Literature DB >> 30152192

Resveratrol and ivacaftor are additive G551D CFTR-channel potentiators: therapeutic implications for cystic fibrosis sinus disease.

Do-Yeon Cho1,2, Shaoyan Zhang1,2, Ahmed Lazrak2,3, Jessica W Grayson1, Jaime A Peña Garcia1, Daniel F Skinner1,2, Dong Jin Lim1,2, Calvin Mackey1,2, Catherine Banks1, Sadis Matalon2,3, Bradford A Woodworth1,2.   

Abstract

BACKGROUND: Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene result in defective Cl- transport and cause chronic bacterial infections in the upper and lower airways of cystic fibrosis (CF) patients. Ivacaftor is a CFTR potentiator that improves Cl- transport in CF patients with at least 1 copy of the G551D mutation. Resveratrol is also a potent CFTR potentiator that increases determinants of mucociliary transport. The objective of this study is to determine whether resveratrol and ivacaftor improve Cl- secretion in G551D CFTR over either agent alone.
METHODS: Fisher rat thyroid cells (FRT) transfected with G551D CFTR and human sinonasal epithelial cells (HSNE) containing the CFTR G551D mutation were subjected to pharmacologic manipulation of transepithelial ion transport in Ussing chambers. Activity was further evaluated using whole-cell patch clamp methods in G551D FRT cells.
RESULTS: In G551D FRT cells, resveratrol (100 μM) and ivacaftor (10 μM) significantly increased Cl- transport (change in short-circuit current, δISC = μA/cm2 ) compared with single-agent and dimethylsulfoxide vehicle controls (resveratrol + ivacaftor 4.97 ± 0.57 vs ivacaftor 0.74 ± 0.12 vs resveratrol 2.96 ± 0.52 vs control 0.74 ± 0.12; p < 0.001). Maximal Cl- secretion (20 μM forskolin) was also significantly enhanced (p < 0.0001). Activity was confirmed in G551D HSNE (resveratrol + ivacaftor 4.48 ± 0.39 vs ivacaftor 1.05 ± 0.11 vs. resveratrol 0.84 ± 0.3 vs control, 0.0 ± 0.02; p < 0.001), and whole-cell patch clamp analysis in G551D FRT cells (resveratrol + ivacaftor -2535 ± 179.3 pA vs ivacaftor -1408.9 ± 101.3 pA vs resveratrol; -766.2 ± 71.2 pA; p < 0.0001).
CONCLUSION: Additive improvement in G551D CFTR-mediated Cl- secretion suggests that resveratrol could enhance ivacaftor therapy in these patients and improve CF-related rhinosinusitis.
© 2018 ARS-AAOA, LLC.

Entities:  

Keywords:  CFTR; CFTR potentiator; G551D; chronic rhinosinusitis; chronic sinusitis; cystic fibrosis; ivacaftor; mucociliary clearance; resveratrol; sinusitis

Mesh:

Substances:

Year:  2018        PMID: 30152192      PMCID: PMC6318032          DOI: 10.1002/alr.22202

Source DB:  PubMed          Journal:  Int Forum Allergy Rhinol        ISSN: 2042-6976            Impact factor:   3.858


  35 in total

1.  Sinonasal inhalation of dornase alfa in CF: A double-blind placebo-controlled cross-over pilot trial.

Authors:  Jochen G Mainz; Isabella Schiller; Christiane Ritschel; Hans-Joachim Mentzel; Joachim Riethmüller; Assen Koitschev; Gerlind Schneider; James F Beck; Baerbel Wiedemann
Journal:  Auris Nasus Larynx       Date:  2010-10-27       Impact factor: 1.863

Review 2.  Chloride channels as drug targets.

Authors:  Alan S Verkman; Luis J V Galietta
Journal:  Nat Rev Drug Discov       Date:  2008-01-19       Impact factor: 84.694

3.  Binding site of activators of the cystic fibrosis transmembrane conductance regulator in the nucleotide binding domains.

Authors:  O Moran; L J V Galietta; O Zegarra-Moran
Journal:  Cell Mol Life Sci       Date:  2005-02       Impact factor: 9.261

4.  Curcumin and genistein additively potentiate G551D-CFTR.

Authors:  Ying-Chun Yu; Haruna Miki; Yumi Nakamura; Akiko Hanyuda; Yohei Matsuzaki; Yoichiro Abe; Masato Yasui; Kazuhiko Tanaka; Tzyh-Chang Hwang; Silvia G Bompadre; Yoshiro Sohma
Journal:  J Cyst Fibros       Date:  2011-03-26       Impact factor: 5.482

5.  Secretin-regulated chloride channel on the apical plasma membrane of pancreatic duct cells.

Authors:  M A Gray; J R Greenwell; B E Argent
Journal:  J Membr Biol       Date:  1988-10       Impact factor: 1.843

6.  Extensive surgical and comprehensive postoperative medical management for cystic fibrosis chronic rhinosinusitis.

Authors:  Frank W Virgin; Steven M Rowe; Mary B Wade; Amit Gaggar; Kevin J Leon; K Randall Young; Bradford A Woodworth
Journal:  Am J Rhinol Allergy       Date:  2012 Jan-Feb       Impact factor: 2.467

7.  Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency.

