ABSTRACT
INTRODUCTION: Light-harvesting chlorophyll a/b-binding (LHCB) protein complexes of photosystem II are integral to the formation of thylakoid structure and the photosynthetic process. They play an important role in photoprotection, a crucial process in leaf development under low-temperature stress. Nonetheless, potential key genes directly related to low-temperature response and albino phenotype have not been precisely identified in tea plant. Moreover, there are no studies simultaneously investigating multiple albino tea cultivars with different temperature sensitivity. OBJECTIVES: The study aimed to clarify the basic characteristics of CsLHCB gene family members, and identify critical CsLHCB genes potentially influential in leaf color phenotypic variation and low-temperature stress response by contrasting green and albino tea cultivars. Concurrently, exploring the differential expression of the CsLHCB gene family across diverse temperature-sensitive albino tea cultivars. METHODS: We identified 20 putative CsLHCB genes according to phylogenetic analysis. Evolutionary relationships, gene duplication, chromosomal localization, and structures were analyzed by TBtools; the physiological and biochemical characteristics were analyzed by protein analysis websites; the differences in coding sequences and protein accumulation in green and albino tea cultivars, gene expression with maturity were tested by molecular biology technology; and protein interaction was analyzed in the STRING database. RESULTS: All genes were categorized into seven groups, mapping onto 7 chromosomes, including three tandem and one segmental duplications. They all own a conserved chlorophyll A/B binding protein domain. The expression of CsLHCB genes was tissue-specific, predominantly in leaves. CsLHCB5 may play a key role in the process of leaf maturation and senescence. In contrast to CsLHCB5, CsLHCB1.1, CsLHCB2, and CsLHCB3.2 were highly conserved in amino acid sequence between green and albino tea cultivars. In albino tea cultivars, unlike in green cultivars, the expression of CsLHCB1.1, CsLHCB1.2, and CsLHCB2 was down-regulated under low-temperature stress. The accumulation of CsLHCB1 and CsLHCB5 proteins was lower in albino tea cultivars. Greater accumulation of CsLHCB2 protein was detected in RX1 and RX2 compared to other albino cultivars. CONCLUSIONS: CsLHCB1.1, CsLHCB1.2, and CsLHCB2 played a role in the response to low-temperature stress. The amino acid sequence site mutation of CsLHCB5 would distinguish the green and albino tea cultivars. The less accumulation of CsLHCB1 and CsLHCB5 had a potential influence on albino leaves. Albino cultivars more sensitive to temperature exhibited lower CsLHCB gene expression. CsLHCB2 may serve as an indicator of temperature sensitivity differences in albino tea cultivars. This study could provide a reference for further studies of the functions of the CsLHCB family and contribute to research on the mechanism of the albino in tea plant.
ABSTRACT
Tea plants (Camellia sinensis) typically contain high-flavonoid phytochemicals like catechins. Recently, new tea cultivars with unique purple-colored leaves have gained attention. These purple tea cultivars are enriched with anthocyanin, which provides an interesting perspective for studying the metabolic flux of the flavonoid pathway. An increasing number of studies are focusing on the leaf color formation of purple tea and this review aims to summarize the latest progress made on the composition and accumulation of anthocyanins in tea plants. In addition, the regulation mechanism in its synthesis will be discussed and a hypothetical regulation model for leaf color transformation during growth will be proposed. Some novel insights are presented to facilitate future in-depth studies of purple tea to provide a theoretical basis for targeted breeding programs in leaf color.
