András Rónai

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Király Kornél; Szalay Balázs; Szalai Judit; Barna István; Gyires Klára; Verbeken Mathieu; Rónai András Z
Intrathecally injected Ile-Pro-Ile, an inhibitor of membrane ectoenzyme dipeptidyl peptidase IV, is antihyperalgesic in rats by switching the enzyme from hydrolase to synthase functional mode to generate endomorphin 2.
Rónai András Z; Király Kornél; Szebeni Andrea; Szemenyei Erzsébet; Prohászka Zoltán; Darula Zsuzsanna; Tóth Géza; Till Ibolya; Szalay Balázs; Kató Erzsébet; Barna István
Immunoreactive endomorphin 2 is generated extracellularly in rat isolated L4,5 dorsal root ganglia by DPP-IV.
Szemenyei Erzsébet; Barna István; Mergl Zsuzsa; Keresztes Attila; Darula Zsuzsanna; Kató Erzsébet; Tóth Géza; Rónai András Z
Detection of a novel immunoreactive endomorphin 2-like peptide in rat brain extracts.

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2009: Király Kornél; Szalay Balázs; Szalai Judit; Barna István; Gyires Klára; Verbeken Mathieu; Rónai András Z
Intrathecally injected Ile-Pro-Ile, an inhibitor of membrane ectoenzyme dipeptidyl peptidase IV, is antihyperalgesic in rats by switching the enzyme from hydrolase to synthase functional mode to generate endomorphin 2.
European journal of pharmacology 2009;620(1-3):21-6.
2009: Rónai András Z; Király Kornél; Szebeni Andrea; Szemenyei Erzsébet; Prohászka Zoltán; Darula Zsuzsanna; Tóth Géza; Till Ibolya; Szalay Balázs; Kató Erzsébet; Barna István
Immunoreactive endomorphin 2 is generated extracellularly in rat isolated L4,5 dorsal root ganglia by DPP-IV.
Regulatory peptides 2009;157(1-3):1-2.
2008: Szemenyei Erzsébet; Barna István; Mergl Zsuzsa; Keresztes Attila; Darula Zsuzsanna; Kató Erzsébet; Tóth Géza; Rónai András Z
Detection of a novel immunoreactive endomorphin 2-like peptide in rat brain extracts.
Regulatory peptides 2008;148(1-3):54-61.
2008: Kató Erzsébet; Lipták Lóránt; Shujaa Nashwan; Mátyus Péter; Gyires Klára; Rónai András Z
alpha2B-adrenoceptor agonist ST-91 antagonizes beta2-adrenoceptor-mediated relaxation in rat mesenteric artery rings.
European journal of pharmacology 2008;580(3):361-5.
2006: Ligeti Melinda; Bösze Szilvia; Csámpai Antal; Gündüz Ozge; Al-Khrasani Mahmud; Rónai András Z; Medzihradszky-Schweiger Hedvig; Benyhe Sándor; Borsodi Anna; Hudecz Ferenc; Magyar Anna
Synthesis of enzymatically resistant nociceptin-related peptides containing a carbamic acid residue.
Journal of peptide science : an official publication of the European Peptide Society 2006;12(7):481-90.
2006: Rónai András Z; Al-Khrasani Mahmoud; Benyhe Sándor; Lengyel Imre; Kocsis László; Orosz György; Tóth Géza; Kató Erzsébet; Tóthfalusi László
Partial and full agonism in endomorphin derivatives: comparison by null and operational model.
Peptides 2006;27(6):1507-13.
2006: Rónai András Z; Szemenyei Erzsébet; Kató Erzsébet; Kocsis László; Orosz György; Al-Khrasani Mahmoud; Tóth Géza
Endomorphin synthesis in rat brain from intracerebroventricularly injected [3H]-Tyr-Pro: a possible biosynthetic route for endomorphins.
Regulatory peptides 2006;134(1):54-60.
2005: Fülöp Katalin; Zádori Zoltán; Rónai András Z; Gyires Klára
Characterisation of alpha2-adrenoceptor subtypes involved in gastric emptying, gastric motility and gastric mucosal defence.
