Effects of Redox and Sulfhydryl Reagents on the Bioelectric Properties of the Giant Axon of the Squid

• Published in: Biophysical journal 1966-09, Vol.6 (5), p.675-689
• Main Authors: Huneeus-Cox, F., Fernandez, H.L., Smith, B.H.
• Format: Article
• Language: English
• Subjects: Action Potentials; Animals; Axons - drug effects; Axons - physiology; Benzoates - pharmacology; Cell Membrane - drug effects; Cysteine - pharmacology; Electric Stimulation; Electrophysiology; Hydrazines - pharmacology; Mercaptoethanol - pharmacology; Mercury - pharmacology; Mollusca; Oxidation-Reduction; Sulfhydryl Compounds - pharmacology
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/S0006-3495(66)86686-9

The effects of internally and externally applied sulfhydryl reagents on the bioelectric properties of the giant axon of the squid Loligo pealeii and Dosidicus gigas were studied. Cysteine-HCl (400 mM, pH 7.3) was used to remove axoplasm from the perfusion channel. Oxidizing agents (1 to 60 mM) tended to increase the duration of the action potential and had a slow, irreversible blocking effect when perfused internally; the membrane potential was little affected. Reducing agents applied internally caused a decrease in the spike duration without affecting its height or the membrane potential, although at high concentrations there was reversible deterioration of the action potential. Both external and internal perfusion of mercaptide-forming reagents caused deterioration in the action and membrane potentials with conduction block occurring in 5 to 45 min. 2-mercaptoethanol reversed the effects. Thiol alkylating reagents, iodoacetate and iodoacetamide, were without effect. N-ethylmaleimide did, however, block. Tests with chelating agents for nonheme iron in the membrane brought about no change in the electrical parameters. The implications of the present findings with regard to the macromolecular mechanism of excitation are discussed.