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PubMedDate not supplied

Epididymal sperm motion as a parameter of male reproductive toxicity: sperm motion, fertility, and histopathology in ethinylestradiol-treated rats.

The present study was designed to characterize the effect of ethinylestradiol (EE) on epididymal sperm motion using a computer-assisted sperm analysis system (CASA), and to elucidate the correlation between sperm motion endpoints and other measures including fertility, histopathologic, and endocrinologic endpoints. EE was orally given to adult male rats at a daily dosage of 10 mg/kg for 3 and 5 d, and at daily dosages of I and 10 mg/kg for 1, 2, 3, and 4 weeks. Changes in sperm motion were first detected after one week of treatment. Of nine sperm motion parameters, the percentage of motile sperm, velocity, and amplitude of the lateral head displacement (ALH) were decreased in the 10 mg/kg dosing group. Accompanying the decreases in those parameters, the male fertility indices in the 10 mg/kg dosing group were reduced after one week of treatment, and no males in this group could impregnate intact females after 2 weeks or more of treatment. The number of sperm heads in the cauda epididymis in the 10 mg/kg dosing group was reduced to about one-half that in the control group after one week of treatment, whereas the total number of homogenization-resistant advanced spermatids in the testis was not altered and only a slight change was detected in the number and morphology of germ cells in the testis. These results suggest that reduction in the number of epididymal sperm and in sperm motion are not secondary to testicular alteration. However, after 3 weeks of treatment, the number of sperm heads in the testis was drastically reduced with severe atrophy of the seminiferous tubules both in the 1 and 10 mg/kg dosing groups. The profiling of epididymal luminal fluid proteins indicated that two major bands that migrated with molecular weights of about 22 and 23 kDa were weakened and their density was reduced to approximately 70% of the control after 5-d and one week treatments in the 10 mg/kg dosing group. Circulating testosterone declined drastically after 3 d of treatment and remained at undetectable levels with a concomitant decline of circulating LH and FSH, suggesting that EE inhibits testosterone secretion immediately via a negative feedback system, and there follow changes in the accessory reproductive organs including the epididymis. These results indicate that EE affects epididymal spermatozoa before testicular germ cells via a testosterone deficiency, when it is administered at extremely high dosages. The reduction in the sperm motion manifested as decreases in the percentage of motile sperm, ALH, and velocity, is considered to be responsible for the onset of infertility. Sperm motion analysis could be particularly useful for detecting the toxic effects of chemicals that act through the endocrinologic system on the epididymis.

Animals↗
PubMed2005

Restricted orientational motion of nitroxides in molecular glasses: direct estimation of the motional time scale basing on the comparative study of primary and stimulated electron spin echo decays.

A comparative study of anisotropic relaxation in two-pulse primary and three-pulse stimulated electron spin echo decays provides a direct way to distinguish fast (correlation time tau(c)<10(-6) s) and slow (tau(c)>10(-6) s) motions. Anisotropic relaxation is detected as a difference of the decay rates for different resonance field positions in anisotropic electron paramagnetic resonance spectra. For fast motion anisotropic relaxation influences the primary echo decay and does not influence the stimulated echo decay. For slow motion it is seen in both two-pulse echo and three-pulse stimulated echo decays. For nitroxide spin probes dissolved in glassy glycerol only fast motion was found below 200 K. Increase of temperature above 200 K results in the appearance of slow motion. Its amplitude increases rapidly with temperature increase. While in glycerol glass slow motion appears above glass transition temperature T(g), in ethanol glass it is observable below T(g). The scenario of motional dynamics in glasses is proposed which involves the broadening of the correlation time distribution with increasing temperature.

Journal Article↗
PubMed1990

[An analysis of the rotational motion in three dimensional motion of the shoulder complex].

An apparatus was developed using a personal computer to measure three dimensional motion including rotation of the shoulder complex quantitatively. Euler angles were introduced to describe three dimensional motions. The rotation angle was calculated by integrating the components of angular velocity vectors of the Euler angles around the long axis of the humerus. Two kinds of measurements were performed on both the normal and contracted shoulders; One is measurement of the rotational motion accompanying abduction, flexion, extension, horizontal flexion and horizontal extension. The other is measurement of three dimensional range of motion and the rotational motion when the shoulder moves as far as possible in three dimensional space (maximum circumduction). External rotation occurred during abduction, and internal rotation occurred during flexion. In maximum circumduction, a linear relationship was found between three dimensional range of motion and the amount of rotational motion.

Humans↗
PubMed2003

Timing accuracy in motion extrapolation: reverse effects of target size and visible extent of motion at low and high speeds.

