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1.
Int J Mol Sci ; 23(3)2022 Jan 23.
Article in English | MEDLINE | ID: mdl-35163167

ABSTRACT

The present study investigated the role of salicylic acid (SA) in regulating morpho-anatomical adaptive responses of a wheat plant to waterlogging. Our pharmacological study showed that treatment of waterlogged wheat plants with exogenous SA promotes the formation axile roots and surface adventitious roots that originate from basal stem nodes, but inhibits their elongation, leading to the formation of a shallow root system. The treatment also enhanced axile root formation in non-waterlogged plants but with only slight reductions in their length and branch root formation. Exogenous SA enhanced the formation of root aerenchyma, a key anatomical adaptive response of plants to waterlogging. Consistent with these results, waterlogging enhanced SA content in the root via expression of specific isochorismate synthase (ICS; ICS1 and ICS2) and phenylalanine ammonia lyase (PAL; PAL4, PAL5 and PAL6) genes and in the stem nodes via expression of specific PAL (PAL5 and PAL6) genes. Although not to the same level observed in waterlogged plants, exogenous SA also induced aerenchyma formation in non-waterlogged plants. The findings of this study furthermore indicated that inhibition of ethylene synthesis in SA treated non-waterlogged and waterlogged plants does not have any effect on SA-induced emergence of axile and/or surface adventitious roots but represses SA-mediated induction of aerenchyma formation. These results highlight that the role of SA in promoting the development of axile and surface adventitious roots in waterlogged wheat plants is ethylene independent while the induction of aerenchyma formation by SA requires the presence of ethylene.


Subject(s)
Plant Roots/drug effects , Salicylic Acid/pharmacology , Triticum/growth & development , Adaptation, Biological/drug effects , Floods , Gene Expression/drug effects , Gene Expression Regulation, Plant/drug effects , Gene Expression Regulation, Plant/genetics , Intramolecular Transferases/genetics , Phenylalanine Ammonia-Lyase/genetics , Plant Roots/metabolism , Salicylic Acid/metabolism , Seedlings/metabolism , Triticum/drug effects , Water
2.
PLoS Biol ; 19(4): e3001190, 2021 04.
Article in English | MEDLINE | ID: mdl-33844686

ABSTRACT

Chemical insecticides have been heavily employed as the most effective measure for control of agricultural and medical pests, but evolution of resistance by pests threatens the sustainability of this approach. Resistance-conferring mutations sometimes impose fitness costs, which may drive subsequent evolution of compensatory modifier mutations alleviating the costs of resistance. However, how modifier mutations evolve and function to overcome the fitness cost of resistance still remains unknown. Here we show that overexpression of P450s not only confers imidacloprid resistance in the brown planthopper, Nilaparvata lugens, the most voracious pest of rice, but also leads to elevated production of reactive oxygen species (ROS) through metabolism of imidacloprid and host plant compounds. The inevitable production of ROS incurs a fitness cost to the pest, which drives the increase or fixation of the compensatory modifier allele T65549 within the promoter region of N. lugens peroxiredoxin (NlPrx) in the pest populations. T65549 allele in turn upregulates the expression of NlPrx and thus increases resistant individuals' ability to clear the cost-incurring ROS of any source. The frequent involvement of P450s in insecticide resistance and their capacity to produce ROS while metabolizing their substrates suggest that peroxiredoxin or other ROS-scavenging genes may be among the common modifier genes for alleviating the fitness cost of insecticide resistance.


Subject(s)
Hemiptera/drug effects , Insecticide Resistance/drug effects , Neonicotinoids/pharmacology , Nitro Compounds/pharmacology , Oryza/parasitology , Peroxiredoxins/physiology , Adaptation, Biological/drug effects , Adaptation, Biological/genetics , Alleles , Animals , Chromosome Mapping , Gene Expression Regulation, Enzymologic/drug effects , Genes, Insect/drug effects , Genes, Modifier/drug effects , Genes, Modifier/physiology , Genetic Association Studies , Genetic Fitness/drug effects , Hemiptera/physiology , Insecticide Resistance/genetics , Insecticides/pharmacology , Oryza/drug effects , Peroxiredoxins/genetics , Reactive Oxygen Species/metabolism , Toxicity Tests
3.
Ecotoxicol Environ Saf ; 212: 112009, 2021 Apr 01.
Article in English | MEDLINE | ID: mdl-33556811

ABSTRACT

Cu pollution is a problem in mining areas in Peru. Here we evaluate the phytoextraction capacity, physiological and proteomic responses of four species growing in copper-contaminated areas in Arequipa, Peru. The plants used in the experiments were obtained by collecting seedlings (Tessaria integrifolia, Bacharis salicifolia), rhizomes (Eleocharis montevidensis) and seeds (Chenopodium murale) along a polluted river. They were exposed to solutions containing 2, 4, 8, 16 and 32 mg Cu L-1 during 20 days. Growth was affected in a concentration-dependent way. According to the tolerance index, B. salicifolia and C. murale were the most sensitive species, but with greater Cu phytoextraction capacity and accumulation in the biomass. The content and ratio of photosynthetic pigments changed differently for each specie and carotenoids level were less affected than chlorophyll. Cu also induced changes in the protein and sugar contents. Antioxidant enzyme activities (catalase and superoxide dismutase) increased with a decrease in the malondialdehyde. There were marked changes in the protein 2D-PAGE profiles with an increase in the abundance of metallothioneins (MT) of class II type I and II. Our results suggest that these species can grow in Cu polluted areas because they developed multiple tolerance mechanisms, such as and MTs production seems a important one.


