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1.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 148-155, 2021.
Article in Chinese | WPRIM | ID: wpr-906375

ABSTRACT

Objective:To screen the active components of sovereign medicinal Achyranthis Bidentatae Radix in Rongjin Niantong formula based on bioinformatics and network pharmacology and observe their effects on therapeutic targets of osteoarthritis (OA) in <italic>in vivo</italic> and <italic>in vitro</italic> animal experiments. Method:The main active components and therapeutic targets of Achyranthis Bidentatae Radix were retrieved from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP), and the differentially expressed genes relevant to OA from the Gene Expression Omnibus (GEO) database for cross analysis. The effects of main active components in Achyranthis Bidentatae Radix on enriched therapeutic targets of rats with OA <italic>in vivo </italic>and <italic>in vitro</italic> were detected by real-time polymerase chain reaction (Real-time PCR) and Western blot. Result:There were 20 active components for Achyranthis Bidentatae Radix against OA, with quercetin being an important one. Among the three target genes, osteopontin (OPN) and plasminogen activator inhibitor-1(PAI-1) were the key ones in the network. Gene Ontology (GO) analysis yielded 227 related terms, involving the regulation of physiological response to trauma (GO: 1903034), negative regulation of trauma response (GO: 1903035), etc. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed 12 related pathways, involving extracellular matrix receptor interaction (hsa04512) and so on. In animal experiments, compared with the normal group, the model group exhibited increased gene and protein expression of OPN and PAI-1. Compared with the model group, the quercetin group displayed decreased gene and protein expression of OPN and PAI-1 (<italic>P</italic><0.05). In cell experiments, the OPN and PAI-1 protein expression levels in the model group were increased as compared with those in the normal group, while the Collagen Ⅱ protein expression was decreased. The OPN and PAI-1 protein expression levels in the quercetin group and the inhibitor group were down-regulated in contrast to those in the model group, whereas the Collagen Ⅱ protein expression levels were up-regulated significantly (<italic>P<</italic>0.05). Conclusion:Achyranthis Bidentatae Radix<italic> </italic>inhibits cartilage degeneration and exerts the preventive and therapeutic effects against OA, which is possibly due to the efficacy of its active component quercetin in down-regulating the expression of OPN and PAI-1 in chondrocytes and up-regulating the Collagen Ⅱ protein expression.

2.
China Journal of Chinese Materia Medica ; (24): 2157-2160, 2008.
Article in Chinese | WPRIM | ID: wpr-252176

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of prim-O-glucosylcimifugin and 4'-O-p-D-glucosyl-5-O-methylvisa-mminol con on the proliferation of smooth muscle cell stimulated by TNF-alpha.</p><p><b>METHOD</b>The primary cell culture method of smooth muscle cell (SMC) was established by attachment-block. The SMC was identificated by immunochemistry method, and the growth curve was drawn by cytometry. The third generation of SMC was adopted in the experiment. The effect of prim-O-glucosylcimif-ugin and 4'-O-beta-D-glucosyl-5-O-methylvisamminol con on the proliferation and cell cycle of SMC was investigated by MTT and flow cytometry respectively.</p><p><b>RESULT</b>TNF-alpha of 5 micro g x L(-1) can stimulate the proliferation of SMC and increase the proportion of G2 phase and S phase in cell cycle which has great significant difference (P < 0.01) compared with control. The three dose groups of prim-O-glucosylcimifugin and 4'-O-beta-D-glucosyl-5-O-methylvisammin-ol con can inhibit the proliferation of SMC and increase the proportion of G0/G1 phase, which has great significant difference (P < 0.01) compared with model group.</p><p><b>CONCLUSION</b>Prim-O-glucosylcimifugin and 4'-O-beta-D-glucosyl-5-O-methylvisamminol con can inhibit the proliferation of SMC stimulated by TNF-alpha.</p>


Subject(s)
Animals , Female , Male , Rats , Cell Proliferation , Cells, Cultured , Drugs, Chinese Herbal , Pharmacology , Monosaccharides , Pharmacology , Myocytes, Smooth Muscle , Cell Biology , Rats, Wistar , Tumor Necrosis Factor-alpha , Pharmacology , Xanthenes , Pharmacology
3.
China Journal of Chinese Materia Medica ; (24): 801-805, 2008.
Article in Chinese | WPRIM | ID: wpr-284387

