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1.
Plant J ; 113(2): 416-429, 2023 01.
Article in English | MEDLINE | ID: mdl-36479950

ABSTRACT

Crop photosynthesis (A) and productivity are often limited by a combination of nutrient stresses, such that changes in the availability of one nutrient may affect the availability of another nutrient, in turn influencing A. In this study, we examined the synergistic effects of phosphorus (P) and potassium (K) on leaf A in a nutrient amendment experiment, in which P and K were added individually or in combination to Brassica napus grown under P and K co-limitation. The data revealed that the addition of P gradually removed the dominant limiting factor (i.e. the limited availability of P) and improved leaf A. Strikingly, the addition of K synergistically improved the overall uptake of P, mainly by boosting plant growth, and compensated for the physiological demand for P by prioritizing investment in metabolic pools of P (P-containing metabolites and inorganic phosphate, Pi). The enlarged pool of metabolically active P was partially associated with the upregulation of Pi regeneration through release from triose phosphates rather than replacement of P-containing lipids. This process mitigated P restrictions on A by maintaining the ATP/NADPH and NADPH/NADP+ ratios and increasing the content and activity of Rubisco. Our findings demonstrate that sufficient K increased Pi-limited A by enhancing metabolic P fractions and Rubisco activity. Thus, ionic synergism may be exploited to mitigate nutrient-limiting factors to improve crop productivity.


Subject(s)
Brassica napus , Phosphorus , Phosphorus/metabolism , Phosphates/metabolism , Potassium/metabolism , Brassica napus/metabolism , Ribulose-Bisphosphate Carboxylase/metabolism , NADP/metabolism , Photosynthesis/physiology , Plant Leaves/metabolism
2.
BMC Res Notes ; 7: 120, 2014 Mar 02.
Article in English | MEDLINE | ID: mdl-24580748

ABSTRACT

BACKGROUND: Hyperglycemia-induced endothelial hyperpermeability is crucial to cardiovascular disorders and macro-vascular complications in diabetes mellitus. The objective of this study is to investigate the effects of green tea polyphenols (GTPs) on endothelial hyperpermeability and the role of nicotinamide adenine dinucleotide phosphate (NADPH) pathway. METHODS: Male Wistar rats fed on a high fat diet (HF) were treated with GTPs (0, 0.8, 1.6, 3.2 g/L in drinking water) for 26 weeks. Bovine aortic endothelial cells (BAECs) were treated with high glucose (HG, 33 mmol/L) and GTPs (0.0, 0.4, or 4 µg/mL) for 24 hours in vitro. The endothelial permeabilities in rat aorta and monolayer BAECs were measured by Evans blue injection method and efflux of fluorescein isothiocyanate (FITC)-dextran, respectively. The reactive oxygen species (ROS) levels in rat aorta and monolayer BAECs were measured by dihydroethidium (DHE) and 2', 7'-dichloro-fluorescein diacetate (DCFH-DA) fluorescent probe, respectively. Protein levels of NADPH oxidase subunits were determined by Western-blot. RESULTS: HF diet-fed increased the endothelial permeability and ROS levels in rat aorta while HG treatments increased the endothelial permeability and ROS levels in cultured BAECs. Co-treatment with GTPs alleviated those changes both in vivo and in vitro. In in vitro studies, GTPs treatments protected against the HG-induced over-expressions of p22phox and p67phox. Diphenylene iodonium chloride (DPI), an inhibitor of NADPH oxidase, alleviated the hyperpermeability induced by HG. CONCLUSIONS: GTPs could alleviate endothelial hyperpermeabilities in HF diet-fed rat aorta and in HG treated BAECs. The decrease of ROS production resulting from down-regulation of NADPH oxidase contributed to the alleviation of endothelial hyperpermeability.