Subject(s)
Adaptation, Biological/drug effects , Copper/toxicity , Environmental Pollutants/toxicity , Metallothionein/metabolism , Plant Development/drug effects , Soil Pollutants/toxicity , Antioxidants/metabolism , Biodegradation, Environmental , Biomass , Chlorophyll/metabolism , Copper/metabolism , Environmental Pollutants/metabolism , Mining , Peru , Plant Roots/drug effects , Plant Roots/growth & development , Plant Roots/metabolism , Proteomics , Seedlings/drug effects , Seedlings/growth & development , Seedlings/metabolism , Soil Pollutants/metabolism , Species Specificity
4.
Plant Cell Physiol ; 62(4): 624-640, 2021 Sep 24.
Article in English | MEDLINE | ID: mdl-33561287

ABSTRACT

Iron (Fe) toxicity is a major challenge for plant cultivation in acidic waterlogged soil environments, where lowland rice is a major staple food crop. Only few studies have addressed the molecular characterization of excess Fe tolerance in rice, and these highlight different mechanisms for Fe tolerance. Out of 16 lowland rice varieties, we identified a pair of contrasting lines, Fe-tolerant Lachit and -susceptible Hacha. The two lines differed in their physiological and morphological responses to excess Fe, including leaf growth, leaf rolling, reactive oxygen species generation and Fe and metal contents. These responses were likely due to genetic origin as they were mirrored by differential gene expression patterns, obtained through RNA sequencing, and corresponding gene ontology term enrichment in tolerant vs. susceptible lines. Thirty-five genes of the metal homeostasis category, mainly root expressed, showed differential transcriptomic profiles suggestive of an induced tolerance mechanism. Twenty-two out of these 35 metal homeostasis genes were present in selection sweep genomic regions, in breeding signatures, and/or differentiated during rice domestication. These findings suggest that Fe excess tolerance is an important trait in the domestication of lowland rice, and the identified genes may further serve to design the targeted Fe tolerance breeding of rice crops.


Subject(s)
Adaptation, Biological/genetics , Iron/toxicity , Oryza/genetics , Plant Proteins/genetics , Adaptation, Biological/drug effects , Crops, Agricultural/genetics , Domestication , Gene Expression Profiling , Gene Expression Regulation, Plant/drug effects , Homeostasis/drug effects , Homeostasis/genetics , India , Iron/metabolism , Oryza/drug effects , Oryza/physiology , Stress, Physiological/drug effects , Stress, Physiological/genetics
5.
Int J Mol Sci ; 23(1)2021 Dec 28.
Article in English | MEDLINE | ID: mdl-35008750

ABSTRACT

Over the last decades, lipotoxicity and glucotoxicity emerged as established mechanisms participating in the pathophysiology of obesity-related type 2 diabetes in general, and in the loss of ß-cell function in particular. However, these terms hold various potential biological processes, and it is not clear what precisely they refer to and to what extent they might be clinically relevant. In this review, we discuss the basis and the last advances of research regarding the role of free fatty acids, their metabolic intracellular pathways, and receptor-mediated signaling related to glucose-stimulated insulin secretion, as well as lipid-induced ß-cell dysfunction. We also describe the role of chronically elevated glucose, namely, glucotoxicity, which promotes failure and dedifferentiation of the ß cell. Glucolipotoxicity combines deleterious effects of exposures to both high glucose and free fatty acids, supposedly provoking synergistic defects on the ß cell. Nevertheless, recent studies have highlighted the glycerolipid/free fatty acid cycle as a protective pathway mediating active storage and recruitment of lipids. Finally, we discuss the putative correspondence of the loss of functional ß cells in type 2 diabetes with a natural, although accelerated, aging process.


Subject(s)
Adaptation, Biological , Glucose/toxicity , Insulin Secretion , Insulin-Secreting Cells/pathology , Lipids/pharmacology , Adaptation, Biological/drug effects , Animals , Humans , Insulin Secretion/drug effects , Insulin-Secreting Cells/drug effects , Insulin-Secreting Cells/ultrastructure , Models, Biological
6.
Int J Mol Sci ; 21(24)2020 Dec 12.
Article in English | MEDLINE | ID: mdl-33322775

ABSTRACT

Since the earliest agricultural attempts, humankind has been trying to improve crop quality and yields, as well as protect them from adverse conditions. Strategies to meet these goals include breeding, the use of fertilisers, and the genetic manipulation of crops, but also an interesting phenomenon called priming or adaptive response. Priming is based on an application of mild stress to prime a plant for another, mostly stronger stress. There are many priming techniques, such as osmopriming, halopriming, or using physical agents. Non-thermal plasma (NTP) represents a physical agent that contains a mixture of charged, neutral, and radical (mostly reactive oxygen and nitrogen species) particles, and can cause oxidative stress or even the death of cells or organisms upon interaction. However, under certain conditions, NTP can have the opposite effect, which has been previously documented for many plant species. Seed surface sterilization and growth enhancement are the most-reported positive effects of NTP on plants. Moreover, some studies suggest the role of NTP as a promising priming agent. This review deals with the effects of NTP treatment on plants from interaction with seed and cell surface, influence on cellular molecular processes, up to the adaptive response caused by NTP.


