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Author Sudoh, Taku| Ikeda, Shuhei| Shigenobu, Keisuke| Tsuzuki, Seiji| Dokko, Kaoru| Watanabe, Masayoshi| Shinoda, Wataru| Ueno, Kazuhide|
Published Date 2023-06-20
Publication Title The Journal of Physical Chemistry C
Volume volume127
Issue issue25
Publisher American Chemical Society (ACS)
Start Page 12295
End Page 12303
ISSN 1932-7447
NCID AA1217589X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 The Authors.
File Version publisher
DOI 10.1021/acs.jpcc.3c02112
Web of Science KeyUT 001016710400001
Related Url isVersionOf https://doi.org/10.1021/acs.jpcc.3c02112
FullText URL fulltext.pdf
Author Miyamoto, Yuki| Hiramoto, Ayami| Iwakuni, Kana| Kuma, Susumu| Enomoto, Katsunari| Nakayama, Naofumi| Baba, Masaaki|
Note This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. This article appeared in Yuki Miyamoto, Ayami Hiramoto, Kana Iwakuni, Susumu Kuma, Katsunari Enomoto, Naofumi Nakayama, Masaaki Baba; Analysis on high-resolution spectrum of the S1–S0 transition of free-base phthalocyanine. J. Chem. Phys. 14 April 2024; 160 (14): 144304. https://doi.org/10.1063/5.0191810 and may be found at https://doi.org/10.1063/5.0191810.| This fulltext file will be available in Apr. 2025.|
Published Date 2024-04-09
Publication Title The Journal of Chemical Physics
Volume volume160
Issue issue14
Publisher AIP Publishing
Start Page 144304
ISSN 0021-9606
NCID AA00694991
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2024 Author(s).
File Version publisher
PubMed ID 38591681
DOI 10.1063/5.0191810
Web of Science KeyUT 001198859200019
Related Url isVersionOf https://doi.org/10.1063/5.0191810
FullText URL fulltext.pdf
Author Naito, Hidefumi| Sumi, Tomonari| Koga, Kenichiro|
Published Date 2024
Publication Title Faraday Discussions
Volume volume249
Publisher Royal Society of Chemistry (RSC)
Start Page 440
End Page 452
ISSN 1359-6640
NCID AA10836538
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © The Royal Society of Chemistry 2024
File Version publisher
PubMed ID 37791511
DOI 10.1039/d3fd00104k
Web of Science KeyUT 001077081700001
Related Url isVersionOf https://doi.org/10.1039/d3fd00104k
JaLCDOI 10.18926/AMO/66912
FullText URL 78_2_095.pdf
Author Itano, Junko| Kiura, Katsuyuki| Maeda, Yoshinobu| Miyahara, Nobuaki|
Abstract The lungs are very complex organs, and the respiratory system performs the dual roles of repairing tissue while protecting against infection from various environmental stimuli. Persistent external irritation disrupts the immune responses of tissues and cells in the respiratory system, ultimately leading to respiratory disease. Neuropeptide Y (NPY) is a 36-amino-acid polypeptide and a neurotransmitter that regulates homeostasis. The NPY receptor is a seven-transmembrane-domain G-protein-coupled receptor with six subtypes (Y1, Y2, Y3, Y4, Y5, and Y6). Of these receptors, Y1, Y2, Y4, and Y5 are functional in humans, and Y1 plays important roles in the immune responses of many organs, including the respiratory system. NPY and the Y1 receptor have critical roles in the pathogenesis of asthma, chronic obstructive pulmonary disease, and idiopathic pulmonary fibrosis. The effects of NPY on the airway immune response and pathogenesis differ among respiratory diseases. This review focuses on the involvement of NPY in the airway immune response and pathogenesis of various respiratory diseases.
