Inhibition by halothane,but not by isoflurane,of oxidative response to opsonized zymosan in whole blood

In an attempt to clarify some apparent discrepancies in reports of the effects of anesthetic agents upon granulocyte function, we studied the effects of halothane and isoflurane, using techniques that allowed us to perform the assays in whole blood and in sealed vials to prevent volatile gas evolution; assay gas concentrations were measured, rather than inferred. Chemiluminescence, superoxide production, and hydrogen peroxide production were assessed after presentation of opsonized zymosan as a phagocytic stimulus. Incubation with halothane led to a highly statistically significant dose-related inhibition of Chemiluminescence (maximum 66%), H₂O₂ production (67%) and ·O ₂ ^– production (61%), within the concentration range observed in blood from patients undergoing general anesthesia. In contrast, the presence of isoflurane led to no statistically significant changes in any of the functions measured. Cells harvested from patients undergoing elective halothane anesthesia showed the same functional inhibition, but for quantitative differences likely due to the inability to control for dilution effects in clinical samples. It has been suggested that halothane anesthesia may be associated with excess mortality in septic patients; although the results we report are readily reversible, their presence during a prolonged anesthesia could be harmful in a patient who is not immunologically normal and/or who is already infected. Careful clinical trials will be necessary to determine if isoflurane is a superior agent in this context.     

Continuous fractionation and solution properties of PVC, 5. Pressure dependence of the viscosity — influence of solvent

Viscosity measurements were carried out as a function of pressure and temperature with solutions of 8 wt.-% PVC (M_w ≈ 75 000) in ten thermodynamically good solvents by means of a Searle-type viscometer. A rollingxyhball viscometer was used for the investigation of the pure solvents. In all cases the viscosity increases in a more or less exponential manner when the pressure is raised. The viscosity ratio f₁₀₀₀ = η_{1000 bar}/η_1bar can be varied by the choice of the solvent from ca. 2 (tetrahydrofuran) to 3,0 (cyclohexanone) at 40°C. For a constant temperature of 40°C, the volumes of activation for the viscous flow of the solutions, V^≠, or f₁₀₀₀ exceed that of the pure solvent, by typically 25%. The dependence of f₁₀₀₀ or V^≠ upon temperature is not very pronounced. However, the greater the f₁₀₀₀-values, the more marked are the temperature effects. The theoretical analysis of the data, including earlier measurements with PS, indicates that three terms contribute to f₁₀₀₀: the basic value (f₁₀₀₀)_s stemming from the pure solvent, the value (f₁₀₀₀)_p which the polymer would contribute under athermal conditions, and finally a thermodynamic term, (f₁₀₀₀)_pa, considering the pull-along effect (i.e. the specific forces a given segment exerts on other segments under variable thermodynamic conditions).     

Messungen zum Aggregationsverhalten perfluorierter Alkansäuren

With the use of various techniques an attempt was made to characterize the aggregates that exist in micellar surfactant solutions of salts of the perfluornonanoic acid. The cmc values of the investigated systems were determined by conductivity and surface tension measurements. Conclusions about the shape of the micellar aggregates were drawn from rheologic and electric birefringence measurements. For the lithium, the ammonium and the tetramethylammonium surfactants the existence of normal micelles with spherical shape and with all surfactant ions lying at the micellar surface was found. The perfluornonanoate surfactants with the ammonium counterions that are partially substituted by alkyl groups showed in all investigations a behaviour that was different from the normal case. It was postulated that these solutions contain emulsion-droplet-like giant micelles with the surfactant ions and counterions solubilized as ion pairs in the interior of the micelles. Some of these giant micelles do not have spherical shape; these solutions showed electric birefringence. In most cases the giant micelles disappeared at higher temperatures. Only normal small micelles with spherical symmetry could then be detected and the measured values were again in the range for values of normal C₈-perfluordetergents. On the basis of the investigated systems reasons and models for the formation of giant micelles are discussed.     

Properties of mouse leukemia viruses. XI. Immunoelectron microscopic studies on viral structural antigens on the cell surface.