European journal of pharmacology 2005;528(1-3):150-7.
2005: Ligeti Melinda; Gündüz Ozge; Magyar Anna; Kató Erzsébet; Rónai András Z; Vita Claudio; Varga Imre; Hudecz Ferenc; Tóth Géza; Borsodi Anna; Benyhe Sándor
Synthesis and biological studies of nociceptin derivatives containing the DTPA chelating group for further labeling with therapeutic radionuclides.
Peptides 2005;26(7):1159-66.
2004: Kocsis László; Orosz György; Magyar Anna; Al-Khrasani Mahmoud; Kató Erzsébet; Rónai Andás Z; Bes Brice; Meunier Jean-Claude; Gündüz Ozge; Tóth Géza; Borsodi Anna; Benyhe Sándor
Nociceptin antagonism: probing the receptor by N-acetyl oligopeptides.
Regulatory peptides 2004;122(3):199-207.
2004: Rónai András Z; Kató Erzsébet; Al-Khrasani Mahmoud; Hajdú Melinda; Müllner Katalin; Elor Guy; Gyires Klára; Fürst Suzanne; Palkovits Miklós
Age and monosodium glutamate treatment cause changes in the stimulation-induced [3H]-norepinephrine release from rat nucleus tractus solitarii-dorsal vagal nucleus slices.
Life sciences 2004;74(13):1573-80.
2004: Tömböly Csaba; Kövér Katalin E; Péter Antal; Tourwé Dirk; Biyashev Dauren; Benyhe Sándor; Borsodi Anna; Al-Khrasani Mahmoud; Rónai András Z; Tóth Géza
Structure-activity study on the Phe side chain arrangement of endomorphins using conformationally constrained analogues.
Journal of medicinal chemistry 2004;47(3):735-43.
2003: Al-Khrasani Mahmoud; Elor Guy; Yusuf Abbas Mamode; Rónai András Z
The effect of endomorphins on the release of 3H-norepinephrine from rat nucleus tractus solitarii slices.
Regulatory peptides 2003;111(1-3):97-101.
2002: Rónai András Z; Gyires Klara; Barna István; Müllner Katalin; Reichart Anikó; Palkovits Miklós
Gyrus cinguli transection abolishes delta-opioid receptor-induced gastroprotection and alters alpha 2 adrenoceptor activity in the lower brainstem in rats.
Brain research 2002;947(1):90-9.
2002: Müllner Katalin; Rónai Andrá Z; Fülöp Katalin; Fürst Susanna; Gyires Klára
Involvement of central K(ATP) channels in the gastric antisecretory action of alpha2-adrenoceptor agonists and beta-endorphin in rats.
European journal of pharmacology 2002;435(2-3):225-9.
2002: Lengyel I; Orosz G; Biyashev D; Kocsis L; Al-Khrasani M; Rónai A; Tömböly Cs; Fürst Zs; Tóth G; Borsodi A
Side chain modifications change the binding and agonist properties of endomorphin 2.
Biochemical and biophysical research communications 2002;290(1):153-61.
2001: Al-Khrasani M; Orosz G; Kocsis L; Farkas V; Magyar A; Lengyel I; Benyhe S; Borsodi A; Rónai A Z
Receptor constants for endomorphin-1 and endomorphin-1-ol indicate differences in efficacy and receptor occupancy.
European journal of pharmacology 2001;421(1):61-7.
2001: Gyires K; Rónai A Z
Supraspinal delta- and mu-opioid receptors mediate gastric mucosal protection in the rat.
The Journal of pharmacology and experimental therapeutics 2001;297(3):1010-5.
2001: Makó E; Rónai A Z
Characterization of kappa and delta opioid receptors in isolated organs by using type/subtype selective agonists and antagonists.
Medical science monitor : international medical journal of experimental and clinical research 2001;7(3):350-6.
2001: Rónai A Z; Gyires K; Barna I; Müllner K; Palkovits M
Neonatal monosodium glutamate treatment abolishes both delta opioid receptor-induced and alpha-2 adrenoceptor-mediated gastroprotection in the lower brainstem in rats.
Journal of physiology, Paris 2001;95(1-6):215-20.
