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Vol. 286, Issue 3, 1183-1190, September 1998
Unit of Pharmacology, Department of Pharmacobiology (S.P.,
A.D.L., D.C.C.), Faculty of Pharmacy, University of Bari, Bari, Italy
and
Department of Pharmacology (C.C., R.J.H.), College of Medicine,
University of Arizona, Tucson, Arizona
A reduction of resting chloride conductance (GCl) and a decrease of the
voltage threshold for contraction are observed during aging in rat
skeletal muscle. The above alterations are also observed in muscle of
adult rat after taurine depletion. As lower levels of taurine were
found by others in aged rats compared to young rats, we tested the
hypothesis that a depletion of taurine may contribute to the alteration
of the electrical and contractile properties we found in skeletal
muscle during aging. This was accomplished by evaluating the potential
benefit of a pharmacological treatment with the amino acid. To this aim
25-mo-old Wistar rats were chronically treated (2-3 mo) with taurine
(1 g/kg p.o. daily) and the effects of such a treatment were evaluated
in vitro on the passive and active membrane electrical
properties of extensor digitorum longus muscle fibers by means of
current-clamp intracellular microelectrode technique.
Excitation-contraction coupling was also evaluated by measuring the
voltage threshold for contraction with the intracellular microelectrode
"point" voltage clamp method. In parallel muscle and blood taurine
contents were determined by high-performance liquid chromatography.
Taurine supplementation significantly raised taurine content in muscle
toward that found in adult rats. Supplementation also significantly
increased GCl vs. the adult value, in parallel the
excitability characteristics (threshold current and latency) related to
this parameter were ameliorated. The increase of GCl induced by taurine
was accompanied by a restoration of the pharmacological sensitivity to
the R(+) enantiomer of 2-(p-chlorophenoxy) propionic acid, a specific
chloride channel ligand. In parallel also the protein kinase C-mediated modulation of the channel was restored; in fact the potency of 4-
-phorbol 12,13-dibutyrate in reducing GCl was lower in
taurine-treated muscles vs. untreated aged, being rather
similar to that observed in adult. The treatment also improved the
mechanical threshold for contraction of striated fibers which in aged
rats is shifted toward more negative potentials, moving it toward the
adult values. Our results suggest that the reduction of taurine content
could play a role in the alteration of electrical and contractile
properties observed during aging. These findings may indicate a
potential application of taurine in ensuring normal muscle function in
the elderly.
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