Role of the Medial Prefrontal Cortex in Cataplexy
- Yo Oishi,
- Rhiannan H. Williams,
- Lindsay Agostinelli,
- Elda Arrigoni,
- Patrick M. Fuller,
- Takatoshi Mochizuki,
- Clifford B. Saper, and
- Thomas E. Scammell
- Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215
-
Author contributions: Y.O., C.B.S., and T.E.S. designed research; Y.O., R.H.W., L.A., and E.A. performed research; P.M.F. contributed unpublished reagents/analytic tools; Y.O., R.H.W., E.A., T.M., C.B.S., and T.E.S. analyzed data; Y.O., R.H.W., E.A., P.M.F., C.B.S., and T.E.S. wrote the paper.
Abstract
Narcolepsy is characterized by chronic sleepiness and cataplexy, episodes of profound muscle weakness that are often triggered by strong, positive emotions. Narcolepsy with cataplexy is caused by a loss of orexin (also known as hypocretin) signaling, but almost nothing is known about the neural mechanisms through which positive emotions trigger cataplexy. Using orexin knock-out mice as a model of narcolepsy, we found that palatable foods, especially chocolate, markedly increased cataplexy and activated neurons in the medial prefrontal cortex (mPFC). Reversible suppression of mPFC activity using an engineered chloride channel substantially reduced cataplexy induced by chocolate but did not affect spontaneous cataplexy. In addition, neurons in the mPFC innervated parts of the amygdala and lateral hypothalamus that contain neurons active during cataplexy and that innervate brainstem regions known to regulate motor tone. These observations indicate that the mPFC is a critical site through which positive emotions trigger cataplexy.
- Received January 31, 2013.
- Revision received April 9, 2013.
- Accepted May 2, 2013.
- Copyright © 2013 the authors 0270-6474/13/339743-09$15.00/0





