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1.
Zhongguo Zhong Yao Za Zhi ; 45(9): 2186-2192, 2020 May.
Article in Chinese | MEDLINE | ID: mdl-32495570

ABSTRACT

Proton nuclear magnetic resonance(~1H-NMR) is used to investigate the effect of Renshenjian Decoction on serum and urine metabolism of type 2 diabetic rats with insulin resistance induced by high-sugar and high-fat diet combined with low-dose streptozotocin(STZ). After the successful establishment of the insulin resistance model of type 2 diabetes, administration for 35 days, the serum and urine of rats were taken. Once the ~1H-NMR data have been collected and processed, PCA and OPLS-DA were used to analyze them. The results show that: compared with the blank group, the contents of methionine, taurine, α-glucose and ß-glucose in the serum of the model group increased significantly(P<0.001), while the contents of 3-hydroxybutyric acid, lactic acid and unsaturated fatty acids decreased significantly(P<0.01). In the model group, the contents of trimethylamine oxide, glycine, α-glucose, ß-glucose, taurine and phosphocholine in urine increased significantly(P<0.05), while the contents of creatine, lactic acid, acetic acid and citric acid decreased significantly(P<0.05). Compared with the model group, the contents of 3-hydroxybutyric acid and unsaturated fatty acids in serum of rats in the treatment group increased significantly(P<0.05), while the contents of taurine, α-glucose and ß-glucose decreased significantly(P<0.01). In the treatment group, the contents of lactic acid, taurine and creatine in urine increased significantly(P<0.05), while the contents of trimethylamine oxide, glycine, α-glucose, ß-glucose and phosphocholine decreased significantly(P<0.01). The results show that Renshenjian Decoction can regulate metabolic disorder and promote the metabolic phenotype to return to the normal range. It displayed therapeutic effect on type 2 diabetic rats with insulin resistance and provided a certain scientific basis for the biological basic research of Renshenjian Decoction by improving insulin resistance in diabetes mellitus.


Subject(s)
Diabetes Mellitus, Experimental , Diabetes Mellitus, Type 2 , Animals , Blood Glucose , Metabolomics , Proton Magnetic Resonance Spectroscopy , Rats , Rats, Sprague-Dawley
2.
Front Plant Sci ; 9: 725, 2018.
Article in English | MEDLINE | ID: mdl-29910821

ABSTRACT

General control non-derepressible-2 (GCN2) is a ubiquitous protein kinase that phosphorylates the α subunit of the eukaryotic initiation factor, eIF2, preventing the initiation of a new cycle of protein synthesis, subsequently reducing the global protein biosynthesis. GCN2 can also regulate the response of plants to biotic and abiotic stresses. In this study, two GCN2 homologs, NtGCN2-1 and NtGCN2-2, were cloned from Nicotiana tabacum, and were predicted to have been derived from their progenitors in N. tomentosiformis and N. sylvestris, respectively. The phosphorylation of NteIF2α could be activated by promoting the expression of NtGCN2 with plant hormones, including salicylic acid (SA), azelaic acid (AZA), methyl jasmonate (MeJA), and by imposition of different stresses (Bemisia tabaci infection, drought, and cold), indicating that NtGCN2 is involved in the response of plants to multiple biotic and abiotic stresses. We also observed that the overexpression of NtGCN2-1 significantly influenced different physiological processes. It promoted seed germination and root elongation. The content of total soluble sugars and reducing sugars were decreased, whereas those of chlorophyll a and b were increased in the GCN2 overexpressing plants. In addition, the overexpressing plants had lower content of reactive oxygen species and exhibited higher antioxidant activities. These physiological alterations could be attributed to the changes in the endogenous phytohormones, decrease in the SA and abscisic acid content, and accumulation of MeJA and AZA. It indicated that the overexpression of NtGCN2 in tobacco, stimulated the plant defense responses via phosphorylation of NteIF2α and regulation of plant hormones, and changes in the antioxidant ability and plant nutrient status.

