Skip to main content
Log in

Identification of the neuroeffector transmitter in jejunal branches of the rabbit mesenteric artery

  • Published:
Naunyn-Schmiedeberg's Archives of Pharmacology Aims and scope Submit manuscript

Summary

Vasoconstriction or excitatory junction potentials (e.j.ps) evoked by nerve stimulation (15 field pulses at 2 Hz every 3 min) were recorded in rabbit isolated jejunal arteries. The resting diameter of the arteries and its decrease in response to stimulation was measured by a photoelectric method. Vasoconstriction was insensitive to prazosin 0.1 or 1 μmol/l. Yohimbine 1 μmol/l considerably enhanced, whereas α,β-methylene ATP (α,β-meATP) 1 μmol/l abolished the contractile response. In order to test the effect of exogenously applied transmitter candidates, noradrenaline (0.1–1 μmol/l) and ATP (10–30 μmol/l) were added in concentrations which evoked a vasoconstriction comparable to that induced by electrical stimulation. The action of noradrenaline was prevented by prazosin 0.1 μmol/l, but was unaffected by both yohimbine 1 μmol/l and α,β-meATP 1 μmol/l. α,β-meATP 1 μmol/l depressed the effect of ATP. The e.j.ps evoked by a train of 15 pulses showed facilitation up to the third response and thereafter depression; a partial summation was also observed. Prazosin 0.1 μmol/l did not change the e j.p. amplitudes. By contrast, when yohimbine 0.1 or 1 μmol/l was added to the prazosin-containing medium, both the late e j.ps in the train and the summation were enhanced in a concentration-dependent manner. α,β-meATP 1 μmol/l almost abolished the e.j.ps. In conclusion, in rabbit jejunal arteries, stimulation of postganglionic sympathetic nerves may release noradrenaline together with ATP which is probably the sole neuroeffector transmitter under our conditions. Transmitter release seems to be modulated by the activation of presynaptic α2-adrenoceptors. Under the stimulation conditions of the present experiments the released transmitter does not activate postsynaptic α1-adrenoceptors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Burnstock G, Kennedy C (1985) Is there a basis for distinguishing two types of P2-purinoceptor? Gen Pharmacol 16:433–440

    Article  CAS  PubMed  Google Scholar 

  • Burnstock G, Warland JJI (1987a) A pharmacological study of the rabbit saphenous artery in vitro: a vessel with a large purinergic contractile response to sympathetic nerve stimulation. Br J Pharmacol 90:111–120

    Google Scholar 

  • Burnstock G, Warland JJI (1987b) P2-purinoceptors of two subtypes in the rabbit mesenteric artery: reactive blue 2 selectively inhibits responses mediated via the P2y but not the P2x purinoceptor. Br J Pharmacol 90:383–391

    Google Scholar 

  • Byrne NG, Large WA (1986) The effect of α,β-methylene ATP on the depolarization evoked by noradrenaline (γ-adrenoceptor response) and ATP in the immature rat basilar artery. Br J Pharmacol 88:6–8 Cheung DW (1982) Two components in the cellular response of rat tail arteries to nerve stimulation. J Physiol (Loud) 328:461468

    Google Scholar 

  • Cheung DW, Fujioka M (1986) Inhibition of the excitatory junction potential in the guinea-pig saphenous artery by ANAPP3. Br J Pharmacol 89:3–5

    Google Scholar 

  • Hirst GDS, Neild TO (1980) Evidence for two populations of excitatory receptors for noradrenaline on arteriolar smooth muscle. Nature 283:767–768

    Google Scholar 

  • Hirst GDS, Neild TO, Silverberg GD (1982) Noradrenaline receptors in the rat basilar artery. J Physiol (Lond) 328:351–360

    Google Scholar 

  • Hollander M, Wolfe DA (1973) Nonparametric statistical methods. John Wiley, New York

    Google Scholar 

  • Holman ME, Surprenant A (1980) An electrophysiological analysis of the effects of noradrenaline and α-receptor antagonists on neuromuscular transmission in mammalian muscular arteries. Br J Pharmacol 71:651–661

    Google Scholar 

  • Illes P, Ramme D, Starke K (1986) Presynaptic opioid δ-receptors in the rabbit mesenteric artery. J Physiol (Lond) 379:217–228

    Google Scholar 

  • Illes P, Nörenberg W (1987) Electrophysiological evidence for an α2-adrenergic inhibitory control of transmitter release in the rabbit mesenteric artery. Eur J Pharmacol (in press)

  • Illes P, Ramme D, Busse R (1987) Photoelectric measurement of neurogenic vasoconstriction in jejunal branches of the rabbit mesenteric artery reveals the presence of presynaptic opioid δ-receptors. Naunyn-Schmiedeberg's Arch Pharmacol 335:701–704

    Google Scholar 

  • Ishikawa S (1985) Actions of ATP and α,β-methylene ATP on neuromuscular transmission and smooth muscle membrane of the rabbit and guinea-pig mesenteric arteries. Br J Pharmacol 86:777–787

    Google Scholar 

  • Kajiwara M, Kitamura K, Kuriyama H (1981) Neuromuscular transmission and smooth muscle membrane properties in the guinea-pig ear artery. J Physiol (Lond) 315:283–302

    Google Scholar 

  • Kennedy C, Saville VL, Burnstock G (1986) The contribution of noradrenaline and ATP to the responses of the rabbit central ear artery to sympathetic nerve stimulation depends on the parameters of stimulation. Eur J Pharmacol 122:291–300

