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Biomedical subjects

A R Blight

Publications and source records attributed to A R Blight.

61 records · Page 4Linked to original sources

Resetting fast phases of head and eye and their linkage in the frog.

(1) Compensatory slow phase movements were evoked by optokinetic, vestibular and combined optokinetic and vestibular stimulation. Superimposed fast phases resetting the position of the head (in space) and of the eye (in head) were recorded with a magnetic field search coil in unrestrained and head fixed frogs, respectively. (2) Head fast phases recorded during optokinetic stimulation covaried in the frequency of their occurrence with slow phase head velocity. Their amplitude was large (average 18.9 +/- 8.9 degrees), maximal velocity increased with amplitude by 6.6 degrees/s/deg, and duration (average 230 +/- 33 ms) was almost independent on amplitude. (3) Ocular fast phases rarely occurred during sinusoidal stimulation and neither optokinetic after nystagmus nor postrotatory nystagmus were observed. Fast phases, evoked by constant velocity optokinetic or acceleratory stimuli, consisted of two components: a primary resetting fast phase and a smaller fast movement in the opposite direction. The primary fast phase had a small amplitude (average 2.2 +/- 1.3 degrees). In different stimulus conditions fast phase parameters were very similar. Maximal velocity increased by 6.5 degrees/s/deg. Duration (average 165 +/- 23.4 ms) was variable. (4) During ocular fast phases the vestibulo-collic and the optokinetic-collic reflexes were suppressed. The slow phase head velocity either became zero or a small head fast phase in the direction of the ocular fast phase occurred. Fast phase head movements were accompanied by an ocular fast phase or by a retraction of one or both eyes, depending on the amplitude of the head fast phase. At the end of a head fast phase eye position was always recentered.

Animals↗

Calcium and the tonic release of transmitter at a non-impulsive synapse in the crab.

Depolarization-transmitter release coupling was studied in the promotor stretch receptor/motoneuron synapse of the crab. Callinectes sapidus, a preparation in which presynaptic action potentials do not occur. Intracellular microelectrode recordings were made from the presynaptic terminal and from the somata of postsynaptic motoneurons while injecting current pulses into the peripheral stretch receptor dendrite with the aid of the sucrose-gap. 1. For short current pulses, the relationship between presynaptic potential and postsynaptic response was found to be similar to that demonstrated in the giant synapse of the squid stellate ganglion, indicating a common reliance on the properties of voltage-dependent calcium channels. 2. The crab synapse was found to be capable of continuous transmission in the range of seconds and minutes without the pronounced depletion of transmitter seen in the squid, and without inactivation of the release process (i.e., the calcium conductance is non-inactivating). 3. A graded, transient response to depolarising current in the presynaptic fibre was found to be calcium-dependent, and probably to reflect the presence of a separate, inactivating calcium conductance. 4. It was concluded that the graded response of the presynaptic membrane could function in helping to compensate for capacitative distortion of receptor potentials decrementally conducted in the sensory dendrite, and was therefore a specialisation for non-impulsive transmission.

Action Potentials↗

Golgi-staining of "primary" and "secondary" motoneurons in the developing spinal cord of an amphibian.

The Golgi technique was used to study the morphology of spinal motoneurons at various stages in the early development of swimming behaviour in embryos and larvae of the palmate newt, Triturus helveticus ((Razoumowsky). The earliest motoneurons stained appeared to be associated with the Mauthner-cell system. The overall morphology of these "primary" motoneurons seems to be similar throughout the lower vertebrates and the distinctive characteristics found in earlier descriptions of those from caudate amphibia were probably due to misinterpretation. At about the time of hatching and development of low-frequency swimming behaviour, other motoneurons were found to innervate the axial musculature, cells with a central morphology different from those of the "primary" type. It was found likely that these "secondary" motoneurons innervate a separate muscle system concerned with tonic and "slow phasic" activity, while "fast phasic" acitivity in rapid swimming is supplied by "primary" cells.

Animals↗