Boyles, M., Murphy, F., Mueller, W., et al. (2022). Development of a standard operating procedure for the DCFH₂-DA acellular assessment of reactive oxygen species produced by nanomaterials. Toxicology Mechanisms and Methods, 32(6), 439-452. https: //doi.org/10.1080/15376516.2022.2029656

[11]. Shilston, J., Gibbon, G., & Banks. (2021). A retrospective case review and development of a standard operating procedure for the airway management of patients with acute high spinal cord injury admitted to adult intensive care in Nottingham University Hospital. Anaesthesia, 76, 113.

[12]. Blasco, H., Nadal-Desbarats, L., Pradat, P. F., et al. (2014). Untargeted 1H-NMR metabolomics in CSF: Toward a diagnostic biomarker for motor neuron disease. Neurology, 82(13), 1167-1174. https: //doi.org/10.1212/WNL.0000000000000274

[13]. Sadhanala, H. K., Pagidi, S., & Gedanken, A. (2021). High quantum yield boron-doped carbon dots: A ratiometric fluorescent probe for highly selective and sensitive detection of Mg2+ions. Journal of Materials Chemistry C, 9(5), 1632–1640. https: //doi.org/10.1039/D0TC05081D

[14]. Dunne, V. G., Bhattachayya, S., Besser, M., et al. (2005). Metabolites from cerebrospinal fluid in aneurysmal subarachnoid haemorrhage correlate with vasospasm and clinical outcome: A pattern-recognition 1H NMR study. NMR in Biomedicine, 18(1), 24-33. https: //doi.org/10.1002/nbm.918

[15]. Kobayashi, R., & Nakae, K. (2025). Editorial: Does big data change neuroscience? Neuroscience Research, 215, 1-2. https: //doi.org/10.1016/j.neures.2025.04.007


Cite this article

Zhou,M. (2025). The Influence of Chemical Precision on Neuroscience Discovery. Theoretical and Natural Science,131,67-73.

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Volume title: Proceedings of ICBioMed 2025 Symposium: Interdisciplinary Frontiers in Pharmaceutical Sciences

ISBN:978-1-80590-291-1(Print) / 978-1-80590-292-8(Online)
Editor:Alan Wang, Xiangdong Xue
Conference date: 11 September 2025
Series: Theoretical and Natural Science
Volume number: Vol.131
ISSN:2753-8818(Print) / 2753-8826(Online)

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References

[1]. Alayli, A. E., Numan, L., Chen, Y., et al. (2023). Sa1407 Procalcitonin as a biomarker for severity of pancreatitis: A systematic review and meta-analysis. Gastroenterology, 164(6), S-384. https: //doi.org/10.1016/S0016-5085(23)01893-0

[2]. Dujmovic, I., & Deisenhammer, F. (2010). Stability of cerebrospinal fluid/serum glucose ratio and cerebrospinal fluid lactate concentrations over 24 h: Analysis of repeated measurements. Clinical Chemistry and Laboratory Medicine, 48(2), 209–212. https: //doi.org/10.1515/CCLM.2010.040

[3]. Floare, C. G., Bogdan, M., Tomoaia-Cotişel, M., et al. (2022). 1H NMR spectroscopic characterization of inclusion complex of desferrioxamine B chelator and β-cyclodextrin. Journal of Molecular Structure, 1248, 131477. https: //doi.org/10.1016/j.molstruc.2021.131477

[4]. Metabolic profiling of CSF: Evidence that early intervention may impact on disease progression and outcome in schizophrenia. (2006). PLoS Medicine, 3(8). Retrieved July 30, 2025, from https: //kns.cnki.net/kcms2/article/abstract?v=tMRSZR5ycIsmHc-Ndz6WgSdBcGK_hW_5Wf9xT9-ga3ILrzOAwVCyG_y7zWW1U0WuEpCBOQxn_kgR3dKlaYV-wIbELzpmZsNT6gp-LKtzDHOXA2TSXFJQFElmMjINZDbO34gB1bVzk5jdb2tE867IhHlULeQGBJAYCA-VxY3PkG3ubbOLazUYZomYOv85RUOfUs8AO0CKerRznWIxSVpwCRAF_8SjMixL

[5]. Jukarainen, N. M., Korhonen, S. P., Laakso, M. P., et al. (2008). Quantification of 1H NMR spectra of human cerebrospinal fluid: A protocol based on constrained total-line-shape analysis. Metabolomics, 4(2), 150-160. https: //doi.org/10.1007/s11306-008-0106-6

[6]. Kuo, C. H., Tsai, M. L., Li, C. H., et al. (2021). Altered pattern of macrophage polarization as a biomarker for severity of childhood asthma. Journal of Inflammation Research, 14, 6011-6023. https: //doi.org/10.2147/JIR.S319754

[7]. Crews, B., Wikoff, W. R., Patti, G. J., et al. (2009). Variability analysis of human plasma and cerebral spinal fluid reveals statistical significance of changes in mass spectrometry-based metabolomics data. Analytical Chemistry, 81(20), 8538–8544. https: //doi.org/10.1021/ac9014947

[8]. Lee, H., Hedtmann, G., Schwab, S., et al. (2021). Effects of a 4-step standard operating procedure for the treatment of fever in patients with acute stroke. Frontiers in Neurology, 12, 614266. https: //doi.org/10.3389/fneur.2021.614266

[9]. Albrecht, B., Voronina, E., Schipke, C., et al. (2020). Pursuing experimental reproducibility: An efficient protocol for the preparation of cerebrospinal fluid samples for NMR-based metabolomics and analysis of sample degradation. Metabolites, 10(6), 251. https: //doi.org/10.3390/metabo10060251

[10]. Boyles, M., Murphy, F., Mueller, W., et al. (2022). Development of a standard operating procedure for the DCFH₂-DA acellular assessment of reactive oxygen species produced by nanomaterials. Toxicology Mechanisms and Methods, 32(6), 439-452. https: //doi.org/10.1080/15376516.2022.2029656

[11]. Shilston, J., Gibbon, G., & Banks. (2021). A retrospective case review and development of a standard operating procedure for the airway management of patients with acute high spinal cord injury admitted to adult intensive care in Nottingham University Hospital. Anaesthesia, 76, 113.

[12]. Blasco, H., Nadal-Desbarats, L., Pradat, P. F., et al. (2014). Untargeted 1H-NMR metabolomics in CSF: Toward a diagnostic biomarker for motor neuron disease. Neurology, 82(13), 1167-1174. https: //doi.org/10.1212/WNL.0000000000000274

[13]. Sadhanala, H. K., Pagidi, S., & Gedanken, A. (2021). High quantum yield boron-doped carbon dots: A ratiometric fluorescent probe for highly selective and sensitive detection of Mg2+ions. Journal of Materials Chemistry C, 9(5), 1632–1640. https: //doi.org/10.1039/D0TC05081D

[14]. Dunne, V. G., Bhattachayya, S., Besser, M., et al. (2005). Metabolites from cerebrospinal fluid in aneurysmal subarachnoid haemorrhage correlate with vasospasm and clinical outcome: A pattern-recognition 1H NMR study. NMR in Biomedicine, 18(1), 24-33. https: //doi.org/10.1002/nbm.918

[15]. Kobayashi, R., & Nakae, K. (2025). Editorial: Does big data change neuroscience? Neuroscience Research, 215, 1-2. https: //doi.org/10.1016/j.neures.2025.04.007