3.
Int J Biol Sci ; 13(4): 471-479, 2017.
Article in English | MEDLINE | ID: mdl-28529455

ABSTRACT

Triple-negative breast cancer (TNBC) is a subtype of breast cancer with a poor prognosis, accounting for approximately 12-24% of breast cancer cases. Accumulating evidence has indicated that there is no effective targeted therapy available for TNBC. Dipalmitoylphosphatidic acid (DPPA) is a bioactive phospholipid. However, the function of DPPA in the growth of TNBC has not yet been studied. In this study, we employed TNBC cells and a subcutaneous tumor model to elucidate the possible effect of DPPA on tumor growth in TNBC. We showed that DPPA significantly inhibited tumor growth in the mouse subcutaneous tumor model and suppressed cell proliferation and angiogenesis in TNBC tumor tissues. This inhibition was mediated partly by suppressing the expression of cyclin B1 (CCNB1), which directly promoted the accumulation of cells in the G2 phase and arrested cell cycle progression in human TNBC. In addition, the inhibition of tumor growth by DPPA may also be mediated by the suppression of tumor angiogenesis in TNBC. This work provides initial evidence that DPPA might be vital as an anti-tumor drug to treat TNBC.


Subject(s)
Apoptosis/drug effects , Cell Proliferation/drug effects , Phosphatidic Acids/pharmacology , Phosphatidic Acids/therapeutic use , Triple Negative Breast Neoplasms/drug therapy , Animals , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Cell Cycle/drug effects , Cell Cycle/genetics , Cell Line , Cell Line, Tumor , Female , Flow Cytometry , G2 Phase/drug effects , G2 Phase/genetics , Humans , Immunoblotting , Male , Mice , Mice, Inbred BALB C , Mice, Nude , Triple Negative Breast Neoplasms/genetics , Triple Negative Breast Neoplasms/metabolism , Xenograft Model Antitumor Assays
4.
Ann Anat ; 200: 79-87, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25819501

ABSTRACT

Many human disorders induce high salinity in tissues and organs, interfering with their normal physiological functions. Using a mouse model, we demonstrated that high salt intake caused infertility. Specifically, we established that high salinity dramatically affects ovarian follicle development and the extent of follicular atresia. However, it did not significantly influence the primordial follicles. TUNEL assays revealed that high salt intake inhibited follicle development by inducing the granulosa and theca cells that surround the oocytes to undergo apoptosis. Furthermore, immunohistological staining for the proliferation markers Ki67 and PH3 showed that high salt intake also repressed granulosa cell proliferation. In vitro testing of granulosa cells also confirmed that high salt significantly repressed cell proliferation and promoted cell apoptosis. In summary, high salt consumption negatively impacts reproductive functions in female mice by interfering with ovarian folliculogenesis.


Subject(s)
Ovarian Follicle/drug effects , Ovarian Follicle/growth & development , Sodium Chloride/toxicity , Animals , Apoptosis/drug effects , Cell Proliferation/drug effects , Female , Follicular Atresia/drug effects , Granulosa Cells/drug effects , In Situ Nick-End Labeling , Infertility, Female/chemically induced , Ki-67 Antigen/metabolism , Mice , Mice, Inbred C57BL , Oocytes/drug effects , Pregnancy , Primary Cell Culture , Theca Cells/drug effects
5.
J Alzheimers Dis ; 43(2): 535-48, 2015.
Article in English | MEDLINE | ID: mdl-25114073

ABSTRACT

Alzheimer's disease (AD) is a progressive neurological disorder that primarily affects memory, and its prevalence is rising. Increasing evidence suggests that dysfunction of the blood-brain barrier (BBB) may be involved in AD and other neurodegenerative diseases. Herein, we report that the permeability of the BBB is increased and that AD-like alterations are present in Slit-2 overexpressing transgenic mice. We found that behavioral change and the corresponding molecular diagnostic markers of AD, such as hippocampal neuron apoptosis, amyloid-ß (Aß) protein deposition, and acetylcholinesterase expression, were increased in the Slit-2 transgenic mice. Moreover, the endothelial cells were dysfunctional, the size of the lateral ventricle cavity increased, and the permeability of the BBB increased. Additionally, there was an increased serum level of glutamate indicating that the BBB is related to AD. Finally, histopathological analysis of other organs in the Slit-2 overexpressing mice did not show any marked abnormalities. These findings demonstrate that Slit2 overexpression may be responsible for AD-like alterations and the increased BBB permeability in these mice. Our study provides a potential novel mechanism for the development of AD.


