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Altered baseline and amphetamine-mediated behavioral profiles in dopamine transporter Cre (DAT-Ires-Cre) mice compared to tyrosine hydroxylase Cre (TH-Cre) mice
Rationale Transgenic mouse lines expressing Cre-recombinase under the regulation of either dopamine transporter (DAT) or tyrosine hydroxylase (TH) promoters are commonly used to study the dopamine (DA) system. While use of the TH promoter appears to have less liability to changes in native gene expr...
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Published in: | Psychopharmacology 2020-12, Vol.237 (12), p.3553-3568 |
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creator | Chohan, Muhammad O. Esses, Sari Haft, Julia Ahmari, Susanne E. Veenstra-VanderWeele, Jeremy |
description | Rationale
Transgenic mouse lines expressing Cre-recombinase under the regulation of either dopamine transporter (DAT) or tyrosine hydroxylase (TH) promoters are commonly used to study the dopamine (DA) system. While use of the TH promoter appears to have less liability to changes in native gene expression, transgene insertion in the DAT locus results in reduced DAT expression and function. This confound is sometimes overlooked in genetically targeted behavioral experiments.
Objectives
We sought to evaluate the suitability of DAT-Ires-Cre and TH-Cre transgenic lines for behavioral pharmacology experiments with DA agonists. We hypothesized that DAT-Ires-Cre expression would impact DAT-mediated behaviors, but no impact of TH-Cre expression would be observed.
Methods
DAT-Ires-Cre and TH-Cre mice bred on mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds were evaluated for novelty-induced, baseline, and amphetamine (AMPH)–induced locomotion, and for AMPH and D1 agonist (SKF-38393)–induced preservative behaviors.
Results
DAT-Ires-Cre mice on both mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds displayed increased novelty-induced activity and decreased AMPH-induced locomotion, with mixed results for AMPH-induced stereotypy. TH-Cre mice on both backgrounds showed typical baseline activity and AMPH-induced stereotypy, with a difference in AMPH-induced locomotion observed only on the mixed background. Both transgenic lines displayed unaltered SKF-38393-induced grooming behavior.
Conclusions
Our findings indicate that the DAT-Ires-Cre transgenic line may lead to confounds for experiments that are dependent on DAT expression. The TH-Cre transgenic line studied here may be a more useful option, depending on background strain, because of its lack of baseline and drug-induced phenotypes. These data highlight the importance of appropriate controls in studies employing transgenic mice. |
doi_str_mv | 10.1007/s00213-020-05635-4 |
format | article |
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Transgenic mouse lines expressing Cre-recombinase under the regulation of either dopamine transporter (DAT) or tyrosine hydroxylase (TH) promoters are commonly used to study the dopamine (DA) system. While use of the TH promoter appears to have less liability to changes in native gene expression, transgene insertion in the DAT locus results in reduced DAT expression and function. This confound is sometimes overlooked in genetically targeted behavioral experiments.
Objectives
We sought to evaluate the suitability of DAT-Ires-Cre and TH-Cre transgenic lines for behavioral pharmacology experiments with DA agonists. We hypothesized that DAT-Ires-Cre expression would impact DAT-mediated behaviors, but no impact of TH-Cre expression would be observed.
Methods
DAT-Ires-Cre and TH-Cre mice bred on mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds were evaluated for novelty-induced, baseline, and amphetamine (AMPH)–induced locomotion, and for AMPH and D1 agonist (SKF-38393)–induced preservative behaviors.
Results
DAT-Ires-Cre mice on both mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds displayed increased novelty-induced activity and decreased AMPH-induced locomotion, with mixed results for AMPH-induced stereotypy. TH-Cre mice on both backgrounds showed typical baseline activity and AMPH-induced stereotypy, with a difference in AMPH-induced locomotion observed only on the mixed background. Both transgenic lines displayed unaltered SKF-38393-induced grooming behavior.