Subject(s)
Adaptation, Biological/drug effects , Crops, Agricultural/drug effects , Germination/drug effects , Plasma Gases/pharmacology , Stress, Physiological/drug effects , Adaptation, Biological/genetics , Crops, Agricultural/genetics , Crops, Agricultural/growth & development , Crops, Agricultural/metabolism , Gene Expression Regulation, Plant/drug effects , Gene Expression Regulation, Plant/genetics , Gene Expression Regulation, Plant/radiation effects , Germination/genetics , Oxidative Stress , Plasma Gases/adverse effects , Plasma Gases/chemistry , Reactive Nitrogen Species/metabolism , Reactive Nitrogen Species/pharmacology , Reactive Oxygen Species/metabolism , Reactive Oxygen Species/pharmacology , Seeds , Stress, Physiological/genetics
7.
J Pharmacol Sci ; 144(3): 129-138, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32921394

ABSTRACT

The traditional Japanese (Kampo) medicines yokukansan (YKS) and yokukansankachimpihange (YKSCH) have similar formulas and the same indications. In animals or cultured cells, the neuropharmacological actions of YKS are sometimes more beneficial than those of YKSCH. Since both drugs are used to treat sleep disorders in Japan, we examined the ameliorative effects of YKS and YKSCH on circadian rhythm disturbance and compared their efficacy using a mouse model of circadian rhythm disruption. Ramelteon was used as the positive control. Ramelteon treatment significantly reversed decreased running wheel activity during the advanced dark phase, indicating facilitation of circadian adaptation. YKS treatment also reversed the activity in the early period of drug treatment; however, it was not statistically significant. YKSCH treatment significantly reversed the decreased activity during the advanced dark phase. Plasma melatonin (MT) levels were significantly increased in the YKSCH but not in the YKS group. The ameliorative effect of YKSCH on rhythm disruption was significantly inhibited by coadministration of the MT2 receptor antagonist. Therefore, the therapeutic effect of YKSCH on circadian rhythm disruption would be attributable, to elevated endogenous MT levels. Taken together, YKS and YKSCH have different pharmacological properties and may be more precisely prescribed depending on patients' psychological symptoms.


Subject(s)
Adaptation, Biological/drug effects , Circadian Rhythm/drug effects , Drugs, Chinese Herbal/pharmacology , Drugs, Chinese Herbal/therapeutic use , Medicine, Kampo , Melatonin/metabolism , Phytotherapy , Sleep Wake Disorders/drug therapy , Animals , Male , Melatonin/blood , Mice, Inbred C3H , Sleep Wake Disorders/etiology , Sleep Wake Disorders/physiopathology
8.
Ecotoxicol Environ Saf ; 203: 111037, 2020 Oct 15.
Article in English | MEDLINE | ID: mdl-32888596

ABSTRACT

Glacier studies as of late have ruffled many eyeballs, exploring this frigid ecology to understand the impact of climate change. Mapquesting the glaciers led to the discovery of concealed world of "psychrophiles" harboring in it. In the present study, the antibiotic resistance genes (ARGs) and heavy metal resistance genes (MRGs) were evaluated through both the culture-dependent and culture-independent methods. Samples were collected from two different glaciers, i.e., debris-covered glacier (Changme Khangpu) and debris-free glacier (Changme Khang). Functional metagenomics of both the glacier samples, provided evidence of presence of resistant genes against various antibiotic groups. Bacitracin resistant gene (bacA) was the predominant ARG in both the glaciers. MRGs in both the glacier samples were diversified as the genes detected were resistant against various heavy metals such as arsenic, tungsten, mercury, zinc, chromium, copper, cobalt, and iron. Unique MRGs identified from Changme Khangpu glacier were resistant to copper (cutA, cutE, cutC, cutF, cueR, copC, and copB) and chromium (yelf, ruvB, nfsA, chrR, and chrA) whereas, from Changme Khang glacier they showed resistance against cobalt (mgtA, dmef, corD, corC, corB, and cnrA), and iron (yefD, yefC, yefB, and yefA) heavy metals. ARGs aligned maximum identity with Gram-negative psychrotolerant bacteria. The cultured bacterial isolates showed tolerance to high concentrations of tested heavy metal solutions. Interestingly, some of the antibiotic resistant bacterial isolates also showed tolerance towards the higher concentrations of heavy metals. Thus, an introspection of the hypothesis of co-occurrence and/co-selection of ARGs and MRGs in such environments has been highlighted here.


