Literature DB >> 25573195

NVP-QBE170: an inhaled blocker of the epithelial sodium channel with a reduced potential to induce hyperkalaemia.

K J Coote1, D Paisley1, S Czarnecki1, M Tweed1, H Watson1, A Young1, R Sugar1, M Vyas1, N J Smith1, U Baettig1, P J Groot-Kormelink1, M Gosling1, R Lock1, B Ethell1, G Williams1, A Schumacher2, J Harris2, W M Abraham3, J Sabater3, C T Poll4, T Faller1, S P Collingwood1, H Danahay1,5.   

Abstract

BACKGROUND AND
PURPOSE: Inhaled amiloride, a blocker of the epithelial sodium channel (ENaC), enhances mucociliary clearance (MCC) in cystic fibrosis (CF) patients. However, the dose of amiloride is limited by the mechanism-based side effect of hyperkalaemia resulting from renal ENaC blockade. Inhaled ENaC blockers with a reduced potential to induce hyperkalaemia provide a therapeutic strategy to improve mucosal hydration and MCC in the lungs of CF patients. The present study describes the preclinical profile of a novel ENaC blocker, NVP-QBE170, designed for inhaled delivery, with a reduced potential to induce hyperkalaemia. EXPERIMENTAL APPROACH: The in vitro potency and duration of action of NVP-QBE170 were compared with amiloride and a newer ENaC blocker, P552-02, in primary human bronchial epithelial cells (HBECs) by short-circuit current. In vivo efficacy and safety were assessed in guinea pig (tracheal potential difference/hyperkalaemia), rat (hyperkalaemia) and sheep (MCC). KEY
RESULTS: In vitro, NVP-QBE170 potently inhibited ENaC function in HBEC and showed a longer duration of action to comparator molecules. In vivo, intratracheal (i.t.) instillation of NVP-QBE170 attenuated ENaC activity in the guinea pig airways with greater potency and duration of action than that of amiloride without inducing hyperkalaemia in either guinea pig or rat. Dry powder inhalation of NVP-QBE170 by conscious sheep increased MCC and was better than inhaled hypertonic saline in terms of efficacy and duration of action. CONCLUSIONS AND IMPLICATIONS: NVP-QBE170 highlights the potential for inhaled ENaC blockers to exhibit efficacy in the airways with a reduced risk of hyperkalaemia, relative to existing compounds.
© 2015 The British Pharmacological Society.

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Year:  2015        PMID: 25573195      PMCID: PMC4439877          DOI: 10.1111/bph.13075

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  44 in total

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2.  Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

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  7 in total

Review 1.  Recent advances in developing therapeutics for cystic fibrosis.

Authors:  Lisa J Strug; Anne L Stephenson; Naim Panjwani; Ann Harris
Journal:  Hum Mol Genet       Date:  2018-08-01       Impact factor: 6.150

Review 2.  The epithelial sodium channel (ENaC) as a therapeutic target for cystic fibrosis.

Authors:  Ren-Jay Shei; Jacelyn E Peabody; Niroop Kaza; Steven M Rowe
Journal:  Curr Opin Pharmacol       Date:  2018-10-16       Impact factor: 5.547

3.  Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel.

Authors:  Nam Soo Joo; Jin Hyeok Jeong; Hyung-Ju Cho; Jeffrey J Wine
Journal:  Sci Rep       Date:  2016-11-10       Impact factor: 4.379

4.  Potentiating TMEM16A does not stimulate airway mucus secretion or bronchial and pulmonary arterial smooth muscle contraction.

Authors:  Henry Danahay; Roy Fox; Sarah Lilley; Holly Charlton; Kathryn Adley; Lee Christie; Ejaz Ansari; Camille Ehre; Alexis Flen; Michael J Tuvim; Burton F Dickey; Colin Williams; Sarah Beaudoin; Stephen P Collingwood; Martin Gosling
Journal:  FASEB Bioadv       Date:  2020-07-01

5.  Preclinical evaluation of the epithelial sodium channel inhibitor BI 1265162 for treatment of cystic fibrosis.

Authors:  Peter Nickolaus; Birgit Jung; Juan Sabater; Samuel Constant; Abhya Gupta
Journal:  ERJ Open Res       Date:  2020-12-07

6.  TMEM16A Potentiation: A Novel Therapeutic Approach for the Treatment of Cystic Fibrosis.

Authors:  Henry L Danahay; Sarah Lilley; Roy Fox; Holly Charlton; Juan Sabater; Brian Button; Clive McCarthy; Stephen P Collingwood; Martin Gosling
Journal:  Am J Respir Crit Care Med       Date:  2020-04-15       Impact factor: 21.405

Review 7.  ENaC inhibition in cystic fibrosis: potential role in the new era of CFTR modulator therapies.

Authors:  Marcus A Mall
Journal:  Eur Respir J       Date:  2020-12-24       Impact factor: 16.671

  7 in total

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