<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(12)</volume><submitter>Bernard A</submitter><funding>Cancéropôle Grand-Sud-Ouest “Projet Emergent 2020”</funding><funding>French ministry of higher education and research</funding><pubmed_abstract>Vincristine (VCR) is responsible for the onset of the VCR-induced peripheral neuropathy (VIPN), associated with neuropathic pain. Several reports have strongly linked the cholecystokinin type 2 receptor (CCK2R) to nociceptive modulation. Thus, our aim was to evaluate the effect of CCK2R blockade on the onset of VIPN, as well as its interaction on VCR anticancer efficacy. VCR was administrated in mice for 8 days (100 µg/kg/d, i.p.). Transcriptomic analysis of the dorsal root ganglia (DRG) was performed at day 7 in VCR and control mice. Proglumide (30 mg/kg/d), a CCK1R and CCK2R antagonist, and Ly225910 (1 mg/kg/d), a selective CCK2R antagonist, were administrated one day before and during VCR treatment. Tactile sensitivity was assessed during treatments. Immunofluorescence and morphological</pubmed_abstract><journal>Pharmaceutics</journal><pagination>2823</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9788598</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Blockade of Cholecystokinin Type 2 Receptors Prevents the Onset of Vincristine-Induced Neuropathy in Mice.</pubmed_title><pmcid>PMC9788598</pmcid><pubmed_authors>Sturtz F</pubmed_authors><pubmed_authors>Demiot C</pubmed_authors><pubmed_authors>Desmouliere A</pubmed_authors><pubmed_authors>Bernard A</pubmed_authors><pubmed_authors>Rovini A</pubmed_authors><pubmed_authors>Richard L</pubmed_authors><pubmed_authors>Danigo A</pubmed_authors><pubmed_authors>Nizou A</pubmed_authors><pubmed_authors>Mroue M</pubmed_authors><pubmed_authors>Bourthoumieu S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Blockade of Cholecystokinin Type 2 Receptors Prevents the Onset of Vincristine-Induced Neuropathy in Mice.</name><description>Vincristine (VCR) is responsible for the onset of the VCR-induced peripheral neuropathy (VIPN), associated with neuropathic pain. Several reports have strongly linked the cholecystokinin type 2 receptor (CCK2R) to nociceptive modulation. Thus, our aim was to evaluate the effect of CCK2R blockade on the onset of VIPN, as well as its interaction on VCR anticancer efficacy. VCR was administrated in mice for 8 days (100 µg/kg/d, i.p.). Transcriptomic analysis of the dorsal root ganglia (DRG) was performed at day 7 in VCR and control mice. Proglumide (30 mg/kg/d), a CCK1R and CCK2R antagonist, and Ly225910 (1 mg/kg/d), a selective CCK2R antagonist, were administrated one day before and during VCR treatment. Tactile sensitivity was assessed during treatments. Immunofluorescence and morphological</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-21T14:16:18.752Z</modification><creation>2025-04-21T14:16:18.752Z</creation></dates><accession>S-EPMC9788598</accession><cross_references><pubmed>36559317</pubmed><doi>10.3390/pharmaceutics14122823</doi></cross_references></HashMap>