Keywords neuropeptide y Y1 receptor airway immune response bronchial epithelial cells respiratory disease
Amo Type Review
Publication Title Acta Medica Okayama
Published Date 2024-04
Volume volume78
Issue issue2
Publisher Okayama University Medical School
Start Page 95
End Page 106
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2024 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 38688827
Web of Science KeyUT 001229151800001
FullText URL fulltext.pdf
Author Matsumoto, Masakazu| Yagasaki, Takuma| Tanaka, Hideki|
Note This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. This article appeared in Masakazu Matsumoto, Takuma Yagasaki, Hideki Tanaka; GenIce-core: Efficient algorithm for generation of hydrogen-disordered ice structures. J. Chem. Phys. 7 March 2024; 160 (9): 094101. https://doi.org/10.1063/5.0198056 and may be found at https://doi.org/10.1063/5.0198056.| This fulltext file will be available in Mar. 2025.|
Published Date 2024-03-01
Publication Title The Journal of Chemical Physics
Volume volume160
Issue issue9
Publisher AIP Publishing
Start Page 094101
ISSN 0021-9606
NCID AA00694991
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2024 Author(s).
File Version publisher
PubMed ID 38426513
DOI 10.1063/5.0198056
Web of Science KeyUT 001178860800001
Related Url isVersionOf https://doi.org/10.1063/5.0198056
JaLCDOI 10.18926/AMO/66664
FullText URL 78_1_001.pdf
Author Sun, Cuiming| Matsukawa, Akihiro|
Abstract Liver fibrosis, which ultimately leads to liver cirrhosis and hepatocellular carcinoma, is a major health burden worldwide. The progression of liver fibrosis is the result of the wound-healing response of liver to repeated injury. Hepatic macrophages are cells with high heterogeneity and plasticity and include tissue-resident macrophages termed Kupffer cells, and recruited macrophages derived from circulating monocytes, spleen and peritoneal cavity. Studies have shown that hepatic macrophages play roles in the initiation and progression of liver fibrosis by releasing inflammatory cytokines/chemokines and pro-fibrogenic factors. Furthermore, the development of liver fibrosis has been shown to be reversible. Hepatic macrophages have been shown to alternately regulate both the regression and turnover of liver fibrosis by changing their phenotypes during the dynamic progression of liver fibrosis. In this review, we summarize the role of hepatic macrophages in the progression and regression of liver fibrosis.
Keywords ERK-MAPK SPRED2 fibrosis macrophages
Amo Type Review
Publication Title Acta Medica Okayama
Published Date 2024-02
Volume volume78
Issue issue1
Publisher Okayama University Medical School
Start Page 1
End Page 8
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2024 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 38419308
Web of Science KeyUT 001203658200006
FullText URL fulltext20240205-01.pdf
Author Tokushige, Keisuke| Abe, Takumi|
Keywords C3-N1' bisindoles bromination umpolung rivularin A alkaloid
Note This is the peer reviewed version of the following article: [K. Tokushige, T. Abe, Chem. Eur. J. 2024, 30, e202302963. https://doi.org/10.1002/chem.202302963], which has been published in final form at [https://doi.org/10.1002/chem.202302963]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.| This fulltext file will be available in Jan. 2025.|
Published Date 2024-01-08
Publication Title Chemistry – A European Journal
Volume volume30
Issue issue11
Publisher Wiley
Start Page e202302963
ISSN 0947-6539
NCID AA11076269
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 Wiley-VCH GmbH
File Version author
PubMed ID 37988219
DOI 10.1002/chem.202302963
Web of Science KeyUT 001142083100001
Related Url isVersionOf https://doi.org/10.1002/chem.202302963
