Feature Extraction and Random Forest to Identify Sheep Behavior from Accelerometer Data

Sensor technologies play an essential part in the agricultural community and many other scientific and commercial communities. Accelerometer signals and Machine Learning techniques can be used to identify and observe behaviours of animals without the need for an exhaustive human observation which is labour intensive and time consuming. This study employed random forest algorithm to identify grazing, walking, scratching, and inactivity (standing, resting) of 8 Hebridean ewes located in Cheshire, Shotwick in the UK. We gathered accelerometer data from a sensor device which was fitted on the collar of the animals. The selection of the algorithm was based on previous research by which random forest achieved the best results among other benchmark techniques. Therefore, in this study, more focus was given to feature engineering to improve prediction performance. Seventeen features from time and frequency domain were calculated from the accelerometer measurements and the magnitude of the acceleration. Feature elimination was utilised in which highly correlated ones were removed, and only nine out of seventeen features were selected. The algorithm achieved an overall accuracy of 99.43% and a kappa value of 98.66%. The accuracy for grazing, walking, scratching, and inactive was 99.08%, 99.13%, 99.90%, and 99.85%, respectively. The overall results showed that there is a significant improvement over previous methods and studies for all mutually exclusive behaviours. Those results are promising, and the technique could be further tested for future real-time activity recognition

A new class of glycomimetic drugs to prevent free fatty acid-induced endothelial dysfunction

Background: Carbohydrates play a major role in cell signaling in many biological processes. We have developed a set of glycomimetic drugs that mimic the structure of carbohydrates and represent a novel source of therapeutics for endothelial dysfunction, a key initiating factor in cardiovascular complications. Purpose: Our objective was to determine the protective effects of small molecule glycomimetics against free fatty acid­induced endothelial dysfunction, focusing on nitric oxide (NO) and oxidative stress pathways. Methods: Four glycomimetics were synthesized by the stepwise transformation of 2,5­dihydroxybenzoic acid to a range of 2,5­substituted benzoic acid derivatives, incorporating the key sulfate groups to mimic the interactions of heparan sulfate. Endothelial function was assessed using acetylcholine­induced, endotheliumdependent relaxation in mouse thoracic aortic rings using wire myography. Human umbilical vein endothelial cell (HUVEC) behavior was evaluated in the presence or absence of the free fatty acid, palmitate, with or without glycomimetics (1µM). DAF­2 and H2DCF­DA assays were used to determine nitric oxide (NO) and reactive oxygen species (ROS) production, respectively. Lipid peroxidation colorimetric and antioxidant enzyme activity assays were also carried out. RT­PCR and western blotting were utilized to measure Akt, eNOS, Nrf­2, NQO­1 and HO­1 expression. Results: Ex vivo endothelium­dependent relaxation was significantly improved by the glycomimetics under palmitate­induced oxidative stress. In vitro studies showed that the glycomimetics protected HUVECs against the palmitate­induced oxidative stress and enhanced NO production. We demonstrate that the protective effects of pre­incubation with glycomimetics occurred via upregulation of Akt/eNOS signaling, activation of the Nrf2/ARE pathway, and suppression of ROS­induced lipid peroxidation. Conclusion: We have developed a novel set of small molecule glycomimetics that protect against free fatty acidinduced endothelial dysfunction and thus, represent a new category of therapeutic drugs to target endothelial damage, the first line of defense against cardiovascular disease