Peptidomic analysis of the anterior temporal lobe and corpus callosum from schizophrenia patients

Schizophrenia is a complex disorder hypothesized to develop from a combination of genetic, neurodevelopmental, and environmental factors. Molecules that are directly involved in the pathogenesis of schizophrenia and may serve as biomarker candidates can be identified with "omics" approaches such as proteomics and peptidomics. In this context, we performed a peptidomic study in schizophrenia postmortem brains, to our knowledge the first such study in schizophrenia patients. We investigated the anterior temporal lobe (ATL) and corpus callosum (CC) by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) and a label-free ion quantification technique based on data-dependent acquisition (DDA). Results indicated alterations in a specific intracellular neurogranin peptide in both the ATL and CC and a decrease of PepH, a fragment of his tone H2B type 1-H intracellular peptide, in the ATL. PepH was tested in serum-deprived Neuro2A cells and showed a protective effect against cell death. Cells were also challenged with lipopolysaccharide (LPS), and PepH was able to prevent the endotoxic effects of LPS. Our data suggest that specific intracellular peptides are altered in schizophrenia patients. The potential biological activity of PepH supports intracellular peptides as novel targets in the study not only of schizophrenia but also of other neuropsychiatric diseases. Biological significance: Psychiatric disorders are considerably more difficult to diagnose in their early stages. Usually, by the time the diagnosis is clear and clinical treatment can be started, the disorder is already established and thus of greater severity. Consequently, the scientific community has been searching for biomarker candidates that can aid the early detection of such disorders and for novel therapeutics to improve treatment or at least delay disease progression. Moreover, key molecules involved in the establishment of psychiatric diseases may help the understanding of their pathogenesis and thus drive the development of more effective treatments. The present work screened peptides that might be possible novel targets to control cell machinery in schizophrenia and identified an intracellular peptide with potential cytoprotective activity. To our knowledge, this is the first peptidomic study in schizophrenia patients.

Cyclic fatigue testing of ProTaper NiTi rotary instruments after clinical use.

PURPOSE: The purpose of this study was to evaluate the cyclic fatigue of ProTaper nickel-titanium (NiTi) rotary instruments (Tulsa Dental, Tulsa, Okla) after multiple clinical uses. STUDY DESIGN: Two hundred twenty-five ProTaper instruments were divided into 3 groups: A = 75 used as controls, B = 75 used in 2 molars (6-8 canals), and C = 75 used in 4 molars (12-16 canals). The number of rotations to breakage and the fractured tip length were recorded for each file and the mean was calculated by ANOVA. RESULTS: No S1-2 or F1-2-3 instrument separated during intracanal use, even if they were reused for a number of cases (x 4 molar cases). CONCLUSION: It is clear that prolonged reuse of NiTi rotary instruments strongly affects instruments' fatigue, but our data suggest the hypothesis that other factors (primarily errors and misuse) may be more accountable for intracanal instrument separation. Further studies could assess the cyclic fatigue of each instrument at different levels of the shaft by altering the radius of curvature.