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Studies have shown that individuals with a consistently cognitively active lifestyle are less vulnerable to A\u03b2 toxicity. Recent research has demonstrated that intrahippocampal A\u03b2 can impact catecholaminergic release and spatial memory. Interestingly, exposure to novelty stimuli has been found to stimulate the release of catecholamines in the hippocampus. However, it remains uncertain whether repeated enhancing catecholamine activity can effectively alleviate cognitive impairment in individuals with Alzheimer's disease.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Objectives<\/jats:title>\n            <jats:p>Our primary aim was to investigate whether repeated exposure to novelty could enable cognitive resilience against A\u03b2. This protection could be achieved by modulating catecholaminergic activity within the hippocampus.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Methods<\/jats:title>\n            <jats:p>To investigate this hypothesis, we subjected mice to three different conditions\u2014standard housing (SH), repeated novelty (Nov), or daily social interaction (Soc) for one month. We then infused saline solution (SS) or A\u03b2 (A\u03b2<jats:sub>1-42<\/jats:sub>) oligomers intrahippocampally and measured spatial memory retrieval in a Morris Water Maze (MWM). Stereological analysis and extracellular baseline dopamine levels using in vivo microdialysis were assessed in independent groups of mice.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Results<\/jats:title>\n            <jats:p>The mice that received A\u03b2<jats:sub>1-42<\/jats:sub> intrahippocampal infusions and remained in SH or Soc conditions showed impaired spatial memory retrieval. In contrast, animals subjected to the Nov protocol demonstrated remarkable resilience, showing strong spatial memory expression even after A\u03b2<jats:sub>1-42<\/jats:sub> intrahippocampal infusion. The stereological analysis indicated that the A\u03b2<jats:sub>1-42<\/jats:sub> infusion reduced the tyrosine hydroxylase axonal length in SH or Soc mice compared to the Nov group. Accordingly, the hippocampal extracellular dopamine levels increased significantly in the Nov groups.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Conclusions<\/jats:title>\n            <jats:p>These compelling results demonstrate the potential for repeated novelty exposure to strengthen the dopaminergic system and mitigate the toxic effects of A\u03b2<jats:sub>1-42<\/jats:sub>. They also highlight new and promising therapeutic avenues for treating and preventing AD, especially in its early stages.<\/jats:p>\n          <\/jats:sec>","DOI":"10.1007\/s00213-024-06650-5","type":"journal-article","created":{"date-parts":[[2024,8,15]],"date-time":"2024-08-15T11:02:08Z","timestamp":1723719728000},"page":"85-100","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Repeated exposure to novelty promotes resilience against the amyloid-beta effect through dopaminergic stimulation"],"prefix":"10.1007","volume":"242","author":[{"given":"Cintia","family":"Vel\u00e1zquez-Delgado","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1503-4097","authenticated-orcid":false,"given":"Eduardo","family":"Hern\u00e1ndez-Ortiz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0005-7627-8433","authenticated-orcid":false,"given":"Lucia","family":"Landa-Navarro","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2248-6596","authenticated-orcid":false,"given":"Miguel","family":"Tapia-Rodr\u00edguez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8066-9078","authenticated-orcid":false,"given":"Perla","family":"Moreno-Castilla","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2056-6119","authenticated-orcid":false,"given":"Federico","family":"Berm\u00fadez-Rattoni","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2024,8,15]]},"reference":[{"key":"6650_CR1","doi-asserted-by":"publisher","first-page":"44","DOI":"10.1016\/j.neulet.2017.10.006","volume":"662","author":"N Adachi","year":"2018","unstructured":"Adachi N, Yoshimura A, Chiba S, Ogawa S, Kunugi H (2018) Rotigotine, a dopamine receptor agonist, increased BDNF protein levels in the rat cortex and hippocampus. 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