The highly selective CRF 2 receptor antagonist K41498 binds to presynaptic CRF 2 receptors in rat brain

• Published in: British journal of pharmacology 2009-02, Vol.136 (6), p.896-904
• Main Authors: Lawrence, A J, Krstew, E V, Dautzenberg, F M, Rühmann, A
• Format: Article
• Language: English
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1038/sj.bjp.0704783

Novel analogues of antisauvagine‐30 (aSvg‐30), a selective antagonist for CRF 2 receptors, have been synthesized and characterized in vitro and in vivo . The analogues were tested for their ability to compete for [ 125 I‐Tyr 0 ]Svg binding and to inhibit Svg‐stimulated adenylate cyclase activity in human embryonic kidney (HEK) 293 cells, permanently transfected with cDNA coding for the human CRF 1 (hCRF 1 ), hCRF 2α and hCRF 2β receptor. One analogue [D‐Phe 11 , His 12 , Nle 17 ]Svg(11‐40), named K41498, showed high affinity binding to hCRF 2α ( K i =0.66±0.03 n M ) and hCRF 2β ( K i =0.62±0.01 n M ) but not the hCRF 1 receptor ( k i =425+50 n M ) and decreased Svg‐stimulated cAMP accumulation in hCRF 2 expressing cells. In conscious Wistar‐Kyoto rats, K41498 (1.84 μg, i.v.) antagonized the hypotensive response to systemic urocortin (1.4 μg, i.v.), but did not block the pressor response to centrally administered urocortin (2.35 μg, i.c.v.). K41498 was subsequently radio‐iodinated, and in autoradiographic studies, specific (sensitive to rat urocortin, astressin and aSvg30, but insensitive to antalarmin) binding of 125 I‐K41498 (100 p M ) was detected in the heart and in selected brain regions including the nucleus tractus solitarius (NTS), spinal trigeminal nucleus, lateral septum and around the anterior and middle cerebral arteries. Following unilateral nodose ganglionectomy, binding of 125 I‐K41498 was reduced by 65% in the ipsilateral NTS, indicative of presynaptic CRF 2 receptors on vagal afferent terminals. These data demonstrate that K41498 is a useful tool to study native CRF 2 receptors in the brain and periphery. British Journal of Pharmacology (2002) 136 , 896–904. doi: 10.1038/sj.bjp.0704783