Document Detail


Regional recruitment of rat diaphragmatic lymphatics in response to increased pleural or peritoneal fluid load.
MedLine Citation:
PMID:  17218349     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The specific role of the diaphragmatic tendinous and muscular tissues in sustaining lymph formation and propulsion in the diaphragm was studied in 24 anaesthetized spontaneously breathing supine rats. Three experimental protocols were used: (a) control; (b) peritoneal ascitis, induced through an intraperitoneal injection of 100 ml kg(-1) of iso-oncotic saline; and (c) pleural effusion, induced through an intrapleural injection of 6.6 ml kg(-1) saline solution. A group of animals (n = 12) was instrumented to measure the hydraulic transdiaphragmatic pressure gradient between the pleural and peritoneal cavities in the three protocols. In the other group (n = 12), the injected iso-oncotic saline was enriched with 2% fluorescent dextrans (molecular mass = 70 kDa); at 30 min from the injections these animals were suppressed and their diaphragm excised and processed for confocal microscopy analysis. In control conditions, in spite of a favourable peritoneal-to-pleural pressure gradient, the majority of the tracer absorbed into the diaphragmatic lymphatic system converges towards the deeper collecting lymphatic ducts. This suggests that diaphragmatic lymph formation mostly depends upon pressure gradients developing between the serosal cavities and the lymphatic vessel lumen. In addition, the tracer distributes to lymph vessels located in the muscular diaphragmatic tissue, suggesting that active muscle contraction, rather than passive tendon stretch, more efficiently enhances local diaphragmatic lymph flow. Vice versa, a prevailing recruitment of the lymphatics of the tendinous diaphragmatic regions was observed in peritoneal ascitis and pleural effusion, suggesting a functional adaptation of the diaphragmatic network to increased draining requirements.
Authors:
Andrea Moriondo; Annalisa Grimaldi; Laura Sciacca; Maria Luisa Guidali; Cristiana Marcozzi; Daniela Negrini
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2007-01-11
Journal Detail:
Title:  The Journal of physiology     Volume:  579     ISSN:  0022-3751     ISO Abbreviation:  J. Physiol. (Lond.)     Publication Date:  2007 Mar 
Date Detail:
Created Date:  2007-03-16     Completed Date:  2007-05-16     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  0266262     Medline TA:  J Physiol     Country:  England    
Other Details:
Languages:  eng     Pagination:  835-47     Citation Subset:  IM    
Affiliation:
Dipartimento di Scienze Biomediche Sperimentali e Cliniche, Università degli Studi dell'Insubria, Via J.H. Dunant 5, 21100 Varese, Italy.
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MeSH Terms
Descriptor/Qualifier:
Acute Disease
Animals
Ascites / metabolism,  physiopathology*
Body Fluids / metabolism
Diaphragm / physiology*
Fluorescent Dyes / pharmacokinetics
Hydrostatic Pressure
Lymphatic System / physiology*
Male
Peritoneal Cavity / physiology*
Pleural Cavity / physiology*
Pleural Effusion / metabolism,  physiopathology*
Rats
Rats, Wistar
Solutions / pharmacokinetics
Chemical
Reg. No./Substance:
0/Fluorescent Dyes; 0/Solutions
Comments/Corrections

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