The action of arginine-specific reagents on ionic and gating currents in frog myelinated nerve
- PMID: 2456783
- DOI: 10.1016/0005-2736(88)90340-9
The action of arginine-specific reagents on ionic and gating currents in frog myelinated nerve
Abstract
(1) The effect of arginine-specific reagents on the sodium current (INa), potassium current (IK) and gating current (Igat) of myelinated nerve fibres was investigated. (2) Externally applied camphorquinone-10-sulfonic acid (Cqs-OH) had little effect, but 50 mM Cqs-OH applied to the cut ends of the fibre progressively reduced the amplitude of INa without significantly altering its time course. After 30 min INa was reduced to 52% (pH 9.0) or 66% (pH 6.75-7.6) of the control value. IK was decreased to a similar extent without changing its kinetics. Igat was less affected than the ionic currents. (3) Externally applied phenylglyoxal markedly reduced INa and Igat, but many fibres were lost during or shortly after the treatment. A few min treatment with 5 mM phenylglyoxal at pH 9 reduced INa to 20% and the on-response of Igat to 69.5%. The effect was to a large extent irreversible. (4) External nitrophenylglyoxal and hydroxyphenylglyoxal significantly reduced INa and were less damaging than phenylglyoxal. INa was decreased to 34.5% by 10 mM nitrophenylglyoxal and to 28.3% by 20 mM hydroxyphenylglyoxal. The effect of nitrophenylglyoxal was little reversible, but that of hydroxyphenylglyoxal to a large extent reversible. 20 mM hydroxyphenylglyoxal reduced the on-response of Igat to 62.5% of the control value, i.e. much less than INa. (5) 5 mM phenylglyoxal, 10 mM nitrophenylglyoxal and 20 mM hydroxyphenylglyoxal shifted the steady-state inactivation curve by 10-15 mV to more negative values of membrane potential but did not affect the descending branch of the INa(E) curve. (6) 20-30 mM glyoxal, 20 mM 1,2-cyclohexanedione and 10 mM 4-hydroxy-3-nitrophenylglyoxal had no effect on INa. (7) The results are compatible with the idea that arginine residues are principal components of the sodium channel macromolecule.
Similar articles
-
The effect of phenylglyoxal on contraction and intramembrane charge movement in frog skeletal muscle.J Physiol. 1990 Feb;421:441-62. doi: 10.1113/jphysiol.1990.sp017954. J Physiol. 1990. PMID: 2348398 Free PMC article.
-
Blocking and modifying actions of octanol on Na channels in frog myelinated nerve.Pflugers Arch. 1985 Oct;405(3):180-7. doi: 10.1007/BF00582558. Pflugers Arch. 1985. PMID: 2415915
-
Carticaine: action of the local anesthetic on myelinated nerve fibres.Eur J Pharmacol. 1980 Mar 7;62(1):73-9. doi: 10.1016/0014-2999(80)90482-3. Eur J Pharmacol. 1980. PMID: 6245896
-
Voltage-dependent conductances of solitary ganglion cells dissociated from the rat retina.J Physiol. 1987 Apr;385:361-91. doi: 10.1113/jphysiol.1987.sp016497. J Physiol. 1987. PMID: 2443669 Free PMC article. Review.
-
Arginyl residues and anion binding sites in proteins.Mol Cell Biochem. 1979 Jul 31;26(2):71-92. doi: 10.1007/BF00232886. Mol Cell Biochem. 1979. PMID: 388184 Review.
Cited by
-
The effect of phenylglyoxal on contraction and intramembrane charge movement in frog skeletal muscle.J Physiol. 1990 Feb;421:441-62. doi: 10.1113/jphysiol.1990.sp017954. J Physiol. 1990. PMID: 2348398 Free PMC article.
-
Structural and developmental differences between three types of Na channels in dorsal root ganglion cells of newborn rats.J Membr Biol. 1990 Jun;116(2):117-28. doi: 10.1007/BF01868670. J Membr Biol. 1990. PMID: 2166163
-
Nifedipine-sensitive intramembrane charge movement in Purkinje cells from mouse cerebellum.J Physiol. 1996 Jan 15;490 ( Pt 2)(Pt 2):363-72. doi: 10.1113/jphysiol.1996.sp021150. J Physiol. 1996. PMID: 8821135 Free PMC article.
-
Effects of sulfhydryl inhibitors on nonlinear membrane currents in frog skeletal muscle fibers.J Gen Physiol. 1993 Mar;101(3):425-51. doi: 10.1085/jgp.101.3.425. J Gen Physiol. 1993. PMID: 7682597 Free PMC article.
-
Divalent cation competition with [3H]saxitoxin binding to tetrodotoxin-resistant and -sensitive sodium channels. A two-site structural model of ion/toxin interaction.J Gen Physiol. 1993 Feb;101(2):153-82. doi: 10.1085/jgp.101.2.153. J Gen Physiol. 1993. PMID: 8384241 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources