Na+ channel and acetylcholine receptor changes in muscle at sites distant from burns do not simulate denervation

Abstract

Nosek, M. T., and J. A. J. Martyn.Na+ channel and acetylcholine receptor changes in muscle at sites distant from burns do not simulate denervation. J. Appl. Physiol. 82(4): 1333–1339, 1997.—Muscle weakness and aberrant responses to neuromuscular relaxants after burn injury are associated with upregulation of acetylcholine receptors (AChRs). Typically, these functional, pharmacological, and biochemical changes occur after denervation, in which transcriptionally mediated qualitative changes in AChRs and Na+ channels and of myogenic regulatory proteins MyoD and myogenin also occur. This study in rats, by an examination of changes in the above-enumerated proteins or their transcripts in the gastrocnemius muscle distant from the burn, verifies whether a denervation-like state exists after burns. Scatchard analysis of [3H]saxitoxin binding revealed no changes in the affinity ( K d) and total number (Bmax) of Na+ channels between control and burn-injured animals at both 7 and 14 days after injury. The mRNA levels of the immature proteins, SkM2 of the Na+ channels and the γ-subunits of AChRs, the increase of which is pathognomic of denervation, were assessed by Northern analysis and were unchanged. The transcripts of mature Na+ channels, SkM1, were significantly increased at day 14after the burn (1.24 ± 0.10 in burn-injured vs. 1.06 ± 0.12 in sham animals, arbitrary units, P= 0.006). Although MyoD levels were increased in burn-injured animals at 14 days (0.21 ± 0.02 vs. 0.15 ± 0.07 arbitrary units, P = 0.05), myogenin levels were unaltered. The absence of changes in AChR transcripts, including α-, δ-, and γ-subunits, indicates that the upregulation of AChR in burns is not transcriptionally mediated. The unaltered levels of transcripts of myogenin, SkM2 of Na+ channels and γ-subunit of AChR, confirm that there is no denervation-like prejunctional (nerve-related) component to explain the muscle weakness or the upregulation of AChRs at sites distant from burns.