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1.
Dose Response ; 11: 558-76, 2013.
Article in English | MEDLINE | ID: mdl-24298231

ABSTRACT

The animal model Caenorhabditis elegans was employed to study polyphenol- and humic substances-induced hormetic changes in lifespan. A detailed insight into the underlying mechanism of hormesis was uncovered by applying whole genome DNA microarray experimentation over a range of quercetin (Q), tannic acid (TA), and humic substances (HuminFeed(®), HF) concentrations. The transcriptional response to all exposures followed a non-linear mode which highlighted differential signaling and metabolic pathways. While low Q concentrations regulated processes improving the health of the nematodes, higher concentrations extended lifespan and modulated substantially the global transcriptional response. Over-represented transcripts were notably part of the biotransformation process: enhanced catabolism of toxic intermediates possibly contributes to the lifespan extension. The regulation of transcription, Dauer entry, and nucleosome suggests the presence of distinct exposure dependent differences in transcription and signaling pathways. TA- and HF-mediated transcript expression patterns were overall similar to each other, but changed across the concentration range indicating that their transcriptional dynamics are complex and cannot be attributed to a simple adaptive response. In contrast, Q-mediated hormesis was well aligned to fit the definition of an adaptive response. Simple molecules are more likely to induce an adaptive response than more complex molecules.

2.
Chemosphere ; 93(6): 1005-8, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23876505

ABSTRACT

Hormetic lifespan extension is, for obvious reasons, beneficial to an individual. But is this effect really cost-neutral? To answer this question, four tannic polyphenols were tested on the nematode Caenorhabditis elegans. All were able to extend the lifespan, but only some in a hormetic fashion. Additional life trait variables including stress resistance, reproductive behavior, growth, and physical fitness were observed during the exposure to the most life extending concentrations. These traits represent the quality of life and the population fitness, being the most important parameters of a hormetic treatment besides lifespan. Indeed, it emerged that each life-extension is accompanied by a constraining effect in at least one other endpoint, for example growth, mobility, stress resistance, or reproduction. Thus, in this context, longevity could not be considered to be attained for free and therefore it is likely that other hormetic benefits may also incur cost-intensive and unpredictable side-effects.


Subject(s)
Caenorhabditis elegans/physiology , Hormesis , Tannins/metabolism , Animals , Phenotype , Stress, Physiological
3.
Front Genet ; 3: 50, 2012.
Article in English | MEDLINE | ID: mdl-22529848

ABSTRACT

Low concentrations of the dissolved leonardite humic acid HuminFeed(®) (HF) prolonged the lifespan and enhanced the thermal stress resistance of the model organism Caenorhabditis elegans. However, growth was impaired and reproduction delayed, effects which have also been identified in response to other polyphenolic monomers, including Tannic acid, Rosmarinic acid, and Caffeic acid. Moreover, a chemical modification of HF, which increases its phenolic/quinonoid moieties, magnified the biological impact on C. elegans. To gain a deep insight into the molecular basis of these effects, we performed global transcriptomics on young adult (3 days) and old adult (11 days) nematodes exposed to two different concentrations of HF. We also studied several C. elegans mutant strains in respect to HF derived longevity and compared all results with data obtained for the chemically modified HF. The gene expression pattern of young HF-treated nematodes displayed a significant overlap to other conditions known to provoke longevity, including various plant polyphenol monomers. Besides the regulation of parts of the metabolism, transforming growth factor-beta signaling, and Insulin-like signaling, lysosomal activities seem to contribute most to HF's and modified HF's lifespan prolonging action. These results support the notion that the phenolic/quinonoid moieties of humic substances are major building blocks that drive the physiological effects observed in C. elegans.

