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1.
Zhongguo Zhong Yao Za Zhi ; (24): 3672-3677, 2021.
Article de Chinois | WPRIM | ID: wpr-888020

RÉSUMÉ

To explore the effect of ophiopogonin D on main fatty acid metabolic enzymes in human cardiomyocyte AC-16,so as to provide reference for cardiovascular protection mechanism and safe clinical application of Ophiopogon japonicus.CCK-8 (cell counting kit-8) was used to detect the effect of different concentrations of ophiopogonin D on the viability of cardiomyocytes.Meanwhile,the effect of different concentrations of ophiopogonin D on the morphology and quantity of cardiomyocytes was observed under microscope.The effect of ophiopogonin D on the mRNA expression of CYP2J2,CYP4F3,CYP4A11,CYP4A22 and CYP4F2 in cardiomyocytes was detected by RT-PCR.Western blot was used to detect the protein expression of CYP4F3 in different concentrations of ophiopogonin D.Compared with the control group,low-concentration ophiopogonin D had no effect on the viability of cardiomyocytes.However,ophiopogonin D with a concentration of higher than 20μmol·L~(-1)could promote the viability.Under the microscope,ophiopogonin D with a concentration of below 100μmol·L~(-1)had no significant effect on the morphology and number of cardiomyocytes.RT-PCR results showed that compared with the control group,5μmol·L~(-1)ophiopogonin D could slightly up-regulate mRNA expressions of CYP2J2 and CYP4F3,while high-concentration ophiopogonin D (10 and 20μmol·L~(-1)) could significantly induce mRNA expressions of CYP2J2and CYP4F3 in a dose-dependent manner (P<0.05).The same concentration of ophiopogonin D had a little effect on the mRNA expressions of CYP4A11,CYP4A22 and CYP4F2.Western blot results showed that 20μmol·L~(-1)ophiopogonin D could significantly induce the protein expression of CYP4F3 in a dose-dependent manner (P<0.05).Based on the above results,ophiopogonin D (less than100μmol·L~(-1)) has no effect on the viability of AC-16 cardiomyocytes.Ophiopogonin D (less than 100μmol·L~(-1)) can selectively induce the expressions of CYP2J2 and CYP4F3,regulate the metabolic pathway of fatty acid signaling molecules,and thus protecting the cardiovascular system.


Sujet(s)
Humains , Acides gras , Myocytes cardiaques , Saponines/pharmacologie , Spirostanes/pharmacologie
2.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;53(7): e9628, 2020. tab, graf
Article de Anglais | LILACS, ColecionaSUS | ID: biblio-1132530

RÉSUMÉ

Ophiopogonin D (OP-D) is the principal pharmacologically active ingredient from Ophiopogon japonicas, which has been demonstrated to have numerous pharmacological activities. However, its protective effect against renal damage in streptozotocin (STZ)-induced diabetic nephropathy (DN) rats remains unclear. The present study was performed to investigate the protective effect of OP-D in the STZ-induced DN rat model. DN rats showed renal dysfunction, as evidenced by decreased serum albumin and creatinine clearance, along with increases in serum creatinine, blood urea nitrogen, TGF-β1, and kidney hypertrophy, and these were reversed by OP-D. In addition, STZ induced oxidative damage and inflammatory response in diabetic kidney tissue. These abnormalities were reversed by OP-D treatment. The findings obtained in the present study indicated that OP-D might possess the potential to be a therapeutic agent against DN via inhibiting renal inflammation and oxidative stress.


