Search PubMed⌕ Search

Biomedical subjects

F E Yates

Publications and source records attributed to F E Yates.

At least 19 recordsLinked to original sources
PubMed2001

Kinetics of human aging: I. Rates of senescence between ages 30 and 70 years in healthy people.

A calculation of loss rates is reported for human structural and functional variables from a substantially larger data set than has been previously studied. Data were collected for healthy, nonsmoking human subjects of both sexes from a literature search of cross-sectional, longitudinal, and cross-sequential studies. The number of studies analyzed was 469, and the total number of subjects was 54,274. A linear model provided a fit of the data, for each variable, that was not significantly different from the best polynomial fit. Therefore, linear loss rates (as a percent decline per year from the reference value at age 30) were calculated for 445 variables from 13 organ systems, and additionally for 24 variables even more integrative, such as maximum oxygen consumption and exercise performance, that express effects of multiple contributing variables and systems. The frequency distribution of the 13 individual system linear loss rates (as percent loss per year) for a very healthy population has roughly a unimodal, right-skewed shape, with mean 0.65, median 0.5, and variance 0.32. (The actual underlying distribution could be a truncated Gaussian, an exponential, Poisson, gamma or some other). The linear estimates of loss rates were clustered between 0% and 2% per year for variables from most organ systems, with exceptions being the endocrine, thermoregulatory, and gastrointestinal systems, for which wider ranges (up to approximately 3% per year) of loss rates were found. We suggest that this set of linear losses over time, observed in healthy individuals between ages (approximately) 30 to 70 years, exposes the underlying kinetics of human senescence, independent of effects of substantial disease.

Adult↗
PubMed2000

Ultradian sleep rhythms of lateral EEG, autonomic, and cardiovascular activity are coupled in humans.

This study compared the dynamics of multiple systems during sleep with earlier results during waking rest. Three consecutive nights of data were collected from three healthy adults for 10 variables: left and right central EEGs; the nasal cycle (NC); beat-to-beat measures of CO, SV, HR, SBP, DBP, MAP, and hemoglobin-oxygen saturation. Time series analysis detected periods at 280-300, 215-275, 165-210, 145-160, 105-140, 70-100, and 40-65 min bins with the greatest spectral power in longer periods. We found significance across subjects with all parameters at 280-300, 105-140 (except left EEG power, left minus right EEG power, and HR), 70-100, and 40-65 min. Significant periods were reported earlier during waking for the NC, pituitary hormones, catecholamines, insulin, and cardiovascular function in five bins at 220-340, 170-215, 115-145, 70-100, and 40-65 min, with 115-145, 70-100, and 40-65 min common across all variables. These results suggest that lateral EEG power during sleep has a common pacemaker (the hypothalamus), or a mutually entrained pacemaker, with the cardiovascular and autonomic nervous systems (ANS), and that the waking ultradians of the neuroendocrine and fuel regulatory hormones may also be coupled to lateral EEG activity. Taken together these results present a new perspective for the Basic Rest-Activity Cycle and the physiology of the ANS-central nervous system during both waking and sleep.

Activity Cycles↗
PubMed1997

Low-frequency ultradian insulin rhythms are coupled to cardiovascular, autonomic, and neuroendocrine rhythms.

Plasma insulin levels were assayed to compare with earlier reported rhythms of the cardiovascular, autonomic, and neuroendocrine systems in 10 resting normal adults over 5-6 h. Our earlier report included time-series analysis for impedance cardiography measures of stroke volume, heart rate, cardiac output, thoracic fluid index, ejection velocity index, and ventricular ejection time; automated cuff measures of systolic, diastolic, and mean arterial pressures; the nasal cycle as a marker of lateralized autonomic tone; and indwelling venous catheters for sampling blood every 7.5 min to assay for adrenocorticotropic hormone, luteinizing hormone, epinephrine, and norepinephrine. Insulin was later assayed from the same plasma samples. Time-series analysis using the fast orthogonal search method of Korenberg detected insulin periodicities at ranges of 220-340, 115-145, 70-100, and 40-65, with significance across subjects at ranges of 115-145, 70-100, and 40-65 min. Significant periods for the other parameters were reported earlier at 220-340, 170-215, 115-145, 70-100, and 40-65 min, with periods at 115-145, 70-100, and 40-65 min dominating across parameters. These results suggest that insulin secretion has a common pacemaker (the hypothalamus) or a mutually entrained pacemaker with the autonomic, cardiovascular, and neuroendocrine systems.

Activity Cycles↗
PubMed1996

Ultradian rhythms of autonomic, cardiovascular, and neuroendocrine systems are related in humans.

Autonomic, cardiovascular, and neuroendocrine activities were monitored for 5-6 h in 10 normal adult resting humans (8 males, 2 females). The nasal cycle, a measure of lateralized autonomic tone, was measured at 4 Hz. Impedance cardiography (BoMed NCCOM3) was used to measure cardiac output, thoracic fluid index, heart rate, ejection velocity index, stroke volume, and ventricular ejection time (averages of 12 heart beats). Systolic, diastolic, and mean arterial pressures were measured with an automated cuff at 7.5-min intervals. Separate blood samples were taken every 7.5 min simultaneously from both arms with the use of indwelling venous catheters. Assays for adrenocorticotropic hormone, luteinizing hormone, norepinephrine, epinephrine, and dopamine were performed on samples from each arm. Time-series analysis, using the fast orthogonal search method of Korenberg, was used to detect variance structure. Significant spectral periods were observed in five windows at 220-340, 170-215, 115-145, 70-100, and 40-65 min. The greatest spectral power was observed in the lower frequencies, but periods at 115-145, 70-100, and 40-65 min were common across variables. Significant correlation coefficients for linear regressions of all paired variables in each subject were observed in 38.87% of the comparisons (subject range, 18.05-48-9.70%) with r > 0.30. These results suggest that either a common oscillator (the hypothalamus) or mutually entrained oscillators regulate these systems.

