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Biomedical subjects

S Rush

Publications and source records attributed to S Rush.

At least 37 records · Page 2Linked to original sources

Treatment of aggressive keratoacanthomas by radiotherapy.

Keratoacanthomas infrequently are treated by radiotherapy. However, keratoacanthomas that are recurrent after surgical excision or whose resection would result in cosmetic deformity may benefit from radiotherapy. Between January 1970 and June 1988, 29 such keratoacanthomas in 18 patients were irradiated. Doses ranged from 3500 cGy in 15 fractions to 5600 cGy in 28 fractions. Measured end points of therapy were (1) initial response, (2) freedom from recurrence, and (3) quality of the subsequent cosmetic appearance (scored as good, fair, or poor). No lesion progressed and all eventually regressed completely. Cosmetic results generally were considered good by both the patient and the referring dermatologist; none of the results was considered poor. Our results demonstrate that radiation is an effective means of treating keratoacanthomas.

Adult↗

Induction of a heat shock gene at the site of tissue injury in the rat brain.

Our objective was to investigate whether localized tissue injury induces expression of a gene encoding the major 70 kd heat shock protein (hsp70) in the mammalian nervous system. A small surgical cut was made in the rat cerebral cortex. By 2 hr postsurgery a dramatic and highly localized induction of hsp70 mRNA was detected at the lesion site using in situ hybridization with labeled riboprobe. By 12 hr the intensity of the signal had diminished, and by 24 hr only a few cells along the walls of the cut demonstrated a high level of hsp70 mRNA. Both neurons and glial cells at the site of the surgical cut responded to tissue injury by induction of hsp70 mRNA. Induction was not observed in other brain regions, nor was the pattern of constitutive expression affected by the surgical procedure.

Animals↗

EMG to torque relationship in rectus abdominis muscle. Results with repeated testing.

Rectus abdominis muscles of young healthy female volunteers were studied to determine both the maximum strength in isometric flexion and the relation between the surface electromyogram (RMS EMG) and torque. Both the upper and lower portions of the abdominal muscle were studied during graded increase and decrease of torque. Repeated testing was performed over 6 weeks. The form of the relation between torque and EMG was better described by a quadratic than by a linear regression relationship, but with considerable variability about the best-fit line. The torque-increasing and torque-decreasing parts of each test were different and were analyzed separately. After 6 weeks of repeated testing, maximum voluntary isometric flexion torque increased 16.8% (P less than 0.01). There was a decrease in the ratio of electromyographic activity to torque production, which was statistically significant in the torque-increasing recordings. These changes in maximum torque and in the EMG-torque relation were attributed to learning through a test-retest effect, rather than to a true change in muscle characteristics. These findings, which show changes in normal subjects undergoing repeated testing, do not support the reliability of isometric strength measurements, or measurements based on RMS EMG recordings, for quantifying abdominal muscle function in patients with back pain, or those undergoing strengthening exercises.

Abdominal Muscles↗

Comparison of acoustic and electrical signals from erectores spinae muscles.

Comparison was made between simultaneous recordings of the electromyogram (EMG) and acoustic myogram (AMG) signals and the torque produced by the lumbar erectores spinae muscles of three healthy subjects while they performed isometric contractions. Repeatability of each signal was studied. The AMG had a relationship to the torque which was more quadratic than linear, whereas that of the EMG was more linear. The coefficient of variability of residuals about a "best-fit" line was 8.55% for torque-increasing EMG recordings and 19.2% for torque-increasing AMG recordings. At the same torque, the EMG was on average about 10% greater for increasing-torque recordings than for decreasing-torque parts of the recordings, but the magnitude of the AMG signal was about 10% less. With repeated testing on the same day, the coefficient of variability of the signal/torque relationship (torque-increasing) was 9% for EMG and 23% for AMG signals. With long-term testing over 2 weeks these coefficients were 23 and 39%, respectively. Correlation analysis showed that the two signal/torque relationships varied independently of each other.

Electromyography↗

Rat and mouse identifier sequences are preferentially but not exclusively located in cortical neuronal genes expressed postnatally.

A genetic element called the identifier (ID) sequence, highly repeated in the rat genome, has previously been reported to be located in the introns of some genes transcribed in the adult rat brain by RNA polymerase II (Pol II). We show that nuclear RNA isolated from neurons of cerebral hemispheres (cortex) of 14-day old rats is enriched more than 10-fold in ID sequences compared to nuclear RNA from liver, kidney, cerebellum, or cortical glia. The developmental onset of the difference is during the first 2 weeks after birth. Mouse cortical neuronal nuclear RNA is similarly enriched in an element related but not identical to the rat ID element, and the enrichment also has postnatal onset. The enriched appearance of ID sequences in transcripts whose expression is increased postnatally in cortical neurons correlates developmentally and spatially with the transcription of ID elements by RNA polymerase III (Pol III) and with a change in chromatin structure.

Animals↗

Trunk extensor EMG-torque relationship.

