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Adenosine 5′‐triphosphate and neuropeptide Y are co‐transmitters in conjunction with noradrenaline in the human saphenous vein
Author(s) -
Racchi Héctor,
Irarrázabal Manuel J,
Howard Michel,
Morán Sergio,
Zalaquett Ricardo,
HuidobroToro J Pablo
Publication year - 1999
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0702396
Subject(s) - prazosin , medicine , guanethidine , suramin , endocrinology , depolarization , adenosine , tetrodotoxin , purinergic receptor , vasoconstriction , vasomotor , neuropeptide y receptor , chemistry , neuropeptide , antagonist , stimulation , receptor
Human saphenous veins were used to assess the cooperative participation of adenosine 5‐triphosphate (ATP), neuropeptide Y (NPY), and noradrenaline (NA) in the vasomotor responses elicited following electrical depolarization of the perivascular nerve terminals. Rings from recently dissected human biopsies were mounted to record isometric muscular contractions; the motor activity elicited in the circular muscle layer following electrical depolarization (2.5–20 Hz, 50 V, 0.5 msec) were recorded. Incubation of the biopsies with either 100 n M tetrodotoxin (TTX) or 1 μ M guanethidine abolished the vasomotor response elicited by electrical nerve depolarization. The independent application of either ATP or NA to vein rings induced concentration‐dependent contractions. Tissue incubation with 30 μ M suramin or 10 n M prazosin produced 10 fold rightward displacements of the α,β‐methylene ATP and NA concentration‐response curves respectively. NPY contracted a limited number of biopsies, the vasoconstriction elicited was completely blocked by 1 μ M BIBP 3226. A 5 min incubation of the biopsies with 10–100 n M NPY synergized, in a concentration‐dependent fashion, both the ATP and the ATP analogue‐induced contractions. Likewise, tissue preincubation with 10 n M NPY potentiated the vasomotor responses evoked with 20–60 n M NA. Neither suramin, BIBP 3226, nor prazosin was individually able to significantly modify the derived frequency‐tension curves. In contrast, the co‐application of 30 μ M suramin and 10 n M prazosin or 30 μ M suramin and 1 μ M BIBP 3226, elicited a significant ( P <0.01) downward displacement of the respective frequency‐tension curves. The simultaneous application of the three antagonists–30 μ M suramin, 1 μ M BIBP 3226 and 10 n M prazosin–caused a significantly greater displacement of the frequency‐tension curve than that achieved in experiments using two of these antagonists. Electrically‐evoked vasomotor activity is blocked to a larger extent by tissue incubation with 2.5 μ M chloroethylclonidine and 30 μ M suramin rather than with 10 n M 5 methyl urapidil and 30 μ M suramin. As a result, the α 1 ‐adrenoceptor involved in the vasomotor activity has tentatively been associated with the α 1B adrenoceptor family subtype. Results support the physiological role of ATP in sympathetic neurotransmission. The present results are consistent with the working hypothesis that human sympathetic vasomotor reflexes involve the coordinated motor action of ATP, NPY, and NA acting on vascular smooth muscle cells. The present results support the concept of sympathetic co‐transmission in the human saphenous vein.British Journal of Pharmacology (1999) 126 , 1175–1185; doi: 10.1038/sj.bjp.0702396