1.Review about structure-function relationships of anthraquinone derivatives from Radix et Rhizoma Rhei.
Jin-Rui ZONG ; Zhi-Mao CHAO ; Zhen-Li LIU ; Jin WANG
China Journal of Chinese Materia Medica 2008;33(20):2424-2427
It review the structure-function relationship of natural anthraquinone derivatives from Radix et Rhizoma Rhei. The anthraquinone derivatives had many identical activities because they have the identical mother nucleus; but the strength of their activities were different, because they have different substitution groups. The anthraquinone derivatives shown the obvious structure-function relationship in many respects, such as antioxygenation, antibiosis, anticancer, the influence of immunity and so on.
Anthraquinones
;
chemistry
;
pharmacology
;
Drugs, Chinese Herbal
;
chemistry
;
pharmacology
;
Molecular Structure
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Rheum
;
chemistry
;
Structure-Activity Relationship
3.Research progress in epigenetic pharmacological effects of rhein.
Zi-Wei ZHU ; Ruo-Nan ZHOU ; Wen-Bin SHANG
China Journal of Chinese Materia Medica 2023;48(24):6545-6550
Rhein, which is one of the main active components of Rheum palmatum, has a range of pharmacological activities such as the regulation of the metabolism of glucose and lipids, anti-inflammatory, anti-tumor, anti-fibrosis, etc. Epigenetics refers to the heritable variation of gene expression without altering the DNA sequence. It is involved in the emergence and development of inflammation, renal fibrosis, diabetes, cancer, atherosclerosis, and other diseases, thus becoming a new strategy for the treatment of many di-seases. A series of studies have shown that epigenetic modification may be a common molecular mechanism of various pharmacological effects of rhein. This paper summarized the effects of rhein on the regulation of epigenetic modification and its underlying mechanisms, which involve the regulation of DNA methylation, protein acetylation, and RNA methylation, so as to provide a basis for the development and application of rhein.
Humans
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Anthraquinones/pharmacology*
;
DNA Methylation
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Epigenesis, Genetic
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Neoplasms/drug therapy*
;
Fibrosis
4.Effects of lovastatin, clomazone and methyl jasmonate treatment on the accumulation of purpurin and mollugin in cell suspension cultures of Rubia cordifolia.
Xing FAN ; Gao-Sheng HU ; Na LI ; Zhi-Fu HAN ; Jing-Ming JIA
Chinese Journal of Natural Medicines (English Ed.) 2013;11(4):396-400
AIM:
To determine the IPP origin of the naphthoquinones (NQs) in Rubia cordifolia, and to evaluate the effects of methyl jasmonate (MeJA) treatment, MEP, and MVA pathway inhibitor treatment on the accumulation of anthraquinones (AQs) and NQs in cell suspension cultures of R. cordifolia.
METHODS:
Cell suspension cultures of R. cordifolia were established. Specific inhibitors (lovastatin and clomazone) and MeJA were supplied to the media, respectively. Treated cells were sampled every three days. Content determination of purpurin (AQs) and mollugin (NQs) were carried out using RP-HPLC. The yield of the two compounds was compared with the DMSO-supplied group and the possible mechanism was discussed.
RESULTS:
Lovastatin treatment increased the yield of purpurin and mollugin significantly. Clomazone treatment resulted in a remarkable decrease of both compounds. In the MeJA-treated cells, the purpurin yield increased, meanwhile, the mollugin yield decreased compared with control.
CONCLUSION
The IPP origin of mollugin in R. cordifolia cell suspension cultures was likely from the MEP pathway. To explain the different effects of MeJA on AQs and NQs accumulation, studies on the regulation and expression of the genes, especially after prenylation of 1,4-dihydroxy-2-naphthoic acid should be conducted.
Acetates
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pharmacology
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Anthraquinones
;
metabolism
;
Cell Culture Techniques
;
Cells, Cultured
;
Cyclopentanes
;
pharmacology
;
Isoxazoles
;
pharmacology
;
Lovastatin
;
pharmacology
;
Oxazolidinones
;
pharmacology
;
Oxylipins
;
pharmacology
;
Pyrans
;
metabolism
;
Rubia
;
drug effects
;
metabolism
5.Impact of otrA expression on morphological differentiation, actinorhodin production, and resistance to aminoglycosides in Streptomyces coelicolor M145.