Subject(s)
Camellia sinensis , Camellia sinensis/genetics , Anthocyanins/metabolism , Plant Proteins/genetics , Plant Breeding , Flavonoids/metabolism , Plant Leaves/metabolism , Tea , Gene Expression Regulation, Plant , TranscriptomeABSTRACT
BACKGROUND: Although dyslipidaemia may have a crucial impact on cardiovascular health in adults, there is a lack of specific data in transitional-age youth. Therefore, this study attempted to evaluate the association of dyslipidaemia with fat-to-muscle ratio (FMR), and establish FMR thresholds for diagnosing dyslipidaemia in transitional-age youth. METHODS: One thousand six hundred sixty individuals aged 16 to 24 years from the baseline of a subcohort in the Northwest China Natural Population Cohort: Ningxia Project were analysed. Anthropometric characteristics were gauged by a bioelectrical impedance analyser, and dyslipidaemia components were measured using a Beckman AU480 chemistry analyser. Additionally, this study used logistic regression to estimate the risk of dyslipidaemia based on FMR quintiles, and calculate the gender-specific ideal cut-off values of dyslipidaemia and its components by the receiver operating characteristic (ROC) curve. RESULTS: Of the 1660 participants, aged 19.06 ± 1.14 years, 558 males and 1102 females. The prevalence of dyslipidaemia was 13.4% and was significantly associated with FMR quintiles among all participants (P < 0.05). The ideal values of FMR in diagnosing dyslipidaemia were 0.2224 for males and 0.4809 for females, while males had a higher AUC than females (0.7118 vs. 0.6656). Meanwhile, high FMR values were significantly associated with adverse outcomes of dyslipidaemia, hypercholesterolemia and hypertriglyceridaemia (P < 0.05). CONCLUSIONS: The FMR was positively correlated with the prevalence of dyslipidaemia. The FMR can be used as an effective body composition index for diagnosing dyslipidaemia, especially in males, and preventive strategies should be initiated in transitional-age youth to decrease obesity-related dyslipidaemia.
Subject(s)
Dyslipidemias , Hyperlipidemias , Adolescent , Adult , Anthropometry , Body Mass Index , Dyslipidemias/diagnosis , Dyslipidemias/epidemiology , Female , Humans , Male , Muscles , ObesityABSTRACT
Squalene is a precursor of steroids with diverse bioactivities. Tea was previously found to contain squalene, but its variation between tea cultivars remains unknown. In this study, tea leaf squalene sample preparation was optimized and the squalene variation among 30 tea cultivars was investigated. It shows that squalene in the unsaponified tea leaf extracts was well separated on gas chromatography profile. Saponification led to a partial loss of squalene in tea leaf extract and so it is not an essential step for preparing squalene samples from tea leaves. The tea leaf squalene content increased with the maturity of tea leaf and the old leaves grown in the previous year had the highest level of squalene among the tested samples. The squalene levels in the old leaves of the 30 tested cultivars differentiated greatly, ranging from 0.289 to 3.682 mg/g, in which cultivar "Pingyun" had the highest level of squalene. The old tea leaves and pruned littering, which are not used in tea production, are an alternative source for natural squalene extraction.
ABSTRACT
Anthracnose is a major leaf disease in tea plant induced by Colletotrichum, which has led to substantial losses in yield and quality of tea. The molecular mechanism with regards to responses or resistance to anthracnose in tea remains unclear. A de novo transcriptome assembly dataset was generated from healthy and anthracnose-infected leaves on tea cultivars "Longjing-43" (LJ43) and "Zhenong-139" (ZN139), with 381.52 million pair-end reads, encompassing 47.78 billion bases. The unigenes were annotated versus Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), National Center for Biotechnology Information (NCBI) non-redundant protein sequences (Nr), evolutionary genealogy of genes: Non-supervised Orthologous Groups (eggNOG) and Swiss-prot. The number of differential expression genes (DEGs) detected between healthy and infected leaves was 1621 in LJ43 and 3089 in ZN139. The GO and KEGG enrichment analysis revealed that the DEGs were highly enriched in catalytic activity, oxidation-reduction, cell-wall reinforcement, plant hormone signal transduction and plant-pathogen interaction. Further studies by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) and high-performance liquid chromatography (HPLC) showed that expression of genes involved in endogenous salicylic acid biosynthesis and also accumulation of foliar salicylic acid are involved in the response of tea plant to anthracnose infection. This study firstly provided novel insight in salicylic acid acting as a key compound in the responses of tea plant to anthracnose disease. The transcriptome dataset in this study will facilitate to profile gene expression and metabolic networks associated with tea plant immunity against anthracnose.
