The Electrical Activity of the Radial Nerve in Diadema antillarum Philippi and Certain Other Echinoids

1968 ◽  
Vol 48 (2) ◽  
pp. 279-289
Author(s):  
N. MILLOTT ◽  
H. OKUMURA
Keyword(s):  
Electrical Activity ◽  
Conduction Velocity ◽  
Radial Nerve ◽  
Diadema Antillarum ◽  
Double Peak ◽  
Slow Potential ◽  
Refractory Periods ◽  
Spine Movement ◽  
Stimulation Of

1. The propagated massed potentials which follow stimulation of the radial nerve in Arbacia, Diadema, Echinus and Paracentrotus are described. 2. Approximate values for the averaged absolute and relative refractory periods and the conduction velocity were obtained. 3. The response of Diadema has a double peak which is shown to represent responses of nerves differing in excitability and conduction velocity. The fast potential is concerned with spine movement. The slow potential is related to inhibition of spine movements excited photically.

Electrical Activity in the Radial Nerve Cord And Ampullae of Sea Urchins

1965 ◽  
Vol 43 (2) ◽  
pp. 247-256
Author(s):  
D. C. SANDEMAN
Keyword(s):  
Electrical Activity ◽  
Nerve Cord ◽  
Action Potentials ◽  
Radial Nerve ◽  
Sea Urchins ◽  
Side Branch ◽  
Single Shock ◽  
Lateral Branches ◽  
Tube Feet ◽  
Stimulation Of

1. A single shock applied through wick electrodes to the isolated radial nerve cord of a sea urchin produces a recordable potential in the cord. The potential is conducted along the cord at a velocity of between 14 and 20 cm./sec. 2. The potential is complex and graded. Two components of the potential can be identified and have different thresholds to stimulation, conduction velocities and amplitudes. They are believed to represent two classes of fibres. 3. The potential is conducted decrementally along the cord and normally cannot be recorded at distances greater than 6o mm. from the stimulus. The amplitude of the potential decays logarithmically falling to half after 7 mm. spread. There is no facilitation of amplitude or distance of spread. 4. Potentials initiated simultaneously at either end of the isolated nerve cord collide and partially occlude each other. 5. Stimulation of a side branch of the nerve cord evokes potentials recordable from only ipsilateral neighbouring side branches and the whole cord. However, contractions of the contralateral ampullae following stimulation of lateral branches reveal spread of the excitation beyond the region of recordable potentials. 6. A single shock to a cord still attached to the test causes contraction of the associated ampullae. One ampulla will contract several times after a single shock, a period of relaxation following each contraction. 7. Electrical activity recorded from the ampullae, and lasting many seconds after the single shock, corresponds with their contractions. The activity is believed to be muscle action potentials. 8. Evidence of a feedback from damaged tube feet to the cord, suppressing ampulla response to cord stimulation, was found.

Stimulation of cyclic AMP formation and nerve electrical activity by octopamine in the terminal abdominal ganglion of the female gypsy moth Lymantria dispar

2006 ◽  
Vol 1071 (1) ◽  
pp. 63-74 ◽  
Author(s):  
Maria C. Olianas ◽  
Paolo Solari ◽  
Luciana Garau ◽  
Anna Liscia ◽  
Roberto Crnjar ◽  
...  
Keyword(s):  
Cyclic Amp ◽  
Electrical Activity ◽  
Gypsy Moth ◽  
Lymantria Dispar ◽  
Abdominal Ganglion ◽  
Stimulation Of

Electronmicroscopic and electrophysiological studies of the teat branch of the XIII thoracic nerve: relationship with lactation in the rat

1988 ◽  
Vol 118 (3) ◽  
pp. 471-483 ◽  
Author(s):  
L. M. Voloschin ◽  
E. Décima ◽  
J. H. Tramezzani
Keyword(s):  
Electrical Stimulation ◽  
Conduction Velocity ◽  
Action Potentials ◽  
Silent Period ◽  
High Amplitude ◽  
Milk Ejection ◽  
Nerve Activity ◽  
Thoracic Nerve ◽  
Myelinated Fibres ◽  
Stimulation Of

