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Publication : GABA promotes interstitial fluid clearance in an AQP4-dependent manner by activating the GABA(A) R.

First Author  Wu C Year  2023
Journal  J Neurochem Volume  166
Issue  3 Pages  560-571
PubMed ID  37282785 Mgi Jnum  J:343660
Mgi Id  MGI:7565921 Doi  10.1111/jnc.15869
Citation  Wu C, et al. (2023) GABA promotes interstitial fluid clearance in an AQP4-dependent manner by activating the GABA(A) R. J Neurochem 166(3):560-571
abstractText  The glymphatic system is a newly discovered perivascular network where cerebrospinal fluid mixes with interstitial fluid, facilitating clearance of protein solutes and metabolic waste from the parenchyma. The process is strictly dependent on water channel aquaporin-4 (AQP4) expressed on the perivascular astrocytic end-feet. Various factors, such as noradrenaline levels related to the arousal state, influence clearance efficiency, highlighting the possibility that other neurotransmitters additionally modulate this process. To date, the specific role of gamma-aminobutyric acid (GABA) in the glymphatic system remains unknown. We used C57BL/6J mice to observe the regulatory effect of GABA on glymphatic pathway by administering a cerebrospinal fluid tracer containing GABA or its GABAA receptor (GABA(A) R) antagonist through cisterna magna injection. Then, we employed an AQP4 knockout mouse model to explore the regulatory effects of GABA on glymphatic drainage and further study whether transcranial magnetic stimulation-continuous theta burst stimulation (cTBS) could regulate the glymphatic pathway through the GABA system. Our data showed that GABA promotes glymphatic clearance in an AQP4-dependent manner by activating the GABA(A) R. Furthermore, cTBS was found to modulate the glymphatic pathway by activating the GABA system. Accordingly, we propose that regulating the GABA system by cTBS could modulate glymphatic clearance and provide new insight for clinical prevention and treatment of abnormal protein deposition-related diseases.
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