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. 2007 Dec 26;27(52):14338–14348. doi: 10.1523/JNEUROSCI.4223-07.2007

Table 1.

Behavioral and anatomical validation

Groups DAT binding Number of TH+ cells l-Dopa
mg 0 min
90 min
P D P D
Control C1 123.9 922 0 0 0 0
C2 154.5 958 0 0 0 0
C3 134.9 1007 0 0 0 0
C4 144.4 935 0 0 0 0
MPTP M1 1.6 137 9 0 0 0
M2 3.4 140 9 0 0 0
M3 2.7 74 8 0 0 0
M4 3.5 198 9 0 0 0
MPTP L1 3.9 127 54 9 0 0 0
l-Dopa :no LID L2 2.9 237 59 11 0 0 0
L3 4.2 169 56 9 0 0 0
L4 5.3 134 50 8 0 0 0
MPTP D1 5.6 217 60 9 0 1 4
l-Dopa LID D2 7.7 106 66 8 0 0 3
D3 0.8 155 53 7 0 0 4
D4 4.1 178 50 8 0 0 3
MPTP D5 3.3 132 52 9 0 1 4
l-Dopa LID D6 3.2 177 51 10 0 0 3
HSV-LacZ D7 4.5 159 58 11 0 1 4
MPTP D8 1.5 107 50 11 0 1 4
l-Dopa LID D9 2.0 141 57 10 0 0 4
HSV-RGS9–2 D10 6.4 206 61 10 0 0 3

Mean age, 3.05 ± 0.05 years; mean weight, 3.1 ± 0.1 kg. No LID, Nondyskinetic; LID, dyskinetic. Extent of lesion is comparable among the MPTP-lesioned groups at both the striatal [dopamine transporter (DAT) binding, femtomoles per milligram of equivalent tissue] and nigral [tyrosine hydroxylase (TH) immunopositive neurons] levels. l-Dopa dose (in milligrams) is given for each individual as well as their mean parkinsonian (P) and mean dyskinetic (D) scores before administration (0 min) and 90 min after administration.