Evidence map›Paper›PMID 41172483›Full record

ArticleJournal of applied oral science : revista FOB2025

Single local injection of 3S-HMGB1 enhances early bone healing and titanium implant osseointegration in type 2 diabetic mice.

Bhuvana Lakkasetter Chandrashekar, Alexandra Arteaga, Evelin Rios, Jimena Mora, Gustavo Pompermaier Garlet, Danieli C Rodrigues, Claudia Cristina Biguetti

Abstract readEvaluation Study
In one paragraph

Article in Journal of applied oral science : revista FOB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Bhuvana Lakkasetter ChandrashekarThe University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, Department of Bioengineering, Richardson, Texas, USA.ORCID http://orcid.org/0000-0001-9059-2844
Alexandra ArteagaThe University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, Department of Bioengineering, Richardson, Texas, USA.ORCID http://orcid.org/0000-0002-8610-5860
Evelin RiosThe University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, Department of Bioengineering, Richardson, Texas, USA.ORCID http://orcid.org/0000-0003-3165-128X
Jimena MoraThe University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, Department of Bioengineering, Richardson, Texas, USA.ORCID http://orcid.org/0009-0005-7016-9818
Gustavo Pompermaier GarletUniversidade de São Paulo, Faculdade de Odontologia de Bauru, Departamento de Ciências Biológicas, Bauru, SP, Brasil.ORCID http://orcid.org/0000-0002-5071-8382
Danieli C RodriguesThe University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, Department of Bioengineering, Richardson, Texas, USA.ORCID http://orcid.org/0000-0002-0389-0833
Claudia Cristina BiguettiThe University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, Department of Bioengineering, Richardson, Texas, USA.ORCID http://orcid.org/0000-0003-4503-3108

Funding

Multifunctional Ionic Liquids Coatings for Dental Implant SurfacesR01DE026736 · NIDCR · UNIVERSITY OF TEXAS DALLAS · PI Danieli Rodrigues · 2017 to 2026
$3.7M
NIDCR NIH HHS R01 DE026736
6 · The paper itself

Abstract

objectiveThis study evaluated the therapeutic potential of a single local injection of 3S-HMGB1 in early osseointegration under diabetic conditions in mice. METHODOLOGY: A total of 48 male 129/Sv mice (24 non-diabetic [ND], 24 diabetic [D]) received titanium implants following maxillary first molar extraction. ND and D mice (n:12) were injected with either saline (control) or 3S-HMGB1 (0.75 mg/kg) into the fresh extraction socket. Osseointegration was evaluated at 7 and 21 days post-implantation using microCT, histology (bone-to-implant contact [BIC] and birefringence), and immunohistochemistry for Runx2 and CXCR4.

resultsND controls exhibited early osteogenic activity, with a predominance of Runx2-positive cells at 7 days and successful osseointegration by 21 days. In contrast, D controls showed reduced numbers of Runx2-positive cells and markedly lower BV/TV, indicating compromised bone healing at 21 days. Treatment with 3S-HMGB1 resulted in significantly increased bone volume at the implant site in D animals (55.6±7.20% vs. 44.6±6.23%) and restored BIC from 44.9±9.32% (D controls) to 61.78±11.31% (D 3S-HMGB1), near ND levels (65.16±7.64%). Both ND and D groups treated with 3S-HMGB1 presented enhanced collagen organization. No significant differences were found in CXCR4 between groups; however, in D animals, a distinct peri-implant staining pattern suggested impaired recruitment despite preserved stem cell niches in the bone marrow.

conclusionsCollectively, our findings indicate that a single injection of redox-stable 3S-HMGB1 may represent a promising regenerative strategy to mitigate early implant failure in diabetes. Future studies should explore sustained delivery approaches to enhance long-term outcomes.

Indexed as

Dental ImplantsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2HMGB1 ProteinOsseointegrationTitaniumWound HealingAnimalsCore Binding Factor Alpha 1 SubunitDental Implantation, EndosseousImmunohistochemistryMaleMiceOsteogenesisReceptors, CXCR4Reference ValuesCore Binding Factor Alpha 1 SubunitDental ImplantsHMGB1 ProteinReceptors, CXCR4Titanium

Identifiers

PMID41172483
PMCPMC13290211

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.