Sujet(s)
Animaux , Mâle , Rats , Saponines/usage thérapeutique , Stress oxydatif/effets des médicaments et des substances chimiques , Ophiopogon/composition chimique , Diabète expérimental/traitement médicamenteux , Néphropathies diabétiques/traitement médicamenteux , Inflammation/prévention et contrôle , Spirostanes/usage thérapeutique , Rat Sprague-Dawley , Streptozocine
3.
Zhongguo Zhong Yao Za Zhi ; (24): 1876-1881, 2019.
Article de Chinois | WPRIM | ID: wpr-773153

RÉSUMÉ

This study is aimed to investigate the intervention effect and possible mechanism of ophiopogonin D( OPD) in protecting cardiomyocytes against ophiopogonin D'( OPD')-induced injury,and provide reference for further research on toxicity difference of saponins from ophiopogonins. CCK-8 assay was used to evaluate the effect of OPD and OPD' on cell viability. The effect of OPD on OPD'-induced cell apoptosis was measured by flow cytometry. Morphologies of endoplasmic reticulum were observed by endoplasmic reticulum fluorescent probe. PERK,ATF-4,Bip and CHOP mRNA levels were detected by Real-time quantitative polymerase chain reaction( PCR) analysis. ATF-4,phosphorylated PERK and e IF2α protein levels were detected by Western blot assay. RESULTS:: showed that treatment with OPD'( 6 μmol·L-1) significantly increased the rate of apoptosis; expressions of endoplasmic reticulum stress related genes were increased. The morphology of the endoplasmic reticulum was changed. In addition,different concentrations of OPD could partially reverse the myocardial cell injury caused by OPD'. The experimental results showed that OPD'-induced myocardial toxicity may be associated with the endoplasmic reticulum stress,and OPD may modulate the expression of CYP2 J3 to relieve the endoplasmic reticulum stress caused by OPD'.


Sujet(s)
Humains , Apoptose , Cardiotoniques , Pharmacologie , Cellules cultivées , Stress du réticulum endoplasmique , Myocytes cardiaques , Saponines , Pharmacologie , Spirostanes , Pharmacologie
4.
Zhongguo Zhong Yao Za Zhi ; (24): 377-384, 2018.
Article de Chinois | WPRIM | ID: wpr-771727

RÉSUMÉ

This study aimed to investigate the effect and mechanism of ophiopogonin D (OP-D) on Ang Ⅱ-induced HUVECs apoptosis, in order to provide a reliable basis for the safety and efficacy of traditional Chinese medicines. The effect of Ang Ⅱ on survival and total proteins content of HUVECs were measured by MTT and Western blotting. The effect of OP-D on Ang Ⅱ-induced lactate dehydrogenase (LDH) release rate in HUVECs was measured by enzyme standard instrument. The effects of OP-D and 11,12-EET on phosphorylation of JNK/c-Jun induced by Ang Ⅱ were measured by Western blot and RT-PCR with the help of JNK specific inhibitor SP600125 and CYP450 isozymes selective inhibitor 6-(2-propargyloxyphenyl) hexanoic acid (PPOH). The cell apoptosis was assayed by flow cytometry. According to the results, different doses of Ang Ⅱ had no significant effect on cell survival; treatment with Ang Ⅱ at 1×10⁻⁶ mol·L⁻¹ could increase the release of LDH (<0.001). The phosphorylation of JNK and c-Jun could be inhibited by the pre-treatment with SP600125, 11,12-EET and OP-D. Pre-treatment with OP-D could significantly reduce the release of LDH induced by Ang Ⅱ stimulation, decrease the expression of caspase-3, and diminish the apoptosis of cells. The protective effect of OP-D was suppressed, when being pretreated with PPOH. The experimental results showed that the apoptosis of HUVECs induced by Ang Ⅱ may be associated with JNK/c-Jun signaling pathway. OP-D-mediated CYP2J2 expression increased 11,12-EET levels, and could remarkably resist Ang Ⅱ-induced injury and apoptosis of cells, which is associated with the maintenance of endothelium homeostasis.


