Crayfish Escape Behaviour: Commands for Fast Movement Inhibit Postural Tone and Reflexes, and Prevent Habituation of Slow Reflexes

1979 ◽  
Vol 79 (1) ◽  
pp. 205-224
Author(s):  
JOHN Y. KUWADA ◽  
JEFFREY J. WINE

Organized behaviour requires central neural mechanisms to prevent the simultaneous occurrence of incompatible movements. We investigated neural pathways in crayfish that suppress slow flexion of the abdomen during rapid flexions (‘tailflips’) produced by a separate set of muscles. The slow flexors are innervated in each half segment of the abdomen by five motor neurones and one peripheral inhibitor. In isolated preparations of the abdominal nervous system, stimulation of identified command neurones, which trigger tailflips in intact animals, inhibited spontaneous activity in the motor neurones to the slow flexors and excited the peripheral inhibitor. These effects are mediated by a population of interganglionic intemeurones interposed between the command cells and the slow flexor efferents. Slow flexor reflexes also were inhibited by escape commands. This inhibition includes pathways that act upon early stages of sensory input. As a result, habituation of reflexes, which normally is produced by repeated stimulation, is abolished if each sensory stimulus is preceded by a burst of impulses in the command neurone.

2021 ◽  
Vol 12 ◽  
Author(s):  
Elena Lorenzi ◽  
Matilde Perrino ◽  
Giorgio Vallortigara

The ability to represent, discriminate, and perform arithmetic operations on discrete quantities (numerosities) has been documented in a variety of species of different taxonomic groups, both vertebrates and invertebrates. We do not know, however, to what extent similarity in behavioral data corresponds to basic similarity in underlying neural mechanisms. Here, we review evidence for magnitude representation, both discrete (countable) and continuous, following the sensory input path from primary sensory systems to associative pallial territories in the vertebrate brains. We also speculate on possible underlying mechanisms in invertebrate brains and on the role played by modeling with artificial neural networks. This may provide a general overview on the nervous system involvement in approximating quantity in different animal species, and a general theoretical framework to future comparative studies on the neurobiology of number cognition.


1993 ◽  
Vol 179 (1) ◽  
pp. 13-30 ◽  
Author(s):  
R. E. Brown ◽  
M. R. Fedde

Mechanoreceptors on or near feather follicles in the wings of birds may provide information about airflow over the wing. We studied discharge characteristics of rapidly and slowly adapting mechanoreceptors associated with propatagial covert feathers, slowly adapting receptors within the alular joint and vibration-sensitive receptors of filoplume follicles attached to the follicles of secondary flight feathers during manual feather movements and during airflow over the wing. Dorsal elevation of covert feathers produced an increase in discharge frequency related to the angle of elevation. Extension of the alula produced an increase in discharge frequency related to the angle of extension. Stimulation of receptors located on the distal half of the follicles of secondary flight feathers by airflow over the wing produced a continuous discharge whose frequency correlated with airflow velocity. There is thus abundant sensory input from the wing to the central nervous system. We conclude that birds have the necessary sensor-feather mechanisms in the wing (1) to detect an imminent stall and the location of the separation point of the airflow from the wing's surface, and (2) to measure airspeed by detecting the frequency of vibration of the secondary flight feathers.


1981 ◽  
Vol 90 (1) ◽  
pp. 231-251
Author(s):  
F. NAGY ◽  
M. MOULINS

1. In the lobster Jasus lalandii the activity of the oesophageal nervous system (monitored through the firing of its main motor neuron, OD1) is modulated by a pair of proprioceptors, the posterior stomach receptors (PSRs). 2. The in vitro preparation used consisted of the oesophageal nervous system, the suboesophageal ganglion and the two PSRs, which provide the only source of sensory input. 3. Stimulation of a PSR activates only the oesophageal oscillator located in the ipsilateral commissural ganglion. 4. When spike conduction is blocked in the ipsilateral connective, the stimulation of a PSR activates the contralateral oesophageal oscillator. Inputs from each PSR project to the different parts of the distributed oesophageal network (in the two commissural ganglia and the oesophageal ganglion), but at a given time only one of the PSRs' projections is effective. 5. The relative efficacy of the PSRs' projections is controlled by the oesophageal motor network itself and requires that the superior oesophageal nerves be intact (sons). 6. The PSRs' inputs are integrated in the suboesophageal ganglion before reaching the oesophageal network. However, this premotor step is not involved in the control of the unilaterality of PSRs' effects. 7. The PSRs are stimulated by at least two different rhythmical muscular sequences of the foregut (the gastric mill sequence and the cardiac sac sequence) and provide a source of rhythmical inputs to the CNS. 8. The oesophageal nervous system exhibits a periodically varying sensitivity to the PSRs' inputs, which is illustrated by a phase-response curve. 9. Each oesophageal oscillator can be entrained by the rhythmical PSRs' inputs over a range of period. This range includes the period of the spontaneous gastric rhythm. 10. It is proposed that the PSRs enable the oesophageal and the gastric mill rhythms to be coordinated through a peripheral loop. The participation of PSRs in the coordination of different motor sequences of the foregut is discussed.


2006 ◽  
Vol 3 (4) ◽  
pp. 297-304
Author(s):  
A. Spiers ◽  
K. Warwick ◽  
M. Gasson ◽  
V. Ruiz

By monitoring signals from the central nervous system, humans can be provided with a novel extra channel of communication that can, for example, be used for the voluntary control of peripheral devices. Meanwhile, stimulation of neural tissue can bring about sensation such as touch, can facilitate feedback from external, potentially remote devices and even opens up the possibility of new sensory input for the individual to experience. The concept of successfully harnessing and stimulating nervous system activity is though something that can only be achieved through an appropriate interface. However, interfacing the nervous system by means of implant technology carries with it many problems and dangers. Further, results achieved may not be as expected or as they at first appear. This paper describes a comparative study investigating different implant types and procedures. It is aimed at highlighting potential problem areas and is intended to provide a useful reference explaining important tolerances and limits.


