2024-03-19T02:55:11Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/1509402021-10-27T12:01:41Zcom_10261_22com_10261_1col_10261_275
DIGITAL.CSIC
author
Rudnicki, Martina
author
Boscá, Lisardo
author
Abdalla, Dulcineia S. P.
funder
Conselho Nacional de Desenvolvimento Científico e Tecnológico (Brasil)
funder
Ministério da Ciência, Tecnologia e Inovação (Brasil)
funder
Instituto Nacional de Ciência e Tecnologia em Toxinas (Brasil)
funder
Ministerio de Ciencia e Innovación (España)
funder
Fundação de Amparo à Pesquisa do Estado de São Paulo
2017-06-06T09:19:50Z
2017-06-06T09:19:50Z
2016
European Journal of Pharmacology 782: 98-106 (2016)
http://hdl.handle.net/10261/150940
10.1016/j.ejphar.2016.04.038
http://dx.doi.org/10.13039/501100003593http://dx.doi.org/10.13039/501100001807http://dx.doi.org/10.13039/501100003545http://dx.doi.org/10.13039/501100004933http://dx.doi.org/10.13039/501100004837
Thiazolidinediones (TZDs) are peroxisome proliferator-activated receptor-γ (PPARγ) agonists used in treating type 2 diabetes that may exhibit beneficial pleiotropic effects on endothelial cells. In this study, we characterized the effects of three new TZDs [GQ-32 (3-biphenyl-4-ylmethyl-5-(4-nitro-benzylidene)-thiazolidine-2,4-dione), GQ-169 (5-(4-chloro-benzylidene)-3-(2,6-dichloro-benzyl)-thiazolidine-2,4-dione), and LYSO-7 (5-(5-bromo-1H-indol-3-ylmethylene)-3-(4-chlorobenzyl)-thiazolidine-2,4-dione)] on endothelial cells. The effects of the new TZDs were evaluated on the production of nitric oxide (NO) and reactive oxygen species (ROS), cell migration, tube formation and the gene expression of adhesion molecules and angiogenic mediators in human umbilical vein endothelial cells (HUVECs). PPARγ activation by new TZDs was addressed with a reporter gene assay. The three new TZDs activated PPARγ and suppressed the tumor necrosis factor α-induced expression of vascular cell adhesion molecule 1 and intercellular adhesion molecule 1. GQ-169 and LYSO-7 also inhibited the glucose-induced ROS production. Although NO production assessed with 4-amino-5-methylamino-2′,7′-difluorofluorescein-FM probe indicated that all tested TZDs enhanced intracellular levels of NO, only LYSO-7 treatment significantly increased the release of NO from HUVEC measured by chemiluminescence analysis of culture media. Additionally, GQ-32 and GQ-169 induced endothelial cell migration and tube formation by the up-regulation of angiogenic molecules expression, such as vascular endothelial growth factor A and interleukin 8. GQ-169 also increased the mRNA levels of basic fibroblast growth factor, and GQ-32 enhanced transforming growth factor-β expression. Together, the results of this study reveal that these new TZDs act as partial agonists of PPARγ and modulate endothelial cell activation and endothelial dysfunction besides to stimulate migration and tube formation.
eng
closedAccess
Inflammation
Endothelial cells
Thiazolidinediones
Angiogenesis
New thiazolidinediones affect endothelial cell activation and angiogenesis
artículo
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URL
https://digital.csic.es/bitstream/10261/150940/1/accesoRestringido.pdf
File
MD5
42637ae8545636bc41605c1740a9a84e
15753
application/pdf
accesoRestringido.pdf