4.
Front Genet ; 3: 48, 2012.
Article in English | MEDLINE | ID: mdl-22493606

ABSTRACT

Recent research has highlighted that the polyphenols Quercetin and Tannic acid are capable of extending the lifespan of Caenorhabditis elegans. To gain a deep understanding of the underlying molecular genetics, we analyzed the global transcriptional patterns of nematodes exposed to three concentrations of Quercetin or Tannic acid, respectively. By means of an intricate meta-analysis it was possible to compare the transcriptomes of polyphenol exposure to recently published datasets derived from (i) longevity mutants or (ii) infection. This detailed comparative in silico analysis facilitated the identification of compound specific and overlapping transcriptional profiles and allowed the prediction of putative mechanistic models of Quercetin and Tannic acid mediated longevity. Lifespan extension due to Quercetin was predominantly driven by the metabolome, TGF-beta signaling, Insulin-like signaling, and the p38 MAPK pathway and Tannic acid's impact involved, in part, the amino acid metabolism and was modulated by the TGF-beta and the p38 MAPK pathways. DAF-12, which integrates TGF-beta and Insulin-like downstream signaling, and genetic players of the p38 MAPK pathway therefore seem to be crucial regulators for both polyphenols. Taken together, this study underlines how meta-analyses can provide an insight of molecular events that go beyond the traditional categorization into gene ontology-terms and Kyoto encyclopedia of genes and genomes-pathways. It also supports the call to expand the generation of comparative and integrative databases, an effort that is currently still in its infancy.

5.
J Nat Prod ; 74(8): 1713-20, 2011 Aug 26.
Article in English | MEDLINE | ID: mdl-21805983

ABSTRACT

The model organism Caenorhabditis elegans was utilized to determine, in vivo, the mode(s) of action of four plant polyphenols, namely, tannic acid (TA), gallic acid (GA), ellagic acid (EA), and catechin (CT). The determination of lifespan, stress resistance, growth, reproduction, eating-related behaviors, antioxidative capacities, and lifespan assays with the mev-1 and the eat-2 mutants as well as in the presence of dead bacteria provided new insights into their action. All four compounds prolonged lifespan, but only TA and CT mediated distinct stress protection. Longevity is unlikely the result of antioxidant capacities but rather due to calorie restriction imitating and hormetic properties in the case of TA and EA or antimicrobial capacities of GA and EA. Furthermore, the prominent "disposable soma theory" is only partly reflected by these polyphenols. In summary, this study underlines the diversity of polyphenolic phytochemicals and their mechanistic background.


Subject(s)
Antioxidants/metabolism , Caenorhabditis elegans/physiology , Ellagic Acid/metabolism , Flavonoids/metabolism , Gallic Acid/metabolism , Longevity , Phenols/metabolism , Tannins/metabolism , Animals , Caenorhabditis elegans/genetics , Caloric Restriction , Catechin/metabolism , Flavonoids/toxicity , Phenols/toxicity , Polyphenols , Reproduction
6.
Biogerontology ; 12(4): 329-47, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21503726

ABSTRACT

Quercetin, Caffeic- and Rosmarinic acid exposure extend lifespan in Caenorhabditis elegans. This comparative study uncovers basic common and contrasting underlying mechanisms: For all three compounds, life extension was characterized by hormetic dose response curves, but hsp-level expression was variable. Quercetin and Rosmarinic acid both suppressed bacterial growth; however, antibacterial properties were not the dominant reason for life extension. Exposure to Quercetin, Caffeic- and Rosmarinic acid resulted in reduced body size, altered lipid-metabolism and a tendency towards a delay in reproductive timing; however the total number of offspring was not affected. An indirect dietary restriction effect, provoked by either chemo-repulsion or diminished pharyngeal pumping was rejected. Quercetin and Caffeic acid were shown to increase the antioxidative capacity in vivo and, by means of a lipofuscin assay, reduce the oxidative damage in the nematodes. Finally, it was possible to demonstrate that the life and thermotolerance enhancing properties of Caffeic- and Rosmarinic acid both rely on osr-1, sek-1, sir-2.1 and unc-43 plus daf-16 in the case of Caffeic acid. Taken together, hormesis, in vivo antioxidative/prooxidative properties, modulation of genetic players, as well as the re-allocation of energy all contribute (to some extent and dependent on the polyphenol) to life extension.


