Abstract
Lobster muscle fibers develop hyperpolarizing responses when subjected to sufficiently strong hyperpolarizing currents. In contrast to axons of frog, toad, and squid, the muscle fibers produce their responses without the need for prior depolarization in high external K(+). Responses begin at a threshold polarization (50 to 70 mv), the potential reaching 150 to 200 mv hyperpolarization while the current remains constant. The increased polarization develops at first slowly, then becomes rapid. It usually subsides from its peak spontaneously, falling temporarily to a potential less hyperpolarized than at threshold for the response. As long as current is applied there can be oscillatory behavior with sequential rise and subsidence of the polarization, repeating a number of times. Withdrawal of current leads to rapid return of the potential to the resting level and a small, brief depolarization. Associated with the latter, but of longer duration, is an increased conductance whose magnitude and duration increase with the antecedent current. Hyperpolarizing responses of lobster muscle fibers are due to increased membrane resistance caused by hyperpolarizing K inactivation. The oscillatory characteristic of the response is due to a delayed superimposed and prolonged increase in membrane permeability, probably for Na(+) and for either K(+) or Cl(-). The hyperpolarizing responses of other tissues also appear to result from hyperpolarizing K inactivation, on which is superimposed an increased conductance for some other ion or ions.
Keywords
CRUSTACEA
IONS
MUSCLES/physiology
MeSH Terms
Animals
Crustacea
Ions
Muscles/physiology
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
REUBEN J P
WERMAN R
GRUNDFEST H
References (16)
16 references, click to expand
-
Graded and all-or-none electrogenesis in arthropod muscle. II. The effects of alkali-earth and onium ions on lobster muscle fibers.
J Gen Physiol. 1961 May;44:997-1027
PMID: 13784437
-
The mechanisms of discharge of the electric organs in relation to general and comparative electrophysiology.
Prog Biophys Biophys Chem. 1957;7:1-85
PMID: 13485186
-
Electrical inexcitability of synapses and some consequences in the central nervous system.
Physiol Rev. 1957 Jul;37(3):337-61
PMID: 13465318
-
Demonstration of two stable states of the nerve membrane in potassium-rich media.
J Physiol. 1959 Oct;148:306-31
PMID: 13836983
-
An analysis of the end-plate potential recorded with an intracellular electrode.
J Physiol. 1951 Nov 28;115(3):320-70
PMID: 14898516
-
Excitation of the squid axon membrane in isosmotic potassium chloride.
Nature. 1959 Jan 24;183(4656):265-6
PMID: 13622770
-
Potassium chloride movement and the membrane potential of frog muscle.
J Physiol. 1960 Apr;151:154-85
PMID: 13791936
-
Ionic mechanisms in electrogenesis.
Ann N Y Acad Sci. 1961 Sep 6;94:405-57
PMID: 13709244
-
Electrophysiology of supramedullary neurons in Spheroides maculatus. I. Orthodromic and antidromic responses.
J Gen Physiol. 1959 Sep;43:159-88
PMID: 13798948
-
The electrical activity of spinal ganglion cells investigated with intracellular microelectrodes.
Jpn J Physiol. 1957 Dec 20;7(4):297-323
PMID: 13501950
-
Resting and action potentials in single nerve fibres.
J Physiol. 1945 Oct 15;104(2):176-95
PMID: 16991677
-
A quantitative description of membrane current and its application to conduction and excitation in nerve.
J Physiol. 1952 Aug;117(4):500-44
PMID: 12991237
-
The electrophysiology and pharmacology of lobster neuromuscular synapses.
J Gen Physiol. 1959 Jul 20;42(6):1301-23
PMID: 13664927
-
Electrophysiology of electric organ in Gymnotus carapo.
J Gen Physiol. 1959 May 20;42(5):1067-104
PMID: 13654750
-
Membrane potentials of the squid giant axon recorded with an inserted antimony microelectrode.
Experientia. 1957 Apr 15;13(4):140-1
PMID: 13447895
-
Nerve excitiation and synaptic transmission.
Annu Rev Physiol. 1960;22:407-32
PMID: 13833517