RT Journal Article
SR Electronic
T1 Expression and Localization of Endothelin Receptors: Implications for the Involvement of Peripheral Glia in Nociception
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP 999
OP 1006
DO 10.1523/JNEUROSCI.21-03-00999.2001
VO 21
IS 3
A1 James D. Pomonis
A1 Scott D. Rogers
A1 Christopher M. Peters
A1 Joseph R. Ghilardi
A1 Patrick W. Mantyh
YR 2001
UL http://www.jneurosci.org/content/21/3/999.abstract
AB The endothelins (ETs) are peptides that have a diverse array of functions mediated by two receptor subtypes, the endothelin A receptor (ETAR) and the endothelin B receptor (ETBR). Pharmacological studies have suggested that in peripheral tissues, ETAR expression may play a role in signaling acute or neuropathic pain, whereas ETBR expression may be involved in the transmission of chronic inflammatory pain. To begin to define the mechanisms by which ET can drive nociceptive signaling, autoradiography and immunohistochemistry were used to examine the distribution of ETAR and ETBR in dorsal root ganglia (DRG) and peripheral nerve of the rat, rabbit, and monkey. In DRG and peripheral nerve, ETAR-immunoreactivity was present in a subset of small-sized peptidergic and nonpeptidergic sensory neurons and their axons and to a lesser extent in a subset of medium-sized sensory neurons. However, ETBR-immunoreactivity was not seen in DRG neurons or axons but rather in DRG satellite cells and nonmyelinating ensheathing Schwann cells. Thus, when ETs are released in peripheral tissues, they could act directly on ETAR-expressing sensory neurons and on ETBR-expressing DRG satellite cells or nonmyelinating Schwann cells. These data indicate that ETs can have direct, nociceptive effects on the peripheral sensory nervous system and that peripheral glia may be directly involved in signaling nociceptive events in peripheral tissues.