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1.
Zhongguo Zhong Yao Za Zhi ; 42(17): 3398-3402, 2017 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-29192453

RESUMO

An Affi-Prep Polymyxin column was combined with a Phenyl Sepharose column and a Sephacryl S-300 column, respectively, to remove the lipopolysaccharides(LPS) in the anti-complementary crude polysaccharides of Houttuynia Herba. The contents of LPS in the polysaccharides were determined by chromogenic tachypleus amebocyte lysate(TAL)method during the procedure of purifying. The anti-complementary activities of the polysaccharides were also compared before and after the removal of LPS. Less remanent LPS was detected after purified using Penyl Sepharose combined with polymyxin column, with the clearance rate of 42.85%. All the columns had no effect on the anti-complementary activity of the polysaccharides. Penyl Sepharose combined with polymyxin column would be sound for LPS removal of the anti-complementary polysaccharides without reducing their bioactivity.


Assuntos
Houttuynia/química , Lipopolissacarídeos/isolamento & purificação , Polissacarídeos/química , Cromatografia , Sefarose
2.
World J Gastroenterol ; 22(48): 10584-10591, 2016 Dec 28.
Artigo em Inglês | MEDLINE | ID: mdl-28082810

RESUMO

AIM: To investigate the pharmacological effect of TongXie-YaoFang (TXYF) formula, a Chinese herbal formula, on Diarrhea-predominant irritable bowel syndrome (D-IBS) rats. METHODS: In a neonatal maternal separation plus restraint stress (NMS + RS) model of D-IBS, male Sprague Dawley rats were randomly divided into two groups (NMS + RS group and TXYF-formula group) with no handlings were used as controls (NH group). Starting from postnatal day 60, rats in TXYF-formula group were administered TXYF-formula (4.92 g/100 g bodyweight) orally twice a day for 14 consecutive days while NH group and NMS + RS group were given distilled water. Using short-circuit current technology, we observed 5-HT-induced changes of current across ion channels, such as cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel, epithelial Na+ channel (ENaC), Ca2+-dependent Cl- channel (CACC), Na+-K+-2Cl- co-transporter (NKCC), and Na+-HCO3- co-transporter (NBC), in the colonic epithelium of three groups after exposure to drugs and specific blockers with a Power Lab System (AD Instruments International). RESULTS: Under basal conditions, the changes of short-circuit current (∆Isc, µA/cm2) induced by 5-HT were similar in NH group and TXYF-formula group, and both higher than NMS + RS group (70.86 µA/cm2 ± 12.32 µA/cm2, 67.67 µA/cm2 ± 11.68 µA/cm2vs 38.8 µA/cm2 ± 7.25 µA/cm2, P < 0.01, respectively). When CACC was blocked by 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid, 5-HT-induced ∆Isc was smaller in NMS + RS group than in NH group and TXYF-formula group, respectively (48.41 µA/cm2 ± 13.15 µA/cm2vs 74.62 µA/cm2 ± 10.73 µA/cm2, 69.22 µA/cm2 ± 11.7 µA/cm2, P < 0.05, respectively). The similar result could be obtained when ENaC was blocked by Amiloride (44.69 µA/cm2 ± 12.58 µA/cm2vs 62.05 µA/cm2 ± 11.26 µA/cm2, 62.11 µA/cm2 ± 12.01 µA/cm2, P < 0.05, respectively). However, when CFTR Cl- channel was blocked by 1,1-dimethyl piperidinium chloride (DPC), 5-HT-induced ∆Isc did not significantly differ in three groups (42.28 µA/cm2 ± 10.61 µA/cm2vs 51.48 µA/cm2 ± 6.56 µA/cm2vs 47.75 µA/cm2 ± 7.99 µA/cm2, P > 0.05, respectively). The similar results could also be obtained in three groups when NBC and NKCC were respectively blocked by their blockers. CONCLUSION: TXYF-formula can regulate the Cl- and HCO3- secretion of colonic mucosa via CFTR Cl- channel, Cl-/HCO3- exchanger, NBC and NKCC co-transporters.


Assuntos
Canais de Cloreto/efeitos dos fármacos , Diarreia/metabolismo , Medicamentos de Ervas Chinesas/farmacologia , Mucosa Intestinal/efeitos dos fármacos , Síndrome do Intestino Irritável/metabolismo , Simportadores de Sódio-Bicarbonato/efeitos dos fármacos , 5-Hidroxitriptofano/farmacologia , Adulto , Amilorida/farmacologia , Animais , Canais de Cloreto/antagonistas & inibidores , Colo/metabolismo , Diarreia/tratamento farmacológico , Diarreia/etiologia , Bloqueadores do Canal de Sódio Epitelial/farmacologia , Humanos , Mucosa Intestinal/metabolismo , Síndrome do Intestino Irritável/tratamento farmacológico , Síndrome do Intestino Irritável/etiologia , Masculino , Privação Materna , Piperidinas/farmacologia , Distribuição Aleatória , Ratos , Ratos Sprague-Dawley , Inibidores de Simportadores de Cloreto de Sódio e Potássio/farmacologia , Simportadores de Sódio-Bicarbonato/antagonistas & inibidores , Simportadores de Cloreto de Sódio-Potássio/efeitos dos fármacos , Estresse Psicológico/complicações , Adulto Jovem
3.
Zhonghua Yi Xue Za Zhi ; 92(15): 1041-4, 2012 Apr 17.
Artigo em Chinês | MEDLINE | ID: mdl-22781645

