A novel physiological property of snake bradykinin-potentiating peptides-Reversion of MK-801 inhibition of nicotinic acetylcholine receptors


Autoria(s): NERY, Arthur A.; TRUJILLO, Cleber A.; LAMEU, Claudiana; KONNO, Katsuhiro; OLIVEIRA, Vitor; CAMARGO, Antonio C. M.; ULRICH, Henning; HAYASHI, Mirian A. F.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

The first naturally occurring angiotensin-converting enzyme (ACE) inhibitors described are pyroglutamyl proline-rich oligopeptides, found in the venom of the viper Bothrops jararaca, and named as bradykinin-potentiating peptides (BPPs). Biochemical and pharmacological properties of these peptides were essential for the development of Captopril, the first active site-directed inhibitor of ACE, currently used for the treatment of human hypertension. However, a number of data have suggested that the pharmacological activity of BPPs could not only be explained by their inhibitory action on enzymatic activity of somatic ACE. In fact, we showed recently that the strong and long-lasting anti-hypertensive effect of BPP-10c [<ENWPHPQIPP] is independent of somatic ACE inhibition. On the other hand, nicotinic acetylcholine receptors expressed in blood vessels have been related to blood pressure regulation. Therefore, we have studied the effects of BPP-10c on acetylcholine receptor function in the PC12 pheochromocytoma cell line, which following induction to neuronal differentiation expresses most of the nicotinic receptor subtypes. BPP-10c did not induce receptor-mediated ion flux, nor potentiated carbamoylcholine-provoked receptor activity as determined by whole-cell recording. This peptide, however, alleviated MK-801-induced inhibition of nicotinic acetylcholine receptor activity. Although more data are needed for understanding the mechanism of the BPP-10c effect on nicotinic receptor activity and its relationship with the anti-hypertensive activity, this work reveals possible therapeutic applications for BPP-10c in establishing normal acetylcholine receptor activity. (C) 2008 Elsevier Inc. All rights reserved.

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP, Brazil

Identificador

PEPTIDES, v.29, n.10, p.1708-1715, 2008

0196-9781

http://producao.usp.br/handle/BDPI/31548

10.1016/j.peptides.2008.06.002

http://dx.doi.org/10.1016/j.peptides.2008.06.002

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

Relação

Peptides

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #Bradykinin-potentiating peptides #Nicotinic acetylcholine receptor #MK-801 inhibition #PC12 pheochromocytoma cells #ANGIOTENSIN-CONVERTING-ENZYME #AGKISTRODON-HALYS-BLOMHOFFII #BOTHROPS-JARARACA #NATRIURETIC PEPTIDE #SMOOTH-MUSCLE #VENOM GLAND #PC12 CELLS #COCAINE #MECHANISM #IDENTIFICATION #Biochemistry & Molecular Biology #Pharmacology & Pharmacy
Tipo

article

original article

publishedVersion