Subject(s)
Antioxidants/pharmacology , Caenorhabditis elegans/drug effects , Animals , Antioxidants/administration & dosage , Base Sequence , Caenorhabditis elegans/genetics , Caenorhabditis elegans/physiology , Caenorhabditis elegans Proteins/genetics , Caffeic Acids/administration & dosage , Caffeic Acids/pharmacology , Cinnamates/administration & dosage , Cinnamates/pharmacology , DNA, Helminth/genetics , Depsides/administration & dosage , Depsides/pharmacology , Dose-Response Relationship, Drug , Gene Expression/drug effects , Genes, Helminth , Heat-Shock Proteins/genetics , Longevity/drug effects , Longevity/genetics , Longevity/physiology , Polyphenols/administration & dosage , Polyphenols/pharmacology , Quercetin/administration & dosage , Quercetin/pharmacology , Rosmarinic Acid
7.
J Gerontol A Biol Sci Med Sci ; 65(6): 626-35, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20413530

ABSTRACT

This study shows that exposure to low concentrations of the polyphenol tannic acid (TA) induces potent life-prolonging properties in Caenorhabditis elegans. In addition, enhanced thermal stress resistance, reduced growth, and slightly increased oxidative stress resistance were observed, although reproductive capacities and pharyngeal pumping rate were not modulated. Exploiting a suite of 14 mutant strains revealed that the mitogen-activated protein kinase kinase SEK-1 (SAPK/ERK kinase) is a key player involved in TA-mediated longevity. It is conceivable that TA mimics pathogen action and therefore activates the SEK-1-mediated pathogen resistance pathway. This pathway is thought to inhibit potential detrimental effects of TA and may also be involved in the longevity process. The observed dose response suggests the presence of a hormesis effect, and the growth impairment is in agreement with the "Disposable Soma Theory." This report underlines the uniqueness of TA-mediated longevity and facilitates a first glimpse into its complex mode of action.


Subject(s)
Caenorhabditis elegans/physiology , Longevity/drug effects , MAP Kinase Kinase 4/metabolism , Tannins/administration & dosage , Animals , Caenorhabditis elegans/drug effects , Caenorhabditis elegans/genetics , Caenorhabditis elegans/growth & development , Dose-Response Relationship, Drug , Hot Temperature , Models, Biological , Mutation/drug effects , Oxidative Stress/drug effects , Pharynx/drug effects , Pharynx/physiology , Reproduction/drug effects , Stress, Physiological/drug effects
8.
Mech Ageing Dev ; 130(8): 477-86, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19501612

ABSTRACT

The flavanol catechin is a ubiquitous metabolite within the plant kingdom. Several health benefits have previously been reported, however, to date, most attention has been devoted to gallated forms of catechin. This study utilized the nematode Caenorhabditis elegans to assess potential life expanding effects of non-gallated catechin. Longevity was observed at three different catechin concentrations, an effect that was neither linked to a specific temperature nor to the viability of the feeding bacteria. Taken all tests into account, hormesis, calorie restriction, as well as the presence of simple antioxidative or antibacterial effects could be excluded. Likewise, the insulin/IGF-1 like signaling pathway and the calmodulin kinase II pathway were not considered to play a major mechanic role. Moreover, stress resistance was enhanced without a marked alteration in reproductive behavior. In addition, lifespan tests with various stress and lifespan relevant mutant strains revealed that the life span extending phenotype was absent in mev-1, daf-2, akt-2 and nhr-8. Finally, catechin elicited a significant reduction in body length, a finding that is in line with the "Disposable Soma Theory". It is proposed that catechin modulates an energy-intensive stress response and repair system that results in reduced body length and an enhanced lifespan.


Subject(s)
Catechin/metabolism , Longevity , Animals , Caenorhabditis elegans , Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism , Caloric Restriction , Flavonoids/chemistry , Free Radicals , Genotype , Insulin/metabolism , Pharynx/pathology , Phenols/chemistry , Phenotype , Polyphenols , Signal Transduction , Temperature , Time Factors
9.
J Am Mosq Control Assoc ; 25(1): 6-17, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19432063