Yan-Fang ZHAO ; Dan-Dan LU ; Andreas BECHTHOLD ; Zheng MA ; Xiao-Ping YU
Journal of Zhejiang University. Science. B 2018;19(9):708-717
otrA resembles elongation factor G (EF-G) and is considered to be an oxytetracycline (OTC)-resistance determinant in Streptomyces rimosus. In order to determine whether otrA also conferred resistance to OTC and other aminoglycosides to Streptomyces coelicolor, the otrA gene from S. rimosus M527 was cloned under the control of the strong ermE* promoter. The resulting plasmid, pIB139-otrA, was introduced into S. coelicolor M145 by intergeneric conjugation, yielding the recombinant strain S. coelicolor M145-OA. As expected S. coelicolor M145-OA exhibited higher resistance levels specifically to OTC and aminoglycosides gentamycin, hygromycin, streptomycin, and spectinomycin. However, unexpectedly, S. coelicolor M145-OA on solid medium showed an accelerated aerial mycelia formation, a precocious sporulation, and an enhanced actinorhodin (Act) production. Upon growth in 5-L fermentor, the amount of intra- and extracellular Act production was 6-fold and 2-fold higher, respectively, than that of the original strain. Consistently, reverse transcription polymerase chain reaction (RT-PCR) analysis revealed that the transcriptional level of pathway-specific regulatory gene actII-orf4 was significantly enhanced in S. coelicolor M145-OA compared with in S. coelicolor M145.
Aminoglycosides/pharmacology*
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Anthraquinones/metabolism*
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Anti-Bacterial Agents/pharmacology*
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Bacterial Proteins/genetics*
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Drug Resistance, Bacterial/genetics*
;
Streptomyces coelicolor/metabolism*
6.Exploring relationship between traditional effects of traditional Chinese medicine and modern pharmacological activities by "co-effect compounds".
Hai-Bo LIU ; Ai-Jun LU ; Bing LIU ; Jia-Ju ZHOU
China Journal of Chinese Materia Medica 2005;30(1):75-78
The compound that distributes in the herbs with one common effect was named as "co-effect compound" (CEC). The CECs of three traditional Chinese medicine(TCM) effects, purgative, relieving pain and clearing heat, had been found and studied. A strong corresponding relationship was found between the pharmacological activities of CECs and the TCM effect they belong to. The study shows that it may be a feasible method to connect traditional effect of TCM with modem pharmacological activity.
Anthraquinones
;
isolation & purification
;
pharmacology
;
Anti-Inflammatory Agents, Non-Steroidal
;
pharmacology
;
Cathartics
;
pharmacology
;
Drugs, Chinese Herbal
;
isolation & purification
;
pharmacology
;
Flavonoids
;
isolation & purification
;
pharmacology
;
Medicine, Chinese Traditional
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Plants, Medicinal
;
chemistry
8.Lipid-lowering effect of seven traditional Chinese medicine monomers in zebrafish system.
Kan CHEN ; Chang-Qian WANG ; Yu-Qi FAN ; Zhi-Hua HAN ; Yue WANG ; Lin GAO ; Hua-Su ZENG
Acta Physiologica Sinica 2017;69(1):55-60
The present study aimed to study lipid-lowering effect of seven traditional Chinese medicine monomers in zebrafish system. Zebrafish were fed with high fat diet to establish a hyperlipemia model, then fasted and bathed with seven traditional Chinese medicine monomers stigmasterol, triacontanol, chrysophanol, vanillic acid, shikimic acid, polydatin and oleanolic acid respectively. The oil red O staining was used to detect the blood lipids of zebrafish. Serum total cholesterol and triglyceride levels were detected to validate the lipid-lowering effect. The result showed that a zebrafish model of hyperlipemia could be established by feeding larvae zebrafish with high fat diet. Among the seven traditional Chinese medicine monomers, chrysophanol had lipid-lowering effect. Chrysophanol significantly reduced serum total cholesterol and triglyceride levels in adult zebrafish fed with high fat diet. Chrysophanol accelerated peristalsis frequency of zebrafish intestine and the excretion of high fat food. It is concluded that chrysophanol has lipid- lowering effect in zebrafish, and the mechanism of the effect may be due to the roles of chrysophanol in reducing lipid absorption from gastrointestinal tract and accelerating the excretion of food.