By varying target size, speed, and extent of visible motion we examined the timing accuracy in motion extrapolation. Small or large targets (0.2 or 0.8 deg) moved at either 2.5, 5, or 10 deg s(-1) across a horizontal path (2.5 or 10 deg) and then vanished behind an occluder. Observers responded when they judged that the target had reached a randomly specified position between 0 and 12 deg. With higher speeds, the timing accuracy (the reverse of absolute error) was better for small than for large targets, and for long than for short visible extents. With low speed, these effects were reversed. In addition, while long visible extents yielded a greater accuracy at high than at low speeds, for short extents the accuracy was much better with the low speed. The findings suggest that, when extrapolating motion with targets and visible extents of different sizes, the visual system implements different scaling algorithms depending on target speed. At higher speeds, processing of visible and occluded motion is likely to share a common scaling mechanism based on velocity transposition. Reverse effects for target size and extent of visible motion at low and high speeds converge with the assumption of two distinct speed-tuned motion-processing mechanisms in human vision.

Humans↗
PubMed1996

Motion sickness susceptibility to optokinetic rotation correlates to past history of motion sickness.

PURPOSE: This study investigated correlations between motion sickness susceptibility to a rotating optokinetic drum and past history of motion sickness. METHOD: There were 49 subjects who filled out a questionnaire on motion sickness history (MSH) who participated in the experiment. Each subject sat in an optokinetic drum for a 12-min baseline and a 12-min drum rotation period. Subjects' motion sickness symptoms (MSS) and electrogastrograms (EGG's) were measured. RESULTS: There were significant correlations between MSH scores and MSS scores during drum rotation (r = 0.5392, p < 0.001), and between MSH scores and EGG 4-9 cycles per minute (cpm) spectral intensity ratios between drum rotation and baseline periods (r = 0.5320, p < 0.001). Further analysis indicated that the mean MSS scores during the drum rotation period were 11.50 for the top 33% MSH scorers, 4.18 for the middle 34% MSH scorers, and 3.63 for the bottom 33% MSH scorers. The mean EGG 4-9 cpm spectral intensity ratios between drum rotation and baseline periods were 2.62 for the top 33% MSH scorers, 1.44 for the middle 34% MSH scorers, and 1.21 for the bottom 33% MSH scorers. CONCLUSION: These results indicated that past history of motion sickness correlates with severity of motion sickness provoked by optokinetic rotation.

Adult↗
PubMed1984

The influence of background motion on the motion aftereffect.

The motion aftereffect caused by adaptation to moving bars is visible in a stationary test pattern consisting of static visual noise (texture). The aftereffect resulting from adaptation to moving bars presented on a background of texture is highly dependent on the direction and velocity of motion of the background during adaptation, and less dependent on the nature of the test pattern. Background motion in the same direction as bar motion during adaptation enhances the aftereffect, whilst a stationary background or background motion in the opposite direction suppresses, and in some cases reverses the direction of, the aftereffect. The influence of background motion is greatest using a textured test pattern, a low adapting texture velocity, and a low grating spatial frequency. The physiological implications of these results are discussed.

Adaptation, Ocular↗
PubMed1993

Motion perception with spatiotemporally matched chromatic and achromatic information reveals a "slow" and a "fast" motion system.

Recent reports dealing with apparent motion challenged the standard view according to which motion processing should be impossible if the visual attributes matched across space and time are processed in independent channels (the similarity principle). The present work examines this possibility insofar as it relates to the spatiotemporal combination of pure chromatic and pure luminance information. The data indicate that the "similarity principle" is indeed infringed at low (< or = 2.5 Hz, i.e. velocities of 2.5 deg/sec for spatial modulations of 1 c/deg, in this study) but not at high (> or = 7.5 Hz) temporal frequencies. The fact that colour and luminance may or may not combine to yield motion perception depending on their temporal modulation reconciliates contradictory results in the literature and supports the idea of two motion systems, a "fast"/specific one, integrating information only from similar subunits, and a "slow"/unspecific one, integrating information across dissimilar subunits (in the present case, across the chromatic and achromatic "domains"). This dichotomy is also supported by the finding that chromatic reverse-phi (i.e. with equiluminant, red and green stimuli) can be observed at medium temporal frequencies but is replaced by direct motion at low temporal frequencies, presumably within the range of the "slow"/unspecific system. Using a modified "minimum motion" technique (referred to as the Reverse-Phi equiluminance method) we present data allowing to assess the relative weights of the two systems as a function of temporal frequency.

Color Perception↗
PubMed1993

Motion contrast and motion integration.

