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PubMed1993

Effect of photoperiod on longevity and metabolic rate in Anopheles quadrimaculatus.

The effect of photoperiod on longevity of nondiapausing members of a species in the mosquito species complex Anopheles quadrimaculatus was tested in laboratory experiments. First-generation adults reared from 2 field collections showed the same trends: those reared under short photoperiod (8 h light: 16 h dark) lived longer than did those reared under long photoperiod (16 h light: 8 h dark). Adult metabolic rates were not consistently related to longevity. In adults reared from the first collection, metabolic rates were higher in long-photoperiod individuals but in adults reared from the second collection, metabolic rates were higher in short-photoperiod individuals. Longevity appears to be another of many insect features that are affected similarly by temperature and photoperiod.

Animals↗

PubMed1996

[Biochemistry of space and time (telomeres, telomerases, and longevity of cell populations and multicellular organisms].

Analysis of recent data on telomeres and telomerases, limitations of proliferative potential of untransformed cells (Hayflick's limit), kinetics and molecular mechanism of cell proliferation and differentiation, and factors that determine the longevity of multicellular organisms suggests that: (i) chromosome end shortening during consecutive divisions of cells that lack telomerase limits cell proliferation beyond Hayflick's limit; (ii) Hayflick's limit can be a manifestation of mechanisms that determine the size of the living organism (it correlates with longevity) but not the longevity of multicellular organisms.

Animals↗

PubMed1997

Association between lactation length and sow reproductive performance and longevity.

OBJECTIVE: To determine whether lactation length was associated with reproductive performance or longevity of sows. DESIGN: Cohort study. SAMPLE POPULATION: Data collected between 1986 and 1992 for sows in 15 breeding herds in Minnesota and Iowa. PROCEDURE: Sows were grouped into 4 genetic line categories according to their sources and 6 parity categories (1, 2, 3, 4, 5 or 6, and > or = 7). Multivariate regression analysis of reproductive performance was conducted, using the general linear model procedure Logistic regression was conducted with a dichotomous response variable for sow longevity (ie, removal from or retention in the herds). Odds ratios were obtained from estimated coefficients of the regression. RESULTS: Herd, genetic line, parity, year, month, and lactation length were significant in statistical models for litter (eg, number of live pigs/litter) and interval (eg, weaning-to-mating interval) traits. Interactions between lactation length and year, lactation length and genetic line, lactation length and parity, and lactation length and genetic line and parity were also significant. Sows removed from herds had a significantly shorter lactation length than did sows of the same parity that were retained in the herds. Sows that had shorter lactation lengths were at higher risk of being removed from the herds than were those that had longer lactation lengths. CLINICAL IMPLICATIONS: Lactation length is associated with reproductive performance and longevity, but genetic line and parity play a role as well. Thus, attention should be paid to genetic lines and parity of sows in the herd when implementing an early weaning production practice.

Animals↗

PubMed1998

Association between longevity and allelic forms of human leukocyte antigens (HLA): population study of aged Italian human subjects.

Several arguments support the idea of a link between longevity and heredity, both in humans and in experimental animals. We have therefore investigated the possibility of an association between the human leukocyte antigens (HLA) and longevity in two groups of Italian subjects: 108 healthy subjects over 85 years old, and 749 healthy blood donors (controls). Only four antigens showed a higher frequency in the elder group: HLA-A31(19), B7, Cw7 and DQ1. These findings suggest an involvement of HLA antigens in human longevity, but the real biological meaning of these results is still unclear.

Aged↗

PubMed1998

Human longevity determinant genes.

Two recent major developments in the molecular biology of lower organisms point to genes as determinants of longevity. The first line of evidence is a selection system that established the participation of genes in aging and subsequently showed longevity to be a polygenic characteristic in Drosophila. The second validation of a genetic role in aging came from studies in which a mutation in an individual gene was found to modulate life span in nematodes. The achievements of genetics in the analysis of aging in mammals are less impressive than they have been for lower organisms, but this situation is changing. Although no genes have yet been directly implicated in prolonging life span in mammals, studies with mice have related immune function to longevity.

