A Novel Poly(3-hexylthiophene) Engineered Interface for Electrochemical Monitoring of Ascorbic Acid During the Occurrence of Glutamate-Induced Brain Cytotoxic Edemas

Author:

Meng Zexuan1,Zhang Yuchan1,Yang Lu1,Zhao Shuang23,Zhou Qiang14,Chen Jiajia1,Sui Jiuxi1,Wang Jian1,Guo Lizhong1,Chang Luyue1,He Jialing2,Wang Guixue23,Zang Guangchao134

Affiliation:

1. Institute of Life Science, and Laboratory of Tissue and Cell Biology, Lab Teaching and Management Center, Chongqing Medical University, Chongqing 400016, China.

2. Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing 400030, China.

3. Jinfeng Laboratory, Chongqing 401329, China.

4. Department of Pathophysiology, Chongqing Medical University, Chongqing, China.

Abstract

Although neuroelectrochemical sensing technology offers unique benefits for neuroscience research, its application is limited by substantial interference in complex brain environments while ensuring biosafety requirements. In this study, we introduced poly(3-hexylthiophene) (P3HT) and nitrogen-doped multiwalled carbon nanotubes (N-MWCNTs) to construct a composite membrane-modified carbon fiber microelectrode (CFME/P3HT-N-MWCNTs) for ascorbic acid (AA) detection. The microelectrode presented good linearity, selectivity, stability, antifouling, and biocompatibility and exhibited great performance for application in neuroelectrochemical sensing. Subsequently, we applied CFME/P3HT-N-MWCNTs to monitor AA release from in vitro nerve cells, ex vivo brain slices, and in vivo living rat brains and determined that glutamate can induce cell edema and AA release. We also found that glutamate activated the N -methyl- d -aspartic acid receptor, which enhanced Na + and Cl inflow to induce osmotic stress, resulting in cytotoxic edema and ultimately AA release. This study is the first to observe the process of glutamate-induced brain cytotoxic edema with AA release and to reveal the mechanism. Our work can benefit the application of P3HT in in vivo implant microelectrode construction to monitor neurochemicals, understand the molecular basis of nervous system diseases, and discover certain biomarkers of brain diseases.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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