Novel peptide calcitonin gene-related peptide antagonists for migraine therapy

Author:

Killoran Patrick M1,Capel Vicky2,D’Aloisio Vera13,Schofield Adam4,Aczél Tímea56,Bölcskei Kata56,Helyes Zsuzsanna5678,von Mentzer Bengt9,Kendall David A19,Coxon Chris R4,Hutcheon Gillian A1ORCID

Affiliation:

1. School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University , Liverpool, L3 3AF , United Kingdom

2. NHS Health Education England , Victoria House, Fulbourn, Cambridge, CB21 5XB , United Kingdom

3. AmbioPharm, Inc. , 1024 Dittman Court, North Augusta, SC 29842 , United States

4. EaStCHEM School of Chemistry, The University of Edinburgh , Joseph Black Building, David, Brewster Road, Edinburgh, EH14 4AS , United Kingdom

5. Department of Pharmacology and Pharmacotherapy, University of Pécs Medical School , Szigeti út 12, Pécs , Hungary

6. Eötvös Lorand Research Network, Chronic Pain Research Group, University of Pécs , Szigeti út 12, Pécs , Hungary

7. PharmInVivo Ltd. , Szondi Gy. u. 10. H-7629 , Pécs , Hungary

8. National Laboratory for Drug Research and Development , Magyar tudósok krt. 2, H-1117 Budapest , Hungary

9. Innovipharm Limited , 2 Woodlands Lane, West Kirby, Wirral, CH48 8D , United Kingdom

Abstract

Abstract Objectives It has previously been shown that the peptide (34Pro,35Phe)CGRP27–37 is a potent calcitonin gene-related peptide, CGRP receptor antagonist, and in this project we aimed to improve the antagonist potency through the structural modification of truncated C-terminal CGRP peptides. Methods Six peptide analogues were synthesized and the anti-CGRP activity confirmed using both in vitro and in vivo studies. Key findings A 10 amino acid-containing peptide VPTDVGPFAF-NH2 (P006) was identified as a key candidate to take forward for in vivo evaluation, where it was shown to be an effective antagonist after intraperitoneal injection into mice. P006 was formulated as a preparation suitable for nasal administration by spray drying with chitosan to form mucoadhesive microcarriers (9.55 ± 0.91 mm diameter) and a loading of 0.2 mg peptide per 20 mg dose. Conclusions The project has demonstrated the potential of these novel small peptide CGRP antagonists, to undergo future preclinical evaluation as anti-migraine therapeutics.

Funder

Innovate UK

Liverpool John Moores University

National Research, Development and Innovation Office of Hungary

Eötvös Lóránd Research Network

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference31 articles.

1. Migraine: the seventh disabler;Steiner;J Headache Pain,2013

2. CGRP inhibitors for migraine prophylaxis: a safety review;Rivera-Mancilla,2020

3. Calcitonin gene related peptide and migraine;Karsan,2015

4. CGRP as the target of new migraine therapies—successful translation from bench to clinic;Edvinsson,2018

5. Calcitonin gene-related peptide modulators—the history and renaissance of a new migraine drug class;Hargreaves,2019

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