PDE3-inhibitor enoximone prevented mechanical ventilation in patients with SARS-CoV-2 pneumonia
Language English Country Great Britain, England Media print-electronic
Document type Case Reports, Journal Article
PubMed
33544007
PubMed Central
PMC7876671
DOI
10.1080/01902148.2021.1881189
Knihovny.cz E-resources
- Keywords
- COVID-19, PDE3-inhibitor, SARS-CoV-2 infection, cytokine storm, enoximone, inflammation, mechanical, ventilation,
- MeSH
- Enoximone therapeutic use MeSH
- COVID-19 Drug Treatment * MeSH
- Phosphodiesterase 3 Inhibitors therapeutic use MeSH
- Intensive Care Units MeSH
- Middle Aged MeSH
- Humans MeSH
- Respiratory Insufficiency therapy MeSH
- SARS-CoV-2 * MeSH
- Aged MeSH
- Respiration, Artificial * MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Names of Substances
- Enoximone MeSH
- Phosphodiesterase 3 Inhibitors MeSH
BACKGROUND: Standard care in severe SARS-CoV-2 pneumonia complicated by severe dyspnea and respiratory failure, consists of symptom reduction, ultimately supported by mechanical ventilation. Patients with severe SARS-CoV-2, a prominent feature of COVID-19, show several similar symptoms to Critical Asthma Syndrome (CAS) patients, such as pulmonary edema, mucus plugging of distal airways, decreased tissue oxygenation, (emergent) exhaustion due to severe dyspnea and respiratory failure. Prior application of elective phosphodiesterase (PDE)3-inhibitors milrinone and enoximone in patients with CAS yielded rapid symptomatic relief and reverted the need for mechanical ventilation, due to their bronchodilator and anti-inflammatory properties. Based on these observations, we hypothesized that enoximone may be beneficial in the treatment of patients with severe SARS-CoV-2 pneumonia and prominent CAS-features. METHODS: In this case report enoximone was administered to four consecutive patients (1 M; 3 F; 46-70 y) with emergent respiratory failure due to SARS-CoV-2 pneumonia. Clinical outcome was compared with three controls who received standard care only. RESULTS: After an intravenous bolus of enoximone 20 mg followed by 10 mg/h via perfusor, a rapid symptomatic relief was observed: two out of four patients recovered within a few hours, the other two (with comorbid COPD GOLD II/III) responded within 24-36 h. Compared to the controls, in the enoximone-treated patients respiratory failure and further COVID-19-related deterioration was reverted and mechanical ventilation was prevented, leading to reduced hospital/ICU time. DISCUSSION: Our preliminary observations suggest that early intervention with the selective PDE3-inhibitor enoximone may help to revert respiratory failure as well as avert mechanical ventilation, and reduces ICU/hospital time in patients with severe SARS-CoV-2 pneumonia. Our findings warrant further research on the therapeutic potential of PDE3-inhibition, alone or in combination with other anti-COVID-19 strategies.
Consultants in Quantitative Methods Eindhoven Netherlands
Department of Pulmonary Medicine Erasmus Medical Centre Rotterdam The Netherlands
Dept of Clinical Pharmacy and Pharmacology UMCG Groningen The Netherlands
Dept of Respiratory Diseases Thomayer Hospital Charles University Prague Czech Republic
See more in PubMed
Chen N, Zhou M, Dong X, et al. . Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020;395(10223):507–513. doi:10.1016/S0140-6736(20)30211-7. PubMed DOI PMC
Bermejo JF, Munoz-Fernandez MA.. Severe acute respiratory syndrome, a pathological immune response to the new coronavirus-implications for understanding of pathogenesis, therapy, design of vaccines, and epidemiology. Viral Immunol. 2004;17(4):535–544. doi:10.1089/vim.2004.17.535. PubMed DOI