Subject(s)
Camellia sinensis/genetics , Colletotrichum/pathogenicity , Gene Expression Profiling/methods , Gene Regulatory Networks , Camellia sinensis/metabolism , Camellia sinensis/microbiology , Gene Expression Regulation, Plant , Gene Ontology , High-Throughput Nucleotide Sequencing , Plant Diseases/genetics , Plant Diseases/microbiology , Plant Leaves/genetics , Plant Proteins/genetics , Salicylic Acid/metabolismABSTRACT
There is epidemiological evidence showing that drinking green tea can lower the risk of esophageal cancer (EC). The effect is mainly attributed to tea polyphenols and their most abundant component, (-)-epigallocatechin-3-gallate (EGCG). The possible mechanisms of tumorigenesis inhibition of EGCG include its suppressive effects on cancer cell proliferation, angiogenesis, DNA methylation, metastasis and oxidant stress. EGCG modulates multiple signal transduction and metabolic signaling pathways involving in EC. A synergistic effect was also observed when EGCG was used in combination with other treatment methods.
Subject(s)
Catechin/analogs & derivatives , Esophageal Neoplasms/drug therapy , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Catechin/chemistry , Catechin/pharmacology , Cell Proliferation/drug effects , DNA Methylation/drug effects , Humans , Polyphenols/chemistry , Signal Transduction/drug effects , TeaABSTRACT
Many in vitro studies have shown that tea catechins had vevarious health beneficial effects. However, inconsistent results between in vitro and in vivo studies or between laboratory tests and epidemical studies are observed. Low bioavailability of tea catechins was an important factor leading to these inconsistencies. Research advances in bioavailability studies involving absorption and metabolic biotransformation of tea catechins were reviewed in the present paper. Related techniques for improving their bioavailability such as nanostructure-based drug delivery system, molecular modification, and co-administration of catechins with other bioactives were also discussed.
Subject(s)
Camellia sinensis/chemistry , Catechin/pharmacokinetics , Animals , Biological Availability , Catechin/chemistry , Drug Delivery Systems , Humans , Nanostructures/administration & dosage , Nanostructures/chemistry , Plant Extracts/chemistry , Plant Extracts/pharmacokineticsABSTRACT
Neurodegenerative disease Alzheimer's disease (AD) is attracting growing concern because of an increasing patient population among the elderly. Tea consumption is considered a natural complementary therapy for neurodegenerative diseases. In this paper, epidemiological studies on the association between tea consumption and the reduced risk of AD are reviewed and the anti-amyloid effects of related bioactivities in tea are summarized. Future challenges regarding the role of tea in preventing AD are also discussed.
