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1.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 610-614, 2018.
Article in English | WPRIM | ID: wpr-773580

ABSTRACT

The present study was designed to further investigate the C steroidal glycosides in Cynanchum plants. Two new steroidal glycosides based on a 13, 14:14, 15-disecopregnane-type aglycone, komaroside P (1) and komaroside Q (2), together with three known compounds (3-5) were isolated from the whole herbs of Cynanchum komarovii. The aglycones of compounds 1 and 2 were two new disecopregnane. Their structures were elucidated on the basis of 1D, 2D NMR spectroscopic data and acid hydrolysis. All the compounds (1-5) showed potent inhibitory activities against human leukemia cell lines (HL-60) with IC values ranging from 16.6 to 26.3 μmol·L, compared to the positive control 5-fluorouracil (6.4 μmol·L).


Subject(s)
Humans , Cell Survival , Cynanchum , Chemistry , Drugs, Chinese Herbal , Chemistry , Pharmacology , Glycosides , Chemistry , Pharmacology , HL-60 Cells , Magnetic Resonance Spectroscopy , Molecular Structure , Steroids , Chemistry , Pharmacology
2.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 610-614, 2018.
Article in English | WPRIM | ID: wpr-812369

ABSTRACT

The present study was designed to further investigate the C steroidal glycosides in Cynanchum plants. Two new steroidal glycosides based on a 13, 14:14, 15-disecopregnane-type aglycone, komaroside P (1) and komaroside Q (2), together with three known compounds (3-5) were isolated from the whole herbs of Cynanchum komarovii. The aglycones of compounds 1 and 2 were two new disecopregnane. Their structures were elucidated on the basis of 1D, 2D NMR spectroscopic data and acid hydrolysis. All the compounds (1-5) showed potent inhibitory activities against human leukemia cell lines (HL-60) with IC values ranging from 16.6 to 26.3 μmol·L, compared to the positive control 5-fluorouracil (6.4 μmol·L).


Subject(s)
Humans , Cell Survival , Cynanchum , Chemistry , Drugs, Chinese Herbal , Chemistry , Pharmacology , Glycosides , Chemistry , Pharmacology , HL-60 Cells , Magnetic Resonance Spectroscopy , Molecular Structure , Steroids , Chemistry , Pharmacology
3.
International Eye Science ; (12): 217-220, 2017.
Article in Chinese | WPRIM | ID: wpr-731455

ABSTRACT

@#AIM: To investigate the effect of NgR mediated oxidative stress on the apoptosis of retinal ganglion cells(RGCs)induced by glucose. <p>METHODS: RGC-5 cell were divided into 3 groups: control group(DMEM high glucose medium+10% fetal calf serum), high glucose group(DMEM high glucose medium+10% fetal calf serum+30mmol/L glucose),NEP1-40 group(DMEM high glucose medium+10% fetal calf serum+30mmol/L glucose+1μmol/L NEP1-40). Detections were performed after 3d culture: the state of cell growth was observed by microscopy. Cell viability was detected by CCK-8 kit. The apoptosis rate of RGC cells was detected by flow cytometry(FCM). The intensity of ROS of the cells were detected by fluorescence microscopy. Intracellular MDA levels and SOD activity were measured by related kits. Western blot was used to detect the expressions of Bcl-2 and Bax proteins. <p>RESULTS: Compared with control group, high glucose group had a poor state and cell viability decreased, cell apoptosis rate significantly increased, ROS and MDA levels were significantly enhanced, SOD activity decreased, and the expression of anti-apoptotic protein Bcl-2 was decreased and the expression of pro apoptotic protein Bax was up-regulated. Compared with glucose group, after NgR expression was inhibited by NEP1-40, the oxidative stress reaction was reduced, Bcl-2/Bax was increased, the cell status was improved, the cell viability was increased, and the apoptosis rate was decreased in the NEP1-40 group(<i>P</i><0.05).<p>CONCLUSION: High concentration of glucose can induce apoptosis of RGC-5 cells by NgR mediated oxidative stress reaction.