2001: Gyires K; Müllner K; Rónai A Z
Activation of central opioid receptors may induce gastric mucosal defence in the rat.
Journal of physiology, Paris 2001;95(1-6):189-96.
2000: Gyires K; Müllner K; Rónai A Z
Functional evidence that gastroprotection can be induced by activation of central alpha(2B)-adrenoceptor subtypes in the rat.
European journal of pharmacology 2000;396(2-3):131-5.
2000: Darula Z; Kövér K E; Monory K; Borsodi A; Makó E; Rónai A; Tourwé D; Péter A; Tóth G
Deltorphin II analogues with 6-hydroxy-2-aminotetralin-2-carboxylic acid in position 1.
Journal of medicinal chemistry 2000;43(7):1359-66.
2000: Gyires K; Rónai A Z; Müllner K; Fürst S
Intracerebroventricular injection of clonidine releases beta-endorphin to induce mucosal protection in the rat.
Neuropharmacology 2000;39(6):961-8.
2000: Makó E; Rónai A Z; Adám G; Juhász G; Ritter L; Lestár B; Crunelli V
Modulation by GABA(B) and delta opioid receptors of neurally induced responses in isolated guinea-pig taenia coli and human colonic circular muscle.
Journal of physiology, Paris 2000;94(2):135-8.
2000: Gyires K; Müllner K; Fürst S; Rónai A Z
Alpha-2 adrenergic and opioid receptor-mediated gastroprotection.
Journal of physiology, Paris 2000;94(2):117-21.
1999: Sartania N; Szatmári I; Orosz G; Rónai A Z; Medzihradszky K; Borsodi A; Benyhe S
Irreversible labelling of the opioid receptors by a melphalan-substituted [Met5]enkephalin-Arg-Phe derivative.
European journal of pharmacology 1999;373(2-3):241-9.
1999: Szatmári I; Orosz G; Rónai A Z; Makó E; Medzihradszky K; Borsodi A
New opioid affinity labels containing maleoyl moiety.
Life sciences 1999;65(17):1795-805.
1999: Rónai A Z; Timár J; Makó E; Erdö F; Gyarmati Z; Tóth G; Orosz G; Fürst S; Székely J I
Diprotin A, an inhibitor of dipeptidyl aminopeptidase IV(EC 3.4.14.5) produces naloxone-reversible analgesia in rats.
Life sciences 1999;64(2):145-52.
1998: Spetea M; Nevin S T; Hosztafi S; Rónai A Z; Tóth G; Borsodi A
Affinity profiles of novel delta-receptor selective benzofuran derivatives of non-peptide opioids.
Neurochemical research 1998;23(9):1211-6.
1998: Pacher P; Kecskemeti V; Ronai A Z; Balogh I; Szalai G; Matkovics B
Changes in cardiac electrophysiology, morphology, tissue biochemistry and vascular reactions in glutathione depleted animals.
Molecular and cellular biochemistry 1998;185(1-2):183-90.
1997: Rónai A Z; Lengyel J; Nagy T; Orosz G; Adlesz V; Racz K; Magyar K
Hip-Arg-Phe-, Hip-Phe-Arg- and Hip-His-Leu-cleaving dipeptidyl carboxypeptidases in human adrenal tumors.
Neuropeptides 1997;31(6):585-8.
1997: Gyires K; Rónai A Z; Tóth G; Darula Z; Fürst S
Analysis of the role of delta opioid receptors in gastroprotection in the rat.
Life sciences 1997;60(16):1337-47.
1996: Sartania N; Benyhe S; Magyar A; Rónai A Z; Medzihradszky K; Borsodi A
Opioid binding profile of morphiceptin, Tyr-MIF-1 and dynorphin-related peptides in rat brain membranes.
Neuropeptides 1996;30(3):225-30.
1995: Rónai A Z; Magyar A; Orosz G; Borsodi A; Benyhe S; Tóth G; Makó E; Kátay E; Babka E; Medzihradszky K
Opioid antagonist properties of the highly delta-receptor-selective BOC-Tyr-Pro-Gly-Phe-Leu-Thr (OtBu) peptide and of its Phe1 and Mel1 analogues.
