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A Mouse Model of Orthopedic Surgery to Study Postoperative Cognitive Dysfunction and Tissue Regeneration
Published on: February 27, 2018
Enhanced meningeal lymphatic drainage alleviates cognitive dysfunction induced by anesthesia and surgery in aged mice
Yaozong Yu1, Xiang Liu1, Ziyi Zang1
1Department of Anesthesiology, Hebei Medical University Third Hospital, Shijiazhuang, 050051, Hebei Province, PR China.
Abstract:
Postoperative cognitive dysfunction (POCD) occurs in elderly surgical patients as a common complication and manifests as cognitive decline. It is associated with neuroinflammation, microglial activation, and impaired metabolic waste clearance-key mechanisms underlying POCD. Meningeal lymphatic vessels (MLVs) facilitate the drainage of cerebrospinal fluid (CSF) and interstitial fluid (IF), regulating brain immune responses and clearing metabolic waste, immune cells, and antigens, thus modulating neuroinflammation. This study investigates whether enhancing meningeal lymphatic drainage mitigates POCD in aged mice. A POCD mouse model was established via tibial fracture surgery under general anesthesia. Meningeal lymphatic drainage was assessed using immunofluorescence, followed by intra-cisterna magna injection of adeno-associated virus (AAV)-vascular endothelial growth factor-c (AAV-VEGF-C) or AAV-mCherry. Cognitive performance, microglial activation, and pro-inflammatory cytokines were evaluated through behavioral tests, western blotting, and immunofluorescence. Anesthesia and surgery impair the function and morphology of MLVs, leading to reduced lymphatic drainage. These changes were associated with elevated hippocampal expression of microglial activation markers ionized calcium-binding adapter molecule 1 (Iba1) and cluster of differentiation 68 (CD68), as well as increased levels of Interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α), which collectively contributed to cognitive impairment. In contrast, AAV-VEGF-C enhanced meningeal lymphatic drainage by promoting lymphangiogenesis and improving function, reduced microglial activation and neuroinflammation, and improved cognitive outcomes. These findings demonstrate that dysfunction of MLVs exacerbates POCD by amplifying neuroinflammation, while enhancing the function of MLVs mitigates these effects. MLVs represent a promising therapeutic target for managing POCD among the aged.
Insights
Surgery impairs brain lymphatic drainage, worsening cognitive decline in aged mice. Enhancing meningeal lymphatic vessels (MLVs) function with VEGF-C improved drainage, reduced neuroinflammation, and restored cognitive function, offering a new therapeutic target for postoperative cognitive dysfunction (POCD).
Area of Science:
- Neuroscience
- Immunology
- Gerontology
Background:
- Postoperative cognitive dysfunction (POCD) is a common complication in elderly surgical patients, characterized by cognitive decline.
- POCD is linked to neuroinflammation, microglial activation, and impaired waste clearance in the brain.
- Meningeal lymphatic vessels (MLVs) are crucial for draining brain fluids, regulating immune responses, and clearing waste, thereby modulating neuroinflammation.
Purpose of the Study:
- To investigate whether enhancing meningeal lymphatic drainage can mitigate POCD in aged mice.
- To determine the role of MLV function in the development of POCD.
Main Methods:
- Established a POCD mouse model using tibial fracture surgery and general anesthesia.
- Assessed meningeal lymphatic drainage via immunofluorescence.
- Administered adeno-associated virus (AAV)-vascular endothelial growth factor-c (AAV-VEGF-C) to enhance MLV function.
- Evaluated cognitive performance, microglial activation (Iba1, CD68), and pro-inflammatory cytokines (IL-1β, TNF-α) using behavioral tests and western blotting.
Main Results:
- Anesthesia and surgery impaired MLV function and morphology, reducing lymphatic drainage.
- This impairment correlated with increased microglial activation and pro-inflammatory cytokines in the hippocampus, leading to cognitive deficits.
- AAV-VEGF-C treatment enhanced MLV drainage, promoted lymphangiogenesis, reduced neuroinflammation, and improved cognitive outcomes.
Conclusions:
- MLV dysfunction exacerbates POCD by amplifying neuroinflammation.
- Enhancing MLV function mitigates POCD and associated neuroinflammation.
- MLVs present a potential therapeutic target for managing POCD in the elderly population.
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