C2D6 measured with unprecedent energy resolution and signal-to-noise ratio are presented. These spectra reveal many new features in core-excited valence and Rydberg states. Detailed vibrational structures are observed in these spectra, providing valuable information on the geometrical and vibrational properties of the core-excited molecules. In addition, C 1s and N 1s core-hole lifetimes are found to be -120 and -135 meV in these molecules with little dependence on their bonding environments. These results and the tentative peak assignments are discussed briefly in terms of the equivalent core model, multielectron excitations, exchange interactions, and the geometry of the excited molecules.

The K-shell excitation spectra of the hydrides water, ammonia, and methane have been measured in photoabsorption experiments using synchrotron radiation in combination with a high-resolution monochromator. For the case of methane, in particular, a wealth of spectral detail is observed which was not accessible in previous studies. The measured excitation energies and relative intensities compare well with values calculated using a complete second-order approximation for the polarization propagator. In order to determine the extent of admixing of valence excitations (i.e., transitions into virtual 0 orbitals) to the Rydberg manifolds, the X-H bond lengths have been varied in the calculations. In the case of H20, the two lowest-energy bands are due to the 0 1s-4a&/3s and 0 1s-2b2/3p transitions and have strong valence character; their width indicates that both excitations are dissociative. The NH3 and ND3 spectra are also broad which is not only due to possible dissociation but also to unresolved vibrational fine structure (v2 mode) and a Jahn-Teller instability. Valence character is concentrated in the lowest excited state in the Rydberg ns manifold, but is distributed more uniformly over the np(e) manifold. The weak dipole-forbidden C 1s -3s ( a & ) transition in CH4 and CD4 is accompanied by vibrational structure due to the v4 mode, indicating that it derives its intensity from vibronic coupling with the C 1s-3p(t2) transition. The structure on the latter band is extremely complicated due to Jahn-Teller coupling and cannot be assigned at present, as is the case for the Rydberg transitions at higher energies. The higher np Rydberg excitations contain considerable valence character. PACS number(s): 33.20.Rm 35.20. -i I. INTRQDUCTIDNE-shell excitation of the CH4, NH3, and H20 molecules has been studied in the past using both electronenergy-loss spectroscopy (EELS) [1 -4] and x-ray absorption spectroscopy [5 -9). Although the spectral resolution obtained with the latter technique has generally been rather modest and could not match that of EELS, recent advances in grazing-incidence monochromator design [10 -14] have resulted in a dramatic improvement of resolution with the "optical" approach. This has been shown in a number of high-resolution K-shell excitation spectra of small molecules reported recently (e.g. , ). In the present paper we describe measurements of the photoabsorption spectrum of gas phase H20, NH3, and CH4 in the near-E-edge region at a resolution sufficiently high to reveal directly the spectral line shape. To substantiate the assignments we have also calculated excitation energies and oscillator strengths using a polarization propagator method [20].In the virtual orbital spectrum of these hydrides and other saturated molecules one expects antibonding valence-type (cr ) orbitals which are the counterparts of the occupied bonding X-H orbitals. An important question is to what extent this antibonding valence character appears in the excitation spectrum. In most of the earlier E-shell studies on the h...

Simvastatin and cerivastatin have been used to investigate the development of statin-induced muscle necrosis in the rat. This was similar for both statins and was treatment-duration dependent, only occurring after 10 days had elapsed even if the dose was increased, and still occurring after this time when dosing was terminated earlier as a result of morbidity. It was then widespread and affected all areas of the muscular system. However, even when myotoxicity was severe, particular individual muscles and some types of fibres within affected muscles were spared consistently. Fibre typing of spared muscles and of acutely necrotic fibres within affected muscles indicated a differential fibre sensitivity to statin-induced muscle necrosis. The fibres showed a necrotic response to statin administration that matched their oxidative/glycolytic metabolic nature: Least sensitive → I ↔ IIA ↔ IID ↔ IIB ← most sensitive. Type I and IIB fibres represent metabolic extremes of a continuum of metabolic properties through the fibre types with type I fibres most oxidative in metabolism and type IIB fibres most glycolytic. In addition, in some (nonnecrotic) glycolytic fibres from muscles showing early multifocal single fibre necrosis the only subcellular alterations present in isolation of any other changes were mitochondrial. These changes were characterised by an increased incidence of vacuolation and the formation of myelinoid vesicular bodies that accumulated in the subsarcolemmal areas. These findings suggest an important early involvement of mitochondria in selective glycolytic muscle fibre necrosis following inhibition of the enzyme HMG-CoA reductase.

The first 42 elements of the Allen Telescope Array (ATA-42) are beginning to deliver data at the Hat Creek Radio Observatory in Northern California. Scientists and engineers are actively exploiting all of the flexibility designed into this innovative instrument for simultaneously conducting surveys of the astrophysical sky and conducting searches for distant technological civilizations. This paper summarizes the design elements of the ATA, the cost savings made possible by the use of COTS components, and the cost/performance trades that eventually enabled this first snapshot radio camera. The fundamental scientific program of this new telescope is varied and exciting; some of the first astronomical results will be discussed.

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The gastrointestinal (GI) tract is an important target organ for the toxicity of xenobiotics. The toxic effects of xenobiotics on this complex, heterogeneous structure have been difficult to model in vitro and have traditionally been assessed in vivo. The explant culture of GI tissue offers an alternative approach. Historically, the organotypic culture of the GI tract proved far more challenging than the culture of other tissues, and it was not until the late 1960s that Browning and Trier described the means by which intestinal tissues could be successfully cultured. This breakthrough provided a tool researchers could utilise, and adapt, to investigate topics such as the pathogenesis of inflammatory intestinal diseases, the effect of growth factors and cytokines on intestinal proliferation and differentiation, and the testing of novel xenobiotics for efficacy and safety. This review considers that intestinal explant culture shows much potential for the application of a relatively under-used procedure in future biomedical research. Furthermore, there appear to be many instances where the technique may provide experimental solutions where both cell culture and in vivo models have been unable to deliver conclusive and convincing findings.

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Transforming growth factor-beta (TGF beta 1) plays a central role in wound healing, so its perturbation by radiation may contribute to the acute and late effects seen in irradiated skin. TGF beta 1 mRNA expression was measured by PCR, in the skin of the CD1 and CBA mouse, exposed to Sr-90 beta from an 11-mm diameter source. TGF beta 1 mRNA expression increased sharply after doses between 1 and 10 Gy and plateaued at approximately 200% above controls after doses between 20 and 50 Gy. Immunohistochemistry showed that the TGF beta 1 protein was confined to the dermis and suprabasal cells with none in basal cells. A dose of 50 Gy produces an acute desquamative reaction in 100% of mice that is resolved in 30 days. After the same dose, TGF beta 1 mRNA expression fell below the controls at 3 h (-9.4% in the CD1 and -44% in the CBA mouse); rose sharply at 6-12 h (+124% CD1, +230% CBA), returned to control levels by 24-48 h, then rose progressively to approximately 200% above the controls between days 7 and 14. TGF beta 1 mRNA expression remained elevated at 100-200% above controls until the end of the experiment at 55 days. The significance of these changes in TGF beta 1 is discussed in the context of the early stress response reaction to radiation, the acute inflammatory and the later chronic fibrosis of the skin.