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Millipore dopamine d1 receptor antagonist r sch23390
Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
Dopamine D1 Receptor Antagonist R Sch23390, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "Intrinsic motivation for singing in songbirds is enhanced by temporary singing suppression and regulated by dopamine"

Article Title: Intrinsic motivation for singing in songbirds is enhanced by temporary singing suppression and regulated by dopamine

Journal: Scientific Reports

doi: 10.1038/s41598-021-99456-w

Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist SCH23390 with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
Figure Legend Snippet: Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist SCH23390 with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).

Techniques Used: Injection

sch23390 selective dopamine d1 receptor antagonist r 1 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h  (Millipore)

 
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    Millipore sch23390 selective dopamine d1 receptor antagonist r 1 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h
    Sch23390 Selective Dopamine D1 Receptor Antagonist R 1 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Tocris sch23390 selective dopamine d1 receptor antagonist r 1 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h
    Sch23390 Selective Dopamine D1 Receptor Antagonist R 1 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h, supplied by Tocris, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    dopamine d1 receptor antagonist sch23390 r sch23390 hydrochloride  (Millipore)

     
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    Millipore dopamine d1 receptor antagonist sch23390 r sch23390 hydrochloride
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    d1 dopamine receptor antagonist r sch 23390 hydrochloride sch23390  (Millipore)

     
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    Millipore d1 dopamine receptor antagonist r sch 23390 hydrochloride sch23390
    D1 Dopamine Receptor Antagonist R Sch 23390 Hydrochloride Sch23390, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h 3 benzazepinehydrochloride  (Merck KGaA)

     
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    Merck KGaA dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h 3 benzazepinehydrochloride
    Dopamine D1 Receptor Antagonist Sch23390 R 7 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h 3 Benzazepinehydrochloride, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h 3 benzazepinehydrochloride  (Millipore)

     
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    Millipore dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h 3 benzazepinehydrochloride
    Dopamine D1 Receptor Antagonist Sch23390 R 7 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h 3 Benzazepinehydrochloride, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 1 phenyl 2 3 4 5 tetrahydro1h benzazepine  (Millipore)

     
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    Millipore dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 1 phenyl 2 3 4 5 tetrahydro1h benzazepine
    Dopamine D1 Receptor Antagonist Sch23390 R 7 Chloro 8 Hydroxy 1 Phenyl 2 3 4 5 Tetrahydro1h Benzazepine, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore dopamine d1 receptor antagonist r sch23390
    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    Dopamine D1 Receptor Antagonist R Sch23390, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    Sch23390 Selective Dopamine D1 Receptor Antagonist R 1 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sch23390 selective dopamine d1 receptor antagonist r 1 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h/product/Millipore
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    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    Sch23390 Selective Dopamine D1 Receptor Antagonist R 1 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h, supplied by Tocris, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore dopamine d1 receptor antagonist sch23390 r sch23390 hydrochloride
    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    Dopamine D1 Receptor Antagonist Sch23390 R Sch23390 Hydrochloride, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dopamine d1 receptor antagonist sch23390 r sch23390 hydrochloride/product/Millipore
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    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    D1 Dopamine Receptor Antagonist R Sch 23390 Hydrochloride Sch23390, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    Dopamine D1 Receptor Antagonist Sch23390 R 7 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h 3 Benzazepinehydrochloride, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    Dopamine D1 Receptor Antagonist Sch23390 R 7 Chloro 8 Hydroxy 3 Methyl 1 Phenyl2 3 4 5 Tetrahydro 1h 3 Benzazepinehydrochloride, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 3 methyl 1 phenyl2 3 4 5 tetrahydro 1h 3 benzazepinehydrochloride/product/Millipore
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    86
    Millipore dopamine d1 receptor antagonist sch23390 r 7 chloro 8 hydroxy 1 phenyl 2 3 4 5 tetrahydro1h benzazepine
    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist <t>SCH23390</t> with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).
    Dopamine D1 Receptor Antagonist Sch23390 R 7 Chloro 8 Hydroxy 1 Phenyl 2 3 4 5 Tetrahydro1h Benzazepine, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist SCH23390 with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).

    Journal: Scientific Reports

    Article Title: Intrinsic motivation for singing in songbirds is enhanced by temporary singing suppression and regulated by dopamine

    doi: 10.1038/s41598-021-99456-w

    Figure Lengend Snippet: Effects of systemic injections of dopamine or opioid antagonists on first song latencies after 5-h LO in young adult birds. ( A ) Schedules of drug injections. Drugs or their vehicles were injected at 30-min preceding the offset of 5-h LO periods. ( B ) Comparisons of first song latencies between a dopamine D1 receptor antagonist SCH23390 with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle (‘Veh’). Each line indicates a single bird. Injections of both lower and higher doses significantly increased first song latencies compared to the vehicle (* p = 0.004, significance level α was corrected to 0.0083 with a Holm-Bonferroni correction for multiple comparisons). ( C ) Comparisons between a dopamine D2 receptor antagonist haloperidol with lower (0.2 mg/kg, top ) and higher (1 mg/kg, bottom ) doses and its vehicle. Injections of the higher dose, but not the lower dose, greatly prolonged the first song latencies (* p = 0.008, corrected α = 0.0125). If no song production was observed during the post-LO period (7-h duration), the data was assigned a time of 7 h (420 min, dashed line). ( D ) Comparisons between an opioid antagonist naloxone with lower (2 mg/kg, top ) and higher (10 mg/kg, bottom ) doses and its vehicle. The effects of naloxone were not significant for either dose ( p = 0.04 and corrected α = 0.0167 for lower dose; p = 0.07 and corrected α = 0.025 for higher dose).

    Article Snippet: Injected drugs and their doses were as follows: the dopamine D1 receptor antagonist R(+)-SCH23390 (Millipore Sigma, D054) dissolved in 0.9% saline (0.2 and 1.0 mg/kg); the dopamine D2 receptor antagonist haloperidol (Millipore Sigma, H1512) stored as stock solution in DMSO at − 20 °C and diluted in 0.9% saline before injection (0.2 and 1.0 mg/kg); the opioid receptor antagonist naloxone hydrochloride dihydrate (Millipore Sigma, N7758) dissolved in 0.9% saline (2 and 10 mg/kg).

    Techniques: Injection