1.Investigation of therapeutic mechanism of Weiweifang on experimental gastric ulcer in rats viewing from metabonomics.
Shu-Ling PENG ; Xiao-Wei LIU ; Zhen-Rui ZHANG
Chinese Journal of Integrated Traditional and Western Medicine 2010;30(10):1073-1077
OBJECTIVETo investigate the therapeutic mechanism of Weiweifang (WWF, a Chinese herbal preparation) on gastric ulcer in rats viewing from metabonomics.
METHODSWistar rats were made to gastric model by acetic acid cauterization and randomized into the model group, the spontaneously healing group and the three WWF treatment groups, and a group of normal rats was set for control. Metabolic spectra of gastric mucosa extraction of rats were acquired with gas chromatography-mass spectrometry (GC-MS) technique. After being pre-processing, data were subjected to partial least squares discriminant analysis (PLS-DA) to discover the biomarkers in rats of the normal group and the model group. The therapeutic effect of WWF on experimental gastric ulcer was assessed by principal component analyses (PCA), and its action of mechanism was explained viewing from the changes of biomarkers.
RESULTSSpectra of biomarkers, including organic acids, fatty acids, amino acids, etc. in model rats were statistically different to those in normal rats, which demonstrated that the energy and substance metabolisms were disordered in rats with gastric ulcer. WWF could cure gastric ulcer effectively by way of regulating the metabolism of gastric mucosa.
CONCLUSIONThe therapeutic mechanism of WWF on experimental gastric ulcer in rats is revealed integrally by metabonomics in this study, displaying prominently the characteristics of Chinese medicine multiple targets comprehensive therapy.
Acetic Acid ; Amino Acids ; metabolism ; Animals ; Drugs, Chinese Herbal ; therapeutic use ; Fatty Acids ; metabolism ; Gas Chromatography-Mass Spectrometry ; Gastric Mucosa ; metabolism ; Male ; Metabolomics ; methods ; Phytotherapy ; Rats ; Rats, Wistar ; Stomach Ulcer ; chemically induced ; drug therapy ; metabolism
2.Spinal Gabapentin and Antinociception: Mechanisms of Action.
Myung Ha YOON ; Jeong Il CHOI ; Seong Wook JEONG
Journal of Korean Medical Science 2003;18(2):255-261
Spinal gabapentin has been known to show the antinociceptive effect. Although several assumptions have been suggested, mechanisms of action of gabapentin have not been clearly established. The present study was undertaken to examine the action mechanisms of gabapentin at the spinal level. Male SD rats were prepared for intrathecal catheterization. The effect of gabapentin was assessed in the formalin test. After pretreatment with many classes of drugs, changes of effect of gabapentin were examined. General behaviors were also observed. Intrathecal gabapentin produced a suppression of the phase 2 flinching, but not phase 1 in the formalin test. The antinociceptive action of intrathecal gabapentin was reversed by intrathecal NMDA, AMPA, D-serine, CGS 15943, atropine, and naloxone. No antagonism was seen following administration of bicuculline, saclofen, prazosin, yohimbine, mecamylamine, L-leucine, dihydroergocristine, or thapsigargin. Taken together, intrathecal gabapentin attenuated only the facilitated state. At the spinal level, NMDA receptor, AMPA receptor, nonstrychnine site of NMDA receptor, adenosine receptor, muscarinic receptor, and opioid receptor may be involved in the antinociception of gabapentin, but GABA receptor, L-amino acid transporter, adrenergic receptor, nicotinic receptor, serotonin receptor, or calcium may not be involved.
Acetic Acids/administration & dosage
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Acetic Acids/metabolism
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Acetic Acids/pharmacology*
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Adrenergic Antagonists/metabolism
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Adrenergic alpha-Antagonists/metabolism
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Analgesics/administration & dosage
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Analgesics/metabolism
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Analgesics/pharmacology*
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Animals
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Atropine/metabolism
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Dihydroergocristine/metabolism
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Enzyme Inhibitors/metabolism
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Excitatory Amino Acid Agonists/metabolism
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GABA Antagonists/metabolism
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Injections, Spinal
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Leucine/metabolism
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Male
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Mecamylamine/metabolism
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Muscarinic Antagonists/metabolism
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N-Methylaspartate/metabolism
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Naloxone/metabolism
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Narcotic Antagonists/metabolism
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Nicotinic Antagonists/metabolism
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Pain Measurement
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Quinazolines/metabolism
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Rats
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Rats, Sprague-Dawley
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Serine/metabolism
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Spinal Cord/drug effects*
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Thapsigargin/metabolism
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Triazoles/metabolism
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alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid/metabolism
3.Lipid synthesis by an acidic acid tolerant Rhodotorula glutinis.
Zhangnan LIN ; Hongjuan LIU ; Jian'an ZHANG ; Gehua WANG
Chinese Journal of Biotechnology 2016;32(3):339-346
Acetic acid, as a main by-product generated in the pretreatment process of lignocellulose hydrolysis, significantly affects cell growth and lipid synthesis of oleaginous microorganisms. Therefore, we studied the tolerance of Rhodotorula glutinis to acetic acid and its lipid synthesis from substrate containing acetic acid. In the mixed sugar medium containing 6 g/L glucose and 44 g/L xylose, and supplemented with acetic acid, the cell growth was not:inhibited when the acetic acid concentration was below 10 g/L. Compared with the control, the biomass, lipid concentration and lipid content of R. glutinis increased 21.5%, 171% and 122% respectively when acetic acid concentration was 10 g/L. Furthermore, R. glutinis could accumulate lipid with acetate as the sole carbon source. Lipid concentration and lipid yield reached 3.20 g/L and 13% respectively with the initial acetic acid concentration of 25 g/L. The lipid composition was analyzed by gas chromatograph. The main composition of lipid produced with acetic acid was palmitic acid, stearic acid, oleic acid, linoleic acid and linolenic acid, including 40.9% saturated fatty acids and 59.1% unsaturated fatty acids. The lipid composition was similar to that of plant oil, indicating that lipid from oleaginous yeast R. glutinis had potential as the feedstock of biodiesel production. These results demonstrated that a certain concentration of acetic acid need not to be removed in the detoxification process when using lignocelluloses hydrolysate to produce microbial lipid by R. glutinis.
Acetic Acid
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Biofuels
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Biomass
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Culture Media
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Fatty Acids
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Hydrolysis
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Industrial Microbiology
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Lignin
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chemistry
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Linoleic Acid
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Lipids
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biosynthesis
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Oleic Acid
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Rhodotorula
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metabolism