Kenyon N, Zeki AA, Albertson TE, Louie S.. Definition of critical asthma syndromes. Clin Rev Allergy Immunol. 2015;48(1):1–6. doi:10.1007/s12016-013-8395-6. PubMed DOI PMC
Kritas SK, Ronconi G, Caraffa A, Gallenga CE, Ross R, Conti P.. Mast cells contribute to coronavirus-induced inflammation: new anti-inflammatory strategy. J Biol Regul Homeost Agents. 2020; 34(1): 9–14. doi:10.23812/20-Editorial-Kritas. PubMed DOI
Beute J. Emergency treatment of status asthmaticus with enoximone. Br J Anaesth. 2014;112(6):1105–1108. doi:10.1093/bja/aeu048. PubMed DOI
Schulz O, Wiesner O, Welte T, et al. . Enoximone in status asthmaticus. ERJ Open Res. 2020;6(1):00367–2019. doi:10.1183/23120541.00367-2019. PubMed DOI PMC
Sobhy A, Eldin DMK, Zaki HV.. The use of milrinone versus conventional treatment for the management of life-threatening bronchial asthma. TOATJ. 2019;13(1):12–17. doi:10.2174/2589645801913010012. DOI
Leeman M, Lejeune P, Melot C, Naeije R.. Reduction in pulmonary hypertension and in airway resistances by enoximone (MDL 17,043) in decompensated COPD. Chest. 1987;91(5):662–666. doi:10.1378/chest.91.5.662. PubMed DOI
Franciosi LG, Diamant Z, Banner KH, et al. . Efficacy and safety of RPL554, a dual PDE3 and PDE4 inhibitor, in healthy volunteers and in patients with asthma or chronic obstructive pulmonary disease: findings from four clinical trials. Lancet Respir Med. 2013;1(9):714–727. doi:10.1016/S2213-2600(13)70187-5. PubMed DOI
Beute J, Lukkes M, Koekoek EP, et al. . A pathophysiological role of PDE3 in allergic airway inflammation. JCI Insight. 2018;3(2)doi:10.1172/jci.insight.94888. PubMed DOI PMC
Santarpino G, Caroleo S, Onorati F, et al. . Inflammatory response to cardiopulmonary bypass with enoximone or steroids in patients undergoing myocardial revascularization: a preliminary report study. CP. 2009;47(02):78–88. doi:10.5414/CPP47078. PubMed DOI
Svensjo E, Andersson KE, Bouskela E, Cyrino FZ, Lindgren S.. Effects of two vasodilatory phosphodiesterase inhibitors on bradykinin-induced permeability increase in the hamster cheek pouch. Agents Actions. 1993;39(1-2):35–41. doi:10.1007/BF01975712. PubMed DOI
Wright LC, Seybold J, Robichaud A, Adcock IM, Barnes PJ.. Phosphodiesterase expression in human epithelial cells. Am J Physiol. 1998;275(4):L694–700. doi:10.1152/ajplung.1998.275.4.L694. PubMed DOI
Surapisitchat J, Beavo JA.. Regulation of endothelial barrier function by cyclic nucleotides: the role of phosphodiesterases. Handb Exp Pharmacol. 2011;(204):193–210. doi:10.1007/978-3-642-17969-3_8 PubMed DOI PMC
Chi CY, Khanh TH, Thoa Le PK, et al. . Milrinone therapy for enterovirus 71-induced pulmonary edema and/or neurogenic shock in children: a randomized controlled trial. Crit Care Med. 2013; 41(7):1754–1760. doi:10.1097/CCM.0b013e31828a2a85. PubMed DOI
Beute J. (Oral) Enoximone in asthma. ERJ Open Res. 2020;6(4):00319–2020. doi:10.1183/23120541.00319-2020. PubMed DOI PMC
Kereiakes D, Chatterjee K, Parmley WW, et al. . Intravenous and oral MDL 17043 (A new inotrope-vasodilator agent) in congestive heart failure: Hemodynamic and clinical evaluation in 38 patients. J Am Coll Cardiol. 1984;4(5):884–889. doi:10.1016/S0735-1097(84)80047-9. PubMed DOI
Metra M, Eichhorn E, Abraham WT, et al. . Effects of low-dose oral enoximone administration on mortality, morbidity, and exercise capacity in patients with advanced heart failure: the randomized, double-blind, placebo-controlled, parallel group ESSENTIAL trials. Eur Heart J. 2009;30(24):3015–3026. doi:10.1093/eurheartj/ehp338. PubMed DOI PMC
