A plant Kunitz-type inhibitor mimics bradykinin-induced cytosolic calcium increase and intestinal smooth muscle contraction

• Published in: Biological chemistry Vol. 393; no. 9; p. 943
• Main Authors: Andrade, Sheila Siqueira, Smaili, Soraya Soubhi, Monteforte, Priscila Totarelli, Miranda, Antônio, Kouyoumdjian, Maria, Sampaio, Misako Uemura, Lopes, Guiomar Silva, Oliva, Maria Luiza V
• Format: Journal Article
• Language: English
• Published: Germany 01-09-2012
• Subjects: Animals; Bauhinia - chemistry; Binding Sites; Bradykinin - analogs & derivatives; Bradykinin - metabolism; Bradykinin - pharmacology; Bradykinin B2 Receptor Antagonists; Calcium - metabolism; Cytosol - metabolism; Drug Interactions; Intestines - drug effects; Intestines - metabolism; Intestines - physiology; Kallikreins - antagonists & inhibitors; Male; Mice; Mice, Knockout; Muscle Contraction - drug effects; Muscle Contraction - physiology; Muscle, Smooth - drug effects; Muscle, Smooth - metabolism; Muscle, Smooth - physiology; Peptides - chemistry; Peptides - pharmacology; Plant Proteins - chemistry; Plant Proteins - pharmacology; Rats, Wistar; Receptor, Bradykinin B1 - metabolism; Receptor, Bradykinin B2 - metabolism; Verapamil - pharmacology
• DOI: 10.1515/hsz-2012-0126
• EISSN: 1437-4315

BbKI is a kallikrein inhibitor with a reactive site sequence similar to that of kinins, the vasoactive peptides inserted in kininogen moieties. This structural similarity probably contributes to the strong interaction with plasma kallikrein, the enzyme that releases, from high-molecular weight kininogen (HMWK), the proinflammatory peptide bradykinin, which acts on B(2) receptors (B(2)R). BbKI was examined on smooth muscle contraction and Ca(2+) mobilization, in which the kallikrein-kinin system is involved. Contrary to expectations, BbKI (1.8 μm) increased [Ca(2+)](c) and contraction, as observed with BK (2.0 μm). Not blocked by B(1) receptors (B(1)R), the BbKI agonistic effect was blocked by the B(2)R antagonist, HOE-140 (6 μm), and the involvement of B(2)R was confirmed in B(2)R-knockout mice intestine. The same tissue response was obtained using a synthetic peptide derived from the BbKI reactive site structure, more resistant than BK to angiotensin I-converting enzyme (ACE) hydrolysis. Depending on the concentration, BbKI has a dual effect. At a low concentration, BbKI acts as a potent kallikrein inhibitor; however, due to the similarity to BK, in high concentrations, BbKI greatly increases Ca(2+) release from internal storages, as a consequence of its interaction with B(2)R. Therefore, the antagonistic and agonistic effects of BbKI may be considered in conditions of B(2)R involvement.