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By Georg Kojda, Murat Bas

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Heterocyclic Supramolecules II

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American Academy of Allergy, Asthma and Immunology, Miami Beach, Florida, 2006: S179 19 Caballero T, C. Lopez-Serrano C. 2006. Anaphylactic reaction and antibodies to DX-88 (kallikrein inhibitor) in a patient with hereditary angioedema. J Allergy Clin Immunol 2006; 117: 476 – 477; discussion 477 31 20 Nussberger J, Cugno M, Amstutz C, Cicardi M, Pellacani A, Agostoni A. 1998. Plasma bradykinin in angio-oedema. Lancet 1998; 351: 1693 – 1697 21 Bork K, Frank J, Grundt B, Schlattmann P, Nussberger J, Kreuz W.

Bradykinin activates the Janus-activated kinase/ signal transducers and activators of transcription (JAK/STAT) pathway in vascular endothelial cells: localization of JAK/STAT signalling proteins in plasmalemmal caveolae. Biochem J 2000; 351: 257 – 264 28 Bae SW, Kim HS, Cha YN, Park YS, Jo SA, Jo I. Rapid increase in endothelial nitric oxide production by bradykinin is mediated by protein kinase A signaling pathway. Biochem Biophys Res Commun 2003; 306: 981 – 987 29 Wang DZ, Chao L, Chao J. Hypotension in transgenic mice overexpressing human bradykinin B2 receptor.

From the evolutionary point of view, kinins exhibit extraordi- narily conserved sequences and are found with only minor modification in all the large classes of vertebrates. This system is of eminent importance in the cardiovascular region since it is known from numerous investigations that there is an interaction between the renin-angiotensin-aldosterone system (RAAS) and the kallikrein-kinin system. The functional interaction between the systems is based on the ability of angiotensin-converting enzyme (ACE) to generate angiotensin II from the precursor angiotensin I as well as to degrade kinins, especially bradykinin, into inactive peptides [8].

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