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Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model

BACKGROUND: We have previously demonstrated that Lactobacillus casei CRL 431 administration improved the resistance to pneumococcal infection in a mouse model. METHODS: This study examined the effects of the oral administration of Lactobacillus casei CRL 431 (L. casei) on the activation of coagulati...

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Autores principales: Haro, Cecilia, Villena, Julio, Zelaya, Hortensia, Alvarez, Susana, Agüero, Graciela
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770469/
https://www.ncbi.nlm.nih.gov/pubmed/19835595
http://dx.doi.org/10.1186/1476-9255-6-28
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author Haro, Cecilia
Villena, Julio
Zelaya, Hortensia
Alvarez, Susana
Agüero, Graciela
author_facet Haro, Cecilia
Villena, Julio
Zelaya, Hortensia
Alvarez, Susana
Agüero, Graciela
author_sort Haro, Cecilia
collection PubMed
description BACKGROUND: We have previously demonstrated that Lactobacillus casei CRL 431 administration improved the resistance to pneumococcal infection in a mouse model. METHODS: This study examined the effects of the oral administration of Lactobacillus casei CRL 431 (L. casei) on the activation of coagulation and fibrinolytic systems as well as their inhibitors during a Streptococcus pneumoniae infection in mice. RESULTS: The alveolo-capillary membrane was damaged and the coagulation system was also activated by the infection. As a consequence, we could see fibrin(ogen) deposits in lung histological slices, increased levels of thrombin-antithrombin complex (TATc) in bronchoalveolar lavage (BAL) and plasma, decrease in prothrombin activity (PT) and prolonged activated partial thromboplastin time test (APTT) values. Factor VII (FVII) and factor X (FX) were decreased in plasma, whereas fibrinogen (F) and factor VIII (FVIII) were increased. The low levels of protein C (PC) in BAL and plasma proved damage on inhibitory activity. The infected animals showed reduced fibrinolytic activity, evidenced by an increase in plasminogen activation inhibitor-1 (PAI-1) in BAL and plasma. The pathogen induced an increase of TNF-α, IL-1β and IL-6 in BAL and serum a few hours after challenge followed by a significant decrease until the end of the assayed period. IL-4 and IL-10 in BAL and serum were also augmented, especially at the end of the experiment. The animals treated with L. casei showed an improvement of alveolo-capillary membrane, lower fibrin(ogen) deposits in lung and decrease in TATc. APTT test and PT, FVII and FX activity were normalized. L. casei group showed lower F levels than control during whole experiment. In the present study no effect of L. casei on the recovery of the inhibitory activity was detected. However, L. casei was effective in reducing PAI-1 levels in BAL and in increasing anti-inflammatory ILs concentration. CONCLUSION: L. casei proved effective to regulate coagulation activation and fibrinolysis inhibition during infection, leading to a decrease in fibrin deposits in lung. This protective effect of L. casei would be mediated by the induction of higher levels of IL-4 and IL-10 which could regulate the anti-inflammatory, procoagulant and antifibrinolytic effects of TNF-α, IL-1β and IL-6.
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spelling pubmed-27704692009-10-30 Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model Haro, Cecilia Villena, Julio Zelaya, Hortensia Alvarez, Susana Agüero, Graciela J Inflamm (Lond) Research BACKGROUND: We have previously demonstrated that Lactobacillus casei CRL 431 administration improved the resistance to pneumococcal infection in a mouse model. METHODS: This study examined the effects of the oral administration of Lactobacillus casei CRL 431 (L. casei) on the activation of coagulation and fibrinolytic systems as well as their inhibitors during a Streptococcus pneumoniae infection in mice. RESULTS: The alveolo-capillary membrane was damaged and the coagulation system was also activated by the infection. As a consequence, we could see fibrin(ogen) deposits in lung histological slices, increased levels of thrombin-antithrombin complex (TATc) in bronchoalveolar lavage (BAL) and plasma, decrease in prothrombin activity (PT) and prolonged activated partial thromboplastin time test (APTT) values. Factor VII (FVII) and factor X (FX) were decreased in plasma, whereas fibrinogen (F) and factor VIII (FVIII) were increased. The low levels of protein C (PC) in BAL and plasma proved damage on inhibitory activity. The infected animals showed reduced fibrinolytic activity, evidenced by an increase in plasminogen activation inhibitor-1 (PAI-1) in BAL and plasma. The pathogen induced an increase of TNF-α, IL-1β and IL-6 in BAL and serum a few hours after challenge followed by a significant decrease until the end of the assayed period. IL-4 and IL-10 in BAL and serum were also augmented, especially at the end of the experiment. The animals treated with L. casei showed an improvement of alveolo-capillary membrane, lower fibrin(ogen) deposits in lung and decrease in TATc. APTT test and PT, FVII and FX activity were normalized. L. casei group showed lower F levels than control during whole experiment. In the present study no effect of L. casei on the recovery of the inhibitory activity was detected. However, L. casei was effective in reducing PAI-1 levels in BAL and in increasing anti-inflammatory ILs concentration. CONCLUSION: L. casei proved effective to regulate coagulation activation and fibrinolysis inhibition during infection, leading to a decrease in fibrin deposits in lung. This protective effect of L. casei would be mediated by the induction of higher levels of IL-4 and IL-10 which could regulate the anti-inflammatory, procoagulant and antifibrinolytic effects of TNF-α, IL-1β and IL-6. BioMed Central 2009-10-16 /pmc/articles/PMC2770469/ /pubmed/19835595 http://dx.doi.org/10.1186/1476-9255-6-28 Text en Copyright © 2009 Haro et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Haro, Cecilia
Villena, Julio
Zelaya, Hortensia
Alvarez, Susana
Agüero, Graciela
Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model
title Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model
title_full Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model
title_fullStr Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model
title_full_unstemmed Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model
title_short Lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model
title_sort lactobacillus casei modulates the inflammation-coagulation interaction in a pneumococcal pneumonia experimental model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770469/
https://www.ncbi.nlm.nih.gov/pubmed/19835595
http://dx.doi.org/10.1186/1476-9255-6-28
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