Subject(s)
Adaptation, Biological/genetics , Anti-Bacterial Agents/toxicity , Drug Resistance, Microbial/genetics , Environmental Pollutants/toxicity , Genes, Bacterial/drug effects , Ice Cover/microbiology , Metals, Heavy/toxicity , Adaptation, Biological/drug effects , Gram-Negative Bacteria/drug effects , Gram-Negative Bacteria/genetics , Ice Cover/chemistry , India , Metagenomics , Sikkim
9.
Ecotoxicol Environ Saf ; 203: 110961, 2020 Oct 15.
Article in English | MEDLINE | ID: mdl-32888621

ABSTRACT

Cadmium (Cd), which seriously affects plant growth and crop production, is harmful to humans. Previous studies revealed ryegrass (Lolium multiflorum Lam.) exhibits Cd tolerance, and may be useful as a potential hyperaccumulator because of its wide distribution. In this study, the physiological and transcriptional responses of two ryegrass cultivars [i.e., high (LmHC) and low (LmLC) Cd tolerance] to Cd stress were investigated and compared. The Cd tolerance of LmHC was greater than that of LmLC at various Cd concentrations. The uptake of Evans blue dye revealed that Cd-induced root cell mortality was higher in LmLC than in LmHC after a 12-h Cd treatment. Furthermore, the content and influx rate of Cd in LmLC roots were greater than in LmHC roots under Cd stress conditions. The RNA sequencing and quantitative real-time PCR data indicated that the Cd transport regulatory genes (ABCG37, ABCB4, NRAMP4, and HMA5) were differentially expressed between the LmLC and LmHC roots. This expression-level diversity may contribute to the differences in the Cd accumulation and translocation between LmLC and LmHC. These findings may help clarify the physiological and molecular mechanisms underlying ryegrass responses to Cd toxicity. Additionally, ryegrass may be able to hyperaccumulate toxic heavy metals during the phytoremediation of contaminated soil.


Subject(s)
Adaptation, Biological , Cadmium/metabolism , Lolium/drug effects , Plant Roots/drug effects , Soil Pollutants/metabolism , Transcription, Genetic/drug effects , Adaptation, Biological/drug effects , Adaptation, Biological/genetics , Biodegradation, Environmental , Cadmium/analysis , Cadmium/toxicity , Genes, Plant , Lolium/chemistry , Lolium/genetics , Plant Roots/chemistry , Plant Roots/genetics , Soil Pollutants/analysis , Soil Pollutants/toxicity
10.
PLoS One ; 15(5): e0232775, 2020.
Article in English | MEDLINE | ID: mdl-32374766

ABSTRACT

Antibacterial photodynamic therapy (aPDT) and antibacterial blue light (aBL) are emerging treatment methods auxiliary to mechanical debridement for periodontitis. APDT provided with near-infrared (NIR) light in conjunction with an indocyanine green (ICG) photosensitizer has shown efficacy in several dental in-office-treatment protocols. In this study, we tested Streptococcus mutans biofilm sensitivity to either aPDT, aBL or their combination dual-light aPDT (simultaneous aPDT and aBL) exposure. Biofilm was cultured by pipetting diluted Streptococcus mutans suspension with growth medium on the bottom of well plates. Either aPDT (810 nm) or aBL (405 nm) or a dual-light aPDT (simultaneous 810 nm aPDT and 405 nm aBL) was applied with an ICG photosensitizer in cases of aPDT or dual-light, while keeping the total given radiant exposure constant at 100 J/cm2. Single-dose light exposures were given after one-day or four-day biofilm incubations. Also, a model of daily treatment was provided by repeating the same light dose daily on four-day and fourteen-day biofilm incubations. Finally, the antibacterial action of the dual-light aPDT with different energy ratios of 810 nm and 405 nm of light were examined on the single-day and four-day biofilm protocols. At the end of each experiment the bacterial viability was assessed by colony-forming unit method. Separate samples were prepared for confocal 3D biofilm imaging. On a one-day biofilm, the dual-light aPDT was significantly more efficient than aBL or aPDT, although all modalities were bactericidal. On a four-day biofilm, a single exposure of aPDT or dual-light aPDT was more efficient than aBL, resulting in a four logarithmic scale reduction in bacterial counts. Surprisingly, when the same amount of aPDT was repeated daily on a four-day or a fourteen-day biofilm, bacterial viability improved significantly. A similar improvement in bacterial viability was observed after repetitive aBL application. This viability improvement was eliminated when dual-light aPDT was applied. By changing the 405 nm to 810 nm radiant exposure ratio in dual-light aPDT, the increase in aBL improved the antibacterial action when the biofilm was older. In conclusion, when aPDT is administered repeatedly to S. mutans biofilm, a single wavelength-based aBL or aPDT leads to a significant biofilm adaptation and increased S. mutans viability. The combined use of aBL light in synchrony with aPDT arrests the adaptation and provides significantly improved and sustained antibacterial efficacy.