Animals
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Anthraquinones
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pharmacology
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Diet, High-Fat
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Fatty Alcohols
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pharmacology
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Glucosides
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pharmacology
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Hyperlipidemias
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drug therapy
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Hypolipidemic Agents
;
pharmacology
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Larva
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Lipids
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blood
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Medicine, Chinese Traditional
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Oleanolic Acid
;
pharmacology
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Shikimic Acid
;
pharmacology
;
Stigmasterol
;
pharmacology
;
Stilbenes
;
pharmacology
;
Vanillic Acid
;
pharmacology
;
Zebrafish
9.The anti-proliferation and anti-migration dual effects of aloe-emodin on KB cells and its mechanism.
Chinese Journal of Stomatology 2009;44(1):50-52
OBJECTIVETo investigate the anti-proliferation and anti-migration dual effects of aloe-emodin on KB cells and its mechanisms.
METHODSKB cells were treated with 2.5, 5, 10, 20 and 40 micromol/L aloe-emodin. Crystal violet assay was used to determine the long-term growth inhibition of aloe-emodin on human oral cancer KB cells. Scratch wound-healing motility assay was used to measure the antimigration effect The protein kinase C alpha and c-myc expression changes in protein levels were detected by Western blotting.
RESULTSA durable cell growth inhibitory effect of aloe-emodin on KB cells was found. Treatment of aloe-emodin resulted in the inhibition of cell migration. The protein kinase C alpha and c-myc in protein levels were decreased upon treatment with aloe-emodin compared with controls.
CONCLUSIONSThe anti-proliferation and anti-migration effects of aloe-emodin on KB cells are associated with the suppression of protein kinase C pathway.
Anthraquinones ; pharmacology ; Cell Movement ; drug effects ; Cell Proliferation ; drug effects ; Genes, myc ; Humans ; KB Cells ; Protein Kinase C ; metabolism
10.Spectrum-effect relationship of total anthraquinone extract of Cassia seeds against fluorouracil-induced liver injury in mice.
Heng WANG ; Mengqi LI ; Shenxing LI ; Jinggan SHI ; Li HUANG ; Suoting CHENG ; Chuncai ZOU ; Haiyan YAN
Journal of Southern Medical University 2023;43(5):825-831
OBJECTIVE:
To investigate the spectrum-effect relationship between the total anthraquinone extract of Cassia seeds and fluorouracil (5-Fu)-induced liver injury in mice and identify the effective components in the extract.
METHODS:
A mouse model of liver injury was established by intraperitoneal injection of 5-Fu, with bifendate as the positive control. The serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) and myeloperoxidase (MPO), superoxide dismutase (SOD) and total antioxidant capacity (T-AOC) in the liver tissue were detected to investigate the effect of the total anthraquinone extract of Cassia seeds (0.4, 0.8 and 1.6 g/kg) on liver injury induced by 5-Fu. HPLC fingerprints of 10 batches of the total anthraquinone extracts were established to analyze the spectrum- effectiveness of the extract against 5- Fu- induced liver injury in mice and screen the effective components using the grey correlation method.
RESULTS:
The 5- Fu- treated mice showed significant differences in liver function parameters from the normal control mice (P < 0.05), suggesting successful modelling. Compared with those in the model group, serum ALT and AST activities were decreased, SOD and T- AOC activities significantly increased, and MPO level was significantly lowered in the mice treated with the total anthraquinone extract (all P < 0.05). HPLC fingerprints of the 31 components in the total anthraquinone extract of Cassia seeds showed good correlations with the potency index of 5-Fu-induced liver injury but with varying correlation strengths. The top 15 components with known correlations included aurantio-obtusina (peak 6), rhein (peak 11), emodin (peak 22), chrysophanol (peak 29) and physcion (peak 30).
CONCLUSION
The effective components in the total anthraquinone extract of Cassia seeds, including aurantio-obtusina, rhein, emodin, chrysophanol, and physcion, are coordinated to produce protective effects against 5-Fu-induced liver injury in mice.
Animals
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Mice
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Emodin
;
Cassia
;
Chemical and Drug Induced Liver Injury, Chronic
;
Anthraquinones
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Antioxidants
;
Fluorouracil/adverse effects*
;
Plant Extracts/pharmacology*