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S Klee

Publications and source records attributed to S Klee.

At least 19 recordsLinked to original sources

Molecular phylogenetic analysis of the Pneumoroidea (Orthoptera, Caelifera): molecular data resolve morphological character conflicts in the basal acridomorpha.

A key transition in the evolution of the insect suborder Caelifera (Orthoptera; Insecta) was from predominantly non-angiosperm-feeding basal lineages to the modern acridomorph fauna (grasshoppers and related insects). However, because of conflicts in the distribution of several complex morphological characters, the relationships of the presumed intermediates, and in particular of the superfamily Pneumoroidea, are presently unclear. We undertook a phylogenetic study of representatives of all of the transitional acridomorph families using mitochondrial and nuclear DNA sequences. No support for pneumoroid monophyly was obtained from nonparametric bootstrap analysis. Furthermore, adopting a maximum-likelihood approach, specific hypotheses of relationships within the Pneumoroidea were firmly rejected using parametric bootstrapping and Kishino-Hasegawa tests. The results indicate that the Pneumoroidea are at best a grade. This distinction implies that the evolution of the proposed pneumoroid synapomorphies, femoro-abdominal stridulation and simple male genital structure, might previously have been misinterpreted as cases of single character gains or losses within lineages. Reconstructions of character states for the femoro-abdominal stridulation indicate that, in fact, multiple losses or gains are equally likely. An important implication of our findings is that, in grasshoppers, auditory tympana may have evolved before stridulation, supporting the argument that the original function of tympana may have been related not to conspecific communication but to predator detection. Overall, the results of this study emphasize the high information content of these minor groups (in this case, the four intermediate families under consideration contain only 0.2% of extant orthopteran species diversity). Our analyses also demonstrate the advantages of model-based methods in analyzing systematic problems and, in particular, of the importance of testing specific phylogenetic hypotheses when a priori support for groupings (e.g., from nonparametric bootstrapping) is marginal.

Animals↗

An investigation into the effect and mechanisms of action of nicotine in inflammatory bowel disease.

OBJECTIVE AND DESIGN: To determine the effect of nicotine on colonic inflammation in the trinitrobenzenesulphonic acid (TNBS) model of inflammatory bowel disease in comparison with sulphasalazine. MATERIALS: Male Wistar rats were used for the in-vivo and ex-vivo studies. In-vitro studies were performed using human leukemia peripheral blood monocyte cells (THP-1 cells) grown in continuous culture. TREATMENT: Rats were given access to either nicotine (5 or 100 microg/mL) or sulphasalazine (375 microg/mL) in their drinking water for 10 or 2 days respectively before and 3 days after TNBS administration. THP-1 cells were treated with nicotine (10(-14) to 10(-11) M) for 2 h before and after stimulation with 3 microg/mL lipopolysaccharide (LPS). METHODS: Inflammation in the TNBS model was assessed by measuring the tissue myeloperoxidase activity, leukotriene B4 concentration, inducible nitric oxide protein expression, the ex-vivo production of tumour necrosis factor alpha (TNFalpha), macroscopic damage score, plasma corticosterone levels and by a qualitative histological evolution. The effect of nicotine on TNFalpha production in LPS stimulated THP-1 monocyte cells in-vitro was also determined. Statistical comparisons were made using the Mann-Whitney U-test for the macroscopic damage score and an ANOVA for all other parameters. RESULTS: TNBS treated rats given access to 100 microg/mL nicotine in their drinking water had a marked reduction in several of the markers of inflammation compared to control TNBS treated rats, but a greater reduction was found at 5 microg/mL nicotine or 375 microg/mL sulphasalazine, the latter producing comparable reductions in inflammation to the low dose nicotine. Nicotine also caused a significant reduction in TNFalpha release from THP-1 cells. CONCLUSIONS: Nicotine reduced inflammation in the TNBS model of colonic damage confirming the use of nicotine in IBD although the choice of dose requires further investigation. The mechanism of action of nicotine does not involve increased corticosterone levels, but may be a consequence of a reduction in TNFalpha or leukotriene B4 production.

