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Biomedical subjects

D Kleinman

Publications and source records attributed to D Kleinman.

At least 37 records · Page 2Linked to original sources

Serum IgG and IgA antibodies specific for Chlamydia trachomatis in salpingitis patients as determined by the immunoperoxidase assay.

The feasibility of applying elevated Chlamydia trachomatis specific IgG antibody and serum IgA antibodies as a non-invasive screening test for C. trachomatis associated salpingitis was analysed in 54 salpingitis patients and 294 apparently healthy women by the single antigen (L2) immunoperoxidase assay (IPA). The prevalence rate of C. trachomatis IgG antibody (titre greater than or equal to 64) was significantly higher in the salpingitis patients in comparison to control (67% versus 23%). The prevalence rate of elevated C. trachomatis IgG titres (greater than or equal to 128, greater than or equal to 256 and greater than or equal to 512) was significantly higher in the salpingitis patients as compared to the controls. For example, at an IgG titre of greater than or equal to 128 the prevalence rate was 57% in the salpingitis patients and 8% in the healthy controls (p less than 0.0001). The prevalence of C. trachomatis IgA antibodies (titre greater than or equal to 16) was significantly higher in salpingitis patients in comparison to controls (37% versus 4%). The prevalence of elevated IgA titres (greater than or equal to 32 and greater than or equal to 64) was found to be significantly higher in salpingitis patients as compared to controls. All the IgG seropositive salpingitis patients were also found to have C. trachomatis IgG antibodies. It appears that testing for IgG antibodies at a serum dilution of 1:128, and for IgA antibodies at a dilution of 1:16 by the IPA test comprises the best combination for the differentiation between the salpingitis patients and apparently healthy controls, and it is suggested that this be used as a marker of active C. trachomatis infection.

Adolescent

The effect of eccentricity and colour on negativity in pattern onset visual evoked potentials.

The effects of stimulus size, eccentricity and colour on the amplitudes of N100 and N130 were investigated in pattern onset VEPs. For black-and-white pattern stimulation, the first set of stimuli was derived from a full dartboard pattern. Central stimulation of various extents was produced by patterns with reduced number of outer rings and for eccentric stimuli a number of central rings were removed from the full pattern. It was found that amplitude of N100 was maximal in VEPs to central stimuli and that it was greatly reduced when eccentric stimulation was applied. The amplitude of N130 showed no significant change in relation to the type of stimulus. When checkerboard stimuli of identical configuration were used for black-and-white pattern stimulation instead of dartboards, systematic changes in peak latencies of N100 were observed in relation to check size. In VEPs to centrally presented small checks the emergence of an early negative peak preceding N100 was recorded at 75 msec. In VEPs to coarse checkerboards presented centrally N100 was often observed with a delayed peak latency of 110 msec. Changes in N130 were not regular when checkerboards with different check sizes were presented centrally. For eccentric checkerboard stimulation, both negative peaks N100 and N130 were revealed. Their peak latencies were similar to those observed in the case of dartboard paracentral stimulation. In VEPs to patterns projected through red or blue filters, regular changes were observed in both negative peaks. Introduction of the red filter led to enhancement of the N100 amplitude in VEPs to dartboard and to checkerboards with fine checks, but it caused no effect on N100 in the VEPs to coarse checkerboards. Introduction of the blue filter led to a decrease in the N100 amplitude in VEPs to dartboard and fine checkerboards and to a slight increase of N100 in VEPs to coarse checkerboards. Changes in N130 were observed only when the blue filter was introduced and they corresponded to those which take place when the level of illumination changes from photopic to mesopic.

Color Perception

Antigenicity of sperm cells after freezing and thawing.

Freezing and thawing is thought to result in removal of spermatozoal membrane antigens. We investigated the presence of sperm antigens before and after freezing and thawing by means of the immunoperoxidase assay (IPAMA), sperm immobilization test (SIT), and separation of proteins by gel electrophoresis. The results of the IPAMA and SIT assays showed no difference in the membrane antigens before and after freezing and thawing. Analysis of surface proteins by gel electrophoresis demonstrated that freezing and thawing did not remove any particular group of proteins from the surface membrane of spermatozoa. According to the evidence of the three tests performed, there is no meaningful removal of antigens from the sperm cell surface membrane by the process of freezing, preservation, and thawing when carried out by the specific methods used. This work does not support the suggestion that in cases of immunologic incompatibility between spermatozoa and cervical mucus it would be possible to overcome the couple's infertility by employing the process of freezing, preservation, and thawing.

Antigens, Surface

Renal clearance of urea, inulin, and p-aminohippurate in heat-acclimated rats.