Aging↗

PubMed1999

Application of hypoosmolar medium to fed-batch culture of hybridoma cells for improvement of culture longevity.

Cell culture longevity in fed-batch culture of hybridomas is often limited by elevated medium osmolality caused by repeated nutrient feeding. Shotwise feeding of 10x Dulbecco's modified Eagle's medium (DMEM) concentrates elevated the osmolality of medium up to 540 mOsm/kg at the end of fed-batch culture of S3H5/gamma2bA2 hybridoma which is known to be lethal to most hybridomas. S3H5/gamma2bA2 hybridoma has been shown to grow without significant growth depression at 219 mOsm/kg in DMEM supplemented with 10% fetal bovine serum. To improve culture longevity in fed-batch cultures of S3H5/gamma2bA2 hybridoma, a hypoosmolar medium (223 mOsm/kg) was used as an initial basal medium. The use of hypoosmolar medium delayed the onset of severe cell death resulting from elevated osmolality and allowed one more addition of 10x DMEM concentrates to the culture. As a result, a final antibody concentration obtained was 121.5 microg/mL which is approximately 1.5-fold higher compared to fed-batch culture using a standard medium (335 mOsm/kg). When compared to batch culture, a more than 5-fold increase in the final antibody concentration was achieved. Taken together, the use of hypoosmolar medium as an initial medium in fed-batch culture improved culture longevity of S3H5/gamma2bA2 hybridoma, resulting in a substantial increase in the final antibody concentration.

Animals↗

PubMed1976

Conditions affecting primary cell cultures of functional adult rat hepatocytes. II. Dexamethasone enhanced longevity and maintenance of morphology.

Primary monolayer cell cultures of adult rat hepatocytes underwent change in morphology and substantial cell loss between 1 and 3 days postinoculation. Dexamethasone-supplementation (1 micronM) of the culture medium maintained the polygonal epithelial morphology of the hepatocytes and increased longevity such that over 80% of the cells survived for 3 days and at least 30% for 8 or 9 days. This enhancement of survival was obtained up to 48 hr postinoculation, but the earlier the time of dexamethason supplementation the greater the effect. Removal of dexamethasone resulted in a decrease in longevity. The positive effect of dexamethasone on longevity was observed following dexamethasone replacement of insulin in supplemented cultures, but the combination of insulin and dexamethasone resulted in poorer survival than with dexamethasone alone. The results are interpreted to indicate that dexamethasone provided a requirement of the in vitro environment for survival and suggest that elaboration of a complex medium is required to maintain hepatocytes in culture.

Animals↗

PubMed2003

Differences in the longevity of topo IIalpha and topo IIbeta drug-stabilized cleavable complexes and the relationship to drug sensitivity.

PURPOSE: DNA topoisomerase II (topo II) is an important cellular target for chemotherapeutic agents. Human cells have two isoforms of topo II (alpha and beta), and both are inhibited by the chemotherapeutic agents etoposide, amsacrine (mAMSA) and mitoxantrone. It is known that the cytotoxic importance of topo IIalpha or topo IIbeta drug-induced complexes differs depending on which drug is present. This study was designed to (a) assess isoform-specific formation and reversal of topo IIalpha and beta cleavable complexes, and (b) determine whether the cytotoxic importance of either isoform was related to differences in the longevity of the complexes. METHODS: Mouse embryonic fibroblasts (MEFs) were used to study the cellular response to the topo II poisons etoposide, mitoxantrone and mAMSA. The longevity of topo IIalpha and beta complexes was determined using the TARDIS assay. This immunofluorescence assay can differentiate between the topo II isoforms and thus allowed us to investigate the persistence and importance of topo IIalpha and beta complexes for the first time. RESULTS: In MEFs treated with etoposide, 50% of topo IIalpha complexes dissociated within 40 min whereas dissociation of topo IIbeta complexes took only 20 min. Disappearance of complexes was a slower process for mitoxantrone-treated cells. The time taken to reduce topo IIalpha and topo IIbeta cleavable complexes by 50% was 10 and 6 h, respectively. In contrast, mAMSA-stabilized topo IIalpha and topo IIbeta cleavable complexes were equally stable (dissociation within 15 min for both isoforms). These stability data were confirmed using an in vitro assay. CONCLUSIONS: We previously demonstrated that topo IIalpha is the major target for etoposide and mitoxantrone but that both topo IIalpha and topo IIbeta are important for mAMSA cytotoxicity. The longevity of the topo IIalpha and beta cleavable complexes shown here is therefore an important factor in determining the cytotoxic sensitivity of either isoform to these drugs.