The integrated surface electromyogram (IEMG) of the lumbar erectores spinae and the torque generated were simultaneously recorded from 27 healthy subjects in the standing posture while they pulled isometrically against resistance provided by a harness around the shoulders. The IEMG-torque ratio (efficiency of electrical activity, or EEA) was used to characterize each subject. Individual recordings showed evidence of nonlinearity of the IEMG-torque relationship in that a statistically better fit to experimental recordings was obtained by using two straight lines with a breakpoint between them. However, with repeated testing, the gradients of these two lines were more variable than the slope of the single straight line fitted to the entire recording. The slope of the best fit line (EEA) was less for recordings made during torque decrease than for increasing-torque recordings. This also showed as a "hysteresis" pattern in the recordings. The coefficient of variability (within subjects) of the EEA was greater in day-to-day testing (24%) than with repeated pulls at the same testing session (14%). This was similar to variability of the maximum generated torque. About 25% of the variability between subjects was found to be due to anthropometric differences. The residual variability of the relationship would limit the accuracy of IEMG as a measure of muscular effort under changing torque conditions. However, the EEA may be useful for characterizing muscle performance, especially when maximum effort cannot be achieved.

Adult↗

Inhibition of the proteolytic contaminant in commercial xanthine oxidase preparations by serum protein fractions.

Commercial xanthine oxidase, widely used for generation of oxygen radicals in vitro, is usually contaminated by proteolytic activity, which limits its utility in studies of oxygen radical damage to protease sensitive substrates. An easily prepared fraction of fetal calf serum was found to inhibit virtually all of the proteolytic contaminant without affecting superoxide generation. The effects attainable with the "purified" enzyme were demonstrated with two protease sensitive targets: proteoglycan subunit from cartilage and fibronectin from human plasma.

Ammonium Sulfate↗

Quantitative comparison of pre-mortem ECG's with those reconstructed from activation data of a revived heart.

The pioneering work of Durrer and associates has made available unique data showing activation isochrones in human hearts. To be certain that the complex experimental procedures do not seriously affect the activation sequence and also to validate accepted basic premises concerning the genesis of the electrocardiogram (ECG), it appears to be essential to show a reasonable correspondence between the subject's ECG before death and ECG's reconstructed from the activation data and heart-lead models. This paper reports the results of such a study. The comparison is evaluated in quantitative terms using several types of correlation coefficient. The significance of these is further evaluated through comparisons of similar coefficients from a random sample of normal records. The correlation coefficient considered to have the most general applicability gives a value of .80; only one subject from the random group showed a higher correspondence. A particular set of leads chosen to minimize the effects of inhomogeneities not accounted for in the modelling process, clearly selected the subject's records from all others with a correlation coefficient of .91 compared to .87, the highest from the random set. Considering the practical limitations on the accuracy of the models underlying these tests, the results are considered, with certain exceptions, to be supportive of the accuracy of the activation experiments and the assumption of a uniform double layer as the ECG source.

Electrocardiography↗

Response of cultured myocardial cells to countershock-type electric field stimulation.

Myocardial cells isolated from 8-day chick embryos were grown in monolayer culture under conditions that produce "standard embryonic" and "adult-type" cells. These cells were subjected to electric field stimulation that had a waveshape and intensities similar to those used in clinical electric countershock procedures. Photocell mechanograms obtained before, during, and after stimulation were correlated with simultaneously measured transmembrane potentials to determine the relationship between membrane polarization and arrhythmia production that occured after the stimulus. The results of these experiments demonstrate that a predictable sequence of mechanical responses occurs after stimuli ranging in intensity from 6 to 200 V/cm. This sequence, which closely resembles that observed in vivo after similar stimulation intensities, consists of a single response (activation), tachyarrhythmia, relaxed arrest followed by transient tachyarrhythmia, arrest with contracture, and cellular fibrillation. This diverse pattern of arrhythmias is associated with a prolonged depolarization of the cell membrane which increases with the intensity of the applied stimulus. It is probable that this depolarization is caused by a transient electromechanical deformation of the cell membrane during the shock. These findings contribute to a better understanding of the causes of the arrhythmias that appear after clinical and experimental electric countershock procedures.

Animals↗

Local potential gradients as a unifying measure for thresholds of stimulation, standstill, tachyarrhythmia and fibrillation appearing after strong capacitor discharges.

The pattern of arrhythmias following capacitor discharges of increasing amplitude, which have been observed by the authors in cultured myocardial cells from chick embryos, was compared to the arrhythmia patterns caused by similar discharges in experimental animals and humans, as reported in the literature. While the absolute voltages and currents causing each type of arrhythmia showed great variation, the scatter decreased considerably when the stimulus level was recalculated on the basis of peak current density in myocardial tissue, and was reduced further when the peak potential gradient at the cell level was used as the common basis of comparison. The similarity in the arrhythmia patterns and in the voltage gradients at which they occur indicates that the mechanism of these arrhythmias may be similar in cultured cells and intact animals and humans.

Action Potentials↗