The adenosine receptor‐mediated inhibition of noradrenaline release possibly involves a N‐protein and is increased by α2‐autoreceptor blockade

British Journal of Pharmacology - Tập 90 Số 2 - Trang 403-412 - 1987
Clemens Allgaier1, Georg Hertting1, Oda Von Kügelgen1
1Institute of Pharmacology, University of Freiburg, Hermann‐Herder‐Str. 5, D‐7800 Freiburg, Federal Republic of Germany

Tóm tắt

The stimulation‐evoked overflow of [3H]‐noradrenaline from slices of the rabbit hippocampus is inhibited by α2‐autoreceptors as well as by adenosine (A1)‐receptors. Slices of rabbit hippocampus were labelled with [3H]‐noradrenaline, superfused continuously and stimulated twice electrically (rectangular pulses; 2 ms, 3 Hz, 24 mA, 5 V cm−1). Treatment of hippocampal slices with N‐ethylmaleimide (NEM, 30 μm; 30 min), which functionally disturbs certain N‐proteins, decreased the inhibitory action of adenosine receptor agonists like (‐)‐N6‐(R‐phenylisopropyl)‐adenosine ((‐)‐PIA) and adenosine on noradrenaline release. Release inhibition caused by (‐)‐PIA (0.03‐1 μm) was antagonized by NEM in a non‐competitive manner in the absence and in the presence of the α2‐adrenoceptor antagonist yohimbine. The adenosine receptor antagonist 8‐phenyltheophylline significantly increased the evoked noradrenaline release by about 15% in control slices by diminishing the inhibitory action of endogenous adenosine. In NEM‐treated slices this effect of 8‐phenytheophylline was not seen. In the presence of (‐)‐PIA (0.1 μm), i.e. under conditions of an increased inhibitory tone, release facilitation by 8‐phenyltheophylline was decreased by NEM compared to that in the respective controls. Occupation of the A1‐receptor with (‐)‐PIA prior to and during the NEM treatment did not protect the A1‐receptor‐coupled signal transduction system from being affected by NEM. In the presence of the α2‐adrenoceptor antagonist yohimbine, the inhibitory action of (‐)‐PIA was strongly increased. The above results suggest the involvement of a regulatory N‐protein in the A1‐receptor‐mediated inhibition of noradrenaline release and an interaction between the α2‐autoreceptor and the A1‐receptor‐coupled signal transduction system, possibly at the level of a N‐protein.

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Tài liệu tham khảo

10.1007/BF00634243

10.1007/BF00506511

Asano T., 1986, Uncoupling of γ‐aminobutyric acid B receptors from GTP‐binding proteins by N‐ethylmaleimide: Effect of N‐ethylmaleimide on purified GTP‐binding proteins, Molecular Pharmac., 29, 244

Boyer J.L., 1984, Differential effect of pertussis toxin on the affinity state for agonists of renal α1‐and α2‐adrenoceptors, J. biol. Chem., 259, 8076, 10.1016/S0021-9258(17)39693-X

10.1073/pnas.80.7.2077

10.1038/314534a0

10.1016/0014-5793(82)80431-6

Cote T.E., 1984, Altered activity of the inhibitory guanyl nucleotide‐binding component (Ni) induced by pertussis toxin. Uncoupling of Ni from receptor with continued coupling of Ni to the catalytic unit, J. biol. Chem., 259, 8693, 10.1016/S0021-9258(17)47207-3

10.1038/316148a0

10.1016/0014-2999(85)90063-9

10.1111/j.1748-1716.1983.tb00022.x

10.1111/j.1476-5381.1985.tb08922.x

10.1111/j.1748-1716.1986.tb07819.x

10.1016/0092-8674(84)90336-2

Harden T.K., 1982, Differential modification of the interaction of cardiac muscarinic cholinergic and beta‐adrenergic receptors with a guanine nucleotide binding component(s), Molec. Pharmac., 21, 570

10.1016/0014-2999(78)90107-3

10.1016/0028-3908(79)90107-2

10.1038/302706a0

10.1038/319670a0

10.1016/0028-3908(84)90074-1

10.1007/BF00506243

10.1016/0028-3908(85)90055-3

10.1007/BF00499902

10.1111/j.1471-4159.1986.tb08499.x

Jakobs K.H., 1982, Uncoupling of α‐adrenoceptor‐mediated inhibition of human platelet adenylate cyclase by N‐ethylmaleimide, J. biol. Chem., 257, 2829, 10.1016/S0021-9258(19)81038-4

Kurose H., 1983, Functional uncoupling of muscarinic receptors from adenylate cyclase in rat cardiac membranes by the active component of islet‐activating protein, pertussis toxin, J. cyclic Nucleotide Res., 9, 305

10.1007/BF00507049

Murayama T., 1983, Loss of the inhibitory function of the guanine nucleotide regulatory component of adenylate cyclase due to its ADP ribosylation by islet‐activating protein, pertussis toxin, in adipocyte membranes, J. biol. Chem., 258, 3319, 10.1016/S0021-9258(18)32863-1

Neer E.J., 1984, Purification and properties of the inhibitory guanine nucleotide regulatory unit of brain adenylate cyclase, J. biol. Chem., 259, 14222, 10.1016/S0021-9258(18)89881-7

10.1111/j.1471-4159.1985.tb05425.x

10.1016/0028-3908(83)90152-1

10.1016/0006-2952(84)90002-9

Ramme D., 1986, Does the blockade of α2‐adrenoceptors unmask previously silent opioid k‐receptors?, Naunyn-Schmiedebergs Arch. Pharmac., 332, R80

10.1038/284017a0

10.1016/0014-2999(84)90475-8

Sternweis P.C., 1984, Isolation of two proteins with high affinity for guanine nucleotides from membranes of bovine brain, J. biol. Chem., 259, 13806, 10.1016/S0021-9258(18)89817-9

10.1007/BF00502457

10.1111/j.1471-4159.1982.tb03954.x

Yeung S.M.H., 1983, Agonist and antagonist affinities for inhibitory adenosine receptors are reciprocally affected by 5′‐guanylylimidodiphosphate or N‐ethylmaleimide, J. biol. Chem., 258, 2334, 10.1016/S0021-9258(18)32928-4