1987 ◽  
Vol 127 (1) ◽  
pp. 295-311
Author(s):  
J. P. C. DUMONT ◽  
J. J. WINE

1. The telson flexor system is homologous to the fast flexor system of anterior ganglia (Dumont & Wine, 1986a), but important differences exist in connections to the telson motor giants (MoGs) (Dumont & Wine, 1986b). In this paper, we describe additional differences in connections to the telson non-giant fast flexor (FF) motor neurones and to the telson flexor inhibitor (FI). 2. The telson FF motor neurones in ganglion 6 (G6) receive inputs similar to those in G4 and G5 (Miller, Hagiwara & Wine, 1985). The escape command neurones (lateral giants, LGs, and medial giants, MGs) in common provide weak disynaptic input via the telson segmental giant (SG6), and relatively strong trisynaptic input via SG2, SG3 and the corollary discharge interneurones 12 and 13. There may also be some direct input from the MGs, but it, as well as the connections from SG6, appears to vary in different preparations. 3. The compound PSP produced in telson FFs by a single LG or MG impulse was suprathreshold in only five of 55 experiments in isolated abdominal nerve cords, but the probability that a motor neurone would fire increased with additional giant axon impulses, showing that temporal summation of excitation outweighed the possible recruitment of inhibition. Firing probability was higher in semi-intact preparations, where at least one posterior telson FF was fired by a single LG impulse 50% of the time. As was pointed out previously (Dumont & Wine, 1986b), telson flexion would disrupt the behaviour pattern expected from LG commands. 4. Two pathways of feedforward inhibition were found which prevent such disruption. The sensory input that recruits the LG also recruits powerful feedforward inhibition of the telson FF motor neurones, which reduces the probability that they will be fired by the LG. The same sensory stimulus also evokes inhibition of FFs in G5, excitation of FFs in G2 and G3, and mixed excitation and inhibition of FFs in G4. In addition, the telson FIs fire at short latency during LG-mediated tailflips. This occurs because the telson FIs are excited by sensory input. In fact, the firing threshold of the telson FIs to sensory input is lower than that of the LGs, at least for electrical stimulation of nerves. When the LGs do fire, they produce additional excitation of the FIs. The telson FIs also are excited by the LGs but not by the MGs. In contrast, the anterior homologues of the telson FIs receive equivalent, delayed excitation from both MGs and LGs, and weaker sensory input, so that they tend to fire only after the peak of flexion (Wine & Mistick, 1977). 5. The predicted net effect of these connections is that the telson flexor muscles should not contract during naturally elicited LG tailflips, and this is consistent with observed behaviour. The results can be interpreted as providing additional examples of potentially maladaptive central connections which are not expressed in behaviour because of feedforward inhibition.


1989 ◽  
Vol 256 (2) ◽  
pp. R554-R559
Author(s):  
J. P. Porter

It was recently reported that electrical stimulation of the hypothalamus could enhance the renin response to reductions in renal perfusion pressure. However, electrical stimulation of brain sites may activate neural pathways that never function physiologically. In the present investigation an external stress in the form of a jet of air to the face was applied to achieve a more physiological activation of the sympathetic nervous system. Conscious restrained rats, instrumented with pneumatic occluding cuffs around the aorta proximal to the renal arteries, were used to determine the relationship between renal perfusion pressure (RPP) and plasma renin activity (PRA) in the control state and in the presence of the stress. The jet of air produced a rightward shift in the relationship between RPP and PRA and also increased the slope, suggesting an enhanced sensitivity. Both the rightward shift and the increase in slope were absent in animals with bilateral renal denervation. In animals with adrenal enucleation, the rightward shift was still present but there was no significant increase in the sensitivity. These data suggest that an external activation of the central nervous system (by a stress) has the potential to modulate the responsiveness of the kidney to nonneural stimuli for renin secretion.


1981 ◽  
Vol 32 (4) ◽  
pp. 213-216 ◽  
Author(s):  
Carlo Ferrari ◽  
Roberto Caldara ◽  
Cristiano Barbieri ◽  
Paolo Testori ◽  
Rosanna Benco ◽  
...  

2012 ◽  
Vol 107 (4) ◽  
pp. 1241-1246 ◽  
Author(s):  
Gary Marsat ◽  
Leonard Maler

To interact with the environment efficiently, the nervous system must generate expectations about redundant sensory signals and detect unexpected ones. Neural circuits can, for example, compare a prediction of the sensory signal that was generated by the nervous system with the incoming sensory input, to generate a response selective to novel stimuli. In the first-order electrosensory neurons of a gymnotiform electric fish, a negative image of low-frequency redundant communication signals is subtracted from the neural response via feedback, allowing unpredictable signals to be extracted. Here we show that the cancelling feedback not only suppresses the predictable signal but also actively enhances the response to the unpredictable communication signal. A transient mismatch between the predictive feedback and incoming sensory input causes both to be positive: the soma is suddenly depolarized by the unpredictable input, whereas the neuron's apical dendrites remain depolarized by the lagging cancelling feedback. The apical dendrites allow the backpropagation of somatic spikes. We show that backpropagation is enhanced when the dendrites are depolarized, causing the unpredictable excitatory input to evoke spike bursts. As a consequence, the feedback driven by a predictable low-frequency signal not only suppresses the response to a redundant stimulus but also induces a bursting response triggered by unpredictable communication signals.


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