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1.
Ann N Y Acad Sci ; 1100: 442-8, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17460209

ABSTRACT

Dietary restriction (DR) delays the onset of age-related deterioration and extends the life span in a variety of model organisms. In many species, age changes in mortality obey the Gompertz equation, which describes an exponential increase with age in age-specific mortality rate. Recently, this model has been used in fruitflies and rodents to investigate the mechanism by which DR reduces adult mortality. We report that food restriction imposed by axenic culture reduces the exponential increase of age-specific mortality of Caenorhabditis elegans. Furthermore, the life span appears largely independent of nutritional status during development, as shown by shifting worms to different food concentrations shortly before adulthood. When DR was exerted after reproduction, a smaller reduction in Gompertzian aging was seen. Thus, the demographic changes exerted by DR in C. elegans resemble those seen in rats, yet are different to those seen in Drosophila and mice.


Subject(s)
Aging , Caloric Restriction , Food Deprivation , Animals , Caenorhabditis elegans , Energy Intake , Longevity , Models, Biological , Models, Theoretical , Time Factors
2.
Aging Cell ; 4(2): 87-95, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15771612

ABSTRACT

The insulin/insulin-like growth factor-1 (Ins/IGF-1) pathway regulates the aging rate of the nematode Caenorhabditis elegans. We describe other features of the three Ins/IGF-1 mutants daf-2, age-1 and aap-1. We show that the investigated Ins/IGF-1 mutants all have a reduced body volume, reduced reproductive capacity, increased ATP concentrations and an elevated stress resistance. We also observed that heat production is lower in these mutants, although the respiration rate was similar or higher compared with wild-type individuals, suggesting a metabolic shift in these mutants.


Subject(s)
Caenorhabditis elegans/physiology , Insulin-Like Growth Factor I/genetics , Insulin/genetics , Adenosine Triphosphate/metabolism , Aging/genetics , Aging/physiology , Animals , Body Size , Caenorhabditis elegans/genetics , Caenorhabditis elegans/metabolism , Heat-Shock Response , Mutation , Oxygen Consumption , Reproduction
3.
Neurobiol Aging ; 26(5): 689-96, 2005 May.
Article in English | MEDLINE | ID: mdl-15708444

ABSTRACT

In Caenorhabditis elegans, metabolism and life expectancy respond to environmental cues of food availability and temperature. Several genes act in a neuroendocrine, DAF-2, insulin/IGF-1 receptor-like pathway in which reduced signaling affects metabolism and increases longevity. Here we describe the effect of reduced DAF-2 signaling on several parameters of metabolism including rates of oxygen consumption and heat output, the calorimetric/respirometric ratio, ATP levels, XTT reduction capacity and accumulation of lipofuscin. We also asked whether the DAF-2 signaling pathway mediates the metabolic and longevity effects of axenic culture medium. We show that both interventions act either antagonistically or in concert, depending on the parameter examined and that axenic culture medium, unlike DAF-2 signaling, does not need DAF-16 for generating these effects. In addition, we provide evidence that DAF-2 signaling controls mitochondrial bioenergetics by adjusting the rate of ATP synthesis to the rate of ATP utilization and by regulating the heat-producing proton leak pathway.


Subject(s)
Aging/metabolism , Food Deprivation/physiology , Mutation , Receptor, Insulin/physiology , Signal Transduction/genetics , Adenosine Triphosphate/metabolism , Age Factors , Animals , Caenorhabditis elegans/metabolism , Caenorhabditis elegans Proteins , Calorimetry, Indirect/methods , Cohort Studies , Female , Germ-Free Life , Lipofuscin/metabolism , Longevity/physiology , Male , Oxygen Consumption , Receptor, Insulin/genetics , Temperature , Tetrazolium Salts/metabolism
4.
Mech Ageing Dev ; 123(11): 1447-56, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12425951

