Augmented sensory‐motor vasodilatation of the rat mesenteric arterial bed after chronic infusion of the P1‐purinoceptor antagonist, DPSPX

1 . The effect of long‐term antagonism of P1‐purinoceptors on vascular function was examined in the perfused mesenteric arterial bed isolated from rats which had received constant infusion of either the non‐selective P1‐purinoceptor antagonist, 1–3‐dipropyl‐8‐sulphophenylxanthine (DPSPX, 30 μg kg−1 h−1, i.p.) or saline for seven days. Sympathetic and sensory‐motor neurotransmission, smooth muscle and endothelial function were assessed. 2 . Basal tone was similar in mesenteric arterial preparations from control and DPSPX‐treated rats. Continuous perfusion with methoxamine (7–70 μm) induced similar increases in tone in control and DPSPX‐treated preparations. In the presence of guanethidine (5 μm), electrical field stimulation (EFS; 1–12 Hz, 60V, 0.1 ms, 30 s) elicited frequency‐dependent vasodilatation due to activation of sensory‐motor nerves. In tissues from DPSPX‐treated rats the nerve‐mediated vasodilator responses were markedly augmented at all frequencies. Maximal relaxation at 8 Hz was 38.34 ± 4.76% (n = 5) in controls and 65.92 ± 3.68% (n = 5) after DPSPX‐treatment (P < 0.01). Adenosine (3 μm) inhibited the frequency‐dependent sensory‐motor neurotransmission similarly in preparations from controls and DPSPX‐treated rats. 3 . In raised‐tone preparations calcitonin gene‐related peptide (CGRP; 5, 15 and 50 pmol), the principal vasodilator transmitter of sensory‐motor nerves in rat mesenteric arteries, produced similar relaxations in control and DPSPX‐treated preparations. Vasodilator responses to the sensory neurotoxin capsaicin (50 and 500 pmol) were also similar between the groups. 4 . Assay of tissue CGRP levels of the superior mesenteric artery by enzyme‐linked immunosorbent assay showed no significant difference in tissue levels of CGRP in controls, 120.25 ± 26.34 pmol g−1 tissue (n = 6) and with DPSPX‐treatment, 82.12 ± 24.42 pmol g−1 tissue (n = 6). 5 . In raised‐tone preparations dose‐dependent endothelium‐dependent vasodilatation to acetylcholine and ATP, and endothelium‐independent vasodilatation to sodium nitroprusside were similar in control and DPSPX‐treated preparations. 6 . EFS (4–32 Hz, 90V, 1 ms, 30 s) elicited frequency‐dependent vasoconstriction due to activation of sympathetic nerves which was similar in controls and in DPSPX‐treated preparations. Adenosine (10 and 30 μm) inhibited sympathetic neurotransmission similarly in control and DPSPX‐treated preparations. Dose‐dependent vasoconstriction to noradrenaline (NA) and ATP, and to KC1 (0.15 mmol) was similar between the groups. 7 . High performance liquid chromatographic analysis of tissue NA showed no significant difference in NA content of the superior mesenteric artery from DPSPX‐treated (1.38 ± 0.09 ng mg−1, n = 6) and control rats (1.46 ± 0.17 ng mg−1, n = 6). 8 . In conclusion, in rats with hypertension due to 7 days treatment with the P1‐purinoceptor antagonist, DPSPX, there is an increase in sensory‐motor vasodilatation of the mesenteric arterial bed. There is no change in sympathetic nerve, endothelial or smooth muscle function. Augmented sensory‐motor neurotransmission, which does not involve a change in postjunctional responsiveness to CGRP or in the CGRP content of sensory‐motor nerves, could be a compensatory change in response to the DPSPX‐induced hypertension.

[1]  G. Burnstock,et al.  Changes in sympathetic neurotransmission and adrenergic control of cardiac contractility during 1,3-dipropyl-8-sulfophenylxanthine-induced hypertension. , 1995, The Journal of pharmacology and experimental therapeutics.

[2]  G. Burnstock,et al.  Enhanced sympathetic neurotransmission in the tail artery of 1,3‐dipropyl‐8‐sulphophenylxanthine (DPSPX)‐treated rats , 1995, British journal of pharmacology.

[3]  G. Burnstock,et al.  Long-term sensory denervation by neonatal capsaicin treatment augments sympathetic neurotransmission in rat mesenteric arteries by increasing levels of norepinephrine and selectively enhancing postjunctional actions. , 1995, The Journal of pharmacology and experimental therapeutics.

[4]  A. Albino-Teixeira,et al.  Hypertension and enhanced β‐adrenoceptor‐mediated facilitation of noradrenaline release produced by chronic blockade of adenosine receptors , 1995, British journal of pharmacology.

[5]  G. Burnstock,et al.  The P1-purinoceptors that mediate the prejunctional inhibitory effect of adenosine on capsaicin-sensitive nonadrenergic noncholinergic neurotransmission in the rat mesenteric arterial bed are of the A1 subtype. , 1993, The Journal of pharmacology and experimental therapeutics.

[6]  M. Lohse,et al.  Adenosine A1 receptor gene structure and regulation in normotensive and spontaneously hypertensive rats. , 1992, European journal of pharmacology.