Subject(s)
Alzheimer Disease/genetics , Alzheimer Disease/pathology , Blood-Aqueous Barrier/physiopathology , Capillary Permeability/genetics , Gene Expression Regulation/genetics , Intercellular Signaling Peptides and Proteins/genetics , Nerve Tissue Proteins/genetics , Aged , Aged, 80 and over , Alzheimer Disease/blood , Amyloid beta-Protein Precursor/genetics , Animals , Blood-Aqueous Barrier/ultrastructure , Disease Models, Animal , Female , Humans , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Microscopy, Electron, Transmission , Middle Aged , Nuclear Magnetic Resonance, Biomolecular
6.
Tumour Biol ; 34(6): 3309-16, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24078452

ABSTRACT

The polymorphism of vitamin D receptor (VDR) gene is demonstrated to affect the activity of its encoding protein and the subsequent downstream effects mediated by vitamin D. Mutations in VDR gene FokI have been suggested in the development of various cancers. Whether the polymorphism of the VDR gene FokI confers risk to ovarian cancer still remains controversial across the published studies in different ethnicity. The aim of this meta-analysis was to determine the role of VDR gene FokI variant in the susceptibility to ovarian cancer. Six publications with 14 individual case-control studies involving a total of 10,964 subjects were finally included into our study after a comprehensive literature search of the PubMed, Embase, Web of Science, and Wanfang databases. The strength of the association between the VDR gene FokI polymorphism and ovarian cancer risk was estimated under the allelic (T vs. C), homozygous (TT vs. CC), additive (CT vs. CC), recessive (TT vs. CC + CT), and dominant (CT + TT vs. CC) gene models. The overall odds ratios (ORs) for the contrast models of T vs. C, TT vs. CC, CT vs. CC, and CT + TT vs. CC indicated that the VDR gene FokI variant was related to an increased risk of ovarian cancer (OR(T vs. C) = 1.09, 95 % confidence interval (CI) 1.03-1.15, P(OR) = 0.004; OR(TT vs. CC) = 1.17, 95 % CI 1.04-1.32, P(OR) = 0.011; OR(CT vs. CC) = 1.10, 95 % CI 1.01-1.20, P(OR) = 0.027; OR(CT + TT vs. CC) = 1.12, 95 % CI 1.03-1.21, P(OR) = 0.007). The stratified analysis among the Caucasians also identified a significant association between the VDR gene FokI polymorphism and the susceptibility to ovarian cancer. The present meta-analysis with large available published data has revealed that the VDR gene FokI polymorphism confers susceptibility to ovarian cancer, particularly among the Caucasian population.


Subject(s)
Genetic Predisposition to Disease/genetics , Ovarian Neoplasms/genetics , Polymorphism, Single Nucleotide , Receptors, Calcitriol/genetics , Binding Sites/genetics , Case-Control Studies , Deoxyribonucleases, Type II Site-Specific/metabolism , Female , Gene Frequency , Genetic Predisposition to Disease/ethnology , Genotype , Humans , Odds Ratio , Ovarian Neoplasms/ethnology , Risk Factors , White People/genetics
7.
Yi Chuan ; 31(7): 748-54, 2009 Jul.
Article in Chinese | MEDLINE | ID: mdl-19586881

