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Yohimbine hydrochloride

Manufactured by Bio-Techne
Sourced in United Kingdom

Yohimbine hydrochloride is a chemical compound used in laboratory research. It is a naturally occurring indole alkaloid derived from the bark of the Pausinystalia yohimbe tree. Yohimbine hydrochloride is commonly used as a research tool in scientific studies, but its specific applications and intended uses are not provided.

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12 protocols using yohimbine hydrochloride

1

Pharmacological Manipulation of Neurochemicals

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The following drugs were kept at −20°C as stock solutions and dissolved in aCSF to their final concentrations on the day of experiments: L-(−)-norepinephrine (+)-bitartrate salt monohydrate (NE, 10-100 μM, Sigma-Aldrich, shielded from light exposure during preparation, storage and application), picrotoxin (PTX, 50 μM, Tocris), prazosin hydrochloride (10 μM, Sigma-Aldrich), (R)-(−)-phenylephrine hydrochloride (100 μM, Sigma-Aldrich), yohimbine hydrochloride (20 μM, Tocris), tetrodotoxin (TTX, 1 μM, Tocris), TNP-ATP triethylammonium salt (10 μM, Tocris), pyridoxalphosphate-6-azophenyl-2′,4’-disulfonic acid tetrasodium salt (PPADS, 100 μM, Tocris).
Fluorocitric acid (FCA, Sigma-Aldrich) was prepared on the day of experiments with DL-fluorocitric acid barium salt (Paulsen et al., 1987 (link)) dissolved in 1 mL of 0.1 M HCl. Two-to-three drops of 0.1 M Na2SO4 was added to precipitate the Ba2+, after which 2 mL of 0.1 M Na2HPO4 was added and the suspension was centrifuged at 1000 g for 5 min. The supernatant was added to the aCSF to achieve a concentration of 100 μM.
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2

Neurotransmitter Stock Solution Preparation

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Dopamine (DA) hydrochloride (1 M stock, H8602, Sigma-Aldrich), serotonin hydrochloride (50 mM stock, 14332, CAY), and L-adrenaline (epinephrine) (5 mM stock, A0173, TCI) were dissolved in 10 mM HCl. L-noradrenaline bitartrate monohydrate (1 M stock, A0906, TCI), sodium L-glutamate monohydrate (10 mM stock, G0188, TCI), 4-aminobutyric acid (100 mM stock, A0282, TCI), histamine (100 mM stock, 18111–71, Nacalai Tesque), acetylcholine chloride (10 mM stock, A6625, Sigma-Aldrich), R( +)-SCH 23390 hydrochloride (10 mM stock, D054, Sigma-Aldrich), and octopamine hydrochloride (10 mM stock, O0413, TCI) were each dissolved separately in distilled water. SKF 81297 hydrobromide (10 mM stock, 1447, TOCRIS), haloperidol hydrochloride (20 mM stock, 0931, TOCRIS), yohimbine hydrochloride (20 mM stock, 1127, TOCRIS), and tyramine (10 mM stock, A0302, TCI) were dissolved in DMSO. Compound solutions were then subdivided into aliquots and stored at − 20 °C until use. A working solution of 1 M DA was stored at 4 °C for 3 weeks prior to use.
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3

Radioligand Binding Assay Protocol

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Dopamine hydrochloride and L-(-)-norepinephrine (+)-bitartrate salt monohydrate were purchased from Sigma. (-) quinpirole hydrochloride, clonidine hydrochloride, 7-OH-PIPAT maleate, RO-105824 dihydrochloride, RX821002 and yohimbine hydrochloride were purchased from Tocris. [3H]RX821002 (63.9 Ci/mmol), [3H]SCH 23390 (81.9 Ci/mmol) and [3H]YM-09151-2 (84.4 Ci/mmol) were from Perkin-Elmer. Pertussis toxin was purchased from Sigma.
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4

Preparation of Psychoactive Drug Solutions

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Yohimbine hydrochloride (Tocris, UK) was dissolved in distilled water. Citalopram hydrobromide (Tocris, UK), buspirone hydrochloride (Sigma, UK) amphetamine (Sigma, UK) and alpha-flupenthixol (Sigma, UK) were dissolved in 0.9 % saline. FG7142 (β-carboline-3-carboxylic acid N-methylamide) and diazepam (both Sigma, UK) were dissolved in 10 % dimethyl sulphoxide (DMSO; BDH Laboratory Supplies, UK), 20 % cremophor EL (Sigma, UK) and 70 % of 0.9 % saline. All drugs were administered at a final volume of 1 ml/kg.
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5

