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Biomedical subjects

R C Howe

Publications and source records attributed to R C Howe.

At least 55 records · Page 3Linked to original sources
PubMed1985

Analysis of the binding and postbinding activities of an inducible cloned CTL line at the population and the single-cell level.

We have analyzed the binding and lytic properties of a cloned CTL line before and after induction with MLC SN. Functional, specific binding by both effector populations could be demonstrated to occur at 20 degrees C; however, lysis required temperatures greater than or equal to 30 degrees C. Approximately 50% of noninduced cells and 70% of induced cells formed specific conjugates with P815 target cells. Conjugate formation approached maximum levels by 30 min at 20 degrees C for both populations. When low cell concentrations were employed for conjugate formation, the difference between SN-induced cells and noninduced cells was more pronounced. Analysis of the postbinding abilities of these populations at the single-cell level revealed that SN-induced cells were considerably more efficient in lysing attached target cells than were noninduced cells; however, significant lysis by the latter could be demonstrated after long periods. When populations which had intermediate cytolytic activity were compared to optimally induced or noninduced cells, apparent dissociation of the binding and postbinding capacities was observed. Cells harvested 4 days after stimulation with allogeneic cells plus SN displayed maximal binding but low postbinding activities. These results are consistent with the possibility that multiple components of the lytic mechanism are affected following induction and that these components may be asynchronously modulated.

Animals↗
PubMed1983

Isolation of alloreactive CTL clones with cyclical changes in lytic activity.

We have isolated two H-2Dd specific CTL clones from CBA anti-DBA/2 MLC that undergo changes in lytic activity against tumor and Con A blast target cells as a consequence of weekly stimulation with irradiated allogeneic cells and conditioned medium from secondary MLC. Lytic activity is highest on days 2 to 3 after stimulation, and lowest on days 5 to 7. CTL that had been irradiated on day 0 before stimulation have significantly greater activity on day 2. Conditioned media alone, in the absence of added allogeneic stimulator cells is capable of supporting, in a dose-dependent fashion, the increase in activity. Collectively, these changes are similar to those described for the induction of lytic activity in nonlytic CTL populations from long-term MLC, and suggest that these cloned lines may be useful to study the modulation of lytic activity of CTL in culture.

Animals↗
PubMed1981

Acute heroin abstinence in man: IV. Sleep--waking state contingencies.

This study investigated the effect of acute heroin withdrawal on the pattern of sleep--waking state sequences. Subjects included drug-dependent patients using pure heroin and drug-free controls. Electrophysiological data were recorded on a 24-hour per day basis for the first 5 - 7 days of withdrawal. EEG records were scored according to standard criteria. Marked increases in the sequential state changes occurred during withdrawal when progressing from awake-with-alpha, stage I, stage II and rapid eye movement (REM) sleep to the awake state. Heroin withdrawal also caused significant decreases in sequential state changes when proceeding from waking or light sleep states into deeper sleep states or into REM sleep. This study revealed that heroin withdrawal caused more abrupt transitions from quiet awake or sleeping conditions into the awake state and impeded progression into slow wave or REM sleep states.

Alpha Rhythm↗
PubMed1980

Acute heroin abstinence in man: I. Changes in behavior and sleep.

The purpose of this study was to examine overt behavioral characteristics and sleep during acute heroin abstinence in man. Both heroine-dependent patients and drug-free control subjects were observed and monitored on a 24-hour per day basis for 5 to 7 days. Observational data were analyzed for frequency of occurrence of various behaviors including the signs and symptoms of withdrawal. Electroencephalographic (EEG) data were scored into awake and sleep stages according to standard techniques. The heroin-dependent subjects generally displayed a higher number of observations across all recording days as compared to the controls. In addition, the signs and symptoms of withdrawal for these patients peaked on day 1 or day 2 and then declined over the remaining recording days. The EEG state data showed an increase in waking and decrease in both slow wave and REM sleep during acute heroin withdrawal. Total sleep was maximally suppressed on withdrawal days 2 and 3 and was still below normal control values on withdrawal days 5 - 7. REM sleep was more disrupted than slow-wave sleep during withdrawal from heroin. Results of this study indicate that heroin withdrawal produces a differential action upon central nervous system structures responsible for the various states of sleep, waking and related behaviors.

