Cited by 176Coagulation, Bradykinin, Polyphosphates, and AngioedemaPineapple and bromelain studiesMast cells and histamine

New topics in bradykinin research

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Maurer, M., Bader, M., Bas, M., Bossi, F., Cicardi, M., Cugno, M., Howarth, P., Kaplan, A. +4 more·2011·Allergy

Abstract

To cite this article: Maurer M, Bader M, Bas M, Bossi F, Cicardi M, Cugno M, Howarth P, Kaplan A, Kojda G, Leeb‐Lundberg F, Lötvall J, Magerl M. New topics in bradykinin research.Allergy2011;66: 1397–1406. Abstract Bradykinin has been implicated to contribute to allergic inflammation and the pathogenesis of allergic conditions. It binds to endothelial B1and B2receptors and exerts potent pharmacological and physiological effects, notably, decreased blood pressure, increased vascular permeability and the promotion of classical symptoms of inflammation such as vasodilation, hyperthermia, oedema and pain. Towards potential clinical benefit, bradykinin has also been shown to exert potent antithrombogenic, antiproliferative and antifibrogenic effects. The development of pharmacologically active substances, such as bradykinin receptor blockers, opens up new therapeutic options that require further research into bradykinin. This review presents current understanding surrounding the role of bradykinin in nonallergic angioedema and other conditions seen by allergists and emergency physicians, and its potential role as a therapeutic target.

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Crossref · 10.1111/j.1398-9995.2011.02686.x

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  • Captopril usage improved accumulation of paclitaxel-loaded nanoparticles in U87 glioma xenograft tumors.

    “Captopril usage has improved the accumulation of paclitaxel-loaded nanoparticles in U87 glioma xenograft tumors [40,41,42].”

    From Approaches to Improve EPR-Based Drug Delivery for Cancer Therapy and Diagnosis (2023) · cites this paper as [41]

    The Pharmacological targeting of the kallikrein-kinin system section says B1 receptor antagonists increase glioma permeability and speculates that this could allow greater entry of cytostatic agents. It does not report captopril use or improved accumulation of paclitaxel-loaded nanoparticles in U87 xenografts. (LLM, conf=0.82)

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References 84 · Cited by 176

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Authors
Maurer, M., Bader, M., Bas, M., Bossi, F., Cicardi, M., Cugno, M., Howarth, P., Kaplan, A., Kojda, G., Leeb‐Lundberg, F., Lötvall, J., & Magerl, M.
Affiliations
  • Stiftung Charité (DE)
  • University of Trieste (IT)
  • University of Milan (IT)
  • University of Southampton (GB)
  • Medical University of South Carolina (US)
  • Düsseldorf University Hospital (DE)
  • University of Gothenburg (SE)
Corresponding author
Maurer, M.
Venue
Allergy
Publisher
Wiley
Published
2011-08-22
Volume
66
Issue
11
Pages
1397-1406
ISSN
  • 0105-4538 (ISSN-L)
  • 1398-9995
OpenAlex
W1942364642
Cited by
176
References
84
Citations by year
2026: 5 · 2025: 8 · 2024: 9 · 2023: 12 · 2022: 11 · 2021: 10 · 2020: 8 · 2019: 11 · 2018: 11 · 2017: 10 · 2016: 10 · 2015: 17 · 2014: 22 · 2013: 22 · 2012: 9
FWCI
2.05
Type
journal article
Language
en
Open access
Locations
  • Allergy (publishedVersion)
  • PubMed (publishedVersion)
  • ArTS Archivio della ricerca di Trieste (University of Trieste https://www.units.it/) (submittedVersion)
  • ePrints Soton (University of Southampton) (submittedVersion)
  • Lund University Publications (Lund University) (submittedVersion)
  • mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
Funders
Shire Human Genetic Therapies
Topics
  • Health Sciences › Medicine › Genetics › Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pineapple and bromelain studies
  • Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
Keywords
bradykinin, bradykinin B1 receptor, bradykinin B2 receptor, allergic inflammation, bradykinin receptor antagonists, antifibrotic effect, vascular permeability, therapeutic target
MeSH terms
Angioedema, Animals, Bradykinin, Humans, Vasodilator Agents, Biomedical Research, Complement C1 Inhibitor Protein, Mice

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