Archives internationales de pharmacodynamie et de thérapie 1995;330(3):361-9.
1995: Rónai A Z; Fehér E; Botyánszki J; Hepp J; Magyar A; Medzihradszky K
Substrate- and inhibitor-specificity of a non-endothelial enzyme which forms [Met5]-enkephalin from [Met5]-enkephalin-Arg6,Phe7 in isolated rabbit ear artery: pharmacological characterization.
Neuropeptides 1995;28(3):137-45.
1994: Orosz G; Rónai A Z; Bajusz S; Medzihradszky K
N-terminally protected penta- and tetrapeptide opioid antagonists based on a pentapeptide sequence found in the venom of Philippine cobra.
Biochemical and biophysical research communications 1994;202(3):1285-90.
1994: Rónai A Z; Hepp J; Magyar A; Borsodi A; Medzihradszky K
Design of opioid peptides for a potential delta-receptor affinity label function: comparison with the mu-specific Tyr-D-Ala-Gly-(Me)Phe-chloromethyl ketone.
Pharmacology 1994;49(2):121-31.
1994: Hollósi M; Majer Z; Rónai A Z; Magyar A; Medzihradszky K; Holly S; Perczel A; Fasman G D
CD and Fourier transform ir spectroscopic studies of peptides. II. Detection of beta-turns in linear peptides.
Biopolymers 1994;34(2):177-85.
1993: Rónai A Z; Magyar A; Medzihradszky K
Kinetic parameters of antagonism by the delta opioid receptor selective peptide antagonist Boc-Tyr-Pro-Gly-Phe-Leu-Thr against selective and non-selective agonists in the mouse vas deferens.
Neuropeptides 1993;25(2):127-9.
1993: Rónai A Z; Botyánszki J; Magyar A; Borsodi A; Benyhe S; Medzihradszky K
Novel, delta-opioid receptor-selective peptide antagonists: demonstration of a possible opioid interaction in the absence of a protonated nitrogen and attempts to locate the protonated nitrogen site.
Archives internationales de pharmacodynamie et de thérapie 1993;323():114-25.
1992: Rónai A Z; Botyánszki J; Hepp J; Medzihradszky K
A novel opioid structure which accepts protonated as well as non-protonated nitrogen: a family of pure, delta receptor selective antagonists.
Life sciences 1992;50(18):1371-8.
1991: Rónai A Z
Bradykinin and angiotensin II inhibit neurotransmission in rabbit ear artery by releasing prostanoids.
European journal of pharmacology 1991;198(1):93-5.
1990: Rónai A Z
Inhibition of neurotransmission by angiotensin I and II in rabbit isolated ear artery.
European journal of pharmacology 1990;179(3):281-6.
1987: Vizi E S; Ronai A; Bernath S
Inhibition by p-nitrophenylphosphate of acetylcholine release induced by Na+-deprivation.
Biochemical pharmacology 1987;36(6):803-7.
1985: Gyüre K; Szentendrei T; Kanyicska B; Fekete M I; Rónai A Z
Dopamine receptor binding of a novel dibenzodioxazocine derivative, EGYT-2509.
Polish journal of pharmacology and pharmacy 1985;37(3):253-61.
1984: Csaba G; Rónai A; Dobozy O; Berzétei I
Impact of neonatal catecholamine treatment on adult response to vasopressin and norepinephrine.
Experimental and clinical endocrinology 1984;84(2):153-8.
1984: Hársing L G; Rónai A Z; Somogyi G T; Umezawa H; Bajusz S; Vizi E S
Met5-enkephalin-Arg6-Phe7 inhibition of noradrenaline and acetylcholine release from peripheral organs.
Journal of autonomic pharmacology 1984;4(1):33-43.
1984: Rónai A Z; Dobozy O; Berzétei I P; Kurgyis J; Csaba G
The effect of neonatal treatment of mice with opioid and dopaminergic agents on the late responsiveness of vasa deferentia to opioids in vitro.
Acta biologica Hungarica 1984;35(1):43-7.
1983: Vizi E S; Ludvig N; Rónai A Z; Folly G
Dissociation of presynaptic alpha 2-adrenoceptors following prazosin administration: presynaptic effect of prazosin.
