Experimental study on protein transmission through the human muscle fascia: preliminary results and application theory in lymphedema.
Identifieur interne : 004B69 ( PubMed/Checkpoint ); précédent : 004B68; suivant : 004B70Experimental study on protein transmission through the human muscle fascia: preliminary results and application theory in lymphedema.
Auteurs : G F Vettorello [Italie] ; M. Rubbini ; C. Nastruzzi ; E. Menegatti ; E. Esposito ; F. Mascoli ; E. Pozza ; A. Cataldi ; I G DoniniSource :
- The Journal of cardiovascular surgery [ 0021-9509 ] ; 1996.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Proteins.
- chemical : Membranes, Artificial.
- metabolism : Fascia, Lymph, Lymphedema.
- Biological Transport, Electrophysiology, Humans, In Vitro Techniques, Leg, Models, Structural, Porosity.
Abstract
The presence of proteins (albumin and globulins) in lymphedematous tissue not only gives rise to colloidosmotic pressure but also produces an electrostatic charge endowing the proteins with individual features and different migration rates. The working hypothesis of the experimental study is to transfer lymph proteins from the upper fascia accumulation area to a subfascial drainage area by subjecting them to an adequate difference in potential. A double chamber, variable volume system with separation wall able to contain a 1 cm square of muscle fascia, was designed and built; the aim of the apparatus was to reproduce the subcutaneus zone separated by the fascia interposition, from the muscle-vascular zone. At the system was applied a variable electric field in six different experiments: 4 using porous synthetic membranes and 2 using human muscle fascia.
PubMed: 8698777
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Cataldi</name></author><author><name sortKey="Donini, I G" sort="Donini, I G" uniqKey="Donini I" first="I G" last="Donini">I G Donini</name></author></analytic><series><title level="j">The Journal of cardiovascular surgery</title><idno type="ISSN">0021-9509</idno><imprint><date when="1996" type="published">1996</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Biological Transport</term><term>Electrophysiology</term><term>Fascia (metabolism)</term><term>Humans</term><term>In Vitro Techniques</term><term>Leg</term><term>Lymph (metabolism)</term><term>Lymphedema (metabolism)</term><term>Membranes, Artificial</term><term>Models, Structural</term><term>Porosity</term><term>Proteins (metabolism)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Fascia (métabolisme)</term><term>Humains</term><term>Jambe</term><term>Lymphe (métabolisme)</term><term>Lymphoedème (métabolisme)</term><term>Maquettes de structure</term><term>Membrane artificielle</term><term>Porosité</term><term>Protéines (métabolisme)</term><term>Techniques in vitro</term><term>Transport biologique</term><term>Électrophysiologie</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Proteins</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Membranes, Artificial</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Fascia</term><term>Lymph</term><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Fascia</term><term>Lymphe</term><term>Lymphoedème</term><term>Protéines</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Biological Transport</term><term>Electrophysiology</term><term>Humans</term><term>In Vitro Techniques</term><term>Leg</term><term>Models, Structural</term><term>Porosity</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Humains</term><term>Jambe</term><term>Maquettes de structure</term><term>Membrane artificielle</term><term>Porosité</term><term>Techniques in vitro</term><term>Transport biologique</term><term>Électrophysiologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The presence of proteins (albumin and globulins) in lymphedematous tissue not only gives rise to colloidosmotic pressure but also produces an electrostatic charge endowing the proteins with individual features and different migration rates. The working hypothesis of the experimental study is to transfer lymph proteins from the upper fascia accumulation area to a subfascial drainage area by subjecting them to an adequate difference in potential. A double chamber, variable volume system with separation wall able to contain a 1 cm square of muscle fascia, was designed and built; the aim of the apparatus was to reproduce the subcutaneus zone separated by the fascia interposition, from the muscle-vascular zone. At the system was applied a variable electric field in six different experiments: 4 using porous synthetic membranes and 2 using human muscle fascia.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">8698777</PMID><DateCreated><Year>1996</Year><Month>09</Month><Day>04</Day></DateCreated><DateCompleted><Year>1996</Year><Month>09</Month><Day>04</Day></DateCompleted><DateRevised><Year>2016</Year><Month>10</Month><Day>26</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0021-9509</ISSN><JournalIssue CitedMedium="Print"><Volume>37</Volume><Issue>4</Issue><PubDate><Year>1996</Year><Month>Aug</Month></PubDate></JournalIssue><Title>The Journal of cardiovascular surgery</Title><ISOAbbreviation>J Cardiovasc Surg (Torino)</ISOAbbreviation></Journal><ArticleTitle>Experimental study on protein transmission through the human muscle fascia: preliminary results and application theory in lymphedema.