Quality considerations with high pressure processing of fresh and value added meat products

Pressure can be applied by high hydrostatic pressure, better known as high pressure processing (HPP), or by hydrodynamic pressure (HDP) in the form of shockwaves to alter quality parameters, such as shelf-life and texture of meat and meat products. The aim of this review is to give an overview of the use of pressure in the meat industry and to highlight its usage as a method to inactivate microorganisms but also a novel strategy to alter the structure and the quality parameters of meat and meat products. Benefits and possibilities of the technologies are presented, as well as how to overcome undesired product changes caused by HPP. The use of hydrodynamic shockwaves is briefly described and a promising newly developed industrial prototype for the generation of shockwaves by underwater explosion is presented.     

Benzo[a]pyrene-Induced Genotoxicity in Rats Is Affected by Co-Exposure to Sudan I by Altering the Expression of Biotransformation Enzymes

The environmental pollutant benzo[a]pyrene (BaP) is a human carcinogen that reacts with DNA after metabolic activation catalysed by cytochromes P450 (CYP) 1A1 and 1B1 together with microsomal epoxide hydrolase. The azo dye Sudan I is a potent inducer of CYP1A1/2. Here, Wistar rats were either treated with single doses of BaP (150 mg/kg bw) or Sudan I (50 mg/kg bw) alone or with both compounds in combination to explore BaP-derived DNA adduct formation in vivo. Using ³²P-postlabelling, DNA adducts generated by BaP-7,8-dihydrodiol-9,10-epoxide were found in livers of rats treated with BaP alone or co-exposed to Sudan I. During co-exposure to Sudan I prior to BaP treatment, BaP-DNA adduct levels increased 2.1-fold in comparison to BaP treatment alone. Similarly, hepatic microsomes isolated from rats exposed to Sudan I prior to BaP treatment were also the most effective in generating DNA adducts in vitro with the activated metabolites BaP-7,8-dihydrodiol or BaP-9-ol as intermediates. DNA adduct formation correlated with changes in the expression and/or enzyme activities of CYP1A1, 1A2 and 1B1 in hepatic microsomes. Thus, BaP genotoxicity in rats in vivo appears to be related to the enhanced expression and/or activity of hepatic CYP1A1/2 and 1B1 caused by exposure of rats to the studied compounds. Our results indicate that the industrially employed azo dye Sudan I potentiates the genotoxicity of the human carcinogen BaP, and exposure to both substances at the same time seems to be hazardous to humans.     

Coumarin-based octopamine phototriggers and their effects on an insect octopamine receptor

We have developed and characterized efficient caged compounds of the neurotransmitter octopamine. For derivatization, we introduced [6-bromo-8-(diethylaminomethyl)-7-hydroxycoumarin-4-yl]methoxycarbonyl (DBHCMOC) and {6-bromo-7-hydroxy-8-[(piperazin-1-yl)methyl]coumarin-4-yl}methoxycarbonyl (PBHCMOC) moieties as novel photo-removable protecting groups. The caged compounds were functionally inactive when applied to heterologously expressed octopamine receptors (AmOctα1R). Upon irradiation with UV-visible or IR light, bioactive octopamine was released and evoked Ca2+ signals in AmOctα1R-expressing cells. The pronounced water solubility of compounds 2-4 in particular holds great promise for these substances as excellent phototriggers of this important neurotransmitter.     

Combustion of Ytterbium Metal

Ytterbium metal powder burns with a luminous vapor phase diffusion flame in oxygen. Consolidated stoichiometric mixtures with both polytetrafluoroethylene and hexachloroethane upon ignition yield intense luminous flames. With UV/Vis spectroscopy of the combustion flames Yb, YbO, YbCl, and YbF species have been identified contributing to the selective emission in the green spectral range. The flame temperatures of ytterbium combustion in oxygen and with halocarbon based oxidizers are in the same range as for comparable magnesium based systems.     

Combination of tagging and tissue phase mapping to accelerate myocardial motion measurements in three directions

Object

Until now, a three-directional velocity field has mostly been obtained by velocity encoding in three directions, which is very time-consuming and hence not usually used in clinical routine. We show the feasibility of combining in-plane tagging with through-plane tissue phase mapping (TPM) to encode a three-directional velocity field at 3 T with reduced overall acquisition time.

Materials and methods

Assessment of a three-directional velocity field was performed for 10 healthy volunteers. The motion patterns obtained by use of five different sequences including three-directional TPM, TPM in the through-plane direction, TPM in the through-plane direction with horizontal or vertical tagging lines, and TPM in the through-plane direction combined with a tagging grid were evaluated and compared.

Results

A three-dimensional velocity field can be obtained in approximately half the acquisition time by combining through-plane TPM with in-plane tagging. Although the velocity information is derived by different means, differences between the information obtained by three-directional TPM encoding and the suggested technique are only minor.

Conclusion

The combination of tagging and TPM enables assessment of the three-directional velocity field in nearly half the time taken when the conventional three-directional TPM sequence is used.