Changes in extracellular potassium concentration in cat spinal cord in response to innocuous and noxious stimulation of legs with healthy and inflamed knee joints

1990 ◽  
Vol 79 (2) ◽  
pp. 283-292 ◽  
Author(s):  
U. Heinemann ◽  
H. G. Schaible ◽  
R. F. Schmidt
Keyword(s):  
Spinal Cord ◽  
Potassium Concentration ◽  
Knee Joints ◽  
Extracellular Potassium ◽  
Noxious Stimulation ◽  
Extracellular Potassium Concentration ◽  
Stimulation Of

Insulin stimulation of an electrogenic pump at high extracellular potassium concentration

1985 ◽  
Vol 249 (1) ◽  
pp. E12-E16
Author(s):  
F. S. Wu ◽  
K. Zierler
Keyword(s):  
Skeletal Muscle ◽  
Potassium Concentration ◽  
Equilibrium Potential ◽  
Extracellular Potassium ◽  
Insulin Stimulation ◽  
Rat Skeletal Muscle ◽  
Extracellular Potassium Concentration ◽  
High K ◽  
Na Ions ◽  
Stimulation Of

There is no agreement about the immediate mechanism by which insulin hyperpolarizes skeletal muscle, adipocytes, and myocardium. Of three candidates, one has been eliminated; the hyperpolarization is not secondary to an increase in intracellular [K]. There are reports that insulin hyperpolarizes by increasing relative permeability to K compared with that to Na ions, and other reports that insulin stimulates an ouabain-sensitive electrogenic Na-K exchange pump. Our evidence has been interpreted to support the former and deny the latter, when rat skeletal muscle is bathed at normal [K]. Crucial evidence for the latter has not been reported: insulin hyperpolarizes to a potential more negative than the K equilibrium potential. We now report that when rat caudofemoralis muscle is incubated with insulin at normal extracellular [K], then depolarized by increasing extracellular [K] to 38.4 mM, by equimolar substitution of KCl for NaCl, there is hyperpolarization compared with potentials of muscles treated similarly with respect to [K] but without insulin. Under these circumstances, the membrane potential in the presence of insulin is more negative than the new K equilibrium potential, and, in contrast to our previous experience with muscles bathed only in normal [K], the hyperpolarization in high [K] is reduced or eliminated by ouabain.

Correlation Between Extracellular Focal Potentials and K+ Potentials Evoked by Primary Afferent Activity

1975 ◽  
Vol 53 (5) ◽  
pp. 912-922 ◽  
Author(s):  
K. Krnjević ◽  
M. E. Morris
Keyword(s):  
Time Course ◽  
Potassium Concentration ◽  
Extracellular Potassium ◽  
Cuneate Nucleus ◽  
Afferent Activity ◽  
Extracellular Potassium Concentration ◽  
Afferent Nerves ◽  
Focal Potentials ◽  
Constant Slope ◽  
Stimulation Of

There is a clear, positive correlation in amplitude between changes in potassium potentials (ΔEK) and focal potentials (ΔV) evoked by tetanic stimulation of afferent nerves in the cuneate nucleus and dorsal horn of cats under Dial anaesthesia or after decerebration. Data obtained with stimulations at various frequencies and intensities, or recording at different positions give a relatively constant slope of ΔV/ΔEK (varying between 0.2 and 0.6 in different experiments). These observations are fully consistent with the possibility that ΔV mainly reflects changes in extracellular potassium concentration caused by the release of K+ from active terminals. Differences in time course of ΔEK and ΔV evoked by single stimuli are a steep function of distance and therefore can be ascribed to the slowness of diffusion, without excluding the possibility of an early additional depolarizing effect by another mechanism.

Effects of dantrolene and D2O on K+-stimulated respiration of skeletal muscle

1982 ◽  
Vol 243 (1) ◽  
pp. C87-C95 ◽  
Author(s):  
D. Erlij ◽  
W. K. Shen ◽  
P. Reinach ◽  
H. Schoen
Keyword(s):  
Skeletal Muscle ◽  
Potassium Concentration ◽  
Extracellular Potassium ◽  
Frog Skeletal Muscle ◽  
Extracellular Potassium Concentration ◽  
Na Efflux ◽  
High Level ◽  
The Relationship ◽  
Peak Increase ◽  
Stimulation Of

We have examined the effects of dantrolene and D2O on the K+-stimulated respiration in frog skeletal muscle. The threshold for K+ stimulation was around 10 mM extracellular potassium concentration ([K+]o). A further marked increase in respiration to levels about ten times the resting level was noted when [K+]o was between 15 and 20 mM. The increase was sustained for hours when [K+]o was less than 20 mM; however, with higher concentrations the stimulation consisted of an initial burst followed by a decline. Dantrolene shifted the relationship between [K+]o and peak increase in respiration toward higher [K+]o by about 10 mM; in addition it nearly completely blocked the sustained component of the increase. D2O, nearly abolished the K+-induced respiration. Neither agent shifted the relationship between [K+]o and membrane potential nor abolished the stimulation of respiration caused by caffeine. Dantrolene did not block the stimulation of Na+ efflux caused by 15 mM K+. The results with these agents are consistent with the proposal that K+-stimulated respiration is due to Ca2+ release into the cytoplasm. In addition, they provide evidence that the stimulated rate of Ca2+ release into the cytoplasm can remain at a persistently high level for hours provided [K+]o does not exceed 20 mM. We calculated that the level of this constant Ca2+ release is about 3.4 X 10(16) ions/(s.cm3).

