Strukturanalytische Untersuchungen zur Altersabhängigkeit der Sensibilität

Zusammenfassung Eine Analyse der Meßwerte von Ronge (1943) über die Reizausnutzung durch das Tastsinnes-Nervensystem der Haut zeigt im Zusammenhang mit einer vorausgegangenen Studie (Scharf und Blumenthal, 1967), daß der Reizerfolg in einer transzendenten Fläche höherer Ordnung in Abhängigkeit vom Lebensalter (oder von der Anzahl der Meissnerschen Tastkörperchen pro Hautflächeneinheit) und vom Reizdruck dargestellt werden kann. In Druckrichtung steigt diese Fläche mit zunehmendem Reizdruck nichtlinear an, in Zeitrichtung oscilliert die Fläche dagegen träge um Normwerte, die beim 20jährigen Menschen realisiert sind. Dabei werden die Altersveränderungen der histologischen Hautstruktur offenbar zur Kompensation der altersabhängigen Verminderungen der Zahl der Tastkörperchen ausgenutzt.

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Summary An analysis of the observations on the Reizausnutzung by nerves of touch (Ronge, 1943) connected to a previous study (Scharf and Blumenthal, 1967) shows that the irritation result may be figured by a transcendental plane of higher order as a function of age (or number of Meissner's corpuscles per area skin) and irritation pressure. Along the pressure axis this non-linear plane is increasing non-linear in dependence on ascending pressure, but along the time axis the plane oscillates lazily round about the norm values which are realized in human beings of about 20 years of age. It seems that the age-dependent changes of histological skin structure are utilized to compensate the age-dependent diminution of touch corpuscle number.

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Mit dankenswerter Unterstützung durch einen Forschungsauftrag des Staatssekretariates für das Hochschulwesen der DDR.

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Numerische Rechnung: Tischrechner Mercedes Cellatron R 44 SM, Leitende Med. techn. Ass. Ruth Pieper (Anatomisches Institut Halle). Programmgesteuerter Digitalrechner ZRA 1, Math, techn. Ass. Friedegund Hüther (Institut für Numerische Mathematik, Halle).

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Graphik: Akad. Bildhauer Hellmut Helwin.     

Mechanism of aluminium-induced porphyrin synthesis in bacteria

In previous studies, aluminium was found to retard bacterial growth and enhance porphyrin formation in Arthrobacter aurescens RS-2. The aim of this study was to establish the mechanism of action of aluminium which leads to increased porphyrin production. Cultures of Arthrobacter aurescens RS-2 were incubated in the absence and presence of 0.74 mm aluminium. After 6 and 24 h of incubation, various parameters of the haem biosynthetic pathway were determined. After 6 h of incubation with aluminium, the activities of the enzymes aminolevulinate synthase (ALAS), aminolevulinate dehydratase (ALAD), porphobilinogen deaminase (PBGD) and uroporphyrinogen decarboxylase (UROD) were increased by 120, 170, 190 and 203%, respectively, while that of ferrochelatase (FC) was found to be unchanged. However, after 24 h of incubation, no change in the activities of ALAS and ALAD was noted, while an about 2-fold increase in PBGD and UROD activities were observed. FC activity was decreased by 63%. It was concluded that aluminium exerts its effect by inducing the enzymes PBGD and UROD rather than by a direct or indirect effect on ALAS. Its effect on the final step in the haem biosynthetic pathway is discussed.     

General relation between variance-time curve and power spectral density for point processes exhibiting 1/f β-fluctuations,with special reference to heart rate variability

Counting statistics in the form of the variance-time curve provides an alternative to spectral analysis for point processes exhibiting 1/f ^β-fluctuations, such as the heart beat. However, this is true only for β<1. Here, the case of general β is considered. To that end, the mathematical relation between the variance-time curve and power spectral density in the presence of 1/f ^β-noise is worked out in detail. A modified version of the variance-time curve is presented, which allows us to deal also with the case β?1. Some applications to the analysis of heart rate variability are given.     

Respiratory phasic effects of inspiratory loading on left ventricular hemodynamics in vagotomized dogs.

Exaggerated inspiratory swings in intrathoracic pressure have been postulated to increase left ventricular (LV) afterload. These predictions are based on measurements of LV afterload by use of esophageal or lateral pleural pressure. Using direct measurements of pericardial pressure, we reexamined respiratory changes in LV afterload. In 11 anesthetized vagotomized dogs, we measured arterial pressure, LV end-systolic (ES) and end-diastolic transmural (TM) pressures, stroke volume (SV), diastolic left anterior descending blood flow (CBF-D), and coronary resistance. Dogs were studied before and while breathing against an inspiratory threshold load of -20 to -25 cmH2O compared with end expiration. Relative to end expiration, SV and LVES TM pressures decreased during inspiration and increased during early expiration, effects exaggerated during inspiratory loading. In all cases, LV afterload (LVES TM pressure) changed in parallel with SV. LV end-diastolic TM pressure did not change. CBF-D paralleled arterial pressure, and there were no changes in coronary resistance. In two dogs, regional LVES segment length paralleled calculated changes in LVES TM pressure. We conclude that 1) LV afterload decreases during early inspiration and increases during early expiration, changes secondary to those in SV; 2) changes in CBF-D are secondary to changes in perfusion pressure during the respiratory cycle; and 3) the use of esophageal or lateral pleural pressure to estimate LV surface pressure overestimates changes in LV TM pressures during respiration.     

Oxygen cost of resistive-loaded breathing in quadriplegia.

We hypothesized that, in quadriplegia, chest wall distortion would increase the energy cost of ventilation. To assess this, we measured the oxygen cost of breathing (VO2 resp) and changes in chest wall configuration during inspiratory resistive-loaded breathing tasks in five quadriplegic and five normal subjects. Each subject performed three breathing tasks that spanned a range of work rates (Wtot). Configurational changes of the abdomen and upper, lower, and transverse rib cage were assessed with magnetometers. We found that 1) in both groups, VO2resp increased linearly with Wtot over the range of tasks performed, 2) the mean slope of the regression line of VO2resp vs. Wtot was greater for quadriplegic than for normal subjects (3.7 +/- 0.8 vs. 2.0 +/- 0.7 ml O2/J, P less than 0.01), 3) efficiency of breathing (Wtot/VO2resp) was less for quadriplegic than for normal subjects (1.9 +/- 0.6 vs. 3.5 +/- 1.4%, P less than 0.001), 4) during inhalation, upper and lower rib cages behaved similarly in the two groups, but the quadriplegic subjects had a decrease in transverse rib cage and a much greater increase in abdomen than normal subjects, and 5) functional residual capacity decreased in normal but not in quadriplegic subjects during the breathing tasks. We conclude that the lesser efficiency of breathing in quadriplegia may be related to the elastic work of chest wall distortion, shorter mean operational diaphragm length, and possibly differences between normal and quadriplegic subjects in mechanical advantage of available inspiratory muscles.