ABSTRACT Electrical stimulation of the XIII thoracic nerve (the 'mammary nerve') causes milk ejection and the release of prolactin and other hormones. We have analysed the route of the suckling stimulus at the level of different subgroups of fibres of the teat branch of the XIII thoracic nerve (TBTN), which innervates the nipple and surrounding skin, and assessed the micromorphology of the TBTN in relation to lactation. There were 844 ± 63 and 868 ± 141 (s.e.m.) nerve fibres in the TBTN (85% non-myelinated) in virgin and lactating rats respectively. Non-myelinated fibres were enlarged in lactating rats; the modal value being 0·3–0·4 μm2 for virgin and 0·4–0·5 μm2 for lactating rats (P > 0·001; Kolmogorov–Smirnov test). The modal value for myelinated fibres was 3–6 μm2 in both groups. The compound action potential of the TBTN in response to electrical stimulation showed two early volleys produced by the Aα- and Aδ-subgroups of myelinated fibres (conduction velocity rate of 60 and 14 m/s respectively), and a late third volley originated in non-myelinated fibres ('C') group; conduction velocity rate 1·4 m/s). Before milk ejection the suckling pups caused 'double bursts' of fibre activity in the Aδ fibres of the TBTN. Each 'double burst' consisted of low amplitude action potentials and comprised two multiple discharges (33–37 ms each) separated by a silent period of around 35 ms. The 'double bursts' occurred at a frequency of 3–4/s, were triggered by the stimulation of the nipple and were related to fast cheek movements visible only by watching the pups closely. In contrast, the Aα fibres of the TBTN showed brief bursts of high amplitude potentials before milk ejection. These were triggered by the stimulation of cutaneous receptors during gross slow sucking motions of the pup (jaw movements). Immediately before the triggering of milk ejection the mother was always asleep and a low nerve activity was recorded in the TBTN at this time. When reflex milk ejection occurred, the mother woke and a brisk increase in nerve activity was detected; this decreased when milk ejection was accomplished. In conscious rats the double-burst type of discharges in Aδ fibres was not observed, possibly because this activity cannot be detected by the recording methods currently employed in conscious animals. During milk ejection, action potentials of high amplitude were conveyed in the Aα fibres of the TBTN. During the treading time of the stretch reaction (SR), a brisk increase in activity occurred in larger fibres; during the stretching periods of the SR a burst-type discharge was again observed in slow-conducting afferents; when the pups changed nipple an abrupt increase in activity occurred in larger fibres. In summary, the non-myelinated fibres of the TBTN are increased in diameter during lactation, and the pattern of suckling-evoked nerve activity in myelinated fibres showed that (a) the double burst of Aδ fibres, produced by individual sucks before milk ejection, could be one of the conditions required for the triggering of the reflex, and (b) the nerve activity displayed during milk-ejection action may result, at least in part, from 'non-specific' stimulation of cutaneous receptors. J. Endocr. (1988) 118, 471–483

Mormyromast electroreceptor organs and their afferent fibers in mormyrid fish. II. Intra-axonal recordings show initial stages of central processing

1990 ◽  
Vol 63 (2) ◽  
pp. 303-318 ◽  
Author(s):  
C. C. Bell
Keyword(s):  
Lateral Line ◽  
Electric Organ Discharge ◽  
Electric Organ ◽  
Direct Stimulation ◽  
Postsynaptic Potentials ◽  
Central Processing ◽  
Refractory Periods ◽  
Synaptic Potentials ◽  
Afferent Fibers ◽  
Stimulation Of

