Full text is available at the source.
Decreased VIP and VPAC2 receptor expression in the biological clock of the R6/2 Huntington's disease mouse
Lower levels of a key brain chemical and its receptor in the internal clock of Huntington’s disease mice
AI simplified
Abstract
A marked reduction in both VIP mRNA and VPAC2 receptor mRNA was found in the SCN of R6/2 mice.
- R6/2 transgenic mice exhibit disrupted circadian rhythms alongside motor and cognitive dysfunctions.
- Altered expression of circadian clock genes occurs in the suprachiasmatic nucleus, the main circadian pacemaker in the brain.
- Decreased levels of vasoactive intestinal polypeptide (VIP) and its receptor VPAC2 coincide with circadian rhythm disruption.
- No neuronal loss in the SCN was observed, suggesting changes in VIP and VPAC2 expression are not due to cell death.
- Impaired VIPergic signaling may contribute to circadian rhythm disruption in R6/2 mice.
AI simplified