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. Author manuscript; available in PMC: 2016 Dec 3.
Published in final edited form as: Neuroscience. 2015 Sep 9;310:12–26. doi: 10.1016/j.neuroscience.2015.09.018

Table 1.

Effect of 6-OHDA and L-DOPA on M1 monoamines and their metabolites

Hemisphere Lesion Treatment DA DOPAC NE 5-HT 5-HIAA
Ipsilateral Sham Vehicle 33 ± 2 43 ± 3 279 ± 22 327 ± 11 3513 ± 234
Contralateral -- 35 ± 3 48 ± 4 305 ± 12 258 ± 13 3551 ± 199
Ipsilateral 6-OHDA Vehicle 29 ± 5 32 ± 7 * 126 ± 50 291 ± 25 3679 ± 289
Contralateral -- 33 ± 2 52 ± 9 343 ± 13 346 ± 79 4212 ± 292
Ipsilateral Sham L-DOPA
(6 mg/kg)
* 94 ± 9 * 85 ± 10 243 ± 14 239 ± 22 3187 ± 135
Contralateral -- 88 ± 4 83 ± 2 270 ± 5 240 ± 16 3484 ± 177
Ipsilateral 6-OHDA L-DOPA
(6 mg/kg)
# § 66 ± 5 # 54 ± 5 § 36 ± 18 664 ± 305 3651 ± 146
Contralateral -- 76 ± 6 99 ± 16 284 ± 20 231 ± 20 3846 ± 242

Rats received unilateral injections of 6-hydroxydopamine (6-OHDA) or sham into the medial forebrain bundle (n = 7 per group). After recovery, rats were treated with daily L-DOPA 6 mg/kg or vehicle (Veh) and decapitated 60 min after final injection. Primary motor cortex tissue was processed via high performance liquid chromatography for concentrations of dopamine (DA), the DA metabolite 3,4-dihydroxyphenylacetic acid (DOPAC), norepinephrine (NE), serotonin (5-HT) or the 5-HT metabolite 5-hydroxyindoleacetic acid (5-HIAA). Reported values are mean pg (of monoamine) per mg (of tissue) ± SEM. Individual planned contrasts were only performed on the ipsilateral hemisphere.

*

p < .05 vs. Sham + Veh;

#

p < .05 vs. 6-OHDA + Veh;

§

p < .05 vs. Sham + L-DOPA.