Jt. Cheng et al., Stimulatory effect of trans-cinnamaldehyde on noradrenaline secretion in guinea-pig ileum myenteric nerve terminals, LIFE SCI, 66(11), 2000, pp. 981-990
The effect of trans-cinnamaldehyde (CNMA) on the release of noradrenaline (
NA)from nerve terminal was investigated using isolated ileal synaptosomes o
f guineapig. Release was determined as the amount of NA, quantified by h.p.
l.c.-electrochemical detection, from samples incubated with CNMA minus that
in parallel blanks treated with same volume of vehicle. CNMA stimulated th
e secretion of NA in a concentration-dependent manner from 5 mu M to 50 mu
M, while the value of lactate dehydrogenase in the incubated medium was not
influenced by CNMA. However, trans-cinnamic acid, cinnamoyl chloride and c
innamamide failed to produce similar effect. Specific action of CNMA can th
us be considered. Guanethidine inhibited the release of NA by CNMA in a con
centration dependent manner. Saxitoxin attenuated the action of CNMA at con
centrations sufficient to block sodium channels. The depolarizing effect of
CNMA on the membrane potential was also illustrated by a concentration-dep
endent increase in the fluorescence of bisoxonol, a potential sensitive dye
. The NA releasing action of CNMA was deleted by removal of calcium chlorid
e from the bathing medium. This action of CNMA was also attenuated by Rp-cA
MP at concentrations sufficient to inhibit the action of cyclic AMP. These
findings suggest that CNMA can depolarize the membrane to result in a calci
um-dependent and cyclic AMP-related release of NA from noradrenergic termin
als.