4.
Acta Academiae Medicinae Sinicae ; (6): 499-503, 2011.
Article in Chinese | WPRIM | ID: wpr-352998

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the feasibility of applying diffusion tensor imaging (DTI)-based arcuate fasciculus tractography and intraoperative arcuate fasciculus navigation for neurosurgery.</p><p><b>METHODS</b>Totally 85 patients with interhemispheric tumors who had undergone intra-operative magnetic resonance imaging (MRI) and neuronavigation were divided into sinistrocerebral tumor (SCT) group (n = 55) and sham group (n = 30). All patients accepted routine MRI and DTI preoperatively. The results from both DTI-based arcuate fasciculus tractography and neuronavigation were applied to guide the surgery. All patients were followed up at 2-4 weeks and 3-6 months postoperatively.</p><p><b>RESULTS</b>All patients smoothly received the pre-operative DTI-based arcuate fasciculus tractography. The three dimensional arcuate fasciculus was successfully integrated with the neuronavigation and achieved microscope heads-up display. Long-term follow-up showed that there were only 4 patients suffered from persistent language dysfunction.</p><p><b>CONCLUSIONS</b>The combined application of DTI-based arcuate fasciculus tractography and intraoperative arcuate fasciculus navigation is feasible for guiding brain surgery. It can improve the surgical outcomes of intracranial tumor involving language functional area. The technology also maximizes the retention of language function and improves the post-operative quality of life.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Brain Neoplasms , General Surgery , Diffusion Magnetic Resonance Imaging , Methods , Diffusion Tensor Imaging , Follow-Up Studies , Monitoring, Intraoperative , Methods , Neuronavigation , Methods
5.
Journal of Southern Medical University ; (12): 805-809, 2011.
Article in Chinese | WPRIM | ID: wpr-332546

ABSTRACT

<p><b>OBJECTIVE</b>To explore the clinical value of intraoperative magnetic resonance imaging (MRI) and functional neuronavigation in the preservation of the language function during microsurgery for lesions near language-related brain regions.</p><p><b>METHODS</b>Sixty-one right-handed patients underwent microsurgical resection of the lesions near the language-related brain regions with the assistance of intraoperative MRI and blood oxygen level- and diffusion tensor imaging-based functional neuronavigation. The patients were divided into 2 groups according to the location of the lesions, namely group A with lesions near the left posterior inferior frontal gyrus and group B with lesions near the left posterior superior temporal gyrus. The aphasia quotient (AQ) of all patients were obtained using Western Aphasia Battery (WAB) before and 2 weeks after the operation.</p><p><b>RESULTS</b>In the 33 patients with a normal AQ score (≥93.8) before the operation, the AQ score underwent no significant changes after the operation (P>0.05). Twenty-eight patients had lowered AQ scores (〈93.8) preoperatively, which were improved significantly after the operation (P<0.01). At 2 weeks after the operation, the language function worsened in 14 patients (23.0%), and only 2 (3.2%) showed a persistent language deficit at 6 months. Of the 61 patients, radical resection of the lesions was achieved in 41 and subtotal resection in 20 patients. The variation of AQ scores after the operation was not found to correlate to the degree of lesion resection, and the patients in group A showed a greater AQ variation than those in group B.</p><p><b>CONCLUSIONS</b>Intraoperative MRI and functional neuronavigation can well demonstrate the structural relations between the lesions, the cortical areas and the fasciculi related to language functions, thus helping to better preserve the language function during microsurgical lesion resection in patients with lesions near language-related brain regions.</p>


Subject(s)
Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Brain Diseases , Pathology , General Surgery , Diffusion Tensor Imaging , Frontal Lobe , Pathology , Language , Magnetic Resonance Imaging , Methods , Microsurgery , Neuronavigation , Methods , Neurosurgical Procedures , Temporal Lobe , Pathology
6.
Acta Pharmaceutica Sinica ; (12): 284-290, 2008.
Article in English | WPRIM | ID: wpr-277861

