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1.
Cell Mol Biol (Noisy-le-grand) ; 66(2): 87-92, 2020 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-32415932

RESUMEN

Cerebral infarction is an acute cerebrovascular disease caused by abnormal blood circulation in the brain. In the present study, we investigate the effect of astragaloside IV on cognitive dysfunction in cerebrally infarcted rats via transforming growth factor-ß (TGF-ß) / Smad signaling pathway. For this purpose, 45 rats were divided into three groups including astragaloside, model, and control. 30 of 45 healthy adult male SD rats were randomly selected to establish an acute cerebral infarction model. 15 modeled rats were enrolled as a model and astragaloside group, and another 15 rats as a blank control group. The rats in the astragaloside group were fed with astragaloside IV according to 1.08 g/kg body weight, and those in the blank group and model group were given matching normal saline. The levels of TGF-ß, Smad1, Smad3 and Smad7 of TGF-ß/Smad signaling transduction pathway at T0 (week 0), T1 (week 3) and T2 (week 6) were determined by enzyme-linked immunosorbent assay (ELISA). The modified neurological severity score (mNSS) was used to evaluate the improvement of cognitive dysfunction in rats. The mNSS of rats with cerebral infarction in the astragaloside group was lower than that in the control group and model group (P< 0.05). While the levels of TGF-ß, Smad1, Smad3 and Smad7 in the astragaloside group were higher than those in the control group and model group (P< 0.05). Astragaloside IV plays an important role in improving cognitive dysfunction in rats with cerebral infarction while affecting the levels of TGF-ß, Smad1, Smad3 and Smad7 and activating TGF-ß / Smad signaling pathway.


Asunto(s)
Infarto Cerebral/tratamiento farmacológico , Saponinas/uso terapéutico , Proteínas Smad/metabolismo , Factor de Crecimiento Transformador beta/metabolismo , Triterpenos/uso terapéutico , Animales , Estudios de Casos y Controles , Infarto Cerebral/patología , Modelos Animales de Enfermedad , Ensayo de Inmunoadsorción Enzimática , Masculino , Ratas , Ratas Sprague-Dawley , Saponinas/farmacología , Índice de Severidad de la Enfermedad , Transducción de Señal/efectos de los fármacos , Proteínas Smad/análisis , Proteína Smad1/análisis , Proteína smad3/análisis , Proteína smad7/análisis , Triterpenos/farmacología
2.
J BUON ; 22(1): 265-269, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28365964

RESUMEN

PURPOSE: The current study was designed to investigate the primary efficacy of esophageal irradiation stents coated with 125I particles in the treatment of elderly patients with advanced esophageal cancer. METHODS: Forty-three elderly patients with advanced esophageal cancer were treated with esophageal stents in the First Affiliated Hospital of Xinxiang Medical University between September 2009 and December 2010. Patients were randomly divided into group A (N=18), treated with irradiation stents, and group B (N=25), treated with ordinary stents. There were no significant intergroup differences in age, lesion length, degree of stenosis, or cancer stage. The stent implantation success rate, relief of dysphagia and complication rate, and survival were assessed. RESULTS: The stent implantation success and short-term dysphagia relief rates were 100.0% in both groups. The mean survival time was 9.8 months and 4.8 months in groups A and B, respectively (p<0.01). However, no significant difference in pain (5/18) or esophageal restenosis (7/25) was found (both p>0.05). CONCLUSION: Dysphagia was relieved and survival was prolonged in advanced esophageal cancer cases treated with 125I particle-coated esophageal stents. This method may be superior to the traditional stents method.


Asunto(s)
Neoplasias Esofágicas/radioterapia , Radioisótopos de Yodo/uso terapéutico , Stents , Anciano , Anciano de 80 o más Años , Trastornos de Deglución/terapia , Neoplasias Esofágicas/mortalidad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Stents/efectos adversos
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