Conclusions
Our findings indicate that the DAT-Ires-Cre transgenic line may lead to confounds for experiments that are dependent on DAT expression. The TH-Cre transgenic line studied here may be a more useful option, depending on background strain, because of its lack of baseline and drug-induced phenotypes. These data highlight the importance of appropriate controls in studies employing transgenic mice.</description><identifier>ISSN: 0033-3158</identifier><identifier>EISSN: 1432-2072</identifier><identifier>DOI: 10.1007/s00213-020-05635-4</identifier><identifier>PMID: 32778904</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine - pharmacology ; Agonists ; Amphetamine - pharmacology ; Amphetamines ; Animals ; Behavior ; Biomedical and Life Sciences ; Biomedicine ; Dopamine ; Dopamine - metabolism ; Dopamine Agonists - pharmacology ; Dopamine D1 receptors ; Dopamine Plasma Membrane Transport Proteins - metabolism ; Dopamine transporter ; Experiments ; Gene expression ; Grooming ; Hydroxylase ; Insertion ; Integrases - genetics ; Locomotion ; Locomotion - drug effects ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Neurosciences ; Novelty ; Original Investigation ; Pharmacology/Toxicology ; Phenotypes ; Preservatives ; Psychiatry ; Recombinase ; Rodents ; Stereotyped behavior ; Stereotyped Behavior - drug effects ; Transgenic mice ; Tyrosine 3-monooxygenase ; Tyrosine 3-Monooxygenase - metabolism</subject><ispartof>Psychopharmacology, 2020-12, Vol.237 (12), p.3553-3568</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020. corrected publication 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020. corrected publication 2020.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-f8efc09faa11f81f4485039e6336b447fcabbce81d71fe3618ae10ad2f93bd4d3</citedby><cites>FETCH-LOGICAL-c419t-f8efc09faa11f81f4485039e6336b447fcabbce81d71fe3618ae10ad2f93bd4d3</cites><orcidid>0000-0002-6349-1076</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32778904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chohan, Muhammad O.</creatorcontrib><creatorcontrib>Esses, Sari</creatorcontrib><creatorcontrib>Haft, Julia</creatorcontrib><creatorcontrib>Ahmari, Susanne E.</creatorcontrib><creatorcontrib>Veenstra-VanderWeele, Jeremy</creatorcontrib><title>Altered baseline and amphetamine-mediated behavioral profiles in dopamine transporter Cre (DAT-Ires-Cre) mice compared to tyrosine hydroxylase Cre (TH-Cre) mice</title><title>Psychopharmacology</title><addtitle>Psychopharmacology</addtitle><addtitle>Psychopharmacology (Berl)</addtitle><description>Rationale
Transgenic mouse lines expressing Cre-recombinase under the regulation of either dopamine transporter (DAT) or tyrosine hydroxylase (TH) promoters are commonly used to study the dopamine (DA) system. While use of the TH promoter appears to have less liability to changes in native gene expression, transgene insertion in the DAT locus results in reduced DAT expression and function. This confound is sometimes overlooked in genetically targeted behavioral experiments.
Objectives
We sought to evaluate the suitability of DAT-Ires-Cre and TH-Cre transgenic lines for behavioral pharmacology experiments with DA agonists. We hypothesized that DAT-Ires-Cre expression would impact DAT-mediated behaviors, but no impact of TH-Cre expression would be observed.
Methods
DAT-Ires-Cre and TH-Cre mice bred on mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds were evaluated for novelty-induced, baseline, and amphetamine (AMPH)–induced locomotion, and for AMPH and D1 agonist (SKF-38393)–induced preservative behaviors.
Results
DAT-Ires-Cre mice on both mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds displayed increased novelty-induced activity and decreased AMPH-induced locomotion, with mixed results for AMPH-induced stereotypy. TH-Cre mice on both backgrounds showed typical baseline activity and AMPH-induced stereotypy, with a difference in AMPH-induced locomotion observed only on the mixed background. Both transgenic lines displayed unaltered SKF-38393-induced grooming behavior.