Drastic Decrease in Isoflurane Minimum Alveolar Concentration and Limb Movement Forces after Thoracic Spinal Cooling and Chronic Spinal Transection in Rats

2005 ◽  
Vol 102 (3) ◽  
pp. 624-632 ◽  
Author(s):  
Steven L. Jinks ◽  
Carmen L. Dominguez ◽  
Joseph F. Antognini
Keyword(s):  
Spinal Cord ◽  
Spinal Cord Injury ◽  
Minimum Alveolar Concentration ◽  
Tail Flick ◽  
Noxious Stimulation ◽  
Partial Recovery ◽  
Spinal Transection ◽  
Thoracic Spinal ◽  
Cord Injury ◽  
Stimulation Of

Background Individuals with spinal cord injury may undergo multiple surgical procedures; however, it is not clear how spinal cord injury affects anesthetic requirements and movement force under anesthesia during both acute and chronic stages of the injury. Methods The authors determined the isoflurane minimum alveolar concentration (MAC) necessary to block movement in response to supramaximal noxious stimulation, as well as tail-flick and hind paw withdrawal latencies, before and up to 28 days after thoracic spinal transection. Tail-flick and hind paw withdrawal latencies were measured in the awake state to test for the presence of spinal shock or hyperreflexia. The authors measured limb forces elicited by noxious mechanical stimulation of a paw or the tail at 28 days after transection. Limb force experiments were also conducted in other animals that received a reversible spinal conduction block by cooling the spinal cord at the level of the eighth thoracic vertebra. Results A large decrease in MAC (to </= 40% of pretransection values) occurred after spinal transection, with partial recovery (to approximately 60% of control) at 14-28 days after transection. Awake tail-flick and hind paw withdrawal latencies were facilitated or unchanged, whereas reflex latencies under isoflurane were depressed or absent. However, at 80-90% of MAC, noxious stimulation of the hind paw elicited ipsilateral limb withdrawals in all animals. Hind limb forces were reduced (by >/= 90%) in both chronic and acute cold-block spinal animals. Conclusions The immobilizing potency of isoflurane increases substantially after spinal transection, despite the absence of a baseline motor depression, or "spinal shock." Therefore, isoflurane MAC is determined by a spinal depressant action, possibly counteracted by a supraspinal facilitatory action. The partial recovery in MAC at later time points suggests that neuronal plasticity after spinal cord injury influences anesthetic requirements.

GABA-Receptor–Independent Dorsal Root Afferents Depolarization in the Neonatal Rat Spinal Cord

1998 ◽  
Vol 79 (5) ◽  
pp. 2581-2592 ◽  
Author(s):  
E. Kremer ◽  
A. Lev-Tov
Keyword(s):  
Spinal Cord ◽  
Dorsal Root ◽  
Gaba Receptor ◽  
Neonatal Rat ◽  
Extracellular Potassium ◽  
Rat Spinal Cord ◽  
Extracellular Potassium Concentration ◽  
Dorsal Roots ◽  
Intact Brain ◽  
Dorsal Root Afferents

Kremer, E. and A. Lev-Tov. GABA-receptor–independent dorsal root afferents depolarization in the neonatal rat spinal cord. J. Neurophysiol. 79: 2581–2592, 1998. Dorsal root afferent depolarization and antidromic firing were studied in isolated spinal cords of neonatal rats. Spontaneous firing accompanied by occasional bursts could be recorded from most dorsal roots in the majority of the cords. The afferent bursts were enhanced after elevation of the extracellular potassium concentration ([K+]e) by 1–2 mM. More substantial afferent bursts were produced when the cords were isolated with intact brain stems. Rhythmic afferent bursts could be recorded from dorsal roots in some of the cords during motor rhythm induced by bath-applied serotonin and N-methyl-d-aspartate (NMDA). Bilaterally synchronous afferent bursts were produced in pairs of dorsal roots after replacing the NaCl in the perfusate with sodium-2-hydroxyethansulfonate or after application of the γ-aminobutyric acid-A (GABAA) receptor antagonist bicuculline with or without serotonin (5-HT) and NMDA. Antidromic afferent bursts also could be elicited under these conditions by stimulation of adjacent dorsal roots, ventrolateral funiculus axons, or ventral white commissural (VWC) fibers. The antidromic bursts were superimposed on prolonged dorsal root potentials (DRPs) and accompanied by a prolonged increase in intraspinal afferent excitability. Surgical manipulations of the cord revealed that afferent firing in the presence of bicuculline persisted in the hemicords after hemisection and still was observed after removal of their ventral horns. Cutting the VWC throughout its length did not perturb the bilateral synchronicity of the discharge. These findings suggest that the activity of dorsal horn neurons is sufficient to produce the discharge and that the bilateral synchronicity can be maintained by cross connectivity that is relayed from side to side dorsal to the VWC. Antagonists of GABAB, 5-HT2/5-HT1C, or glutamate metabotropic group II and III receptors could not abolish afferent depolarization in the presence of bicuculline. Depolarization comparable in amplitude to DRPs, could be produced in tetrodotoxin-treated cords by elevation of [K+]e to the levels reported to develop in the neonatal rat spinal cord in response to dorsal root stimulation. A mechanism involving potassium transients produced by neuronal activity therefore is suggested to be the major cause of the GABA-independent afferent depolarization reported in our study. Possible implications of potassium transients in the developing and the adult mammalian spinal cord are discussed.

Sign in / Sign up

Export Citation Format

Share Document