Titanium dioxide dental implants surfaces related oxidative stress in bone remodeling: a systematic review

被引:19
作者
Abdulhameed, Elaf Akram [1 ,2 ]
Al-Rawi, Natheer H. [3 ]
Omar, Marzuki [1 ]
Khalifa, Nadia [2 ]
Samsudin, A. B. Rani [3 ]
机构
[1] Univ Sains Malaysia, Sch Dent Sci, Kota Baharu, Kelantan, Malaysia
[2] Univ Sharjah, Coll Dent Med, Prevent & Restorat Dent, Sharjah, U Arab Emirates
[3] Univ Sharjah, Oral & Craniofacial Hlth Sci, Sharjah, U Arab Emirates
关键词
Angiogenesis; Nanoparticles; Nanotube; ROS; Osteogenesis; TiO2; IN-VITRO; OSTEOGENESIS; NANOTUBES; TISSUE; ACCURACY;
D O I
10.7717/peerj.12951
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background. Titanium dioxide dental implants have a controversial effect on reactive oxygen species (ROS) production. ROS is necessary for cellular signal transmission and proper metabolism, but also has the ability to cause cell death as well as DNA, RNA, and proteins damage by excessive oxidative stress. This study aimed to systematically review the effect of titanium dioxide dental implant-induced oxidative stress and its role on the osteogenesis-angiogenesis coupling in bone remodeling. Methods. This systematic review was performed conforming to preferred reporting items for systematic review and meta-analysis (PRISMA) model. Four different databases (PubMed, Science Direct, Scopus and Medline databases) as well as manual searching were adopted. Relevant studies from January 2000 till September 2021 were retrieved. Critical Appraisal Skills Programme (CASP) was used to assess the quality of the selected studies. Results. Out of 755 articles, only 14 which met the eligibility criteria were included. Six studies found that titanium dioxide nanotube (TNT) reduced oxidative stress and promoted osteoblastic activity through its effect on Wnt, mitogen-activated protein kinase (MAPK) and forkhead box protein O1 (FoxO1) signaling pathways. On the other hand, three studies confirmed that titanium dioxide nanoparticles (TiO(2)NPs) induce oxidative stress, reduce ostegenesis and impair antioxidant defense system as a significant negative correlation was found between decreased SIR3 protein level and increased superoxide (O-2(center dot-)). Moreover, five studies proved that titanium implant alloy enhances the generation of ROS and induces cytotoxicity of osteoblast cells via its effect on NOX pathway. Conclusion. TiO(2)NPs stimulate a wide array of oxidative stress related pathways. Scientific evidence are in favor to support the use of TiO2 nanotube-coated titanium implants to reduce oxidative stress and promote osteogenesis in bone remodeling. To validate the cellular and molecular cross talk in bone remodeling of the present review, well-controlled clinical trials with a large sample size are required.
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