Furck AK, Bentley S, Bartsota M, Rigby ML, Slavik Z.. Oral Enoximone as an Alternative to Protracted Intravenous Medication in Severe Pediatric Myocardial Failure. Pediatr Cardiol. 2016; 37(7):1297–1301. doi:10.1007/s00246-016-1433-4. PubMed DOI
Londino JD, Lazrak A, Collawn JF, Bebok Z, Harrod KS, Matalon S.. Influenza virus infection alters ion channel function of airway and alveolar cells: mechanisms and physiological sequelae. Am J Physiol Lung Cell Mol Physiol. 2017;313(5):L845–L58. doi:10.1152/ajplung.00244.2017. PubMed DOI PMC
Liu S, Yu C, Yang F, Paganini-Hill A, Fisher MJ.. Phosphodiesterase inhibitor modulation of brain microvascular endothelial cell barrier properties. J Neurol Sci. 2012;320(1-2):45–51. doi:10.1016/j.jns.2012.06.005. PubMed DOI PMC
Kosutova P, Mikolka P, Balentova S, Adamkov M, Calkovska A, Mokra D.. Effects of PDE3 inhibitor olprinone on the respiratory parameters, inflammation, and apoptosis in an experimental model of acute respiratory distress syndrome. Int J Mol Sci. 2020; 21(9).doi:10.3390/ijms21093382. PubMed DOI PMC
Cervin A, Lindgren S.. The effect of selective phosphodiesterase inhibitors on mucociliary activity in the upper and lower airways in vitro. Auris Nasus Larynx. 1998;25(3):269–276. doi:10.1016/S0385-8146(98)00010-8. PubMed DOI
Penmatsa H, Zhang W, Yarlagadda S, et al. . Compartmentalized cyclic adenosine 3',5'-monophosphate at the plasma membrane clusters PDE3A and cystic fibrosis transmembrane conductance regulator into microdomains. Mol Biol Cell. 2010;21(6):1097–1110. doi:10.1091/mbc.e09-08-0655. PubMed DOI PMC
Liu S, Veilleux A, Zhang L, et al. . Dynamic activation of cystic fibrosis transmembrane conductance regulator by type 3 and type 4D phosphodiesterase inhibitors. J Pharmacol Exp Ther. 2005;314(2):846–854. doi:10.1124/jpet.105.083519. PubMed DOI
Beute J, Ganesh K, Nastiti H, et al. . PDE3 inhibition reduces epithelial mast cell numbers in allergic airway inflammation and attenuates degranulation of basophils and mast cells. Front Pharmacol. 2020;11(470).doi:10.3389/fphar.2020.00470. PubMed DOI PMC
Diamant Z, Timmers MC, van der Veen H, Booms P, Sont JK, Sterk PJ.. Effect of an inhaled neutral endopeptidase inhibitor, thiorphan, on airway responsiveness to leukotriene D4 in normal and asthmatic subjects. Eur Respir J. 1994;7(3):459–466. doi:10.1183/09031936.94.07030459. PubMed DOI
Ding S, Zhang J, Yin S, et al. . Inflammatory cytokines tumour necrosis factor-α and interleukin-8 enhance airway smooth muscle contraction by increasing L-type Ca2+ channel expression. Clin Exp Pharmacol Physiol. 2019; 46(1):56–64. doi:10.1111/1440-1681.13030. PubMed DOI
Horby P, Lim WS, et al. . Dexamethasone in hospitalized patients with Covid-19 - preliminary report. N Engl J Med. 2020.doi:10.1056/NEJMoa2021436. PubMed DOI PMC
Giorgi M, Cardarelli S, Ragusa F, et al. . Phosphodiesterase inhibitors: Could they be beneficial for the treatment of COVID-19? Int J Mol Sci. 2020; 21(15): 5338.doi:10.3390/ijms21155338 PubMed DOI PMC
Dalamaga M, Karampela I, Mantzoros CS.. Commentary: Phosphodiesterase 4 inhibitors as potential adjunct treatment targeting the cytokine storm in COVID-19. Covid-19 in Metabolism. 2020;109(154282). doi:10.1016/j.metabol.2020.154282. PubMed DOI PMC
Santaniello A, Vigone B, Beretta L.. Letter to the editor: Immunomodulation by phosphodiesterase-4 inhibitor in COVID-19 patients. Metabolism - Metabolism. 2020;110:154300. VolOpen AccessPublished:June 20, doi:10.1016/j.metabol.2020.154300. PubMed DOI PMC
Hameid RA, Cormet-Boyaka E, Kuebler WM, Uddin M, Berdiev BK.. SARS-CoV-2 may hijack GPCR signaling pathways to dysregulate lung ion and fluid transport. Am J Physiol Lung Cell Mol Physiol. 2021. doi:10.1152/ajplung.00499.2020. PubMed DOI PMC