scholarly journals The Control of Photo-Pigmentary Responses in Eyeless Catfish

1938 ◽  
Vol 15 (3) ◽  
pp. 363-370
Author(s):  
URSULA WYKES

1. In common with certain other teleosts and lacertilians, eyeless Amiurus nebulosus and Fundulus heteroclitus show a pigmentary response to changes in intensity of illumination. The melanophores contract in the darkness and expand in bright light. The control of this photic response was investigated in Amiurus. 2. The contraction in darkness was not obtained in areas denervated by section of spinal nerves nor in the posterior part of the body after section of the cord. The response is therefore under the control of nervous reflexes passing through the brain. A similar melanophore contraction can be obtained by electrical stimulation of the cord at extremely low frequencies. 3. The response remained in pinealectomized animals. Photoreceptors may possibly be located in the skin or the wall of the diencephalon may be sensitive to light. 4. After hypophysectomy the response continues but the degree of melanophore expansion in bright light is diminished. The expanding hormone of the pituitary is therefore important in that it augments a melanophore response which is under nervous control.

1971 ◽  
Vol 55 (1) ◽  
pp. 205-212 ◽  
Author(s):  
C. P. GALT ◽  
G. O. MACKIE

1. Reversal of the water current through the pharynx of Oikopleura is brought about by a change in the action of the cilia of the two stigmatal ciliated rings. These ‘ciliary reversals’ occur synchronously in the two ciliated rings and can be evoked by the addition of particulate material to the incoming water or by tactile or electrical stimulation of the lips. 2. Nerves run from the lips via the brain to individual ciliated cells, and it is therefore likely that the ciliated cells are under nervous control. 3. At each ciliary reversal an electrical potential can be picked up on the body surface. The same events are recorded by microelectrodes inserted into the ciliated rings. The microelectrode recordings resemble intracellular recordings, and the reversal potentials are considered to represent depolarizations of the membranes of the ciliated cells. 4. Ciliary reversals continue after removal of the brain, suggesting the existence of a peripheral pacemaker.


1889 ◽  
Vol 35 (149) ◽  
pp. 23-44 ◽  
Author(s):  
Francis Warner

(1) Movement in mau has long been a subject of profitable study. Visible movement in the body is produced by muscular contraction following upon stimulation of the muscles by efferent currents passing from the central nerve-system. Modern physiological experiments have demonstrated that when a special brain-area discharges nerve-currents, these are followed by certain visible movements or contraction of certain muscles corresponding. So exact are such reactions, as obtained by experiment upon the brain-areas, that movements similar to those produced by experimental excitation of a certain brain-area may be taken as evidence of action in that area, or as commencing in discharge from that area (see Reinforcement of Movements, 35; Compound Series of Movements, 34).


Author(s):  
Martin E. Atkinson

The cranial nerves are the most important neural structures relevant to dental students and practitioners. The cranial nerves are the nerve supply to all the structures in the head and neck and underpin of the anatomy and function of these regions—the head and neck will not work without them. In a wider context, correct functioning of the cranial nerves is a very good indicator of the health or otherwise of the CNS; it may be necessary to test the function of some, or even all, of the cranial nerves at times to assess neural function. In addition, many of the cranial nerves may be involved in various diseases of the head and neck. As outlined in Chapter 3, 12 pairs of cranial nerves arising from the brain form one major component of the peripheral nervous system, the 31 pairs of spinal nerves forming the other. Each pair of cranial nerves has a name and number. Conventionally, they are numbered using the Roman numerals I to XII. The nerves are numbered from one to 12, according to their origin from the brain; nerves with the lowest numbers arise from the most anterior aspect of the brain (the forebrain) whereas those with highest numbers arise from the lowest part (the medulla). Several aspects of any nerve anywhere in the body are required to d escribe its anatomy and function in complete detail: • Its origins and terminations in the CNS; • Its neuronal components—are they motor, sensory, or autonomic? • Its course to and from its target tissues; • Its distribution to specific areas and structures through specific branches; • Its overall functions and specific functions of its component parts. In addition, if the clinical significance is going to be appreciated, we w ill also need to consider: • The effects of damage or disease on the nerve; • Its important relationships to other structures; • How to test whether the nerve is functioning correctly. Given that there are 12 pairs of nerves, does a competent dentist need to know everything in the two lists about every cranial nerve? The answer, you will be relieved to hear, is ‘no’.


