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At least 1,711 records · Page 95Linked to original sources
PubMed1989

Flash evoked potentials in the ectostriatum of the zebra finch: a current source-density analysis.

Recent research has demonstrated that ipsilaterally visually evoked potentials (VEPs) can be measured within the ectostriatum, the telencephalic target area of the tectofugal visual pathway in birds. In this paper we systematically measured contra- and ipsilateral VEPs within the ectostriatal complex to obtain more detailed information on the processing of contra- and ipsilateral stimuli. The similarity of neighbouring VEPs at equal depth and a comparison of a one dimensional and a three dimensional analysis of current source-densities (CSDs) for identical coordinates suggested that a one dimensional current source-density analysis might be applicable. The one dimensional current source-density analysis demonstrated largely corresponding patterns in the sink-source sequences of the current source-density depth profiles for the contra- and ipsilateral stimulus responses. The occurrence of a large sink in the centre of the ectostriatal core, together with the results of multiunit recordings, shows that the ectostriatal core is the location of the generators for both the contra- and the ipsilaterally evoked responses. The occurrence of macroscopic sinks and sources and the fact that VEPs can be recorded from the ectostriatum shows that there is a higher degree of order in the ectostriatum than has been previously demonstrated by anatomical methods. The time coincidence between the maximum spike rate of multiunit responses, the negative peak of the evoked potential, and the large central sink demonstrates that the influence of ipsi- as well as of contralateral stimuli is predominantly excitatory.

Animals↗
PubMed1988

Enucleation enhances ipsilateral flash evoked responses in the ectostriatum of the zebra finch (Taeniopygia guttata castanotis Gould).

The tectofugal pathway in birds has been reported to process primarily information from the contralateral eye. Although this pathway has access to the contralateral hemisphere by various connections, electrophysiological recordings up to now have failed to demonstrate any excitatory influence of visual stimulation in the higher stations of this pathway. This study is the first to demonstrate an excitatory projection from the ipsilateral eye to the telencephalic projection area of the tectofugal pathway by recordings of visually evoked potentials in the ectostriatum. The excitatory projection probably leads from the eye to the contralateral tectum opticum, then recrosses back to the nucleus rotundus of the ipsilateral side where it reaches the ectostriatum. In normal birds, the ipsilateral stimulus responses in the ectostriatum are smaller in amplitude and have a longer latency than responses to contralateral stimuli. In unilaterally enucleated birds, the ipsilateral response is enhanced in the ectostriatum and can be detected in the nucleus rotundus, too. The results suggest that in normal birds the ipsilateral response is inhibited to a high degree by spontaneous activity of the contralateral eye. Possibly, this counterbalanced inhibition provides a mechanism for weighting information from the left and right eye field in order to ensure adequate processing of stimuli.

Animals↗
PubMed1980

Flashing tomosynthesis--a new tomographic method.

A new tomographic method called tomosynthesis and its first clinical results are presented. The method is based on classical tomography. All information necessary for the tomography of an object is obtained in one procedure without moving the X-ray tube, the film, or the object. Thus the investigation requires only a few seconds.

Humans↗
PubMed1978

Off-components in response to brief light flashes in the oscillatory potential of the human electroretinogram.

Amplitudes and implicit times of the several oscillatory potentials (OP's) in the human electroretinogram have been studied in relation to temporal, adaptive and spectral stimulus variables. The last of the OP-wavelets responds differently from the preceding ones; its implicit time shortens with increase in stimulus frequency or adaptive illumination, whereas that of the preceding OP's is prolonged or stays constant. Moreover, the last OP-wavelet is time locked with the stimulus offset, whereas the others are not. This can be confirmed by linear subtraction of responses to an isolated stimulus onset from responses to stimuli of variable durations. These results indicate, that the last oscillatory potential is related to the light offset and is presumably generated by the retinal off-elements described in single cell recordings.

Adaptation, Physiological↗
PubMed1987

Rapid FLASH NMR imaging.

Nuclear magnetic resonance (NMR) spectroscopy and imaging provide new tools for non-invasive investigations of living systems. Recent developments in rapid NMR imaging now offer considerable improvements for both scientific applications and medical diagnosis. Using fast imaging sequences cross-sectional images may be recorded within seconds and, therefore, become free from motional artifacts due to breathing or peristalsis. New functional imaging experiments include dynamic studies of the application of paramagnetic contrast agents or ECG-synchronized recordings of cardiac NMR movies. Superior anatomical information is achieved by three-dimensional NMR imaging with measuring times of minutes rather than hours.

Arm↗
PubMed1978

Proteolysis and flash photolysis of bacteriorhodopsin in purple membrane fragments.

Pronase treatment of aqueous suspensions of purple membrane fragments from H.halobium leads to the cleavage of bacteriorhodopsin. The protein fragments remaining in the membrane after treatment with relatively small concentrations of enzyme (2% w/w) in normal daylight range in molecular weight from 20,000--21,000 daltons, indicating that cleavage occurs mainly near the extremities of the protein chain. At higher enzyme concentrations the relative amounts of protein fragments having smaller molecular weight increase. Generally, the relative loss of retinal chromophore is larger than that of protein and thus the retinal binding site seems to be located near one of the chain ends that is cleaved off by enzyme. Irradiation with white light during the time of proteolysis (at both low and high enzyme concentrations) results in extensive cleavage, so that under certain conditions no high molecular weight components can be detected in SDS-polyacrylamide gels. It, therefore, appears that parts of the bacteriorhodopsin chain become more exposed to enzyme digestion when the purple membrane is illuminated. Enzyme treated aqueous purple membrane fragment suspensions still show photocycle activity. The main consequence of proteolysis is a pronounced appearance of biphasicity in the decay of M412 and the regeneration of bR570. Simultaneously the yield of O660 is reduced. As with untreated purple membrane, the correlation between the rates of decay of M412 and regeneration of bR570 is greatest when the yield of O660 is lowest.

Bacterial Proteins↗
PubMed1994

Measurement of intracellular Ca2+ concentration using Indo-1 during simultaneous flash photolysis to release Ca2+ from DM-nitrophen.

We have constructed a modular instrument to measure intracellular [Ca2+] ([Ca2+]i) in single isolated cells while simultaneously imposing step changes in [Ca2+]i using "caged Ca2+". By combining the outputs of a xenon arc lamp with a frequency-tripled (Nd:YAG) laser, the instrument can operate with low maintained illumination to measure [Ca2+]i using a ratiometric Ca(2+)-sensitive fluorophore and also activate the release of Ca2+ from a caged-Ca2+ compound with a high energy pulse of ultraviolet light. This instrument is simple to assemble, introduces little electrical noise, provides a wide range of illumination power, produces only moderate photobleaching of the Ca2+ indicator and can be readily adapted to diverse cellular preparations. We demonstrate the use of this system to measure step changes in [Ca2+]i in adult rat ventricular myocytes and a human embryonic kidney cell line (293 cells) in culture.

Acetates↗