Subject(s)
Adaptation, Biological/drug effects , Anti-Bacterial Agents/pharmacology , Biofilms/drug effects , Indocyanine Green/pharmacology , Photochemotherapy/methods , Photosensitizing Agents/pharmacology , Streptococcus mutans/drug effects , Adaptation, Biological/radiation effects , Bacterial Load/drug effects , Bacterial Load/radiation effects , Biofilms/radiation effects , Humans , Microbial Viability/drug effects , Microbial Viability/radiation effects , Oral Hygiene/methods , Periodontitis/drug therapy , Streptococcus mutans/radiation effects
11.
PLoS Pathog ; 16(5): e1008431, 2020 05.
Article in English | MEDLINE | ID: mdl-32379814

ABSTRACT

Bacteria are well known for their extremely high adaptability in stressful environments. The clinical relevance of this property is clearly illustrated by the ever-decreasing efficacy of antibiotic therapies. Frequent exposures to antibiotics favor bacterial strains that have acquired mechanisms to overcome drug inhibition and lethality. Many strains, including life-threatening pathogens, exhibit increased antibiotic resistance or tolerance, which considerably complicates clinical practice. Alarmingly, recent studies show that in addition to resistance, tolerance levels of bacterial populations are extremely flexible in an evolutionary context. Here, we summarize laboratory studies providing insight in the evolution of resistance and tolerance and shed light on how the treatment conditions could affect the direction of bacterial evolution under antibiotic stress.


Subject(s)
Adaptation, Biological/drug effects , Bacteria/drug effects , Drug Resistance, Bacterial/drug effects , Adaptation, Biological/genetics , Adaptation, Physiological/drug effects , Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial/genetics , Drug Resistance, Microbial/drug effects , Evolution, Molecular
12.
J Environ Sci Health B ; 55(5): 429-437, 2020.
Article in English | MEDLINE | ID: mdl-32065017

ABSTRACT

We evaluated the real effects of pollutants through a multi-generation study. We tested whether short-term exposure (48 h) of successive (first and second) generations of Chironomus yoshimatsui neonates (<24-h-old) to two acetylcholinesterase inhibitor insecticides, pyraclofos, and pirimicarb, would change insecticide sensitivity and life-cycle parameters over four generations. Additionally, we tested whether acetylcholinesterase (AChE) activity levels would be associated with this sensitivity change. Sensitivities (48 h EC50 value, using immobility as the endpoint) in chironomids (<24-h-old) and insect life-cycle parameters (the number of larvae per egg mass and adult size) were investigated. Parental chironomids produced larvae that were less sensitive than those in the control group following the two 48 h pirimicarb exposure events, whereas exposure to pyraclofos did not affect sensitivity. The AChE activity in larvae with low sensitivity to pirimicarb was significantly higher than that in the control. Thus, increased AChE activity might be associated with low sensitivity. The life-cycle parameters in chironomids recovered from the effects of pyraclofos and pirimicarb suggested they could adapt to the insecticides by changing biomass allocation. Our study suggested potential chemical risks of insecticide stress and how aquatic organisms adapt to it.


Subject(s)
Carbamates/toxicity , Chironomidae/drug effects , Cholinesterase Inhibitors/toxicity , Insecticides/toxicity , Organothiophosphates/toxicity , Pyrimidines/toxicity , Adaptation, Biological/drug effects , Animals , Chironomidae/physiology , Ecotoxicology/methods , Larva/drug effects , Water Pollutants, Chemical/toxicity
13.
Phytomedicine ; 68: 153143, 2020 Mar.
Article in English | MEDLINE | ID: mdl-32018209

ABSTRACT

BACKGROUND: Rhodiola rosea L. (Crassulaceae) has been used for years in the traditional medicine of several countries as an adaptogen drug, able to preserve homeostasis in response to stress stimuli. Currently R. rosea roots and rhizome are classified as a traditional herbal medicinal product for temporary relief of symptoms of stress, such as fatigue and sensation of weakness by the European Medicines Agency. HYPOTHESIS/PURPOSE: Increasing evidences suggest the involvement of neuroinflammation in response to stress. However, whether the modulation of neuroinflammatory parameters could be involved in the anti-stress effect of R. rosea has been barely studied. Thus, the aim of this work is to investigate the possible modulation of molecular inflammatory processes elicited by a R. rosea roots and rhizome ethanolic extract in an in vitro model of corticotropin releasing hormone (CRH)-stimulated BV2 microglial cells. METHODS: BV2 cells were stimulated with CRH 100 nM and changes in cell viability, cytokines production and heat shock protein 70 (HSP70) levels were evaluated. Intracellular pathways related to inflammation, such as nuclear factor kappa-light-chain enhancer of activated B cells (NF-κB) nuclear translocation and mitogen-activated protein kinases (MAPK) activation were also analyzed. RESULTS: We found that R. rosea extract (2.7% m/m rosavin and 1% m/m salidroside) 20 µg/ml was able to counteract the neuroinflammatory effect of CRH by inhibiting NF-κB nuclear translocation with a mechanism of action involving the modulation of mitogen-activated protein kinase-activated protein kinase 2 (MKK2), extracellular signal-regulated kinase 1/2 (ERK 1/2) and c-Jun n-terminal kinase (JNK), resulting in a reduction of HSP70 expression. CONCLUSION: This work expands the knowledge of the intracellular mechanisms involved in R. rosea anti-stress activity and may be useful for the study of other adaptogen drugs.


