The Ionic Basis of the Fast Action Potentials in the Isolated CerebroVisceral Connective of Anodonta Cygnea

1969 ◽  
Vol 51 (2) ◽  
pp. 297-318
Author(s):  
ALBERT D. CARLSON ◽  
J. E. TREHERNE

1. The large axons in the cerebro-visceral connective have been shown to function for appreciable periods in preparations bathed in sodium-free non-electrolyte solutions. 2. The results of experiments on the effects of organic monovalent cations and anions, together with observations on the effects of tetrodotoxin, procaine and manganous ions and the changes in conduction velocity in tris chloride and dextran solutions indicate that the action potentials are, nevertheless, mediated by conventional sodium-dependent mechanisms. 3. Radioisotope experiments show that there is a small fraction, of approx. 0.5 mM/kg. tissue, which does not exchange rapidly with the 22Na in the bathing medium and which can be depleted by stimulation in sodium-free solutions. 4. On the basis of these observations it is suggested that there is sequestered extra-axonal sodium fraction which can be utilized by the large axons to maintain action potentials in preparations bathed in sodium-free solutions.

1969 ◽  
Vol 50 (3) ◽  
pp. 711-722
Author(s):  
J. E. TREHERNE ◽  
DEFOREST MELLON ◽  
ALBERT D. CARLSON

The compound action potentials recorded in cerebro-visceral connectives consisted of a large homogeneous slow component, with a conduction velocity of between 0·03 and 0·04 m.sec-1, together with a variable rapidly conducting component, showing spikes with maximum velocities in the region of 0·4-0·5 m.sec-1. 2. Comparison of the square of the conduction velocity, for the various components of the compound action potential, with distribution of axon diameters in the connective showed that the small axons (0·1-0·3µ in diameter) contributed to the slow component, the larger axons (2·0-6·0 µ in diameter) forming the initial rapidly conducting spikes. 3. The small axons showed a rapid loss of function in preparations bathed in isotonic sucrose solutions. The larger axons, however, continued to function for appreciable periods in isotonic solutions of non-electrolytes. 4. The larger axons were rapidly and reversibly blocked by dilute tetrodotoxin. Additional evidence is also presented which suggests that the action potentials associated with the axons are sodium-dependent and do not depend upon any appreciable involvement of calcium ions in carrying the action current. 5. Both the large and the small axons appear to be relatively accessible to small ions and molecules in the bathing medium. The results are discussed in relation to the possible physiological mechanisms involved in the function of the larger axons in sodium-free solutions.


1972 ◽  
Vol 57 (1) ◽  
pp. 41-53
Author(s):  
D. B. SATTELLE

1. The compound action potential recorded from the pleural-supraintestinal connective of Viviparus contectus consists of a large, slow component with an average conduction velocity of about 0.02 m/sec (at 23° C) and a faster component with a conduction velocity of 0.10 m/sec (at 23° C) for the fastest fibres. 2. Both fast and slow action potentials are rapidly abolished by the substitution of tris chloride and choline chloride for the sodium salts of normal Ringer. Tetrodotoxin, applied at 10-5M rapidly abolishes action potentials in all fibres. It is, therefore, concluded that a largely sodium-dependent mechanism of spike generation operates in all axons of the connective. 3. Lithium ions effectively substitute for sodium ions in maintaining the fast action potentials for extended periods, whereas tetraethylammonium ions do not. 4. When the calcium chloride of normal Ringer is replaced by sucrose, magnesium chloride or barium chloride, conduction of fast action potentials is maintained. A small increase in the sensitivity of all axons to tetrodotoxin is observed in calcium-free Ringer; a slight reduction in the spike amplitude of fast action potentials follows the application of manganous ions at 5 mM/l in normal Ringer. It is concluded that any possible contribution of calcium to the generation of the action current of the fast action potential is very small compared to that of sodium. 5. All axons of the connective function for extended periods in sodium-free (dextran) Ringer. Under these conditions, tetrodotoxin blocks conduction in all fibres at concentrations of 10-6M, suggesting that function in dextran Ringer is maintained by a sodium-dependent mechanism.