Acute Disease↗
PubMed1980

Acute heroin abstinence in man. III. Effect upon waking and slow wave sleep.

The purpose of this study was to evaluate the effects of acute heroin withdrawal on waking behavior and slow wave sleep. Data were collected from drug-dependent patients who were using pure heroin and from drug-free controls. All data were recorded on a 24-hour per day basis for 5 - 7 consecutive days. EEG records were manually scored according to standard criteria. The heroin-dependent patients during withdrawal showed approximately a 26% decrease in slow wave sleep and an 18% increase in waking behavior. The awake state in the heroin-dependent patients during withdrawal also displayed an increase in number of episodes and number of state shifts, and a decrease in duration and sleep onset latency. In addition, the slow wave sleep categories during withdrawal generally showed an increase in sleep onset latency and interstate interval and a decrease in number of episodes. These results indicate that heroin withdrawal is associated with a marked disruption of the central nervous system mechanisms responsible for maintenance of the normal sleep--waking cycle. Analyses of the pattern of this disruption will further aid in understanding the withdrawal syndrome.

Electroencephalography↗
PubMed1980

Acute heroin abstinence in man: II. Alterations in rapid eye movement (REM) sleep.

The purpose of this study was to examine the effects of withdrawal from heroin upon rapid eye movement (REM) sleep. Subjects included both heroin-dependent patients and drug-free controls. The drug users were young males who had an average daily intake of approximately 973 mg of 92 - 98% pure heroin before entering the study. All electrophysiological data were obtained via a telemetry system on a 24-hour per day basis for 5 to 7 consecutive days. EEG records were scored into the standard awake and sleep states. Results showed a marked decrease in total amount of REM sleep during heroin withdrawal. This total decrease was associated with a decrease in duration of individual REM episodes and a large decrease in the number of occurrences of REM sleep. The heroin-dependent patients during withdrawal also showed a prolonged latency from sleep onset to first REM episode and a reduced number of REM shifts per 24-hour period. No significant difference in REM sleep interval was observed between the control subjects and drug users. Some of the overt behavioral characteristics associated with heroin withdrawal may be indirectly related to the concurrent loss in REM sleep as observed in this study.

Electroencephalography↗
PubMed1979

A method for transition smoothing of sleep--waking states.

A method was developed for sequential redistribution of short-duration sleep--waking states into the long-duration behavioral state(s) that surrounds these intervals. This methodological approach is useful in determination of general sleep--waking patterns such as state durations, interstate intervals, and sleep--waking cycles. The redistribution sequences had no effect on total amount of sleep or waking categories, but did decrease stage 1 with successive redistribution steps. Examination of the slope of the curve (number of occurrences or mean epoch duration divided by successive redistributions) can be used to determine the appropriate "smoothing" for electroencephalogram (EEG) state data via location of the breakpoint in the curve. The low-pass redistribution technique has been particularly useful for smoothing large volumes of EEG state data for subsequent analyses without significantly changing the various sleep-waking states.

Adult↗
PubMed1979

Distribution of Lyb-4.1 and other membrane antigens on murine lymphoid tumors.

The distribution of membrane antigens on 6 DBA/2-derived tumors (L1210, L5178Y, P815, ABLS 11, ABLS 12, and ABLS 13) was studied by direct cytotoxicity and quantitative absorption assays. Lyb-4.1 antigen was found solely on the L1210 tumor. Iad antigens were absent from all tumors, and H-2Kd and H-2Dd antigens were present on all tumors. Immunoglobulin was adsorbed to the ascites tumors and lost after 3 days or more in tissue culture. These studies were performed to characterize the distribution of DBA/2 membrane antigens on DBA/2-derived tumors as a base line for functional and chemical studies with these tumors and with their solubilized proteins.

