Effect of several bicyclic peptide and cyclic pseudopeptide tachykinin NK2 receptor antagonists in the human isolated urinary bladder

S. Giuliani, R. Patacchini, M. Lazzeri, G. Benaim, D. Turini, L. Quartara, C. A. Maggi

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

1. We have studied several tachykinin NK2 receptor antagonists, bearing a monocyclic pseudopeptide (MEN 10,508, MEN 10,573, MEN 10,581, MEN 10,612, MEN 10,619, and MEN 10,677), or bicyclic peptide (MEN 10,627, MEN 10,692, MEN 10,771, MEN 10,882 and MEN 10,993) structure, an the human isolated urinary bladder detrusor muscle against neurokinin A as an agonist, and compared their affinities in this preparation with those for NK2 receptors expressed in the rabbit isolated pulmonary artery and hamster isolated trachea. 2. In the human bladder, all the antagonists tested produced a concentration-dependent and competitive antagonism of neurokinin A-mediated contractions: among the cyclic pseudopeptides MEN 10,677 (pK(B) = 8.0) was the most potent antagonist, while among the bicyclic analogues it was MEN 10,993 (pK(B) = 8.8). 3. In general, the bicyclic peptide antagonists tested were more potent than the monocyclic pseudopeptide compounds, either in the human urinary bladder or in the rabbit pulmonary artery or hamster trachea, showing a nanomolar affinity for the human NK2 receptor. 4. A highly significant correlation was found between the estimated pK(B) values of all the antagonists tested in the human urinary bladder and rabbit pulmonary artery (r2 = 0.94, n = 12, P <0.01), whereas no linear correlation was found between pK(B) values measured in the human urinary bladder and hamster trachea (r2 = 0.52, n = 12, P > 0.05): these observations provide further pharmacological evidence for receptor homology between the human and rabbit NK2 receptor. 5. The present results point out the class of NK2 receptor antagonists bearing a bicyclic peptide structure, like MEN 10,627, as candidates for testing in pathological conditions, such as bladder hyperactivity, for which preclinical evidence indicates that a therapeutic effect could result from the block of the tachykinin NK2 receptor.

Original languageEnglish
Pages (from-to)251-259
Number of pages9
JournalJournal of Autonomic Pharmacology
Volume16
Issue number5
Publication statusPublished - 1996

Fingerprint

Tachykinin Receptors
Cyclic Peptides
Urinary Bladder
Pulmonary Artery
Rabbits
Neurokinin A
Trachea
Cricetinae
Peptides
Therapeutic Uses
Pharmacology
Muscles

ASJC Scopus subject areas

  • Pharmacology
  • Neuroscience(all)

Cite this

Effect of several bicyclic peptide and cyclic pseudopeptide tachykinin NK2 receptor antagonists in the human isolated urinary bladder. / Giuliani, S.; Patacchini, R.; Lazzeri, M.; Benaim, G.; Turini, D.; Quartara, L.; Maggi, C. A.

In: Journal of Autonomic Pharmacology, Vol. 16, No. 5, 1996, p. 251-259.

Research output: Contribution to journalArticle

Giuliani, S. ; Patacchini, R. ; Lazzeri, M. ; Benaim, G. ; Turini, D. ; Quartara, L. ; Maggi, C. A. / Effect of several bicyclic peptide and cyclic pseudopeptide tachykinin NK2 receptor antagonists in the human isolated urinary bladder. In: Journal of Autonomic Pharmacology. 1996 ; Vol. 16, No. 5. pp. 251-259.
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T1 - Effect of several bicyclic peptide and cyclic pseudopeptide tachykinin NK2 receptor antagonists in the human isolated urinary bladder

AU - Giuliani, S.

AU - Patacchini, R.

AU - Lazzeri, M.

AU - Benaim, G.

AU - Turini, D.

AU - Quartara, L.

AU - Maggi, C. A.

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AB - 1. We have studied several tachykinin NK2 receptor antagonists, bearing a monocyclic pseudopeptide (MEN 10,508, MEN 10,573, MEN 10,581, MEN 10,612, MEN 10,619, and MEN 10,677), or bicyclic peptide (MEN 10,627, MEN 10,692, MEN 10,771, MEN 10,882 and MEN 10,993) structure, an the human isolated urinary bladder detrusor muscle against neurokinin A as an agonist, and compared their affinities in this preparation with those for NK2 receptors expressed in the rabbit isolated pulmonary artery and hamster isolated trachea. 2. In the human bladder, all the antagonists tested produced a concentration-dependent and competitive antagonism of neurokinin A-mediated contractions: among the cyclic pseudopeptides MEN 10,677 (pK(B) = 8.0) was the most potent antagonist, while among the bicyclic analogues it was MEN 10,993 (pK(B) = 8.8). 3. In general, the bicyclic peptide antagonists tested were more potent than the monocyclic pseudopeptide compounds, either in the human urinary bladder or in the rabbit pulmonary artery or hamster trachea, showing a nanomolar affinity for the human NK2 receptor. 4. A highly significant correlation was found between the estimated pK(B) values of all the antagonists tested in the human urinary bladder and rabbit pulmonary artery (r2 = 0.94, n = 12, P <0.01), whereas no linear correlation was found between pK(B) values measured in the human urinary bladder and hamster trachea (r2 = 0.52, n = 12, P > 0.05): these observations provide further pharmacological evidence for receptor homology between the human and rabbit NK2 receptor. 5. The present results point out the class of NK2 receptor antagonists bearing a bicyclic peptide structure, like MEN 10,627, as candidates for testing in pathological conditions, such as bladder hyperactivity, for which preclinical evidence indicates that a therapeutic effect could result from the block of the tachykinin NK2 receptor.

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