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Type 2 diabetes mellitus (T2DM) is a common comorbidity among Parkinsons disease (PD) patients. Yet, little is known about dysregulated pathways that are unique in PD patients with T2DM. We applied high-resolution metabolomic profiling in serum samples of 636 PD and 253 non-PD participants recruited from Central California. We conducted an initial discovery metabolome-wide association and pathway enrichment analysis. After adjusting for multiple testing, in positive (or negative) ion mode, 30 (25) metabolic features were associated with T2DM in both PD and non-PD participants, 162 (108) only in PD participants, and 32 (7) only in non-PD participants. Pathway enrichment analysis identified 17 enriched pathways associated with T2DM in both the PD and non-PD participants, 26 pathways only in PD participants, and 5 pathways only in non-PD participants. Several amino acid, nucleic acids, and fatty acid metabolisms were associated with T2DM only in the PD patient group suggesting a possible link between PD and T2DM.

BACKGROUND: Pesticide exposure has consistently been associated with Parkinsons disease (PD) onset. Yet, fewer epidemiologic studies have examined whether pesticides influence PD motor and non-motor symptom progression. OBJECTIVES: Using a geographic information system tool that integrates agricultural pesticide use reports and land use records to derive ambient exposures at residences and workplaces, we assessed associations between specific pesticides previously related to PD onset with PD symptom progression in two PD patient cohorts living in agricultural regions of California. METHODS: We calculated the pounds of pesticide applied agriculturally near each participants residential or occupational addresses from 1974 to the year of PD diagnosis, using a geographic information system tool that links the California Pesticide Use Reports database to land use data. We examined 53 pesticides selected a priori as they have previously been associated with PD onset. We longitudinally followed two PD patient cohorts (PEG1 N = 242, PEG2 N = 259) for an average of 5.0 years (SD ± 3.5) and 2.7 years (SD ± 1.6) respectively and assessed PD symptoms using the movement disorder specialist-administered Unified Parkinsons disease Rating Scale part III (UPDRS), Mini-Mental State Examination (MMSE), and Geriatric Depression Scale (GDS). Weighted time-to-event regression models were implemented to estimate effects. RESULTS: Ten agricultural pesticides, including copper sulfate (pentahydrate), 2-methyl-4-chlorophenoxyacetic acid (MCPA) dimethylamine salt, tribufos, sodium cacodylate, methamidophos, ethephon, propargite, bromoxynil octanoate, monosodium methanearsonate (MSMA), and dicamba, were associated with faster symptom progression. Among these pesticides, residential or workplace proximity to higher amounts of copper sulfate (pentahydrate) and MCPA (dimethylamine salt) was associated with all three progression endpoints (copper sulfate: HRs = 1.22-1.36, 95 % CIs = 1.03-1.73; MCPA: HRs = 1.27-1.35, 95 % CIs = 1.02-1.70). CONCLUSIONS: Our findings suggest that pesticide exposure may not only be relevant for PD onset but also PD progression phenotypes. We have implicated ten specific pesticide active ingredients in faster PD motor and non-motor decline.

Ionic liquids have excellent properties such as low vapor pressure, non-flammation, good stability and high solubility, making them promising for applications in many fields such as food, chemicals and medicine. This article outlines the main physical and chemical properties of the substance, lists its applications in the food industry as a solvent, catalyst, and extractant for separation, purification, and analysis of food components, and provides an overview of its toxicological safety related to ecological and human health risks at the microbial, plant, and animal levels, which will provide a reference for scientific application and safety management of imidazole ionic liquids in the food industry.

Ethylene‐vinyl acetate (EVA) hot‐melt adhesives featured good thermal stability, strong weather resistance and fast bonding speed, are of great concern to the industry and engineering fields. However, the weak bond strength and poor reusability severely hinder their application under harsh conditions. Herein, the hydrolyzed EVA (EVOH) copolymers with rich hydroxyl groups are fabricated by an EVA hydrolysis reaction, and their mechanical properties, environmental adaptability, and reusability were systematically evaluated. As a result, the shear strengths measured by bonding the stainless steel plates can reach up to 16.4 MPa at room temperature (25°C) and 13.1 MPa at ultra‐low temperature (−196°C), indicating the good bonding performance of EVOH. Besides, owing to the excellent dynamic reversibility and thermal stability, it can obtain 92% of shear strength retention rate after 10 reuses, which is the highest value reported so far. In addition, the hydroxyl‐rich EVOH delivers good solvent and corrosion resistance that can be widely used for bonding various materials. Therefore, this research provide new lightspots for developing environmentally friendly hot‐melt adhesives with excellent bonding properties, corrosion resistance, and reusability. [ABSTRACT FROM AUTHOR]

The formation of solid electrolyte interphase (SEI) and lithium ion intercalation are two crucial processes in lithium ion batteries. Given the complexity and challenges involved in investigating real batteries, a combination of model batteries comprising well-defined ultrathin graphite electrodes with surface-sensitive techniques can provide valuable information on these processes. Here, a comparative study of the performance of batteries using regular- and high-concentration electrolytes (RCE and HCE) is presented, aided by a myriad of correlative surface science techniques. It is found that the SEI formed in HCE possesses a thinner organic layer and more inorganic substances. Such an effective SEI protects the graphite electrode and facilitates the processes of Li+ intercalation/deintercalation, thereby improving the reversibility and cycling stability of the battery, superior to those with RCE. Moreover, the battery performance can be readily tuned by switching the electrolytes. The good cycling stability of the battery can still be maintained in RCE after the preformation of a robust SEI on the ultrathin graphite electrode in HCE. This work highlights the importance of electrolyte-modulated SEI formation to battery performance and provides powerful platforms to comprehensively study the SEI formation and ion intercalation processes. [ABSTRACT FROM AUTHOR]