1980 ◽  
Vol 84 (1) ◽  
pp. 149-160
Author(s):  
D. H. Bauer ◽  
L. S. Demski

A pattern of dark vertical bands is a characteristic agonistic display in the green sunfish, Lepomis cyanellus and the bluegill, L. macrochirus. The rapidity with which the display can appear and disappear indicates that it is neurally controlled. Electrical stimulation of the brain was carried out in anaesthetized green sunfish and bluegills to map those regions from which this colour change can be elicited. Banding was evoked by stimulation of sites near the midline in the preoptic area, ventral thalamic-dorsal hypothalmic transition zone, the midbrain tegmentum (just dorsal to the nucleus prerotundus pars medialis), in and near the torus semicricularis, in the basal midbrain (region of the crossing tectobulbar tracts), and in the rostral basomedial medulla. A ‘transition’ zone was located basally in the middle medulla, caudal to which only paling was evoked. Areas found to be negative for evoked banding included the telencephalic lobe, the inferior lobe of the hypothalamus, the optic tract, the optic tectum, the body and valvula of the cerebellum and the caudal medulla. It is postulated that the vertical banding pattern is made up of a separate, selectively controlled system of dermal melanophores. The possible neural mechanisms controlling banding are discussed.


1923 ◽  
Vol 6 (1) ◽  
pp. 73-76 ◽  
Author(s):  
A. R. Moore

Coordinated swimming movements in Yungia are not dependent upon the presence of the brain. The neuromuscular mechanism necessary for spontaneous movement and swimming is complete in the body of the animal apart from the brain. Normally this mechanism is set in motion by sensory stimulation arriving by way of the brain. The latter is a region of low threshold and acts as an amplifier by sending the impulses into a great number of channels. When the head is cut off these connections with the sensorium are broken, consequently peripheral stimulation does not have its usual effect. If, however, the motor nerves are stimulated directly as by mechanical stimulation of the median anterior region, then swimming movements result. Also if the threshold of the entire nervous mechanism is lowered by phenol or by an increase in the ion ratios See PDF for Equation and See PDF for Equation then again peripheral stimulation throws the neuromuscular mechanism into activity and swimming movements result.


Author(s):  
Edward R. Howard

Joseph Lister (1827–1912) acquired a lifelong interest in histology and experimental physiology while a student at University College London between 1848 and 1852. His first two publications in 1853 were histological studies of the contractile tissue of the iris and the skin. Studies of inflammation in 1855 progressed to experiments on the nervous control of arteries, using techniques of peripheral nerve division, spinal cord section and needle stimulation of the brain. This interest in nervous mechanisms led to innovative experiments on gut motility and the autonomic nervous system, from which he inferred that sympathetic nerve control was mediated via intrinsic neuronal plexuses in the gut wall, a mode of action confirmed 100 years later, in 1964–65. It is not generally known that Lister was elected FRS for this early experimental work and that his early commitment to experimental science and microscopy was the background to his later work on the development of surgical antisepsis.


1967 ◽  
Vol 46 (3) ◽  
pp. 475-485
Author(s):  
D. C. SANDEMAN

1. Damage to the statocysts or section of the oesophageal connectives of Carcinus causes repeated ‘spontaneous’ eye withdrawals or ‘blinking’ on the damaged side. 2. When the eyes and brain are isolated from the body, repetitive blinking persists and concomitant bursts of large impulses appear in a single motor axon in the optic tract. The length of these bursts varies from 80 to 180 impulses and the interburst intervals from 5 to 60 sec. There is no obvious correlation between burst length and interburst interval. 3. The bursts are inhibited by stimulating the inside half of the ipsilateral oesophageal connective or initiated by stimulation of the oculomotor and tegumentary nerves. If stimulated with a continuous train of pulses these pathways also cause an increase or decrease in the interburst intervals. 4. The actively spiking portion of the eye-withdrawal motor neuron extends into the brain at least as far as the tegumentary/antennary neuropile. Here it is particularly sensitive to cathodal stimulation, yielding trains of spikes to maintained d.c. stimulation. This point is considered to be near the spike initiating locus for the bursts.


1886 ◽  
Vol s2-26 (104) ◽  
pp. 573-589
Author(s):  
ALICE JOHNSON ◽  
LILIAN SHELDON