Activity Cycles↗
PubMed1990

Blood pressure levels and variance assessed by ambulatory monitoring: optimal parameters.

We obtained multiple ambulatory blood pressure monitoring (ABPM) records over five years from two trained, normotensive subjects experienced in wearing the apparatus. The resulting time series data on systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rate (HR) were used to suggest optimal parameters for monitoring by two instruments (Colin Medical Instruments ABPM-630 and Del Mar Avionics Pressurometer) and to compare two indirect methods (auscultatory and oscillometric). A 10-min sampling interval day and night provided sufficient density of data to support spectral analysis for ultradian rhythms in the frequency range of one cycle per hour to one cycle per 9 h on a 24-h record. Rhythms with major periods of approximately 3, 6, and 9 h were variously found in 94 normotensive subjects, aged 20 to 95 years, including the two trained subjects. When the monitoring period was extended to 72 h, the circadian (approximately 24 h) rhythm could be more sharply defined, as well as a 12-h harmonic. In some studies the two trained subjects wore two monitors, one on each arm, set to read simultaneously. From the simultaneous measurements on both arms, it was shown that averaging across three points (30 min of record) reduced the coefficient of variation between the two simultaneous records to 6% or less. Auscultatory and oscillometric methods were equally reliable. Echocardiographic data were obtained in five normotensive subjects and compared to their ABPM data. The ABPM records provided additional information about cardiovascular function not merely duplicating that obtained by acute stress tests, such as exercise or cold pressor responses, or echocardiography. Standards for ABPM are suggested.

Adult↗
PubMed1990

Ultradian adrenocortical and circulatory oscillations in conscious dogs.

We examined adrenal blood flow, cortisol secretion rate, concentration of cortisol in adrenal venous blood, mean arterial blood pressure, and heart rate in unrestrained conscious dogs, sampling at 15-20 s, 5 min, or 10 min during experiments lasting from 30 min to 8 h. Time history analysis designed for short, noisy time series detected three significant ultradian oscillatory periods: approximately 3, 6, and 90 min. Circulatory variables (systemic mean arterial pressure, heart rate, and adrenal blood flow) showed all three. Cortisol secretion rate showed the 3- and 90-min oscillations but not the 6-min oscillation. Adrenal glucocorticoid secretion rate and adrenal blood flow were not strongly coupled. However, at one extreme of blood flow (close to zero) and at the opposite extreme (very high blood flow stimulated by adrenocorticotropic hormone) adrenal blood flow and cortisol secretion were tightly coupled. In the normal physiological range, the multiperiodic, rhythmic organization of circulatory variables and adrenal glucocorticoid function arises from independent or only weakly coupled oscillators, not necessarily harmonically related, manifesting near-periodicity with wobble and intermittency.

Activity Cycles↗
PubMed1986

Similarity principles and intrinsic geometries: contrasting approaches to interspecies scaling.

We criticize standard allometric approaches on the grounds that they emphasize scaling to one variable at a time, whereas chemically reactive hydrodynamic systems involved in pharmacokinetic phenomena are of higher dimension. We show that attempts based on mechanical similitude to set a dosage that would be equivalent across species (for example, from mouse to humans) lead to ambiguous results. Another failing of standard allometry may be its incapability to accommodate the neoteny of Homo sapiens, even though it helped discover the phenomenon. The retarded development in our species implied by neoteny can most clearly be seen in the evidence that both our brain size and our lifespan lie well above the allometric curve for Class Mammalia for these features. In contrast to allometry, which proposes a search for scaling coefficients through invariant external measurement reference frames, we propose a search for transformations of coordinate space coefficients in an intrinsic geometry for the mammalian body plan.

Aging↗
PubMed1983

Dynamic regulation of mean arterial pressure: special role of renal resistances.

In this paper the general properties of homeostatic variables are discussed, and it is shown that mean state regulation must be defined over some stated epoch and that the variance associated with such regulation can permit maximum/minimum variations of 2:1. Dynamic regulation is then contrasted with (automatic) control, and mean systemic arterial pressure (MSAP) in mammals is shown to be under dynamic regulation in the long run, although it may be under control in the short run. The discussion is next developed around the branching rules for mammalian arterial trees. The heart and lymphatic system are introduced as separate, zero-back-pressure, sump pumps that "ground" central venous pressure and interstitial pressure, respectively. Hydraulic flow arguments, combined with arterial tree branching rules, are used to demonstrate the short-circuit character of the renal circulation, and the peculiar distribution of pressure drops within it. From that peculiar distribution it is proposed that there is a nonanatomic, functional resistance located approximately at the region of efferent arterioles, which adds 15 mm Hg of hydrostatic pressure, upstream, to the central arteries. The chief aim of the paper is to raise certain questions about inconsistencies in data about renal circulation, to suggest a resolution, and to show how MSAP is set at (approximately) 100 mm Hg.

Animals↗