Investigation of the optimal dose for experimental lipopolysaccharide-induced recognition memory impairment: behavioral and histological studies
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Background: Lipopolysaccharide (LPS) administration is one of the most commonly used methods for inducing inflammation in animal models. Several animal studies have investigated the effects of acute and chronic peripheral administration of LPS on cognitive impairment. However, no previous study has compared the effects of different doses of chronically administered LPS on recognition memory performance. Aim: Here, we aimed to investigate the optimal dose of chronically administered LPS for the induction of recognition memory impairment in mice. Materials and methods: LPS at different doses (0.25, 0.50 and 0.75 mg/kg) was administered to SWR/J mice daily for 7 days. On day 9, the open field, novel object recognition and novel arm discrimination behavioral tests were performed. Additionally, prefrontal cortical histological examination was conducted. Results: Compared with the control group, mice injected with 0.75 mg/kg LPS notably showed no object preference (familiar vs. novel), a reduction in the discrimination index, and spatial recognition impairment. Administration of the 0.25 and 0.50 mg/kg doses of LPS showed a preference for the novel object compared with the familiar object, had no significant impact on the discrimination index, and caused spatial recognition impairment. These behavioral results are in line with the histological examination of the prefrontal cortex, which revealed that the 0.75 mg/kg dose produced the most histological damage. Conclusions: Our findings suggest that for chronic peripheral administration of LPS, 0.75 mg/kg is the optimal dose for inducing neuroinflammation-associated recognition memory deficits.
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Inflammation model mice exhibit a decline in cognitive function.
“It has been reported that inflammation model mice exhibit a decline in cognitive function (Alzahrani et al. 2022; Borikar et al. 2022; Skrzypczak-Wiercioch and Sałat 2022).”
From Astrocyte-specific inhibition of the primary cilium suppresses C3 expression in reactive astrocyte (2024) · cites this paper as Alzahrani et al. 2022
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Astrocyte-specific inhibition of the primary cilium suppresses C3 expression in reactive astrocyte
Muhamad, N. A., Masutani, K., Furukawa, S., Yuri, S., Toriyama, M., Matsumoto, C., Itoh, S., Shinagawa, Y., Isotani, A., Toriyama, M., et al. (2024) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-024-01482-5 · Cited by 8 · see citing works
- Authors
- Alzahrani, N. A., Bahaidrah, K. A., Mansouri, R. A., Alsufiani, H. M., & Alghamdi, B. S.
- Affiliations
- King Abdulaziz University (SA)
- Corresponding author
- Alzahrani, Noor Ahmed
- ORCID
- Venue
- Journal of Integrative Neuroscience
- Publisher
- IMR Press
- Published
- 2022-03-21
- Volume
- 21
- Issue
- 2
- Pages
- 49-49
- ISSN
- 0219-6352 (ISSN-L)
- 1757-448X
- OpenAlex
- W4220661307
- Cited by
- 34
- References
- 4
- Citations by year
- 2026: 12 · 2025: 6 · 2024: 10 · 2023: 5 · 2022: 1
- FWCI
- 1.91
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Journal of Integrative Neuroscience (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- lipopolysaccharide, dose optimization, recognition memory impairment, neuroinflammation, novel object recognition, spatial recognition, cognitive impairment, mouse model
- MeSH terms
- Animals, Inflammation, Lipopolysaccharides, Memory Disorders, Recognition, Psychology, Mice, Cognitive Dysfunction
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