1. A solid post-anal gut is formed behind the blastopore (anus), growing out into the tail, and fusing with the undifferentiated tissues at its posterior end. The fusion of hypoblast and epiblast in this region represents the neurenteric canal. 2. In the Frog the post-anal gut is at first hollow, but afterwards becomes solid. 3. The stomodæum and pituitary body are derived from a solid ingrowth of the inner layer of the epiblast. The hind part of this ingrowth fuses with the front wall of the fore-gut, but the perforation to form the actual mouth does not appear till after hatching. The pituitary body grows upwards as a solid cord, and applies itself to the infundibulum in the ordinary manner. 4. From the hind border of the stomodæum proceeds a solid rod of cells, which constitutes the thyroid body, and is developed from the cells of the middle ventral line of the foregut. 5. The development of the peripheral nervous system is preceded by the appearance of a neural ridge, extending along the whole length of the body. 6. The spinal nerves grow out from the neural ridge, and pass downwards between the neural canal and muscle plates. 7. The cranial nerves also grow out from the neural ridge, but are nearer to the surface than the spinal nerves, owing to the absence of muscle plates in the head. 8. When each has attained a certain length it fuses with a thickening of the epiblast, situated some distance above the level of the notochord. (This is the case with the 5th, 7th, and 9th nerves, and probably also with the vagus.) 9. At the point of fusion there is a thickening of the nervetrunk, forming a ganglion, which afterwards recedes from the surface, remaining, however, attached to the sense organ by a nerve. 10. The main trunk of the nerve passes on, and, in the cases of the 7th and 9th nerves, fuses again with the epiblast of the dorsal wall of the corresponding gill-cleft. Later, the nerve becomes detached from the epiblast, and gives off two branches, one behind and one in front of the gill-cleft. 11. The 5th nerve has no such second (ventral) fusion with the epiblast, but divides below its first (dorsal) fusion into two branches, the superior and inferior maxillary. 12. In the Frog a neural ridge is present at an early stage, just after the closure of the neural canal. The facio-auditory nerve grows out of the brain, and it is therefore probable that the other cranial nerves have the same origin. N.B.--Our figures are diagrammatic in so far that the outlines of the cells were not perfectly apparent in all sections. This appeared to us to be due to bad preservation, as the better the specimens were preserved the more distinct and complete were the cell outlines. It was generally possible to draw them accurately with a camera and Zeiss obj. D, OC. 2. We have therefore represented them throughout as distinct.


1959 ◽  
Vol 36 (1) ◽  
pp. 62-71 ◽  
Author(s):  
G. H. SATCHELL

1. Inflation of the pharynx of a dogfish causes an inhibition of respiration manifested as a reduction in rate and amplitude. 2. Tetanic stimulation of the central end of a cut branchial nerve also inhibits respiration. 3. These inhibitory responses differ in their greater regularity and duration from the transient inhibition arising from stimulation elsewhere in the body. 4. Both normal respiration and inflation cause the discharge of receptors whose impulses pass up the vagus nerve. The pattern of firing of these receptors during an inflation corresponds to the pattern, of inhibition. 5. Brief inflations are more effective in securing inhibition if they arrive at a time when the receptors are not being caused to fire by a normal inspiration. 6. Cutting the branchial branches of the IXth and Xth nerves eliminates the pause between successive respirations and increases the respiratory rate. 7. These pauses can be made to reappear by periodically stimulating the central end of a cut branchial nerve. 8. Section of the brain between the medulla and the mesencephalon increases the sensitivity to inflation. 9. Inhibitory afferents run in all branchial branches of the IXth and Xth nerves and in the pre-spiracular branch of the VIIth nerve. 10. It is suggested that in its response to vagotomy the dogfish resembles a medullary mammal.


1994 ◽  
Vol 191 (1) ◽  
pp. 247-256
Author(s):  
G Ferguson ◽  
J Messenger ◽  
B Budelmann

Rotation (roll or pitch) of a cuttlefish away from its normal orientation produces countershading reflexes (CSRs) that consist of chromatophore expansion on the ventral body surface. When rotation is in the roll plane, the CSR has two components on each side of the body. The first (component A) consists of a unilateral expansion of chromatophores on the uppermost latero-ventral edge of the mantle, the underside of the upper fin and the uppermost side of the head; it occurs when the angle of rotation is less than 90°. Further rotation (from approximately 90° to approximately 180°) adds the second component (component B): a unilateral expansion of the chromatophores on the upper half of the ventral surface of the mantle, funnel, head and arms. When rotation is in the pitch plane, chromatophores expand on the posterior part of the ventral mantle and fins when the head is down; when the head is up, chromatophores expand on the ventral surface of the arms, head and funnel and on the anterior part of the ventral mantle and fins. The pitch CSR is always bilateral. Destruction of the gravity or the angular acceleration receptor systems of the statocysts demonstrates that it is the gravity receptor systems that drive the CSRs. Unilateral destruction of the gravity receptor systems shows that the pitch CSR is driven bilaterally, whereas the roll CSR is driven unilaterally. Components A and B of the roll CSR are driven by input from the ipsilateral statocyst, but component A is additionally driven by light. Brain lesions provide evidence that the pathways for the CSRs run through the lateral basal lobes in the supraoesophageal part of the brain.


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