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Biomedical subjects

H Grundfest

Publications and source records attributed to H Grundfest.

At least 37 records · Page 2Linked to original sources
PubMed1968

Correlated morphological and physiological studies on isolated single muscle fibers. II. The properties of the crayfish transverse tubular system: localization of the sites of reversible swelling.

Living muscle fibers of crayfish become dark during efflux of Cl(-). This change in appearance is correlated with occurrence of vacuolation in the fixed fibers. The vacuoles begin at and are mainly confined to the terminals of the transverse tubular system (TTS) which are in diadic contact with the sarcoplasmic reticulum (SR). In electron micrographs swellings more than 1 micro in diameter may be seen connected to the sarcolemma or sarcolemmal invaginations by relatively unswollen tubules about 300-500 A wide. Darkening of the living fibers can be reversed by causing an influx of Cl(-). Vacuoles are then absent in the fixed preparations. These findings accord with the conclusion that the membrane of the TTS is anion permselective. Localization of the selectivity to the membrane of the terminals of the TTS strengthens the hypothesis that a channeling of current flow is responsible for initiation of excitation-contraction coupling. During the swelling, and upon its reversal, the area of the membrane of the terminals must change reversibly by about two to four orders of magnitude. The absence of changes in the dimensions of the unit membrane indicates that the expansion of the membrane and its subsequent shrinkage involve reversible incorporation of cytoplasmic material into the membrane phase.

Chlorides↗
PubMed1968

Permeability of alkali metal cations in lobster muscle. A comparison of electrophysiological and osmometric analyses.

Single muscle fibers from lobster walking legs are effectively impermeable to Na, but are permeable to K. They shrink in hyperosmotic NaCl; they swell in low NaCl media which are hyposmotic or which are made isosmotic with the addition of KCl. In conformity, the membrane potential is relatively insensitive to changes in external Na, while it responds according to the Nernst relation for changes in external K. When the medium is made isosmotic or hyperosmotic with RbCl the volume and membrane potential changes are of essentially the same magnitudes as those in media enriched with KCl. The time courses for attaining equilibrium are slower, indicating that Rb is less permeant than K. Substitution of CsCl for NaCl (isosmotic condition) produces no change in volume of the muscle fiber. Addition of CsCl (hyperosmotic condition) causes a shrinkage which attains a steady state, as is the case in hyperosmotic NaCl. Osmotically, therefore, Cs appears to be no more permeant than is Na. However, the membrane depolarizes slowly in Cs-enriched media and eventually comes to behave as an ideal Cs electrode. Thus, the electrode properties of the lobster muscle fiber membrane may not depend upon the diffusional relations of the membrane and ions, and the osmotic permeability of the membrane for a given cation may not correspond with the electrophysiologically deduced permeability. Comparative data on the effects of NH(4) and Li are also included and indicate several other degrees of complexity in the cell membrane.

Animals↗
PubMed1968

Effects of lithium on different membrane components of crayfish stretch receptor neurons.

Unlike several other varieties of input membrane, that of the crayfish stretch receptor develops a generator potential in response to stretch when all the Na of the medium is replaced with Li. However, Li depolarizes the receptor neuron, the soma membrane becoming more depolarized than that of the axon. During exposure to Li the cell usually fires spontaneously for a period, and when it becomes quiescent spike electrogenesis fails in the soma but persists in the axon. These effects are seen in the rapidly adapting as well as the slowly adapting cells. The block of spike electrogenesis of the soma membrane is only partly due to the Li-induced depolarization and a significant role must be ascribed to a specific effect of Li.

Animals↗
PubMed1968

Analysis of spike electrogenesis of Eel electroplaques with phase plane and impedance measurements.

Eel electroplaques provide experimental conditions in which registration of phase plane trajectories (dV/dt vs. V) and impedance measurements with an AC Wheatstone bridge, in conjunction with spike electrogenesis describe quantitatively the ionic processes of the electrogenesis. Thus, these data employing as they do measurements of transients, permit an independent test of the validity of the assumptions which underlie the Hodgkin-Huxley equivalent circuit: independent ionic channels with fixed ionic batteries and exhibiting time-variant conductance changes with different kinetics for the different channels. The analysis accords with earlier findings on voltage-clamped electroplaques and this agreement confirms the validity of the equivalent circuit despite the fact that the current-voltage characteristics of the axons and electroplaques differ profoundly. As for squid axons, the equivalent circuit of the electroplaques has four branches: a capacity and three ionic channels. One of the latter is an invariant leak channel (G(L)) of high conductance. A K channel (G(K)) is fully open at rest, but rapidly undergoes inactivation when the cell is depolarized by more than 40 mv. G(L) and G(K) have a common inside negative emf (E(K)). A Na channel (G(Na)) with an inside positive emf (E(Na)) is closed at rest, but opens transiently upon depolarization.