[7]  I. Azevedo,et al.  Does adenosine malfunction play a role in hypertension? , 1992, Pharmacological research.

[8]  R. Panek,et al.  Evidence for a functional tissue renin-angiotensin system in the rat mesenteric vasculature and its involvement in regulating blood pressure. , 1991, The Journal of pharmacology and experimental therapeutics.

[9]  A. Albino-Teixeira,et al.  Long-term administration of 1,3-dipropyl-8-sulfophenylxanthine causes arterial hypertension. , 1991, European journal of pharmacology.

[10]  W. Osswald Mediation by adenosine of the trophic effects exerted by the sympathetic innervation of blood vessels. , 1991, Journal of neural transmission. Supplementum.

[11]  A. Saito,et al.  Age-related decrease of calcitonin gene-related peptide-containing vasodilator innervation in the mesenteric resistance vessel of the spontaneously hypertensive rat. , 1990, Circulation research.

[12]  A. Saito,et al.  Changes in calcitonin gene-related peptide (CGRP)-containing vasodilator nerve activity in hypertension , 1990, Brain Research.

[13]  T. Westfall,et al.  Inhibition of periarterial nerve stimulation-induced vasodilation of the mesenteric arterial bed by CGRP (8-37) and CGRP receptor desensitization. , 1990, Biochemical and biophysical research communications.

[14]  A. Albino-Teixeira,et al.  Purine agonists prevent trophic changes caused by sympathetic denervation. , 1990, European journal of pharmacology.

[15]  R. M. Lee,et al.  Increased sympathetic innervation in the cerebral and mesenteric arteries of hypertensive rats. , 1990, Canadian journal of physiology and pharmacology.

[16]  G. Burnstock The fifth Heymans memorial lecture-Ghent, February 17, 1990. Co-transmission. , 1990, Archives internationales de pharmacodynamie et de therapie.

[17]  H. Nilsson,et al.  Transmitter characteristics of small mesenteric arteries from the rat. , 1990, Acta physiologica Scandinavica.

[18]  T. Lüscher,et al.  Impaired endothelium-dependent relaxations in hypertensive resistance arteries involve cyclooxygenase pathway. , 1990, The American journal of physiology.

[19]  A. Saito,et al.  Adrenergic modulation of calcitonin gene-related peptide (CGRP)-containing nerve-mediated vasodilation in the rat mesenteric resistance vessel , 1990, Brain Research.

[20]  J. de Champlain Pre- and postsynaptic adrenergic dysfunctions in hypertension. , 1990, Journal of hypertension. Supplement : official journal of the International Society of Hypertension.

[21]  E. Jackson,et al.  Adenosine-angiotensin II interactions. Part I. Role of adenosine in regulating angiotensin II-induced potentiation of noradrenergic neurotransmission and angiotensin II-induced vasoconstriction. , 1989, The Journal of pharmacology and experimental therapeutics.

[22]  R. Head Hypernoradrenergic innervation: its relationship to functional and hyperplastic changes in the vasculature of the spontaneously hypertensive rat. , 1989, Blood vessels.

[23]  G. Burnstock,et al.  Progressive changes in adrenergic, serotonergic, and peptidergic nerves in proximal colon of streptozotocin-diabetic rats. , 1988, Gastroenterology.

[24]  K. Goto,et al.  Calcitonin gene-related peptide acts as a novel vasodilator neurotransmitter in mesenteric resistance vessels of the rat , 1988, Nature.

[25]  E. Daniel,et al.  Peptide‐Containing Nerves Around Blood Vessels of Stroke‐Prone Spontaneously Hypertensive Rats , 1988, Hypertension.

[26]  C. Maggi,et al.  The sensory-efferent function of capsaicin-sensitive sensory neurons. , 1988, General pharmacology.

[27]  E. Jackson Role of adenosine in noradrenergic neurotransmission in spontaneously hypertensive rats. , 1987, The American journal of physiology.

[28]  R. Yamamoto,et al.  Is presynaptic modulation of norepinephrine release altered in the mesenteric vasculature of adult spontaneously hypertensive rats? , 1987, Blood vessels.

[29]  R. Stitzel,et al.  Perfusion of the intact and partially isolated rat mesenteric vascular bed: application to vessels from hypertensive and normotensive rats. , 1986, Blood vessels.

[30]  T. Westfall,et al.  Effect of low sodium diet on the facilitatory effect of angiotensin on 3H-norepinephrine release in the rat portal vein. , 1985, Blood vessels.

[31]  C. Su,et al.  Involvement of the vascular renin-angiotensin system in beta adrenergic receptor-mediated facilitation of vascular neurotransmission in spontaneously hypertensive rats. , 1984, The Journal of pharmacology and experimental therapeutics.

[32]  T. Scott,et al.  The correlation between the development of sympathetic innervation and the development of medial hypertrophy in jejunal arteries in normotensive and spontaneously hypertensive rats. , 1983, Journal of the autonomic nervous system.

[33]  B. Zimmerman Adrenergic facilitation by angiotensin: does it serve a physiological function? , 1981, Clinical science.