Animals↗

Far-infrared spectroscopy of CH3OD in highly excited torsional states and the atlas of the Fourier transform spectra in the range 200-350 cm(-1).

The high resolution Fourier transform far-infrared (FIR) spectrum of the torsion rotation band of CH3OD has been analyzed for the highly excited torsion states (n > or = 2) in the vibrational ground state. The spectrum shows splitting of the lines due to strong torsional-rotational-vibrational interactions in the molecule. Assignments were possible for rotational sub-bands in the torsional state as high as n = 4 and for K values up to 8 and J values of up to approximately 30 in most cases, for all the symmetry species. For the third excited torsional state n = 3 assignments were possible to K = 10. The data were analyzed with the help of the energy expansion model, which has been proven very successful in methanol. The state dependent expansion parameters are presented. These molecular parameters were able to reproduce the observed wavenumbers almost to within experimental accuracy of 0.0002 cm(-1) for clean unblended lines. These expansion coefficients should prove valuable in the calculation of precise energy values for excited torsional states up to n = 4, which is way above the torsional barrier. The detailed high-resolution spectral atlas of CH3OD has been presented in the range 200-350 cm(-1). This atlas is an extension of our earlier atlas in the range 20-205 cm(-1). The availability of this atlas in the journal will be very valuable for spectroscopists and astrophysicists seeking information in the infrared (IR) region in the laboratory and in outer space.

Deuterium↗

Evidence for a trigger function of valproic acid in xenobiotic-induced hepatotoxicity.

The influence of the antiepileptic drug, valproic acid (2-n-propylpentanoic acid), on the hepatocellular capacity, to cope with an extrinsic oxidative stress was investigated. Freshly isolated rat hepatocytes exposed to therapeutic concentrations of valproic acid (0.25-1.0 mmol/l) were less resistant than controls, as evidenced by a significant cytotoxic response after challenge of the cells with a non-toxic dose of allyl alcohol (2-propen-1-ol). Valproic acid alone was not toxic to hepatocytes even at ten times higher concentrations (10 mmol/l), suggesting that cell damage was not a mere additive effect. Incubation with valproic acid plus allyl alcohol induced an irreversible depletion of hepatocellular glutathione, in contrast to allyl alcohol alone which induced a transient loss. Hepatocytes treated with valproic acid plus allyl alcohol were protected by N-acetylcysteine, a precursor of glutathione. These findings indicate that valproic acid affects hepatocellular defence mechanisms and suggest that a predisposition of hepatocytes to oxidative stress may play a role in the fatal hepatotoxicity of valproic acid in epileptic patients.

Acetylcysteine↗

Perturbations Involving nu1 of NCCN.

From high-resolution infrared spectra of 14N12C12C14N, 14N13C13C14N, and 15N12C12C15N, we find that the levels 1000(0)0(0), 1000(0)1(1), 1000(0)2(0,2), and 1000(0)3(1,3) have very pronounced perturbations. Our analysis shows that these perturbations are due to a vibrational resonance among the levels 1000(0)0(0), 0102(0)2(0), and 0102(0)2(2) in the one case, and equivalent levels with one or more additional quanta of nu5 in the other three cases. The resonance constant for the perturbation involving nu1 is 0.25 cm-1. It has the dependence on v5 and l5 that is expected for the sextic potential constant, K124455, although it seems too large for such a high-order constant. The Deltal (or Deltak) = 2 interaction between, for instance, 1000(0)0(0) and 0102(0)2(2e) is shown to be primarily due to the l-type resonance mixing of the 0102(0)2(0) and 0102(0)2(2e) states. The resonance is nearly "turned off" for the 1000(0)2(0,2) and 1000(0)3(1,3) states of 14N13C13C14N because there are no level crossings between the interacting states and the band centers are too far away to have an obvious effect, although careful analysis shows that the perturbation can be seen in their effective centrifugal distortion constants. The spectrum of 15N12C12C15N shows level crossings only in the case of the 1000(0)1(1), 1000(0)2(0,2), and 1000(0)3(1,3) states. Copyright 1999 Academic Press.

