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1.
Int Endod J ; 51(5): 522-528, 2018 May.
Article in English | MEDLINE | ID: mdl-28329416

ABSTRACT

AIM: To evaluate the resistance to cyclic fatigue of ProTaper Next (PTN; Dentsply Sirona, Ballaigues, Switzerland), Revo-S (Micro-Mega, Besançon, France), Mtwo (Sweden & Martina, Padova, Italy), Twisted Files (TF, SybronEndo, Orange, CA, USA) and EndoWave (J Morita Corporation, Osaka, Japan) used in continuous rotation or in reciprocation of Optimum Torque Reverse motion (OTR). METHODOLOGY: A total of 120 nickel-titanium files were tested. Twenty-four instruments for each brand were divided into two groups (n = 12) on the basis of the motion tested: continuous rotation (Group 1) or reciprocation of OTR motion (Group 2). Resistance to cyclic fatigue was determined by recording time to fracture (TtF) in a stainless steel artificial canal with a 60° angle of curvature and 5 mm radius of curvature. The TtF data were analysed by using two-way analysis of variance (anova) and Bonferroni's post hoc tests at 0.05. RESULTS: Mtwo and TF had significantly higher TtF when compared with all other instruments, both in continuous rotation and in reciprocation of OTR motion (P < 0.0001 and P < 0.05, respectively). No difference was observed between Mtwo and TF (P > 0.05), in both motions. PTN was associated with higher cyclic fatigue resistance than Revo-S and EndoWave, both in continuous rotation and in reciprocation of OTR motions (P < 0.0001). No difference was observed between Revo-S and EndoWave, in both motions (P > 0.05). Reciprocating OTR motion improved TtF of all instruments (P < 0.0001). CONCLUSIONS: Reciprocation of OTR motion improved significantly cyclic fatigue resistance of all instruments tested compared with continuous rotation. Mtwo and TF had significantly higher cyclic fatigue than the other instruments, in both continuous rotation and reciprocation of OTR motion.


Subject(s)
Alloys , Root Canal Therapy/instrumentation , Equipment Failure , Equipment Failure Analysis , Humans , Microscopy, Electron, Scanning , Motion
2.
Parasite Immunol ; 39(11)2017 Nov.
Article in English | MEDLINE | ID: mdl-28929498

ABSTRACT

Visceral leishmaniosis is a zoonotic disease that is transmitted by Lutzomyia longipalpis sandflies. Dogs are the main peri-urban reservoir of the disease, and progression of canine leishmaniosis is dependent on the type of immune response elaborated against the parasite. Type 1 immunity is characterized by effective cellular response, with production of pro-inflammatory cytokines such as tumour necrosis factor alpha (TNF-α). In contrast, Type 2 immunity is predominantly humoral, associated with progression of the disease and mediated by anti-inflammatory cytokines such as interleukin 10 (IL-10). Although seemly important in the dynamics of leishmaniosis, other gene products such as toll-like receptor 2 (TRL-2) and inducible nitric oxide synthase (iNOS) exert unclear roles in the determination of the type of immune response. Given that the dog skin serves as a micro-environment for the multiplication of Leishmania spp., we investigated the parasite load and the expression of TLR-2, iNOS, IL-10 and TNF-α in the skin of 29 infected and 8 control dogs. We found that increased parasite load leads to upregulation of TLR-2, IL-10 and TNF-α, indicating that abundance of these transcripts is associated with infection. We also performed a xenodiagnosis to demonstrate that increased parasitism is a risk factor for infectiousness to sandflies.


Subject(s)
Dog Diseases/parasitology , Interleukin-10/biosynthesis , Leishmania infantum/immunology , Leishmaniasis, Visceral/veterinary , Nitric Oxide Synthase Type II/biosynthesis , Toll-Like Receptor 2/biosynthesis , Tumor Necrosis Factor-alpha/biosynthesis , Animals , Disease Reservoirs/parasitology , Dog Diseases/diagnosis , Dogs , Insect Vectors/parasitology , Interleukin-10/immunology , Leishmania infantum/pathogenicity , Leishmaniasis, Visceral/parasitology , Nitric Oxide Synthase Type II/immunology , Parasite Load , Psychodidae/parasitology , Skin/parasitology , Skin/pathology , Toll-Like Receptor 2/immunology , Tumor Necrosis Factor-alpha/immunology , Zoonoses
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