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. Author manuscript; available in PMC: 2013 Apr 11.
Published in final edited form as: J Immunol. 2011 Feb 18;186(7):4443–4454. doi: 10.4049/jimmunol.1002449

Table 1.

Salemeterol treatment increased the turn-over rate of dopamine in the mouse striatum in MPTP Parkinson’s disease model

DA (Mean ± SE) DOPAC (Mean ± SE) % (DOPAC/DA) HVA (Mean ± SE) % (HVA/DA)
Saline control 748.5 ± 76.7 123.0 ± 14.3 16.4 107.1 ± 4.26 14.3
MPTP 266.0 ± 22.18 81.33 ± 10.2 30.5 73.11 ± 5.66 27.4
Salmeterol (10 ug/kg/day) 668.6 ± 67.05 193.3 ± 28.0 28.8 101.9 ± 7.81 16.5
MPTP + Salmeterol (1ug/kg/day) 214.1± 16.89 148.2 ± 9.7 69.2 85.68 ± 2.68 39.7
MPTP + Salmeterol (10ug/kg/day) 205.6 ± 16.23 165.9 ± 8.8 80.5 97.18 ± 5.77 47.3

For 6 consecutive days, 8-wk-old C57BL/6 male mice received daily MPTP injections (15 mg/kg of MPTP·HCl (14.52 mg/kg as a base), s.c.). Salmeterol (1or 10 μg/kg/day) was given by continuous infusion (via an Alzet mini-pump) for 2 weeks starting at two days before the first MPTP injection. Mice used as controls received an equal volume of 0.9% saline. The mice were euthanized 21 days after the last MPTP/saline treatment with an i.p. injectionof 120 mg/kg pentobarbital and then perfused through the left ventricle with saline. Striatum region was dissected for the analysis of levels of DA and its metabolites, DOPAC and HVA. The trun-over rates were expressed by the ratio of DOPAC/DA and HVA/DA. The values of the DA, DOPAC and HVA are expressed as ng/100 mg of wet weight. Numbers of animal are 5–8 per group.