Journal
CHEMICAL ENGINEERING JOURNAL
Volume 430, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.133090
Keywords
Hyaluronan; Neuregulin 1; Neuroinflammation; Animal model; Alzheimer's disease; Naked mole rats brain microenvironment
Categories
Funding
- National Natural Science Foundation of China [51773050, 51903067]
- Heilongjiang Postdoctoral Fund [LBHZ18068]
- China Postdoctoral Science Foundation [2018 M641837]
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Neuroinflammation plays a crucial role in the progression of Alzheimer's disease by triggering neuropathological amyloid-l3 deposition. Utilizing the unique brain microenvironment characteristics of naked mole rats, researchers developed an injectable hydrogel to alter the brain environment and successfully mitigated Alzheimer's disease progression in mice, showing potential for early intervention strategies.
Neuroinflammation is one of the major processes that trigger neuropathological amyloid-l3 (Al3) deposition and contribute to Alzheimer's disease (AD) progression. Naked mole rats, which are the longest living rodents and exhibit negligible senescence, have a special brain microenvironment characterized by high-molecular-mass hyaluronan (HMM-HA) and high levels of neuregulin 1 (NRG1), which are related to resistance to neuroinflammation and Al3 deposition, leading to protection from AD. Thus, mimicking the unique brain microenvironment of the naked mole rat as a strategy for AD treatment is of critical interest. Here, naked mole rat HMMHA and NRG1 were used to establish an injectable neuroinflammation-responsive triglycerol monostearate (TM)HA-NRG1 hydrogel to alter the brain microenvironment in the early to late stages of AD. Intracerebroventricular (ICV) delivery of the hydrogel resulted in significant mitigation of Al3 plaque formation and complement C1q deposition in the hippocampus. Interestingly, we found that C1q deposition on pericytes was probably associated with capillary dysfunction. Furthermore, continuous intervention obviously reduced C1q deposition on pericytes and improved the oxygen supply to the brain. Importantly, in 16-month-old AD mice, cognitive decline was significantly ameliorated after TM-HA-NRG1 hydrogel treatment. Thus, the work reported here provides a potential early intervention strategy for retarding later AD progression.
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