Abstract
Azide (0.2 to 5.0 mM) and chloretone (2.0 to 15.0 mM) reversibly inhibited 20 to 90 per cent of the resting respiration of frog sciatic nerves, and caused a loss of potassium and a gain of sodium in this tissue. The changes in ionic contents that developed after 5 or 10 hours were roughly correlated with the degree of respiratory depression, but the time courses of these changes were different with the two reagents. In azide these changes appeared to begin immediately, while in chloretone, at concentrations between 3.0 and 5.0 mM, the ionic shifts developed after a delay of several hours. Fifteen millimolar chloretone produced immediate changes in ionic contents several times greater than those produced by anoxia. The changes in ionic distribution produced in 5 hours by anoxia, 5.0 mM azide, or 5.0 mM chloretone were at least partially reversible; those produced by 15.0 mM chloretone were irreversible. With the exception of 15.0 mM chloretone the ionic shifts produced by these reagents may be due primarily to the depression of the respiration, although there are indications that azide acts, in addition, by another pathway. Concentrations of azide or chloretone that depressed the resting rate of oxygen consumption more than 50 per cent produced a slow conduction block, while 15.0 mM chloretone blocked conduction within 15 minutes.
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Selected References
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- BRINK F., Jr, BRONK D. W., CARLSON F. D., CONNELLY C. M. The oxygen uptake of active axons. Cold Spring Harb Symp Quant Biol. 1952;17:53–67. doi: 10.1101/sqb.1952.017.01.008. [DOI] [PubMed] [Google Scholar]
- CARLSON F. D., BRINK F., Jr, BRONK D. W. A continuous flow respirometer utilizing the oxygen cathode. Rev Sci Instrum. 1950 Nov;21(11):923–932. doi: 10.1063/1.1745465. [DOI] [PubMed] [Google Scholar]
- CHANCE B., WILLIAMS G. R. Respiratory enzymes in oxidative phosphorylation. VI. The effects of adenosine diphosphate on azide-treated mitochondria. J Biol Chem. 1956 Jul;221(1):477–489. [PubMed] [Google Scholar]
- CRESCITELLI F. Nerve sheath as a barrier to the action of certain substances. Am J Physiol. 1951 Aug;166(2):229–240. doi: 10.1152/ajplegacy.1951.166.2.229. [DOI] [PubMed] [Google Scholar]
- DAINTY J., KRNJEVIC K. The rate of exchange of 24Na in cat nerves. J Physiol. 1955 Jun 28;128(3):489–503. doi: 10.1113/jphysiol.1955.sp005320. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DE NO LORENTE R. Observations on the properties of the epineurium of frog nerve. Cold Spring Harb Symp Quant Biol. 1952;17:299–315. doi: 10.1101/sqb.1952.017.01.028. [DOI] [PubMed] [Google Scholar]
- FENN W. O., GERSCHMAN R. The loss of potassium from frog nerves in anoxia and other conditions. J Gen Physiol. 1950 Jan 20;33(3):195–203. doi: 10.1085/jgp.33.3.195. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FITZHUGH R. Effects of azide and electrical polarization on refractory period in frog nerve. J Cell Physiol. 1954 Aug;44(1):117–140. doi: 10.1002/jcp.1030440111. [DOI] [PubMed] [Google Scholar]
- FOULKES E. C. Cation transport in yeast. J Gen Physiol. 1956 May 20;39(5):687–704. doi: 10.1085/jgp.39.5.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FRANKENHAEUSER B., HODGKIN A. L. The after-effects of impulses in the giant nerve fibres of Loligo. J Physiol. 1956 Feb 28;131(2):341–376. doi: 10.1113/jphysiol.1956.sp005467. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GREENGARD P., BRINK F., Jr, COLOWICK S. P. Some relationships between action potential, oxygen consumption and coenzyme content in degenerating peripheral axons. J Cell Physiol. 1954 Dec;44(3):395–420. doi: 10.1002/jcp.1030440304. [DOI] [PubMed] [Google Scholar]
- HUXLEY A. F., STAMPFLI R. Direct determination of membrane resting potential and action potential in single myelinated nerve fibers. J Physiol. 1951 Feb;112(3-4):476–495. doi: 10.1113/jphysiol.1951.sp004545. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KEYNES R. D., MAISEL G. W. The energy requirement for sodium extrusion from a frog muscle. Proc R Soc Lond B Biol Sci. 1954 May 27;142(908):383–392. doi: 10.1098/rspb.1954.0031. [DOI] [PubMed] [Google Scholar]
- KEYNES R. D. The ionic fluxes in frog muscle. Proc R Soc Lond B Biol Sci. 1954 May 27;142(908):359–382. doi: 10.1098/rspb.1954.0030. [DOI] [PubMed] [Google Scholar]
- KRNJEVIC K. Some observations on perfused frog sciatic nerves. J Physiol. 1954 Feb 26;123(2):338–356. doi: 10.1113/jphysiol.1954.sp005055. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LING G., GERARD R. W. The membrane potential and metabolism of muscle fibers. J Cell Physiol. 1949 Dec;34(3):413–438. doi: 10.1002/jcp.1030340307. [DOI] [PubMed] [Google Scholar]
- LOOMIS W. F., LIPMANN F. Inhibition of phosphorylation by azide in kidney homogenate. J Biol Chem. 1949 May;179(1):503–503. [PubMed] [Google Scholar]
- Michaelis M., Quastel J. H. The site of action of narcotics in respiratory processes. Biochem J. 1941 Apr;35(4):518–533. doi: 10.1042/bj0350518. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SHANES A. M., BERMAN M. D. Kinetics of ion movement in the squid giant axon. J Gen Physiol. 1955 Nov 20;39(2):279–300. doi: 10.1085/jgp.39.2.279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SHANES A. M., BERMAN M. D. Penetration of the desheathed toad sciatic nerve by ions and molecules. II. Kinetics. J Cell Physiol. 1955 Apr;45(2):199–240. doi: 10.1002/jcp.1030450205. [DOI] [PubMed] [Google Scholar]
- SHANES A. M. Effects of sheath removal on bullfrog nerve. J Cell Physiol. 1953 Apr;41(2):305–311. doi: 10.1002/jcp.1030410208. [DOI] [PubMed] [Google Scholar]
- SHANES A. M. Factors in nerve functioning. Fed Proc. 1951 Sep;10(3):611–621. [PubMed] [Google Scholar]
- SHANES A. M. Sodium exchange through the epineurium of the bullfrog sciatic. J Cell Physiol. 1954 Feb;43(1):99–105. doi: 10.1002/jcp.1030430108. [DOI] [PubMed] [Google Scholar]