Animals↗
PubMed1967

Crayfish muscle: permeability to sodium induced by calcium depletion.

Membrane of crayfish muscle fibers becomes selectively permeable to sodium when the calcium concentration of the bathing medium is reduced. Removal of calcium or its reduction below 1 or 2 millimole per liter causes large transient depolarizations up to 70 millivolts in amplitude. They resemble pro longed action potentials and occur only in the presence of sodium. The responses are abolished when tris(hydroxymethyl)aminomethane or lithium is substituted for sodium, and are blocked by tetrodotoxin even in the presence of sodium.

Animals↗
PubMed1967

Crayfish muscle fiber: ionic requirements for depolarizing synaptic electrogenesis.

Presence of sodium in the bathing medium is not essential for the electrically excitable depolarizing electrogenesis of crayfish muscle fibers, production of action potentials being dependent on calcium. The depolarizing electrogenesis of the excitatory synaptic membrane component does require sodium, however, and this ion cannot be replaced by lithium as it can in spike electrogenesis of many cells. Ionophoretic applications of glutamate, which in the presence of sodium depolarize the cell by activating the excitatory synaptic membrane, are without effect in the absence of sodium. Not only is there no depolarization, but the membrane conductance also remains unchanged. Thus, in the absence of inward movement of sodium across the synaptic membrane there is also no outward movement of potassium. Accordingly, it seems that increased conductance for potassium is not an independent process in the synaptic membrane, whereas it is independent of sodium activation in spike electrogenesis. Chloride activation is independent, however; increase in conductance and the electrogenesis of the inhibitory synaptic component are not affected by the absence of sodium. Implications of these findings regarding the structure of differently excitable membrane components are discussed.

Animals↗
PubMed1966

Analysis of depolarizing and hyperpolarizing inactivation responses in gymnotid electroplaques.

In electroplaques of several gymnotid fishes hyperpolarizing or depolarizing currents can evoke all-or-none responses that are due to increase in membrane resistance as much as 10- to 12-fold. During a response the emf of the membrane shifts little, if at all, when the cell either is at its normal resting potential, or is depolarized by increasing external K, and in the case of depolarizing responses when either Cl or an impermeant anion is present. Thus, the increase in resistance is due mainly, or perhaps entirely, to decrease in K permeability, termed depolarizing or hyperpolarizing K inactivation, respectively. In voltage clamp measurements the current-voltage relation shows a negative resistance region. This characteristic accounts for the all-or-none initiation and termination of the responses demonstrable in current clamp experiments. Depolarizing inactivation is initiated and reversed too rapidly to measure with present techniques in cells in high K. Both time courses are slowed in cells studied in normal Ringer's. Once established, the high resistance state is maintained as long as an outward current is applied. Hyperpolarizing inactivation occurs in normal Ringer's or with moderate excess K. Its onset is more rapid with stronger stimuli. During prolonged currents it is not maintained; i.e., there is a secondary increase in conductance. Hyperpolarizing inactivation responses exhibit a long refractory period, presumably because of persistence of this secondary increase in conductance.

Animals↗
PubMed1966

Osmometrically determined characteristics of the cell membrane of squid and lobster giant axons.

Lobster and squid giant nerve fibers respond differently when subjected to osmotic challenges. The axons proper, as distinct from the total (fiber) complex formed by the axon and connective sheath, both behave as "fast" osmometers for changes in the concentration of NaCl, but the maximum degree of swelling in hyposmotic media is by about 60% in lobster and only by 20% in squid. The relative volume intercepts of the van't Hoff relation are about 0.2 for lobster and 0.4 for squid. The sheaths of both axons undergo only small, apparently passive changes in volume. Lobster axons are permeable to Cl, but squid axons are impermeable to this anion. Lobster axons are also permeable to glycerol. The implications of the data as to the nature of volume regulation of cells are discussed.

Animals↗