1988 ◽  
Vol 118 (3) ◽  
pp. 471-483 ◽  
Author(s):  
L. M. Voloschin ◽  
E. Décima ◽  
J. H. Tramezzani

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


1972 ◽  
Vol 56 (2) ◽  
pp. 493-499
Author(s):  
N. J. LANE ◽  
J. E. TREHERNE

1. Ultrastructural observations on the uptake of an exogenous tracer substance, horseradish peroxidase (M.W. 40,000), have shown that this large molecule can penetrate the neural lamella in intact cerebro-visceral connectives of the lamellibranch, Anodonta cygnea. 2. Peroxidase molecules were also observed to penetrate between the intercellular clefts formed by adjacent membranes of the underlying peripheral glial cell layer and to move extensively into the underlying extracellular spaces. 3. These observations confirm the results of previous electrophysiological, radioisotopic and ultrastructural investigations indicating that a relatively rapid exchange of water-soluble ions and molecules occurs between the blood, or bathing medium, and the extracellular fluid bathing the axon surfaces in intact connectives.


1974 ◽  
Vol 60 (3) ◽  
pp. 653-671
Author(s):  
D. B. SATTELLE

1. A mean resting potential of -53.3 (S.D. ±2.7) mV has been obtained for 23 neurones of the parietal and visceral ganglia of Limnaea stagnalis (L.). Changes in the resting potential of between 28 and 43 mV accompany tenfold changes in [K+0]. A modified constant-field equation accounts for the behaviour of most cells over the range of external potassium concentrations from 0-5 to 10.o mM/1. Mean values have been estimated for [K+1, 56.2 (S.D.± 9-0) mM/1 and PNa/PK, 0-117 (S.D.±0-028). 2. Investigations on the ionic basis of action potential generation have revealed two cell types which can be distinguished according to the behaviour of their action potentials in sodium-free Ringer. Sodium-sensitive cells are unable to support action potentials for more than 8-10 min in the absence of sodium. Sodium slopes of between 29 and 37 mV per decade change in [Na+0] have been found for these cells. Tetrodotoxin (5 x 10-5 M) usually blocks action potentials in these neurones. Calcium-free inger produces a marked reduction in the overshoot potential and calcium slopes of about 18 mV per decade change in [Ca2+o] are found. Manganous chloride only partially reduces the action potential overshoot in these cells at concentrations of 10 mM/l. 3. Sodium-insensitive neurones maintain action potentials in the absence of external sodium. Stimulation only slightly reduces the amplitude of the action potential under these conditions and such cells are readily accessible to potassium ions in the bathing medium. A calcium-slope of 29 mV per decade change in [Ca2+o] has been observed in these cells in the absence of external sodium. 4. It is concluded that both sodium and calcium ions can be involved in the generation of the action potential in neurones of Limnaea stagnate, their relative contribution varying in different cells.


1999 ◽  
Vol 277 (2) ◽  
pp. H826-H833 ◽  
Author(s):  
Seiko Tanabe ◽  
Toshio Hata ◽  
Masayasu Hiraoka

To explore a possible ionic basis for the prolonged Q-T interval in women compared with that in men, we investigated the electrophysiological effects of estrogen in isolated guinea pig ventricular myocytes. Action potentials and membrane currents were recorded using the whole cell configuration of the patch-clamp technique. Application of 17β-estradiol (10–30 μM) significantly prolonged the action potential duration (APD) at 20% (APD20) and 90% repolarization (APD90) at stimulation rates of 0.1–2.0 Hz. In the presence of 30 μM 17β-estradiol, APD20 and APD90 at 0.1 Hz were prolonged by 46.2 ± 17.1 and 63.4 ± 11.7% of the control ( n = 5), respectively. In the presence of 30 μM 17β-estradiol the peak inward Ca2+ current ( I CaL) was decreased to 80.1 ± 2.5% of the control ( n = 4) without a shift in its voltage dependence. Application of 30 μM 17β-estradiol decreased the rapidly activating component of the delayed outward K+ current ( I Kr) to 63.4 ± 8% and the slowly activating component ( I Ks) to 65.8 ± 8.7% with respect to the control; the inward rectifier K+ current was barely affected. The results suggest that 17β-estradiol prolonged APD mainly by inhibiting the I Kcomponents I Krand I Ks.