Amsacrine↗

PubMed1999

Longevity of cast gold inlays and partial crowns--a retrospective study at a dental school clinic.

From 1963 to 1993, 890 patients were treated with 3518 cast gold restorations by students and postgraduate dentists. The longevity of these restorations was studied retrospectively using the patient files. Longevity was calculated using the method described by Kaplan and Meier. After the observation period, 111 (3.2%) of the examined restorations were not in place anymore. The most frequent reasons for failure were caries (33.7%), lack of retention (32.7%), endodontic treatment (29.6%), insufficient marginal adaptation (3.1%) and extraction (1%). The cumulative survival rate and a 95% interval of confidence was calculated for all restorations and for each of the locations and surfaces included in the trial. The 10-year survival rate for occlusal inlays was, 76.1% (12.1) for MO inlays 88.3% (4.2), for DO inlays 83.4% (4.6), for MOD inlays 87.5% (2.4), for partial crowns 86.1% (3.3) and 85.7% (1.7) for all restorations. Based on the statistical method used, the cast gold restorations demonstrated satisfactory longevity results.

Adult↗

PubMed1988

Epicardial ventricular pacemaker electrode longevity in children.

While epicardially implanted electrodes remain the most widely used in children for ventricular pacing, their expected longevity remains unknown. The longevity of 126 such electrodes implanted from January 1970 through December 1985 was evaluated in 81 children followed up for 1 to 192 months (median 63). Age at initial implant was 1 day to 18 years. Each child had from 1 to 5 electrodes implanted; 85 electrodes were of the sutureless helical type and 41 were of the suture-fixated type. Electrode failure, defined as loss of capture with a high pacing threshold found at operation or sensing failure, occurred in 38 electrodes from 1 to 157 months postimplant (median 37). Mode of failure was high threshold with high impedance (n = 15), low impedance (n = 6), complete inability to pace (n = 8), sensing failure (n = 2) or high threshold with no measure of impedance (n = 7). Actuarial life table analysis of electrode longevity showed a 88 +/- 3% (standard error of the estimate) survival rate at 6 months with no significant decrease until 53 months (75 +/- 5%, p less than 0.05). There was then a gradual steady decrease to 49 +/- 7% by 101 months. From 101 to 157 months no significant decrease occurred. Survival rate decrease was greatest within the first 6 month period postimplant (-12%). Electrodes surviving to 6 months are highly likely to survive until 53 months. Of those surviving to 53 months, 74% should survive to 120 months.

Adolescent↗

PubMedDate not supplied

Recent progress in testing the longevity determinant and dysdifferentiation hypotheses of aging.

An overview of the longevity determinant and dysdifferentiation hypotheses is presented, highlighting some of the major postulates and predictions. Results of recent experiments testing these hypotheses are discussed, including the search for specific longevity determinant genes and evidence that cancer and aging may have common causative mechanisms of action and control. Regulation of oxidative stress is considered a potential longevity determinant mechanism and methods and results testing this prediction are reviewed. Possibility of enhancing protective mechanisms against oxidative stress is discussed by way of intervention of central regulatory mechanisms of antioxidants using the cyclase-arachidonic acidcyclooxygenase (GAC model).

Journal Article↗

PubMedDate not supplied

Gompertz mortality analysis: aging, longevity hormesis and toxicity.

