Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Crotamine Pharmacology Revisited: Novel Insights Based on the Inhibition of K-V Channels

Texto completo
Autor(es):
Peigneur, Steve [1] ; Orts, Diego J. B. [2] ; Prieto da Silva, Alvaro R. [3] ; Oguiura, Nancy [4] ; Boni-Mitake, Malvina [5] ; de Oliveira, Eduardo B. [6] ; Zaharenko, Andre J. [3] ; de Freitas, Jose C. [2] ; Tytgat, Jan [1]
Número total de Autores: 9
Afiliação do(s) autor(es):
[1] Katholieke Univ Leuven, Toxicol Lab, Louvain - Belgium
[2] Univ Sao Paulo, Inst Biociencias, Dept Fisiol, Sao Paulo - Brazil
[3] Inst Butantan, Genet Lab, Sao Paulo - Brazil
[4] Inst Butantan, Lab Ecol & Evolucao, Sao Paulo - Brazil
[5] Comissao Nacl Energia Nucl, Inst Pesquisas Energet & Nucl, Sao Paulo - Brazil
[6] Univ Sao Paulo, Dept Biochem & Immunol, Ribeirao Preto Med Sch, Sao Paulo - Brazil
Número total de Afiliações: 6
Tipo de documento: Artigo Científico
Fonte: MOLECULAR PHARMACOLOGY; v. 82, n. 1, p. 90-96, JUL 2012.
Citações Web of Science: 33
Resumo

Crotamine, a 5-kDa peptide, possesses a unique biological versatility. Not only has its cell-penetrating activity become of clinical interest but, moreover, its potential selective antitumor activity is of great pharmacological importance. In the past, several studies have attempted to elucidate the exact molecular target responsible for the crotamine-induced skeletal muscle spasm. The aim of this study was to investigate whether crotamine affects voltage-gated potassium (K-V) channels in an effort to explain its in vivo effects. Crotamine was studied on ion channel function using the two-electrode voltage clamp technique on 16 cloned ion channels (12 K-V channels and 4 Na-V channels), expressed in Xenopus laevis oocytes. Crotamine selectively inhibits K-V 1.1, K-V 1.2, and K-V 1.3 channels with an IC50 of similar to 300 nM, and the key amino acids responsible for this molecular interaction are suggested. Our results demonstrate for the first time that the symptoms, which are observed in the typical crotamine syndrome, may result from the inhibition of K-V channels. The ability of crotamine to inhibit the potassium current through K-V channels unravels it as the first snake peptide with the unique multifunctionality of cell-penetrating and antitumoral activity combined with K-V channel-inhibiting properties. This new property of crotamine might explain some experimental observations and opens new perspectives on pharmacological uses. (AU)

Processo FAPESP: 09/07128-7 - Neurotoxinas de anêmonas do mar como ferramentas para o estudo da fisiologia de canais voltagem - dependentes de potássio
Beneficiário:Diego Jose Orts y Belato
Linha de fomento: Bolsas no Brasil - Mestrado