1. Physiologically and morphologically identified primary afferent fibers from mormyromast electroreceptor organs were recorded intracellularly. The fiber recordings were made from the nerve root of the posterior lateral line nerve, where the fibers enter the brain, and from the electrosensory lateral line lobe (ELL), near the central terminals of the fibers. 2. The intracellular recordings reveal a variety of potentials, synaptic and nonsynaptic, in addition to the large orthodromic action potentials from the periphery. The goal of the present study was to describe and interpret these various potentials in mormyromast afferent fibers as a first step in understanding the processing of electrosensory information in ELL. 3. Three types of synaptic potentials were recorded inside mormyromast afferent fibers: 1) electric organ corollary discharge (EOCD) excitatory postsynaptic potentials (EPSPs), driven by the motor command that elicits the electric organ discharge (EOD); 2) EPSPs evoked by electrosensory stimulation of electroreceptors in the skin near the electroreceptor from which the recorded fiber originates or by direct stimulation of an electrosensory nerve; and 3) inhibitory postsynaptic potentials (IPSPs) evoked by electrosensory stimulation of more distant electroreceptors. These synaptic potentials can be attributed to synaptic input to postsynaptic cells in ELL that is observed inside the afferent fibers because of electrical synapses between the fibers and the postsynaptic cells. 4. The peripherally evoked EPSPs could frequently be shown to be unitary. The unitary EPSPs were identical to the orthodromic spikes in originating from a single electroreceptor, in threshold, and in latency shift with increasing stimulus intensity. These similarities suggest that the unitary EPSPs are electrotonic EPSPs caused by impulses in other mormyromast afferent fibers that terminate on some of the same postsynaptic cells as the recorded fiber. The peripherally evoked IPSPs had a longer latency than the EPSPs or orthodromic spikes, requiring the presence of an inhibitory interneuron. 5. The peripherally evoked EPSPs, both unitary and nonunitary, show absolute refractory periods of 3-8 ms, followed by relative refractory periods of approximately 8 ms, when tested with two identical stimuli to a nerve. These refractory periods are interpreted as because of refractoriness in the fine preterminal branches of the axonal arbor. 6. A depolarizing afterpotential is commonly associated with the orthodromic spike and probably results from the successful propagation of the spike into the entire terminal arbor. The depolarizing afterpotential has a refractory period that is similar to that of the peripherally evoked EPSPs and that is also interpreted as refractoriness in the fine preterminal branches.(ABSTRACT TRUNCATED AT 400 WORDS)

Mechanical sensitivity of group III and IV afferents from posterior articular nerve in normal and inflamed cat knee

1986 ◽  
Vol 55 (4) ◽  
pp. 635-643 ◽  
Author(s):  
P. Grigg ◽  
H. G. Schaible ◽  
R. F. Schmidt
Keyword(s):  
Sciatic Nerve ◽  
Knee Joint ◽  
Conduction Velocity ◽  
Mechanical Stimulation ◽  
Dorsal Root ◽  
Receptive Fields ◽  
Group Iv ◽  
Mechanical Sensitivity ◽  
Group Iii ◽  
Stimulation Of

Recordings were performed from sciatic nerve or dorsal root filaments in 28 cats to study single group III (conduction velocity 2.5-20 m/s) and group IV (conduction velocity less than 2.5 m/s) units supplying the knee joint via the posterior articular nerve (PAN). In seven of these cats the knee joint had been inflamed artificially. Recordings from sciatic nerve filaments revealed responses to local mechanical stimulation of the joint in only 3 of 41 group IV units and in 12 of 18 group III units from the normal joint. In the inflamed joint 14 of 36 group IV units and 24 of 36 group III units were excited with local mechanical stimulation. In recordings from dorsal root filaments (normal joint) 4 of 11 group IV units and 7 of 13 group III units were activated by stimulating the joint locally. In the normal joint four group IV units (recorded from dorsal root filaments) responded only to rotations against the resistance of the tissue, whereas the majority of the fibers did not respond even to forceful movements. Group III units with local mechanosensitivity in the normal joint reacted strongly or weakly to movements in the working range of the joint or only to movements against resistance of the tissue. In the inflamed joint, group IV fibers (recorded in sciatic nerve filaments) with detectable receptive fields responded strongly to gentle movements or only to movements against resistance of tissue. Some did not react to movements. Group III units reacted strongly or weakly to gentle movements or only to movements against resistance of the tissue.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals Towards fungal computer

