Jd. Troadec et al., ATP-EVOKED INCREASES IN [CA2-2X2 PURINOCEPTOR(](I) AND PEPTIDE RELEASE FROM RAT ISOLATED NEUROHYPOPHYSEAL TERMINALS VIA A P), Journal of physiology, 511(1), 1998, pp. 89-103
1. The effect of externally applied ATP on cytosolic free Ca2+ concent
ration ([Ca2+](i)) was tested in single isolated rat neurohypophysial
nerve terminals by fura-2 imaging. The release of vasopressin (AVP) an
d oxytocin (OT) upon ATP stimulation was also studied from a populatio
n of terminals using specific radioimmunoassays. 2. ATP evoked a susta
ined [Ca2+](i) increase, which was dose dependent in the 1-100 mu M ra
nge (EC50 = 4.8 mu M). This effect was observed in only similar to 40%
of the terminals. 3. Interestingly, ATP, in the same range (EC50 = 8.
6 mu M), evoked AVP, but no significant OT, release from these termina
ls. 4. Both the [Ca2+](i) increase and AVP release induced by ATP were
highly and reversibly inhibited by suramin, suggesting the involvemen
t of a P-2 purinergic receptor in the ATP-induced responses. yridoxal-
5-phosphate-6-azophenyl-2',4'-disulphonic acid (PPADS), another P-2 pu
rinergic receptor antagonist, strongly reduced the ATP-induced [Ca2+](
i) response. 5. To further characterize the receptor, different agonis
ts were tested, with the following efficacy: ATP = 2-methylthio-ATP >
ATP-gamma-S > alpha,beta-methylene-ATP > ADP. The compounds adenosine,
AMP, beta,gamma-methylene-ATP and UTP were ineffective. 6. The ATP-de
pendent [Ca2+](i) increase was dependent on extracellular Ca2+ concent
ration ([Ca2+](o)). Fluorescence-quenching experiments with Mn2+ showe
d that externally applied ATP triggered a Mn2+ influx. The ATP-induced
[Ca2+](i) increase and AVP release were independent of and additive t
o a K+-induced response, in addition to being insensitive to Cd2+. The
ATP-induced [Ca2+](i) increase was strongly reduced in the presence o
f Gd3+. These results suggest that the observed [Ca2+](i) increases we
re elicited by Ca2+ entry through a P-2X channel receptor rather than
via a voltage-dependent Ca2+ channel. 7. We propose that ATP, co-relea
sed with neuropeptides, could act as a paracrine-autocrine messenger,
stimulating, via Ca2+ entry through a P-2X2 receptor, the secretion of
AVP, in particular, from neurohypophysial nerve terminals.