Subject(s)
Endothelium, Vascular/drug effects , NADPH Oxidases/metabolism , Polyphenols/pharmacology , Reactive Oxygen Species/metabolism , Signal Transduction/drug effects , Tea/chemistry , Animals , Aorta/cytology , Blotting, Western , Capillary Permeability/drug effects , Cattle , Cell Membrane Permeability/drug effects , Cells, Cultured , Diet, High-Fat , Dose-Response Relationship, Drug , Endothelial Cells/drug effects , Endothelial Cells/metabolism , Endothelial Cells/physiology , Endothelium, Vascular/metabolism , Endothelium, Vascular/physiology , Glucose/pharmacology , Male , NADH, NADPH Oxidoreductases/antagonists & inhibitors , NADH, NADPH Oxidoreductases/metabolism , NADPH Oxidases/antagonists & inhibitors , Onium Compounds/pharmacology , Rats , Rats, Wistar
3.
PLoS One ; 8(1): e53796, 2013.
Article in English | MEDLINE | ID: mdl-23342006

ABSTRACT

OBJECTIVE: Hypoadiponectinemia contributes to the development of obesity and related disorders such as diabetes, hyperlipidemia, and cardiovascular diseases. In this study we investigated the effects of green tea polyphenols (GTPs) on adiponectin levels and fat deposits in high fat (HF) fed rats, the mechanism of signaling pathway was explored as well. METHODS AND RESULTS: Male Wistar rats were fed with high-fat diet. GTPs (0.8, 1.6, 3.2 g/L) were administered via drinking water. Serum adiponectin and insulin were measured by ELISA, mRNA levels of adiponectin and PPARγ in visceral adipose tissue (VAT) were determined by Real-time PCR, protein levels of PPARγ, phospho (p) - PPARγ, extracellular signal regulated kinase (erk) 1/2 and p-erk1/2 in VAT were determined by western blot. GTPs treatment attenuated the VAT accumulation, hypoadiponectinemia and the decreased mRNA level of adiponectin in VAT induced by HF. Decreased expression and increased phosphorylation of PPARγ (the master regulator of adiponectin), and increased activation of erk1/2 were observed in HF group, and these effects could be alleviated by GTPs treatment. To explore the underlying mechanism, VAT was cultured in DMEM with high glucose to mimic the hyperglycemia condition in vitro. Similar to the results of in vivo study, decreased adiponectin levels, decreased expression and increased phosphorylation of PPARγ, and elevated erk1/2 phosphorylation in cultured VAT were observed. These effects could be ameliorated by co-treatment with GTPs or PD98059 (a selective inhibitor of erk1/2). CONCLUSION: GTPs reduced fat deposit, ameliorated hypoadiponectinemia in HF-fed rats, and relieved high glucose-induced adiponectin decrease in VAT in vitro. The signaling pathway analysis indicated that PPARγ regulation mediated via erk1/2 pathway was involved.


Subject(s)
Adiponectin/metabolism , Extracellular Signal-Regulated MAP Kinases/metabolism , Intra-Abdominal Fat/drug effects , PPAR gamma/metabolism , Polyphenols/pharmacology , Signal Transduction/drug effects , Tea/chemistry , Adiponectin/blood , Adiponectin/genetics , Animals , Body Weight/drug effects , Diet, High-Fat/adverse effects , Down-Regulation/drug effects , Extracellular Signal-Regulated MAP Kinases/antagonists & inhibitors , Intra-Abdominal Fat/cytology , Intra-Abdominal Fat/metabolism , Male , Mitogen-Activated Protein Kinase 1/antagonists & inhibitors , Mitogen-Activated Protein Kinase 1/metabolism , Mitogen-Activated Protein Kinase 3/antagonists & inhibitors , Mitogen-Activated Protein Kinase 3/metabolism , PPAR gamma/genetics , Phosphorylation/drug effects , Protein Kinase Inhibitors/pharmacology , Rats , Rats, Wistar
4.
Zhong Yao Cai ; 32(4): 500-3, 2009 Apr.
Article in Chinese | MEDLINE | ID: mdl-19645231

ABSTRACT

OBJECTIVE: To establish the standard for quality control of Fructus Hordei germinatus, Fructus Oryzae germinatus and Fructus Setariae germinatus. METHODS: The digital microscope and infrared spectroscopy were used in the pharmacognostical study. RESULTS: Distinguished differences were found on morphological and microscopical features of these three crude drugs. Whereas, their infrared spectrums were basically all the same. CONCLUSION: The study provides a convenient, effect method for the identification of these three medicinal materials.


