Avacir Casanova Andrello

Climate change and the impacts related to nonbiodegradable synthetic materials highlight the need for sustainable alternatives. Biopolymers from renewable sources show great potential for producing hydrogels, which are three-dimensionally crosslinked materials with high water absorption. In this work, super-absorbent biodegradable hydrogels were produced via single-step reactive extrusion using mixtures of starch, gelatin, cellulose, and xanthan gum, with glycerol as a plasticizer, and citric acid as a crosslinking agent. Pelleted hydrogels were obtained with water absorption between 290% and 363%. Reactive extrusion promoted the formation of new ester and amide bonds, confirmed by FT-IR. Citric acid was effective as a crosslinker, and higher citric acid content (3%) produced samples with greater swelling, supported by the porous internal structure observed. Preliminary agricultural tests showed that the formulation with the highest citric acid content, when added to soil at 5%, significantly increased water-holding capacity and resulted in the highest germination rate of maize seeds. Overall, the extrusion process proved efficient, scalable, and environmentally friendly for producing biodegradable hydrogels for agricultural applications.

Several instrumentations systems are available in the market and it is necessary to assess their behavior in curved root canals. Aim: To analyze the ability of two manual instrumentation techniques to center mesial root canals of mandibular molars, studied by computed microtomography (micro-CT). Materials and Method: Twenty mesial root canals of mandibular molars were matched based on similar morphological dimensions using micro-CT evaluation and divided in 2 groups (n=10): (1) Crown-down technique with Gates-Glidden drills and K-Flexofiles and (2) M manual NiTi rotary system. Changes in volume, surface area and canal transportation were compared using an unpaired t-test with a 5% significance level. Results: No significant differences were observed between groups regarding volume surface area after root canal preparation (p>0.05). Variation in the centroid differed between groups in the total canal length, and in the cervical and middle thirds, with better centralization for the M files (p<0.05). Conclusions: Both manual instrumentation techniques had similar volume and surface area variation. Both techniques left unprepared canal areas with similar values. M manual NiTi files caused minor canal transportation.

This study assessed the effect of composite resins, aggregated or not with S-PRG particles, and the use of toothpaste in controlling demineralization and bacterial growth. Human molars were distributed into 3 groups: control (CT) – sound teeth, Beautifil Bulk Restorative System (aggregated with S-PRG) (BB), Filtek One Bulk Fill (without S-PRG) (FB). Teeth destined for groups BB and FB previously received Class I preparations (4 × 4 × 4 mm), followed by single-increment restorations. All teeth were sectioned mesiodistally, with all specimens subjected to cariogenic challenge for 5 days, including microcosm biofilm formation. Half of each tooth was exposed to toothpaste (CTF, BBF, FBF). The loss of microhardness was assessed considering the initial microhardness as 100% on enamel, dentin, and composite resin substrates. Colony Forming Units (CFU/mL) were counted in 3 media. Data analysis used one-way ANOVA, Tukey HSD test, and paired t-test (α = 0.05). Toothpaste significantly reduced CFU/mL for total bacteria and genus Streptococcus (p < 0.05), with no significant difference for Streptococcus mutans. Enamel microhardness was positively affected by toothpaste. Both restorative systems controlled enamel demineralization, with FB and FBF outperforming BB and BBF. There was minor degradation of both composite resins, between 10% and 22%. Toothpaste effectively reduced microorganisms, irrespective of the composite resin. Regarding demineralization control, both restorative systems, with and without S-PRG particles, were effective on enamel.

Background: Periodontitis can induce systemic inflammation, and it may affect the testicles and male reproductive performance. This study investigated the effects of periodontitis on the testicles, reproductive performance, and offspring development in male rats.Methods: Male Wistar rats were induced with periodontitis by ligating their first molars. After 14 days of inducing periodontal lesions, the animals were observed for an additional 54 days, corresponding to a complete cycle of spermatogenesis. Rats from the periodontitis group (GP, n = 12) and the control group (GC, n = 12) were paired with healthy females (n = 48) for 10 days, equivalent to 2 estrous cycles. Post‐mating, the males underwent microtomographic, histological, and reproductive parameter assessments.Results: Microtomographic analysis revealed higher porosity around the first molar in GP (26 ± 6%) and greater distance between the amelocemental junction and the alveolar bone (1.37 [1.12–1.90] mm), indicative of bone resorption. GP also exhibited significant decreases in final body weight, reduced Sertoli and Leydig cell counts, and lowered testosterone levels compared to GC. Significant morphological alterations in sperm tails were observed in GP compared to GC.Conclusions: Periodontitis adversely affected reproductive performance, evoking, and offspring development in male rats. These findings highlight the systemic impacts of periodontal disease on male reproductive health in an animal model.Plain Language Summary: Our study investigated how periodontitis can affect male reproductive health in rats and offspring development. We induced periodontitis in male rats and, after a full cycle of sperm production, these rats were mated with healthy females. We observed that the rats with periodontitis had worse reproductive performance compared to the control group without periodontitis. Additionally, the offspring of the rats with periodontitis showed signs of compromised intrauterine development and a higher incidence of congenital malformations. These results highlight that the inflammation caused by periodontitis can have adverse effects beyond the mouth, significantly impacting male reproductive health and offspring development. These findings suggest the need for further research into the clinical implications of periodontitis on reproductive health.

