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Pramipexole dihydrochloride

Manufactured by Bio-Techne
Sourced in United States

Pramipexole dihydrochloride is a chemical compound used in laboratory settings. It functions as a dopamine receptor agonist, primarily targeting the D2 and D3 subtypes of dopamine receptors.

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2 protocols using pramipexole dihydrochloride

1

Pramipexole and Cocaine Administration

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Pramipexole dihydrochloride was purchased from Tocris (Minneapolis, MN, USA), and cocaine hydrochloride was provided by the Drug Supply Program at the National Institute on Drug Abuse (Bethesda, MD). Both pramipexole and cocaine were dissolved in sterile, physiologic saline. Cocaine was administered intravenously (IV) in a volume of 0.1 ml/kg, whereas pramipexole was administered IP in a volume of 1 ml/kg.
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2

Pharmacological Pretreatment in 6-OHDA Rat Model

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The following drugs were used: benserazide hydrochloride, 3,4-dihydroxy-l-phenylalanine (L-DOPA), 6-hydroxydopamine hydrochloride (6-OHDA) and desipramine hydrochloride (Sigma-Aldrich, St. Louis, MO, USA), pramipexole dihydrochloride (Tocris, Bristol, UK) and reboxetine mesylate (Abcam Biochemicals, Cambridge, UK). 6-OHDA was dissolved in saline containing 0.02% ascorbic acid and locally injected in the brain. Desipramine (25 mg/kg, i.p.), pramipexole (0.6 mg/kg, s.c.), reboxetine (20 mg/kg, i.p.) and L-DOPA [10 mg/kg, i.p.; administered together with the peripheral DOPA decarboxylase inhibitor, benserazide (7.5 mg/kg)] were dissolved in saline. All drugs were injected in a volume of 10 ml/kg. Desipramine was administered 30 min before the injection of 6-OHDA. The other drugs were administered for four consecutive days preceding the experiment. The animals were tested 30 min after the last drug administration.
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