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J Nutr Biochem ; 82: 108398, 2020 08.
Artículo en Inglés | MEDLINE | ID: mdl-32402912

RESUMEN

Neointimal hyperplasia is a prominent pathological phenomenon in the process of stent restenosis. Abnormal proliferation and migration of vascular smooth muscle cells (VSMCs) play major pathological processes involved in the development of restenosis. l-Theanine, one of the major amino acid components in green tea, has been reported to improve vascular function. Here we display the effects of l-theanine on neointima formation and the underlying mechanism. In the rat carotid-artery balloon-injury model, l-theanine greatly inhibited neointima formation and prevented VSMCs from a contractile phenotype switching to a synthetic phenotype. In vitro study showed that l-theanine significantly inhibited PDGF-BB-induced VSMC proliferation and migration, which was comparable with the effect of l-theanine on AngII-induced VSMC proliferation and migration. Western blot analysis demonstrated that l-theanine suppressed PDGF-BB and AngII-induced reduction of SMA and SM22α and increment of OPN, suggesting that l-theanine inhibited the transformation of VSMCs from contractile to the synthetic phenotype. Further experiments showed that l-theanine exhibits potential preventive effects on neointimal hyperplasia and related vascular remodeling via inhibition of phosphorylation of Elk-1 and activation of MAPK1. The present study provides the new experimental evidence that l-theanine has potential clinical application as an anti-restenosis agent for the prevention of restenosis.


Asunto(s)
Traumatismos de las Arterias Carótidas/patología , Glutamatos/farmacología , Músculo Liso Vascular/efectos de los fármacos , Neointima/prevención & control , Animales , Becaplermina/farmacología , Traumatismos de las Arterias Carótidas/metabolismo , Movimiento Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Células Cultivadas , Reestenosis Coronaria/prevención & control , Modelos Animales de Enfermedad , Hiperplasia/tratamiento farmacológico , Masculino , Proteína Quinasa 1 Activada por Mitógenos/metabolismo , Miocitos del Músculo Liso/efectos de los fármacos , Neointima/patología , Fenotipo , Ratas , Ratas Sprague-Dawley , Transducción de Señal/efectos de los fármacos , Té/química , Proteína Elk-1 con Dominio ets/metabolismo
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