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RESEARCH PAPER / 2025-12-10

Ganoderma lucidum polysaccharides target the gut-brain axis: Unveiling a novel mechanism for ameliorating aging-induced cognitive impairment and oxidative stress.

Youmeng Chen, Xiaoxiong Zeng, Xinrong Gong, Yili Chen, Xin Zhang, Songmei Luo

Department of Food Science and Engineering, Ningbo University, Ningbo, 315211, PR China; Department of Pharmacy, Lishui Central Hospital, The Fifth Hospital Affiliated to Wenzhou Medical University, Lishui, 323000, PR China. · pubmed

Abstract

With the rapid progression of global population aging, the incidence of cognitive dysfunction-related disorders is steadily increasing. In recent years, growing attention has been directed toward the interaction between the gut microbiota and the central nervous system (CNS). The gut-brain axis (GBA), as a bidirectional communication pathway, plays an increasingly recognized role in regulating cognitive functions. Ganoderma lucidum polysaccharides (GLP), a traditional medicinal and edible substance, can regulate gut microbiota homeostasis and short-chain fatty acid (SCFAs) levels through the GBA. GLP reduces the Firmicutes/Bacteroidetes ratio, significantly increases the abundance of Lactobacillus, and further suppresses oxidative stress and inflammatory responses by controlling microglial overactivation and neuroinflammation, thereby enhancing the expression of synapse-associated proteins and brain-derived neurotrophic factor (BDNF). Consequently, GLP shows potential for improving cognitive dysfunction. This review systematically summarizes the bioactivities of GLP, explores the neurodegenerative mechanisms of aging, and proposes the possibility that GLP mitigates aging-induced inflammation and improves cognitive function via modulation of the gut microbiota.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

Ganoderma lucidum polysaccharides may improve cognitive dysfunction by modulating the gut-brain axis and reducing oxidative stress. The paper addresses mechanisms that could mitigate aging-induced cognitive decline, aligning with longevity research goals.

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