Clearance values of urea, inulin, and p-aminohippurate (PAH) were measured in heat-acclimated (HA) rats exposed for 3 wk to 35 degrees C, in control rats (C) exposed to 23 degrees C, and in HA rats deacclimated (DA) for 3 wk. In HA rats, urea clearance was lower by 73%, inulin clearance by 61%, and PAH clearance by 56%, compared with C rats. The clearance values of these substances returned to the control values in DA rats. The data suggest that the low clearance values reflect both reduced renal blood flow and possible changes in the capacity of the glomeruli for filtration and the tubules for either reabsorption or secretion.

Acclimatization

Infection of endometrial cells with human cytomegalovirus.

In order to understand the mechanism of congenital human cytomegalovirus (CMV) infection we studied the effect of CMV on epithelial cell culture of the endometrium. Endometrial cells proved to be sensitive to CMV as indicated by morphologic alterations, success to support growth of infectious virus and positive immunoperoxidase staining. The infected cells were enlarged, multinuclear and revealed intranuclear inclusions. Electron microscopy detected the presence of the viral particles in the CMV-infected endometrial cells. The possibility that CMV infection of the endometrial cells may play a role in transmitting the virus to the embryo will be discussed.

Cells, Cultured

The undesirable effects of various changes of monoplane occlusion on complete denture retention.

The most commonly seen undesirable alterations to the occlusal plane, when using monoplane occlusion with nonanatomic teeth, have been outlined verbally and graphically. The introduction of dislodging forces to denture retention brought about by these variations in the monoplane have been examined, as well as methods for their correction. The order of presentation of undesirable alterations to the occlusal plane is a guide for a step-by-step correction of these changes. It provides the practitioner with a sequential checklist for correcting undesirable occlusal changes in monoplane denture occlusion with nonanatomic teeth.

Dental Occlusion, Balanced

Human endometrium in cell culture: a new method for culturing human endometrium as separate epithelial and stromal components.

The present study describes a simple method for culturing human endometrium as separate epithelial and stromal components. Fifty-two samples of normal human endometrium have been initiated in tissue culture: endometrium from both the proliferative and luteal phases of the menstrual cycle showed satisfactory growth in vitro with a success rate of about 94%. Epithelial cultures remained viable for 60 days, while from stromal cells it was possible to establish cell lines. Both cell types possessed estrogen receptors. Epithelial cells showed no clear estrogen or progesterone response. Our observations suggest that this simple method for culturing human endometrium may serve as a tool in further investigations.

Connective Tissue

The effect of background illumination on pattern onset visual evoked potentials.

The early part (first 200 msec) of pattern onset VEPs elicited by a dartboard pattern was studied in conditions of varying level of background illumination. The effect of pattern adaptation and pattern blurr was also studied. The observed complex behaviour of the main negativity within this part of the VEP can be best described in terms of a composite of two independent negative peaks labelled N100 and N130. In high luminance conditions peak N100 was dominant and the presence of N130 was indicated only by a 'notch' on the rising slope of the negativity. As luminance decreased the situation was reversed and N130 became a dominant feature of the negative wave. This finding did not depend on the particular choice of reference site. For checkerboard stimulation the same features were present, but variability of the VEP wave form was greater than in the case of dartboard stimulation. Present results relate the well-known pattern specific properties of the negativity in onset VEPs to N100 only, whereas N130 is not pattern specific. Lower and upper half-field stimulation produced peaks of opposite polarity at 100 msec but no change was observed in polarity of N130. These findings support the suggestion that these two parts of the negativity in pattern onset VEPs may have different cortical sources.

Adaptation, Physiological

N1-P2 correlates of reaction time at the single-trial level.

Using a template-matching pattern recognition technique evaluated in an earlier paper, the amplitude and latency of the N1-P2 wave of the vertex visual evoked potential was established on each trial of a reaction time task. This single-trial physiological information correlated meaningfully with trial-by-trial changes in performance, providing further indication of the validity and practicability of a single-trial approach to the analysis of human EP data.

Acoustic Stimulation

Potentiation of the habituation of human brain potentials.

A single-trial analysis, using the cross-covariance function to locate and quantify individual visual evoked potentials (VEPs), is employed to assess run-by-run changes in the habituation function of the N1-P2 wave of the vertex VEP. The characteristic exponential form of this function is shown to be less pronounced later in the experimental session. This finding is adduced as evidence of potentiation of VEP habituation and as such is argued to provide further justification for considering VEP habituation as genuine habituation in Thompson and Spencer's (1966) system.

Cerebral Cortex

Contradiction of auditory and visual information by brain stimulation.

Cats with permanently implanted electrodes were trained to discriminate between trains of flashes or clicks at two different repetition frequencies. After substantial overtraining with these sensory stimuli, high levels of stimulus generalization were obtained to electrical stimulation of the reticular formation at either frequency stimultaneously with contradictory flicker or click stimulation at the opposite frequency resulted in control of the behavior by the reticualr stimulus. Lateral geniculate stimulation failed to show this effect.

Acoustic Stimulation