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1.
Genome ; 66(4): 80-90, 2023 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-36763968

RESUMEN

Polygonatum cyrtonema Hua is a traditional Chinese herb medicine, and it is widely distributed in China. The intrageneric taxonomy and phylogenetic relationships within Polygonatum have long been controversial due to their morphological similarity and lacking special DNA barcodes. In this paper, the complete chloroplast genome is a relatively conserved quadripartite structure including a large single copy region of 84 711 bp, a small single copy region of 18 210 bp, and a pair of inverted repeats region of 26 142 bp. A total of 342 simple sequence repeats were identified, and most of them were found to be composed of A/T, including 126 mono-nucleotides and 179 di-nucleotides. Nucleotide diversity was analyzed and eight highly variable regions (psbl∼trnT-CGU, atpF∼atpH, trnT-GGU∼psbD, psaJ∼rps20, trnL-UAG∼ndhD, ndhG∼ndhl, ndhA, and rpl32∼ccsA) were identified as potential molecular markers. Phylogenetic analysis based on the whole chloroplast genome showed that P. cyrtonema, within the family Asparagaceae, is closely related to Polygonatum sibiricum and Polygonatum kingianum. The sequence matK, trnT-GGU & ccsA, and ndhG∼ndhA were identified as three DNA barcodes. The assembly and comparative analysis of P. cyrtonema complete chloroplast genome will provide essential molecular information about the evolution and molecular biology for further study.


Asunto(s)
Genoma del Cloroplasto , Plantas Medicinales , Polygonatum , Filogenia , Polygonatum/genética , Plantas Medicinales/genética , China
2.
Artículo en Chino | MEDLINE | ID: mdl-23290644

RESUMEN

OBJECTIVE: To investigate the effect of prostaglandins E1 combined with Xuebijing injection on the expression of transforming growth factor-ß1 (TGF-ß1) and tumor necrosis factor-α (TNF-α) in rats with acute pulmonary interstitial fibrosis. METHODS: A rat model of pulmonary interstitial fibrosis was established by intratracheal injection of bleomycin (1 ml/kg). One hundred and eight Wistar rats were randomly divided into six groups with 18 in each group, which were normal control group, model group, hormone (methylprednisolone) treatment group, Xuebijing treatment group, prostaglandin E1 treatment group and combination treatment group (prostaglandin E1 and Xuebijing injection). Except for those in the normal control group, the rats in each group were sacrificed on the 7th, 14th and 28th day after treatment. The TGF-ß1 expression in lung tissue was measured by immunohistochemical staining. The TNF-α concentration in bronchoalveolar lavage fluid (BALF) of rat model was determined by enzyme-linked immunosorbent assay. RESULTS: The combination treatment group showed significantly more macrophages with TGF-ß1 expression in lung tissue at each time point, as compared with the model group, Xuebijing treatment group, methylprednisolone treatment group and prostaglandin E1 treatment group (P < 0.05). On the 7th day, the TNF-α concentration in BALF in the combination treatment group was significantly lower than those in the model group, methylprednisolone treatment group and prostaglandin E1 treatment group (P < 0.05); on the 14th day, the TNF-α concentration in BALF in the combination treatment group was significantly lower than that in the model group (P < 0.05); on the 28th day, the levels of TNF-α in the prostaglandin E1 treatment group and combination treatment group were significantly lower than that in the model group (P < 0.05). CONCLUSION: Prostaglandin E1 combined with Xuebijing injection may significantly inhibit TGF-ß1 expression in the lung tissue of rats with acute pulmonary interstitial fibrosis, which reduces alveolar inflammatory response.


Asunto(s)
Alprostadil/farmacología , Medicamentos Herbarios Chinos/farmacología , Fibrosis Pulmonar/metabolismo , Factor de Crecimiento Transformador beta1/metabolismo , Alprostadil/administración & dosificación , Animales , Líquido del Lavado Bronquioalveolar/química , Medicamentos Herbarios Chinos/administración & dosificación , Femenino , Masculino , Metilprednisolona/administración & dosificación , Metilprednisolona/farmacología , Fibrosis Pulmonar/patología , ARN Mensajero/genética , Ratas , Ratas Wistar , Factor de Necrosis Tumoral alfa/metabolismo
3.
Zhongguo Wei Zhong Bing Ji Jiu Yi Xue ; 18(2): 105-8, 2006 Feb.
Artículo en Chino | MEDLINE | ID: mdl-16512643

RESUMEN

OBJECTIVE: To investigate the protective effects of the integrated traditional Chinese and western medicine Xuebijing injection on stress-induced organ damage in rabbits. METHODS: Forty rabbits were randomly divided into four groups: the control group, the model group, the western medicine group, and the Xuebijing group. The stress-induced organ damage model was replicated by soak the rabbits in water, the animals in the western medicine group and Xuebijing group received injection of lytic cocktail and Xuebijing, respectively. The changes in cortisol (Cor), thromboxane A(2) (TXA(2)), endothelin (ET), nitric oxide synthase (NOS) were determined at different time points in all the groups. The pathologic changes of the gastric mucosa, the adrenal gland and the cardiac muscle cell were observed. RESULTS: The content of Cor increased significantly in model group (P<0.01). The content of Cor decreased in the western medicine group and Xuebijing group, the changes showed no significant difference between two groups (P>0.05). The contents of ET, TXA(2) decreased and NOS increased in Xuebijing group compared with the western medicine group, the differences were significant (all P<0.05). The pathological changes of the gastric mucosa, the adrenal gland and the cardiac myocyte were less marked in Xuebijing group, compared with the western medicine group, the difference was significant (P<0.05). CONCLUSION: Xuebijing has better protective effects on stress-induced organ damage.


Asunto(s)
Glándulas Suprarrenales/patología , Medicamentos Herbarios Chinos/farmacología , Mucosa Gástrica/patología , Miocitos Cardíacos/patología , Estrés Fisiológico , Glándulas Suprarrenales/efectos de los fármacos , Animales , Modelos Animales de Enfermedad , Endotelinas/sangre , Mucosa Gástrica/efectos de los fármacos , Hidrocortisona/sangre , Miocitos Cardíacos/efectos de los fármacos , Óxido Nítrico Sintasa/sangre , Conejos , Distribución Aleatoria , Tromboxano A2/sangre
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