Sujet(s)
Humains , Angiotensine-II , Apoptose , Acides arachidoniques , Métabolisme , Cellules cultivées , Cytochrome P-450 enzyme system , Métabolisme , Cellules endothéliales de la veine ombilicale humaine , Biologie cellulaire , Phosphorylation , Saponines , Pharmacologie , Transduction du signal , Spirostanes , Pharmacologie
5.
Article de Anglais | WPRIM | ID: wpr-317048

RÉSUMÉ

<p><b>OBJECTIVE</b>To investigate the effects of ophiopogonin D on human breast cancer MCF-7 cells.</p><p><b>METHODS</b>Cell viability was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and colony formation experiments. Cell cycle was measured with cell cycle flow cytometry and a living cell assay. Apoptosis and terminal deoxynucleoitidyl transferase-mediated dUTP nick end labeling assays were performed to detect the apoptosis of MCF-7 cells induced by ophiopogonin D. Finally, Western blotting was used to explore the mechanism.</p><p><b>RESULTS</b>Exposure of cells to ophiopogonin D resulted in marked decreases in viable cells and colony formation with a dose-dependent manner. Treatment of these cells with ophiopogonin D also resulted in cell cycle arrest at the G(2)/M phase, and increased apoptosis. Mechanistically, ophiopogonin D-induced G(2)/M cell cycle arrest was associated with down-regulation of cyclin B1. Furthermore, activation of caspase-8 and caspase-9 was involved in ophiopogonin D-induced apoptosis.</p><p><b>CONCLUSION</b>The data suggested that ophiopogonin D inhibits MCF-7 cell growth via the induction of cell cycle arrest at the G(2)/M phase.</p>


Sujet(s)
Humains , Apoptose , Prolifération cellulaire , Points de contrôle de la phase G2 du cycle cellulaire , Points de contrôle de la phase M du cycle cellulaire , Cellules MCF-7 , Saponines , Pharmacologie , Spirostanes , Pharmacologie
6.
Yao Xue Xue Bao ; (12): 1117-1123, 2014.
Article de Chinois | WPRIM | ID: wpr-299159

RÉSUMÉ

This study aimed to examine whether ophiopogonin D (OP-D) is capable of protecting cardiomyocytes against DOX-induced injury and the mechanisms involved. H9c2 cells were cultured. MTT assay was used to evaluate cell viability and toxicity. Mito-tracker as fluorescence probe was used to measure ROS content raised from mitochondria. The mRNA and protein expression of ATF6alpha, GRP78 and CHOP were analyzed using real-time PCR and Western blotting, respectively. The results showed that a significant endoplasmic reticulum stress (ERS) was induced upon exposure of H9c2 cells to DOX as indicated by the increase in the expression of ERS related proteins, which was paralleled with the accumulation of reactive oxygen species (ROS) and decrease in the viability of H9c2 cells. Whereas, DOX-induced ROS accumulation and up-regulation of ERS related proteins were partially abolished by pretreatment with OP-D. Consequently, a DOX-induced ERS was mitigated by application of OP-D. Similarly, DOX-induced decrease in cell viability was partially attenuated by either inhibiting CHOP or pretreatment with N-acetylcysteine (NAC), an antioxidant. Moreover, cardiac ultrastructural abnormalities seen in mouse receiving DOX injections were obviously ameliorated by pretreatment of OP-D. Taken together, the present study proved that OP-D protects cardiomyocytes against DOX-induced injury, at least in part, through reducing ROS accumulation and alleviating ERS.


Sujet(s)
Animaux , Souris , Rats , Acétylcystéine , Facteur de transcription ATF-6 , Métabolisme , Antioxydants , Lignée cellulaire , Survie cellulaire , Doxorubicine , Stress du réticulum endoplasmique , Protéines du choc thermique , Métabolisme , Mitochondries , Métabolisme , Myocytes cardiaques , Espèces réactives de l'oxygène , Métabolisme , Saponines , Pharmacologie , Spirostanes , Pharmacologie , Facteur de transcription CHOP , Métabolisme , Régulation positive
7.
Article de Anglais | WPRIM | ID: wpr-812198

