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. 2003 Jun 9;139(3):575–584. doi: 10.1038/sj.bjp.0705284

Figure 2.

Figure 2

Antagonism of the L-163,255-induced decrease in gCl (upper panel) and gK (lower panel) by [D-Lys-3]-GHRP-6 (GHS-receptor antagonist), staurosporine and chelerythrine (PKC inhibitors) and U73122 (PLC inhibitor) following in vitro application in the EDL muscle fibres of adult rats. The bars show the mean values of gCl and gK (±s.e.m.), from the number of fibres indicated within brackets (two to four rats), recorded in the absence and in the presence of L-163,255 (50 μM) alone and after the addition of L-163,255 to muscle preparations previously incubated for 30 min to 1 h with [D-Lys-3]-GHRP-6 (100 μM), staurosporine (1 μM), chelerythrine (1 μM), or U73122 (10 μM). *Significantly different with respect to the value recorded in the absence of drug (P<0.05 or less).