Conclusions
Our findings indicate that the DAT-Ires-Cre transgenic line may lead to confounds for experiments that are dependent on DAT expression. The TH-Cre transgenic line studied here may be a more useful option, depending on background strain, because of its lack of baseline and drug-induced phenotypes. These data highlight the importance of appropriate controls in studies employing transgenic mice.</description><subject>2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine - pharmacology</subject><subject>Agonists</subject><subject>Amphetamine - pharmacology</subject><subject>Amphetamines</subject><subject>Animals</subject><subject>Behavior</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Dopamine Agonists - pharmacology</subject><subject>Dopamine D1 receptors</subject><subject>Dopamine Plasma Membrane Transport Proteins - metabolism</subject><subject>Dopamine transporter</subject><subject>Experiments</subject><subject>Gene expression</subject><subject>Grooming</subject><subject>Hydroxylase</subject><subject>Insertion</subject><subject>Integrases - genetics</subject><subject>Locomotion</subject><subject>Locomotion - drug effects</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Neurosciences</subject><subject>Novelty</subject><subject>Original Investigation</subject><subject>Pharmacology/Toxicology</subject><subject>Phenotypes</subject><subject>Preservatives</subject><subject>Psychiatry</subject><subject>Recombinase</subject><subject>Rodents</subject><subject>Stereotyped behavior</subject><subject>Stereotyped Behavior - drug effects</subject><subject>Transgenic mice</subject><subject>Tyrosine 3-monooxygenase</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><issn>0033-3158</issn><issn>1432-2072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kctu1DAUhi1ERYeBF2CBLLEpCxffkjjL0XBppUrdDGvrJD5mUiVxsDMV8zY8Kp6mUIlFvbEsf_9_Lj8h7wS_FJxXnxLnUijGJWe8KFXB9AuyElpJJnklX5IV50oxJQpzTl6ndMfz0Ua_IudKVpWpuV6R35t-xoiONpCw70akMDoKw7THGYb8ZgO6DuYTgXu470KEnk4x-K7HRLuRujA9gHSOMKYpxOxHtxHpxefNjl1HTCy_PtKha5G2YZjgVG4OdD7GkE7C_dHF8OvY5w4W4e7qSfKGnHnoE759vNfk-9cvu-0Vu7n9dr3d3LBWi3pm3qBvee0BhPBGeK1NwVWNpVJlo3XlW2iaFo1wlfCoSmEABQcnfa0ap51ak4vFN8_284BptkOXWux7GDEckpV5r6YotK4z-uE_9C4c4pi7y1SllBZlXvyayIVq85gpordT7AaIRyu4PeVnl_xszs8-5Gd1Fr1_tD40efH_JH8Dy4BagJS_xh8Yn2o_Y_sHJEGnRQ</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Chohan, Muhammad O.</creator><creator>Esses, Sari</creator><creator>Haft, Julia</creator><creator>Ahmari, Susanne E.</creator><creator>Veenstra-VanderWeele, Jeremy</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6349-1076</orcidid></search><sort><creationdate>20201201</creationdate><title>Altered baseline and amphetamine-mediated behavioral profiles in dopamine transporter Cre (DAT-Ires-Cre) mice compared to tyrosine hydroxylase Cre (TH-Cre) mice</title><author>Chohan, Muhammad O. ; Esses, Sari ; Haft, Julia ; Ahmari, Susanne E. ; Veenstra-VanderWeele, Jeremy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-f8efc09faa11f81f4485039e6336b447fcabbce81d71fe3618ae10ad2f93bd4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine - pharmacology</topic><topic>Agonists</topic><topic>Amphetamine - pharmacology</topic><topic>Amphetamines</topic><topic>Animals</topic><topic>Behavior</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Dopamine Agonists - pharmacology</topic><topic>Dopamine D1 receptors</topic><topic>Dopamine Plasma Membrane Transport Proteins - metabolism</topic><topic>Dopamine transporter</topic><topic>Experiments</topic><topic>Gene expression</topic><topic>Grooming</topic><topic>Hydroxylase</topic><topic>Insertion</topic><topic>Integrases - genetics</topic><topic>Locomotion</topic><topic>Locomotion - drug effects</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Neurosciences</topic><topic>Novelty</topic><topic>Original Investigation</topic><topic>Pharmacology/Toxicology</topic><topic>Phenotypes</topic><topic>Preservatives</topic><topic>Psychiatry</topic><topic>Recombinase</topic><topic>Rodents</topic><topic>Stereotyped behavior</topic><topic>Stereotyped Behavior - drug effects</topic><topic>Transgenic mice</topic><topic>Tyrosine 3-monooxygenase</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chohan, Muhammad O.