I. Dubuc et al., THE NONPEPTIDE NEUROTENSIN ANTAGONIST, SR-48692 USED AS A TOOL TO REVEAL PUTATIVE NEUROTENSIN RECEPTOR SUBTYPES, British Journal of Pharmacology, 112(2), 1994, pp. 352-354
The nonpeptide neurotensin (NT) antagonist, SR 48692, was recently sho
wn to inhibit NT binding to the cloned rat and human NT receptor and t
o antagonize NT effects in a variety of in vitro and in vivo assays. H
ere, we show that, in contrast to its antagonistic action on NT-induce
d hypomotility in the rat, SR 48692 failed to antagonize NT-induced hy
pothermia and analgesia in the mouse and rat. We suggest that these ef
fects might be mediated through a subtype of SR 48692-insensitive NT r
eceptor.