56 research outputs found

    Metabolomic profiles of myocardial ischemia under treatment with salvianolic acid B

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    <p>Abstract</p> <p>Background</p> <p><it>Radix Salvia miltiorrhiza </it>(<it>Danshen</it>) has been used as a principal herb in treating cardiovascular diseases in Chinese medicine. Salvianolic acid B (SA-B), a water-soluble active component of <it>Danshen</it>, was found to have anti-myocardial ischemia (anti-MI) effect. This study aims to investigate mechanisms of SA-B on MI.</p> <p>Methods</p> <p>Five conventional Western medicines (isosorbide dinitrate, verapamil, propranolol, captopril and trimethazine) with different mechanisms for treating cardiovascular diseases were selected as positive references to compare with SA-B in changing of the metabolomic profiles in MI rats under treatment. Potential mechanisms of SA-B were further investigated in H9C2 cell line.</p> <p>Results</p> <p>The metabolomic profiles between SA-B- and propranolol-treated MI rats were similar, since there was a big overlap between the two groups in the PLS-DA score plot. Finally, it was demonstrated that SA-B exhibited a protective effect on MI mainly by decreasing the concentration of cyclic adenosine monophosphate (cAMP) and Ca<sup>2+ </sup>and inhibiting protein kinase A (PKA).</p> <p>Conclusion</p> <p>SA-B and propanolol exhibited similar metabolomic profiles, indicating that the two drugs might have a similar mechanism.</p

    Serum proteomic, peptidomic and metabolomic profiles in myasthenia gravis patients during treatment with Qiangji Jianli Fang

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    BACKGROUND: Qiangji Jianli Fang (QJF) has been used for treatment of myasthenia gravis (MG) in China. However, our understanding of the effects of QJF against MG at the molecular level is limited. This study aims to investigate the effects of QJF treatment of MG patients on the protein, peptide and metabolite levels in serum. METHODS: High-throughput proteomic, peptidomic and metabolomic techniques were applied to investigate serum samples from 21 healthy individuals and 47 MG patients before and after QJF treatment via two-dimensional gel electrophoresis, matrix-assisted laser desorption/ionization time of flight mass spectrometry and liquid chromatography Fourier transform mass spectrometry, respectively. RESULTS: After QJF treatment, the expression levels of peptides m/z 1865.019, 2021.128 and 1211.668 of complement C3f increased (P = 0.004, P = 0.001 and P = 0.043, respectively), while that of peptide m/z 1739.931 of component C4b decreased (P = 0.043), in the serum of MG patients. The levels of γ-aminobutyric acid (P = 0.000) and coenzyme Q4 (P = 0.000) resumed their normal states. CONCLUSION: QJF could inhibit the activity of the complement system and restore the normal levels of metabolites

    Serum Amino Acids in Association with Prevalent and Incident Type 2 Diabetes in A Chinese Population

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    We aimed to simultaneously examine the associations of both essential and non-essential amino acids with both prevalent and incident type 2 diabetes in a Chinese population. A case-control study was nested within the Singapore Chinese Health Study. Participants included 144 cases with prevalent and 160 cases with incident type 2 diabetes and 304 controls. Cases and controls were individually matched on age, sex, and date of blood collection. Baseline serum levels of 9 essential and 10 non-essential amino acids were measured using liquid chromatography tandem mass spectrometry. We identified that five essential (isoleucine, leucine, lysine, phenylalanine, and valine) and five non-essential (alanine, glutamic acid, glutamine, glycine, and tyrosine) amino acids were associated with the prevalence of type 2 diabetes; four essential (isoleucine, leucine, tryptophan, and valine) and two non-essential (glutamine and tyrosine) amino acids were associated with the incidence of type 2 diabetes. Of these, valine and tyrosine independently led to a significant improvement in risk prediction of incident type 2 diabetes. This study demonstrates that both essential and non-essential amino acids were associated with the risk for prevalent and incident type 2 diabetes, and the findings could aid in diabetes risk assessment in this Chinese population

