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Provedor de dados:  BJMBR
País:  Brazil
Título:  Antagonism by hemoglobin of effects induced by L-arginine in neuromuscular preparations from rats
Autores:  Ambiel,C.R.
Alves-Do-Prado,Wilson
Data:  2001-04-01
Ano:  2001
Palavras-chave:  Skeletal muscle
Nitric oxide
Tetanic fade
L-arginine
D-arginine
Hemoglobin
Resumo:  Nitric oxide (NO)-synthase is present in diaphragm, phrenic nerve and vascular smooth muscle. It has been shown that the NO precursor L-arginine (L-Arg) at the presynaptic level increases the amplitude of muscular contraction (AMC) and induces tetanic fade when the muscle is indirectly stimulated at low and high frequencies, respectively. However, the precursor in muscle reduces AMC and maximal tetanic fade when the preparations are stimulated directly. In the present study the importance of NO synthesized in different tissues for the L-Arg-induced neuromuscular effects was investigated. Hemoglobin (50 nM) did not produce any neuromuscular effect, but antagonized the increase in AMC and tetanic fade induced by L-Arg (9.4 mM) in rat phrenic nerve-diaphragm preparations. D-Arg (9.4 mM) did not produce any effect when preparations were stimulated indirectly at low or high frequency. Hemoglobin did not inhibit the decrease of AMC or the reduction in maximal tetanic tension induced by L-Arg in preparations previously paralyzed with d-tubocurarine and directly stimulated. Since only the presynaptic effects induced by L-Arg were antagonized by hemoglobin, the present results suggest that NO synthesized in muscle acts on nerve and skeletal muscle. Nevertheless, NO produced in nerve and vascular smooth muscle does not seem to act on skeletal muscle.
Tipo:  Info:eu-repo/semantics/other
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2001000400017
Editor:  Associação Brasileira de Divulgação Científica
Relação:  10.1590/S0100-879X2001000400017
Formato:  text/html
Fonte:  Brazilian Journal of Medical and Biological Research v.34 n.4 2001
Direitos:  info:eu-repo/semantics/openAccess
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