The sublethal toxic effects of pyriproxyfen, an insect juvenile hormone analog (JHA) insecticide, on the circulating metabolite balance in the Neotropical brown stink bug, Euschistus heros, one of the main agronomic pests in South America, were investigated. Our objectives were to evaluate changes in the baseline levels of lipids and carbohydrates, along with three selected micro-elements—nickel (Ni), copper (Cu), and zinc (Zn)—in the hemolymph of adult E. heros, following the application of a predetermined LC₃₀ of pyriproxyfen (single topical application) in fourth-instar nymphs (N4). Hemolymph was sampled using glass capillaries, with the resulting concentrations of lipids and carbohydrates determined through vanillin- and anthrone-positive reactions, respectively, and micro-element analysis was performed through total reflection X-ray fluorescence (TXRF) spectrometry. Lipids are the main and more stable energy metabolites for E. heros, with a proportion of 2:1 compared to carbohydrate levels. A remarkable sensitivity of carbohydrate levels to sublethal pyriproxyfen exposure, irrespective of sex, was observed. Baseline micro-element levels based on untreated control insects indicate sex-based differences in Ni and Zn, but not in Cu, concentrations. After insecticide exposure, the levels of these micro-elements were variable, with Ni and Zn generally decreasing and Cu decreasing in females but nearly doubling in males. The observed disproportion in lipids, carbohydrates, and inorganic micro-elements suggests potential physiological shifts triggered by pyriproxyfen activity in E. heros during late juvenile stages.

Introduction Traumatized teeth may undergo calcific metamorphosis of the pulp, a factor which makes endodontic treatment difficult due to the total or partial obliteration of the root canal.

Introduction: Endometriosis is a chronic inflammatory disease that affects ∼10% of women. A significant fraction of patients experience limited or no efficacy with current therapies. Tissue adjacent to endometriosis lesions often exhibits increased neurite and vascular density, suggesting that disease pathology involves neurotrophic activity and angiogenesis. Objectives: We aim to evaluate the potential for key tyrosine-kinase-receptor-coupled neurotrophic molecules to contribute to endometriosis-associated pain in mice. Methods: The levels of VEGFR1 regulators (VEGFA, VEGFB, PLGF, and sVEGFR1) were quantified by ELISA in peritoneal fluid from endometriosis patients undergoing surgery and used to calculate VEGFR1 occupancy. We used genetic depletion, neutralizing antibody, and pharmacological approaches to specifically block ligand (NGF or BDNF) or neurotrophic receptor (VEGFR1, TRKs) in a murine model of endometriosis-associated pain. Endometriosis-associated pain was determined using the von Frey filaments method, quantification of spontaneous abdominal pain-related behavior, and thermal discomfort. Diseases parameters were evaluated by lesion size and prevalence. Results: We found that entrectinib (pan-Trk inhibitor) or anti-NGF treatments reduced evoked pain, spontaneous pain, and thermal discomfort. In contrast, even though receptor occupancy revealing that VEGFR1 agonist levels are sufficient to support pain, blocking VEGFR1 signaling via antibody or tamoxifen-induced knockout did not reduce pain or lesion size in mice. Targeting BDNF-TrkB with an anti-BDNF antibody also proved ineffective. Conclusions: This suggests NGF-TrkA signaling, but not BDNF-TrkB or VEGF-VEGFR1, mediates endometriosis-associated pain. Moreover, entrectinib blocks endometriosis-associated pain and reduces lesion sizes. Our results also indicated that entrectinib-like molecules are promising candidates for endometriosis treatment. Credit author statement: Conceptualization: T.H. Zaninelli, V. Fattori, and M.S. Rogers; investigation and data curation: T.H. Zaninelli, V. Fattori, O.K. Heintz, K.R. Wright; A.C. Andrello, W.A. Verri Jr, M.S. Rogers; funding acquisition: M.S. Rogers,, S.A. Missmer, R.M. Anchan; methodology: T.H. Zaninelli, V. Fattori, and M.S. Rogers; human sample collection: S.A. Missmer, A.F. Vitonis, K.L. Terry, R.M. Anchan; animal breading and VEGFR1 ablation: D. Sim and H. Bukhari; resources: A.C. Andrello; D. Bree, T. Zheng, J. Wagner, W.A. Verri Jr, and M.S. Rogers; project administration: T.H. Zaninelli; supervision: V. Fattori, W.A. Verri Jr, and M.S. Rogers; visualization: T.H. Zaninelli, V. Fattori, W.A. Verri Jr, and M.S. Rogers; writing–original draft: T.H. Zaninelli; writing – editing and reviewing: all authors. All authors have read and approved the final version of the manuscript.