European journal of pharmacology 1983;95(3-4):287-90.
1983: Földes J; Török K; Székely J I; Borvendég J; Karczag I; Tolna J; Marosfi S; Váradi A; Gara A; Rónai A Z
Human tolerability studies with D-Met2,Pro5-enkephalinamide.
Life sciences 1983;33 Suppl 1():769-72.
1983: Rónai A Z; Serfózó P; Hársing L G; Vizi S E
The conversion of Met-enkephalin-Arg6, Phe7 to Met-enkephalin in rabbit ear artery.
Life sciences 1983;33 Suppl 1():101-4.
1982: Rónai A Z; Hársing L G; Berzétei I P; Bajusz S; Vizi E S
[Met5]enkephalin-Arg-Phe ACTS on vascular opiate receptors.
European journal of pharmacology 1982;79(3-4):337-8.
1981: Rónai A Z; Berzétei I P; Kurgyis J
Opioid effects in developing rat vas deferens.
Cellular and molecular neurobiology 1981;1(4):335-42.
1981: Rónai A Z; Berzétei I P; Bajusz S; Székely J I
The in vitro pharmacology of D-Met2,Pro5-enkephalinamide.
The Journal of pharmacy and pharmacology 1981;33(8):534-5.
1981: Rónai A Z; Berzétei I P; Székely J I; Miglécz E; Kurgyis J; Bajusz S
Enkephalin-like character and analgesia.
European journal of pharmacology 1981;69(3):263-71.
1980: Bajusz S; Rónai A Z; Székely J I; Turán A; Juhász A; Patthy A; Miglécz E; Berzétei I
Enkephalin analogs containing amino sulfonic acid and amino phosphonic acid residues at position 5.
FEBS letters 1980;117(1):308-10.
1980: Soós J; Berzétei I; Bajusz S; Rónai A Z
Correlation between circular dichroism data and biological activities of 2,5 substituted enkephalin analogues.
Life sciences 1980;27(2):129-33.
1980: Bajusz S; Rónai A Z; Székely J I; Miglécz E; Berzétei I
Further enhancment of analgesic activity: enkephalin analogs with terminal guanidino group.
FEBS letters 1980;110(1):85-7.
1980: Csaba G; Rónai A; László V; Darvas Z; Berzétei I
Amplification of hormone receptors by neonatal oxytocin and vasopressin treatment.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 1980;12(1):28-31.
1980: Székely J I; Miglécz E; Rónai A Z
Biphasic effects of a potent enkephalin analogue (D-Met2,Pro5)-enkephalinamide and morphine on locomotor activity in mice.
Psychopharmacology 1980;71(3):299-301.
1979: Rónai A Z; Székely J I; Berzétei I; Miglécz E; Bajusz S
Tetrapeptide-amide analogues of enkephalin: the role of C-terminus in determining the character of opioid activity.
Biochemical and biophysical research communications 1979;91(4):1239-49.
1979: Székely J I; Miglécz E; Dunai-Kovács Z; Tarnawa I; Rónai A Z; Gráf L; Bajusz S
Attenuation of morphine tolerance and dependence by alpha-melanocyte stimulating hormone(alpha-MSH).
Life sciences 1979;24(21):1931-8.
1979: Rónai A Z; Berzétei I; Székely J I; Gráf L; Bajusz S
Kinetic studies in isolated organs: tools to design analgesic peptides and to analyze their receptor effects.
Pharmacology 1979;18(1):18-24.
1978: Székely J I; Dunai-Kovács Z; Miglécz E; Rónai A Z; Bajusz S
In vivo antagonism by naloxone of morphine, beta-endorphin and a synthetic enkephalin analog.
The Journal of pharmacology and experimental therapeutics 1978;207(3):878-83.
1978: Bajusz S; Patthy A; Kenessey A; Gráf L; Székely J I; Rónai A Z
Is there correlation between analgesic potency and biodegradation of enkephalin analogs?
Biochemical and biophysical research communications 1978;84(4):1045-53.
1977: Rónai A Z; Berzétei I; Bajusz S
Differentiation between opioid peptides by naltrexone.