ABSTRACT

<p><b>OBJECTIVE</b>To observe the protective effects of catechin morphon (GCG and EGCG) on hypoxia-reoxygenation induced injury in myocardial cells and to explore the mechanisms.</p><p><b>METHOD</b>In cultured neonatal rat cardiomyocytes, we investigated the preconditioning protection by GCG and EGCG on the spontaneous beating, the survival rate, the release of LDH, MDA, SOD, GSH-Px and the ATP enzyme activity of cardiomyocyte cellular membrane in cultured rat cardiomyocytes treated during the reoxygenation 1h following hypoxia 3 h. The blocking agent of protien kinase C staurosporine (10 nmol x L(-1)) or the deactivator of Gi/o protein pertussis toxin (PTX, 200 microg x mL(-1)) were added before the catechin treatment.</p><p><b>RESULTS</b>Preconditioning by GCG and EGCG increased the spontaneous beating and the survival rate, and decreased the release of LDH and MDA with the rise of SOD and ATP enzyme activity. Inhibition of PKC by staurosporine and Gi/o protein by PTX abolished the protection by catechin with the reduction of the beating, survival rate and activity of SOD, and the increase of the release of LDH and MDA. The results indicated that the activation of signal transduction pathway from PKC and Gi/o protein seemed to be involved in the cardioprotection of preconditioning by GCG and EGCG.</p><p><b>CONCLUSION</b>The protection by GCG and EGCG on hypoxia-reoxygenation injury in cultured neonatal rat cardiomyocytes is found, which is related with scavenging of free radicals, and PKC Gi/o signal transduction pathway.</p>


Subject(s)
Animals , Female , Rats , Cardiotonic Agents , Chemistry , Pharmacology , Catechin , Chemistry , Pharmacology , Free Radicals , Metabolism , Hypoxia , Myocytes, Cardiac , Metabolism , Pathology , Oxygen , Metabolism , Protein Kinase C , Metabolism , Proteins , Metabolism , Signal Transduction , Survival Rate
4.
China Journal of Chinese Materia Medica ; (24): 2513-2517, 2008.
Article in Chinese | WPRIM | ID: wpr-283849

ABSTRACT

<p><b>OBJECTIVE</b>To observe the antioxidant effects of water extract of Carthamus tinctorius on ox-LDL induced injury in rat cardiac microvascular endothelial cell and detecting oxygen derived free radicals (OFR) to explore the antioxidant mechanisms.</p><p><b>METHOD</b>By using the third generation of rat cardiac microvascular endothelial cells (rCMEC), the protection of water extract of C. tinctorius was investigated after ox-LDL (100 mg x L(-1) induced damage. The supernatant was collected for detecting lactate dehydrogenase (LDH), malondialdehyde (MDA), superoxide dismutase (SOD), xanthine oxidase (XOD), glutathione peroxidase (GSH-Px), nitric oxide (NO), nitric oxide synthase (NOS) activity, and cell suspension was collected for detecting reactive oxygen species (ROS) by electron spin resonance (ESR).</p><p><b>RESULT</b>Water extract of C. tinctorius increased the rCMEC survival rate, reduced LDH, MDA and XOD levels, and improved SOD, GSH-Px and NOS activity, while in the cell suspension ROS signal decreased significantly.</p><p><b>CONCLUSION</b>Water extract of C. tinctorius has antioxidation. The mechanisms are likely related with scavenging of free radicals, enhancing its clearance, enhancing endogenous antioxidant activity.</p>


Subject(s)
Animals , Rats , Carthamus tinctorius , Chemistry , Drugs, Chinese Herbal , Chemistry , Pharmacology , Electron Spin Resonance Spectroscopy , Methods , Endothelial Cells , Metabolism , Enzyme Activation , Glutathione Peroxidase , Metabolism , L-Lactate Dehydrogenase , Metabolism , Lipoproteins, LDL , Pharmacology , Microvessels , Cell Biology , Nitric Oxide Synthase , Metabolism , Rats, Wistar , Reactive Oxygen Species , Metabolism , Superoxide Dismutase , Metabolism , Water , Chemistry , Xanthine Oxidase , Metabolism
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