Enhancement of noradrenaline release by angiotensin II and bradykinin in mouse atria: evidence for cross-talk between G(q/11) protein- and G(i/o) protein-coupled receptors

Br J Pharmacol. 2000 Mar;129(6):1095-102. doi: 10.1038/sj.bjp.0703167.

Abstract

1. The interaction between alpha(2)-autoreceptors and receptors for angiotensin (AT(1)) and bradykinin (B(2)) was studied in mouse isolated atria. The preparations were labelled with [(3)H]-noradrenaline and then superfused with desipramine-containing medium and stimulated electrically. 2. Angiotensin II (10(-11) - 10(-7) M), angiotensin III (10(-10) - 10(-6) M) and bradykinin (10(-11) - 10(-7) M) enhanced the evoked overflow of tritium when preparations were stimulated with conditions that led to marked alpha(2)-autoinhibition (120 pulses at 3 Hz), but not when stimulated with conditions that led to little alpha(2)-autoinhibition (20 pulses at 50 Hz). 3. Blockade of alpha-adrenoceptors by phentolamine (1 or 10 microM) reduced or abolished the effect of angiotensin II and bradykinin on the overflow response to 120 pulses at 3 Hz. 4. Addition of the delta-opioid agonist [D-Ser(2)]-leucine enkephalin-Thr (DSLET, 0.1 microM), or of neuropeptide Y (0.1 microM), together with phentolamine, restored the effect of angiotensin II and bradykinin. 5. The beta-adrenoceptor agonist terbutaline (10(-9) - 10(-4) M) enhanced the evoked overflow of tritium irrespective of the degree of autoinhibition. 6. The experiments show that (i) a marked prejunctional facilitatory effect of angiotensin and bradykinin in mouse isolated atria requires prejunctional alpha(2)-autoinhibition; (ii) in the absence of alpha(2)-autoinhibition, activation of other prejunctional G(i/o) protein-coupled receptors, namely opioid and neuropeptide Y receptors, restores a marked effect of angiotensin II and bradykinin; and (iii) the facilitatory effect of terbutaline is not dependent upon the degree of alpha(2)-autoinhibition. The findings indicate that the major part of the release-enhancing effect elicited through prejunctional G(q/11) protein-coupled receptors is due to disruption of an ongoing, alpha(2)-autoreceptor-triggered G(i/o) protein mediated inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Angiotensin II / pharmacology*
  • Angiotensin III / pharmacology
  • Animals
  • Atrial Function
  • Bradykinin / pharmacology*
  • Calcium / physiology
  • Electric Stimulation
  • Electrophysiology
  • Enkephalin, Leucine / analogs & derivatives
  • Enkephalin, Leucine / pharmacology
  • GTP-Binding Proteins / drug effects
  • GTP-Binding Proteins / physiology*
  • Heart / drug effects*
  • Heart / physiology
  • Heart Atria / drug effects
  • Heart Atria / metabolism
  • In Vitro Techniques
  • Male
  • Mice
  • Myocardium / metabolism*
  • Neuropeptide Y / pharmacology
  • Norepinephrine / metabolism*
  • Receptor Cross-Talk / drug effects*
  • Receptors, Adrenergic, alpha-2 / drug effects
  • Receptors, Angiotensin / drug effects
  • Terbutaline / pharmacology

Substances

  • Adrenergic beta-Agonists
  • Neuropeptide Y
  • Receptors, Adrenergic, alpha-2
  • Receptors, Angiotensin
  • Angiotensin II
  • Angiotensin III
  • Enkephalin, Leucine
  • enkephalin, Ser(2), Leu(5), Thr(6)-
  • GTP-Binding Proteins
  • Terbutaline
  • Bradykinin
  • Calcium
  • Norepinephrine