ÿþ <html> <head> <title>Abstact: Whisking is controlled</title> </head> <body bgcolor="#ffffff"> <cite><font size=4> J Neurophysiol. 2010 Nov;104(5):2532-42. Epub 2010 Sep 15. </cite></font><br> <h3><strong> Cannabinoids reveal separate controls for whisking amplitude and timing in rats. </h3></strong> <br> <h4> Pietr MD, Knutsen PM, Shore DI, Ahissar E, Vogel Z. <br> </h4> Department of Neurobiology, The Weizmann Institute of Science, Rehovot, Israel. <br> <p> Whisking is controlled by multiple, possibly functionally segregated, motor <br> sensory-motor loops. While testing for effects of endocannabinoids on whisking, <br> we uncovered the first known functional segregation of channels controlling whisking <br> amplitude and timing. Channels controlling amplitude, but not timing, were modulated <br> by cannabinoid receptor type 1 (CB1R). Systemic administration of CB1R agonist <br> ”(9)-tetrahydrocannabinol (”(9)-THC) reduced whisking spectral power across all <br> tested doses (1.25-5 mg/kg), whereas whisking frequency was affected at only very high <br> doses (5 mg/kg). Concomitantly, whisking amplitude and velocity were significantly <br> reduced in a dose-dependent manner (25-43 and 26-50%, respectively), whereas cycle <br> duration and bilateral synchrony were hardly affected (3-16 and 3-9%, respectively). <br> Preadministration of CB1R antagonist SR141716A blocked ”(9)-THC-induced kinematic <br> alterations of whisking, and when administered alone, increased whisking amplitude and <br> velocity but affected neither cycle duration nor synchrony. These findings indicate <br> that whisking amplitude and timing are controlled by separate channels and that <br> endocannabinoids modulate amplitude control channels.<br>