4.5 Article

Saponins from Panax japonicus alleviate HFD-induced impaired behaviors through inhibiting NLRP3 inflammasome to upregulate AMPA receptors

期刊

NEUROCHEMISTRY INTERNATIONAL
卷 148, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2021.105098

关键词

Saponins from panax japonicus; High fat diet; Impaired behavior; NLRP3 inflammasome; AMPA receptor

资金

  1. National Natural Science Foundation of China [NSFC81673778]
  2. Research Fund for Excellent Dissertation of China Three Gorges University [2020SSPY102]
  3. Hubei Province Key Laboratory of Occupational Hazard Identification and Control, Wuhan University of Science and Technology [OHIC2020K01]

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Obesity is associated with behavioral changes such as cognitive decline and depression, with saponins from panax japonicus showing anti-inflammatory effects in a mouse model of diet-induced obesity. The study found that obese mice exhibited behavioral disturbances, neuroinflammation, and neuronal degeneration, which were partly linked to NLRP3 inflammasome activation. Treatment with SPJ alleviated the cognitive impairment and depression-like behaviors induced by high fat diet by suppressing neuroinflammation and modulating AMPA receptors signaling pathway.
Obesity is characterized by a condition of low-grade chronic inflammation that facilitates development of numerous comorbidities and dysregulation of brain homeostasis. It is reported that obesity can lead to behavioral alterations such as cognitive decline and depression-like behaviors both in humans and rodents. Saponins from panax japonicus (SPJ) have been reported to exhibit anti-inflammatory action in mouse model of diet-induced obesity. We evaluated the neuroprotection of SPJ on high fat diet (HFD) induced impaired behaviors such as memory deficit and depressive-like behaviors, and explored the underlying mechanisms. 6-week male Balb/c mice were divided into normal control group (NC, 17% total calories from fat), HFD group (60% total calories from fat), and HFD treated with SPJ groups (orally gavaged with dosages of 15 mg/kg and 45 mg/kg), respectively. After treatment for 16 weeks, behavioral tests were performed to evaluate the cognition and depression-like behaviors of the mice. The underling mechanisms of SPJ on HFD-induced impaired behaviors were investigated through histopathological observation, Western blot analysis and immunofluorescence. Our results showed that HFD-fed mice caused behavioral disorders, neuronal degeneration as well as elevated neuroinflammation, which was partly involved in NLRP3 inflammasome that finally resulted in decreased protein levels of AMPA receptors and down-regulated phosphorylated levels of CaMKII and CREB in cortex and hippocampus. All the above changes in cortex and hippocampus induced by HFD were mitigated by SPJ treatment. SPJ treatment alleviated HFD-induced recognitive impairment and depression-like behaviors of mice, which could be partly due to the capacity of SPJ to mitigate neuroinflammation through inhibition of NLRP3 inflammasome and upregulation of AMPA receptors signaling pathway.

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