Subject(s)
Drugs, Chinese Herbal/chemistry , Edible Grain/anatomy & histology , Seeds/anatomy & histology , Drugs, Chinese Herbal/standards , Edible Grain/ultrastructure , Hordeum/anatomy & histology , Hordeum/ultrastructure , Oryza/anatomy & histology , Oryza/ultrastructure , Pharmacognosy , Powders , Quality Control , Seeds/ultrastructure , Setaria Plant/anatomy & histology , Setaria Plant/ultrastructure , Spectroscopy, Fourier Transform Infrared
5.
J Nutr Biochem ; 20(12): 1021-7, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19195865

ABSTRACT

Caveolin-1 (Cav-1), a negative regulator of endothelial nitric oxide synthase (eNOS), influences various aspects of the cardiovascular functions. We had reported that a high-fat diet up-regulated aortic Cav-1 expressions in rats. In this study, we investigated the effects of green tea polyphenols (GTPs) on endothelial Cav-1 expression and phosphorylation in vitro. Bovine aortic endothelial cells (BAECs) were treated with 4 microg/ml GTPs for 0, 4, 8, 12, 16 and 24 h, and with 0, 0.04, 0.4, 4 and 40 microg/ml GTPs for 16 h, respectively. Cav-1 protein and mRNA were detected using Western blot and reverse transcriptase polymerase chain reaction. Cav-1 protein expression was down-regulated after treatment of BAECs with 4 microg/ml GTPs for 12, 16 and 24 h. And decrease in the level of Cav-1 mRNA was observed after GTP treatment for 4 and 8 h. GTPs (0.04-4 microg/ml) down-regulate Cav-1 protein expressions and mRNA levels dose dependently. PD98059, an inhibitor of extracellular signal-regulated kinase 1/2 (ERK1/2), up-regulated Cav-1 expression in BAECs alone and abolished the down-regulation effects of GTPs in BAECs while pretreatment with it. Inhibition of p38 mitogen-activated protein kinase (p38MAPK) with SB203580, which down-regulates Cav-1 expression in BAECs alone, deteriorated the Cav-1 down-regulating effects by GTPs. In addition to the effects on expression of Cav-1, GTP treatment inhibited phosphorylation of Cav-1 [tyrosine 14 (Tyr14)]. These data indicate that GTPs down-regulate gene expression of Cav-1 time- and dose- dependently via activating ERK1/2 and inhibiting p38MAPK signaling.


Subject(s)
Catechin/analogs & derivatives , Caveolin 1/biosynthesis , Endothelium, Vascular/drug effects , MAP Kinase Kinase 2/metabolism , Mitogen-Activated Protein Kinase 3/metabolism , p38 Mitogen-Activated Protein Kinases/metabolism , Animals , Catechin/pharmacology , Cattle , Down-Regulation , Endothelium, Vascular/metabolism , Flavonoids/pharmacology , Imidazoles/pharmacology , Nitric Oxide Synthase Type III/metabolism , Pyridines/pharmacology , RNA, Messenger/metabolism , Tea/chemistry
6.
Zhong Yao Cai ; 28(2): 89-91, 2005 Feb.
Article in Chinese | MEDLINE | ID: mdl-15981873

ABSTRACT

OBJECTIVE: To identify Chinese drug Beimu from its fake species. METHOD: IR spectra was obtained by Fourier Transform Infrared Spectroscopy (FTIR) and clustering analysis was adopted for authentication. RESULT: There were significant differences between Beimu and its fake species. CONCLUSION: The established method was quick, sensitive and accurate. It could be used for the differentiation of different species of Beimu materials and their fake species.


Subject(s)
Fritillaria/classification , Plants, Medicinal/classification , Spectroscopy, Fourier Transform Infrared/methods , China , Cluster Analysis , Drug Contamination , Pharmacognosy , Quality Control
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