Potential probiotic (L. plantarum, L. pentosus, P. pentosaceus, W. cibaria and L. rhamnosus) alleviates memory impairment in lipopolysaccharide‐induced cognitive dysfunction and neurotoxicity in mice brain via protection against neuroinflammation and neurodegeneration

Background The impact of probiotics as gut and immunological modulator in restoring gut microbial balance and immune cells expression have generated much attention in the health sector. Its inhibitory effect on bacterial translocation and associated neural inflammatory processes has been reported. H...

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Veröffentlicht in:Alzheimer's & dementia 2024-12, Vol.20 (S6), p.n/a
Hauptverfasser: Obisesan, Abiola Oluwatosin, Dodo, Samuel O, Adeniyi, Funmilayo Racheal, Olayinka, Juliet Nnenda, Adeoluwa, Olusegun Adebayo, Fafure, Adedamola O
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container_end_page n/a
container_issue S6
container_start_page
container_title Alzheimer's & dementia
container_volume 20
creator Obisesan, Abiola Oluwatosin
Dodo, Samuel O
Adeniyi, Funmilayo Racheal
Olayinka, Juliet Nnenda
Adeoluwa, Olusegun Adebayo
Fafure, Adedamola O
description Background The impact of probiotics as gut and immunological modulator in restoring gut microbial balance and immune cells expression have generated much attention in the health sector. Its inhibitory effect on bacterial translocation and associated neural inflammatory processes has been reported. However, there is scarcity of data on its neuroprotective impact against neuroinflammation‐associated neurodegeneration and memory impairment. Therefore, we tested the neuroprotective capabilities of the probiotic strains against lipopolysaccharide (LPS)‐induced neurotoxicity and memory impairment in mice. Method Forty eight mice (n = 12) weighing 25 ‐ 30 g were randomly classified into four groups consisting of probiotic strains (107 CFU/ml, orally), donepezil (3 mg/kg, intraperitoneally (i.p.)), normal saline (10 ml/kg, orally), and LPS (0.25 mg/kg i.p) group. LPS was injected 60 min after treatments for seven days. Novel object recognition (NORT) and Y‐maze tests were performed 24 h following the last treatment to assess cognitive functions. Dendritic spine of the dentate gyrus was stained with Golgi cox. Immunohistochemistry detected brain‐derived neurotrophic factor (BDNF) expression as well as Iba 1 and amyloid beta activation in the hippocampus and prefrontal cortex, while enzyme‐linked immunosorbent assay was used to measure neuroinflammation (tumor necrosis factor‐α (TNF‐α), interleukin‐1 beta (IL‐1β), interleukin‐12 (IL‐12), and interferon gamma (IFN‐γ)) and oxidative stress biomarkers (glutathione (GSH) and malondialdehyde (MDA)). Result Probiotics reduced elevation of pro‐inflammatory cytokines, MDA levels and enhanced GSH levels in the brain. Probiotic strains enhanced BDNF expressions, reduced microglia and amyloid beta activation in the hippocampus and prefrontal cortex of LPS‐induced mice. Conclusion These finding show that probiotic strains may possess neuroprotective effect against LPS‐induced cognitive impairment and neurodegeneration via antioxidant and anti‐inflammatory mechanisms.
doi_str_mv 10.1002/alz.089920
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Its inhibitory effect on bacterial translocation and associated neural inflammatory processes has been reported. However, there is scarcity of data on its neuroprotective impact against neuroinflammation‐associated neurodegeneration and memory impairment. Therefore, we tested the neuroprotective capabilities of the probiotic strains against lipopolysaccharide (LPS)‐induced neurotoxicity and memory impairment in mice. Method Forty eight mice (n = 12) weighing 25 ‐ 30 g were randomly classified into four groups consisting of probiotic strains (107 CFU/ml, orally), donepezil (3 mg/kg, intraperitoneally (i.p.)), normal saline (10 ml/kg, orally), and LPS (0.25 mg/kg i.p) group. LPS was injected 60 min after treatments for seven days. Novel object recognition (NORT) and Y‐maze tests were performed 24 h following the last treatment to assess cognitive functions. Dendritic spine of the dentate gyrus was stained with Golgi cox. Immunohistochemistry detected brain‐derived neurotrophic factor (BDNF) expression as well as Iba 1 and amyloid beta activation in the hippocampus and prefrontal cortex, while enzyme‐linked immunosorbent assay was used to measure neuroinflammation (tumor necrosis factor‐α (TNF‐α), interleukin‐1 beta (IL‐1β), interleukin‐12 (IL‐12), and interferon gamma (IFN‐γ)) and oxidative stress biomarkers (glutathione (GSH) and malondialdehyde (MDA)). Result Probiotics reduced elevation of pro‐inflammatory cytokines, MDA levels and enhanced GSH levels in the brain. Probiotic strains enhanced BDNF expressions, reduced microglia and amyloid beta activation in the hippocampus and prefrontal cortex of LPS‐induced mice. Conclusion These finding show that probiotic strains may possess neuroprotective effect against LPS‐induced cognitive impairment and neurodegeneration via antioxidant and anti‐inflammatory mechanisms.