Publication:
Biomechanical restoration potential of pentagalloyl glucose after arterial extracellular matrix degeneration

dc.contributor.coauthorPatnaik, Sourav S.
dc.contributor.coauthorPillalamarri, Narasimha Rao
dc.contributor.coauthorRomero, Gabriela
dc.contributor.coauthorEscobar, G. Patricia
dc.contributor.coauthorSprague, Eugene
dc.contributor.coauthorFinol, Ender A.
dc.contributor.departmentDepartment of Mechanical Engineering
dc.contributor.kuauthorPişkin, Şenol
dc.contributor.kuprofileResearcher
dc.contributor.otherDepartment of Mechanical Engineering
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.yokid148702
dc.date.accessioned2024-11-09T22:58:21Z
dc.date.issued2019
dc.description.abstractThe objective of this study was to quantify pentagalloyl glucose (PGG) mediated biomechanical restoration of degenerated extracellular matrix (ECM). Planar biaxial tensile testing was performed for native (N), enzyme-treated (collagenase and elastase) (E), and PGG (P) treated porcine abdominal aorta specimens (n = 6 per group). An Ogden material model was fitted to the stress-strain data and finite element computational analyses of simulated native aorta and aneurysmal abdominal aorta were performed. The maximum tensile stress of the N group was higher than that in both E and P groups for both circumferential (43.78 +/- 14.18 kPa vs. 10.03 +/- 2.68 kPa vs. 13.85 +/- 3.02 kPa; p = 0.0226) and longitudinal directions (33.89 +/- 8.98 kPa vs. 9.04 +/- 2.68 kPa vs. 14.69 +/- 5.88 kPa; p = 0.0441). Tensile moduli in the circumferential direction was found to be in descending order as N > P > E (195.6 +/- 58.72 kPa > 81.8 +/- 22.76 kPa > 46.51 +/- 15.04 kPa; p = 0.0314), whereas no significant differences were found in the longitudinal direction (p = 0.1607). PGG binds to the hydrophobic core of arterial tissues and the crosslinking of ECM fibers is one of the possible explanations for the recovery of biomechanical properties observed in this study. PGG is a beneficial polyphenol that can be potentially translated to clinical practice for preventing rupture of the aneurysmal arterial wall.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsorshipU.S. National Institutes of Health Award [R01HL121293]
dc.description.sponsorshipAmerican Heart Association Collaborative Sciences Award [16CSA28480006] This work has been supported by a U.S. National Institutes of Health Award (R01HL121293) and an American Heart Association Collaborative Sciences Award (16CSA28480006). The use of the ANSYS biaxial curve fitting tool is gratefully acknowledged through an educational licensing agreement with Ansys Inc.
dc.description.volume6
dc.identifier.doi10.3390/bioengineering6030058
dc.identifier.eissn2306-5354
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85082441073
dc.identifier.urihttp://dx.doi.org/10.3390/bioengineering6030058
dc.identifier.urihttps://hdl.handle.net/20.500.14288/7702
dc.identifier.wos488013600004
dc.keywordsPentagalloyl glucose
dc.keywordsAneurysm
dc.keywordsEnzyme
dc.keywordsBiomechanics
dc.keywordsAorta
dc.languageEnglish
dc.publisherMdpi
dc.sourceBioengineering-Basel
dc.subjectBiotechnology
dc.subjectApplied microbiology
dc.subjectEngineering
dc.subjectBiomedical engineering
dc.titleBiomechanical restoration potential of pentagalloyl glucose after arterial extracellular matrix degeneration
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0002-8799-9472
local.contributor.kuauthorPişkin, Şenol
relation.isOrgUnitOfPublicationba2836f3-206d-4724-918c-f598f0086a36
relation.isOrgUnitOfPublication.latestForDiscoveryba2836f3-206d-4724-918c-f598f0086a36

Files