</creatorcontrib><creatorcontrib>Esses, Sari</creatorcontrib><creatorcontrib>Haft, Julia</creatorcontrib><creatorcontrib>Ahmari, Susanne E.</creatorcontrib><creatorcontrib>Veenstra-VanderWeele, Jeremy</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chohan, Muhammad O.</au><au>Esses, Sari</au><au>Haft, Julia</au><au>Ahmari, Susanne E.</au><au>Veenstra-VanderWeele, Jeremy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Altered baseline and amphetamine-mediated behavioral profiles in dopamine transporter Cre (DAT-Ires-Cre) mice compared to tyrosine hydroxylase Cre (TH-Cre) mice</atitle><jtitle>Psychopharmacology</jtitle><stitle>Psychopharmacology</stitle><addtitle>Psychopharmacology (Berl)</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>237</volume><issue>12</issue><spage>3553</spage><epage>3568</epage><pages>3553-3568</pages><issn>0033-3158</issn><eissn>1432-2072</eissn><abstract>Rationale
Transgenic mouse lines expressing Cre-recombinase under the regulation of either dopamine transporter (DAT) or tyrosine hydroxylase (TH) promoters are commonly used to study the dopamine (DA) system. While use of the TH promoter appears to have less liability to changes in native gene expression, transgene insertion in the DAT locus results in reduced DAT expression and function. This confound is sometimes overlooked in genetically targeted behavioral experiments.
Objectives
We sought to evaluate the suitability of DAT-Ires-Cre and TH-Cre transgenic lines for behavioral pharmacology experiments with DA agonists. We hypothesized that DAT-Ires-Cre expression would impact DAT-mediated behaviors, but no impact of TH-Cre expression would be observed.
Methods
DAT-Ires-Cre and TH-Cre mice bred on mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds were evaluated for novelty-induced, baseline, and amphetamine (AMPH)–induced locomotion, and for AMPH and D1 agonist (SKF-38393)–induced preservative behaviors.
Results
DAT-Ires-Cre mice on both mixed 129S6/C57BL/6 and pure C57BL/6 backgrounds displayed increased novelty-induced activity and decreased AMPH-induced locomotion, with mixed results for AMPH-induced stereotypy. TH-Cre mice on both backgrounds showed typical baseline activity and AMPH-induced stereotypy, with a difference in AMPH-induced locomotion observed only on the mixed background. Both transgenic lines displayed unaltered SKF-38393-induced grooming behavior.
Conclusions
Our findings indicate that the DAT-Ires-Cre transgenic line may lead to confounds for experiments that are dependent on DAT expression. The TH-Cre transgenic line studied here may be a more useful option, depending on background strain, because of its lack of baseline and drug-induced phenotypes. These data highlight the importance of appropriate controls in studies employing transgenic mice.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32778904</pmid><doi>10.1007/s00213-020-05635-4</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-6349-1076</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine - pharmacology Agonists Amphetamine - pharmacology Amphetamines Animals Behavior Biomedical and Life Sciences Biomedicine Dopamine Dopamine - metabolism Dopamine Agonists - pharmacology Dopamine D1 receptors Dopamine Plasma Membrane Transport Proteins - metabolism Dopamine transporter Experiments Gene expression Grooming Hydroxylase Insertion Integrases - genetics Locomotion Locomotion - drug effects Male Mice Mice, Inbred C57BL Mice, Transgenic Neurosciences Novelty Original Investigation Pharmacology/Toxicology Phenotypes Preservatives Psychiatry Recombinase Rodents Stereotyped behavior Stereotyped Behavior - drug effects Transgenic mice Tyrosine 3-monooxygenase Tyrosine 3-Monooxygenase - metabolism |
title | Altered baseline and amphetamine-mediated behavioral profiles in dopamine transporter Cre (DAT-Ires-Cre) mice compared to tyrosine hydroxylase Cre (TH-Cre) mice |
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