RESUMO
Bearing faults are one kind of primary failure in rotatory machines. To avoid economic loss and casualties, it is important to diagnose bearing faults accurately. Vibration-based monitoring technology is widely used to detect bearing faults. Graph signal processing methods promising for the extraction of the fault features of bearings. In this work, graph multi-scale permutation entropy (MPEG) is proposed for bearing fault diagnosis. In the proposed method, the vibration signal is first transformed into a visibility graph. Secondly, a graph coarsening method is used to generate coarse graphs with different reduced sizes. Thirdly, the graph's permutation entropy is calculated to obtain bearing fault features. Finally, a support vector machine (SVM) is applied for fault feature classification. To verify the effectiveness of the proposed method, open-source and laboratory data are used to compare conventional entropies and other graph entropies. Experimental results show that the proposed method has higher accuracy and better robustness and de-noising ability.
RESUMO
The post-translational modification of cysteine through redox reactions, especially S-sulfhydration, plays a critical role in regulating protein activity, interactions, and spatial arrangement. This review focuses on the impact of protein S-sulfhydration on vascular function and its implications in vascular diseases. Dysregulated S-sulfhydration has been linked to the development of vascular pathologies, including aortic aneurysms and dissections, atherosclerosis, and thrombotic diseases. The H2S signaling pathway and the enzyme cystathionine γ-lyase (CSE), which is responsible for H2S generation, are identified as key regulators of vascular function. Additionally, potential therapeutic targets for the treatment of vascular diseases, such as the H2S donor GYY4137 and the HDAC inhibitor entinostat, are discussed. The review also emphasizes the antithrombotic effects of H2S in regulating platelet aggregation and thrombosis. The aim of this review is to enhance our understanding of the function and mechanism of protein S-sulfhydration modification in vascular diseases, and to provide new insights into the clinical application of this modification.