Biomedical subjects
Publications and source records attributed to S Leeman.
A comparative study of the ultrasound appearances of the thigh with the static B scan showed consistent differences in 10 children with muscular dystrophy compared with 40 healthy controls. This non-invasive technique could be useful in assessing the extent of pathological change in dystrophic patients and could prove a valuable diagnostic aid.
The effects of continuous wave ultrasound on three different classes of biosystems have been investigated at a frequency of 1.5 MHz. The criteria for cavitation are given, and these are applied to experimentally observed growth retardation of plant roots, cell death and DNA degradation in bacteria and pyknosis of human lymphocytes. An attempt is being made to find common physical mechanisms for all these biological responses, and cavitation processes in particular are examined here. A description is given of the techniques used to monitor the presence of cavitation, and indirect evidence, drawn from pulsed field and elevated pressure experiments, is presented to show that other-non-linear processes are also operative.
The effect of an imcomplete field of view on the reconstruction of objects from their projections is considered. An exact analytical method is used to calculate the reconstruction of an impulse and an annulus which lie out the field of view of an imaging device. A general impression of the effects of truncating the projections of any object may be obtained from these calculations of elemental objects.
Human tissues show dispersive ultrasound absorption, and it is important to understand how ultrasound pulses in the diagnostic frequency range, 1-10 MHz, propagate in such media. An uncomplicated wave-equation model for human soft tissues is postulated, and its dispersion law for absorption is demonstrated to be compatible with existing experimental findings. Propagative solutions for the simple one-dimensional, homogeneous case (no scattering) are derived. It is shown that the transmitted pulse consists of an undistorted, damped replica of the incident pulse, plus a depth-dependent, time-extended 'rumble', both of which travel at a fixed, finite velocity through the medium. The constancy of this (signal) velocity reconciles the predicted velocity dispersion with the observed weakness of such an effect in many tissues, and some consequences for the measurement of both velocity and absorption are indicated.
Human lymphocyte cultures are exposed to 1.5 MHz continuous wave ultrasound, and it is demonstrated that cell death, as monitored by pyknosis, follows immediately on sonication at intensities within the usual therapeutic range (less than 1.7 W/cm2,spatial average). The number of cells affected is determined by the ultrasound intensity only, but the rate at which they proceed through their pyknosis cycle is modified by both the intensity and the duration of exposure. There is a clear indication of an intensity threshold for the effect approximately 1.1 W/cm2. Pulsed 1.5 MHz ultrasound (70 mus, 1 :1 pulses, 1.7 W/cm2 space-time average) results in a 15-20 hour delay in the measurable response to sonication. It is shown that the intracellular presence of a lysosomal-enzyme inhibitor strongly modifies the course of the ultrasound action. Evidence is presented to suggest that the basic interaction mechanism is via a cavitation process, but there are some difficulties with this interpretation, which are also discussed.
A practical method of assessing ultrasonic A-scan pulse-echo scanner performance is described, which relies upon the identification and quantitation of an overall system transfer function. The mapping of reflecting elements into an image is then described by this transfer function, and indices of system performance, and particularly resolution and range accuracy, are developed in terms of the shape of the transfer function. Some advantages of this method compared to more conventional methods of assessing scanner performance are discussed.
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1. Substance P (SP) was measured in acid acetone extracted plasma of cats using a sensitive radioimmunoassay. The immunoreactive material was submitted to ion exchange chromatography and at least 90% of immunoreactivity co-chromatographed with synthetic SP. 2. The level of immunoreactive SP (I-SP) in extracted plasma of the cat was 69.3 +/- 9.8 fmol/ml with values ranging from 2.5 to 165 fmol/ml. Evisceration of the cats caused a decrease of I-SP levels from 70.8 +/- 30.8 fmol/ml to 20.8 +/- 9.9 15 min and to 26.8 +/- 19.7 fmol/ml 60 min after the operation. 3. Ligation of intestinal blood vessels led to a fall in I-SP levels from 58.7 +/- 11.5 to 25.9 +/- 4.1 fmol/ml within 15 min. 4. No difference between I-SP values in portal (71.8 +/- 11.2 fmol/ml) and peripheral plasma (68.3 +/- 12.1 fmol/ml) was found under the conditions in which these experiments were performed. 5. It is concluded that a major part of circulating immunoreactive SP originates from the intestine.
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The binding of neurotensin to synaptic membranes from rat brain was studied at 24 degrees with the use of [3H]neurotensin. The binding was found to be highly specific, saturable, and reversible. Values for KD of 2 nM and 0.9 nM were derived from equilibrium and kinetic experiments, respectively. Virtually no degradation of neurotensin was observed in the incubation medium after exposure to synaptic membranes under the conditions of the binding studies. Competitive inhibition of [3H]neurotensin binding by partial sequences of neurotensin revealed that the addition of the residue arginine-8 to the neurotensin-(9-13)-pentapeptide increases about 500-fold the relative binding potency, whereas the remaining portion of the NH2-terminal region is mainly responsible for full pharmacological potency; the COOH-terminal leucyl residue is essential for binding.
The propagation of ultrasound pulses in inhomogeneous media is described, and it is shown that they are scattered by fluctuations in density and compressibility. It is proposed that some of the echoes recorded by diagnostic pulse echo equipment are produced in this way. The precise form of the acoustic field backscattered from tissues is calculated using realistic approximations about the nature of tissue inhomogeneitics and the form of the pulses used. It is shown that only limited information about tissue structure is contained in these signals, and the restrictions imposed by the use of typical pulses are indicated. The implications of this analysis for methods of tissue characterization and clinical imaging are discussed.
The factors contributing to the structure (i.e. amplitude and shape) of echoes from major reflecting boundaries in tissues are reviewed. It is shown that the pulsed nature of a scanner's emitted sound field introduces complex variations in echo shape which are not usually taken into account. Moreover, echo structure is strongly modified by the geometry of the interface and not only by the physical composition of the adjacent materials. These effects are shown to be characteristic of the basic reflection process with pulsed fields. The influence of some receiver transfer properties on the displayed echo is also indicated. It is suggested that the analysis of sound fields scattered from small-scale internal structures (echo ensemble analysis) is a preferred method of tissue characterization.
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