Subject(s)
Alzheimer Disease/prevention & control , Amyloid beta-Peptides/antagonists & inhibitors , Brain/drug effects , Neuroprotective Agents/therapeutic use , Plant Extracts/therapeutic use , Tea , Age Factors , Aged , Aged, 80 and over , Alzheimer Disease/epidemiology , Alzheimer Disease/metabolism , Alzheimer Disease/pathology , Amyloid beta-Peptides/metabolism , Animals , Brain/metabolism , Brain/pathology , Camellia sinensis/chemistry , Cognition/drug effects , Humans , Memory/drug effects , Middle Aged , Nerve Degeneration , Neuroprotective Agents/isolation & purification , Oxidative Stress/drug effects , Plant Extracts/isolation & purification , Prognosis , Protective Factors , Recommended Dietary Allowances , Risk FactorsABSTRACT
Neuropeptide FF (NPFF) interacts with specific receptors to regulate diverse biological processes. Its modulatory effect in the immune field, however, has not been fully explored yet. Here, we report that NPFF2 receptors may be functionally expressed in two immune cell models, the primary peritoneal macrophage and RAW 264.7 macrophage. Firstly, the mRNA levels of NPFF2 receptor were up-regulated in macrophages when treated with LPS for 24 to 72 h. Subsequently, our data hinted that NPFF regulates the viability of both kinds of macrophages. After treatment with RF9, a reported antagonist for both NPFF receptors, delayed or inhibited the NPFF-induced macrophages viability augmentation, suggesting the involvement of NPFF2 receptor. Furthermore, down-regulation of nitric oxide (NO) synthases (NOSs) partially significantly inhibited the viability augmentation of macrophages induced by NPFF, implying a nitric oxide synthases- dependent pathway is involved. However, the NOSs are not the only route by which NPFF affects the viability of macrophages. Pharmacological inhibitors of NF-κB signal pathway also blocked the NPFF-induced macrophages growth, suggesting the involvement of the NF-κB signal pathway. The regulation activity of NPFF for macrophages suggests that NPFF could act as a potential hormone in the control of immune system. Collectively, our data provide new evidence about the immune modulatory effect of NPFF, which will be helpful in extending the scope of NPFF functions.
Subject(s)
Immunologic Factors/immunology , Macrophages/immunology , Oligopeptides/immunology , Receptors, Neuropeptide/immunology , Animals , Cell Line , Cell Survival , Lipopolysaccharides/immunology , Macrophages/cytology , Macrophages/metabolism , Macrophages, Peritoneal/cytology , Macrophages, Peritoneal/immunology , Macrophages, Peritoneal/metabolism , Male , Mice , Mice, Inbred C57BL , NF-kappa B/immunology , Nitric Oxide Synthase/immunology , RNA, Messenger/genetics , Receptors, Neuropeptide/genetics , Up-RegulationABSTRACT
The environmental pollution and food safety problems caused by phthalic acid esters (PAEs) have been attracted 'extensive attention around the world. As a large PAEs producer and consumer, China is facing severe PAEs environmental pollution problems. This paper reviewed the present pollution status of six PAEs classified by the U.S. Environmental Protection Agency as the priority pollutants in China farmland soils, analyzed the sources of these six PAEs in this country, and discussed the absorption and accumulation characteristics of the PAEs in different crops as well as the bio-toxic effects of PAEs pollutants. The PAEs concentrations in China farmland soils are significantly higher those in the farmland soils of the United States and European countries. The main sources of PAEs in China farmland soils are atmospheric deposition, agricultural films, sewage sludge application, and wastewater irrigation. There exist significant differences in the characteristics of PAEs absorption, accumulation, and distribution among different crops. PAEs not only have negative effects on soil quality, crop growth, and crop physiological and biochemical properties, but also possess bio-accumulative characteristics. The weaknesses in current researches were pointed out, and the suggestions for the further researches were given, e. g., to expand the scope of PAEs pollution survey, to explore the toxic mechanisms of PAEs on crops, and to develop the techniques for in situ remediation of PAEs-polluted soils.
Subject(s)
Crops, Agricultural/growth & development , Environmental Monitoring , Phthalic Acids/analysis , Soil Pollutants/analysis , China , Diethylhexyl Phthalate/analysis , Esters/analysis , Plasticizers/analysisABSTRACT
Surface soil (0-20 cm) and peanut kernel samples were collected in four main peanut producing areas of Shandong Province, and the contents of six PAEs chemicals that classified by the U. S. Environmental Protection Agency as priority pollutants were determined by gas chromatography (GC). The results indicated that the total concentration of six PAEs (sigma PAEs) ranged from 0.34 to 2.81 mg x kg(-1), and the mean was 1.22 mg x kg(-1). In four different areas, the order of sigmaPAEs concentration in soil was hilly area of middle southern Shandong > western plain of Shandong > Jiaodong Peninsula > northern plain of Shandong. The concentration of DBP in four main peanut producing areas of Shandong Province seriously exceeded the control limit in USA. The content of PAEs ranged from 0.17 to 0.66 mg x kg(-1) in peanut kernels, with the average value 0.34 mg x kg(-1) which was less than the suggested targets in USA and Europe and of low health risk. DEHP and DBP were the main components of PAEs both in soils and peanut kernels, with higher percentage content and detection rate. The sigma PAEs contents in soils or peanut kernels under plastic mulching were significantly higher than that of open field cultivation pattern. The PAEs concentrations in peanut kernels and soils had significant correlation, with the Pearson coefficient 0. 786 (sigma PAEs), 0.747 (DBP) and 0.511 (DEHP), respectively.
