神经保护
医学
炎症性肠病
药理学
小胶质细胞
炎症
芍药苷
神经炎症
海马结构
CD86
纳米载体
嗜中性
肠易激综合征
生物利用度
神经药理学
免疫学
神经退行性变
补体系统
硝苯地平
药品
疾病
神经科学
肠粘膜
控制释放
作者
Jing Lu,Kangyu Jin,Bing Chen,Ruoxi Wang,Fengling Hu,Shaohua Hu,Danni Zhong,X Li,M M Zhou
标识
DOI:10.1002/advs.202523551
摘要
Inflammatory bowel disease (IBD) is frequently complicated by comorbid depression and anxiety, creating a therapeutic vicious cycle that is currently managed with fragmented, non-integrated treatments. Here, we introduce a colon-targeted, pH-responsive hydrogel microalgal system (CV@PA-gel) designed for synergistic treatment of IBD and its psychiatric comorbidities. This engineered platform co-encapsulates the natural neuroprotective agent paeoniflorin (PA) and the gut-microbiota modulator Chlorella vulgaris (CV) within a genipin-crosslinked carboxymethyl chitosan/sodium alginate matrix. The CV@PA-gel exhibits minimal drug release in the stomach but provides sustained, targeted release in the colon, significantly enhancing the oral bioavailability and intestinal retention of its cargo. In a murine model of chronic colitis, CV@PA-gel outperforms free PA by more effectively restoring gut barrier integrity, ameliorating systemic and hippocampal inflammation, and rescuing anxiety-, depressive-like, and cognitive behaviors. Mechanistically, our findings suggest that gut-derived systemic inflammation is associated with complement C3 activation and subsequent microglia-mediated polarization of neurotoxic A1 astrocytes in the hippocampus, leading to synaptic loss. PA, delivered precisely by the hydrogel, directly suppresses this cascade by inhibiting microglial release of key A1-inducing factors. Our work establishes a versatile biomaterials strategy for disrupting the gut-brain axis pathology, offering a powerful platform for the simultaneous management of intestinal and neuropsychiatric disorders.
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