P. Karoon et al., ENHANCED SYMPATHETIC NEUROTRANSMISSION IN THE TAIL ARTERY OF 1,3-DIPROPYL-8-SULPHOPHENYLXANTHINE (DPSPX)-TREATED RATS, British Journal of Pharmacology, 116(2), 1995, pp. 1918-1922
1 Sympathetic neurotransmission and noradrenaline content of the tail
artery of Wistar rats treated for 7 days with the adenosine antagonist
, 1,3-dipropyl-8-sulphophenylxanthine (DPSPX), were examined. 2 Systol
ic blood pressure of the DPSPX-treated rats (164.0 +/- 2.9 mmHg; n = 6
) was significantly greater than saline-treated controls (140.0 +/- 2.
8 mmHg; n = 5) after 7 days treatment. 3 The presser responses of the
arterial rings to transmural nerve stimulation (65 V, 0.1 ms, 4-64 Hz,
for 1 s) were markedly enhanced in the DPSPX-treated compared with th
e saline-treated animals. Both noradrenergic and purinergic components
of perivascular sympathetic neurotransmission were enhanced during DP
SPX-induced hypertension. 4 Vasoconstrictor responses to exogenous nor
adrenaline (0.1-300 mu M) and adenosine 5'-triphosphate (0.01-3 mM) we
re unaffected after DPSPX treatment, indicating prejunctional alterati
on of sympathetic cotransmission during DPSPX-induced hypertension. 5
Acute exposure to DPSPX (10 mu M) did not modify vasoconstrictor respo
nses to transmural nerve stimulation, thus supporting the claim that t
he enhancement of sympathetic neurotransmission only results from long
-term DPSPX treatment.6 The noradrenaline content of the tail arteries
of DPSPX-treated (4.498 +/- 0.26 ng cm(-1); n = 4) was significantly
greater than saline-treated (3.440 +/- 0.30 ng cm(-1); n = 5) animals.
7 These findings show that chronic inhibition of the actions of endog
enous adenosine by DPSPX results in an elevation of systolic blood pre
ssure accompanied by enhanced sympathetic cotransmission and enhanced
noradrenaline content of the rat tail artery.