Syncoilin is a 64-kDa intermediate filament protein expressed in skeletal muscle and enriched at the perinucleus, sarcolemma, and myotendinous and neuromuscular junctions. Due to its pattern of cellular localization and binding partners, syncoilin is an ideal candidate to be both an important structural component of myocytes and a potential mediator of inherited myopathies. Here we present a report of a knockout mouse model for syncoilin and the results of an investigation into the effect of a syncoilin null state on striated muscle function in 6-8-week-old mice. An analysis of proteins known to associate with syncoilin showed that ablation of syncoilin had no effect on absolute expression or spatial localization of desmin or alpha dystrobrevin. Our syncoilin-null animal exhibited no differences in cardiotoxin-induced muscle regeneration, voluntary wheel running, or enforced treadmill exercise capacity, relative to wild-type controls. Finally, a mechanical investigation of isolated soleus and extensor digitorum longus indicated a potential differential reduction in muscle strength and resilience. We are the first to present data identifying an increased susceptibility to muscle damage in response to an extended forced exercise regime in syncoilin-deficient muscle. This study establishes a second viable syncoilin knockout model and highlights the importance of further investigations to determine the role of syncoilin in skeletal muscle.

Soil samples from a potentially contaminated site were prepared and analysed for their copper, nickel and zinc contents by both inductively coupled plasma (ICP) spectrometry and x-ray fluorescence (XRF) spectrometry. Results obtained by XRF spectrometry were either comparable with or slightly higher than those obtained by ICP. However, when the results obtained by the two techniques were compared with the threshold values for contamination by the three metals, then each set of results led to the same conclusion with respect to the categorization of the site. Comparability between the two techniques was thus demonstrated and either may be used to screen soil for phytotoxic metals.

The study evaluated the biological and analytical variance in plasma zinc from 36 adults 60-88 yr of age. Blood samples were taken by finger-prick from each subject on d 1, 2, 3, 8, and 15. Days 1, 2, and 3 were selected to describe daily variation; 1, 8, and 15 were selected to describe weekly variation. Plasma Zn was analyzed by flame atomic absorption using a microinjection technique. Variation was partitioned into analytical, intraindividual, and interindividual components using analysis of variance. The interindividual variability was generally greater than the intraindividual variability. The variability for plasma zinc was about 30% and was substantially greater than reported for younger populations. This variability could not be attributed to the covariates examined, including zinc intake from food and supplements, serum albumin, and C-reactive protein. The variability would affect the accuracy of plasma zinc status based on a blood sample collected on a single day. With the microtechnique used in this study, 8 sample days would be needed to estimate plasma Zn with 95% confidence level and 20% level of accuracy.

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