Animals↗
PubMed1979

Internal synthesis of p23,30 by several lymphoid malignancies.

The aim of this study was to prove the internal synthesis of p23,30 antigen (HLA-D related determinant) on human leukemias and lymphomas on which it has been detected with complement-dependent cytotoxic assays. Murine Ia antigens similar to p23,30 antigen are found on many subsets of cells in the mouse (B lymphocytes, macrophages, allogeneically activated T lymphocytes) and on intercellularly transferred immunoregulatory molecules, which may be adsorbed to other cells. The question exists whether the p23,30 antigen, which occurs on a wide range of human leukemias, is internally synthesized by these tumors or, in some instances, is synthesized by normal lymphocytes and is adsorbed to the leukemic cells. The expression of p23,30 antigen on a limited series of human leukemias and lymphomas was detected by a complement dependent, cytotoxicity assay. The internal synthesis of p23,30 antigen and p44,12 (HLA-A and -B antigens and beta2-microglobulin) was confirmed by immunoprecipitation and these antigens from [35S]methionine labeled, detergent solubilized membranes of tumor cells. In each instance, the synthesis of p23,30 antigen by the malignant cells was confirmed. The distribution of p23,30 antigen (and 1a antigen) on subsets of normal cells and in immunoregulatory molecules was reviewed. In view of these findings, the role of p23,30 antigen in the diagnosis of subsets of human hematologic malignancies was reconsidered.

Antigens, Surface↗
PubMed1978

Analysis of tonic muscle activity and muscle cramps during hemodialysis.

A problem associated with some patients undergoing hemodialysis is the presence of muscle cramps. As the etiology of these cramps is still unknown, the purpose of this study was to evaluate tonic muscle activity and muscle cramps during hemodialysis. Forty-six complete dialysis treatment sessions were studied. Electromyographic (EMG) activity was recorded from a leg muscle in patients who cramped and control patients who did not cramp. EMG was analyzed via a minicomputer for each minute of recording time. Results indicated the mean muscle cramp latency from start of dialysis was 248 minutes. Average muscle cramp was 10 minutes in duration and took three minutes to develop and seven minutes to fully dissipate. Tonic EMG activity in patients with muscle cramps showed a continued increase throughout the latter part of dialysis whereas the control patients showed a continual decline. The results suggest that the latent increase in EMG activity may be causally related to muscle cramps and may be a useful predictor as to the onset of muscle cramps during hemodialysis.

Electromyography↗
PubMed1978

Heterogeneity in the membrane proteins of human lymphoid cell lines as seen in sodium dodecyl sulfate-polyacrylamide electrophoresis slab gels.

The proteins of [35S]methionine-labeled membranes of six human lymphoid cell lines were examined by electrophoresis in sodium dodecyl sulfate-polyacrylamide gradient slab gels in order to identify molecular differences among these tumors. The lymphoid cells were internally labeled with [35S]methionine, their membranes were isolated, and the reduced and alkylated membrane proteins were treated electrophoretically in sodium dodecyl sulfate-polyacrylamide gradient slab gels. The gel patterns of over 100 membrane proteins per cell were highly complex but reproducible and, in that sense, constituted fingerprints of the individual tumors. Several proteins occurred uniquely on one or a few tumors. Some protein bands were identified to be serologically recognized membrane antigens by electrophoresis of immunopurified antigen in parallel to membrane samples. p44,12, a complex of proteins with molecular weights of 44,000 and 12,000 (HLA-A and -B antigens and beta2-microglobulin), and p29,34, (HLA-D antigen) were identified in this manner. High-resolution sodium dodecyl sulfate-polyacrylamide gradient gel electrophoresis can be used to catalog and describe lymphocyte membrane proteins and perhaps to identify subsets of lymphoid cancers.

Antigens, Neoplasm↗