FullText URL fulltext20240130-01.pdf
Author Miyazaki, Yusuke| Shinoda, Wataru|
Note This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Chemical Information and Modeling, copyright © 2023 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jcim.3c01611.| This fulltext file will be available in Dec. 2024.|
Published Date 2023-12-29
Publication Title Journal of Chemical Information and Modeling
Volume volume64
Issue issue2
Publisher American Chemical Society (ACS)
Start Page 532
End Page 542
ISSN 1549-9596
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 American Chemical Society
File Version author
PubMed ID 38156656
DOI 10.1021/acs.jcim.3c01611
Web of Science KeyUT 001146739900001
Related Url isVersionOf https://doi.org/10.1021/acs.jcim.3c01611
FullText URL fulltext20240109-03.pdf
Author Yamada, Koji| Tsubogo, Tetsu| Kanazawa, Hikaru| Ishizuka, Sayaka| Ohyama, Koutaro| Kaida, Masaki| Abe, Takumi|
Keywords hemiaminals indoles ring-switch thiazolo[4.5-b]indoles thioamides
Note This is the peer reviewed version of the following article: [K. Yamada, T. Tsubogo, H. Kanazawa, S. Ishizuka, K. Ohyama, M. Kaida, T. Abe, Eur. J. Org. Chem. 2024, 27, e202301130. https://doi.org/10.1002/ejoc.202301130], which has been published in final form at [https://doi.org/10.1002/ejoc.202301130]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.| This fulltext file will be available in Dec. 2024.|
Published Date 2023-12-19
Publication Title European Journal of Organic Chemistry
Volume volume27
Issue issue4
Publisher Wiley
Start Page e202301130
ISSN 1434-193X
NCID AA1118165X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 Wiley-VCH GmbH
File Version author
DOI 10.1002/ejoc.202301130
Web of Science KeyUT 001127624500001
Related Url isVersionOf https://doi.org/10.1002/ejoc.202301130
FullText URL fulltext20231128-01.pdf
Author Mitsudo, Koichi| Okumura, Yasuyuki| Sato, Eisuke| Suga, Seiji|
Keywords electrocatalysis electrochemistry electrosynthesis indirect electrolysis mediator
Note This is the peer reviewed version of the following article: [K. Mitsudo, Y. Okumura, E. Sato, S. Suga, Eur. J. Org. Chem. 2023, 26, e202300835. https://doi.org/10.1002/ejoc.202300835], which has been published in final form at [https://doi.org/10.1002/ejoc.202300835]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.| This fulltext file will be available in Nov. 2024.|
Published Date 2023-11-13
Publication Title European Journal of Organic Chemistry
Volume volume26
Issue issue47
Publisher Wiley
Start Page e202300835
ISSN 1434-193X
NCID AA1118165X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 Wiley-VCH GmbH
File Version author
DOI 10.1002/ejoc.202300835
Web of Science KeyUT 001100702300001
Related Url isVersionOf https://doi.org/10.1002/ejoc.202300835
FullText URL fulltext.pdf
Author Khazan, Negar| Kim, Kyu Kwang| Hansen, Jeanne N.| Singh, Niloy A.| Moore, Taylor| Snyder, Cameron W. A.| Pandita, Ravina| Strawderman, Myla| Fujihara, Michiko| Takamura, Yuta| Jian, Ye| Battaglia, Nicholas| Yano, Naohiro| Teramoto, Yuki| Arnold, Leggy A.| Hopson, Russell| Kishor, Keshav| Nayak, Sneha| Ojha, Debasmita| Sharon, Ashoke| Ashton, John M.| Wang, Jian| Milano, Michael T.| Miyamoto, Hiroshi| Linehan, David C.| Gerber, Scott A.| Kawar, Nada| Singh, Ajay P.| Tabdanov, Erdem D.| Dokholyan, Nikolay V.| Kakuta, Hiroki| Jurutka, Peter W.| Schor, Nina F.| Rowswell-Turner, Rachael B.| Singh, Rakesh K.| Moore, Richard G.|
Published Date 2022-04-11
Publication Title Journal of Medicinal Chemistry
Volume volume65
Issue issue8
Publisher American Chemical Society (ACS)
Start Page 6039
End Page 6055
ISSN 0022-2623
NCID AA00702411
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 The Authors.