    Serum osmolality and ions, and gill Na+/K+-ATPase of spottedtail goby Synechogobius ommaturus (R.) in response to acute salinity changes

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    This study was carried out to determine the effects of abrupt salinity change on osmoregulatory ability of the spottedtail goby Synechogobius ommaturus. 720 juvenile fish (65.3 ± 11.8 g) were transferred to 200 L tanks (with 40 juveniles in each tank), in which salinities were abruptly changed from 10 to 20, 30, 40, 50 and freshwater. Survival rate, serum osmolality, electrolytes (Na+, Cl−, and K+) and gill Na+/K+-ATPase (NKA) activity were assessed successively in 528 h. Results showed serum osmolality, ion concentrations and gill Na+/K+-ATPase activity increased significantly when fish were transferred to salinity 40 and 50 and all fish in these groups died by the end of the experiment. Serum osmolality, Na+, Cl− and K+ in fish transferred to a salinity of 20, 30 and freshwater were not affected and no mortality was detected. Compared with the control group, a significantly decrease of NKA activity happened in the freshwater group, but the activity in 20 and 30 groups was not affected significantly. The results indicated that S. ommaturus could adapt rapidly and maintain homeostasis in a wide range of salinities (from freshwater to salinity 30) and this species may be suitable for aquaculture in estuarine and coastal areas where rapid salinity fluctuations commonly occur. Keywords: Osmolality, Gill, Na+/K+-ATPase, Synechogobius ommaturu

    Angular Dependence of the Spin Photocurrent in a Spin Light Emitting Diode

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    International audienceWe study the photogenerated spin currents in a spin light emitting diode when the device is excited under circularly polarized light. The device is based on a In 0 1 Ga 0 9 As quantum well embedded in a p-in junction. The spin filtering is performed owing to a Co-Fe-B/MgO electrode with out-of-plane magnetization. The helicity-dependent photocurrent is explored as a function of the incident and azimuth angles of the incoming light wave vector with respect to the magnetization direction of the ferromagnetic electrode. The results are interpreted as a simple phenomenological model described in the paper, which demonstrates it is an efficient way to detect the remanent < (remnant?) magnetic moment of the ferromagnetic electrode at room temperature

    RuvBL2 Is Involved in Histone Deacetylase Inhibitor PCI-24781-Induced Cell Death in SK-N-DZ Neuroblastoma Cells

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    <div><p>Neuroblastoma is the second most common solid tumor diagnosed during infancy. The survival rate among children with high-risk neuroblastoma is less than 40%, highlighting the urgent needs for new treatment strategies. PCI-24781 is a novel hydroxamic acid-based histone deacetylase (HDAC) inhibitor that has high efficacy and safety for cancer treatment. However, the underlying mechanisms of PCI-24781 are not clearly elucidated in neuroblastoma cells. In the present study, we demonstrated that PCI-24781 treatment significantly inhibited tumor growth at very low doses in neuroblastoma cells SK-N-DZ, not in normal cell line HS-68. However, PCI-24781 caused the accumulation of acetylated histone H3 both in SK-N-DZ and HS-68 cell line. Treatment of SK-N-DZ with PCI-24781 also induced cell cycle arrest in G2/M phase and activated apoptosis signaling pathways via the up-regulation of DR4, p21, p53 and caspase 3. Further proteomic analysis revealed differential protein expression profiles between non-treated and PCI-24781 treated SK-N-DZ cells. Totally 42 differentially expressed proteins were identified by MALDI-TOF MS system. Western blotting confirmed the expression level of five candidate proteins including prohibitin, hHR23a, RuvBL2, TRAP1 and PDCD6IP. Selective knockdown of RuvBL2 rescued cells from PCI-24781-induced cell death, implying that RuvBL2 might play an important role in anti-tumor activity of PCI-24781 in SK-N-DZ cells. The present results provide a new insight into the potential mechanism of PCI-24781 in SK-N-DZ cell line.</p></div
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