Response-selective C5a agonists: differential effects on neutropenia and hypotension in the rat

被引:29
作者
Short, AJ
Paczkowski, NJ
Vogen, SM
Sanderson, SD
Taylor, SM [1 ]
机构
[1] Univ Queensland, Dept Physiol & Pharmacol, St Lucia, Qld 4072, Australia
[2] Univ Nebraska, Med Ctr, Eppley Inst Res Canc & Allied Dis, Omaha, NE 68198 USA
关键词
C5a; C5a agonist; neutropenia; hypotension;
D O I
10.1038/sj.bjp.0702847
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Some in vivo activities of two complement C5a agonist analogues have been evaluated by measuring changes in blood pressure and neutropenia in the rat and comparing the results with their receptor affinities in peritoneal macrophages and polymorphonuclear leucocytes (PMNs). In vitro C5a receptor (C5aR) binding experiments showed that YSFKPMPLaR and YSFKD(NMeNle)PlaR had similar affinities for the macrophage C5aR (IC50 0.2, 0.1 mM respectively). In PMNs, the affinity of YSFKPMPLaR (IC50 0.1 mM) was similar to that in macrophages, whereas the affinity of YSFKD(NMeNle)PLaR for the PMN C5aR was > 100mM. Given i.v., YSFKD(NMeNle)PLaR had similar activity to YSFKPMPLaR on blood pressure but did not cause neutropenia.. These results demonstrate selectivity of a new C5a agonist in vitro, which is paralleled in vivo. The results suggest the possibility of developing selective agonists of C5a for in vivo use in humans.
引用
收藏
页码:511 / 514
页数:4
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