Literature DB >> 23460288

New renin inhibitor VTP-27999 alters renin immunoreactivity and does not unfold prorenin.

Manne Krop1, Xifeng Lu, Koen Verdonk, Maarten A D H Schalekamp, Jeanette M G van Gool, Brian M McKeever, Richard Gregg, A H Jan Danser.   

Abstract

Renin inhibitors like aliskiren not only block renin but also bind prorenin, thereby inducing a conformational change (like the change induced by acid) allowing its recognition in a renin-specific assay. Consequently, aliskiren can be used to measure prorenin. VTP-27999 is a new renin inhibitor with an aliskiren-like IC50 and t1/2, and a much higher bioavailability. This study addressed (pro)renin changes during treatment of volunteers with VTP-27999 or aliskiren. Both drugs increased renin immunoreactivity. Treatment of plasma samples from aliskiren-treated subjects with excess aliskiren yielded higher renin immunoreactivity levels, confirming the presence of prorenin. Unexpectedly, this approach did not work in VTP-27999-treated subjects, although an assay detecting the prosegment revealed that their blood still contained prorenin. Subsequent in vitro analysis showed that VTP-27999 increased renin immunoreactivity for a given amount of renin by ≥ 30% but did not unfold prorenin. Yet, it did bind to acid-activated, intact prorenin and then again increased immunoreactivity in a renin assay. However, no such increase in immunoreactivity was seen when measuring acid-activated prorenin bound to VTP-27999 with a prosegment-directed assay. The VTP-27999-induced rises in renin immunoreactivity could be competitively prevented by aliskiren, and antibody displacement studies revealed a higher affinity of the active site-directed antibodies in the presence of VTP-27999. In conclusion, VTP-27999 increases renin immunoreactivity in renin immunoassays because it affects the affinity of the active site-directed antibody. Combined with its lack of effect on prorenin, these data show that VTP-27999 differs from aliskiren. The clinical relevance of these results needs to be established.

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Year:  2013        PMID: 23460288     DOI: 10.1161/HYPERTENSIONAHA.111.00967

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  2 in total

Review 1.  New developments in the pharmacological treatment of hypertension: dead-end or a glimmer at the horizon?

Authors:  Ludovit Paulis; Romana Rajkovicova; Fedor Simko
Journal:  Curr Hypertens Rep       Date:  2015-06       Impact factor: 5.369

2.  Colocalization of the (Pro)renin Receptor/Atp6ap2 with H+-ATPases in Mouse Kidney but Prorenin Does Not Acutely Regulate Intercalated Cell H+-ATPase Activity.

Authors:  Arezoo Daryadel; Soline Bourgeois; Marta F L Figueiredo; Ana Gomes Moreira; Nicole B Kampik; Lisa Oberli; Nilufar Mohebbi; Xifeng Lu; Marcel E Meima; A H Jan Danser; Carsten A Wagner
Journal:  PLoS One       Date:  2016-01-29       Impact factor: 3.240

  2 in total

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