Journal Article↗

Climbing the Bending Vibrational Ladder in D13C15N by Hot Gas Emission Spectroscopy.

Using a newly constructed Fourier transform emission apparatus, we have measured the threefold substituted HCN isotopomer, D13C15N, at 1370 K in the range from 450 to 700 cm-1. We could assign hot bands with upper states up to Kvl2 = 12(12). The assignments have been verified for states up to v2 = 5 by fitting with earlier room temperature absorption measurements of overtone and hot bands. The intensities are shown to be in qualitative agreement with the expected intensity pattern for such emission spectra. All the measurements for D13C15N have been combined in a single least-squares fit that includes approximately 2700 rovibrational lines which have a root-mean-square deviation on the order of 0.000 4 cm-1. The spectroscopic constants for the bending states v2 = 1, ellipsis,12 are reported, as well as for some combination states involving the other vibrational modes. We also give the spectroscopic constants of various states of DCN, D13C14N, and D12C15N which where obtained from room temperature absorption measurements. Copyright 1999 Academic Press.

Journal Article↗

Absolute Line Intensities for the nu6 Band of H2O2.

The purpose of this work was to obtain reliable absolute intensities for the nu6 band of H2O2. It was undertaken because strong discrepancies exist between the different nu6 band intensities which are presently available in the literature (A. Perrin, A. Valentin, J.-M. Flaud, C. Camy-Peyret, L. Schriver, A. Schriver, and P. Arcas, J. Mol. Spectrosc. 1995. 171, 358), (R. May, J. Quant. Radiat. Transfer 1991. 45, 267), and (R. L. Sams, personal communication). The method which was chosen in the present work was to measure simultaneously the far-infrared absorptions and the nu6 absorptions of H2O2. Consequently, Fourier transform spectra of H2O2 were recorded at Giessen in a spectral range (370-1270 cm-1) which covers both the R branch of the torsion-rotation band and the P branch of the nu6 band which appear at low and high wavenumbers, respectively. From the low wavenumber data, the partial pressure of H2O2 present in the cell during the recording of the spectra was determined by calibrating the observed absorptions in the torsion-rotation band with intensities computed using the permanent H2O2 dipole moment measured by Stark effect (A. Perrin, J.-M. Flaud, C. Camy-Peyret, R. Schermaul, M. Winnewisser, J.-Y. Mandin, V. Dana, M. Badaoui, and J. Koput, J. Mol. Spectrosc. 1996. 176, 287-296) and [E. A. Cohen and H. M. Pickett, J. Mol. Spectrosc. 1981. 87, 582-583). In the high frequency range, this value of the partial pressure of H2O2 was used to measure absolute line intensities in the nu6 band. Finally, the line intensities in the nu6 band were fitted using the theoretical methods described in detail in our previous works. Using these new results on line intensities together with the line position parameters that we obtained previously, a new synthetic spectra of the nu6 band was generated, leading to a total band intensity of 0.185 x 10(-16) cm-1/(molecule.cm-2) at 296 K. It has to be pointed out that the new line intensities agree to within the experimental uncertainties with the individual line intensity measurements performed previously by May and by Sams. Copyright 1999 Academic Press.

Journal Article↗

Simultaneous Rovibrational Analysis of the nu(2), nu(3), nu(5), and nu(6) Bands of H(3)(12)CF.

A total of 4892 transition wavenumbers of the nu(2), nu(3), nu(5), and nu(6) fundamental bands of H(3)(12)CF and 1469 frequencies of the rotational transitions in the v(2) = 1, v(3) = 1, v(5) = 1, and v(6) = 1 vibrational states have been fitted simultaneously by taking explicitly into account various Coriolis interactions, l-type interactions, and alpha-resonance terms between and within the vibrational states. The standard deviation of the fit using 71 parameters was 8.10 x 10(-5) cm(-1) for the infrared data and 0.198 MHz for the rotational data. This study clearly shows that in order to obtain a really quantitative fit of the highly precise data of vibration-rotational and rotational spectroscopy, it is necessary to fit all the data simultaneously using a variational approach. The deperturbed values of the upper state rotational constants differ significantly from those obtained previously in fitting the nu(3) and nu(6) bands as isolated bands and the nu(2)/nu(5) bands by a variational approach. This is important for the precise determination of the equilibrium structure of methyl fluoride (J. Demaison, J. Breidung, W. Thiel, and D. Papousek, Struct. Chem., in press). Besides this, the results can be used in further studies of the reduced Hamiltonians for more complicated systems of interacting vibrational levels. Copyright 1999 Academic Press.

