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Извлечено: 997 / 997 (100.0%) Средняя confidence: 0.13
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Xijiaqi Formula attenuates cognitive dysfunction by inhibiting neuroinflammation and promoting neuroplasticity in rats with chronic heart failure.

PMID: 41571368 · DOI: 10.1016/S1875-5364(26)61078-3 · Chinese journal of natural medicines, 2026 · Jie Chen, Xuefen Wu, Qian Zhang, Hongcai Shang, Wanting Li, Linnan Zhou, Xinyu Chu, Guiyang Xia, Huan Xia, Xiaohong Wei,
📄 Abstract

Chronic heart failure (CHF) impairs cognitive function. Xijiaqi Formula (XJQ), a traditional Chinese medicine (TCM) used clinically to treat CHF, demonstrates potential for improving cognition in CHF patients. However, its precise mechanism in treating post-CHF cognitive dysfunction remains unclear. This study systematically investigates XJQ's effects on post-CHF cognitive dysfunction and the underlying mechanisms. The components of XJQ were identified through liquid chromatography-mass spectrometry. CHF was induced in rats via ligation of the left anterior descending coronary artery, followed by six weeks of XJQ treatment. Cardiac function was evaluated through echocardiography and hemodynamic parameters, while cognitive function was assessed using Morris water maze (MWM) and open field tests (OFT). XJQ treatment enhanced both cardiac and cognitive functions in CHF rats. Network pharmacology identified 12 core active components of XJQ and indicated its effect on cognitive dysfunction involved regulating synapses, inflammation, and phosphodiesterase 4 (PDE4)-dependent cyclic adenosine monophosphate (cAMP) signaling. XJQ inhibited microglial and astrocyte activation, decreased proinflammatory cytokines, and mitigated neuronal damage. Notably, XJQ promoted synaptic repair and dendritic growth by downregulating PDE4 and upregulating cAMP, protein kinase A (PKA), cAMP-response element binding protein (CREB), brain-derived neurotrophic factor (BDNF), PSD95, and synapsin I levels. Molecular docking and Bio-layer interferometry assays confirmed direct binding of quercetin, kaempferol, isorhamnetin, and darutoside to PDE4. In conclusion, XJQ alleviates neuroinflammation and enhances synaptic plasticity to improve cognitive dysfunction in CHF rats via the PDE4/cAMP/PKA/CREB signaling pathway. These findings provide valuable insight into the heart-brain axis.

Confidence: 0.18 · 9 полей извлечено
Идентификация (6 полей)
Target
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Alt. target
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Protein family
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Functional class
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Subcellular loc.
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Isoforms (metab/obesity)
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Механизм действия (21 полей)
Mechanism
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Mutations (obesity/lean)
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Activity (obesity)
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Activity temporal
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Energy balance
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Appetite
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Fat metabolism
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Lipolysis
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Thermogenesis
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Muscle metabolism
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Inflammation
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Glucose metabolism
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AA metabolism
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Hormonal pathways
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Cell death
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Adipocyte fibrosis
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Upstream (biochem)
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Upstream (physiol)
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Downstream (biochem)
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Downstream (physiol)
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PTMs
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Экспрессия (8 полей)
Tissue expression
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In vitro
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In vivo
CHF rat model treated with XJQ; assessed cardiac function (echocardiography, hemodynamics) and cognitive function (Morris water maze, open field test); measured neuroinflammation markers and synaptic plasticity proteins
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In silico
Network pharmacology identified 12 core active components and predicted involvement of synapses, inflammation, and PDE4/cAMP signaling; molecular docking confirmed binding of quercetin, kaempferol, isorhamnetin, darutoside to PDE4
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Genetic association
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Ex vivo
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Animal model
Rats with chronic heart failure induced by ligation of left anterior descending coronary artery
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Diet/model
CHF rat model (ligation of left anterior descending coronary artery) treated with XJQ for six weeks
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Клиника (11 полей)
Drug
Xijiaqi Formula
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Indication
chronic heart failure
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Patient subgroups
patients with chronic heart failure and cognitive dysfunction
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Safety concerns
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Off-target
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Trial stage
preclinical
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Pharma competitors
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AE severity
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MOA weight loss
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Endpoints
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Approved
False
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