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1.
Zhongguo Zhong Yao Za Zhi ; 43(11): 2190-2198, 2018 Jun.
Article in Chinese | MEDLINE | ID: mdl-29945367

ABSTRACT

The point of this study is to explore and investigate mechanisms of Buyang Huanwu decoction for treatment of cerebral infarction (CI) using a network pharmacology approach. First, TCMSP database, DrugBank database and PharmMapper server were used and combined with oral bioavailability and drug analysis to screen the components of Buyang Hanwu decoction and predict the potential targets. Then, Cytoscape 3.5.1 software was used to construct compounds-targets network and the protein-protein interaction (PPI) networks for targets of compounds and CI-related targets and merge the two PPI networks to acquire active targets. Finally, gene ontology (GO) and KEGG pathway analysis of active targets were carried out by DAVID online analysis tool and KOBAS 3.0 software. In total of 150 screened compounds and 232 potential targets were obtained. And in total of 208 active targets were finally determined by merging networks. Results indicated that Buyang Huanwu decoction might have a role in treating CI by regulating some biological processes including response to drug, aging, response to hypoxia, and blood coagulation, and some molecular function, such as protein binding, enzyme binding and serine-type endopeptidase activity. The mechanisms might be concerned with PI3K-Akt signaling pathway, TNF signaling pathway, HIF-1 signaling pathway and cAMP signaling pathway. Among them, the regulation of PI3K-Akt signaling pathway might be one of the most crucial mechanisms.


Subject(s)
Cerebral Infarction/drug therapy , Drugs, Chinese Herbal/therapeutic use , Signal Transduction , Databases, Pharmaceutical , Humans , Phosphatidylinositol 3-Kinases
2.
J Sci Food Agric ; 96(1): 215-22, 2016 Jan 15.
Article in English | MEDLINE | ID: mdl-25582752

ABSTRACT

BACKGROUND: The present study was undertaken to investigate the effects of fermentation concentrate of Hericium caput-medusae (Bull.:Fr.) Pers. (HFC) on growth performance, digestibility, intestinal microbiology, and intestinal morphology in broiler chickens. A total of 600 male Arbor Acres broilers were randomly divided into five dietary treatments (20 broilers per pen with six pens per treatment): CON (basal diet), ANT (basal diet supplemented with 5 mg kg(-1) flavomycin) and HFC (basal diet supplemented with 6, 12, and 18 g kg(-1) HFC). The experimental lasted for 42 days. RESULTS: The results revealed that the average daily gain [linear (L), P < 0.01; quadratic (Q), P < 0.01] of broilers increased when the HFC levels increased during the starter (days 1-21), finisher (days 22-42), and the overall experiment period (days 1 to 42). In the small intestinal digesta and the caecum digesta, the Escherichia coli count (L, P < 0.05; Q, P < 0.001) decreased while the Lactobacilli count (L, P < 0.01; Q, P < 0.001) and Bifidobacteria count (L, P < 0.001; Q, P < 0.001) increased when the HFC levels increased. The crude protein digestibility of broilers (L, P < 0.01; Q, P < 0.001) increased when the HFC levels increased. In the duodenum, jejunum, and ileum of broilers, the villus height and villus height to crypt depth ratio (L, P < 0.001; Q, P < 0.001) increased when the HFC levels increased. CONCLUSION: Dietary supplementation with HFC increased gut Lactobacilli and Bifidobacteria counts and inhibited E. coli growth, improved nutrient utilisation and intestine villus structure, and thus improved the growth of broilers.


Subject(s)
Bacteria/drug effects , Basidiomycota , Chickens/growth & development , Dietary Proteins/metabolism , Dietary Supplements , Digestion , Intestines/drug effects , Animals , Bacteria/growth & development , Basidiomycota/metabolism , Chickens/metabolism , Chickens/microbiology , Diet , Fermentation , Intestinal Mucosa/metabolism , Intestines/anatomy & histology , Intestines/microbiology
3.
J Sci Food Agric ; 95(2): 267-74, 2015 Jan.
Article in English | MEDLINE | ID: mdl-24771556