File Version publisher
PubMed ID 35404047
DOI 10.1021/acs.jmedchem.1c01878
Web of Science KeyUT 000797573100012
Related Url isVersionOf https://doi.org/10.1021/acs.jmedchem.1c01878
JaLCDOI 10.18926/AMO/65750
FullText URL 77_4_395.pdf
Author Pavlovic, Marko| Babic, Dragan| Rastovic, Pejana| Arapovic, Jurica| Martinac, Marko| Jakovac, Sanja| Barbaric, Romana|
Abstract We investigated the relationship between serum tumor necrosis factor-alpha (TNF-α) levels and psychopathological symptoms, clinical and socio-demographic characteristics and antipsychotic therapy in individuals with schizophrenia. TNF-α levels were measured in 90 patients with schizophrenia and 90 healthy controls matched by age, gender, smoking status, and body mass index. The Positive and Negative Syndrome Scale (PANSS) was used to assess the severity of psychopathology in patients. No significant differences in TNF-α levels were detected between the patients and controls (p=0.736). TNF-α levels were not correlated with total, positive, negative, general, or composite PANSS scores (all p>0.05). A significant negative correlation was observed between TNF-α levels and the PANSS cognitive factor (ρ=−0.222, p=0.035). A hierarchical regression analysis identified the cognitive factor as a significant predictor of the TNF-α level (beta=−0.258, t=−2.257, p=0.027). There were no significant differences in TNF-α levels among patients treated with different types of antipsychotics (p=0.596). TNF-α levels correlated positively with the age of onset (ρ=0.233, p=0.027) and negatively with illness duration (ρ=−0.247, p=0.019) and antipsychotic treatment duration (ρ=−0.256, p=0.015). These results indicate that TNF-α may be involved in cognitive impairment in schizophrenia, and would be a potential clinical-state marker in schizophrenia.
Keywords tumor necrosis factor-alpha schizophrenia psychopathology immune system
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2023-08
Volume volume77
Issue issue4
Publisher Okayama University Medical School
Start Page 395
End Page 405
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2023 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 37635140
Web of Science KeyUT 001163659800010
JaLCDOI 10.18926/AMO/65749
FullText URL 77_4_387.pdf
Author Kataoka, Takahiro| Habu, Hiroshi| Tanaka, Ayumi| Naoe, Shota| Murakami, Kaito| Fujimoto, Yuki| Yukimine, Ryohei| Takao, Soshi| Mitsunobu, Fumihiro| Yorifuji, Takashi| Yamaoka, Kiyonori|
Abstract No epidemiological studies have examined the health effects of daily bathing in radon hot springs. In this cross-sectional study, we investigated the associations between radon hot spring bathing and health conditions. The target population was 5,250 adults ≥ 20 years old in the town of Misasa, Japan. We collected information about the participants’ bathing habits and alleviation of a variety of disease symptoms, and their self-rated health (SRH). Unadjusted and adjusted odds ratios (ORs) and 95% confidence intervals (CI) were calculated. In both the adjusted and unadjusted models of hypertension, significant associations between the > 1×/week hot spring bathing and the alleviation of hypertension symptoms were observed compared to the group whose hot spring bathing was <1×/week: adjusted model, OR 5.40 (95%CI: 1.98-14.74); unadjusted model, 3.67 (1.50-8.99) and for gastroenteritis: adjusted model, 9.18 (1.15-72.96); unadjusted model, 7.62 (1.59-36.49). Compared to the no-bathing group, higher SRH was significantly associated with both bathing < 1×/week: unadjusted model, 2.27 (1.53-3.37) and > 1×/week: adjusted model, 1.91 (1.15-3.19). These findings suggest that bathing in radon hot springs is associated with higher SRH and the alleviation of hypertension and gastroenteritis.
