The corridor test, which was originally developed for studies of unilateral sensorimotor impairments in rats, was adapted here for experiments in mice. This test has several attractive features: it does not require any specialised training or equipment and, in contrast to, e.g., the stepping test, does not involve any direct contact with the animal learn more during testing. Moreover, the motivational aspect of the task (sugar pellets) makes it useful for repeated testing and does not require any time-consuming off-line assessment,

which is the case with the cylinder test. These features make the corridor task attractive for studies involving assessment of functional changes over time, such as in neurorestorative studies and cell transplantation experiments, which have already been reported for rats (Dowd et al., 2005a,b; Torres et al., 2008). Our own preliminary observations suggest that the deficits observed in intranigral 6-OHDA-lesioned

mice in the corridor task and the apomorphine- and amphetamine-induced rotation tests can be at least partially rescued with an intrastriatal transplant of embryonic ventral mesencephalic tissue (S. Grealish and A. Björklund, unpublished results). This is consistent with a recent study that has reported recovery in amphetamine- and apomorphine-induced rotation following intrastriatal transplantation of midbrain neural stem cells (Parish Olaparib cell line et al., 2008). Based on the results presented here we propose the following criteria for stiripentol the determination of lesion severity in 6-OHDA-lesioned mice: Mice with severe lesions, defined as an overall loss of > 80% of the TH+ innervation in the striatum (dorsal and ventral striatum combined), are characterised by 20% retrievals of pellets in the corridor task on the side contralateral to the lesion and 3 contralateral turns/min in response to 0.1 mg/kg apomorphine, s.c.. These mice will in most, but not all, cases score 6 ipsilateral turns per minute in response to an i.p. injection of 5 mg/kg amphetamine. Mice exhibiting

this magnitude of impairment are expected to display > 85% TH+ cell loss in SN and > 45% TH+ cell loss in VTA. Mice with intermediate lesions, defined as an overall 60–80% TH+ denervation of striatum, are defined by 21–40% retrievals of pellets, contralaterally, in the corridor task. These mice will show a similar response to amphetamine as mice with severe lesions, and may or may not display contralateral rotations in response to apomorphine. The magnitude of TH+ cell loss in these animals is likely to be > 85% in the SN and > 20% in the VTA. Mice with mild lesions, defined as < 60% denervation of the striatum, are difficult to distinguish from intact mice as they show only minor deficits in the corridor task (40–45% contralateral pellet retrievals) and little to no rotational asymmetry in the apomorphine and amphetamine tests. In these mice TH+ cell loss in the midbrain is typically < 50%.