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3 protocols using 8 cpt

1

Neurite Outgrowth Assay with Cerebellar Granule Neurons

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For priming experiments, CGN were treated with 1 mM dbcAMP (Calbiochem; positive control), or with 8-CPT (Tocris) at concentrations of 0.25, 0.5, and 1 mM. Neurons were plated in poly-L-lysine (PLL)-coated 24-well culture dishes at a density of 1×106 neurons per well and incubated for 16 hours. Neurons were then trypsinized, and used in neurite outgrowth assays. Additional CGN were treated with 0.5 or 1 mM 8-CPT, or 1 mM dbcAMP and used immediately in neurite outgrowth assays.
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2

Neurophysiological Experiment Reagents

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Pharmacological agents were purchased from:

Sigma Aldrich—BAPTA, bicuculline methobromide, TTX, paraformaldehyde, tannic acid, tergitol, d-serine and all the salts used to prepare the internal and external solutions; Tocris Bioscience—(+)-MK-801 maleate, D-AP5, 8-CPT, and CPA. Bio-Rad—glutaraldehyde.

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3

Pharmacological Agents for Neuroscience Research

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Pharmacological agents were purchased from: Sigma Aldrich - BAPTA, d-serine, TTX, sodium fluoracetate, CPA, and all the salts used to prepare the internal and external solutions; Tocris Bioscience - (+)-MK-801 maleate, d-AP5, 8-CPT, cPTIO, l-glutamic acid, LY367385, LY341495, MPEP, 2-AG, AM251, L-NAME, DETA NONOate, Nimodipine, Thapsigargin, THL, GDPβS, Calphostin C, Bicuculline, and SCH50911. These compounds were dissolved in water except 8-CPT, 2-AG, AM251, THL, Nimodipine, and Thapsigargin that were dissolved in dimethyl sulphoxide.
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