Keywords radon hot spring bathing habit self-rated health cross-section study
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2023-08
Volume volume77
Issue issue4
Publisher Okayama University Medical School
Start Page 387
End Page 394
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2023 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 37635139
Web of Science KeyUT 001163659800003
JaLCDOI 10.18926/AMO/65741
FullText URL 77_4_359.pdf
Author Koshida, Tomohiro| Maruta, Toyoaki| Tanaka, Nobuhiko| Hidaka, Kotaro| Kurogi, Mio| Nemoto, Takayuki| Yanagita, Toshihiko| Takeya, Ryu| Tsuneyoshi, Isao|
Abstract Pulsed radiofrequency (PRF) is a safe method of treating neuropathic pain by generating intermittent electric fields at the needle tip. Resiniferatoxin (RTX) is an ultrapotent agonist of transient receptor potential vanilloid subtype-1 (TRPV1) receptors. We investigated the mechanism of PRF using a rat model of RTX-induced neuropathic pain. After administering RTX intraperitoneally, PRF was applied to the right sciatic nerve. We observed the changes in TRPV1, calcitonin gene-related peptide (CGRP), and brain-derived neurotrophic factor (BDNF) in the dorsal root ganglia by western blotting. Expressions of TRPV1 and CGRP were significantly lower in the contralateral (RTX-treated, PRF-untreated) tissue than in control rats (p<0.0001 and p<0.0001, respectively) and the ipsilateral tissues (p<0.0001 and p<0.0001, respectively). BDNF levels were significantly higher in the contralateral tissues than in the control rats (p<0.0001) and the ipsilateral tissues (p<0.0001). These results suggest that, while TRPV1 and CGRP are decreased by RTX-induced neuronal damage, increased BDNF levels result in pain development. PRF may promote recovery from neuronal damage with concomitant restoration of TRPV1 and CGRP, and exert its analgesic effect by reversing BDNF increase. Further research is required to understand the role of TRPV1 and CGRP restoration in improving mechanical allodynia.
Keywords pulsed radiofrequency resiniferatoxin transient receptor potential vanilloid subtype-1 (TRPV1) calcitonin gene-related peptide (CGRP) brain-derived neurotrophic factor (BDNF)
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2023-08
Volume volume77
Issue issue4
Publisher Okayama University Medical School
Start Page 359
End Page 364
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2023 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 37635135
Web of Science KeyUT 001163659800011
FullText URL fulltext20230721-01.pdf
Author Yamada, Iori| Terasaki, Hidenori| Urakawa, Satoru| Kondo, Tadashi| Machida, Akihiko| Tange, Yoshinori| Higo, Yuji|
Keywords Fe alloy Sound velocity Liquid Core Mercury Light element
Note The version of record of this article, first published in Physics and Chemistry of Minerals, is available online at Publisher’s website: http://dx.doi.org/10.1007/s00269-023-01243-8|
Published Date 2023-07-01
Publication Title Physics and Chemistry of Minerals
Volume volume50
Issue issue3
Publisher Springer Science and Business Media LLC
Start Page 19
ISSN 0342-1791
NCID AA00773930
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © The Author(s) 2023
File Version publisher
DOI 10.1007/s00269-023-01243-8
Web of Science KeyUT 001020912400001
Related Url isVersionOf https://doi.org/10.1007/s00269-023-01243-8
JaLCDOI 10.18926/AMO/65489
FullText URL 77_3_243.pdf
Author Shibata, Yusuke| Eguchi, Jun| Wada, Jun|
Abstract Brown adipose tissue (BAT) plays a critical role in metabolic homeostasis. BAT dysfunction is associated with the development of obesity through an imbalance between energy expenditure and energy intake. The nuclear receptor peroxisome proliferator-activated receptor gamma (PPARγ) is the master regulator of adipogenesis. However, the roles of PPARγ and thiazolidinediones (TZDs) in the regulation of BAT metabolism remain unclear. TZDs, which are selective PPARγ activators, improve systemic insulin resistance in animals and humans. In the present study, we generated brown adipocyte-specific PPARγ-deficient mice (BATγKO) to examine the in vivo roles of PPARγ and TZDs in BAT metabolism. In electron microscopic examinations, brown adipocyte-specific PPARγ deletion promoted severe whitening of brown fat and morphological alteration of mitochondria. Brown adipocyte-specific PPARγ deletion also reduced mRNA expression of BAT-selective genes. Although there was no difference in energy expenditure between control and BATγKO mice in calorimetry, norepinephrine-induced thermogenesis was impaired in BATγKO mice. Moreover, pioglitazone treatment improved diet-induced insulin resistance in the control mice but not in the BATγKO mice. These findings suggest that BAT PPARγ is necessary for the maintenance of brown adipocyte function and for the insulin-sensitizing action of TZDs.