</ArticleTitle><Pagination><MedlinePgn>345-51</MedlinePgn></Pagination><Abstract><AbstractText>The presence of proteins (albumin and globulins) in lymphedematous tissue not only gives rise to colloidosmotic pressure but also produces an electrostatic charge endowing the proteins with individual features and different migration rates. The working hypothesis of the experimental study is to transfer lymph proteins from the upper fascia accumulation area to a subfascial drainage area by subjecting them to an adequate difference in potential. A double chamber, variable volume system with separation wall able to contain a 1 cm square of muscle fascia, was designed and built; the aim of the apparatus was to reproduce the subcutaneus zone separated by the fascia interposition, from the muscle-vascular zone. At the system was applied a variable electric field in six different experiments: 4 using porous synthetic membranes and 2 using human muscle fascia.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Vettorello</LastName><ForeName>G F</ForeName><Initials>GF</Initials><AffiliationInfo><Affiliation>Dipartimento di Scienze Biomediche e Terapie Avanzate (Sez. di Clinica Chirurgica, University of Ferrara, Italy.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Rubbini</LastName><ForeName>M</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Nastruzzi</LastName><ForeName>C</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Menegatti</LastName><ForeName>E</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Esposito</LastName><ForeName>E</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Mascoli</LastName><ForeName>F</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Pozza</LastName><ForeName>E</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Cataldi</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Donini</LastName><ForeName>I G</ForeName><Initials>IG</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Italy</Country><MedlineTA>J Cardiovasc Surg (Torino)</MedlineTA><NlmUniqueID>0066127</NlmUniqueID><ISSNLinking>0021-9509</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008567">Membranes, Artificial</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011506">Proteins</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D001692" MajorTopicYN="N">Biological Transport</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004594" MajorTopicYN="N">Electrophysiology</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005205" MajorTopicYN="N">Fascia</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D066298" MajorTopicYN="N">In Vitro Techniques</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007866" MajorTopicYN="N">Leg</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008196" MajorTopicYN="N">Lymph</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008567" MajorTopicYN="N">Membranes, Artificial</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008961" MajorTopicYN="N">Models, Structural</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016062" MajorTopicYN="N">Porosity</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011506" MajorTopicYN="N">Proteins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1996</Year><Month>8</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1996</Year><Month>8</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1996</Year><Month>8</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">8698777</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Italie</li></country></list><tree><noCountry><name sortKey="Cataldi, A" sort="Cataldi, A" uniqKey="Cataldi A" first="A" last="Cataldi">A. Cataldi</name><name sortKey="Donini, I G" sort="Donini, I G" uniqKey="Donini I" first="I G" last="Donini">I G Donini</name><name sortKey="Esposito, E" sort="Esposito, E" uniqKey="Esposito E" first="E" last="Esposito">E. Esposito</name><name sortKey="Mascoli, F" sort="Mascoli, F" uniqKey="Mascoli F" first="F" last="Mascoli">F. Mascoli</name><name sortKey="Menegatti, E" sort="Menegatti, E" uniqKey="Menegatti E" first="E" last="Menegatti">E. Menegatti</name><name sortKey="Nastruzzi, C" sort="Nastruzzi, C" uniqKey="Nastruzzi C" first="C" last="Nastruzzi">C. Nastruzzi</name><name sortKey="Pozza, E" sort="Pozza, E" uniqKey="Pozza E" first="E" last="Pozza">E. Pozza</name><name sortKey="Rubbini, M" sort="Rubbini, M" uniqKey="Rubbini M" first="M" last="Rubbini">M. Rubbini</name></noCountry><country name="Italie"><noRegion><name sortKey="Vettorello, G F" sort="Vettorello, G F" uniqKey="Vettorello G" first="G F" last="Vettorello">G F Vettorello</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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