<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(2)</volume><submitter>Norevik CS</submitter><funding>Norges Forskningsråd</funding><funding>Norges Teknisk-Naturvitenskapelige Universitet</funding><funding>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior</funding><funding>Helse Midt-Norge</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Exercise training promotes brain plasticity and is associated with protection against cognitive impairment and Alzheimer's disease (AD). These beneficial effects may be partly mediated by blood-borne factors. Here we used an in vitro model of AD to investigate effects of blood plasma from exercise-trained donors on neuronal viability, and an in vivo rat model of AD to test whether such plasma impacts cognitive function, amyloid pathology, and neurogenesis.&lt;h4>Methods&lt;/h4>Mouse hippocampal neuronal cells were exposed to AD-like stress using amyloid-β and treated with plasma collected from human male donors 3 h after a single bout of high-intensity exercise. For in vivo studies, blood was collected from exercise-trained young male Wistar rats (high-intensity intervals 5 days/week for 6 weeks). Transgenic AD rats (McGill-R-Thy1-APP) were injected 5 times/fortnight for 6 weeks at 2 months or 5 months of age with either (a) plasma from the exercise-trained rats, (b) plasma from sedentary rats, or (c) saline. Cognitive function, amyloid plaque pathology, and neurogenesis were assessed. The plasma used for the treatment was analyzed for 23 cytokines.&lt;h4>Results&lt;/h4>Plasma from exercised donors enhanced cell viability by 44.1% (p = 0.032) and reduced atrophy by 50.0% (p &lt; 0.001) in amyloid-β-treated cells. In vivo exercised plasma treatment did not alter cognitive function or amyloid plaque pathology but did increase hippocampal neurogenesis by ∼3 fold, regardless of pathological stage, when compared to saline-treated rats. Concentrations of 7 cytokines were significantly reduced in exercised plasma compared to sedentary plasma.&lt;h4>Conclusion&lt;/h4>Our proof-of-concept study demonstrates that plasma from exercise-trained donors can protect neuronal cells in culture and promote adult hippocampal neurogenesis in the AD rat brain. This effect may be partly due to reduced pro-inflammatory signaling molecules in exercised plasma.</pubmed_abstract><journal>Journal of sport and health science</journal><pagination>245-255</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10980897</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exercised blood plasma promotes hippocampal neurogenesis in the Alzheimer's disease rat brain.</pubmed_title><pmcid>PMC10980897</pmcid><pubmed_authors>Miguel-Dos-Santos R</pubmed_authors><pubmed_authors>Witter MP</pubmed_authors><pubmed_authors>Ryan L</pubmed_authors><pubmed_authors>Tari AR</pubmed_authors><pubmed_authors>Jacobsen K</pubmed_authors><pubmed_authors>Scrimgeour N</pubmed_authors><pubmed_authors>Kobro-Flatmoen A</pubmed_authors><pubmed_authors>Norevik CS</pubmed_authors><pubmed_authors>Huuha AM</pubmed_authors><pubmed_authors>Rosbjorgen RN</pubmed_authors><pubmed_authors>Moreira JBN</pubmed_authors><pubmed_authors>Skender B</pubmed_authors><pubmed_authors>Hildegard Bergersen L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exercised blood plasma promotes hippocampal neurogenesis in the Alzheimer's disease rat brain.</name><description>&lt;h4>Background&lt;/h4>Exercise training promotes brain plasticity and is associated with protection against cognitive impairment and Alzheimer's disease (AD). These beneficial effects may be partly mediated by blood-borne factors. Here we used an in vitro model of AD to investigate effects of blood plasma from exercise-trained donors on neuronal viability, and an in vivo rat model of AD to test whether such plasma impacts cognitive function, amyloid pathology, and neurogenesis.&lt;h4>Methods&lt;/h4>Mouse hippocampal neuronal cells were exposed to AD-like stress using amyloid-β and treated with plasma collected from human male donors 3 h after a single bout of high-intensity exercise. For in vivo studies, blood was collected from exercise-trained young male Wistar rats (high-intensity intervals 5 days/week for 6 weeks). Transgenic AD rats (McGill-R-Thy1-APP) were injected 5 times/fortnight for 6 weeks at 2 months or 5 months of age with either (a) plasma from the exercise-trained rats, (b) plasma from sedentary rats, or (c) saline. Cognitive function, amyloid plaque pathology, and neurogenesis were assessed. The plasma used for the treatment was analyzed for 23 cytokines.&lt;h4>Results&lt;/h4>Plasma from exercised donors enhanced cell viability by 44.1% (p = 0.032) and reduced atrophy by 50.0% (p &lt; 0.001) in amyloid-β-treated cells. In vivo exercised plasma treatment did not alter cognitive function or amyloid plaque pathology but did increase hippocampal neurogenesis by ∼3 fold, regardless of pathological stage, when compared to saline-treated rats. Concentrations of 7 cytokines were significantly reduced in exercised plasma compared to sedentary plasma.&lt;h4>Conclusion&lt;/h4>Our proof-of-concept study demonstrates that plasma from exercise-trained donors can protect neuronal cells in culture and promote adult hippocampal neurogenesis in the AD rat brain. This effect may be partly due to reduced pro-inflammatory signaling molecules in exercised plasma.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-04T02:10:57.177Z</modification><creation>2025-04-04T20:15:31.791Z</creation></dates><accession>S-EPMC10980897</accession><cross_references><pubmed>37500010</pubmed><doi>10.1016/j.jshs.2023.07.003</doi></cross_references></HashMap>