</description><identifier>ISSN: 1552-5260</identifier><identifier>EISSN: 1552-5279</identifier><identifier>DOI: 10.1002/alz.089920</identifier><identifier>PMID: 39782609</identifier><language>eng</language><publisher>Hoboken: John Wiley and Sons Inc</publisher><subject>Drug Development</subject><ispartof>Alzheimer's &amp; dementia, 2024-12, Vol.20 (S6), p.n/a</ispartof><rights>2024 The Alzheimer's Association. published by Wiley Periodicals LLC on behalf of Alzheimer's Association.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11713413/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11713413/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids></links><search><creatorcontrib>Obisesan, Abiola Oluwatosin</creatorcontrib><creatorcontrib>Dodo, Samuel O</creatorcontrib><creatorcontrib>Adeniyi, Funmilayo Racheal</creatorcontrib><creatorcontrib>Olayinka, Juliet Nnenda</creatorcontrib><creatorcontrib>Adeoluwa, Olusegun Adebayo</creatorcontrib><creatorcontrib>Fafure, Adedamola O</creatorcontrib><title>Potential probiotic (L. plantarum, L. pentosus, P. pentosaceus, W. cibaria and L. rhamnosus) alleviates memory impairment in lipopolysaccharide‐induced cognitive dysfunction and neurotoxicity in mice brain via protection against neuroinflammation and neurodegeneration</title><title>Alzheimer's &amp; dementia</title><description>Background The impact of probiotics as gut and immunological modulator in restoring gut microbial balance and immune cells expression have generated much attention in the health sector. Its inhibitory effect on bacterial translocation and associated neural inflammatory processes has been reported. However, there is scarcity of data on its neuroprotective impact against neuroinflammation‐associated neurodegeneration and memory impairment. Therefore, we tested the neuroprotective capabilities of the probiotic strains against lipopolysaccharide (LPS)‐induced neurotoxicity and memory impairment in mice. Method Forty eight mice (n = 12) weighing 25 ‐ 30 g were randomly classified into four groups consisting of probiotic strains (107 CFU/ml, orally), donepezil (3 mg/kg, intraperitoneally (i.p.)), normal saline (10 ml/kg, orally), and LPS (0.25 mg/kg i.p) group. LPS was injected 60 min after treatments for seven days. Novel object recognition (NORT) and Y‐maze tests were performed 24 h following the last treatment to assess cognitive functions. Dendritic spine of the dentate gyrus was stained with Golgi cox. Immunohistochemistry detected brain‐derived neurotrophic factor (BDNF) expression as well as Iba 1 and amyloid beta activation in the hippocampus and prefrontal cortex, while enzyme‐linked immunosorbent assay was used to measure neuroinflammation (tumor necrosis factor‐α (TNF‐α), interleukin‐1 beta (IL‐1β), interleukin‐12 (IL‐12), and interferon gamma (IFN‐γ)) and oxidative stress biomarkers (glutathione (GSH) and malondialdehyde (MDA)). Result Probiotics reduced elevation of pro‐inflammatory cytokines, MDA levels and enhanced GSH levels in the brain. Probiotic strains enhanced BDNF expressions, reduced microglia and amyloid beta activation in the hippocampus and prefrontal cortex of LPS‐induced mice. 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Its inhibitory effect on bacterial translocation and associated neural inflammatory processes has been reported. However, there is scarcity of data on its neuroprotective impact against neuroinflammation‐associated neurodegeneration and memory impairment. Therefore, we tested the neuroprotective capabilities of the probiotic strains against lipopolysaccharide (LPS)‐induced neurotoxicity and memory impairment in mice. Method Forty eight mice (n = 12) weighing 25 ‐ 30 g were randomly classified into four groups consisting of probiotic strains (107 CFU/ml, orally), donepezil (3 mg/kg, intraperitoneally (i.p.)), normal saline (10 ml/kg, orally), and LPS (0.25 mg/kg i.p) group. LPS was injected 60 min after treatments for seven days. Novel object recognition (NORT) and Y‐maze tests were performed 24 h following the last treatment to assess cognitive functions. Dendritic spine of the dentate gyrus was stained with Golgi cox. Immunohistochemistry detected brain‐derived neurotrophic factor (BDNF) expression as well as Iba 1 and amyloid beta activation in the hippocampus and prefrontal cortex, while enzyme‐linked immunosorbent assay was used to measure neuroinflammation (tumor necrosis factor‐α (TNF‐α), interleukin‐1 beta (IL‐1β), interleukin‐12 (IL‐12), and interferon gamma (IFN‐γ)) and oxidative stress biomarkers (glutathione (GSH) and malondialdehyde (MDA)). Result Probiotics reduced elevation of pro‐inflammatory cytokines, MDA levels and enhanced GSH levels in the brain. Probiotic strains enhanced BDNF expressions, reduced microglia and amyloid beta activation in the hippocampus and prefrontal cortex of LPS‐induced mice. Conclusion These finding show that probiotic strains may possess neuroprotective effect against LPS‐induced cognitive impairment and neurodegeneration via antioxidant and anti‐inflammatory mechanisms.</abstract><cop>Hoboken</cop><pub>John Wiley and Sons Inc</pub><pmid>39782609</pmid><doi>10.1002/alz.089920</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record>
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title Potential probiotic (L. plantarum, L. pentosus, P. pentosaceus, W. cibaria and L. rhamnosus) alleviates memory impairment in lipopolysaccharide‐induced cognitive dysfunction and neurotoxicity in mice brain via protection against neuroinflammation and neurodegeneration
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