The hazard function, denoted h(x), is the probability of death during an interval of time [Formula: see text], assuming survival to the beginning of the interval. Brues and Sacher provided both theoretical and experimental support for the assumption that h(x) is an exponential function of the mean intensity of physiologic injury for a homogeneous mammalian population provided an adequate diet, kept free of preventable disease and maintained under favorable, uniform conditions. Consequently, the Napierian logarithm of the hazard function, the 'Gompertzian', is proportional to the mean intensity of physiologic injury under the aforementioned conditions. Investigation of Gompertzian values therefore affords a simple and convenient measure of the mean population time course of aging, toxicity and beneficial life-enhancing effects (e.g., longevity hormesis and slowing of the aging process). (The word 'hormesis' has been applied to various forms of 'stimulation' elicited by low doses of otherwise toxic agents.) Using this method of analysis, reversible toxicity, reversible reduction in physiologic injury (longevity 'hormesis'), irreversible toxicity and irreversible reduction in aging (via caloric restriction) are all reviewed. It is demonstrated that these effects may superimpose upon one another, the most common combination following administration of mild to moderate doses of a toxic agent being irreversible toxicity combining with longevity hormesis.

Journal Article↗

PubMed2005

[Pacemaker longevity. Replacement of the device].

Life expectancy of patients implanted with cardiac pacemakers has largely increased, so that generator replacement is becoming an important part of the activity in most of the implanting centers. In more than 70% of the cases, the indication for pacemaker replacement is normal battery depletion. Since the new devices are more and more sophisticated and smaller, longevity optimization becomes a real challenge. The main determinant of pacemaker longevity is the output programmed for the pulse generator. It mainly depends on the output voltage and duration settings. The pacing impedance and the percentage of time with pacing are other major determinants of pacemaker longevity. Each manufacturer provides specific policy but the battery voltage and internal impedance are the more accurate and easy-to-obtain battery depletion parameters. The magnet rate is still frequently used but is less valuable since it can drop abruptly at the end of battery life. The complication rate of pacemaker replacement is three-fold higher than the one of first implant. Infections, skin erosions and lead related complications are not uncommon. The replacement should be systematically preceded by the checking of several points including the patient's pacemaker dependency, the necessity to replace or extract one or several leads, the venous system status, the compatibility between the new generator and the leads and the necessity to upgrade the pacing system or to change the pacemaker pocket.

Device Removal↗

PubMed2006

A retrospective clinical study on longevity of posterior composite and amalgam restorations.

OBJECTIVES: The purpose of this study was to evaluate retrospectively the longevity of class I and II amalgam and composite resin restorations placed in a general practice. METHODS: Patient records of a general practice were used for collecting the data for this study. From the files longevity and reasons for failure of 2867 class I and II amalgam and composite resin restorations placed in 621 patients by two operators between 1990 and 1997 were recorded in 2002. RESULTS: 912 amalgam restorations (502 by operator 1 and 410 by operator 2) and 1955 posterior composite resin restorations (1470 by operator 1 and 485 by operator 2) were placed. One hundred and eighty-two amalgam and 259 posterior composite resin restorations failed during the observation period. The main reasons for failure of the restorations were caries (34%), endodontic treatment (12%) and fracture of the tooth (13%). Life tables calculated from the data reveal a survival for composite resin of 91.7% at 5 years and 82.2% at 10 years. For amalgam the survival is 89.6% at 5 years and 79.2% at 10 years. Cox-regression analysis resulted in a significant effect of the amount of restored surfaces on the survival of the restorations. No significant effect of operator, material as well as combination of material and operator was found. SIGNIFICANCE: In the investigated general practice, two dentists obtained comparable longevity for amalgam and composite resin restorations.

Acid Etching, Dental↗

PubMed2007

Increased longevity of hematopoiesis in continuous bone marrow cultures derived from NOS1 (nNOS, mtNOS) homozygous recombinant negative mice correlates with radioresistance of hematopoietic and marrow stromal cells.