2018 ◽  
Vol 8 (6) ◽  
pp. 20180029 ◽  
Author(s):  
Andrew Adamatzky
Keyword(s):  
Electrical Activity ◽  
Information Transfer ◽  
Chemical Stimulation ◽  
Reliable Indicator ◽  
Mycelium Network ◽  
Logical Functions ◽  
Stimulation Of

We propose that fungi Basidiomycetes can be used as computing devices: information is represented by spikes of electrical activity, a computation is implemented in a mycelium network and an interface is realized via fruit bodies. In a series of scoping experiments, we demonstrate that electrical activity recorded on fruits might act as a reliable indicator of the fungi’s response to thermal and chemical stimulation. A stimulation of a fruit is reflected in changes of electrical activity of other fruits of a cluster, i.e. there is distant information transfer between fungal fruit bodies. In an automaton model of a fungal computer, we show how to implement computation with fungi and demonstrate that a structure of logical functions computed is determined by mycelium geometry.

scholarly journals Co-Ordination of Pedal-Disk Detachment in the Sea Anemone Calliactis Parasitica

1969 ◽  
Vol 51 (2) ◽  
pp. 387-396
Author(s):  
I. D. MCFARLANE
Keyword(s):  
Electrical Stimulation ◽  
Electrical Activity ◽  
Mechanical Stimulation ◽  
Average Frequency ◽  
Conduction System ◽  
Identical Stimulus ◽  
Slow Conduction ◽  
Calliactis Parasitica ◽  
Behavioural Sequence ◽  
Stimulation Of

1. Electrical activity has been recorded from the sphincter region of Calliactis parasitica during the behavioural sequence in which the anemone detaches from the substrate and attaches to a Buccinum shell. The ectodermal slow-conduction system (SS1) fires repetitively, the majority of observed pulses occurring in the period prior to detachment (a typical example is 25 SS1pulses at an average frequency of 1 pulse/7 sec.). Shell-tentacle contact is essential for stimulation of SS1activity. 2. Mechanical stimulation of the column excites the SS1, and 30 stimuli at a frequency of about one shock/5 sec. give pedal disk detachment. 3. Electrical stimulation of the ectoderm excites the SS1and about 30 stimuli at frequencies between one shock/3 sec. and one shock/9 sec. produce detachment. Detachment and the SS1 have an identical stimulus threshold. It is concluded that detachment is co-ordinated by the SS1.

Primate nucleus gracilis neurons: responses to innocuous and noxious stimuli

1988 ◽  
Vol 59 (3) ◽  
pp. 886-907 ◽  
Author(s):  
D. G. Ferrington ◽  
J. W. Downie ◽  
W. D. Willis
Keyword(s):  
Conduction Velocity ◽  
Dynamic Range ◽  
Subcutaneous Tissue ◽  
Receptive Fields ◽  
High Threshold ◽  
Spinothalamic Tract ◽  
Sinusoidal Vibration ◽  
Nucleus Gracilis ◽  
Pressure Sensitive ◽  
Stimulation Of

