In the present study, we aimed to compare the detoxifying effects of two fat emulsions containing either long-chain triglyceride or a mixture of medium-chain and long-chain triglycerides in the propafenone-poisoned rat model. Rats were randomly divided into 3 groups according to the fat emulsions used: long-chain triglyceride-based fat emulsion (LL) group; medium-chain and long-chain triglyceride-based fat emulsion (ML) group; normal saline (NS) group. Propafenone was continuously pumped (velocity=70 mg/kg per h) until the mean blood pressure dropped to 50% of basal level. Then, LL/ML fat emulsions or NS was intravenously infused instantly with a loading-dose (1.5 mL/kg) and a maintenance dose (0.25 mL/kg per min) for 1 h. Subsequently, the propafenone was added to plasma (3.5 μg/mL) in vitro, mixed with three doses of LL or ML (1, 2, or 4%). Finally, after centrifugation, the concentration of propafenone was measured. Rats treated with LL exhibited accelerated recovery, characterized by higher blood pressure and heart rate. Rats in both the LL and ML groups demonstrated decreased propafenone in plasma (time-points: 15, 25, and 60 min). However, rats that received LL showed lower propafenone in myocardial tissue at the end of detoxification treatment. Rats in the ML group had the lowest value of pH, the minimum content of HCO3-, and the highest production of lactic acid at the end. In the in vitro experiments, propafenone decreased more dramatically in the LL group compared to the ML group. Long-chain triglyceride fat emulsion had a better effect on treating propafenone poisoning in rats.

The pitting corrosion of three duplex steels (DSS), SAF2205, SAF2507, Z3CN20.09M thermally aged at 350 - 500 ℃ for 5500 h was investigated by the means of electrochemical techniques. The pitting potential (Ep) of thermally aged Z3CN20.09M specimens decreased with increasing of ageing temperature, however, the Ep of SAF2205 and SAF2507 thermally aged specimens decreased first and reached the lowest value at 450 ℃ and then increased slightly. The electrochemical impedance spectroscopy results are coincident with the potentiodynamic polarisation testing results. The variation in the charge transfer resistance of specimens coincided with the Ep values. There is little influence of low temperature (below 350 ℃) on resistance to pitting of SAF2205 and SAF2507 DSS. But, the pitting resistance of them degrades drastically ageing at higher temperature above 450 ℃. The deterioration in pitting resistance of thermally aged DSS specimens mainly attributes to the precipitation of Cr-rich α′ phases which affected by temperature markedly. At the range of 350 -500 ℃, the temperature the higher, the precipitation of Cr-rich α′ phases the more. The formation of G phases and the healing process during the long thermal ageing at 500 ℃ is the other reasons for the change in pitting resistance.

Human contrast sensitivity is considered in relation to the responses delivered by retinal ganglion cells of the primate to luminance and chromatic contrast. At different temporal frequencies, response amplitude relative to response variability determines the limit to sensitivity of a single ganglion cell. This can be related to specific models of central detection mechanisms. Both for luminance and chromatic contrast, psychophysical sensitivity to temporal modulation can be achieved by summation of activity of just a few cells that provide input to a detection mechanism. This analysis is then extended to a spatial context. Several sets of data indicate that, in spatial terms, detection mechanisms are of limited spatial extent, and that, at least in the case of luminance patterns, eye movements play a critical role in contrast detection.