RÉSUMÉ

A competitive enzyme-linked immunosorbent assay (ELISA) was developed to determine ruscogenin (RUS) by using the monoclonal antibody (McAb). The monoclonal antibody against RUS, secreted from the established hybridoma cell lines, was identified as being of the IgG1 isotype. The McAb exhibited high specificity to RUS, showing a very slight cross reactivity with diosgenin (15.7%), and no cross-reactivity to sarsasapogenin, diammonium glycyrrhizinate, oleanolic acid and notoginsenoside R1. The established ELISA, at an IC50 value of 157.55 ng·mL(-1) and a detection limit (IC20) of 20.57 ng·mL(-1), was compared with HPLC analyses, and a good correlation between ELISA and HPLC-ELSD analyses of RUS in the extract of Radix Ophiopogonis was obtained. The experimental data indicated that the ELISA method exhibits more advantages over HPLC-ELSD, such as low detection limit, high specificity, low background, and no requirement for sample pre-treatment, and is more suitable for the determination of natural components in Chinese traditional medicines and in biological samples for pharmacokinetic studies.


Sujet(s)
Anticorps monoclonaux , Médicaments issus de plantes chinoises , Test ELISA , Méthodes , Sensibilité et spécificité , Spirostanes
8.
Article de Anglais | WPRIM | ID: wpr-812296

RÉSUMÉ

AIM@#To investigate the chemical constituents of Dioscorea zingiberensis C. H. Wright.@*METHODS@#The compounds were isolated by various chromatographic techniques, and the structures of the new steroidal saponins were elucidated by extensive 1D- and 2D-NMR, MS, and IR spectral analysis.@*RESULTS@#The 70% EtOH extract of the rhizomes of Dioscorea zingiberensis afforded two new steroidal saponins, zingiberenosides A (1) and B (2), along with eight known analogues, 3β, 26-dihydroxy-25(R)-furosta-Δ(5, 20(22))-diene-3-O-α-L- rhamnopyranosyl-(1→2)-O-β-D-glucopyranoside (3), methyl parvifloside (4), deltoside (5), methyl deltoside (6), zingiberensis new saponin (7), deltonin (8), progenin III (9) and diosgenin-diglucoside (10).@*CONCLUSION@#Two new steroidal saponins were isolated from Dioscorea zingiberensis and their structures determined.


Sujet(s)
Dioscorea , Chimie , Diosgénine , Chimie , Structure moléculaire , Extraits de plantes , Chimie , Rhizome , Chimie , Saponines , Chimie , Spirostanes , Chimie , Stéroïdes , Chimie
9.
Yao Xue Xue Bao ; (12): 855-859, 2013.
Article de Chinois | WPRIM | ID: wpr-259540

RÉSUMÉ

This study is to investigate the antitumor activity of ophiopogonin B (OP-B). MTT assay, flow cytometric analysis, acridine orange staining, Lyso-Tracker Red staining and HeLa-GFP-LC3 transfect cells assay were used to detect the proliferation activity, apoptosis and autophagy of HeLa cells. The results showed that OP-B exerted potent antiproliferative activity on HeLa cells, the cell growth inhibition effect of OP-B was not due to apoptosis and OP-B could induce autophagy of HeLa cells. OP-B also induced the protein expression up-regulation of Beclin-1 and promoted LC3 I transformation LC3 II, which were representative proteins of autophagy. Furthermore, 3-MA, an inhibitor of autophagy, not only inhibited OP-B-mediated autophagy but also almost completely reversed the antiproliferative effect of OP-B, suggesting that the growth inhibition effect of OP-B was autophagy dependent. Western blotting demonstrated that OP-B inhibited the phosphorylation of Akt and its' downstream vital protein, such as mTOR and p70S6K. In addition, OP-B also induced the protein expression up-regulation of PTEN, which is a negative regulation protein for Akt/mTOR signaling pathway. However, OP-B did not affect the protein expression of total Akt. Collectively, the antitumor effects of OP-B were autophagy-dependent via repression Akt/mTOR signaling pathway. Therefore, OP-B is a prospective inhibitor of Akt/mTOR and may be used as an alternative compound to treat cervical carcinoma.