1. Recordings were made from 67 neurons in the nucleus gracilis (NG) of anesthetized macaque monkeys. All of the cells were activated antidromically from the ventral posterior lateral (VPL) nucleus of the contralateral thalamus. Stimuli used to activate the cells orthodromically were graded innocuous and noxious mechanical stimuli, including sinusoidal vibration and thermal pulses. 2. The latencies of antidromic action potentials following stimulation in the VPL nucleus were significantly shorter for cells in the caudal compared with the rostral NG. The mean minimum afferent conduction velocity of the afferent conduction velocity of the afferent fibers exciting the NG cells was 52 m/s, as judged from the latencies of the cells to orthodromic volleys evoked by electrical stimulation of peripheral nerves. The overall conduction velocity of the pathway from peripheral nerve to thalamus was approximately 40 m/s. 3. Cutaneous receptive fields on the distal hindlimb usually occupied an area equivalent to much less than a single digit. However, a few cells had receptive fields up to or exceeding the area of the foot. 4. NG cells were classified by their responses to graded mechanical stimulation of the skin as low threshold (LT) or wide dynamic range (WDR). No high-threshold NG cells were found. A special subcategory of pressure-sensitive LT (SA) neurons was recognized. Many of these cells were maximally responsive to maintained indentation of the skin. The sample of NG cells differed from the population of primate spinothalamic and spinocervicothalamic pathways so far examined, in having a larger proportion of LT neurons and a smaller proportion of WDR cells. A few NG cells responded best to manipulation of subcutaneous tissue. 5. Discriminant analysis permitted the NG cells to be assigned to classes determined by a k-means cluster analysis of the responses of a reference set of 318 primate spinothalamic tract (STT) cells. There were four classes of cells based on normalized responses of individual neurons and another four classes based upon responses compared across the population of cells. The NG cells were allocated to the various categories in different proportions than either primate STT cells or spinocervicothalamic neurons, consistent with the view that the functional roles of these somatosensory pathways differ. 6. Some of the pressure-sensitive NG cells were excited when the skin was stretched, suggesting an input from type II slowly adapting (Ruffini) mechanoreceptors.(ABSTRACT TRUNCATED AT 400 WORDS)

scholarly journals Glucose stimulates somatostatin secretion in pancreatic δ-cells by cAMP-dependent intracellular Ca2+ release

2019 ◽  
Vol 151 (9) ◽  
Author(s):  
Geoffrey Denwood ◽  
Andrei Tarasov ◽  
Albert Salehi ◽  
Elisa Vergari ◽  
Reshma Ramracheya ◽  
...  
Keyword(s):  
Electrical Activity ◽  
Secretory Vesicles ◽  
Glucose Levels ◽  
Somatostatin Secretion ◽  
Elevated Glucose ◽  
Mouse Islets ◽  
Underlying Mechanisms ◽  
Fold Stimulation ◽  
Cyclase Activator ◽  
Stimulation Of

Somatostatin secretion from pancreatic islet δ-cells is stimulated by elevated glucose levels, but the underlying mechanisms have only partially been elucidated. Here we show that glucose-induced somatostatin secretion (GISS) involves both membrane potential-dependent and -independent pathways. Although glucose-induced electrical activity triggers somatostatin release, the sugar also stimulates GISS via a cAMP-dependent stimulation of CICR and exocytosis of somatostatin. The latter effect is more quantitatively important and in mouse islets depolarized by 70 mM extracellular K+, increasing glucose from 1 mM to 20 mM produced an ∼3.5-fold stimulation of somatostatin secretion, an effect that was mimicked by the application of the adenylyl cyclase activator forskolin. Inhibiting cAMP-dependent pathways with PKI or ESI-05, which inhibit PKA and exchange protein directly activated by cAMP 2 (Epac2), respectively, reduced glucose/forskolin-induced somatostatin secretion. Ryanodine produced a similar effect that was not additive to that of the PKA or Epac2 inhibitors. Intracellular application of cAMP produced a concentration-dependent stimulation of somatostatin exocytosis and elevation of cytoplasmic Ca2+ ([Ca2+]i). Both effects were inhibited by ESI-05 and thapsigargin (an inhibitor of SERCA). By contrast, inhibition of PKA suppressed δ-cell exocytosis without affecting [Ca2+]i. Simultaneous recordings of electrical activity and [Ca2+]i in δ-cells expressing the genetically encoded Ca2+ indicator GCaMP3 revealed that the majority of glucose-induced [Ca2+]i spikes did not correlate with δ-cell electrical activity but instead reflected Ca2+ release from the ER. These spontaneous [Ca2+]i spikes are resistant to PKI but sensitive to ESI-05 or thapsigargin. We propose that cAMP links an increase in plasma glucose to stimulation of somatostatin secretion by promoting CICR, thus evoking exocytosis of somatostatin-containing secretory vesicles in the δ-cell.

Sign in / Sign up

Export Citation Format

Share Document