ABSTRACT

Mutation in any of the four clock genes (clk-1, clk-2, clk-3, gro-1) causes an average slowing down of many temporal processes, and an increase of mean life span. The latter effect has been linked to the slow phenotype, and it has been reasoned that any reduction of the rate of living would reduce the load of oxidative damage, which is thought to drive the ageing process. To test this model we measured several parameters describing metabolic output in wild type worms and all four Clk mutants. We found no gross changes in metabolic output, as assessed from oxygen consumption and heat production rates, lucigenin-mediated light production capacity, ATP content, and lipofuscin autofluorescence. Catalase and superoxide dismutase (SOD) were variably altered, but not cooperatively, as would be expected to enhance reactive oxygen species (ROS) scavenging activity. Thus we conclude that the prolonged life span of Clk mutants cannot be attributed to reduced metabolic rate or an increased activity of the major antioxidant enzymes catalase and SOD.


Subject(s)
Alkyl and Aryl Transferases/genetics , Caenorhabditis elegans Proteins/genetics , Energy Metabolism/physiology , Helminth Proteins/genetics , Mutation/physiology , Telomere-Binding Proteins/genetics , Acridines/metabolism , Adenosine Triphosphate/metabolism , Animals , Caenorhabditis elegans , Catalase/metabolism , Fluorescence , Lipofuscin/physiology , Longevity , Luminescent Measurements , Oxygen Consumption , Superoxide Dismutase/metabolism , Thermogenesis
5.
Exp Gerontol ; 37(8-9): 1015-21, 2002.
Article in English | MEDLINE | ID: mdl-12213552

ABSTRACT

The nematode Caenorhabditis elegans responds to unfavourable environmental conditions by arresting development and entering diapause as a dauer larva. Dauers can survive several times the normal life span and the duration of the dauer state has no effect on postdauer life span. This led to the suggestion that dauers are non-ageing, and that dauers eventually perish as the consequence of depletion of stored nutrients. We have investigated physiological changes associated with long-term diapause survival, and found that dauer larvae slowly develop senescence-like symptoms, including decrease of metabolic capacity, aconitase enzyme activity, and ATP stores, and increase of lipofuscin- and oxidised flavin-specific fluorescence. However, these changes are reversed when the dauers recover. Thus senescence can occur before attainment of reproductive maturity, and furthermore, is reversible. Other life processes, including respiration rate and heat output, remain unaltered over four weeks of diapause at 24 degrees C. Possible determinants of the enhanced life maintenance include increased resistance to oxidative stress provided by enhanced superoxide dismutase and catalase activities, and a shift to a highly reducing redox status.


Subject(s)
Aging/physiology , Caenorhabditis elegans/physiology , Longevity , Adenosine Triphosphate/metabolism , Animals , Larva/physiology , Lipofuscin/biosynthesis , Oxygen Consumption , Superoxide Dismutase/metabolism
6.
Syst Appl Microbiol ; 25(4): 603-10, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12583721

ABSTRACT

Microbial mats, growing in Antarctic lakes constitute unique and very diverse habitats. In these mats microorganisms are confronted with extreme life conditions. We isolated 746 bacterial strains from mats collected from ten lakes in the Dry Valleys (lakes Hoare and Fryxell), the Vestfold Hills (lakes Ace, Druzhby, Grace, Highway, Pendant, Organic and Watts) and the Larsemann Hills (lake Reid), using heterotrophic growth conditions. These strains were investigated by fatty acid analysis, and by numerical analysis, 41 clusters, containing 2 to 77 strains, could be delineated, whereas 31 strains formed single branches. Several fatty acid groups consisted of strains from different lakes from the same region, or from different regions. The 16S rRNA genes from 40 strains, representing 35 different fatty acid groups were sequenced. The strains belonged to the alpha, beta and gamma subclasses of the Proteobacteria, the high and low percent G+C Gram-positives, and to the Cytophaga-Flavobacterium-Bacteroides branch. For strains representing 16 fatty acid clusters, validly named nearest phylogenetic neighbours showed pairwise sequence similarities of less than 97%. This indicates that the clusters they represent, belong to taxa that have not been sequenced yet or as yet unnamed new taxa, related to Alteromonas, Bacillus, Clavibacter, Cyclobacterium, Flavobacterium, Marinobacter, Mesorhizobium, Microbacterium, Pseudomonas, Saligentibacter, Sphingomonas and Sulfitobacter.


