2. Academic Validation
  3. Agomelatine Targets Aquaporin-4 Polarization to Rescue Glymphatic Dysfunction in Parkinson's Disease

Agomelatine Targets Aquaporin-4 Polarization to Rescue Glymphatic Dysfunction in Parkinson's Disease

  • Neurosci Bull. 2025 Nov 18. doi: 10.1007/s12264-025-01543-9.
Shisi Wang # 1,  Dan Wu # 2,  Guoming Chen # 1,  Jun Yuan 1,  Lu Zheng 1,  Xuehong Huang 1,  Xu Liu 1,  Zhuang Kang 2,  Yiwei Feng 1,  Jialu Zhang 3,  Wei Cai 4 5,  Zhengqi Lu 6,  Lei Wei 7
Affiliations

Affiliations

  • 1 Department of Neurology, Mental and Neurological Disease Research Center, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.
  • 2 Department of Radiology, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.
  • 3 GE Healthcare, MR Research, Beijing, 100176, China.
  • 4 Department of Neurology, Mental and Neurological Disease Research Center, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China. [email protected].
  • 5 Guangdong Provincial Key Laboratory of Brain Function and Disease, Guangzhou, 510630, China. [email protected].
  • 6 Department of Neurology, Mental and Neurological Disease Research Center, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China. [email protected].
  • 7 Department of Neurology, Mental and Neurological Disease Research Center, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China. [email protected].
  • # Contributed equally.
PMID: 41251938 DOI: 10.1007/s12264-025-01543-9
Abstract

Melatonin deficiency in Parkinson's disease (PD) patients correlates with impaired glymphatic function as measured by diffusion tensor imaging along the perivascular space (DTI-ALPS) index, suggesting circadian-regulated waste clearance as a therapeutic target. Unlike previous studies focusing on agomelatine's (AGM) antidepressant and sleep-regulating properties, we demonstrate its novel mechanism in PD treatment through glymphatic enhancement. Retrospective clinical analysis of PD patients revealed that AGM administration restored glymphatic function and improved motor performance. In 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced (MPTP) PD models, AGM alleviated glymphatic dysfunction and anxiety-like behaviors while reducing PD pathology. Crucially, AGM promoted aquaporin-4 (AQP4) polarization at astrocytic endfeet, as evidenced by RNA Sequencing showing enhanced gap junction-related gene expression. The brain and muscle ARNT-like 1 (BMAL1)-mediated transcriptional regulation emerged as the key pathway underlying these effects. Our findings establish AGM as the first melatoninergic agent targeting the glymphatic-AQP4 axis in PD, shifting therapeutic strategies from symptomatic relief to disease modification. This provides clinical rationale for repurposing circadian regulators to decelerate PD progression through enhanced protein clearance.

Keywords

Agomelatine; Aquaporin-4; Glymphatic system; Parkinson’s disease.

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