Subject(s)
Corticotropin-Releasing Hormone/metabolism , Inflammation/drug therapy , Plant Extracts/pharmacology , Rhodiola/chemistry , Adaptation, Biological/drug effects , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Cell Line , Cell Survival/drug effects , Corticotropin-Releasing Hormone/pharmacology , Glucosides/pharmacology , HSP70 Heat-Shock Proteins/metabolism , Inflammation/metabolism , Inflammation/pathology , JNK Mitogen-Activated Protein Kinases/metabolism , MAP Kinase Signaling System/drug effects , Mice , Microglia/cytology , Microglia/drug effects , NF-kappa B/metabolism , Phenols/pharmacology , Plant Extracts/chemistry , Plant Roots/chemistry , Plants, Medicinal/chemistry , Rhizome/chemistry , Stress, Physiological/drug effects
14.
FASEB J ; 34(1): 399-409, 2020 01.
Article in English | MEDLINE | ID: mdl-31914606

ABSTRACT

The liver plays a key role during fasting to maintain energy homeostasis and euglycemia via metabolic processes mainly orchestrated by the insulin/glucagon ratio. We report here that fasting or calorie restriction protocols in C57BL6 mice promote a marked decrease in the hepatic protein levels of G protein-coupled receptor kinase 2 (GRK2), an important negative modulator of both G protein-coupled receptors (GPCRs) and insulin signaling. Such downregulation of GRK2 levels is liver-specific and can be rapidly reversed by refeeding. We find that autophagy, and not the proteasome, represents the main mechanism implicated in fasting-induced GRK2 degradation in the liver in vivo. Reducing GRK2 levels in murine primary hepatocytes facilitates glucagon-induced glucose production and enhances the expression of the key gluconeogenic enzyme Pck1. Conversely, preventing full downregulation of hepatic GRK2 during fasting using adenovirus-driven overexpression of this kinase in the liver leads to glycogen accumulation, decreased glycemia, and hampered glucagon-induced gluconeogenesis, thus preventing a proper and complete adaptation to nutrient deprivation. Overall, our data indicate that physiological fasting-induced downregulation of GRK2 in the liver is key for allowing complete glucagon-mediated responses and efficient metabolic adaptation to fasting in vivo.


Subject(s)
Adaptation, Biological/drug effects , Autophagy , Fasting , G-Protein-Coupled Receptor Kinase 2/metabolism , Glucagon/pharmacology , Liver/metabolism , Animals , G-Protein-Coupled Receptor Kinase 2/genetics , Gastrointestinal Agents/pharmacology , Homeostasis , Liver/drug effects , Liver/pathology , Male , Mice , Mice, Inbred C57BL , Signal Transduction
15.
Front Immunol ; 11: 608895, 2020.
Article in English | MEDLINE | ID: mdl-33708192

ABSTRACT

Involvement of gut microbiota in pulmonary disease by the gut-lung axis has been widely observed. However, the cross-talk messengers between respiratory mucosal immunity and gut microbiota are largely unknown. Using selective pharmacologic destruction of gut microenvironment mouse models, we found gut microbiota displayed significantly lower alpha diversity and relative abundance of bacteria in Gentamicin treated mice. Metagenomic studies revealed functional differences in gut bacteria in altering metabolic profiles in mice blood. Branched-chain amino acids (BCAAs) are the essential factors linked between gut and lung. During this process, selective destruction of gut microbiota by Gentamicin induced high levels of BCAAs, and the high levels of BCAAs impacted the lung immunity against influenza virus. In vivo, Gentamicin-treated mice or mice fed with high BCAAs diets displayed reduced survival. At the sites of infection, the number of CD11b+Ly6G+ cells decreased, and CD8+ T cells increased accompanied by exuberant expression of pro-inflammatory cytokines could result in tissue damage. CD11b+Ly6G+ cells transplantation conferred remarkable protection from influenza virus infections. In vitro, BCAAs promoted bone marrow-derived cells differentiation to dendritic cells. Taken together, these findings demonstrate that Gentamicin induced disruption of the gut microbiota leads to increased BCAA levels that suppress CD11b+Ly6c+ cell development in association with overactive CD8+ T responses which may contribute to enhanced severity of the viral infection.


Subject(s)
Adaptation, Biological/drug effects , Amino Acids, Branched-Chain/metabolism , Gastrointestinal Microbiome/drug effects , Gentamicins/pharmacology , Orthomyxoviridae Infections/metabolism , Adaptation, Biological/physiology , Animals , CD11b Antigen/metabolism , CD8-Positive T-Lymphocytes/drug effects , CD8-Positive T-Lymphocytes/metabolism , Cell Differentiation/drug effects , Chickens , Cytokines/metabolism , Dendritic Cells/drug effects , Dendritic Cells/metabolism , Gastrointestinal Microbiome/physiology , Humans , Inflammation/metabolism , Mice , Mice, Inbred BALB C , Microbiota/drug effects , Orthomyxoviridae/pathogenicity
16.
Int J Mol Sci ; 20(24)2019 Dec 12.
Article in English | MEDLINE | ID: mdl-31842355