Immunoelectron microscopic studies confirmed most of the results of the cytotoxic tests reported by Hunsmann et al. (Hunsmann, et al. (1976). Virology69, 157–168). GP71 and P12 viral structural antigens could be demonstrated on the surface of murine C-virus-producing but not on nonproducing transformed K Balb, MSV85 and HT-1 cells. GP71 serum revealed a type- and group-specific reactivity but failed to demonstrate an interspecies antigenic determinant, probably because of its relatively low corresponding titer. P12 antiserum reacted mainly type specifically. By this method, P10, P15, and P31 antigens were not detectable in significant amounts with the possible exception of P31 antigen on the highly producing FLV-Eveline cell. GP71 antigen occurred on the viral surface as well as on nonbudding areas of the cell membrane. P12 antigen was absent on virus particles but relatively abundant on nonbudding areas of the cell surface. No difference in the distribution of type- and group-specific determinants of GP71 was recognizable, and no clusters of the antigens studied were observed on the membrane under the conditions used. Based on these results it is suggested that among the virus structural antigens only GP71 and P12 antigens are integral surface constituents of the cells investigated and that none of the antigenic determinants studied represents a murine C-virus-induced tumor-specific cell surface antigen (TSSA). The relation of viral structural antigens to cell surface and soluble antigens described earlier and the significance of the results for possible preparation of vaccines are discussed.     

Only minor spinal motor reflex effects from feline group IV muscle nociceptors

The contribution of group III and IV muscle nociceptors activated by injection of KCl or bradykinin into the muscle artery (i.a.) of the gastrocnemius-soleus muscle to spinal motor reflex pathways was investigated in high spinal cats. Group I-III fibres were completely blocked by TTX, leaving group IV-fibre conduction intact. Thus, effects from i.a. KCl or bradykinin injection persisting after TTX were attributed to TTX resistant group IV fibres while the contribution of group III fibres was approximately defined by the difference between those effects and the control effects before TTX. Confirming former findings the chemical activation of group III and IV muscle afferents induced distinct reflex facilitation of the flexor posterior biceps semitendinosus and inhibition of the extensor quadriceps. After the block of all myelinated fibres by TTX the same stimuli induced only minor reflex effects mediated by the persistently conducting TTX resistant group IV afferents. It is concluded that the main functional meaning of group IV muscle afferents, which respond preferentially with a higher threshold to mechanical stimuli, is probably less related to reflex motor control than that of group III afferents.     

Verfahren zur automatischen Messung von Enzymkinetiken

Zusammenfassung Es wird ein neues Verfahren zur automatischen Untersuchung von Enzymkinetiken angegeben. Die Umsatzgeschwindigkeit einer Enzymreaktion in Abhängigkeit von jeweils einer veränderlichen Größe wird hierbei am durchlaufenden Reaktionsgemisch kontinuierlich gemessen und registriert. Unabhängige Veränderliche kann eine Konzentration (z. B. Substrat-, Coenzym-, Wasserstoffionenkonzentration) oder die Temperatur sein. Am Beispiel der Ermittlung einer Aktivitäts-pS-Kurve (Koordinaten:v=Umsatzgeschwindigkeit;pS=negativer Logarithmus der Substratkonzentration) wird das Verfahren im Einzelnen beschrieben. Unsere Methode eignet sich bisher zur Untersuchung von Enzymen, deren Umsatz durch Messung der Lichtabsorption erfaßbar ist. Als Beispiel werden Aktivitäts-pS-Kurven von Lactatdehydrogenase aus menschlichem Herzmuskel- und Leberhomogenisat sowie von Kaninchenmuskel-LDH gezeigt und die ermittelten Michaeliskonstanten angegeben.     

Über Funktionsänderungen markhaltiger Kaltblüternerven nach Adrenalektomie und Zufuhr rindenwirksamer Steroide in Abhängigkeit von der Ionenverteilung

Ohne ZusammenfassungBenutzte Symbole und Abkürzungen NNR Nebennierenrinde - DOCA Desoxycorticosteronacetat - K _i intracelluläres Kalium (sinngemäß für Natrium) - K _a extracelluläres Kalium (sinngemäß für Natrium) - Q Ladung - E _m Membranruhepotential - _m Zeitkonstante der Membran - R _m Membranwiderstand - C _m Membrankapazität     

Erholungserfolge bei Kindern in Höhenklima

Zusammenfassung 1.Beobachtungen aus der Gewichtskurve lassen einen klimatischen Einflu\ auf die Zunahme möglich erscheinen. 2. Der Hämoglobingehalt war nach dem Aufenthalt in 55% gesteigert; bei der Nachuntersuchung nach 6 Wochen zeigte sich in 47 % ein Erfolg gegenÜber dem Anfangswert. 3. Untersuchungen mit dem Ergographen ergaben eine Erhöhung der Muskelkraft und Verringerung der ErmÜdbarkeit. 4. Es fand eine gewisse Anpassung der Herztätigkeit au eine Arbeitsleistung statt. 5. Die Vitalkapazität hat in 47% zugenommen. 6. Die Reaktion der Vasomotoren auf Kältereiz war verkÜrzt.