Author/Authors :
Azhdari-Zarmehri، Hassan نويسنده Department of Physiology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran , , Semnanian، Saeed نويسنده Department of Physiology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran , , Fathollahi، Yaghoub نويسنده Department of Physiology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran ,
Abstract :
The rostral ventromedial medulla (RVM) acts a key role in the descending inhibitory
pain modulation. Neuropeptide orexin-A (ORXA) is confined to thousands of neurons
in the lateral hypothalamus (LH). While RVM gets the orexinergic projections, the
orexin receptors are also expressed in this structure. The aim of this study was to
specify the cellular effects of ORXA on RVM neurons in vitro by using the whole cell
patch-clamp recording. RVM neurons were classified into three types based on their
electrophysiological characteristics. Type 1 neurons exhibited an irregular spontaneous
activity which was interrupted by periods of pause in 25% of recorded neurons.
Type 2 neurons did not show any spontaneous baseline activity (53.8% of recorded
neurons). Type 3 neurons fired repetitively without interruption (51.2% of recorded
neurons). ORXA had either inhibitory or excitatory effects on 53.8% (7/13) of type 1
neurons. ORXA excited 46.4% (13/28) of type 2 neurons and 27.3% (3/11) of type 3
neurons. The excitatory effect of ORXA observed in type 2 neurons was suppressed
by an orexin 1 receptor (OXR1) antagonist, SB-334867. Briefly, we hypothesized
that the ORXA mediated excitation and/or inhibition in RVM neurons might work as a
mechanism to modulate pain processing by orexinergic neurons.