RESUMO

OBJECTIVE: To summarize the clinical efficacies and experiences of using rapid pore cranial drilling and external ventricular drainage (EVD) in the treatment of ventricular hemorrhage caused by thalamic hemorrhage. METHODS: Retrospective analysis was conducted for 401 patients at 5 hospitals from May 1983 to December 2010. They underwent EVD with an infusion of urokinase for intraventricular hemorrhage caused by thalamic hemorrhage. There were 212 males and 189 females with an age range of 19 - 78 years. RESULTS: After a 1-month therapy, the outcomes were cure 147/401 (36.7%), improvement 192/401 (47.9%) and others (death and against-advice discharge) 62/401 (15.4%). After 1-3-month treatment, their prognoses were evaluated by activity of daily living (ADL): ADLI 147/401, ADLII 82/401, ADLIII 76/401, ADLIV 19/401, ADLV 15/401, death 43/401 and against-advice discharge 19/401. During a follow-up period of 1 - 3 years, 274 patients showed the following outcomes: ADLI 122/243, ADLII 63/243, ADLIII 58/243 while 31 patients died from pulmonary infection. CONCLUSION: The procedure of EVD (including an infusion of urokinase) with rapid pore cranial drilling is preferred treatment for ventricular hemorrhage caused by thalamic hemorrhage.


Assuntos
Hemorragia Cerebral/cirurgia , Drenagem/métodos , Adulto , Idoso , Hemorragia Cerebral/patologia , Ventrículos Cerebrais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Tálamo/patologia , Resultado do Tratamento , Ativador de Plasminogênio Tipo Uroquinase/uso terapêutico , Adulto Jovem
4.
J Asian Nat Prod Res ; 14(6): 592-5, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22587799

RESUMO

A polysaccharide, isolated and purified from the aqueous extract of nettle plant Urtica fissa, was found to consist of D-glucose and D-arabinose. Molecular weight was determined to be Mn 4140. The NMR experiments (¹H, ¹³C, ¹H--¹H COSY, TOCSY, HSQC, NOESY, and HMBC) revealed the structure as the following repeating unit: -->6)-α-D-Glcp-(1-->6)-α-D-Glcp-(1-->6)-ß-D-Glcp--(1-->5)-ß-D-Araf-(1-->3)-ß-D-Glcp-(1-->


Assuntos
Medicamentos de Ervas Chinesas/isolamento & purificação , Ressonância Magnética Nuclear Biomolecular/métodos , Polissacarídeos/química , Polissacarídeos/isolamento & purificação , Urticaceae/química , Sequência de Carboidratos , Medicamentos de Ervas Chinesas/química , Raízes de Plantas/química
5.
J Asian Nat Prod Res ; 11(11): 951-7, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20183259

RESUMO

Three polysaccharides were isolated from the roots of Urtica fissa by extraction, ultrafiltration, anion-exchange, and gel-filtration chromatography. The structures were characterized using acetylation, methylation, and spectral methods (GCMS, NMR). All three polysaccharides are mainly composed of D-arabinofuranosyl, D-galactopyranosyl, D-glucopyranosyl residues with different structural characteristics. Polysaccharide A of MW 5.2 x 10(3) contained a linear chain of 1-linked beta-D-glucopyranosyl, 1,6-linked beta-D-glucopyranosyl, 1,6-linked alpha-galactopyranosyl, and 1,5-linked beta-arabinofuranosyl moieties. Polysaccharide B of MW 7.7 x 10(4) possessed a chain consisting of 1,5-linked alpha-D-arabinofuranosyl, 1,3-linked beta-D-mannopyranosyl, 1,6-linked beta-D-glucopyranosyl, and 1,6-linked alpha-D-galactopyranosyl residues, but 4-O of alpha-D-galactopyranosyl residues were branched by terminal beta-D-glucopyranosyl residues. Polysaccharide C of MW 5.3 x 10(4) composed of a chain of 1,5-linked alpha-D-arabinofuranosyl, 1,4-linked beta-D-galactopyranosyl, 1,5-linked beta-D-xylopyranosyl, 1,4-linked beta-D-mannopyranosyl, 1-linked beta-D-glucopyranosyl residues, and the terminal beta-D-glucopyranosyl residues are attached to 3-O positions of 1,6-linked alpha-D-glucopyranosyl residues.


Assuntos
Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/isolamento & purificação , Polissacarídeos/química , Polissacarídeos/isolamento & purificação , Urticaceae/química , Cromatografia Gasosa-Espectrometria de Massas , Ressonância Magnética Nuclear Biomolecular , Raízes de Plantas/química
6.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao ; 25(1): 88-92, 2003 Feb.
Artigo em Chinês | MEDLINE | ID: mdl-12905617

RESUMO

In order to explore the new methods of biological treatment of human gliomas, this project is to study the biological properties of gliomas from four different aspects, the results show that there is a IL-6 autocrine loop in human gliomas and the growth of gliomas will be inhibited when the autocrine loop is broken. There is a magnificent predominant expression of Th2 cytokines in human gliomas and human glioma cells, the switching of Th2 to Th1 can inhibit the proliferation of glioma cells. The dosage of 100 micrograms/ml of erythromycin is the best of therapeutic effect. Angiostatin can not only inhibit the vascular endothelial growth, but also have the inhibitory role on the growth of glioma cells in vivo. The above studies have provided some new ideas and will be very helpful for the treatment of glioma patients.


Assuntos
Neoplasias Encefálicas/metabolismo , Glioma/metabolismo , Interleucina-6/metabolismo , Angiostatinas/farmacologia , Animais , Terapia Biológica , Neoplasias Encefálicas/terapia , Resistencia a Medicamentos Antineoplásicos , Glioma/terapia , Humanos , Interleucina-6/genética , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Células Th1/metabolismo , Células Th2/metabolismo
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