ABSTRACT

The aim of the study is to investigate chemical constituents of the leaves of Pieris japonica. The isolation and purification of the constituents were performed by various chromatography and spectral analysis. Three new phenolic glucosides, erythro-syringoylglycerol 4-O-beta-D-glucoside (1), 1-(2-beta-D-glucopyranoxyl-4-methoxyl-6-hydroxyphenyl)-3-hydroxyl-l-propanone (3), erythro-l-(4-hydroxyl-3-methoxyphenyl)-2-[4-(3-beta-D-glucopyranoxypropyl)-2 ,6-dimethoxyphenoxy]-1, 3-propanediol (4), along with five known phenolic glucosides, syringoylglycerol 8-O-beta-D-glucoside (2), magnolenin C (5), syringaresinol mono-beta-D-glucoside (6), 3-(4-hydroxyl-3-methyphenyl)-1 -propanol-l-O-beta-D-glucoside (7) and 3, 5-dimethoxyl-4-hydroxybenzyl alcohol 4-O-beta-D-glucoside (8) were isolated and identified from the plant leaves. Compounds 1 and 2 inhibited significantly (P <0.01) the proliferation of murine T and B cells at concentration of 1 x 10(-6) mol L(-1), in vitro.


Subject(s)
Ericaceae , Chemistry , Glucosides , Chemistry , Immunosuppressive Agents , Chemistry , Lignans , Chemistry , Phenols , Chemistry , Plant Leaves , Chemistry , Plants, Medicinal , Chemistry
7.
China Journal of Chinese Materia Medica ; (24): 2604-2606, 2007.
Article in English | WPRIM | ID: wpr-324323

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the chemical constituents from aerial part of Curcuma wenyujin.</p><p><b>METHOD</b>Compounds were isolated by repeated column chromatography on silica gel. Their structures were elucidated on the basis of spectral analysis and comparison with literature data.</p><p><b>RESULT</b>Six compounds were isolated and identified as codonolactone (1), voleneol (2), octacosanoic acid (3), beta-sitosterol (4), mangdesisterol (5), and daucosterol (6).</p><p><b>CONCLUSION</b>Compounds 1, 2, and 5 were isolated from the plant for the first time.</p>


Subject(s)
Curcuma , Chemistry , Fatty Acids , Chemistry , Phytosterols , Chemistry , Plant Components, Aerial , Chemistry , Plants, Medicinal , Chemistry , Sesquiterpenes , Chemistry , Sitosterols , Chemistry
8.
Acta Pharmaceutica Sinica ; (12): 439-441, 2004.
Article in Chinese | WPRIM | ID: wpr-302791

ABSTRACT

<p><b>AIM</b>To study the chemical constituents of Knoxia corymbosa Willd.</p><p><b>METHODS</b>Chromatography was used to isolate and purify the chemical constituents, their structures were identified by spectral analysis.</p><p><b>RESULTS</b>Four flavonol glycosides were identified as quercetin-7-O-alpha-L-arabinosyl-3-O-beta-D-6"-acetylglucopyranoside (1), kaempferol-7-O-alpha-L-arabinosyl-3-O-beta-D-glucopyranoside (2), quercetin-3-O-beta-D-glucopyranoside (3), quercetin-3-O-beta-D-6"-acetylglucopyranoside (4).</p><p><b>CONCLUSION</b>Compound 1 is a new flavonol glycoside. The other flavonol glycosides were isolated from Knoxia corymbosa Willd for the first time.</p>


Subject(s)
Glucosides , Chemistry , Molecular Conformation , Molecular Structure , Plants, Medicinal , Chemistry , Quercetin , Chemistry , Rubiaceae , Chemistry
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