1.Effect of concentration of catalpol and 5-hydroxymethyl-2-furaldehyde from processing of Rehmanniae Radix.
Mei-fen ZHU ; Xiang-qian LIU ; Oh JU-HEE ; Yook CHANG-SOO ; Lee JE-HYUN
China Journal of Chinese Materia Medica 2007;32(12):1155-1157
OBJECTIVETo study on effect of concentration of catalpol and 5-hydroxy methyl-2-furaldehyde (5-HMF) from Rehmanniae Radix at various processing.
METHODThe Rehmanniae Radix was dried and prepared from the steaming process with 10% ethanol, 50% ethanol at 90 degrees C and 100 degrees C each other. And the changes of catalpol and 5-HMF was determinated. The extraction of 5-HMF and catalpol was sonicated in 30% methanol for 2 h. The analysis of 5-HMF and catalpol was conducted by HPLC with reversed-phase C-18 column and detected under UV 284 nm, 204 nm. Elution was carried out at 1.0 mL min(-1) with 3% acetonitrile.
RESULTFrom this analysis, we found out that the content of catalpol was decreased with the number of processing times, and content of 5-HMF was increased with the number of processing times at various processing. The temperature and concentration of ethanol can effect on content of catalpol and 5-HMF at processing. The Cooked Rehmanniae Radix processed at 100 degrees C, 10% ethanol is best. And the content of 5-HMF processed for more than 7 times was accorded with standard of Korea phamcopoetia.
CONCLUSIONAnalyze the effect of concentration of catalpol and 5-HMF from Rehmanniae Radix at various processing, and provide the foundation for further study.
Chromatography, High Pressure Liquid ; Ethanol ; Furaldehyde ; analogs & derivatives ; analysis ; Glucosides ; analysis ; Hot Temperature ; Iridoid Glucosides ; Iridoids ; analysis ; Plant Tubers ; chemistry ; Plants, Medicinal ; chemistry ; Rehmannia ; chemistry ; Technology, Pharmaceutical ; methods
2.Chemical Constituents from Leaves of Pileostegia viburnoides Hook.f.et Thoms.
Xiao Jun LI ; Zu Zhen LIU ; Kwan Woo KIM ; Xiang WANG ; Zhi LI ; Youn Chul KIM ; Chang Soo YOOK ; Xiang Qian LIU
Natural Product Sciences 2016;22(3):154-161
Phytochemical investigation on the leaves of Pileostegia viburnoides Hook.f.et Thoms led to the isolation of twenty-five compounds, and their structures were identified as n-dotriacontane (1), taraxeryl acetate (2), friedelin (3), epifriedelinol (4), canophyllal (5), stigmast-4-en-3-one (6), stigmasterol (7), (24R)-5A-stigmastane-3,6-dione (8), ursolic acid (9), pomolic acid (10), umbelliferone (11), 4-epifriedelin (12), n-octatriacontanol (13), β-amyrin (14), α-amyrin (15), taraxerol (16), nonadecanol (17), friedelane (18), arachic acid (19), protocatechuic acid (20), n-pentatriacontanol (21), hexadecanoic acid (22), vincosamide (23), daucosterol (24), and skimming (25), respectively. To our best knowledge, compounds 1, 2, 12, 13, 17 - 19 and 21-23 were new within Saxifragaceae family. Compounds 15, 16, and 20 were produced from this genus for the first time. Compounds 4, 14 and 25 were first obtained from species P. viburnoides and compounds 3, 5 - 11, and 24 were achieved from the leaves of P. viburnoides for the first time. Furthermore, the anti-neuroinflammatory activity of these isolates was evaluated.
Coumarins
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Humans
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Palmitic Acid
;
Saxifragaceae
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Stigmasterol
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Triterpenes
3.Nitric Oxide(NO) in Inflammatory Arthritis.