European journal of pharmacology 1977;45(4):393-4.
1977: Gráf L; Cseh G; Barát E; Ronai A Z; Székely J I; Kenessey A; Bajusz S
Structure-function relationships in lipotropins.
Annals of the New York Academy of Sciences 1977;297():63-83.
1977: Gráf L; Kenessey A; Berzétei I; Rónai A Z
Demonstration of beta-lipotropin activating enzyme in porcine pituitary.
Biochemical and biophysical research communications 1977;78(3):1114-23.
1977: Székely J I; Rónai A Z; Dunai-Kovács Z; Miglécz E; Berzétri I; Bajusz S; Gráf L
(D-met2, pro5)-enkephalinamide: a potent morphine-like analgesic.
European journal of pharmacology 1977;43(3):293-4.
1977: Vizi S E; Rónai A; Hársing L; Knoll J
Inhibitory effect of dopamine on acetylcholine release from caudate nucleus.
Polish journal of pharmacology and pharmacy 1977;29(3):201-11.
1977: Bajusz S; Rónai A Z; Székely J I; Gráf L; Dunai-Kovács Z; Berzétei I
A superactive antinociceptive pentapeptide, (D-Met2, Pro5)-enkephalinamide.
FEBS letters 1977;76(1):91-2.
1977: Szkely J I; Rónai A Z; Dunai-Kovács Z; Miglécz E; Bajusz S; Gráf L
Cross tolerance between morphine and beta-endorphin in vivo.
Life sciences 1977;20(7):1259-64.
1977: Rónai A; Gráf L; Székely I; Dunai-Kovács Z; Bajusz S
Differential behaviour of LPH-(61-91)-peptide in different model systems: comparison of the opioid activities of LPH-(61-91)-peptide and its fragments.
FEBS letters 1977;74(2):182-4.
1977: Ronai A Z; Foldes F F; Hahn E F; Fishman J
Orientation of the oxygen atom at C-6 as a determinant of agonistic activity in the oxymorphone series.
The Journal of pharmacology and experimental therapeutics 1977;200(3):496-500.
1977: Székely J I; Rónai A Z; Dunai-Kovács Z; Gráf L; Bajusz S
C-terminal fragment (residues 61-91) of beta-lipotropin: is it the natural opiate-like neurohormon of the brain?
Experientia 1977;33(1):54-5.
1976: Illés P; Rónai A; Knoll J
Inhibition of neuromuscular transmission by prostaglandin E1 in the circular muscle of the guinea-pig vas deferens.
Medical biology 1976;54(6):400-5.
1976: Graf L; Szekely J I; Ronai A Z; Dunai-Kovacs Z; Bajusz S
Comparative study on analgesic effect of Met5-enkephalin and related lipotropin fragments.
Nature 1976;263(5574):240-2.
1976: Rónai A Z; Székely J I; Gráf L; Dunai-Kovács Z; Bajusz S
Morphine-like analgesic effect of a pituitary hormone, beta-lipotropin.
Life sciences 1976;19(5):733-8.
1976: Gráf L; Rónai A; Bajusz S; Csheh G; Székely J I
Opioid agonist activity of beta-lipotropin fragments: a possible biological source of morphine-like substances in the pituitary.
FEBS letters 1976;64(1):181-4.
1976: Bajusz S; Rónai A Z; Székely J I; Dunai-Kovács Z; Berzétei I; Gráf L
Enkephalin analogs with enhanced opiate activity.
Acta biochimica et biophysica; Academiae Scientiarum Hungaricae 1976;11(4):305-9.
1975: Rónai A Z; Vizi S E
The effect of lithium treatment on the acetylcholine content of rat brain.
Biochemical pharmacology 1975;24(19):1819-20.
1974: Knoll J; Zséli J; Rónai A; Vizi E S
Effect of azidomorphine and related substances on the intestinal motility.
Pharmacology 1974;12(4-5):283-9.
1972: Vizi E S; Illés P; Rónai A; Knoll J
Effect of lithium on acetylcholine release and synthesis.
Neuropharmacology 1972;11(4):521-30.

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