<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>43(1)</volume><submitter>Sakai Y</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Pyrrolidinophenone derivatives (PPs) are amphetamine-like designer drugs containing a pyrrolidine ring, and their adverse effects resemble those of methamphetamine (METH). Microglial activation has been recently suggested as a key event in eliciting the adverse effects against dysfunction of the central nervous system. The aim of this study is to clarify the mechanisms of microglial activation induced by PPs.&lt;h4>Methods&lt;/h4>We employed the human microglial cell line HMC3 to assess microglial activation induced by PPs and evaluated the capacities for proliferation and interleukin-6 (IL-6) production that are characteristic features of the activation events.&lt;h4>Results&lt;/h4>The WST-1 assay indicated that viability of HMC3 cells was increased by treatment with sublethal concent</pubmed_abstract><journal>Forensic toxicology</journal><pagination>142-154</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11782452</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>α-Pyrrolidinooctanophenone facilitates activation of human microglial cells via ROS/STAT3-dependent pathway.</pubmed_title><pmcid>PMC11782452</pmcid><pubmed_authors>Hattori J</pubmed_authors><pubmed_authors>Suenami K</pubmed_authors><pubmed_authors>Sakai Y</pubmed_authors><pubmed_authors>Jimbo S</pubmed_authors><pubmed_authors>Takayama T</pubmed_authors><pubmed_authors>Nagai A</pubmed_authors><pubmed_authors>Matsumura T</pubmed_authors><pubmed_authors>Michiue T</pubmed_authors><pubmed_authors>Morikawa Y</pubmed_authors><pubmed_authors>Ikari A</pubmed_authors><pubmed_authors>Matsunaga T</pubmed_authors></additional><is_claimable>false</is_claimable><name>α-Pyrrolidinooctanophenone facilitates activation of human microglial cells via ROS/STAT3-dependent pathway.</name><description>&lt;h4>Purpose&lt;/h4>Pyrrolidinophenone derivatives (PPs) are amphetamine-like designer drugs containing a pyrrolidine ring, and their adverse effects resemble those of methamphetamine (METH). Microglial activation has been recently suggested as a key event in eliciting the adverse effects against dysfunction of the central nervous system. The aim of this study is to clarify the mechanisms of microglial activation induced by PPs.&lt;h4>Methods&lt;/h4>We employed the human microglial cell line HMC3 to assess microglial activation induced by PPs and evaluated the capacities for proliferation and interleukin-6 (IL-6) production that are characteristic features of the activation events.&lt;h4>Results&lt;/h4>The WST-1 assay indicated that viability of HMC3 cells was increased by treatment with sublethal concent</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-04T14:05:36.535Z</modification><creation>2025-04-04T14:05:36.535Z</creation></dates><accession>S-EPMC11782452</accession><cross_references><pubmed>39652148</pubmed><doi>10.1007/s11419-024-00708-x</doi></cross_references></HashMap>