Sujet(s)
Humains , Adénine , Pharmacologie , Antinéoplasiques d'origine végétale , Pharmacologie , Apoptose , Protéines régulatrices de l'apoptose , Métabolisme , Autophagie , Bécline-1 , Prolifération cellulaire , Relation dose-effet des médicaments , Cellules HeLa , Protéines membranaires , Métabolisme , Protéines associées aux microtubules , Métabolisme , Ophiopogon , Chimie , Phosphohydrolase PTEN , Métabolisme , Phosphorylation , Plantes médicinales , Chimie , Protéines proto-oncogènes c-akt , Métabolisme , Ribosomal Protein S6 Kinases, 70-kDa , Métabolisme , Saponines , Pharmacologie , Transduction du signal , Spirostanes , Pharmacologie , Sérine-thréonine kinases TOR , Métabolisme , Régulation positive
10.
Yao Xue Xue Bao ; (12): 619-623, 2012.
Article de Chinois | WPRIM | ID: wpr-276270

RÉSUMÉ

An unusual novel C27-steroidal glycoside sulfate was isolated from the underground organs of Liriope graminifolia (Linn.) Baker with three known compounds. Their chemical structures were determined by spectral analysis, including HR-MS, 1D and 2D NMR as (25S)-ruscogenin 1-sulfate-3-O-alpha-L-rhamnopyranoside (1), (25S)-ruscogenin 1-O-beta-D-xylopyranosyl-3-O-alpha-L-rhamnopyranoside (2), hesperidin (3), and 4', 7-dihydroxy-5-methoxyflavanone (4). Compound 1 has cytotoxic activities against K562 and HL60 cells with IC50 values of 18.6 microg x mL(-1) and 16.5 microg x mL(-1), respectively.


Sujet(s)
Humains , Antinéoplasiques d'origine végétale , Chimie , Pharmacologie , Prolifération cellulaire , Médicaments issus de plantes chinoises , Chimie , Pharmacologie , Hétérosides , Chimie , Pharmacologie , Cellules HL-60 , Hespéridine , Chimie , Pharmacologie , Concentration inhibitrice 50 , Cellules K562 , Liriope , Chimie , Tubercules , Chimie , Plantes médicinales , Chimie , Spirostanes , Chimie , Pharmacologie
11.
Yao Xue Xue Bao ; (12): 443-446, 2011.
Article de Chinois | WPRIM | ID: wpr-348936

RÉSUMÉ

Nonaqueous capillary electrophoresis is used for the determination of the contents of diosgenin and ruscogenin in Radix Ophiopogonis. The operating buffer was composed of 20 mmol x L(-1) Na2B4O7-HCl (pH 7.61) in 70% methanol. The applied voltage was 25 kV and detection potential was at +0.70 V. With these conditions, the components were successfully separated. The content of diosgenin in Radix Ophiopogonis was 0.018 mg x g(-1) and ruscogenin was 0.008 mg x g(-1). The average recoveries of diosgenin and ruscogenin were 102% and 99.2%, respectively. A new method of the quality control of diosgenin and ruscogenin in Radix Ophiopogonis is provided.


