Whether or not in vivo acne transfer of gastrin gene into skeletal muscle b
y electroporation could modify gastrin secretion was examined. The expressi
on plasmid vector, either pMEPrGaspA encoding the rat gastrin acne or pEGFP
-N1 encoding the GFP reporter gene was injected into M. rectus abdominis bf
rats or M. biceps formis of mice. Subsequently, square electric pulses of
direct current were applied six times at 25 V with a loading period of 100
msec per pulse. Clear foreign gene expression in the skeletal muscle was de
monstrated by. both GFP fluorescence and immunostaining of rat gastrin. Tim
e course changes in plasma gastrin levels after transfection revealed that
in rats, gastrin gene transfer significantly increased the plasma gastrin l
evel for 4 weeks post-transfection (P<0.05), but the difference diminished
at the end of the 10-week period. In mice, plasma gastrin level elevated si
milarly for 3 weeks, and pH of gastric contents decreased in the gastrin ge
ne transfected group compared with the control counterpart (P<0.05). These
findings suggest that localized in vivo gene transfer by electroporation al
lows skeletal muscle to become an artificial endocrine tissue for hormonal
manipulation of animals.