Although the lateral habenula (LHb) is involved in the regulation of multiple brain functions and this region expresses abundant M-type
potassium channel (M-channel) subunits Kv7.2 and Kv7.3, the role of M-channels in regulating working memory is unclear, particularly in
Parkinson's disease (PD). Here we tested the effects of activation and blockade of LHb M-channels on working memory by the T-maze rewarded alternation test in rats with unilateral
6-hydroxydopamine lesions of the substantia nigra compacta (SNc). The SNc lesion induced working memory impairment, increased the firing rate of LHb neurons, decreased
dopamine (DA) level in the ventral medial prefrontal cortex (vmPFC) and reduced the expression of Kv7.2 subunit in the LHb. Intra-LHb injection of M-channel activator
retigabine induced enhancement of working memory in SNc
sham-lesioned and SNc-lesioned rats; conversely, the injection of M-channel blocker
XE-991 impaired working memory in the two groups of rats. However, doses producing significant effects in SNc-lesioned rats were higher than those in SNc
sham-lesioned rats. Further, intra-LHb injection of
retigabine decreased the firing rate of LHb neurons and increased release of DA and
serotonin (5-HT) in the vmPFC, while
XE-991 increased the firing rate and decreased DA and
5-HT release in the two groups of rats. Compared with SNc
sham-lesioned rats, the duration of M-channel activation and blockade action on the firing rate of the neurons and release of DA and
5-HT was significantly shortened in SNc-lesioned rats, which was consistent with reduced expression of Kv7.2 subunit in the LHb after lesioning the SNc. Collectively, these findings suggest involvement of LHb Kv7.2 subunit-containing M-channels in working memory impairment in SNc-lesioned rats, and that enhanced or impaired working memory after activation or blockade of M-channels in the LHb is related to the changes in the firing activity of LHb neurons and DA and
5-HT release in the vmPFC.