Biphasic regulation of development of the high-affinity saxitoxin receptor by innervation in rat skeletal muscle

Scott J Sherman, William A. Catterall

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

Specific binding of 3H-saxitoxin (STX) was used to quantitate the density of voltage-sensitive sodium channels in developing rat skeletal muscle. In adult triceps surae, a single class of sites with a KD = 2.9 nM and a density of 21 fmol/mg wet wt was detected. The density of these high-affinity sites increased from 2.0 fmol/mg wet wt to the adult value in linear fashion during days 2-25 after birth. Denervation of the triceps surae at day 11 or 17 reduced final saxitoxin receptor site density to 10.4 or 9.2 fmol/mg wet wt, respectively, without changing KD. Denervation of the triceps surae at day 5 did not alter the subsequent development of saxitoxin receptor sites during days 5-9 and accelerated the increase of saxitoxin receptor sites during days 9-13. After day 13, saxitoxin receptor development abruptly ceased and the density of saxitoxin receptor sites declined to 11 fmol/mg wet wt. These results show that the regulation of high-affinity saxitoxin receptor site density by innervation is biphasic. During the first phase, which is independent of continuing innervation, the saxitoxin receptor density increases to 47-57% of the adult level. After day 11, the second phase of development, which is dependent on continuing innervation, gives rise to the adult density of saxitoxin receptors.

Original languageEnglish (US)
Pages (from-to)753-768
Number of pages16
JournalJournal of General Physiology
Volume80
Issue number5
DOIs
StatePublished - Nov 1 1982
Externally publishedYes

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Saxitoxin
Skeletal Muscle
Denervation
Sodium Channels
Parturition

ASJC Scopus subject areas

  • Physiology

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Biphasic regulation of development of the high-affinity saxitoxin receptor by innervation in rat skeletal muscle. / Sherman, Scott J; Catterall, William A.

In: Journal of General Physiology, Vol. 80, No. 5, 01.11.1982, p. 753-768.

Research output: Contribution to journalArticle

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