Sang Cheol BAE ; Dong Yook KIM ; Tae Hwan KIM ; Jae Bum JUN ; Sung Soo JUNG ; In Hong LEE ; Dae Hyun YOO ; Seong Yoon KIM ; Eun Young LEE ; Sung Yeoul CHANG
Korean Journal of Medicine 1997;52(1):32-41
OBJECTIVES:Nitric Oxide(NO) is a toxic, inorganic, gaseous free radical produced during the metabolism of L-Arginine by NO synthase(NOS). It has been implicated in a rapidly growing number of physiological and pathophysiological processes such as cytotoxic effects against microbes and tumor cells, blood vessel dilation and neurotransmitter. Recently there is growing evidence implicating NO in immune regulation, inflammation, autoimmunity, and arthritis. We performed this study to determine a role for nitric oxide in inflammatory arthritis especially rheumatoid arthritis(RA). METHODS: We measured (1) the concentrations of nitrite, a breakdown product of nitric oxide, in serum and synovial fluid from patients with RA and osteoarthritis(OA) and in the serum of controls (2) the concentrations of nitrite in the supernatant of cultured synovial tissue with RA and OA and (3) determined whether human chondrocytes and synoviocytes can synthesize nitric oxide and if so, how production is regulated by cytokines and antirheumatic drugs. RESULTS: 1) Serum nitrite concentrations in patients with RA and OA were higher than in controls. In both disease groups synovial fluid nitrite was higher than serum nitrite. Serum and synovial fluid nitrite concenrations in RA were higher than those in OA. However, those findings are not statistically significant. 2) Although these findings are not statistically significant, the concentration of nitrite in the supernatant of cultured synavial tissue with RA was higher than that in OA. 3) IL-1beta and TNF-alpah induced the biosynthesis of NO by chondrocytes and synoviocytes. IGF-1 and TGF-beta failed to provoke the production of NO. The biosynthesis of NO required an induction period of approximately 6 hours and was inhibited by L-NMMA and cycloheximide. Dexamethasone, indomethacin, gold sodium thiomalate and methotrexate had no effect on the induction of NO biosynthesis. CONCLUSION: These results suggest a role for nitric oxide as an inflommatory mediator in inflammatory arthritis.
Antirheumatic Agents
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Arginine
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Arthritis*
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Arthritis, Rheumatoid
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Autoimmunity
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Blood Cells
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Chondrocytes
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Cycloheximide
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Cytokines
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Dexamethasone
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Gold Sodium Thiomalate
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Humans
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Indomethacin
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Inflammation
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Insulin-Like Growth Factor I
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Metabolism
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Methotrexate
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Neurotransmitter Agents
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Nitric Oxide
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omega-N-Methylarginine
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Synovial Fluid
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Transforming Growth Factor beta
4.Treatment outcome of postoperative radiotherapy for retroperitoneal sarcoma.
Hyun Jin LEE ; Si Yeol SONG ; Tae Won KWON ; Jeong Hwan YOOK ; Song Cheol KIM ; Duck Jong HAN ; Choung Soo KIM ; Hanjong AHN ; Heung Moon CHANG ; Jin Hee AHN ; Eun Jin JWA ; Sang Wook LEE ; Jong Hoon KIM ; Eun Kyung CHOI ; Seong Soo SHIN ; Seung Do AHN
Radiation Oncology Journal 2011;29(4):260-268
PURPOSE: To evaluate the treatment outcome and prognostic factor after postoperative radiotherapy in retroperitoneal sarcoma. MATERIALS AND METHODS: Forty patients were treated with surgical resection and postoperative radiotherapy for retroperitoneal sarcoma from August 1990 to August 2008. Treatment volume was judged by the location of initial tumor and surgical field, and 45-50 Gy of radiation was basically delivered and additional dose was considered to the high-risk area. RESULTS: The median follow-up period was 41.4 months (range, 3.9 to 140.6 months). The 5-year overall survival (OS) was 51.8% and disease free survival was 31.5%. The 5-year locoregional recurrence free survival was 61.9% and distant metastasis free survival was 50.6%. In univariate analysis, histologic type (p = 0.006) was the strongest prognostic factor for the OS and histologic grade (p = 0.044) or resection margin (p = 0.032) had also effect on the OS. Histologic type (p = 0.004) was unique significant prognostic factor for the actuarial local control. CONCLUSION: Retroperitoneal sarcoma still remains as a poor prognostic disease despite the combined modality treatment including surgery and postoperative radiotherapy. Selective dose-escalation of radiotherapy or combination of effective chemotherapeutic agent must be considered to improve the treatment result especially for the histopathologic type showing poor prognosis.
Disease-Free Survival
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Follow-Up Studies
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Humans
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Neoplasm Metastasis
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Prognosis
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Recurrence
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Sarcoma
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Treatment Outcome
5.Analysis of TCR Vfi Gene Repertoire in Patients with Rheumatoid Arthritis.