Journal Article↗

A contribution to safety assessment of veterinary drug residues: in vitro/ex vivo studies on the intestinal toxicity and transport of covalently bound residues.

1. The gastrointestinal fate of protein-bound residues of the model compound furazolidone (FZD) was investigated in vitro and ex vivo. Protein-bound residues were generated in rat liver microsomes, isolated by solvent extraction and digested with 0.5% hydrochloric acid and Pronase E. 2. During digestion, 3-amino-2-oxazolidinone (AOZ), the side chain of furazolidone, was partly released from bound residues. 3. The absorption of free AOZ and digested protein-bound residues was tested in isolated perfused rat gut segments (IPGS) and in the intestinal cell line Caco-2. Free AOZ was transfered both in the IPGS model and in Caco-2 monolayer cultures, while no indications for passage of bound residues were obtained. 4. No acute toxicity of AOZ or digested food residues respectively was observed in gut segments and Caco-2 cells at concentrations that were substantially above maximum residue levels to be expected in food of animal origin after administration of therapeutic doses. 5. The results demonstrate that digestive processes can alter the chemical nature of drug residues and yield degradation products that may be bioavailable for the consumer. Thus, the covalent binding of xenobiotics to macromolecular tissue constituents cannot necessarily be regarded as an irreversible endpoint of residue bioavailability and toxicity.

Animals↗

Infrared Spectrum of 15N13C13C15N near 2100 cm-1

The high resolution infrared spectrum of the linear centro-symmetric molecule 13C215N2 (cyanogen) has been measured in the region from 1950 to 2150 cm-1. The nu3 fundamental band and the difference band nu1-nu5 were observed in that region. Hot-band transitions arising from the nu5, 2nu5, 3nu5, and nu4 levels were also measured with the nu3 band. The nu3 fundamental band and first hot band for 15N12C13C15N were also measured. Copyright 1998 Academic Press. Copyright 1998Academic Press

Journal Article↗

The Far-Infrared Spectrum of ClNO2 Studied by High-Resolution Fourier-Transform Spectroscopy.

The far-infrared spectrum of nitryl chloride was studied using high-resolution Fourier-transform spectroscopy in the 300-525 cm-1 region. Vibrational band centers of fundamental, hot, and difference bands were determined. Furthermore, rotational and centrifugal distortion constants up to fourth order for the nu3 bands of 35ClNO2 and 37ClNO2 (centered at 370 and 364 cm-1, respectively) were obtained. The nu5 fundamental of ClNO2 (predicted around 410 cm-1) is very weak and overlapped by difference bands. Copyright 1998 Academic Press.

Journal Article↗

The Far Infrared Spectrum of HOCl: Line Positions and Intensities.

The far infrared spectrum of HOCl has been recorded at high resolution between 20 and 360 cm-1 by means of Fourier transform spectroscopy, and it was possible to observe pure rotation lines involving rotational levels with high Ka quantum numbers (up to Ka = 9). These lines combined with microwave and tunable far infrared data available in the literature were least squares fitted using a Watson-type Hamiltonian. The fitting leads to precise sets of rotational and centrifugal distortion constants for the ground states of both isotopomers HO35Cl and HO37Cl. Also relative line intensities were measured and their fitting allowed the determination of rotational corrections to the b-component of the permanent transition moment. Finally, to get Hamiltonian constants consistent with the newly determined ground state constants for the (100), (010), (001) vibrational states, available data concerning the nu1, nu2, and nu3 bands were refitted. Three interesting points are to be stressed. For the (001) state, we were able to complete the existing data with rotation lines observed in our spectra up to rather high Ka values (Ka = 7). For HO35Cl, we were able to show that some (010) and (100) levels are perturbed by levels of the (002) and (030) states, respectively, through Coriolis-type interactions. This allows the determination of the band centers of these two dark states. Copyright 1998 Academic Press.