OBJECTIVE: Neuronal nitric oxide synthase (NOS1, mitochondrial NOS, neuronal NOS) homozygous deletion recombinant negative mice demonstrate ionizing irradiation resistance in vivo, attributable to the decrease in mitochondrial-localized production of peroxynitrite, a potent lipid toxic free radical species resulting from the combination of nitric oxide and superoxide. The present studies were designed to determine whether reduced mitochondrial generation of toxic radical oxygen species in NOS1-/- mice also increased the longevity of hematopoiesis in continuous bone marrow cultures and conferred radioresistance to cells in vitro. MATERIALS AND METHODS: Long-term bone marrow cultures (LTBMCs) were established from NOS1-/- and NOS1+/+ littermate mice. Radiation resistance of hematopoietic and marrow stromal cells was measured. Cell cycle analysis and measurement of glutathione and glutathione peroxidase were carried out on irradiated clonal bone marrow stromal cell lines. RESULTS: A significant increase in longevity of hematopoiesis was detected in NOS1-/- mouse LTBMCs for over 64 weeks in culture compared to 20 weeks for NOS1+/+ mouse LTBMCs (p < 0.001). Permanent bone marrow stromal cell lines derived from NOS1-/- mouse LTBMCs demonstrated increased radioresistance in vitro reflected by an increased shoulder on the survival curve with n = 32.15 +/- 1.21 compared to NOS1+/+ cells n = 10.47 +/- 3.2 (p = 0.0026), interleukin-3-dependent NOS1-/- hematopoietic progenitor cell lines also demonstrated decreased apoptosis after 10 Gy irradiation. Both pre- and postirradiation stabilization of the cellular antioxidant pool was detected in NOS1-/- cells. NOS1-/- cells showed a prolonged G1 cell cycle arrest after 10 Gy. CONCLUSIONS: Prolonged hematopoiesis in LTBMCs correlates with intrinsic radioresistance of hematopoietic and marrow stromal cells from NOS1-/- mice. The data confirm the importance to hematopoiesis of mitochondrial localized nitric oxide in both radioresistance and longevity of hematopoiesis in continuous bone marrow cultures.

Animals↗

PubMed2006

Preadaptation to efficient respiratory maintenance is essential both for maximal longevity and the retention of replicative potential in chronologically ageing yeast.

Only recently have the studies of yeast ageing started to focus on the S288c-derived strains used extensively in genomics and on the longest lifespans. Chronological longevity (stationary (G(0)) survival) of such strains is greater when cells are pre-grown on a respiratory carbon source, as compared to when they are pre-grown on glucose (the latter a respiration-repressing sugar). Prior adaptation to efficient respiratory maintenance also ensures that such chronologically aged yeast cells still display a full replicative lifespan should they reenter the cell cycle. In contrast, cells that are pre-grown on glucose exhibit marked and progressive losses of replicative potential as they age chronologically in stationary phase. Increasing the respiratory activity in glucose-grown cultures by HAP4 gene overexpression increased survival and reversed the loss of replicative potential during a subsequent stationary phase. Adaptation to efficient respiratory maintenance is therefore important, not just for maximal longevity, but also for the maintenance of a full replicative lifespan by chronologically ageing cultures of yeast. In such respiration-adapted cultures, losses of the Sch9 protein kinase or Yca1 caspase both shortened lifespan. In contrast loss of Yap1, the major transcriptional regulator of the oxidative stress response, generated a small increase in chronological lifespan in certain strain backgrounds. It would appear, therefore, that any induction of oxidative stress response genes in chronologically ageing yeast is not operating to generate an increase in longevity, even though such protective effects might be expected from the increased proxidant status of these cells over time.

Adaptation, Physiological↗

PubMed2005

Longevity and failure load of ceramic veneers with different preparation designs after exposure to masticatory simulation.

