Reverse transcription-polymerase chain reaction and western immunoblot anal
yses were performed to demonstrate the presence of beta-arrestin-1 in rat d
orsal root ganglion. beta-Arrestin-1 existed as two alternatively spliced v
ariants, although predominantly in its untruncated form. Several factors af
fected the visualization of the truncated version on a sodium dodecyl sulfa
te-polyacrylamide gel; however, the isoform was clearly detected on a two-d
imensional gel. We further localized beta-arrestin-1 immunoreactivity in th
e sensory neurons of the 5th lumbar dorsal root ganglia. beta-arrestin-1-im
munoreactive neurons accounted for approximate to 60% of the sensory neuron
s, and approximate to 88% of the beta-Arrestin-1 immunoreactive neurons fel
l into a category of small neurons having a diameter of 10-30 mu m.
Members of the arrestin superfamily play crucial roles in the desensitizati
on of G protein-coupled receptors. Our data demonstrating the presence of b
eta-arrestin-1 in the rat dorsal root ganglion at both messenger RNA and pr
otein levels support the idea that beta-arrestin-1 participates in receptor
desensitization in the sensory neurons. Furthermore, because small-size ne
urons of dorsal root ganglion are often implicated in nociception, the pred
ominant presence of beta-arrestin-1 immunoreactivity in small-size sensory
neurons suggests that beta-arrestin-1 may have a role modulating nociceptiv
e signals. (C) 1999 IBRO. Published by Elsevier Science Ltd.