    Google Scholar 

  • Kuriyama H, Makita Y (1983) Modulation of noradrenergic transmission in the guinea-pig mesenteric artery: an electrophysiological study. J Physiol (Lond) 335:609–627

    Google Scholar 

  • Medgett IC, Langer SZ (1984) Heterogeneity of smooth muscle alpha adrenoceptors in rat tail artery in vitro. J Pharmacol Exp Ther 229:823–830

    Google Scholar 

  • Meldrum LA, Burnstock G (1983) ATP acts as a co-transmitter with noradrenaline in sympathetic nerves supplying the guineapig vas deferens. Eur J Pharmacol 92:161–163

    Google Scholar 

  • Mishima S, Miyahara H, Suzuki H (1984) Transmitter release modulated by α-adrenoceptor antagonists in the rabbit mesenteric artery: a comparison between noradrenaline outflow and electrical activity. Br J Pharmacol 83:537–547

    Google Scholar 

  • Muramatsu I (1986) Evidence for sympathetic, purinergic transmission in the mesenteric artery of the dog. Br J Pharmacol 87:478–480

    Google Scholar 

  • Muramatsu I, Kigoshi S, Oshita M (1984) Nonadrenergic nature of prazosin-resistant, sympathetic contraction in the dog mesenteric artery. J Pharmacol Exp Ther 229:532–538

    Google Scholar 

  • Neild TO, Zelcer E (1982) Noradrenergic neuromuscular transmission with special reference to arterial smooth muscle. Prog Neurobiol 19:141–158

    Google Scholar 

  • Nilsson H, Sjöblom N, Folkow B (1985) Interaction between prejunctional α2-receptors and neuronal transmitter reuptake in small mesenteric arteries from the rat. Acta Physiol Scand 125:245–252

    Google Scholar 

  • Ramme D, Illes P, Späth L, Starke K (1986) Blockade of α2-adrenoceptors permits the operation of otherwise silent opioid κ-receptors at the sympathetic axons of rabbit jejunal arteries. Naunyn-Schmiedeberg's Arch Pharmacol 334:48–55

    Google Scholar 

  • Schabert A, Bauer RD, Busse R (1980) Photoelectric device for the recording of diameter changes of opaque and transparent blood vessels in vitro. Pfügers Arch 385:239–242

    Google Scholar 

  • Sneddon P, Burnstock G (1984) Inhibition of excitatory junction potentials in guinea-pig vas deferens by α,β-methylene-ATP: further evidence for ATP and noradrenaline as cotransmitters. Eur J Pharmacol 100:85–90

    Google Scholar 

  • Sneddon P, Burnstock G (1985) ATP as a co-transmitter in rat tail artery. Eur J Pharmacol 106:149–152

    Google Scholar 

  • Sneddon P, Westfall DP (1984) Pharmacological evidence that adenosine triphosphate and noradrenaline are co-transmitters in the guinea-pig vas deferens. J Physiol (Lond) 347: 561–580

    Google Scholar 

  • Sneddon P, Westfall DP, Fedan JS (1982) Cotransmitters in the motor nerves of the guinea-pig vas deferens: electro-physiological evidence. Science 218:693–695

    Google Scholar 

  • Snedecor GW, Cochran WG (1967) Statistical methods. The Iowa State University Press, Ames

    Google Scholar 

  • Starke K (1981) α-Adrenoceptor subclassification. Rev Physiol Biochem Pharmacol 88:199–236

    Google Scholar 

  • Stjärne L, Astrand P (1984) Discrete events measure single quanta of adenosine 5′-triphosphatc secreted from sympathetic nerves of guinea-pig and mouse vas deferens. Neuroscience 13: 21–28

    Google Scholar 

  • Stjärne L, Astrand P (1985) Relative pre- and postjunctional roles of noradrenaline and adenosine 5′-triphosphate as neurotransmitters of the sympathetic nerves of guinea-pig and mouse vas deferens. Neuroscience 14:929–946

    Google Scholar 

  • Suzuki H (1983) An electrophysiological study of excitatory neuromuscular transmission in the guinea-pig main pulmonary artery. J Physiol (Loud) 336:47–59

    Google Scholar 

  • Suzuki H (1985) Electrical responses of smooth muscle cells of the rabbit ear artery to adenosine triphosphate. J Physiol (Lond) 359:401–415

    Google Scholar 

  • Suzuki H, Mishima S, Miyahara H (1984) Effects of reserpine on electrical responses evoked by perivascular nerve stimulation in the rabbit ear artery. Biomed Res 5:259–266

    Google Scholar 

  • Vidal M, Hicks PE, Langer SZ (1986) Differential effects of α,β-methylene ATP on responses to nerve stimulation in SHR and WKY tail arteries. Naunyn-Schmiedeberg's Arch Pharmacol 332:384–390

    Google Scholar 

  • von Kiigelgen I, Starke K (1985) Noradrenaline and adenosine triphosphate as co-transmitters of neurogenic vasoconstriction in rabbit mesenteric artery. J Physiol (Lond) 367:435–455

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Send offprint requests to P. Illes

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ramme, D., Regenold, J.T., Starke, K. et al. Identification of the neuroeffector transmitter in jejunal branches of the rabbit mesenteric artery. Naunyn-Schmiedeberg's Arch Pharmacol 336, 267–273 (1987). https://doi.org/10.1007/BF00172677

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00172677

key words

Navigation