Authors:  Bradford A Woodworth
Journal:  Laryngoscope       Date:  2015-05-06       Impact factor: 3.325

8.  Exposure to cigarette smoke condensate reduces calcium activated chloride channel transport in primary sinonasal epithelial cultures.

Authors:  Frank W Virgin; Christopher Azbell; Daniel Schuster; Jumin Sunde; Shaoyan Zhang; Eric J Sorscher; Bradford A Woodworth
Journal:  Laryngoscope       Date:  2010-07       Impact factor: 3.325

9.  Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study.

Authors:  Edward F McKone; Scott S Emerson; Karen L Edwards; Moira L Aitken
Journal:  Lancet       Date:  2003-05-17       Impact factor: 79.321

10.  Porcine nasal epithelial cultures for studies of cystic fibrosis sinusitis.

Authors:  Nichole Dean; Neel K Ranganath; Brandon Jones; Shaoyan Zhang; Daniel Skinner; Steven M Rowe; Eric J Sorscher; Bradford A Woodworth
Journal:  Int Forum Allergy Rhinol       Date:  2014-04-14       Impact factor: 3.858

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  7 in total

1.  Controlled delivery of ciprofloxacin and ivacaftor via sinus stent in a preclinical model of Pseudomonas sinusitis.

Authors:  Dong-Jin Lim; Justin McCormick; Daniel Skinner; Shaoyan Zhang; Jeffrey B Elder; John G McLemore; Mark Allen; John Martin West; Jessica W Grayson; Steven M Rowe; Bradford A Woodworth; Do-Yeon Cho
Journal:  Int Forum Allergy Rhinol       Date:  2019-12-23       Impact factor: 3.858

2.  Ivacaftor restores delayed mucociliary transport caused by Pseudomonas aeruginosa-induced acquired cystic fibrosis transmembrane conductance regulator dysfunction in rabbit nasal epithelia.

Authors:  Do-Yeon Cho; Shaoyan Zhang; Daniel F Skinner; Dong Jin Lim; Catherine Banks; Jessica W Grayson; Guillermo J Tearney; Steven M Rowe; Bradford A Woodworth
Journal:  Int Forum Allergy Rhinol       Date:  2021-10-26       Impact factor: 5.426

3.  Resveratrol restores intracellular transport in cystic fibrosis epithelial cells.

Authors:  Binyu Lu; Deborah A Corey; Thomas J Kelley
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2020-04-08       Impact factor: 5.464

4.  Mutation-specific dual potentiators maximize rescue of CFTR gating mutants.

Authors:  Guido Veit; Dillon F Da Fonte; Radu G Avramescu; Aiswarya Premchandar; Miklos Bagdany; Haijin Xu; Dennis Bensinger; Daniel Stubba; Boris Schmidt; Elias Matouk; Gergely L Lukacs
Journal:  J Cyst Fibros       Date:  2019-10-31       Impact factor: 5.482

Review 5.  Role of inflammation and oxidative stress in tissue damage associated with cystic fibrosis: CAPE as a future therapeutic strategy.

Authors:  Victor Emanuel Miranda Soares; Thiago Inácio Teixeira do Carmo; Fernanda Dos Anjos; Jonatha Wruck; Sarah Franco Vieira de Oliveira Maciel; Margarete Dulce Bagatini; Débora Tavares de Resende E Silva
Journal:  Mol Cell Biochem       Date:  2021-09-16       Impact factor: 3.396

6.  Impact of Cystic Fibrosis Transmembrane Conductance Regulator Therapy on Chronic Rhinosinusitis and Health Status: Deep Learning CT Analysis and Patient-reported Outcomes.

Authors:  Daniel M Beswick; Stephen M Humphries; Connor D Balkissoon; Matthew Strand; Eszter K Vladar; David A Lynch; Jennifer L Taylor-Cousar
Journal:  Ann Am Thorac Soc       Date:  2022-01

Review 7.  Antibiotic eluting sinus stents.

Authors:  Harrison M Thompson; Dong-Jin Lim; Catherine Banks; Jessica W Grayson; Samrath Ayinala; Do-Yeon Cho; Bradford A Woodworth
Journal:  Laryngoscope Investig Otolaryngol       Date:  2020-07-11
  7 in total

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