Evidence map›Paper›PMID 36778044›Full record

ArticleExperimental and therapeutic medicine2023

G‑CSF delays tooth extraction socket bone healing via the inhibition of bone turnover in mice.

Masayuki Oshitani, Kazuki Takaoka, Miho Ueta, Kohei Tomimoto, Hirokazu Hattori, Naomichi Yoneda, Koji Yamanegi, Kazuma Noguchi, Hiromitsu Kishimoto

Abstract read
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Article in Experimental and therapeutic medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Masayuki OshitaniDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Kazuki TakaokaDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Miho UetaDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Kohei TomimotoDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Hirokazu HattoriDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Naomichi YonedaDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Koji YamanegiDepartment of Pathology, School of Medicine, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Kazuma NoguchiDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.
Hiromitsu KishimotoDepartment of Oral and Maxillofacial Surgery, Hyogo Medical University, Nishinomiya, Hyogo 663-8501, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Granulocyte colony-stimulating factor (G-CSF) regulates the survival, proliferation and differentiation of all cells in the neutrophil lineage, and is consequently used for neutropenic conditions. Upon G-CSF administration, osteoblasts and osteocytes are suppressed, and the support system allowing hematopoietic stem cells to remain in the microenvironment is diminished. The present study focused on and investigated G-CSF as a regulatory factor of bone remodeling. The aim of the present study was to investigate the effect of G-CSF administration on the bone healing of tooth extraction sockets. Significant differences in the bone volume fraction, and trabecular separation of the proximal femurs and alveolar septa were observed between the G-CSF and control (saline-treated) groups. The trabecular bone of the femur and alveolar septa was reduced in the G-CSF group compared with that in the control group. In addition, serum procollagen type 1 N-terminal propeptide levels, a marker of bone formation, were lower in the G-CSF group compared with in the control group. Fibrous connective tissues and immature bone were observed in the extraction socket, and bone healing was delayed in the G-CSF group compared with that in the control group. The bone area in the extraction socket 6 days after tooth extraction was significantly smaller in the G-CSF group (23.6%) than that in the control group (45.1%). Furthermore, G-CSF administration reduced the number of canaliculi per osteocyte and inhibited the connection of osteocyte networks. Consequently, osteoblast activation was inhibited and bone remodeling changed to a state of low bone turnover in the G-CSG group. Analysis of bone formation parameters revealed that the G-CSF group exhibited a lower mineral apposition rate compared with in the control group. In conclusion, these findings indicated that G-CSF may delay bone healing of the socket after tooth extraction.

Indexed as

bone healingbone remodelingbone turnovergranulocyte colony-stimulating factortooth extraction

Identifiers

PMID36778044
PMCPMC9910036

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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 OpenQuestion graph.