ABSTRACT

Strigolactones (SLs) and karrikins (KARs) are both butenolide molecules that play essential roles in plant growth and development. SLs are phytohormones, with SLs having known functions within the plant they are produced in, while KARs are found in smoke emitted from burning plant matter and affect seeds and seedlings in areas of wildfire. It has been suggested that SL and KAR signaling may share similar mechanisms. The α/ß hydrolases DWARF14 (D14) and KARRIKIN INSENSITIVE 2 (KAI2), which act as receptors of SL and KAR, respectively, both interact with the F-box protein MORE AXILLARY GROWTH 2 (MAX2) in order to target SUPPRESSOR OF MAX2 1 (SMAX1)-LIKE/D53 family members for degradation via the 26S proteasome. Recent reports suggest that SLs and/or KARs are also involved in regulating plant responses and adaptation to various abiotic stresses, particularly nutrient deficiency, drought, salinity, and chilling. There is also crosstalk with other hormone signaling pathways, including auxin, gibberellic acid (GA), abscisic acid (ABA), cytokinin (CK), and ethylene (ET), under normal and abiotic stress conditions. This review briefly covers the biosynthetic and signaling pathways of SLs and KARs, compares their functions in plant growth and development, and reviews the effects of any crosstalk between SLs or KARs and other plant hormones at various stages of plant development. We also focus on the distinct responses, adaptations, and regulatory mechanisms related to SLs and/or KARs in response to various abiotic stresses. The review closes with discussion on ways to gain additional insights into the SL and KAR pathways and the crosstalk between these related phytohormones.


Subject(s)
4-Butyrolactone/analogs & derivatives , Adaptation, Biological/drug effects , Furans/metabolism , Lactones/metabolism , Plant Development/drug effects , Plant Growth Regulators/pharmacology , Pyrans/metabolism , Stress, Physiological/drug effects , 4-Butyrolactone/pharmacology , Furans/chemistry , Lactones/chemistry , Plant Physiological Phenomena , Pyrans/chemistry , Signal Transduction , Structure-Activity Relationship
17.
Mar Pollut Bull ; 149: 110536, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31543481

ABSTRACT

Heavy metal stress changes the morphological and anatomical structure of plant organs. In this study, we determined the anatomical changes and Cd distribution in the roots of Aegiceras corniculatum (L.) Blanco (Black mangrove) under Cd stress. The results showed that Cd levels in A. corniculatum root tissues decreased in the following order: endodermis > pith > xylem > epidermis and exodermis > phloem > cortex. The endodermis secondary casparian strip replaces exodermis casparian strip and plays a role in the "retardation mechanism", which sort of compensates for the missing exodermis retardation effect. The xylem and pith both show high affinity for Cd and contain enriched Cd. This creates a low-Cd environment for phloem and protects the nutrient transport function of the vasculature against Cd toxicity. The present study provides new evidences suggesting that Cd regional enrichment and anatomical structure changes are an adaptive strategy of mangrove plants to HM tolerance.


Subject(s)
Cadmium/pharmacokinetics , Cadmium/toxicity , Plant Roots/drug effects , Primulaceae/drug effects , Adaptation, Biological/drug effects , Cadmium/analysis , Microscopy, Electron, Scanning , Plant Epidermis/drug effects , Plant Epidermis/metabolism , Plant Roots/anatomy & histology , Plant Roots/metabolism , Primulaceae/anatomy & histology , Primulaceae/metabolism , Spectrometry, X-Ray Emission , Stress, Physiological , Tissue Distribution , Water Pollutants, Chemical/pharmacokinetics , Water Pollutants, Chemical/toxicity , Wetlands , Xylem/drug effects , Xylem/metabolism
18.
PLoS One ; 14(8): e0221881, 2019.
Article in English | MEDLINE | ID: mdl-31469877

ABSTRACT

Flavodoxins are small electron transfer proteins containing flavin mononucleotide (FMN) as a prosthetic group, which play an important role during oxidative stress or iron limitation. The aims of this study were the identification and characterization of flavodoxins in the model aromatic-degrader Paraburkholderia xenovorans LB400 and the analyses of their protective effects during oxidative stress induced by paraquat and H2O2. Two genes (BxeA0278 and BxeB0391) encoding flavodoxins (hereafter referred to as fldX for flavodoxin from P. xenovorans), were identified at the LB400 major and minor chromosome. Genomic context of the flavodoxin-encoding genes showed genes encoding membrane proteins, transporters, and proteins involved in redox processes and biosynthesis of macromolecules. A secondary structure prediction of both LB400 flavodoxins showed the characteristic flavodoxin structure of five ß-sheets intercalated with five α-helices. FldX1 contains a loop intercalated in the fifth ß-strand, which indicates that it belongs to the long-chain flavodoxins, whereas FldX2 is a short-chain flavodoxin. A phylogenetic analysis of 73 flavodoxins from 43 bacterial genera revealed eight clusters (I-VIII), while FldX1 and FldX2 grouped separately within a long-chain and a short-chain flavodoxin clades. FldX1 and FldX2 were overexpressed in P. xenovorans. Interestingly, the strain overexpressing the long-chain flavodoxin FldX1 (p2-fldX1) showed a faster growth in glucose than the control strain. The recombinant strain overexpressing the long-chain flavodoxin FldX1 (p2-fldx1) exposed to paraquat (20 mM) possessed lower susceptibility to growth inhibition on plates and higher survival in liquid medium than the control strain. The strains overexpressing the flavodoxins FldX1 and FldX2 showed higher survival during exposure to 1 mM paraquat (>95%) than the control strain (68%). Compared to the control strain, strains overexpressing FldX1 and FldX2 showed lower lipid peroxidation (>20%) after exposure to 1 mM paraquat and a lower protein carbonylation (~30%) after exposure to 1 mM H2O2 was observed. During exposure to paraquat, strain p2-fldx1 downregulated the katG4, hpf, trxB1 and ohr genes (> 2-fold), whereas strain p2-fldx2 upregulated the oxyR and ahpC1 genes (> 2-fold). In conclusion, the flavodoxins FldX1 and FldX2 of P. xenovorans LB400 conferred protection to cells exposed to the oxidizing agents paraquat and H2O2.


