The physical degradation of AlGaN/GaN high electron mobility transistors during OFF-state stress experiments has been systematically studied. Oxide particles and stringers were found to form along the gate edge of stressed devices. When the gate electrode is removed, pits are seen to have formed underneath each particle. The observed room-temperature oxidation process is strongly dependent on the duration of the electrical stressing and the electric field. Moreover, the oxidation can be significantly reduced in vacuum (3 × 10−5 Torr), with a corresponding 30% reduction of current collapse. Finally, a degradation process with electric-field-driven oxidation of the AlGaN surface has been proposed.

The roles of reactive oxygen species (ROS), extracellular signal-regulated kinase 1/2 (ERK 1/2) and mitochondrial permeability transition pore (mPTP) in sevoflurane postconditioning induced cardioprotection against ischemia-reperfusion injury in Langendorff rat hearts were investigated. When compared with the unprotected hearts subjected to 30 min of ischemia followed by 1 h of reperfusion, exposure of 3% sevoflurane during the first 15 min of reperfusion significantly improved functional recovery, decreased infarct size, reduced lactate dehydrogenase and creatine kinase-MB release, and reduced myocardial malondialdehyde production. However, these protective effects were abolished in the presence of either ROS scavenger N-acetylcysteine or ERK 1/2 inhibitor PD98059, and accompanied by prevention of ERK 1/2 phosphorylation and elimination of inhibitory effect on mPTP opening. These findings suggested that sevoflurane postconditioning protected isolated rat hearts against ischemia-reperfusion injury via the recruitment of the ROS-ERK 1/2-mPTP signaling cascade.

The role of C-X-C motif chemokine 10 (CXCL10), a pro-inflammatory factor, in the development of acute respiratory distress syndrome (ARDS) remains unclear. In this study, we explored the role of CXCL10 and the effect of CXCL10 neutralization in lipopolysaccharide (LPS)-induced ARDS in rats. The expression of CXCL10 and its receptor chemokine receptor 3(CXCR3) increased after LPS induction. Moreover, neutralization of CXCL10 ameliorated the severity of ARDS by reducing pulmonary edema, inhibiting the release of inflammatory mediators (IFN-γ, IL-6 and ICAM-1) and limiting inflammatory cells (neutrophils, macrophages, CD8+ T cells) influx into the lung, with a reduction in CXCR3 expression in neutrophils and macrophages. Therefore, CXCL10 could be a potential therapeutic target in LPS-induced ARDS.

In single guinea‐pig ventricular myocytes, we examined the stoichiometry of Na+‐Ca2+ exchange (NCX) by measuring the reversal potential (ENCX) of NCX current (INCX) and intracellular Ca2+ concentration ([Ca2+]i) with the whole‐cell voltage‐clamp technique and confocal microscopy, respectively. With given ionic concentrations in the external and pipette solutions, the predicted ENCX were −73 and −11 mV at 3:1 and 4:1 stoichiometries, respectively. ENCX measured were −69 ± 2 mV (n= 11), −47 ± 1 mV (n= 14) and −15 ± 1 mV (n= 15) at holding potentials (HP) of −73, −42 and −11 mV, respectively. Thus, ENCX almost coincided with HP, indicating that [Ca2+]i and/or [Na+]i changed due to INCX flow. Shifts of ENCX (ΔENCX) were measured by changing [Ca2+]o or [Na+]o. The measured values of ΔENCX were almost always smaller than those expected theoretically at a stoichiometry of either 3:1 or 4:1. Using indo‐1 fluorescence, [Ca2+]i measured under the whole‐cell voltage‐clamp supported a 3:1 but not 4:1 stoichiometry. To prevent Ca2+ accumulation, we inhibited INCX with Ni2+ and re‐examined ENCX during washing out Ni2+. With HP at predicted ENCX at a 3:1 stoichiometry, ENCX developed was close to predicted ENCX and did not change with time. However, with HP at predicted ENCX for a 4:1 stoichiometry, ENCX developed initially near a predicted ENCX for a 3:1 stoichiometry and shifted toward ENCX for a 4:1 stoichiometry with time. We conclude that the stoichiometry of cardiac NCX is 3:1.

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Ulinastatin inhibits the release of inflammatory medium and reduces the inflammatory response during CPB. Tranexamic acid can effectively inhibit the fibrinolytic hyperfunction caused by CPB and thus decreases postsurgical bleeding. In addition, it exhibits a minor anti-inflammatory response. As a consequence, a combined treatment of ulinastatin and tranexamic acid reduces postsurgical bleeding and shortens postoperative hospital stay in patients undergoing heart valve replacement surgery.

The two-dimensional spatial distribution of structural degradation of AlGaN/GaN high electron mobility transistors was investigated under high-power electrical stressing using atomic force and scanning electron microscopy. It was found that pits form on the surface of the GaN cap layer at the edges of the gate fingers in the middle of the device. The average pit area and density increase gradually from the edge to the center of the fingers and are more common along inner fingers than fingers. It was also found that pit formation and growth are thermally activated.