Sung Soo JUNG ; Kwan Pyo HONG ; Dong Yook KIM ; Tae Hwan KIM ; In Hong LEE ; Jae Bum JUN ; Sang Cheol BAE ; Dae Hyun YOO ; Seong Yoon KIM ; Eun Young LEE ; Sung Yeoul CHANG ; Young Gyu CHAI
The Journal of the Korean Rheumatism Association 1996;3(1):11-31
OBJECTIVES: Polymerase chain reaction (PCR) technology was eamine synovial fluid and peripheral T cells in patients with rheumatoid arthritis(RA) to determine the preferential usage of the T cell receptor(TCR) variable region(V) gene. METHODS: Oligonucleotide primers specific for individual TCR Vfi gene families were used to amplify the TCR gene products in a semiquantitative assay of their relative utilization in unselected T cell populations. RESULTS: The result of Vfi utilization was generally heterogenous, similar with previous reports. However, the mean expression of Vfi16 and Vfi18 in RA was more preferentially utilized compared to normal donors. The usage of Vfi in peripheral blood from 3 patients with RA demonstrated restrictions in Vfi16, Vfi 20 and Vfi18 genes, respectively. Analyses of synovial fluid resulted in restriction in Vfi12, Vfi20 and Vfi20, respectively. Although there was no significant pattern of skewed Vfi gene mean usage when comparing the synovial fluids with the peripheral blood T cells from RA patients, there were significant biased Vfi genes, Vfi12, V~I and Vfi20, each 3 patients. As the HLA type is a determining factor in shaping TCR repertoire of peripheral T cells, we compared the Vfi utilization in HLA-DR4 expressing groups that have susceptibility and gene dosage effect in disease progression. It was a little different that comparing the pattern of Vfi usage in peripheral blood and synovial fluid from RA patients between HLA-DR4 positive and negative group. CONCLUSION: The results were consistent with the conclusion that the increased Vfi family T cells infiltrate synovium and are dependent on each patient and may be involved in inducing and maintaining the synovitis that characterizes RA. The different outcome of each patient may be due to the difference in disease duration, genetic background and geographic region. A more important factor may be the stage of disease, because epitope 'induced immune reaction may change over time. Therefore, selecting patients early in the course of disease may be important and may facilitate the need for more in-depth TCR analysis in the future.
Arthritis, Rheumatoid*
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Bias (Epidemiology)
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Disease Progression
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DNA Primers
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Gene Dosage
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Genes, T-Cell Receptor
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HLA-DR4 Antigen
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Humans
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Polymerase Chain Reaction
;
Synovial Fluid
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Synovial Membrane
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Synovitis
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T-Lymphocytes
;
Tissue Donors
6.Cytotoxicity and anti-inflammatory effects of root bark extracts of Acanthopanax henryi.
Jong-Hwan KIM ; Xiang-Qian LIU ; Ling DAI ; Chang-Soo YOOK ; Kyung-Tae LEE
Chinese Journal of Natural Medicines (English Ed.) 2014;12(2):121-125
AIM:
To investigate the cytotoxicity, anti-inflammatory activity, and action mechanism of root bark extracts of Acanthopanax henryi.
METHOD:
The hot methanol extract of the root bark of A. henryi was subjected to XAD-4 column chromatography eluting with a gradient of methanol in water. The cytotoxicity and anti-inflammatory effects of the MeOH fractions were evaluated on the inhibition on lipopolysaccharide (LPS)-induced nitric oxide, prostaglandin E2, interleukin-1β, and interleukin-6 production in RAW 264.7 macrophages.
RESULTS:
The 80% MeOH fraction was a better inhibitor of LPS-induced NO, PGE2, IL-1β, and IL-6 production, and expression of inducible nitric oxide synthase (iNOS) at the protein levels in a concentration-dependent manner.
CONCLUSION
The 80% MeOH fraction of A. henryi root bark has significant anti-inflammatory activity. This provides a pharmacological basis for clinical application for the treatment of inflammation.
Animals
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Anti-Inflammatory Agents
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pharmacology
;
therapeutic use
;
Dinoprostone
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metabolism
;
Dose-Response Relationship, Drug
;
Eleutherococcus
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Inflammation
;
chemically induced
;
drug therapy
;
metabolism
;
Interleukin-1beta
;
metabolism
;
Interleukin-6
;
metabolism
;
Lipopolysaccharides
;
Macrophages
;
drug effects
;
metabolism
;
Mice
;
Nitric Oxide
;
metabolism
;
Nitric Oxide Synthase Type II
;
metabolism
;
Phytotherapy
;
Plant Bark
;
Plant Extracts
;
pharmacology
;
therapeutic use
;
Plant Roots