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- Title
Pharmacological characterization of the cardiovascular effect of Nibethione: ex vivo, in vivo and in silico studies.
- Authors
Sánchez-Recillas, Amanda; Navarrete-Vázquez, Gabriel; Hidalgo-Figueroa, Sergio; Bonilla-Hernández, Marcos; Ortiz-Andrade, Rolffy; Ibarra-Barajas, Maximiliano; Yáñez-Pérez, Víctor; Carlos Sánchez-Salgado, Juan
- Abstract
Objective This work describes the vasorelaxant and antihypertensive effects and the mechanism of action on vascular smooth muscle cells of Nibethione, a synthetic thiazolidinedione derivative. Additionally, evidence of its cytotoxicity is assessed. Methods Nibethione (NB) was synthesized, and its vasorelaxant effect and mechanism of action were assessed through ex vivo experiments. Molecular docking studies were used to predict the mode of interaction with L-type Ca2+ channel, and in vivo antihypertensive activity was assayed on spontaneously hypertensive rats (SHR). The cytotoxicity potential was evaluated in porcine aortic endothelial cells (PAECs) from primary explants. Key findings Nibethione vasorelaxant effect was efficient on KCl (80 mM) and NE-contraction. This effect was deleteriously modified in the presence of potassium channel block drugs, while the maximal contraction induced with NE was significantly decreased by NB; the CaCl2-induced contraction was abolished entirely. In vivo experiments showed that NB decreased diastolic blood pressure in 20.3 % after its administration on SHR. The molecular docking showed that NB blocks L-type Ca2+ channel, and in vitro tests showed that NB did not produce cytotoxic activity on PAECs (IC50 >1000 µM). Conclusions Nibethione showed in vivo antihypertensive and ex vivo vasorelaxant effects with implication of voltage-dependent L-type Ca2+ channel blocking, and this may contribute to the research of novel antihypertensive drugs.
- Subjects
VASCULAR smooth muscle; POTASSIUM channels; MOLECULAR docking; IN vivo studies; BLOOD pressure; AORTA; ANGIOTENSIN I
- Publication
Journal of Pharmacy & Pharmacology, 2021, Vol 73, Issue 11, p1186
- ISSN
0022-3573
- Publication type
Article
- DOI
10.1111/jphp.13295