Sujet(s)
Diosgénine , Électrophorèse capillaire , Méthodes , Ophiopogon , Chimie , Racines de plante , Chimie , Plantes médicinales , Chimie , Contrôle de qualité , Spirostanes
12.
Zhongguo Zhong Yao Za Zhi ; (24): 2508-2510, 2010.
Article de Chinois | WPRIM | ID: wpr-279411

RÉSUMÉ

<p><b>OBJECTIVE</b>To develop an HPLC-ELSD method for the determination of 25 (R, S) ruscogenin 1-O-[beta-D-glucopyranosyl (1 --> 2)] [beta-D-xylopyranosyl (1 --> 3)] beta-D-fucopyranoside in the tuberous roots of Liriope muscari from different habitats and different harvest time.</p><p><b>METHOD</b>A Shimadzu C18 column (4.6 mm x 150 mm, 5 microm) with a solvent system consisting of acetonirile-water (46: 54) was used, and detected by ELSD. The temperature of drift tube was 94 degrees C and the nebulizer nitrogen flow rate was 2.5 L x min(-1).</p><p><b>RESULT</b>The calibration curve of 25 (R, S) ruscogenin 1-O-[beta-D-glucopyranosyl (1 --> 2)] [beta-D-xylopyranosyl (1 --> 3)] beta-D-fucopyranoside showed good linearity in the range of 1.02-12.228 microg and the average recovery was 100.80%, with RSD of 1.8%. 10 batches of L. muscari from different habitats were analyzed, and the contents were 0.25% - 0.41%. The contents of 15 batches from different harvest time were 0.13%-0.38%.</p><p><b>CONCLUSION</b>The method is simple, rapid and sensitive, and can be used for determination of 25 (R, S) ruscogenin 1-O-[beta-D-glucopyranosyl (1 --> 2)] [beta-D-xylopyranosyl (1 --> 3)] beta-D-fucopyranoside in L. muscari. It provides the valuable basis for quality assessment of L. muscari.</p>


Sujet(s)
Chromatographie en phase liquide à haute performance , Méthodes , Écosystème , Liliaceae , Chimie , Liriope , Chimie , Spectroscopie par résonance magnétique , Méthodes , Données de séquences moléculaires , Structure moléculaire , Préparations à base de plantes , Chimie , Pharmacologie , Racines de plante , Chimie , Physiologie , Structures de plante , Chimie , Saponines , Chimie , Spirostanes , Chimie , Pharmacologie , Triterpènes
13.
Zhongguo Zhong Yao Za Zhi ; (24): 1504-1507, 2007.
Article de Chinois | WPRIM | ID: wpr-287930

RÉSUMÉ

<p><b>OBJECTIVE</b>To study the accumulation of active ingredients, the absorption and transformation of N, P and K in Anemarrhena asphodeloides and provide basis for determination of the harvest time and fertilizing.</p><p><b>METHOD</b>Samples were collected in different phrases and the weight of dry matter, the content of N, P and K of different organs and the content of sarsasapogenin were determined.</p><p><b>RESULT</b>Absorption of N, P and K started by the root and rhizoma after July. At the end of August, the N and K of the aerial part transfered largely into rhizome. The content of sarsasapogenin in rhizome was the highest in early spring.</p><p><b>CONCLUSION</b>Additional fertilizer is helpful to increase the yield in July of the second year after the transplantation. The quality is the best when harvest in early spring.</p>


Sujet(s)
Absorption , Anemarrhena , Métabolisme , Engrais , Azote , Pharmacocinétique , Phosphore , Pharmacocinétique , Parties aériennes de plante , Métabolisme , Racines de plante , Métabolisme , Plantes médicinales , Métabolisme , Potassium , Pharmacocinétique , Rhizome , Métabolisme , Saisons , Spirostanes , Métabolisme
14.
Rev. Fac. Farm. (Merida) ; 29: 31-8, 1994. tab
Article de Espagnol | LILACS | ID: lil-151537

RÉSUMÉ

Un estudio sistemático de la cromatografía de gases espectrometría de masas de capturas de iones de espirostenos y furosteno relacionadoshidroxilados en el anillo F, libres o como derivados de TMS, es reportado. Las interacciones ión o iónmolécula están presentes en algunos casos siendo resuelto mediante la sililación


Sujet(s)
Chromatographie en phase gazeuse , Chromatographie d'échange d'ions , Spectrométrie de masse , Sapogénines , Spirostanes
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