ABSTRACT

Phytochrome 3 (PHY3) is a novel chimeric photoreceptor that can respond to both red/far red and blue light. Using this photoreceptor, some cryptogams could enhance light sensitivity under low light environment. But PHY3 sequence information is still extremely limited. In the present study, a full-length PHY3 genomic sequence was cloned from a fern Allantodia dilatata (Bl.) Ching by inverse PCR approaches. Sequence analysis showed that introns were absent in the gene. It contained a 4 278 bp open reading frame, encoding a deduced protein of 1 425 amino acid residues with a theoretical isoelectric point (pI) of 6.29 and a calculated molecular mass about 157 kDa. Protein domain search and structure analyses indicated that PHY3 originated from the recombination of two different photoreceptors. Its N-terminal section consisted of a putative functional phytochrome chromophore-binding domain including PAS, GAF, and PHY, whereas the C-terminal region possessed a nearly complete phototropin motif with two LOV and one STKc domains.


Subject(s)
Ferns/genetics , Light , Photoreceptors, Plant/chemistry , Photoreceptors, Plant/genetics , Phytochrome/chemistry , Phytochrome/genetics , Cloning, Molecular , Color , Evolution, Molecular , Models, Molecular , Photoreceptors, Plant/metabolism , Phytochrome/metabolism , Protein Conformation , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Sequence Analysis, DNA
8.
BMC Evol Biol ; 9: 130, 2009 Jun 11.
Article in English | MEDLINE | ID: mdl-19519899

ABSTRACT

BACKGROUND: Ferns have generally been neglected in studies of chloroplast genomics. Before this study, only one polypod and two basal ferns had their complete chloroplast (cp) genome reported. Tree ferns represent an ancient fern lineage that first occurred in the Late Triassic. In recent phylogenetic analyses, tree ferns were shown to be the sister group of polypods, the most diverse group of living ferns. Availability of cp genome sequence from a tree fern will facilitate interpretation of the evolutionary changes of fern cp genomes. Here we have sequenced the complete cp genome of a scaly tree fern Alsophila spinulosa (Cyatheaceae). RESULTS: The Alsophila cp genome is 156,661 base pairs (bp) in size, and has a typical quadripartite structure with the large (LSC, 86,308 bp) and small single copy (SSC, 21,623 bp) regions separated by two copies of an inverted repeat (IRs, 24,365 bp each). This genome contains 117 different genes encoding 85 proteins, 4 rRNAs and 28 tRNAs. Pseudogenes of ycf66 and trnT-UGU are also detected in this genome. A unique trnR-UCG gene (derived from trnR-CCG) is found between rbcL and accD. The Alsophila cp genome shares some unusual characteristics with the previously sequenced cp genome of the polypod fern Adiantum capillus-veneris, including the absence of 5 tRNA genes that exist in most other cp genomes. The genome shows a high degree of synteny with that of Adiantum, but differs considerably from two basal ferns (Angiopteris evecta and Psilotum nudum). At one endpoint of an ancient inversion we detected a highly repeated 565-bp-region that is absent from the Adiantum cp genome. An additional minor inversion of the trnD-GUC, which is possibly shared by all ferns, was identified by comparison between the fern and other land plant cp genomes. CONCLUSION: By comparing four fern cp genome sequences it was confirmed that two major rearrangements distinguish higher leptosporangiate ferns from basal fern lineages. The Alsophila cp genome is very similar to that of the polypod fern Adiantum in terms of gene content, gene order and GC content. However, there exist some striking differences between them: the trnR-UCG gene represents a putative molecular apomorphy of tree ferns; and the repeats observed at one inversion endpoint may be a vestige of some unknown rearrangement(s). This work provided fresh insights into the fern cp genome evolution as well as useful data for future phylogenetic studies.


Subject(s)
Evolution, Molecular , Ferns/genetics , Genome, Chloroplast , Phylogeny , Base Composition , Base Sequence , Chloroplasts/genetics , Chromosome Inversion , Comparative Genomic Hybridization , DNA, Plant/genetics , Gene Order , Genes, Plant , Genome, Plant , Molecular Sequence Data , RNA, Transfer/genetics , Repetitive Sequences, Nucleic Acid , Sequence Analysis, DNA
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