Carbonic anhydrase inhibition ameliorates inflammation and experimental pulmonary hypertension

Hannes Hudalla, Zoe Michael, Nicolas Christodoulou, Gareth R. Willis, Angeles Fernandez-Gonzalez, Evgenia J. Filatava, Paul Dieffenbach, Laura E. Fredenburgh, Robert S. Stearman, Mark W. Geraci, Stella Kourembanas, Helen Christou

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Inflammation and vascular smooth muscle cell (VSMC) phenotypic switching are causally linked to pulmonary arterial hypertension (PAH) pathogenesis. Carbonic anhydrase inhibition induces mild metabolic acidosis and exerts protective effects in hypoxic pulmonary hypertension. Carbonic anhydrases and metabolic acidosis are further known to modulate immune cell activation. To evaluate if carbonic anhydrase inhibition modulates macrophage activation, inflammation, and VSMC phenotypic switching in severe experimental pulmonary hypertension, pulmonary hypertension was assessed in Sugen 5416/hypoxia (SU/Hx) rats after treatment with acetazolamide or ammonium chloride (NH4Cl). We evaluated pulmonary and systemic inflammation and characterized the effect of carbonic anhydrase inhibition and metabolic acidosis in alveolar macrophages and bone marrow–derived macrophages (BMDMs). We further evaluated the treatment effects on VSMC phenotypic switching in pulmonary arteries and pulmonary artery smooth muscle cells (PASMCs) and corroborated some of our findings in lungs and pulmonary arteries of patients with PAH. Both patients with idiopathic PAH and SU/Hx rats had increased expression of lung inflammatory markers and signs of PASMC dedifferentiation in pulmonary arteries. Acetazolamide and NH4Cl ameliorated SU/Hx-induced pulmonary hypertension and blunted pulmonary and systemic inflammation. Expression of carbonic anhydrase isoform 2 was increased in alveolar macrophages from SU/Hx animals, classically (M1) and alternatively (M2) activated BMDMs, and lungs of patients with PAH. Carbonic anhydrase inhibition and acidosis had distinct effects on M1 and M2 markers in BMDMs. Inflammatory cytokines drove PASMC dedifferentiation, and this was inhibited by acetazolamide and acidosis. The protective antiinflammatory effect of acetazolamide in pulmonary hypertension is mediated by a dual mechanism of macrophage carbonic anhydrase inhibition and systemic metabolic acidosis.

Original languageEnglish (US)
Pages (from-to)512-524
Number of pages13
JournalAmerican Journal of Respiratory Cell and Molecular Biology
Volume61
Issue number4
DOIs
StatePublished - Oct 1 2019

Fingerprint

Carbonic Anhydrases
Pulmonary Hypertension
Macrophages
Acidosis
Muscle
Acetazolamide
Pulmonary Artery
Inflammation
Smooth Muscle Myocytes
Cell Dedifferentiation
Vascular Smooth Muscle
Bone
Alveolar Macrophages
Rats
Bone and Bones
Lung
Chemical activation
Cells
Pneumonia
Ammonium Chloride

Keywords

  • Acetazolamide
  • Acidosis
  • Carbonic anhydrases
  • Lung
  • Macrophages

ASJC Scopus subject areas

  • Molecular Biology
  • Pulmonary and Respiratory Medicine
  • Clinical Biochemistry
  • Cell Biology

Cite this

Hudalla, H., Michael, Z., Christodoulou, N., Willis, G. R., Fernandez-Gonzalez, A., Filatava, E. J., ... Christou, H. (2019). Carbonic anhydrase inhibition ameliorates inflammation and experimental pulmonary hypertension. American Journal of Respiratory Cell and Molecular Biology, 61(4), 512-524. https://doi.org/10.1165/rcmb.2018-0232OC

Carbonic anhydrase inhibition ameliorates inflammation and experimental pulmonary hypertension. / Hudalla, Hannes; Michael, Zoe; Christodoulou, Nicolas; Willis, Gareth R.; Fernandez-Gonzalez, Angeles; Filatava, Evgenia J.; Dieffenbach, Paul; Fredenburgh, Laura E.; Stearman, Robert S.; Geraci, Mark W.; Kourembanas, Stella; Christou, Helen.

In: American Journal of Respiratory Cell and Molecular Biology, Vol. 61, No. 4, 01.10.2019, p. 512-524.

Research output: Contribution to journalArticle

Hudalla, H, Michael, Z, Christodoulou, N, Willis, GR, Fernandez-Gonzalez, A, Filatava, EJ, Dieffenbach, P, Fredenburgh, LE, Stearman, RS, Geraci, MW, Kourembanas, S & Christou, H 2019, 'Carbonic anhydrase inhibition ameliorates inflammation and experimental pulmonary hypertension', American Journal of Respiratory Cell and Molecular Biology, vol. 61, no. 4, pp. 512-524. https://doi.org/10.1165/rcmb.2018-0232OC
Hudalla, Hannes ; Michael, Zoe ; Christodoulou, Nicolas ; Willis, Gareth R. ; Fernandez-Gonzalez, Angeles ; Filatava, Evgenia J. ; Dieffenbach, Paul ; Fredenburgh, Laura E. ; Stearman, Robert S. ; Geraci, Mark W. ; Kourembanas, Stella ; Christou, Helen. / Carbonic anhydrase inhibition ameliorates inflammation and experimental pulmonary hypertension. In: American Journal of Respiratory Cell and Molecular Biology. 2019 ; Vol. 61, No. 4. pp. 512-524.
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