MicroRNA-134-5p (MiR-134-5p) has been proposed as a promising novel biomarker for the diagnosis of acute myocardial infarction (AMI). However, the biological role of miR-134-5p in ischemic cardiomyocytes has been little disclosed yet. Expression of miR-134-5p and X-linked inhibitor of apoptosis protein (XIAP) was detected using RT-qPCR and western blot. Oxidative stress and cell apoptosis were determined by enzyme-linked immunosorbent assays, 3-(4, 5-dimethylthiazole-2-y1)-2, 5-biphenyl tetrazolium bromide assay, flow cytometry, western blot, and terminal-deoxynucleoitidyl transferase-mediated nick end labeling (TUNEL). The interaction between miR-134-5p and XIAP was confirmed by luciferase reporter assay. Expression of miR-134-5p was upregulated in serum of AMI patients and hypoxia/reoxygenation (H/R)-induced cardiomyocytes (AC16 and HCM). MiR-134-5p downregulation could inhibit H/R-mediated release of lactic dehydrogenase enzyme (LDH) and malondialdehyde (MDA), and promote superoxide dismutase (SOD) and glutathione peroxidase (GSH-PX) levels. Meanwhile, cell viability was increased, while the apoptosis rate and TUNEL positive cells were inhibited by miR-134-5p downregulation in H/R-treated AC16 and HCM cells. Mechanically, XIAP was downregulated and targeted by miR-134-5p in H/R-induced cardiomyocytes in vitro. Overexpression of XIAP inhibited oxidative stress and cell apoptosis in H/R-treated AC16 and HCM cells, which was similar to miR-134-5p knockdown. Moreover, downregulation of XIAP could partially reverse the effect of miR-134-5p knockdown in H/R-induced cardiomyocytes. Knockdown of miR-134-5p protected cardiomyocytes from H/R-induced oxidative stress and apoptosis in vitro through targeting XIAP.The prototypical reactivity profiles of transition metal dihydrogen complexes (M-H2 ) are well-characterized with respect to oxidative addition (to afford dihydrides, M(H)2 ) and as acids, heterolytically delivering H+ to a base and H- to the metal. In the course of this study we explored plausible alternative pathways for H2 activation, namely direct activation through H-atom or hydride transfer from the σ-H2 adducts. To this end, we describe herein the reactivity of an isostructural pair of a neutral S= 1 / 2 and an anionic S=0 Co-H2 adduct, both supported by a trisphosphine borane ligand (P3B ). The thermally stable metalloradical, (P3B )Co(H2 ), serves as a competent precursor for hydrogen atom transfer to t Bu3 ArO⋅ . What is more, its anionic derivative, the dihydrogen complex [(P3B )Co(H2 )]1- , is a competent precursor for hydride transfer to BEt3 , establishing its remarkable hydricity. The latter finding is essentially without precedent among the vast number of M-H2 complexes known.Heterojunction engineering is a fundamental strategy to develop efficient electrocatalysts for the oxygen reduction reaction by tuning electronic properties through interfacial cooperation. In this study, a heterojunction electrocatalyst consisting of bimetallic carbide Co3 ZnC and cobalt encapsulated within N-doped carbon nanotubes (Co3 ZnC/Co@NCNTs) is synthesized by a facile two-step ion exchange-thermolysis pathway. Co3 ZnC/Co@NCNTs effectively promotes interfacial charge transport between the different components with optimizes adsorption and desorption of intermediate products at the heterointerface. In situ-grown N-doped carbon nanotubes (NCNTs) not only improve the electrical conductivity but also suppress the oxidation of transition metal nanoparticles in alkaline media. Moreover, the abundant nitrogen types (pyridinic N, Co-Nx , and graphitic nitrogen) in the carbon skeleton provide more active sites for oxygen adsorption. Benefitting from this optimized structure, Co3 ZnC/Co@NCNTs hybrid not only demonstrates excellent oxygen reduction activity, with a half-wave potential of 0.83 V and fast mass transport with limited current density of 6.23 mA cm-2 , but also exhibits superior stability and methanol tolerance, which surpass those of commercial Pt/C catalysts. This work provides an effective heterostructure for interfacial electronic modulation to improve electrocatalytic performance. Sarcopenia is an objective measure of patient frailty and is a predictor of adverse surgical outcomes. We hypothesized that sarcopenia is associated with increased surgical site occurrence (SSO) and hernia occurrences in patients undergoing oncologic abdominal wall reconstruction. Consecutive patients who underwent abdominal wall reconstruction (AWR) for an abdominal wall ablative defect at a single center from 2005 to 2015 were evaluated. The total psoas index (TPI) was used to define sarcopenia. The primary endpoint of the study was hernia occurrence; (SSO) was a secondary outcome measure. Eighty-six patients met the inclusion criteria. Multivariate analysis demonstrated that sarcopenia increased the risk of hernia more than threefold, trending toward significance (OR = 3.3; 95% CI 0.69-15.4; P = .13). Multivariate logistic regression demonstrated that preoperative radiotherapy (OR = 4.8, 95% CI 1.4-16; P = .01) and obesity (OR = 4.9, 95% CI 1.5-16.3; P =.009) were independent predictors of developing an SSO. Sarcopenia, as defined by TPI, is correlated with hernia occurrence, but not SSO. These findings emphasize the importance of preoperative fitness and nutritional optimization and provide useful information for preoperative counseling and risk stratification.Sarcopenia, as defined by TPI, is correlated with hernia occurrence, but not SSO. These findings emphasize the importance of preoperative fitness and nutritional optimization and provide useful information for preoperative counseling and risk stratification.This study aimed the optical imaging of malignant and normal skin tissues with multimodal wide-field fluorescence polarization imaging (WF) technique, by using methylene blue as fluorescence dye. We present optical imaging of skin tissues by different techniques, including reflectance, fluorescence, and polarization imaging for early detection of skin cancer. KU-0060648 cell line We collected the reflectance confocal images at 390 and 500 nm. For wide-field fluorescence images, specimens were stimulated at 640 nm and images were collected between 670 and 710 nm. The correlation of the regarded optical modalities with histopathology (H&E), their potentials, capabilities, and limitations to detect skin lesions are discussed. The advantages of multimodal imaging of skin tissues are analyzed to divulge possibilities for precise tumor boundary detection and their classification for malignant and nonmalignant skin tissues. Prior to imaging, the cells were stained in aqueous MB (a dye approved by FDA).