When a moving aperture contains a drifting grating, the perception of aperture movement is strongly affected by the grating movement. We have studied this interaction, using a moving circular patch of sinusoidal grating matched to the background in mean luminance. The circular window, or aperture, could be defined either by an abrupt transition from a full-contrast grating to the background (hard aperture) or by a two-dimensional Gaussian fall-off in contrast (soft aperture). The grating movement could be controlled independently of the aperture motion. Subjects judged the direction of the aperture movement (i.e. the movement of the patch as a whole). We find that an illusory motion of a stationary aperture can be induced depending on the direction of the grating drift. A hard aperture presented in the fovea appears to move in the direction opposite the grating movement, demonstrating simultaneous motion contrast. However, a soft aperture presented in the periphery appears to move in the same direction as the drifting grating, demonstrating motion integration (assimilation). These results are discussed in the context of interactions between short-range and long-range motion mechanisms and with respect to the significance of boundaries in determining the figure-ground relationship of motion signals.

Contrast Sensitivity↗
PubMed1995

Motion aftereffect after monocular adaptation to filled-in motion at the blind spot.

Although the blind spot encodes no visual information, one never perceives an odd blob or blank there, but sees a complete scene of the world even when viewing monocularly. This phenomenon called "filling-in" might be related to mechanisms essential to surface perception, but the neural representation has still been unclear. To determine at what stage the computation for filling-in is established in the visual system, whether prolonged observation of a filled-in motion including the blind spot of one eye could cause motion aftereffect at the corresponding visual field of the other eye was examined. The result was positive--interocular transfer of motion aftereffect was obtained at the tested eye. This finding suggests the possibility that real motion and filled-in motion share a common motion pathway in an early stage in the human visual system.

Adaptation, Ocular↗
PubMed1994

Is global motion really based on spatial integration of local motion signals?

Previous studies have shown that a random-dot kinematogram (RDK) comprising dots, each of which takes a random walk in direction or speed over time, can appear to flow in a single direction. This has been interpreted as evidence for the existence of a co-operative network linking neurons sensitive to different directions/speeds and different spatial locations. We have investigated the possibility that global motion perception in such patterns might simply reflect motion energy detection at a coarse spatial scale (such that many dots fall in the receptive field of one energy detector) without the need to encode local dot motions on a fine spatial scale and then integrate their motions over space. We created random-walk RDKs and then spatially high-pass filtered them to remove low spatial frequencies. Perception of global motion was unimpaired for both direction and speed random walks, showing that the phenomenon is not reliant on low spatial frequencies and must, therefore, involve integration of local motion signals across space, as originally postulated.

Discrimination, Psychological↗
PubMed2005

Technical note: validation of a motion analysis system for measuring the relative motion of the intermediate component of a tripolar total hip arthroplasty prosthesis.

Tripolar total hip arthroplasty (THA) prosthesis had been suggested as a method to reduce the occurrence of hip dislocation and microseparation. Precisely measuring the motion of the intermediate component in vitro would provide fundamental knowledge for understanding its mechanism. The present study validates the accuracy and repeatability of a three-dimensional motion analysis system to quantitatively measure the relative motion of the intermediate component of tripolar total hip arthroplasty prostheses. Static and dynamic validations of the system were made by comparing the measurement to that of a potentiometer. Differences between the mean system-calculated angle and the angle measured by the potentiometer were within +/-1 degrees . The mean within-trial variability was less than 1 degrees . The mean slope was 0.9-1.02 for different angular velocities. The dynamic noise was within 1 degrees . The system was then applied to measure the relative motion of an eccentric THA prosthesis. The study shows that this motion analysis system provides an accurate and practical method for measuring the relative motion of the tripolar THA prosthesis in vitro, a necessary first step towards the understanding of its in vivo kinematics.

Algorithms↗
PubMed2005

Greater losses in sensitivity to second-order local motion than to first-order local motion after early visual deprivation in humans.

We compared sensitivity to first-order versus second-order local motion in patients treated for dense central congenital cataracts in one or both eyes. Amplitude modulation thresholds were measured for discriminating the direction of motion of luminance-modulated (first-order) and contrast modulated (second-order) horizontal sine-wave gratings. Early visual deprivation, whether monocular or binocular, caused losses in sensitivity to both first- and second-order motion, with greater losses for second-order motion than for first-order motion. These findings are consistent with the hypothesis that the two types of motion are processed by different mechanisms and suggest that those mechanisms are differentially sensitive to early visual input.

Adolescent↗
PubMed2006

Cross-fixation transfer of motion aftereffects with expansion motion.

It has been shown that motion aftereffect (MAE) not only is present at the adapted location but also partially transfers to nearby non-adapted locations. However, it is not clear whether MAE transfers across the fixation point. Since cells in area MSTd have receptive fields that cover both sides of the fixation point and since many MSTd cells, but not cells in earlier visual areas, prefer complex motion patterns such as expansion, we tested cross-fixation transfer of MAE induced by expanding random-dots stimuli. We also used rightward translational motion for comparison. Subjects adapted to motion patterns on a fixed side of the fixation point. Dynamic MAE was then measured with a nulling procedure at both the adapted site and the mirror site across the fixation point. Subjects' eye fixation during stimulus presentation was monitored with an infrared eye tracker. At the adapted site, both the expansion and the translation patterns generated strong MAEs, as expected. However, only the expansion pattern, but not translation pattern, generated significant MAE at the mirror site. This remained true even after we adjusted stimulus parameters to equate the strengths of the expansion MAE and translation MAE at the adapted site. We conclude that there is cross-fixation transfer of MAE for expansion motion but not for translational motion.

