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Humulus japonicus attenuates LPS-and scopolamine-induced cognitive impairment in mice

Authors :
Jun Go
Hye-Yeon Park
Da Woon Lee
So-Young Maeng
In-Bok Lee
Yun Jeong Seo
Jin-Pyo An
Won Keun Oh
Chul-Ho Lee
Kyoung-Shim Kim
Source :
Laboratory Animal Research. 38
Publication Year :
2022
Publisher :
Springer Science and Business Media LLC, 2022.

Abstract

Background Neuroinflammation plays an important role in cognitive decline and memory impairment in neurodegenerative disorders. Previously, we demonstrated that Humulus japonicus (HJ) has anti-inflammatory effects in rodent models of Alzheimer’s disease and Parkinson’s disease. The present study aimed to examine the protective potential of HJ extracts against lipopolysaccharide (LPS)-induced cognitive impairment and scopolamine-induced amnesia in mouse models. Cognitive improvement of mice was investigated by novel object recognition test. For analyzing effects on neuroinflammation, immunohistochemistry and quantitative real-time polymerase chain reaction (qRT-PCR) assays were performed. Results We found that the oral administration of HJ significantly improved cognitive dysfunction induced by LPS in a novel object recognition test. The LPS-induced activation of microglia was notably decreased by HJ treatment in the cortex and hippocampus. HJ administration with LPS also significantly increased the mRNA expression of interleukin (IL)-10 and decreased the mRNA expression of IL-12 in the parietal cortex of mice. The increased expression of LPS-induced complement C1q B chain (C1bq) and triggering receptor expressed on myeloid cells 2 (Trem2) genes was significantly suppressed by HJ treatment. In addition, HJ administration significantly improved novel object recognition in a scopolamine-induced amnesia mouse model. Conclusions These findings revealed that HJ has a beneficial effect on cognitive impairment and neuroinflammation induced by systemic inflammation and on amnesia induced by scopolamine in mice.

Details

ISSN :
22337660
Volume :
38
Database :
OpenAIRE
Journal :
Laboratory Animal Research
Accession number :
edsair.doi.dedup.....40d80a5d69e9f5cecddc01527302943c