Subject(s)
Arachis/chemistry , Esters/analysis , Phthalic Acids/analysis , Soil Pollutants/analysis , Soil/chemistry , ChinaABSTRACT
Neuropeptide FF (NPFF) has been reported to play important roles in regulating diverse biological processes. However, little attention has been focused on the downstream signal transduction pathway of NPFF. Here, we used the differentiated neuroblastoma cell line, dSH-SY5Y, which endogenously expresses hNPFF2 receptor, to investigate the signal transduction downstream of NPFF. In particular we investigated the regulation of the extracellular signal-regulated protein kinase (ERK) and the nuclear factor kappa B (NF-κB) pathways by NPFF in these cells. NPFF rapidly and transiently stimulated ERK. H89, a selective inhibitor of cyclic AMP-dependent protein kinase A (PKA), inhibited the NPFF-activated ERK pathway, indicating the involvement of PKA in the NPFF-induced ERK activation. Down-regulation of nitric oxide synthases also attenuated NPFF-induced ERK activation, suggesting that a nitric oxide synthase-dependent pathway is involved. Moreover, the core upstream components of the NF-κB pathway were also significantly activated in response to NPFF, suggesting that the NF-κB pathway is involved in the signal transduction pathway of NPFF. Collectively, these data demonstrate that nitric oxide synthases are involved in the signal transduction pathway of NPFF, and provide the first evidence for the interaction between NPFF and the NF-κB pathway. These advances in our interpretation of the NPFF pathway mechanism will aid the comprehensive understanding of its function and provide novel molecular insight for further study of the NPFF system.
Subject(s)
Extracellular Signal-Regulated MAP Kinases/metabolism , NF-kappa B/metabolism , Oligopeptides/pharmacology , Cell Differentiation/drug effects , Cell Line/drug effects , Humans , Isoquinolines/pharmacology , Nitric Oxide/metabolism , Protein Kinase Inhibitors/pharmacology , Receptors, Neuropeptide/genetics , Receptors, Neuropeptide/metabolism , Signal Transduction , Sulfonamides/pharmacologyABSTRACT
As the increasing emergence of multi-drug resistant tumor cells, there is an urgent need for developing new chemotherapeutic agents. NK-lysin was a novel effector of cytotoxic T cells and natural killer (NK) cells and had broad antimicrobial activity. In this study, we developed a core region of NK-lysin termed NK-18, and studied its antitumor activity and possible action mode. Our results showed that NK-18 (with 18 amino acids) possesses potent antitumor activity against bladder and prostate cancer cells by disrupting the integrity of cell membrane, but has negligible hemolysis activity against mouse erythrocytes. In addition, CD spectra was employed to study its conformation in membrane mimicking environment. NK-18 takes a standard α-helical conformation in membrane mimicking environment, which could be accounted for its more potent antitumor activity compared with its low α-helical content homologous derivatives. These findings together with its shorter amino acid sequence and lower synthesis cost suggest that NK-18 could present an alternative therapeutic strategy to cancer chemotherapy and play a promising role in fighting the multi-drug resistant tumors.
