تفاعل #586098

ord-d8e95ead20ff49c283dd4c9a23a270d3

معادلة التفاعل

NCCC1=CC=C(O)C(O)C1
[3H]Dopamine
CN1CCCC1c1cccnc1
nicotine
NCCc1ccc(O)c(O)c1
Dopamine

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITthe suspension was incubated at 37° C. for another 10 min
  2. 2
    workup.WAITPerfusion buffer (room temperature) was pumped into the chambers at a rate of 3 mL/min for a wash period of 8 min
  3. 3
    أخرىFractions (12 sec each) were continuously collected from each chamber throughout the experiment
  4. 4
    أخرىThe perfusate was collected directly into scintillation vials, to which scintillation fluid
  5. 5
    workup.ADDITIONwas added

الإجراء التجريبي

The synaptosomal suspension was incubated for 10 min at 37° C. to restore metabolic activity. [3H]Dopamine ([3H]DA, specific activity=28.0 Ci/mmol, NEN Research Products) was added at a final concentration of 0.1 μM and the suspension was incubated at 37° C. for another 10 min. Aliquots of tissue (50 μL) and perfusion buffer (100 μL) were loaded into the suprafusion chambers of a Brandel Suprafusion System (series 2500, Gaithersburg, Md.). Perfusion buffer (room temperature) was pumped into the chambers at a rate of 3 mL/min for a wash period of 8 min. Test compound (10 μM) or nicotine (10 μM) was then applied in the perfusion stream for 40 sec. Fractions (12 sec each) were continuously collected from each chamber throughout the experiment to capture basal release and agonist-induced peak release and to re-establish the baseline after the agonist application. The perfusate was collected directly into scintillation vials, to which scintillation fluid was added. [3H]DA released was quantified by scintillation counting. For each chamber, the integrated area of the peak was normalized to its baseline.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07767193B2uspto-grants-2010_08