ABSTRACT

The Culex pipiens complex consists of several species, subspecies, forms, races, physiological variants, or biotypes according to different authors and includes the 2 holarctic variants Cx. pipiens biotype pipiens and Cx. pipiens biotype molestus. Differences in morphological characters are overlapping and thus are delimited in their taxonomic value, even when behavioral and reproductive specializations are apparent. Our enzyme electrophoretic study included 7 geographic populations of Cx. pipiens biotype pipiens and 7 of the biotype molestus from several European countries. For comparison, 5 populations of Culex quinquefasciatus from Asia, Africa, and North America were examined. The aim was an assessment of the extent of genetic differences between local populations of the biotypes pipiens and molestus versus the degree of differentiation between geographic populations of both groups. Culex torrentium, Cx. modestus, Culex stigmatosoma, and Culex territans were studied for comparison as taxonomical well-defined species. The population genetic analyses revealed much higher genetic distances between local populations of Cx. pipiens biotype pipiens and Cx. pipiens biotype molestus compared to the low differentiation between geographic populations within each taxon. The UPGMA analysis and F-statistics position the geographic populations in discrete monophyletic clusters. Gene flow between local populations of the biotypes pipiens and molestus could be shown to be lower than gene flow between geographically distant populations within each of the 2 groups, leading to the conclusion that Cx. pipiens biotype molestus could be a distinct taxon. Culex quinquefasciatus could be diagnosed as genetically well separated, in particular by the diagnostic enzyme marker MDH (NADP). Two genetic enzyme markers were identified to differentiate Cx. torrentium from Cx. pipiens s.l. Culex modestus, Cx. stigmatosoma, and Cx. territans showed considerable genetic distances to the species of the Culex pipiens complex and between each other, and several genetic markers could be identified.


Subject(s)
Culex/genetics , Genetic Variation , Phylogeny , Animals , Breeding , Culex/classification , Culex/enzymology , Europe , Female , Gene Flow , Gene Frequency , Genetic Drift , Genetic Markers , Insect Proteins/genetics , Male , Sexual Behavior, Animal , Species Specificity
10.
Biogerontology ; 10(5): 565-78, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19043800

ABSTRACT

The nematode Caenorhabditis elegans responds to flavonoid-rich diets with improved health and longevity. The precise mechanism(s) responsible for this remains to be identified, but is believed to be linked to the highly antioxidative properties of flavonoids. This study provides a dissection of lifespan modulation by the flavonoid quercetin. In detail, quercetin was shown not to act as a simple antimicrobial agent or exclusively via radical scavenging capacities. Likewise, lifespan extension had no effect on reproduction and body length. Furthermore, neither a caloric restriction mimetic nor a sirtuin (sir-2.1) dependence was identified as a likely mode of action. However, four genes were pinpointed to be required for the quercetin derived lifespan extension, namely age-1, daf-2, unc-43 and sek-1. The latter two have, to date, not been linked to quercetin-mediated lifespan extension.


Subject(s)
Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans , Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism , Longevity/drug effects , MAP Kinase Kinase 4/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Quercetin/pharmacology , Receptor, Insulin/metabolism , Animals , Antioxidants/pharmacology , Caenorhabditis elegans/drug effects , Caenorhabditis elegans/physiology , Caenorhabditis elegans Proteins/genetics , Calcium-Calmodulin-Dependent Protein Kinase Type 2/genetics , Caloric Restriction , Diet , Life Expectancy , MAP Kinase Kinase 4/genetics , Mutation , Oxidative Stress , Phosphatidylinositol 3-Kinases/genetics , Receptor, Insulin/genetics , Signal Transduction/physiology , Temperature
11.
Mech Ageing Dev ; 129(10): 611-3, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18692520

ABSTRACT

The polyphenol quercetin has recently been found to extend lifespan and increase stress resistance in the nematode Caenorhabditis elegans. The forkhead transcription factor DAF-16 has previously been linked to these effects. However, by using a daf-16(mgDf50) mutant strain, we show that quercetin exposure leads to increased mean lifespans up to 15%. Furthermore, quercetin-treated daf-16(mgDf50) worms show an enhanced resistance to thermal and oxidative stress. Our data reveal that DAF-16 is not obligatorily required for quercetin-mediated longevity and stress resistance.


Subject(s)
Antioxidants/pharmacology , Caenorhabditis elegans Proteins/genetics , Caenorhabditis elegans Proteins/physiology , Longevity/genetics , Mutation , Quercetin/pharmacology , Transcription Factors/genetics , Transcription Factors/physiology , Animals , Caenorhabditis elegans , Dose-Response Relationship, Drug , Forkhead Transcription Factors , Gene Expression Profiling , Longevity/drug effects , Oxidative Stress , Temperature , Time Factors
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