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Hemoglobin Protects Enamel against Intrinsic Enamel Erosive Demineralization

dc.contributor.authorCarvalho, Thamyris Souza
dc.contributor.authorAraújo, Tamara Teodoro
dc.contributor.authorOliveira Ventura, Talita Mendes
dc.contributor.authorDionizio, Aline
dc.contributor.authorFrazão Câmara, João Victor
dc.contributor.authorMoraes, Samanta Mascarenhas
dc.contributor.authorLeme, Júlia Chaparro
dc.contributor.authorGrizzo, Larissa Tercilia
dc.contributor.authorCrusca, Edson [UNESP]
dc.contributor.authorTanaka Shibao, Priscila Yumi
dc.contributor.authorMarchetto, Reinaldo [UNESP]
dc.contributor.authorHenrique-Silva, Flavio
dc.contributor.authorPessan, Juliano Pelim [UNESP]
dc.contributor.authorRabelo Buzalaf, Marília Afonso
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionSão Carlos Federal University
dc.date.accessioned2025-04-29T18:36:51Z
dc.date.issued2024-01-10
dc.description.abstractIntroduction: This study investigated the changes in the acquired enamel pellicle (AEP) proteome when this integument is formed in vivo after treatment with sugarcane-derived cystatin (CaneCPI-5), hemoglobin (HB), and a statherin-derived peptide (StN15), or their combination and then exposed to an intrinsic acid challenge. The effectiveness of these treatments in preventing intrinsic erosion was also evaluated. Methods: Ten volunteers, after prophylaxis, in 5 crossover phases, rinsed with the following solutions (10 mL, 1 min): control (deionized water-H2O) – group 1, 0.1 mg/mL CaneCPI-5 – group 2, 1.0 mg/mL HB – group 3, 1.88 × 10−5 M StN15 – group 4, or a blend of these – group 5. Following this, AEP formation occurred (2 h) and an enamel biopsy (10 µL, 0.01 M HCl, pH 2.0, 10 s) was conducted on one incisor. The biopsy acid was then analyzed for calcium (Arsenazo method). The vestibular surfaces of the other teeth were treated with the same acid. Acid-resistant proteins in the residual AEP were then collected and analyzed quantitatively via proteomics. Results: Compared to control, treatment with the proteins/peptide, mixed or isolated, markedly enhanced acid-resistant proteins in the AEP. Notable increases occurred in pyruvate kinase PKM (11-fold, CaneCPI-5), immunoglobulins and submaxillary gland androgen-regulated protein 3B (4-fold, StN15), Hb, and lysozyme C (2-fold, StN15). Additionally, a range of proteins not commonly identified in the AEP but known to bind calcium or other proteins were identified in groups treated with the tested proteins/peptide either in isolation or as a mixture. The mean (SD, mM) calcium concentrations released from enamel were 3.67 ± 1.48a, 3.11 ± 0.72a, 1.94 ± 0.57b, 2.37 ± 0.90a, and 2.38 ± 0.45a for groups 1–5, respectively (RM-ANOVA/Tukey, p < 0.05). Conclusions: Our findings demonstrate that all treatments, whether using a combination of proteins/peptides or in isolation, enhanced acid-resistant proteins in the AEP. However, only HB showed effectiveness in protecting against intrinsic erosive demineralization. These results pave the way for innovative preventive methods against intrinsic erosion, using “acquired pellicle engineering” techniques.en
dc.description.affiliationDepartment of Biological Sciences Bauru School of Dentistry University of São Paulo
dc.description.affiliationDepartment of Biochemistry and Technology Institute of Chemistry São Paulo State University (UNESP)
dc.description.affiliationDepartment of Genetics and Evolution São Carlos Federal University
dc.description.affiliationDepartment of Preventive and Restorative Dentistry School of Dentistry Araçatuba São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Biochemistry and Technology Institute of Chemistry São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Preventive and Restorative Dentistry School of Dentistry Araçatuba São Paulo State University (UNESP)
dc.format.extent90-107
dc.identifierhttp://dx.doi.org/10.1159/000536200
dc.identifier.citationCaries Research, v. 58, n. 2, p. 90-107, 2024.
dc.identifier.doi10.1159/000536200
dc.identifier.issn1421-976X
dc.identifier.issn0008-6568
dc.identifier.scopus2-s2.0-85187024088
dc.identifier.urihttps://hdl.handle.net/11449/298347
dc.language.isoeng
dc.relation.ispartofCaries Research
dc.sourceScopus
dc.subjectAcquired enamel pellicle
dc.subjectHemoglobin
dc.subjectProteomics
dc.subjectTooth wear
dc.titleHemoglobin Protects Enamel against Intrinsic Enamel Erosive Demineralizationen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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