Keywords PPARγ brown adipose tissue thiazolidinediones
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2023-06
Volume volume77
Issue issue3
Publisher Okayama University Medical School
Start Page 243
End Page 254
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2023 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 37357625
Web of Science KeyUT 001026279600002
FullText URL K0006824_abstract_review.pdf K0006824_summary.pdf
Author Wang, Yaming|
Published Date 2023-03-24
Content Type Thesis or Dissertation
Grant Number 甲第6824号
Granted Date 2023-03-24
Thesis Type Doctor of Philosophy in Dental Science
Grantor 岡山大学
language English
Copyright Holders © The Royal Society of Chemistry 2021
FullText URL K0006817_abstract_review .pdf K0006817_fulltext.pdf K0006817_summary.pdf
Author ANADA, Risa|
Published Date 2023-03-24
Content Type Thesis or Dissertation
Grant Number 甲第6817号
Granted Date 2023-03-24
Thesis Type Doctor of Philosophy in Dental Science
Grantor 岡山大学
language English
Copyright Holders © The Royal Society of Chemistry 2023
FullText URL fulltext20230508-02.pdf
Author Formica, Michele| Rogova, Tatiana| Shi, Heyao| Sahara, Naoto| Ferko, Branislav| Farley, Alistair J. M.| Christensen, Kirsten E.| Duarte, Fernanda| Yamazaki, Ken| Dixon, Darren J.|
Note The version of record of this article, first published in Nature Chemistry, is available online at Publisher’s website: http://dx.doi.org/10.1038/s41557-023-01165-6|
Published Date 2023-05-01
Publication Title Nature Chemistry
Volume volume15
Issue issue5
Publisher Springer Science and Business Media LLC
Start Page 714
End Page 721
ISSN 1755-4330
NCID AA12391432
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © The Author(s) 2023
File Version publisher
PubMed ID 37127757
DOI 10.1038/s41557-023-01165-6
Related Url isVersionOf https://doi.org/10.1038/s41557-023-01165-6
JaLCDOI 10.18926/AMO/64122
FullText URL 76_6_715.pdf
Author Mohammed Zahedul Islam Nizami| Gorduysus, Melahat| Shinoda-Ito, Yuki| Yamamoto, Tadashi| Nishina, Yuta| Takashiba, Shogo| Arias, Zulema|
Abstract The failure of endodontic treatment is directly associated with microbial infection in the root canal or periapical areas. An endodontic sealer that is both bactericidal and biocompatible is essential for the success of root canal treatments. This is one of the vital issues yet to be solved in clinical dental practice. This in vitro study assessed the effectiveness of graphene oxide (GO) composites GO-CaF2 and GO-Ag-CaF2 as endodontic sealer materials. Dentin slices were coated with either the GO-based composites or commonly used root canal sealers (non-eugenol zinc oxide sealer). The coated slices were treated in 0.9% NaCl, phosphate-buffered saline (PBS), and simulated body fluid (SBF) at 37˚C for 24 hours to compare their sealing effect on the dentin surface. In addition, the radiopacity of these composites was examined to assess whether they complied with the requirements of a sealer for good radiographic visualization. Scanning electron microscopy showed the significant sealing capability of the composites as coating materials. Radiographic images confirmed their radiopacity. Mineral deposition indicated their bioactivity, especially of GO-Ag-CaF2, and thus it is potential for regenerative application. They were both previously shown to be bactericidal to oral microbes and cytocompatible with host cells. With such a unique assemblage of critical properties, these GO-based composites show promise as endodontic sealers for protection against reinfection in root canal treatment and enhanced success in endodontic treatment overall.
Keywords bioactive sealer graphene oxide mineral deposition antimicrobial activity radiopacity
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2022-12
Volume volume76
Issue issue6
Publisher Okayama University Medical School
Start Page 715
End Page 721
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2022 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 36549774
Web of Science KeyUT 000905195100012