Analgesic and Anti-inflammatory Protocol

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Atropine, carrageenan, acetylsalicylic acid, indomethacin, formaldehyde and L-nitro arginine methyl ester (L-NAME) were purchased from Sigma (St Louis, MO, USA). Yohimbine hydrochloride was purchased from Tocris (Ellisville, MO, USA). Tramadol, naloxone, amitriptyline hydrochloride and morphine sulfate were donated by Cristália Produtos Químicos e Farmacêuticos Ltda (Itapira, SP, Brazil). ASE was dissolved in distilled water (10 mg.ml−1, stock solution).
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6

Pharmacological Manipulation of Neurochemicals

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The following drugs were kept at −20°C as stock solutions and dissolved in aCSF to their final concentrations on the day of experiments: L-(−)-norepinephrine (+)-bitartrate salt monohydrate (NE, 10-100 μM, Sigma-Aldrich, shielded from light exposure during preparation, storage and application), picrotoxin (PTX, 50 μM, Tocris), prazosin hydrochloride (10 μM, Sigma-Aldrich), (R)-(−)-phenylephrine hydrochloride (100 μM, Sigma-Aldrich), yohimbine hydrochloride (20 μM, Tocris), tetrodotoxin (TTX, 1 μM, Tocris), TNP-ATP triethylammonium salt (10 μM, Tocris), pyridoxalphosphate-6-azophenyl-2′,4’-disulfonic acid tetrasodium salt (PPADS, 100 μM, Tocris).
Fluorocitric acid (FCA, Sigma-Aldrich) was prepared on the day of experiments with DL-fluorocitric acid barium salt (Paulsen et al., 1987 (link)) dissolved in 1 mL of 0.1 M HCl. Two-to-three drops of 0.1 M Na2SO4 was added to precipitate the Ba2+, after which 2 mL of 0.1 M Na2HPO4 was added and the suspension was centrifuged at 1000 g for 5 min. The supernatant was added to the aCSF to achieve a concentration of 100 μM.
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7

Intravenous and Intraperitoneal Methamphetamine Administration

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Methamphetamine hydrochloride (purity 99%; METH, ‘ice’) was sourced from the Australian Government Analytical Laboratories (Pymble, NSW). For IVSA, METH was dissolved in saline (0.9%) at a dose of 0.1 mg/kg per 0.05 mL infusion and filtered through a Millipore syringe filter (0.45 µm). For intraperitoneal (IP) injection, METH was administered at a dose of 1 mg/kg and at a volume of 1 mL/kg. Yohimbine hydrochloride was sourced from Tocris Bioscience (Bristol, UK), was dissolved in distilled water at a dose of 0.625 mg/kg or 1.25 mg/kg and was administered at a volume of 2 mL/kg.
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8

Pharmacological Agents for Neuroscience Research

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ARC-239, BRL-44408, clonidine hydrochloride, dexmedetomidine hydrochloride, efaroxan hydrochloride, guanabenz acetate, guanfacine hydrochloride, idazoxan hydrochloride, JP-1302, prazosin hydrochloride, rauwolscine hydrochloride, RS-79948, RX-821002, terazosin, UK-14304, WB-4101 and yohimbine hydrochloride were acquired from Tocris (Ellisville, MO). Atipamezole was from Orion Corporation (Espoo, Finland) and isoflurane was from Abbott Diagnostics (Chicago, IL). All other chemicals were obtained from Sigma-Aldrich (St. Louis, MO).
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9

Stimulants and Neuropeptide Effects

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Methamphetamine hydrochloride (METH) was purchased from the Australian Government Analytical Laboratories (Australia), oxytocin from China Peptides (China) and yohimbine hydrochloride from Tocris Bioscience (United Kingdom). For intraperitoneal (i.p.) injections, METH was injected at a volume of 1 ml/kg, whilst oxytocin and yohimbine were injected at 2 ml/kg.
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10

Evaluation of Oxaliplatin and Mitragynine

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Oxaliplatin was obtained from Temple University Hospital Pharmacy (Philadelphia, PA) as a 6 mg/ml concentration stock solution and diluted in sterile water (B. Braun Medical Inc., Irvine, CA). Mitragynine (MG) was obtained from Cayman Chemical Company (Ann Arbor, MI) with molecular weight and purity (>97.3 %) additionally confirmed by Dr. Allen Reitz (Fox Chase Chemical Diversity Center, Doylestown, PA). MG was dissolved in a vehicle of 20 % Tween 80 / 80 % sterile water. Naltrexone hydrochloride (NTX), prazosin hydrochloride (PRZ), and propranolol hydrochloride (PROP) were obtained from Sigma-Aldrich (St. Louis, MO) and dissolved in sterile water. Yohimbine hydrochloride (YOH) was purchased from Tocris Bioscience (Bristol, UK) and dissolved in sterile water. All drugs were administered intraperitoneally (IP) at a volume of 10 ml/kg.
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