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To address this issue, we studied the responses of\n                      <jats:styled-content style=\"fixed-case\">D1CT<\/jats:styled-content>\n                      \u20107 mice to two critical components of\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      pathophysiology: the exacerbation of tic\u2010like behaviours in response to stress and the presence of sensorimotor gating deficits, which are thought to reflect the perceptual alterations causing the tics.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Experimental Approach<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">D1CT<\/jats:styled-content>\n                      \u20107 and wild\u2010type (\n                      <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>\n                      ) littermates were subjected to a 20\u2009min session of spatial confinement (\n                      <jats:styled-content style=\"fixed-case\">SC<\/jats:styled-content>\n                      ) within an inescapable, 10\u2009cm wide cylindrical enclosure. Changes in plasma corticosterone levels, tic\u2010like behaviours and other spontaneous responses were measured.\n                      <jats:styled-content style=\"fixed-case\">SC<\/jats:styled-content>\n                      \u2010exposed mice were also tested for the prepulse inhibition (\n                      <jats:styled-content style=\"fixed-case\">PPI<\/jats:styled-content>\n                      ) of the startle response (a sensorimotor gating index) and other\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      \u2010related behaviours, including open\u2010field locomotion, novel object exploration and social interaction and compared with non\u2010confined counterparts.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Key Results<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">SC<\/jats:styled-content>\n                      produced a marked increase in corticosterone concentrations in both\n                      <jats:styled-content style=\"fixed-case\">D1CT<\/jats:styled-content>\n                      \u20107 and\n                      <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>\n                      mice. In\n                      <jats:styled-content style=\"fixed-case\">D1CT<\/jats:styled-content>\n                      \u20107, but not\n                      <jats:styled-content style=\"fixed-case\">WT<\/jats:styled-content>\n                      mice,\n                      <jats:styled-content style=\"fixed-case\">SC<\/jats:styled-content>\n                      exacerbated tic\u2010like and digging behaviours, and triggered\n                      <jats:styled-content style=\"fixed-case\">PPI<\/jats:styled-content>\n                      deficits and aggressive responses. Conversely, SC did not modify locomotor activity or novel object exploration in\n                      <jats:styled-content style=\"fixed-case\">D1CT<\/jats:styled-content>\n                      \u20107 mice. Both tic\u2010like behaviours and\n                      <jats:styled-content style=\"fixed-case\">PPI<\/jats:styled-content>\n                      impairments in\n                      <jats:styled-content style=\"fixed-case\">SC<\/jats:styled-content>\n                      \u2010exposed\n                      <jats:styled-content style=\"fixed-case\">D1CT<\/jats:styled-content>\n                      \u20107 mice were inhibited by standard\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      therapies and\n                      <jats:styled-content style=\"fixed-case\">\n                        D\n                        <jats:sub>1<\/jats:sub>\n                      <\/jats:styled-content>\n                      dopamine receptor antagonism.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions and Implications<\/jats:title>\n                    <jats:p>\n                      These findings collectively support the translational and construct validity of\n                      <jats:styled-content style=\"fixed-case\">D1CT<\/jats:styled-content>\n                      \u20107 mice with respect to\n                      <jats:styled-content style=\"fixed-case\">TS<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Linked Articles<\/jats:title>\n                    <jats:p>\n                      This article is part of a themed section on Updating Neuropathology and Neuropharmacology of Monoaminergic Systems. To view the other articles in this section visit\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/bph.v173.13\/issuetoc\">http:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/bph.v173.13\/issuetoc<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bph.13243","type":"journal-article","created":{"date-parts":[[2015,7,14]],"date-time":"2015-07-14T12:43:27Z","timestamp":1436877807000},"page":"2111-2121","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":53,"title":["The\n                    <scp>D1CT<\/scp>\n                    \u20107 mouse model of\n                    <scp>T<\/scp>\n                    ourette syndrome displays sensorimotor gating deficits in response to spatial confinement"],"prefix":"10.1111","volume":"173","author":[{"given":"Sean 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