Subject(s)
Bacteria/classification , Fresh Water/microbiology , Water Microbiology , Antarctic Regions , Bacteria/genetics , Bacteria/isolation & purification , Base Sequence , Biomass , Fatty Acids/analysis , Fatty Acids/classification , Genetic Variation , Molecular Sequence Data , Phylogeny , RNA, Ribosomal, 16S/analysis
7.
Exp Gerontol ; 37(12): 1359-69, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12559405

ABSTRACT

Dietary restriction (DR) is the most consistent means of extending life span throughout the animal kingdom. Multiple mechanisms by which DR may act have been proposed but none are clearly predominant. We asked whether metabolic rate and stress resistance is altered in Caenorhabditis elegans in response to DR. DR was imposed in two complementary ways: by growing wild-type worms in liquid medium supplemented with reduced concentrations of bacteria and by using eat-2 mutants, which have a feeding defect. Metabolic rate was not reduced when we fed wild-type worms reduced food and was up-regulated in the eat-2 mutants in liquid culture, as assessed by oxygen consumption rate and heat production. The specific activity levels of the antioxidant enzymes superoxide dismutase (SOD) and catalase showed small increases when we reduced food in wild-type worms, but restricted worms acquired no elevated protection against paraquat and hydrogen peroxide. eat-2 mutants showed elevated specific activities of SOD and catalase relative to wild type in liquid culture. These results indicate that the effects imparted by DR and the eat-2 mutation are not identical, and they contradict, at least in C. elegans, the widespread belief that CR acts by lowering the rate of metabolism.


Subject(s)
Caenorhabditis elegans/metabolism , Food Deprivation/physiology , Oxygen Consumption/physiology , Thermogenesis/physiology , Aging/metabolism , Animals , Caenorhabditis elegans/genetics , Catalase/metabolism , Eating/physiology , Feeding and Eating Disorders/genetics , Feeding and Eating Disorders/physiopathology , Helminth Proteins/genetics , Mutation , Superoxide Dismutase/metabolism
8.
Exp Gerontol ; 37(12): 1371-8, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12559406

ABSTRACT

Culture in axenic medium causes two-fold increases in the length of development and adult life span in Caenorhabditis elegans. We asked whether axenic medium imposes dietary restriction (ADR), and causes changes in metabolic activity and stress resistance. Eat mutants, which have a reduced food intake, were studied in parallel with wild-type worms to assess potential synergistic actions of axenic culture and food restriction. We found that axenic culture enhances metabolic activity as assessed by mass-specific oxygen consumption rate and heat production. Axenic culture also caused higher activities of the antioxidant enzymes superoxide dismutase and catalase, and led to increased resistance to high temperature, which was further exacerbated by mutation in eat-2. These results show that axenic medium up-regulates a variety of somatic maintenance functions including oxidative and thermal stress resistance and that food restriction due to axenic growth and to mutation in eat-2 are very similar but not identical.


Subject(s)
Caenorhabditis elegans/metabolism , Food Deprivation/physiology , Oxygen Consumption/physiology , Stress, Physiological/metabolism , Thermogenesis/physiology , Aging/physiology , Animals , Catalase/metabolism , Culture Media , Eating/physiology , Feeding and Eating Disorders/genetics , Feeding and Eating Disorders/physiopathology , Helminth Proteins/genetics , Longevity , Mutation , Superoxide Dismutase/metabolism , Up-Regulation
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