Journal Article↗

Simultaneous Rovibrational Analysis of the nu2, nu3, nu5, and nu6 Bands of H313CF.

A total of 6071 transition wavenumbers of the nu2, nu3, nu5, and nu6 fundamental bands of H313CF and 1689 frequencies of the rotational transitions in the v2 = 1, v3 = 1, v5 = 1, and v6 = 1 vibrational states have been fitted simultaneously by taking into account various Coriolis interactions, l-type interactions, and alpha-resonance terms between and within the vibrational states. The standard deviation of the fit using 75 parameters was final sigma = 7.63 x 10(-5) cm-1 for the infrared data and 0.150 MHz for the rotational data. The possibility of obtaining a quantitative fit of the very precise data of high-resolution Fourier transform and submillimeter-wave spectroscopy for a semirigid symmetric top molecule is discussed. Copyright 1998 Academic Press.

Journal Article↗

[Pharmacotherapy of degenerative joint diseases in dogs].

The pharmacological treatment of degenerative joint diseases is restricted essentially to the alleviation of acute symptoms of activated arthropathies. Suitable compounds are the non-steroidal and steroidal antiinflammatory drugs, which however do not allow long-term therapy due to their overall catabolic effects on cartilage metabolism. Since causally acting drugs are not available, the progressive course of the disease cannot be prevented so far. Natural components of the cartilage's matrix, being recommended as so-called chondroprotective drugs, do not fulfill the expectation of a remission of the degenerative process. Indeed, regarding the necessity of multiple local applications of these drugs, they are not superior to antiinflammatory drugs. Provided careful dosing and surveillance of untoward gastrointestinal effects, non-steroidal antiinflammatory agents still are the drugs of first choice.

Animals↗

Intensity Measurements of Deltal > 1 Transitions of Several Isotopomers of HCN

The intensities of the forbidden Q-branch transitions 02(2f)0-00(0)0, 12(2f)0-00(0)0, and 02(2f)1-00(0)0 for HCN have been measured. The intensities of the 02(2f)0-00(0)0 transitions of DCN, D13C15N, and H12C15N were also measured, as well as the 02(2f)1-00(0)0 transitions of H12C15N and H13C15N. These Q-branch transitions are forbidden even when the effects of l-type resonance are considered so they must get their intensity from some other Coriolis interactions. The much stronger P- and R-branch lines for the e levels of these same vibrational transitions were also measured and they are shown to get most of their intensity from l-type resonance. However, the same Coriolis resonance that gives intensity to the Q-branch transitions seems to affect the DeltaJ = ±1 transitions as shown by the difference in the intensities of the DeltaJ = +1 and DeltaJ = -1 transitions. Measurements of the intensity of the 03(3e)0-00(0)0 and 03(3f)0-00(0)0 transitions shows that they derive most, but perhaps not all, of their intensity from l-type resonance. An unsuccessful search for forbidden DeltaJ = 0, e-e transitions for the strong 10(0)0-00(0)0 band shows that there is no detectable mixing of the e and f levels. Copyright 1997 Academic Press. Copyright 1997Academic Press

Journal Article↗

Effect of tachykinin receptor inhibition in the brain on cardiovascular and behavioral responses to stress.

