<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao Q</submitter><funding>MEXT | Japan Society for the Promotion of Science</funding><funding>The University President’ Discretionary Expenses</funding><funding>Nakatomi Foundation</funding><funding>Toyama Dai-ichi Bank Scholarship Foundation</funding><funding>Takeda Science Foundation</funding><funding>Toyama Prefecture Human Resources Development Foundation</funding><funding>Tamura Science and Technology Foundation</funding><pagination>ENEURO.0121-22.2022</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9159529</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(3)</volume><pubmed_abstract>The dorsal raphe (DR) nucleus contains many tyrosine hydroxylase (TH)-positive neurons which are regarded as dopaminergic (DA) neurons. These DA neurons in the DR and periaqueductal gray (PAG) region (DA&lt;sup>DR-PAG&lt;/sup> neurons) are a subgroup of the A10 cluster, which is known to be heterogeneous. This DA population projects to the central nucleus of the amygdala (CeA) and the bed nucleus of the stria terminalis (BNST) and has been reported to modulate various affective behaviors. To characterize, the histochemical features of DA&lt;sup>DR-PAG&lt;/sup> neurons projecting to the CeA and BNST in mice, the current study combined retrograde labeling with Fluoro-Gold (FG) and histological techniques, focusing on TH, dopamine transporter (DAT), vasoactive intestinal peptide (VIP), and vesicular glut</pubmed_abstract><journal>eNeuro</journal><pubmed_title>Histochemical Characterization of the Dorsal Raphe-Periaqueductal Grey Dopamine Transporter Neurons Projecting to the Extended Amygdala.</pubmed_title><pmcid>PMC9159529</pmcid><funding_grant_id>JP21K0674601</funding_grant_id><funding_grant_id>JP19H04212</funding_grant_id><funding_grant_id>JP19K06459</funding_grant_id><funding_grant_id>17H02223</funding_grant_id><funding_grant_id>JP21H0258901</funding_grant_id><funding_grant_id>JP19K16192</funding_grant_id><funding_grant_id>JP21H02592</funding_grant_id><funding_grant_id>JP21K07489</funding_grant_id><funding_grant_id>JP19K09918</funding_grant_id><funding_grant_id>22K09663</funding_grant_id><funding_grant_id>JP20H0341001</funding_grant_id><funding_grant_id>JP18KK0468</funding_grant_id><funding_grant_id>JP20K09209</funding_grant_id><funding_grant_id>JP20K21664</funding_grant_id><funding_grant_id>22K15795</funding_grant_id><funding_grant_id>JP19K24241</funding_grant_id><pubmed_authors>Ito T</pubmed_authors><pubmed_authors>Konno K</pubmed_authors><pubmed_authors>Yamasaki M</pubmed_authors><pubmed_authors>Ohtsuka S</pubmed_authors><pubmed_authors>Yamamoto R</pubmed_authors><pubmed_authors>Hioki H</pubmed_authors><pubmed_authors>Ono M</pubmed_authors><pubmed_authors>Soko C</pubmed_authors><pubmed_authors>Zhao Q</pubmed_authors><pubmed_authors>Kato N</pubmed_authors><pubmed_authors>Watanabe M</pubmed_authors><pubmed_authors>Hori Y</pubmed_authors><pubmed_authors>Furuyama T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Histochemical Characterization of the Dorsal Raphe-Periaqueductal Grey Dopamine Transporter Neurons Projecting to the Extended Amygdala.</name><description>The dorsal raphe (DR) nucleus contains many tyrosine hydroxylase (TH)-positive neurons which are regarded as dopaminergic (DA) neurons. These DA neurons in the DR and periaqueductal gray (PAG) region (DA&lt;sup>DR-PAG&lt;/sup> neurons) are a subgroup of the A10 cluster, which is known to be heterogeneous. This DA population projects to the central nucleus of the amygdala (CeA) and the bed nucleus of the stria terminalis (BNST) and has been reported to modulate various affective behaviors. To characterize, the histochemical features of DA&lt;sup>DR-PAG&lt;/sup> neurons projecting to the CeA and BNST in mice, the current study combined retrograde labeling with Fluoro-Gold (FG) and histological techniques, focusing on TH, dopamine transporter (DAT), vasoactive intestinal peptide (VIP), and vesicular glut</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May-Jun</publication><modification>2025-04-06T04:01:53.308Z</modification><creation>2025-04-06T04:01:53.308Z</creation></dates><accession>S-EPMC9159529</accession><cross_references><pubmed>35580986</pubmed><doi>10.1523/ENEURO.0121-22.2022</doi></cross_references></HashMap>