Subject(s)
Antimicrobial Cationic Peptides/pharmacology , Antineoplastic Agents/pharmacology , Animals , Cell Line, Tumor , Circular Dichroism , Hemolysis/drug effects , Humans , Mice , Microscopy, Confocal , Microscopy, Electron, ScanningABSTRACT
Polybia-MPI (MPI), a short cationic α-helical antimicrobial peptide, exhibited excellent anticancer activity and selectivity in vitro in our previous studies. To improve its in vivo application, we synthesized an analog (MPI-1) of MPI by replacing the C terminal amide -[CO-NH(2)] with thioamide -ψ[CS-NH(2)]. Although there is just one atom difference, the MPI-1 exhibited some surprising properties. In vitro studies revealed that MPI-1 exhibited relatively high lytic activity over MPI, whereas its stability to enzymatic degradation in serum was improved remarkably. Despite the enhanced toxicity in vitro, MPI-1 exhibited significantly lower mortality to mice than MPI at 75 mg/kg. Importantly, in vivo anticancer activity study indicated that MPI-1 could remarkably suppress the growth of sarcoma xenograft tumors more efficiently than MPI. Therefore, the significantly improved anticancer activity and predominantly lower in vivo toxicity might allow MPI-1 to be a good candidate for future anticancer treatment.
Subject(s)
Antimicrobial Cationic Peptides , Antineoplastic Agents , Insect Proteins , Neoplasms/drug therapy , Thioamides/chemistry , Animals , Antimicrobial Cationic Peptides/chemistry , Antimicrobial Cationic Peptides/therapeutic use , Antineoplastic Agents/chemistry , Antineoplastic Agents/therapeutic use , Cell Line , Drug Screening Assays, Antitumor , Humans , Insect Proteins/chemistry , Insect Proteins/therapeutic use , Mice , Treatment Outcome , Wasp Venoms/chemistryABSTRACT
The actinomycin D (AMD) analogs in which the D-valine residues (the second amino acid residue in the cyclic depsipeptide of AMD) and the N-methyl-L-valine residues (the fifth amino acid residue in the cyclic depsipeptide of AMD) were replaced with D-Phe or l- and D-forms N-methylvalines, N-methylisoleucine, N-methylleucine, N-methylphenylalanine, N-methylalanine, and sarcosine were synthesized. The antimicrobial activity and cytotoxic activities of these compounds in vitro were investigated. The results showed that most D-valine substituted analogs had much lower antimicrobial activity and cytotoxic activities in vitro than AMD itself, but three N-methyl-L-valine substituted analogs had comparable or even more remarkable cytotoxic activities in vitro than AMD. Acute toxicities and antitumor effects of the N-methyl-L-valine substituted analogs in mice were also examined. The result showed that the acute toxicity of compound 4 L-methylleucine(5)-AMD analog is comparable to AMD itself and that of compound 3(L-Methylisoleucine(5)-AMD analog) is slightly more toxic, about 1.25-fold than AMD. However, the acute toxicity of compound 5 D-methylleucine5-AMD analog is about 2-fold lower than AMD. This suggested that the N-methyl-D-amino acid replacement in the cyclic ring might play a vital role in their decreased acute toxicities, and perhaps the N-methyl-D-leucine substituent is more favorable, though there may be a slight loss of antitumor activity. This finding may be helpful for the design and development of more potent antitumor agents together with low acute toxicity, and suggests that the N-methyl-D-leucine substituent has the potential to be used as antitumor drug lead.