ABSTRACT

BACKGROUND: The present study was conducted to investigate the lipid-lowering effect of polysaccharides from the submerged fermentation concentrate of Hericium caput-medusae (Bull.:Fr.) Pers. (HFCP) in broilers. A total of 480 female Arbor Acres broilers were randomly divided into four dietary treatments, each consisting of six pens as replicates, and fed diets containing 0 (control), 1, 3 or 5 g kg(-1) HFCP. RESULTS: The results revealed that the average daily gain of broilers increased (linear (L), P < 0.01; quadratic (Q), P < 0.01) when the HFCP levels increased. The serum cholesterol, triglyceride and low-density lipoprotein cholesterol levels decreased (Q, P < 0.05) while the high-density lipoprotein cholesterol level increased (Q, P < 0.05) when the HFCP levels increased. The caecum Escherichia coli count and pH decreased (Q, P < 0.01) while the lactobacilli count and bifidobacteria count increased (L, P < 0.05; Q, P < 0.05) when the HFCP levels increased. The propionic acid and butyric acid concentrations increased (L, P < 0.001; Q, P < 0.001) while the abdominal fat rate and liver fat content decreased (L, P < 0.01; Q, P < 0.05) when the HFCP levels increased. CONCLUSION: Dietary supplementation with HFCP may lead to the development of low abdominal fat of broilers as demanded by health-conscious consumers.


Subject(s)
Adipose Tissue/drug effects , Agaricales/chemistry , Chickens/metabolism , Dietary Carbohydrates/pharmacology , Lipids/blood , Meat/analysis , Polysaccharides/pharmacology , Adipose Tissue/metabolism , Animals , Bacteria/metabolism , Body Fat Distribution , Butyric Acid/metabolism , Cecum/drug effects , Cecum/microbiology , Chickens/growth & development , Chickens/microbiology , Dietary Supplements , Female , Fermentation , Humans , Hydrogen-Ion Concentration , Intra-Abdominal Fat/metabolism , Liver/drug effects , Liver/metabolism , Propionates/metabolism
4.
Food Chem Toxicol ; 59: 145-52, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23770344

ABSTRACT

Oxidative stress has been considered as a major cause of cell damage in various neurodegenerative disorders. One of the reasonable strategies for delaying the disease's progression is to prevent reactive oxygen species (ROS) mediated cellular injury by dietary or pharmaceutical augmentation of free radical scavengers. Isocampneoside II (ICD) is an active phenylethanoid glycoside isolated from the medicinal hardwood genus Paulownia. This study was designed to explore free radical scavenging potential of ICD in different in vitro systems and its protective role in hydrogen peroxide (H2O2)-induced oxidative stress and apoptotic death in cultured rat pheochromocytoma (PC12) cells. The results showed ICD eliminated approximately 80.75% superoxide radical at the concentration of 0.1mg/ml and inhibited metal chelating by 22.07% at 8 mg/ml. Additionally, ICD showed a strong ability on reducing power and provided protection against oxidative protein damage induced by hydroxyl radicals. Pretreatment of PC12 cells with ICD prior to H2O2 exposure elevated cell viability, enhanced activity of superoxide dismutase and catalase, and decreased levels of malondialdehyde and intracellular ROS. Furthermore, ICD inhibited cell apoptosis and Bax/Bcl-2 ratio induced by H2O2. These findings suggested ICD may be considered as a potential antioxidant agent and should encourage for further research in neurodegenerative diseases.


Subject(s)
Antioxidants/pharmacology , Apoptosis/drug effects , Caffeic Acids/pharmacology , Disaccharides/pharmacology , Glycosides/pharmacology , Lipid Peroxidation/drug effects , Neurons/drug effects , Neuroprotective Agents/pharmacology , Oxidative Stress/drug effects , Animals , Apoptosis Regulatory Proteins/biosynthesis , Apoptosis Regulatory Proteins/genetics , Apoptosis Regulatory Proteins/metabolism , Cell Survival/drug effects , Chelating Agents/pharmacology , Gene Expression Regulation/drug effects , Hydrogen Peroxide/antagonists & inhibitors , Hydrogen Peroxide/toxicity , Nerve Tissue Proteins/biosynthesis , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Neurons/enzymology , Neurons/metabolism , Oxidants/antagonists & inhibitors , Oxidants/toxicity , Oxidation-Reduction , Oxidoreductases/metabolism , PC12 Cells , Rats , Reactive Oxygen Species/antagonists & inhibitors , Reactive Oxygen Species/metabolism
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