Abstract
1. The ionic requirements of the somatic and axonal action potentials of `H' neurones of the snail Cryptomphallus aspersa were studied using intracellular micro-electrodes.
2. The overshoot of the somatic action potential increased by 10 mV for a tenfold increase in [Ca2+]o. In calcium-free media the action potential decreased gradually to values of 50 to 90% of the control and they could be completely eliminated with 2 mM-EGTA. The maximum rate of rise also varied with [Ca2+]o.
3. After 2 hr in sodium-free solution the somatic action potential decreased 6% in overshoot and 24% in rate of rise.
4. The somatic action potential was not affected by TTX, 5 × 10-6 g/ml. Procaine, 18 mM, reduced its rate of rise but did not eliminate it whereas 30 mM-CoCl2 did.
5. The size of the axonal action potential increased with increased [Na+]o, but decreased with an increase in [Ca2+]o.
6. Procaine, 18 mM, abolished the axonal action potential whereas it was not affected by TTX, 5 × 10-6 g/ml., nor, usually, by 30 mM-CoCl2.
7. The results obtained by studying the compound action potential of the nerves were similar to those from axonal action potentials.
8. The possibility that the somatic action potential is mainly calcium dependent while the axonal action potential is mainly produced by sodium is discussed.
Full text
PDF














Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- ABBOTT B. C., PARNAS I. ELECTRICAL AND MECHANICAL RESPONSES IN DEEP ABDOMINAL EXTENSOR MUSCLES OF CRAYFISH AND LOBSTER. J Gen Physiol. 1965 May;48:919–931. doi: 10.1085/jgp.48.5.919. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BULBRING E., KURIYAMA H. Effects of changes in the external sodium and calcium concentrations on spontaneous electrical activity in smooth muscle of guinea-pig taenia coli. J Physiol. 1963 Apr;166:29–58. doi: 10.1113/jphysiol.1963.sp007089. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FATT P., GINSBORG B. L. The ionic requirements for the production of action potentials in crustacean muscle fibres. J Physiol. 1958 Aug 6;142(3):516–543. doi: 10.1113/jphysiol.1958.sp006034. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GERASIMOV V. D. VLIIANIE IZMENENI I INONNOGO SOSTAVA SREDY NA PROTSESSY VOZBUZHDENIIA GIGANTSKIKH NERVNYKH KLETOK ULITKI. Fiziol Zh SSSR Im I M Sechenova. 1964 Apr;50:457–463. [PubMed] [Google Scholar]
- HAGIWARA S., NAKA K. I. THE INITIATION OF SPIKE POTENTIAL IN BARNACLE MUSCLE FIBERS UNDER LOW INTRACELLULAR CA++. J Gen Physiol. 1964 Sep;48:141–162. doi: 10.1085/jgp.48.1.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagiwara S., Nakajima S. Differences in Na and Ca spikes as examined by application of tetrodotoxin, procaine, and manganese ions. J Gen Physiol. 1966 Mar;49(4):793–806. doi: 10.1085/jgp.49.4.793. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagiwara S., Takahashi K. Surface density of calcium ions and calcium spikes in the barnacle muscle fiber membrane. J Gen Physiol. 1967 Jan;50(3):583–601. doi: 10.1085/jgp.50.3.583. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Iwasaki S., Satow Y. Sodium- and calcium-dependent spike potentials in the secretory neuron soma of the X-organ of the crayfish. J Gen Physiol. 1971 Feb;57(2):216–236. doi: 10.1085/jgp.57.2.216. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kao C. Y. Tetrodotoxin, saxitoxin and their significance in the study of excitation phenomena. Pharmacol Rev. 1966 Jun;18(2):997–1049. [PubMed] [Google Scholar]
- Koketsu K., Nishi S. Calcium spikes of nerve cell membrane: role of calcium in the production of action potentials. Nature. 1968 Feb 3;217(5127):468–469. doi: 10.1038/217468b0. [DOI] [PubMed] [Google Scholar]
- Krishtal O. A., Magura I. S. Calcium ions as inward current carriers in mollusc neurones. Comp Biochem Physiol. 1970 Aug 15;35(4):857–866. doi: 10.1016/0010-406x(70)90080-0. [DOI] [PubMed] [Google Scholar]
- Meves H. The ionic requirements for the production of action potentials in helix pomatia neurones. Pflugers Arch. 1968;304(3):215–241. doi: 10.1007/BF00592126. [DOI] [PubMed] [Google Scholar]
- Moreton R. B. Ionic mechanism of the action potentials of giant neurones of Helix aspersa. Nature. 1968 Jul 6;219(5149):70–71. doi: 10.1038/219070a0. [DOI] [PubMed] [Google Scholar]
- NARAHASHI T., MOORE J. W., SCOTT W. R. TETRODOTOXIN BLOCKAGE OF SODIUM CONDUCTANCE INCREASE IN LOBSTER GIANT AXONS. J Gen Physiol. 1964 May;47:965–974. doi: 10.1085/jgp.47.5.965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakamura Y., Nakajima S., Grundfest H. The action of tetrodotoxin on electrogenic components of squid giant axons. J Gen Physiol. 1965 Jul;48(6):975–996. [PubMed] [Google Scholar]
- Niedergerke R., Orkand R. K. The dependence of the action potential of the frog's heart on the external and intracellular sodium concentration. J Physiol. 1966 May;184(2):312–334. doi: 10.1113/jphysiol.1966.sp007917. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Niedergerke R., Orkand R. K. The dual effect of calcium on the action potential of the frog's heart. J Physiol. 1966 May;184(2):291–311. doi: 10.1113/jphysiol.1966.sp007916. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozeki M., Freeman A. R., Grundfest H. The membrane components of crustacean neuromuscular systems. I. Immunity of different electrogenic components to tetrodotoxin and saxitoxin. J Gen Physiol. 1966 Jul;49(6):1319–1334. doi: 10.1085/jgp.0491319. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TAUC L., GERSCHENFELD H. M. Cholinergic transmission mechanisms for both excitation and inhibition in molluscan central synapses. Nature. 1961 Oct 28;192:366–367. doi: 10.1038/192366a0. [DOI] [PubMed] [Google Scholar]
- TAUC L., HUGHES G. M. Modes of initiation and propagation of spikes in the branching axons of molluscan central neurons. J Gen Physiol. 1963 Jan;46:533–549. doi: 10.1085/jgp.46.3.533. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TAUC L. Site of origin and propagation in spike in the giant neuron of Aplysia. J Gen Physiol. 1962 Jul;45:1077–1097. doi: 10.1085/jgp.45.6.1077. [DOI] [PMC free article] [PubMed] [Google Scholar]
