The Orbiting Astrophysical Spectrometer In Space (OASIS)

The Orbiting Astrophysical Observatory In Space (OASIS) is an Advanced Concept currently under study at NASA as a mission for the next decade. The goal of the OASIS mission is to identify a local site or sites where galactic cosmic rays (GCR) originate and are accelerated. The mission will also allow GCR data to be used to investigate how elements are made and distributed in the galaxy and to improve our understanding of supernovae and the nucleosynthesis of the heavy elements. OASIS consists of two instruments that provide complementary data on the location and nature of the source(s) through investigating the composition of ultra-heavy nuclei ( ) and the energy spectrum of electrons. In particular OASIS will measure the relative abundances in the actinide group ( ) to determine the age of the -process material in GCRs. The presence of young r-process material would indicate that GCRs are a sample of the interstellar medium in OB associations. OASIS will measure the electron spectrum to 10 TeV. The energy where this spectrum ends will tell us the distance to the nearest GCR source(s). OASIS will look for spectral features and anisotropy in the high energy electron spectrum that are expected to appear when only a few of the nearest astrophysical sources can contribute to the electron flux. Spectral features may also suggest dark matter decay products. We anticipate that these measurements will lead to the identification of the nearest cosmic ray electron source and provide a crucial test of the OB association model for the origin of GCR nuclei

Hydrogen sulfide cytoprotective signaling is endothelial nitric oxide synthase-nitric oxide dependent

Previous studies have demonstrated that hydrogen sulfide (H(2)S) protects against multiple cardiovascular disease states in a similar manner as nitric oxide (NO). H(2)S therapy also has been shown to augment NO bioavailability and signaling. The purpose of this study was to investigate the impact of H(2)S deficiency on endothelial NO synthase (eNOS) function, NO production, and ischemia/reperfusion (I/R) injury. We found that mice lacking the H(2)S-producing enzyme cystathionine γ-lyase (CSE) exhibit elevated oxidative stress, dysfunctional eNOS, diminished NO levels, and exacerbated myocardial and hepatic I/R injury. In CSE KO mice, acute H(2)S therapy restored eNOS function and NO bioavailability and attenuated I/R injury. In addition, we found that H(2)S therapy fails to protect against I/R in eNOS phosphomutant mice (S1179A). Our results suggest that H(2)S-mediated cytoprotective signaling in the setting of I/R injury is dependent in large part on eNOS activation and NO generation

Calcineurin links mitochondrial elongation with energy metabolism.

Canonical protein phosphatase 3/calcineurin signaling is central to numerous physiological processes. Here we provide evidence that calcineurin plays a pivotal role in controlling systemic energy and body weight homeostasis. Knockdown of calcineurin in Drosophila melanogaster led to a decrease in body weight and energy stores, and increased energy expenditure. In mice, global deficiency of catalytic subunit Ppp3cb, and tissue-specific ablation of regulatory subunit Ppp3r1 from skeletal muscle, but not adipose tissue or liver, led to protection from high-fat-diet-induced obesity and comorbid sequelæ. Ser637 hyperphosphorylation of dynamin-related protein 1 (Drp1) in skeletal muscle of calcineurin-deficient mice was associated with mitochondrial elongation into power-cable-shaped filaments and increased mitochondrial respiration, but also with attenuated exercise performance. Our data suggest that calcineurin acts as highly conserved pivot for the adaptive metabolic responses to environmental changes such as high-fat, high-sugar diets or exercise

2020 Cornell Nutrition Conference Proceedings

Complete proceedings of manuscripts written for the 2020 Cornell Nutrition ConferenceDepartment of Animal Scienc