The neurokinins, substance P (SP) and neurokinin A (NKA) represent natural, nonspecific ligands of NK1 and NK2 receptors. In our study in conscious rats, we tested the hypothesis that neurokinins, especially SP, are used by neuronal circuits to generate cardiovascular and behavioral responses to stress by using the selective, high-affinity, nonpeptide antagonists of NK1 and NK2 receptors, CP-96, 345, RP 67580 and SR 48968, respectively, Formalin injected s.c. through a chronically implanted catheter in the region of the lower leg was used as a stress stimulus. The antagonists and their inactive enantiomers, RP 68651 and SR 48965, as a control for nonspecific activity, were injected intracerebroventricularly (i.c.v.) 10 min before the s.c. injection of formalin. Formalin (2.5%, 50 microliters, s.c.) induced a marked increase in mean arterial pressure (MAP) and heart rate (HR) as well as hind limb grooming/biting (HG) as the dominant behavioral manifestation. Pretreatment with the NK1 receptor antagonist, CP-96,345 (5 nmol, i.c.v.), significantly attenuated only the HR (-54%; P < .01) but not the MAP response to formalin. The NK1 receptor antagonist, RP 67580, injected i.c.v. at doses of 100, 500 and 2500 pmol significantly reduced both, the MAP and HR responses to formalin by maximally 63% (P < .01) and 52% (P < .01), respectively. In a separate set of experiments, we compared the effect of the individual and simultaneous blockade of central NK1 and NK2 receptors on the cardiovascular and behavioral responses to formalin stress. Pretreatment with RP 67580 (100 pmol, i.c.v.) attenuated the MAP (-30%; P < .05), HR (-40%; P < .01) and HG (P < .05) responses to formalin. The NK2 receptor antagonist, SR 48968 (650 pmol, i.c.v.), affected neither the cardiovascular nor the behavioral responses. i.c.v. pretreatment with both tachykinin receptor antagonists (RP 67580: 100 pmol; SR 48968: 650 pmol) reduced the MAP, HR and HG responses to formalin to the same extent as RP 67580 alone. Pretreatment with the inactive enantiomers, RP 68651 (100 pmol, i.c.v.) and SR 48965 (650 pmol, i.c.v.) did not alter the cardiovascular and behavioral responses to formalin. Our results demonstrate that centrally administered NK1 receptor antagonists inhibit the cardiovascular and behavioral reactions in response to a noxious stimulus. They provide first pharmacological evidence that endogenous SP acts as mediator of stress responses in the brain.

Animals↗

The Ethylene Hot Band Spectrum near 3000 cm-1

A new hot band spectrum of ethylene has been recorded from 2970 to 3015 cm-1 at low rotational temperatures in a seeded molecular jet, using vibrational energy transfer from SF6 to C2H4. An IR-IR double resonance technique has been applied to pump the lower states and subsequently probe the hot bands. Two new hot bands, nu10 + nu11 - nu10 and nu7 + nu11 - nu7, have been found. The weak hot band starting from nu7 has been identified by direct labeling of some rotational levels in the nu7 manifold. High resolution FTIR spectra at ambient and at elevated temperatures have been recorded, too; it has thus become possible to extend the analysis to higher rotational quantum numbers. The previously analyzed nu9 + nu10 level has been reinvestigated and a b-type Coriolis interaction with the nearby nu7 + nu11 state has been observed. Rotational energy levels of nu7 + nu11 and of nu9 + nu10 have been fitted simultaneously, taking into account the local perturbations due to five dark states. From the shift of all K not equal 0 levels to higher frequencies in the nu10 + nu11 state, a global a-type Coriolis interaction with nu8 + 2nu12 has been identified.

Journal Article↗

Infrared Transitions of H12C14N and H12C15N between 500 and 10 000 cm-1

We have measured the Fourier transform spectrum (FTS) of two isotopomers of hydrogen cyanide (H12C14N and H12C15N) from 500 to 10 000 cm-1. The infrared data have been combined with earlier published microwave and submillimeter-wave measurements. From this analysis new vibration-rotation energy levels and constants are given, based on the observation of a number of new vibrational levels, especially for H12C15N. The Coriolis interaction involving Deltav3 = -1, Deltav2 = 3, and Deltal = &plusmn;1 has been observed for a great many levels and in some cases the assignments of laser transitions allowed by this interaction are more clearly shown. New vibration-rotation constants are given that allow one to predict the transition wavenumbers for most of the transitions below 10 000 cm-1 with accuracies of about 0.5 cm-1 or better. Values are given for the power series expansion of the l-type resonance constants and for the centrifugal distortion constants, as well as the usual vibrational and rotational constants.

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