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. 2011 Nov 23;2:71. doi: 10.3389/fneur.2011.00071

Table 1.

Details on the drugs used for pre-treatment.

Drug used for pre-treatment Drug classification and purpose Dose (μmol/kg), time before 4-AP Reference for function or effective dose
TEA BKCa inhibitor, to test 4-AP KV selectivity 35 Berg and Koteng (1997)
Glibenclamide KATP inhibitor, to test 4-AP KV selectivity 40 Berg and Koteng (1997)
Hexamethonium chloride Peripheral nAChR antagonist, ganglion blockade 37 Wassermann (1971), Berg (2005)
Atropine sulfate Mainly peripheral mAChR antagonist 6.9, −20 min Vargas and Ringdahl (1990), Berg (2002)
Scopolamine hydrobromide Mainly central mAChR antagonist 2.4, −30 min Vargas and Ringdahl (1990), Berg (2002)
Reserpine Depletes sympathetic nerves of norepinephrine 2 × 8.2, i.p.,
−48 + −24 h
Berg (2002)
Phentolamine Non-selective αAR antagonist 6.3 Berg (2002, 2005)
Prazosin α1AR antagonist 0.24 Berg (2003, 2005)
Yohimbine α2AR antagonist 5 Berg (2003)
Nadolol Peripheral β1 + 2AR antagonist 8.5 Berg et al. (2010)
SR59230A β3AR antagonist 10, −5 min Malinowska and Schlicker (1997), Berg et al. (2010)
Desipramine hydrochloride Inhibits norepinephrine reuptake 44, i.p., −4.5 h Miralles et al. (2002), Berg et al. (2009)

SR59230A was from Tocris Bioscience, Bristol, UK; the remaining drugs from Sigma Chemical Co., St. Louis, MO, USA. The drugs were administered i.v. as bolus injections (0.6–1 ml/kg) 10 min prior to 4-AP, unless otherwise indicated.