Alteplase and DNase for the treatment of pleural empyema in rats.


Journal

Pulmonary pharmacology & therapeutics
ISSN: 1522-9629
Titre abrégé: Pulm Pharmacol Ther
Pays: England
ID NLM: 9715279

Informations de publication

Date de publication:
04 2019
Historique:
received: 01 05 2017
revised: 18 11 2018
accepted: 03 01 2019
pubmed: 17 1 2019
medline: 17 4 2019
entrez: 17 1 2019
Statut: ppublish

Résumé

Adjunctive intrapleural fibrinolytic is an option to treat empyema at fibrinopurulent stage, but there is controversy about which should be use. Our objective is to evaluate the action of alteplase and/or desoxyribonuclease at physical and chemical properties in vitro pus derived from an experimental induced empyema in rats. Streptococcus pneumoniae was introduced into the pleural cavity by thoracentesis through pleural pressure monitor. Animals were euthanized after 24 h, with macroscopic thoracic evaluation and measurement of amount of intrapleural liquid that was posteriorly stored at -80 °C. Selected samples were randomly distributed into four groups, then thawed at room temperature before exposure to one of the following: G1 = alteplase (n = 12), G2 = DNase (n = 12), G3 = alteplase + DNase (n = 12), or G4 = saline (n = 6). The mean molecular size in the fluid portion of the empyema was evaluated using dynamic light scattering; viscosity of the empyema fluid was measured using the drip method. Macroscopic showed purulent liquid, with fibrin and septation, with mean volume of 4.16 ml (0.5-8 ml). All samples were culture-positive for Streptococcus pneumoniae. Comparing with control, all experimental groups presented reduction of larger than 135 nm molecular size, but there was only significant difference with alteplase (p = 0,02). Viscosity reduced at all experimental groups, but increased at control. DNase group presented negative median (-5 mPa/s) of viscosity, and differed significantly from that observed in the control group (p = 0.04). Alteplase, DNase and alteplase + DNase changed significantly physical and chemical properties of experimental empyema at fibrinopurulent phase: alteplase reduced molecular size larger than 135 nm and DNase reduced viscosity.

Sections du résumé

BACKGROUND AND OBJECTIVES
Adjunctive intrapleural fibrinolytic is an option to treat empyema at fibrinopurulent stage, but there is controversy about which should be use. Our objective is to evaluate the action of alteplase and/or desoxyribonuclease at physical and chemical properties in vitro pus derived from an experimental induced empyema in rats.
METHODS
Streptococcus pneumoniae was introduced into the pleural cavity by thoracentesis through pleural pressure monitor. Animals were euthanized after 24 h, with macroscopic thoracic evaluation and measurement of amount of intrapleural liquid that was posteriorly stored at -80 °C. Selected samples were randomly distributed into four groups, then thawed at room temperature before exposure to one of the following: G1 = alteplase (n = 12), G2 = DNase (n = 12), G3 = alteplase + DNase (n = 12), or G4 = saline (n = 6). The mean molecular size in the fluid portion of the empyema was evaluated using dynamic light scattering; viscosity of the empyema fluid was measured using the drip method.
RESULTS
Macroscopic showed purulent liquid, with fibrin and septation, with mean volume of 4.16 ml (0.5-8 ml). All samples were culture-positive for Streptococcus pneumoniae. Comparing with control, all experimental groups presented reduction of larger than 135 nm molecular size, but there was only significant difference with alteplase (p = 0,02). Viscosity reduced at all experimental groups, but increased at control. DNase group presented negative median (-5 mPa/s) of viscosity, and differed significantly from that observed in the control group (p = 0.04).
CONCLUSIONS
Alteplase, DNase and alteplase + DNase changed significantly physical and chemical properties of experimental empyema at fibrinopurulent phase: alteplase reduced molecular size larger than 135 nm and DNase reduced viscosity.

Identifiants

pubmed: 30648619
pii: S1094-5539(17)30122-0
doi: 10.1016/j.pupt.2019.01.001
pii:
doi:

Substances chimiques

Fibrinolytic Agents 0
Deoxyribonucleases EC 3.1.-
Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-4

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

Mario Gehlen (M)

Pediatric Surgeon, Conceição Children's Hospital and Mãe de Deus University Hospital, Canoas, Brazil.

Jose Carlos Fraga (JC)

Department of Surgery, School of Medicine, Federal University of Rio Grande do Sul (UFRGS). Pediatric Surgeon, Head of Pediatric Surgery Service, Pediatric Thoracic Surgery Unit, Clinical Hospital of Porto Alegre (HCPA), Brazil. Electronic address: jfraga@hcpa.edu.br.

Sergio Luis Amantea (SL)

Department of Pediatrics, Federal University of Health Sciences of Porto Alegre (UFCSPA). Pediatric Pneumologist, Head of Emergency Department, Santo Antônio Children Hospital, Porto Alegre, Brazil.

Nadya P Silveira (NP)

School of Chemistry, Federal University of Rio Grande do Sul. Head of the Rio Grande do Sul State Foundation for Research Support (FAPERGS), Brazil.

Jane Kulczynski (J)

Pathology Department, UFRGS. Head of Pathology Service at the Clinical Hospital of Porto Alegre, Brazil.

Eliane Roesch (E)

Microbiology and Molecular Biology Unit, Clinical Pathology Service, Clinical Hospital of Porto Alegre, Brazil.

Kalyana G Portal (KG)

School of Medicine, UFRGS. Research Assistant Scholarship Recipient (PIBIC), Clinical Hospital of Porto Alegre, Brazil.

Paulo R Sanches (PR)

Biomedical Engineer, Clinicas Hospital of Porto Alegre, Brazil.

Articles similaires

1.00
Humans Yoga Low Back Pain Female Male
Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice

Classifications MeSH