2003 ◽  
Vol 17 (2) ◽  
pp. 126-131 ◽  
Author(s):  
Belmiro Cavalcanti do Egito Vasconcelos ◽  
Cosme Gay Escoda ◽  
Ricardo José de Holanda Vasconcellos ◽  
Riedel Frota Sá Nogueira Neves

The aim of this study was to evaluate standardized conduction velocity data for uninjured facial nerve and facial nerve repaired with autologous graft nerves and synthetic materials. An evaluation was made measuring the preoperative differences in the facial nerve conduction velocities on either side, and ascertaining the existence of a positive correlation between facial nerve conduction velocity and the number of axons regenerated postoperatively. In 17 rabbits, bilateral facial nerve motor action potentials were recorded pre- and postoperatively. The stimulation surface electrodes were placed on the auricular pavilion (facial nerve trunk) and the recording surface electrodes were placed on the quadratus labii inferior muscle. The facial nerves were isolated, transected and separated 10 mm apart. The gap between the two nerve ends was repaired with autologous nerve grafts and PTFE-e (polytetrafluoroethylene) or collagen tubes. The mean of maximal conduction velocity of the facial nerve was 41.10 m/s. After 15 days no nerve conduction was evoked in the evaluated group. For the period of 2 and 4 months the mean conduction velocity was approximately 50% of the normal value in the subgroups assessed. A significant correlation was observed between the conduction velocity and the number of regenerated axons. Noninvasive functional evaluation with surface electrodes can be useful for stimulating and recording muscle action potentials and for assessing the functional state of the facial nerve.


1975 ◽  
Vol 62 (1) ◽  
pp. 231-241
Author(s):  
RR Bennett ◽  
PB Buchan ◽  
JE Treherne

Exposure to sodium-deficient (tris) saline caused an appreciable decline in the sodium content of intact connectives in the absence of equivalent reduction in the amplitude of the recorded action potentials. Return of sodium-depleted connectives to normal saline resulted in a rapid recovery of axonal function despite only a partial (less than 70%) recovery in sodium content. Replacement of sodium ions by those of lithium in the bathing medium resulted in a substantial accumulation of this cation. Lithium movements exhibited a marked asymetry, no significant decline in concentration being observed upon return to normal saline. These results are tentatively interpreted in terms of an exchangeable glial sodium fraction and are discussed in relation to extra-axonal sodium regulation.


2006 ◽  
Vol 96 (6) ◽  
pp. 2963-2971 ◽  
Author(s):  
Philip M. Lang ◽  
Gila Moalem-Taylor ◽  
David J. Tracey ◽  
Hugh Bostock ◽  
Peter Grafe

Activity-dependent fluctuations in axonal excitability and changes in interspike intervals modify the conduction of trains of action potentials in unmyelinated peripheral nerve fibers. During inflammation of a nerve trunk, long stretches of axons are exposed to inflammatory mediators such as 5-hydroxytryptamine [5-HT]. In the present study, we have tested the effects of m-chlorophenylbiguanide (mCPBG), an agonist at the 5-HT(3) serotonin receptor, on activity- and potential-dependent variations in membrane threshold and conduction velocity of unmyelinated C-fiber axons of isolated rat sural nerve segments. The increase in axonal excitability during application of mCPBG was much stronger at higher frequencies of action potentials and/or during axonal membrane hyperpolarization. The effects on the postspike recovery cycle also depended on the rate of stimulation. At an action potential frequency of 1 Hz or in hyperpolarized axons, mCPBG produced a loss of superexcitability. In contrast, at 0.33 Hz, a small increase in the postspike subexcitability was observed. Similar effects on excitability changes were found when latency instead of threshold was recorded, but only at higher action potential frequencies: at 1.8 Hz, mCPBG increased conduction velocity and reduced postspike supernormality. The latter effect would increase the interspike interval if pairs of action potentials were conducted along several cm in an inflamed nerve trunk. These data indicate that activation of axonal 5-HT(3) receptors not only enhances membrane excitability but also modulates action potential trains in unmyelinated, including nociceptive, nerve fibers at high impulse rates.


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