Subject(s)
Adaptation, Biological/drug effects , Betaproteobacteria/drug effects , Betaproteobacteria/physiology , Flavodoxin/genetics , Hydrogen Peroxide/pharmacology , Oxidative Stress/drug effects , Paraquat/pharmacology , Amino Acid Sequence , Computational Biology/methods , Flavodoxin/chemistry , Flavodoxin/metabolism , Gene Expression Regulation, Bacterial , Genome, Bacterial , Genomics/methods , Phylogeny
19.
Int J Mol Sci ; 20(14)2019 Jul 23.
Article in English | MEDLINE | ID: mdl-31340536

ABSTRACT

Molecular mechanisms that are the base of the strategies adopted by Mediterranean plants to cope with the challenges imposed by limited or excessive solar radiation during the summer season have received limited attention. In our study, conducted on C. incanus plants growing in the shade or in full sunlight, we performed measurements of relevant physiological traits, such as leaf water potential, gas exchange and PSII photochemistry, RNA-Seq with de-novo assembly, and the analysis of differentially expressed genes. We also identified and quantified photosynthetic pigments, abscisic acid, and flavonoids. Here, we show major mechanisms regulating light perception and signaling which, in turn, sustain the shade avoidance syndrome displayed by the 'sun loving' C. incanus. We offer clear evidence of the detrimental effects of excessive light on both the assembly and the stability of PSII, and the activation of a suite of both repair and effective antioxidant mechanisms in sun-adapted leaves. For instance, our study supports the view of major antioxidant functions of zeaxanthin in sunny plants concomitantly challenged by severe drought stress. Finally, our study confirms the multiple functions served by flavonoids, both flavonols and flavanols, in the adaptive mechanisms of plants to the environmental pressures associated to Mediterranean climate.


Subject(s)
Adaptation, Biological/drug effects , Cistus/radiation effects , Gene Expression Regulation, Plant , Photosystem II Protein Complex/genetics , Plant Leaves/radiation effects , RNA, Plant/genetics , Abscisic Acid/metabolism , Adaptation, Biological/genetics , Antioxidants/metabolism , Chlorophyll/biosynthesis , Cistus/genetics , Cistus/metabolism , DNA Damage , DNA Repair , DNA, Plant/genetics , DNA, Plant/metabolism , Flavonoids/biosynthesis , Light Signal Transduction/genetics , Mediterranean Region , Photosynthesis/genetics , Photosystem II Protein Complex/metabolism , Plant Leaves/genetics , Plant Leaves/metabolism , RNA, Plant/metabolism , Sequence Analysis, RNA , Solar Energy , Sunlight , Water/metabolism , Zeaxanthins/biosynthesis
20.
Trends Cancer ; 5(6): 365-390, 2019 06.
Article in English | MEDLINE | ID: mdl-31208698

ABSTRACT

Most Phase II and III clinical trials in head and neck cancer (HNC) combine two or more treatment modalities, which are based, in part, on knowledge of the molecular mechanisms of innate and acquired resistance to monotherapy. In this review, we describe the range of tumor-cell autonomously derived (intrinsic) and tumor-microenvironment-derived (extrinsic) acquired-resistance mechanisms to various FDA-approved monotherapies for HNC. Specifically, we describe how tumor cells and the tumor microenvironment (TME) respond to radiation, chemotherapy, targeted therapy (cetuximab), and immunotherapies [programmed cell death 1 (PD-1) inhibitors] and adapt to the selective pressure of these monotherapies. Due to the diversity of adaptive responses to monotherapy, monitoring the response to treatment in patients is critical to understand the path that leads to resistance and to guide the optimal therapeutic drug combinations in the clinical setting. We envisage that applying such a rationale-based therapeutic strategy will improve treatment efficacy in HNC patients.


Subject(s)
Adaptation, Biological , Head and Neck Neoplasms/therapy , Adaptation, Biological/drug effects , Adaptation, Biological/radiation effects , Antineoplastic Agents/pharmacology , Antineoplastic Agents/therapeutic use , Biomarkers, Tumor , Clinical Trials as Topic , Drug Resistance, Neoplasm , Head and Neck Neoplasms/etiology , Head and Neck Neoplasms/metabolism , Head and Neck Neoplasms/pathology , Humans , Immunotherapy , Molecular Targeted Therapy , Radiation Tolerance , Radiotherapy , Signal Transduction , Treatment Outcome , Tumor Microenvironment/drug effects , Tumor Microenvironment/genetics , Tumor Microenvironment/immunology , Tumor Microenvironment/radiation effects
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