| Literature DB >> 26615828 |
Wilmer H Perera Córdova1, Suzana Guimarães Leitão2, Geraldino Cunha-Filho3, Roberto Alonso Bosch4, Isel Pascual Alonso4, Rogelio Pereda-Miranda5, Rodrigo Gervou3, Natália Araújo Touza3, Luis Eduardo M Quintas3, François Noël3.
Abstract
Parotoid gland secretions of toad species are a vast reservoir of bioactive molecules with a wide range of biological properties. Herein, for the first time, it is described the isolation by preparative reversed-phase HPLC and the structure elucidation by NMR spectroscopy and/or mass spectrometry of nine major bufadienolides from parotoid gland secretions of the Cuban endemic toad Peltophryne fustiger: ψ-bufarenogin, gamabufotalin, bufarenogin, arenobufagin, 3-(N-suberoylargininyl) marinobufagin, bufotalinin, telocinobufagin, marinobufagin and bufalin. In addition, the secretion was analyzed by UPLC-MS/MS which also allowed the identification of azelayl arginine. The effect of arenobufagin, bufalin and ψ-bufarenogin on Na(+)/K(+)-ATPase activity in a human kidney preparation was evaluated. These bufadienolides fully inhibited the Na(+)/K(+)-ATPase in a concentration-dependent manner, although arenobufagin (IC50 = 28.3 nM) and bufalin (IC50 = 28.7 nM) were 100 times more potent than ψ-bufarenogin (IC50 = 3020 nM). These results provided evidence about the importance of the hydroxylation at position C-14 in the bufadienolide skeleton for the inhibitory activity on the Na(+)/K(+)-ATPase. Published by Elsevier Ltd.Entities:
Keywords: 1D and 2D NMR spectroscopy; Bufadienolides; HRESIMS; Na(+)/K(+) ATPase; Peltophryne fustiger; UPLC-MS/MS; Western Giant toad
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Year: 2015 PMID: 26615828 DOI: 10.1016/j.toxicon.2015.11.015
Source DB: PubMed Journal: Toxicon ISSN: 0041-0101 Impact factor: 3.033