Subject(s)
Antibiotics, Antineoplastic/chemistry , Antibiotics, Antineoplastic/pharmacology , Cell Line, Tumor/drug effects , Dactinomycin/analogs & derivatives , Dactinomycin/pharmacology , Depsipeptides/chemistry , Depsipeptides/genetics , Depsipeptides/pharmacology , Amino Acid Substitution , Amino Acids/metabolism , Animals , Anti-Infective Agents/chemistry , Anti-Infective Agents/metabolism , Anti-Infective Agents/therapeutic use , Antibiotics, Antineoplastic/metabolism , DNA Fragmentation , Dactinomycin/metabolism , Depsipeptides/metabolism , Drug Screening Assays, Antitumor , Humans , Mice , Microbial Sensitivity Tests , Molecular StructureABSTRACT
With a reddish paddy soil as test materials, soil profile nitrogen storage in long-term different fertilization system (1990-2006) have been investigated. The result indicated that recycling of organic matter significantly increased the soil profile C storage (ranged from 57.7 to 66.2 t/hm2), and it was increased by 18.7-27.2 t/hm2 compared with the soil profile C storage of 1990. But it was increased by 5.4 t/hm2 with only application of chemical fertilizers. Saturated carbon storage of paddy soils was 84.0 t/hm2, and the C sequestration potential ranged from 17.8-43.7 t/hm2 compared with the current soil profile carbon storage. The result showed that there was a significant relationship between soil bulk density and depth changes of profile soil. The organic C storage would be greatly underestimated by 20.6% or 11.3% if we only take 20 cm or 23 cm as the standard depth in the estimating method for organic C storage, it also would be underestimated the difference of treatments. The combined application of chemical fertilizer and organic matter is optimal for agricultural field based onsoil organic C storage and the carbon sequestration potential.
Subject(s)
Carbon/analysis , Fertilizers , Oryza/growth & development , Soil/analysis , Agriculture/methods , China , Ecosystem , Organic Chemicals/analysisABSTRACT
To have a deep understanding on the mechanisms of cadmium (Cd) toxicity on peanut plants is of theoretical and practical significances for the selection and utilization of Cd-resistant peanut germ plasm resources. With fourteen peanut varieties as test materials and taking the chlorophyll content of functional leaves, malondialdehyde (MDA) content and cell membrane permeability of roots and leaves, and oxidative vitality of roots at flowering stage as test physiological parameters, a sand culture experiment was conducted in an artificial climate chamber to investigate the physiological responses of different peanut varieties to six levels of Cd stress. The results showed that within the range of 0-60 mg Cd x L(-1) addition, the chlorophyll content of functional leaves and the oxidative vitality of roots decreased significantly with increasing Cd addition, while the MDA content and cell membrane permeability of leaves and roots were in adverse. The cell membrane permeability of roots and leaves was the most sensitive physiological parameter, while the chlorophyll content of functional leaves was the least sensitive one in the responses of peanut plant to Cd stress. In the linear regression equations describing the relationships between test physiological parameters and Cd concentrations in nutrient solution, the absolute value of slope (b)/intercept (a) ratio, /b/a/, could better describe the sensitivity of peanut plants to Cd stress. It was known from the integrative evaluation of /b/a/ values and the cluster analysis of sensitivity that among the fourteen peanut varieties, "Zhonghua-4", "Xiangnong-55" and "Xiangnong-3010-w" were highly sensitive to Cd stress (first grade), "Lainong-29", "Xiangnongxiaoguo-w2-7", "Fenghua-2", "Lainong-13", "Yuhua-15" and "Fenghua-3" were sensitive (second grade), "Xiangnong-312", "Qiyangxiaozi" and "Pingdu-01" were less sensitive (third grade), while "Huayu-20" and "Huayu-23" were insensitive (forth grade).
