Plasma bradykinin concentrations during septic shock determined by a novel LC-MS/MS assay.


Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 08 11 2018
revised: 21 02 2019
accepted: 21 02 2019
pubmed: 26 2 2019
medline: 14 6 2019
entrez: 26 2 2019
Statut: ppublish

Résumé

Bradykinin is an important mediator of inflammation and vascular permeability and could have an important role in the development of septic shock. Measurement of bradykinin by immunological methods may suffer from interference and lack of specificity. We developed and validated a liquid chromatography mass spectrometry assay (LC-MS/MS) for plasma bradykinin. We used plasma samples from healthy volunteers (n = 19) and patients with septic shock (n = 47). Stable isotope bradykinin internal standard was added to samples before solid-phase extraction and quantification by LC-MS/MS. Stability of bradykinin was studied for 12 months. Our assay has good sensitivity (0.1 nmol/l) and a wide linear range (0.1-1000 nmol/l). Bradykinin added to plasma was stable for 12 months at -20 °C when a mixture of protease inhibitors was added at sampling but degraded during repeated freezing and thawing. Bradykinin concentration in plasma from septic shock patients (<0.1-0.6 nmol/l) did not change significantly during shock and recovery but differed slightly from that in healthy individuals (0.5-1.1 nmol/l). Our bradykinin assay was successfully used to determine bradykinin concentrations in plasma samples. Intensive care unit patients with septic shock had low concentrations of plasma bradykinin during both shock and recovery phases.

Sections du résumé

BACKGROUND BACKGROUND
Bradykinin is an important mediator of inflammation and vascular permeability and could have an important role in the development of septic shock. Measurement of bradykinin by immunological methods may suffer from interference and lack of specificity. We developed and validated a liquid chromatography mass spectrometry assay (LC-MS/MS) for plasma bradykinin.
METHODS METHODS
We used plasma samples from healthy volunteers (n = 19) and patients with septic shock (n = 47). Stable isotope bradykinin internal standard was added to samples before solid-phase extraction and quantification by LC-MS/MS. Stability of bradykinin was studied for 12 months.
RESULTS RESULTS
Our assay has good sensitivity (0.1 nmol/l) and a wide linear range (0.1-1000 nmol/l). Bradykinin added to plasma was stable for 12 months at -20 °C when a mixture of protease inhibitors was added at sampling but degraded during repeated freezing and thawing. Bradykinin concentration in plasma from septic shock patients (<0.1-0.6 nmol/l) did not change significantly during shock and recovery but differed slightly from that in healthy individuals (0.5-1.1 nmol/l).
CONCLUSIONS CONCLUSIONS
Our bradykinin assay was successfully used to determine bradykinin concentrations in plasma samples. Intensive care unit patients with septic shock had low concentrations of plasma bradykinin during both shock and recovery phases.

Identifiants

pubmed: 30802439
pii: S0009-8981(19)30085-3
doi: 10.1016/j.cca.2019.02.023
pii:
doi:

Substances chimiques

Bradykinin S8TIM42R2W

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20-24

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Mikael Lindström (M)

HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. Electronic address: mikael.lindstrom@hus.fi.

Miia Valkonen (M)

Division of Intensive Care Medicine, Department of Anesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Niina Tohmola (N)

HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Risto Renkonen (R)

HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland; Faculty of Medicine, University of Helsinki, Finland.

Tomas Strandin (T)

Faculty of Medicine, University of Helsinki, Finland.

Antti Vaheri (A)

Faculty of Medicine, University of Helsinki, Finland.

Outi Itkonen (O)

HUSLAB, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

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Classifications MeSH