Dentifrices containing H(2)O-reactive bioactive glasses alleviate hypersensitivity in teeth via the blockage of open dentinal tubules. Here, the ability of two such products to release Ca(2+) ions into human saliva was investigated, together with their influence on the status of this biofluid's (1)H NMR-detectable biomolecules. Human salivary supernatants were equilibrated with increasing volumes of those derived from each dentifrice (5.00 min at 37 degrees C). These biofluids were also equilibrated at 37 degrees C with a preselected quantity of the intact products (samples were collected at increasing timepoints). Salivary Ca(2+) concentrations were monitored by a (1)H NMR technique involving ethylenediamine tetra-acetate addition and/or atomic absorption spectrometry. Added Ca(2+)- and dentifrice supernatant volume (DSV)-induced modifications to the salivary (1)H NMR profile were explored by spectral titration. Data acquired demonstrated added DSV-dependent increases in salivary Ca(2+) concentrations and (Ca(2+)-independent) modifications to the intensities of selected salivary (1)H NMR signals, particularly those of the malodorous amines methyl-, dimethyl-, and trimethylamines, which were diminished by up to 80% of their prior values. Time-dependent elevations in salivary Ca(2+) level were observed on equilibration with the intact dentifrices. Added Ca(2+) ions exerted a concentration-dependent influence on a range of resonances (including those of citrate, succinate, pyruvate, and lactate). These data provide valuable information regarding the mechanisms of action of the products tested.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/jbm.b.31377 | DOI Listing |
Dental Press J Orthod
December 2024
São Leopoldo Mandic School of Dentistry, Department of Molecular Biology (Campinas/SP, Brazil).
Objective: This systematic review aimed to analyze the literature on changes in endogenous salivary biomarkers of pain, anxiety, stress, and inflammation related to tooth movement during orthodontic treatment of children and adolescents.
Material And Methods: An electronic search was performed in nine databases to identify quasi-experimental studies, without restricting publication language and year. Two reviewers extracted the data and assessed the individual risk of bias using the JBI tools, and the certainty of evidence using the GRADE tool.
Sci Transl Med
December 2024
Department of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Sjögren's disease (SjD) is an autoimmune disorder characterized by progressive salivary and lacrimal gland dysfunction, inflammation, and destruction, as well as extraglandular manifestations. SjD is associated with autoreactive B and T cells, but its pathophysiology remains incompletely understood. Abnormalities in regulatory T (T) cells occur in several autoimmune diseases, but their role in SjD is ambiguous.
View Article and Find Full Text PDFFront Mol Biosci
November 2024
Department of Dentistry, Institute of Oral Biology, University of Oslo, Oslo, Norway.
Background: Secretion of saliva is controlled by autonomic nerve signals via regulation of Ca-dependent ion transport across acinar cell membranes. Oxidative stress may affect this process, leading to a decrease in saliva production. This study investigates elements of the Ca regulatory pathway and their vulnerability to hydrogen peroxide-induced oxidative stress.
View Article and Find Full Text PDFFunction (Oxf)
October 2024
Department of Molecular Pathobiology, New York University College of Dentistry, New York, USA.
Ca2+ signaling via the store operated Ca2+ entry (SOCE) mediated by STIM1 and STIM2 proteins and the ORAI1 Ca2+ channel is important in saliva fluid secretion and has been associated with Sjogren's disease (SjD). However, there are no studies addressing STIM1/2 dysfunction in salivary glands or SjD in animal models. We report that mice lacking Stim1 and Stim2 (Stim1/2K14Cre(+)) in salivary glands exhibited reduced Ca2+ levels and hyposalivate.
View Article and Find Full Text PDFFree Radic Biol Med
November 2024
Department of Orthopaedics, The First Affiliated Hospital of Jinan University, No. 613 11 West Huangpu Avenue, Tianhe District, Guangzhou, Guangdong, 510630, China.
Rationale: Difficulty in skin wound healing is a concern for diabetic patients across the world. Impaired mitochondrial dysfunction and aging-related vascular dysfunction in human umbilical vein endothelial cells (HUVECs) caused by oxidative stress are major impediments to diabetic wound healing. However, research on skin repair at the mechanistic level by improving mitochondrial function and inhibiting oxidative stress-induced HUVEC senescence remains lacking.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!