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3 protocols using terazosin hydrochloride

1

Electrophysiology and Behavioral Experiments: Drug Preparations

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In electrophysiological experiments, l-noradrenaline bitartrate monohydrate (NA; Tokyo Chemical Industry, Tokyo, Japan), CNQX (Alomone Labs, Jerusalem, Israel), dl-AP-5 (AP-5; Tocris Bioscience, Bristol, UK), terazosin hydrochloride (Sigma, St. Louis, MO, USA), atipamezole hydrochloride (Wako, Osaka, Japan), timolol maleate (Sigma), and phenylephrine hydrochloride (Wako) were dissolved in distilled water. Picrotoxin (Sigma) was dissolved in dimethyl sulfoxide. These drug solutions were diluted with standard Ringer’s solution before use. Kynurenic acid hydrate (KYNA; Tokyo Chemical Industry) was dissolved in standard Ringer’s solution. In behavioral experiments, Picrotoxin, NA, and terazosin (Tocris) were dissolved in phosphate-buffered saline (PBS). Picrotoxin injection into the cortex has been reported to elicit seizures29 (link). The doses of drugs were chosen based on the previous studies26 (link),30 (link)–32 (link).
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2

Pharmacological Screening Compound Acquisition

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Leflunomide, teriflunomide, tolvaptan and BTP2 were purchased from Tocris Bioscience (Bristol, UK). Omeprazole, lansoprazole, rufinamide, prazosin hydrochloride, terazosin hydrochloride, flutamide, roflumilast and propidium iodide were purchased from Sigma-Aldrich (Dorset, UK). Conivaptan hydrochloride was purchased from Selleckchem (distributed by Stratech, Suffolk, UK) and OAG was purchased from Cayman Chemicals (distributed by Cambridge Bioscience, Cambridge, UK). All molecules were of ≥98% purity certified by the vendors.
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3

Radioligand Binding Assay for Alpha-Adrenoceptors

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[ 3 H]-Prazosin (85 Ci/mmol), [ 3 H]-8-OH-DPAT (154.2 Ci/mmol), [ 3 H]-p-MPPF (74.2 Ci/mmol), and [ 3 H]-YM-09151-2 (81.1 Ci/mmol) were purchased from PerkinElmer. Alfuzosin hydrochloride, doxazosin mesylate, tamsulosin hydrochloride, and terazosin hydrochloride were purchased from Sigma-Aldrich (St. Louis, MO), and silodosin was from ShangHai Biochempartner (China). LDT5 hydrochloride ((1-(2-methoxyphenyl)-4-[2-(3,4-dimethoxyphenyl) ethyl] piperazine monohydrochloride) was synthesized as previously described for other N-phenylpiperazine derivatives (Romeiro et al., 2011) . Stock solutions (1 and 10 mM) were made in sterile deionized water (LDT5) or 100% DMSO (Sigma-Aldrich) and then diluted in water. At the final concentration used (no more than 0.1%), DMSO had no effect in our assays.
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