Figural Aftereffect↗
PubMed2001

Cortical responses to object-motion and visually-induced self-motion perception.

We investigated the spatiotemporal cortical dynamics during the perception of object-motion and visually-induced self-motion perception in six normal subjects, using a 143-channel neuromagnetometer. Object-motion specific tasks evoked early transient activity over the right temporooccipital cortex, while self-motion perception, or vection, additionally was followed by sustained bilateral activity in the temporoparietal area. The specific signal distributions suggest to represent the different perceptual modes of object-motion and self-motion sensation.

Adult↗
PubMed2003

Can spatial and temporal motion integration compensate for deficits in local motion mechanisms?

We studied the motion perception of a patient, AMG, who had a lesion in the left occipital lobe centered on visual areas V3 and V3A, with involvement of underlying white matter. As shown by a variety of psychophysical tests involving her perception of motion, the patient was impaired at motion discriminations that involved the detection of small displacements of random-dot displays, including local speed discrimination. However, she was unimpaired on tests that required spatial and temporal integration of moving displays, such as motion coherence. The results indicate that she had a specific impairment of the computation of local but not global motion and that she could not integrate motion information across different spatial scales. Such a specific impairment has not been reported before.

Brain Mapping↗
PubMed2000

A slowly moving foreground can capture an observer's self-motion--a report of a new motion illusion: inverted vection.

We investigated interactions between foreground and background stimuli during visually induced perception of self-motion (vection) by using a stimulus composed of orthogonally moving random-dot patterns. The results indicated that, when the foreground moves with a slower speed, a self-motion sensation with a component in the same direction as the foreground is induced. We named this novel component of self-motion perception 'inverted vection'. The robustness of inverted vection was confirmed using various measures of self-motion sensation and under different stimulus conditions. The mechanism underlying inverted vection is discussed with regard to potentially relevant factors, such as relative motion between the foreground and background, and the interaction between the mis-registration of eye-movement information and self-motion perception.

Adult↗
PubMed2002

Deficits of motion transparency perception in adult developmental dyslexics with normal unidirectional motion sensitivity.

We assessed motion integration ability in seven adult developmental dyslexics using unidirectional and bidirectional (transparent) random dot kinematograms (RDKs) that varied in the number of frames. All adult dyslexics performed as well as normally reading age-matched controls with unidirectional RDKs, regardless of frame number. However, using orthogonal motion transparent stimuli, deficits were obvious in six dyslexics and depended on frame number. Whereas controls needed on average only 4.4 frames (144 ms) to identify both directions correctly on 75% of presentations, dyslexics needed on average 14.6 frames (483 ms) to achieve this level of performance. Even though a unidirectional motion task failed to reveal processing abnormalities in adult dyslexics, the motion transparency task was effective at revealing significant perceptual dysfunction, suggesting that performance on this task is a better psychophysical indicator of visual motion deficits in dyslexia. This finding provides little support for the magnocellular deficit hypothesis and, rather, points to abnormality within dorsal extrastriate cortical areas that subserve the integration and segmentation of complex motion signals.

Adult↗
PubMed1997

Adaptation to motion of a second-order pattern: the motion aftereffect is not a general result.

It has become apparent from recent work that the spatial frequency and orientation content of the first-order (luminance) carrier is very important in determining the properties of a second-order (contrast) modulation of that carrier. In light of this we examined whether there was any evidence for a motion aftereffect in one-dimensional second-order patterns containing only two sinusoidal luminance components: a spatial beat. The stimuli were either 1 cpd luminance sinusoids or 1 cpd luminance beats modulating a carrier sinusoid of 5 cpd. The magnitude of any motion aftereffect, or any directionally specific effect of adaptation, was measured for all combinations of first and second-order test and adapting patterns. Both flickering and non-flickering stimuli were used. The results indicate that a motion aftereffect is only induced by first-order adapting stimuli, and likewise, is only measurable in first-order test stimuli. We find no evidence for any directionally specific effect of adaptation in second-order stimuli, whether the test is counterphased or otherwise. These results apparently conflict with recent reports of a second-order induced motion aftereffect, but are consistent with many other findings which show differences between the detection of motion for first and second-order stimuli. We conclude that the induction of a motion aftereffect for second-order stimuli is not a general result and is critically dependent upon (amongst other things) the local properties of the stimulus, including the spatial frequency and orientation content of the first-order carrier.

Adaptation, Ocular↗