<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carmen-Orozco RP</submitter><funding>NIAID NIH HHS</funding><funding>FIC NIH HHS</funding><funding>Cienciactiva Peru</funding><funding>Innóvate Perú</funding><funding>National Institutes of Health</funding><pagination>e0009295</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8104410</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The parasite Taenia solium causes neurocysticercosis (NCC) in humans and is a common cause of adult-onset epilepsy in the developing world. Hippocampal atrophy, which occurs far from the cyst, is an emerging new complication of NCC. Evaluation of molecular pathways in brain regions close to and distant from the cyst could offer insight into this pathology.&lt;h4>Methods&lt;/h4>Rats were inoculated intracranially with T. solium oncospheres. After 4 months, RNA was extracted from brain tissue samples in rats with NCC and uninfected controls, and cDNA was generated. Expression of 38 genes related to different molecular pathways involved in the inflammatory response and healing was assessed by RT-PCR array.&lt;h4>Results&lt;/h4>Inflammatory cytokines IFN-γ, TNF-α, and IL-1, together wit</pubmed_abstract><journal>PLoS neglected tropical diseases</journal><pubmed_title>Changes in inflammatory gene expression in brain tissue adjacent and distant to a viable cyst in a rat model for neurocysticercosis.</pubmed_title><pmcid>PMC8104410</pmcid><funding_grant_id>5D43TW006581</funding_grant_id><funding_grant_id>D43 TW006581</funding_grant_id><funding_grant_id>U19 AI129909</funding_grant_id><funding_grant_id>118‐2015‐FONDECYT</funding_grant_id><funding_grant_id>U19AI129909 - TMRC program</funding_grant_id><funding_grant_id>N-135 PNICP - PIAP 2015</funding_grant_id><pubmed_authors>Sutherland G</pubmed_authors><pubmed_authors>Delgado-Kamiche AD</pubmed_authors><pubmed_authors>Davila-Villacorta DG</pubmed_authors><pubmed_authors>Celiz RH</pubmed_authors><pubmed_authors>Cysticercosis Working Group in Peru</pubmed_authors><pubmed_authors>Verastegui MR</pubmed_authors><pubmed_authors>Carmen-Orozco RP</pubmed_authors><pubmed_authors>Gilman RH</pubmed_authors><pubmed_authors>Trompeter G</pubmed_authors><pubmed_authors>Gavidia C</pubmed_authors><pubmed_authors>Garcia HH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Changes in inflammatory gene expression in brain tissue adjacent and distant to a viable cyst in a rat model for neurocysticercosis.</name><description>&lt;h4>Background&lt;/h4>The parasite Taenia solium causes neurocysticercosis (NCC) in humans and is a common cause of adult-onset epilepsy in the developing world. Hippocampal atrophy, which occurs far from the cyst, is an emerging new complication of NCC. Evaluation of molecular pathways in brain regions close to and distant from the cyst could offer insight into this pathology.&lt;h4>Methods&lt;/h4>Rats were inoculated intracranially with T. solium oncospheres. After 4 months, RNA was extracted from brain tissue samples in rats with NCC and uninfected controls, and cDNA was generated. Expression of 38 genes related to different molecular pathways involved in the inflammatory response and healing was assessed by RT-PCR array.&lt;h4>Results&lt;/h4>Inflammatory cytokines IFN-γ, TNF-α, and IL-1, together wit</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-05T16:17:46.977Z</modification><creation>2022-02-10T10:27:20.414Z</creation></dates><accession>S-EPMC8104410</accession><cross_references><pubmed>33905419</pubmed><doi>10.1371/journal.pntd.0009295</doi></cross_references></HashMap>