Subject(s)
Arachis/genetics , Arachis/physiology , Cadmium/toxicity , Chlorophyll/analysis , Genetic Variation , Malondialdehyde/metabolism , Plant Leaves/chemistry , Plant Roots/enzymology , Species SpecificityABSTRACT
As the frequent emergency of resistant tumor cells during treatment, the development of new agents with new modes of action attracts a great deal of interest. Polybia-MPI was a short cationic alpha-helical amphiphilic peptide that has selective toxicity toward cancer cells but no hemolytic activity. Its target selectivity is based on the binding preference to membranes containing anionic phospholipids by electrostatic driving. Its ability to make PI and trypan blue permeate into tumor cells at the same rate (within minutes), suggests a killing mechanism that involves plasma membrane perturbation. SEM and confocal microscopy experiments verified that the cell died as a result of acute injury and bursting, suggesting necrosis. As compared to the conventional chemotherapy, polybia-MPI targets at the cell membrane rather than enters into the cell to exert its action. So it is difficult for tumor cells to develop resistance to polybia-MPI during treatment and its action is not affected by the common multi-drug resistant mechanism. Although this is an initial study that looked at its in vitro activity rather than the in vivo activity, with the increasing resistance of conventional chemotherapy, polybia-MPI may offer a novel therapeutic strategy in the treatment of multi-drug resistant cancer.
Subject(s)
Anti-Infective Agents/pharmacology , Antineoplastic Agents/pharmacology , Insect Proteins/pharmacology , Insect Proteins/therapeutic use , Animals , Annexin A5/metabolism , Antineoplastic Agents/therapeutic use , Cell Death/drug effects , Cell Division/drug effects , Cell Line, Tumor/drug effects , Cell Membrane/drug effects , Cell Membrane/pathology , Cell Survival/drug effects , Drug Resistance, Multiple/drug effects , Flow Cytometry , HL-60 Cells/drug effects , Humans , Leukemia L1210/drug therapy , Mice , Necrosis , Peptides/pharmacology , Peptides/therapeutic use , WaspsABSTRACT
A 16-year long-term fertilization experiment was conducted on paddy soil derived from red earth to investigate the effects of different fertilization patterns on the concentrations of soil organic nitrogen (N) components. When chemical fertilizers were applied only, the soil nitrogen content was slightly influenced. Organic fertilization, especially its combination with chemical fertilization, could significantly increase the contents of soil mineralizable N and organic nitrogen by 55.2% and 38.8%, respectively. In addition, organic fertilization could significantly improve the components of acid hydrolysable N, and lead to the increase of ammonium N (AN) , amino sugar N (ASN), and hydrolysable unidentified N (HUN) by 36.5%, 68.4%, and 73.9%, respectively. When the organic fertilization was combined with chemical fertilization, soil amino acid N content was increased by 71.1%, while HUN content was decreased by 34.5%. In all fertilization treatments, the cumulative amount of soil mineralized N increased with increasing incubation time. The content of soil mineralized N under organic fertilization and its combination with chemical fertilization was higher than that under chemical fertilization.
Subject(s)
Fertilizers , Nitrogen/chemistry , Oryza/growth & development , Soil/analysis , Agriculture/methods , Nitrogen/analysis , Organic Chemicals/analysis , Quaternary Ammonium Compounds/analysis , Quaternary Ammonium Compounds/chemistry , Time FactorsABSTRACT
Leu5AMD ([D-Val2, L-MeLeu5]2 AMD) is a novel actinomycin D (AMD) analog, in which both N-methylvalines were replaced by N-methylleucines. In the present study, an attempt has been made to investigate the effects of Leu5AMD on the proliferation of human gastric carcinoma cell line SGC-7901. The results showed that Leu5AMD inhibited the proliferation and induces apoptosis in SGC-7901 cells in a dose-dependent manner. Apoptosis induced by Leu5AMD was further confirmed by annexin V-FITC/PI dual staining assay. After treatment with Leu5AMD, the loss of mitochondrial potential and the decrease of bcl-2 gene expression were observed in apoptotic cells, suggesting that Leu5AMD may be involved in mitochondria and bcl-2 related apoptotic pathway. In addition, the in vivo antitumor effects of Leu5AMD on S-180 bearing mice and the acute toxicity on healthy mice were investigated. Treatment with Leu5AMD markedly suppressed the growth of Sarcoma xenograft. These results suggest that Leu5AMD may be used as a promising chemotherapeutical agent for patients affected by gastric carcinoma and other solid cancer.