One-Way Localized Adiabatic Passage in an Acoustic System.

Stimulated adiabatic passage utilizes radiation pulses to efficiently and selectively transfer population between quantum states, via an intermediate state that is normally decaying. In this Letter, we propose the analog of stimulated adiabatic passage in an acoustic system. It is realized with cavities that correlate through adiabatically time-varying couplings, where the cavities and time-varying couplings mimic discrete states and radiation pulses, respectively. With appropriate arrangements of coupling actions, an acoustic wave can be efficiently transferred from the initial excited cavity to the target cavity in the forward direction, immune to the intermediate dark cavity. On the other hand, for the backward propagation, the acoustic energy is perfectly localized in the intermediate dark cavity and completely dissipated. We analytically, numerically, and experimentally demonstrate such unidirectional sound localization and unveil the essential role of zero-eigenvalue eigenstates in the adiabatic passage process.

Observation of low-loss broadband supermode propagation in coupled acoustic waveguide complex.

We investigate analytically, numerically, and experimentally the low-loss supermode propagation in a coupled acoustic waveguide complex within a broadband. The waveguide complex is implemented with air channels coupled via an ultrathin metafluid layer. We analytically derive the field distribution of incident sound needed for producing acoustic supermodes, and verify the periodically revival propagation in coupled waveguide systems numerically and experimentally. We find out that the supermode wavelength becomes longer for higher mode order or lower frequency. We have also demonstrated the robust propagation of supermodes in broadband. Our scheme can in principle be extended to three dimensions and the ultrasound regime with simplicity and may promote applications of high-fidelity signal transfer in complicated acoustic networks.

[The protective effect of exenatide on the renal injury in diabetic rats].

OBJECTIVE: To investigate the protective effect of exenatide (Ex) on the renal injury in streptozotocin-induced diabetic rats. METHODS: Sprague-Dawley rats were randomly divided into 2 groups:normal control group (NC group, n=8) and model group. Model group was injected with low dose of streptozotocin (30 mg·kg-1) after the rats were fed with high fat and high glucose diet for 4 weeks. Seventy-two hours later, rats of blood glucose level ≥ 16.7 mmol·L-1 were divided into diabetes mellitus group (DM, n=10) and two exenatide-treated groups (Ex groups,3 or 6µg·kg-1, n=8). Ex groups subcutaneously injected with exenatide for 12 weeks, but NC group and DM group were injected with the same volume of solvent. Changes in glycolipid metabolism and renal function such as serum creatinine (Scr), urine creatinine (Ucr), blood urea nitrogen (BUN), 24 hour urine micro-albumin (24 h UMA)in the 4 groups of rats were determined and creatinine clearance rate (Ccr) were calculated. Renal oxidative stress parameters such as superoxide dismutase (SOD), malondialdehyde(MDA), glutathione per-oxidase (GSH-Px) were measured. Hematoxylin-eosin (HE) staining was used to examine pathological morphology in the renal tissues and ELISA was performed to determine the level of advanced glycation end products(AGEs), the glycosylation end product in renal tissues. RESULTS: Compared to the DM group,glycolipid metabolic abnormalities in the exenatide-treated groups were significantly ameliorated with lower levels of blood glucose,HbAlc, cholesterol and triglyceride (P < 0.05). The renal function index was markedly improved (P < 0.05) with Ccr reduced, indicating a high glomerular filtration status. Meanwhile, exenatide treatment improved the diabetes-induced pathological changes in renal morphology, substantially increased the activities of SOD and GSH-Px, and reduced the levels of MDA and AGEs. CONCLUSIONS: Exe-natide has the renal protective effect probably by the mechanisms of inhibition of AGEs production and reduction of oxidative stress in the renal tissues of diabetic rats.

A pseudogene-signature in glioma predicts survival.

Pseudogene was recognized as a potential tumor suppressor or oncogene in varies of diseases, however its roles in glioma have not been investigated. Our study was to identify the pseudogene-signature that predicted glioma survival. Using a pseudogene-mining approach, we performed pseudogene expression profiling in 183 glioma samples from the Chinese Glioma Genome Atlas (CGGA) and set it as the training set. We found a six-pseudogene signature correlated with patients' clinical outcome via bioinformatics analyses (P ≤ 0.01), and validated it in the Repository of Molecular Brain Neoplasia Data (REMBRANDT) containing 350 cases. A formula calculating the risk score based on the six-pseudogene signature was introduced and the patients of CGGA set were classified into high-risk group and low-risk group with remarkably different survival (P < 0.001) based on their scores. The prognostic value of the signature was confirmed in the REMBRANDT set. Though the function of these pseudogenes is not clear, the identification of the prognostic pseudogenes indicated the potential roles of pseudogenes in glioma pathogenesis and they may have clinical implications in treating glioma.