STATEMENT OF PROBLEM: Laminate veneers are widely used in the management of unesthetic anterior teeth. However, limited information is available regarding the influence of preparation design on longevity of ceramic veneers. PURPOSE: This study evaluated the influence of preparation design on longevity and failure load of ceramic veneers bonded to human maxillary central incisors after cyclic loading and thermal cycling in a dual-axis masticatory simulator. MATERIAL AND METHODS: Sixty-four caries-free maxillary central incisors were divided into 4 groups (n = 16). The control group remained unprepared (NP). For Group WP, a window preparation was made. Specimens in Group IOP were prepared with an incisal overlap of 2 mm without palatal chamfer. For Group CVP, specimens were prepared with a complete-veneer design of 3-mm incisal reduction and 2-mm palatal extension. Forty-eight IPS Empress 1 ceramic veneers were bonded adhesively with dual-polymerizing composite (Variolink II). All specimens were subjected to cyclic mechanical loading (1.2 million cycles, cycle frequency 1.3 Hz, invariable palatal load 49 N) and thermal cycling (5 degrees C-55 degrees C, dwell time 60 seconds, 5500 cycles) in a masticatory simulator. Failure was defined by bulk fracture of a specimen. Subcritical crack patterns were observed. Surviving specimens were loaded in a universal testing machine until fracture. The failure-load values (N) (1.5 mm/min crosshead speed) were automatically recorded by controlling software. Statistical analysis of data was performed by Kruskal-Wallis analysis of variance (alpha = .05) and pairwise Wilcoxon rank sum tests (alpha = .05). RESULTS: Three specimens from group NP, 1 specimen each from the WP and CVP groups, and 2 specimens from group IOP fractured during fatigue. After 1.2 million cycles, the highest crack rates were observed for complete veneers and originated in the palatal concavity extending to the facial surface. The median (interquartile range = x .25 - x .75 ) failure loads (N) were as follows: NP 713.3 (404.4-777.1), WP 549.5 (477.5-597.7), IOP 695.3 (400.0-804.6), and CVP 519.2 (406.1-732.9). No significant differences in longevity and failure load were demonstrated between natural teeth and teeth restored with ceramic veneers ( P = .555). CONCLUSION: Maxillary teeth restored with the 3 types of IPS Empress 1 veneers showed fracture resistance similar to that of unprepared incisors ( P = .555).

Aluminum Silicates↗

PubMed2005

Phosphorous retention capacity of filter media for estimating the longevity of constructed wetland.

The filter medium could be selected and the longevity of the filter medium by the phosphorus saturation could be predicted in the constructed wetland system, accordingly proposing the scheme to remove the phosphorus for a long period. The phosphorus adsorption capacities of various filter media were investigated in relation to the size and types of filter media to screen the optimal condition. The objective of this study was to evaluate the constructed wetland longevity by improving P adsorption capacity. The maximum P adsorption capacities of filter media A (4--10 mm), B (2--4 mm), and C (0.1--2 mm) were 7.7, 11.6, and 22.5 mg/kg, respectively, showing that they increased as the filter media size decreased. Among the experimental media, the optimal filter media size was 0.1--2 mm. When Ca, Mg, Al and Fe were added to the filter medium C, which is the optimal filter medium, the addition of Ca improved mostly the P adsorption capacity. In the alternative proposal to use these facts, the oyster shell was added to the filter medium and the P adsorption capacity was examined: adding 2% oyster shell increased the P adsorption capacity from 23 to 36 mg/kg. In the column where the oyster shell was mixed, when the oyster shell content was 5%, 10%, 20%, 40%, 60%, 80%, and 100% in the filter medium C, the respective saturation times of the P adsorption were about 6, 9, 17, 30, 43, 56, and 70 days. When the oyster shell content was 0%, 5%, 10%, 20%, 40%, 60%, 80%, and 100% after 1 month in the column, the P adsorption amount was about 180, 600, 1560, 4280, 6157, 7089, 7519, and 7925 mg/kg, respectively. The increment of the P adsorption amount was small if the oyster shell content was 60% or more, because the filter medium with more than 60% oyster shell content did not approach the saturation time by the P adsorption yet. The P adsorption amount for 60%, 80%, and 100% could be predicted as about 9702, 12,879, and 16,056 mg/kg, respectively. The largest amount of extracted P in the filter media with oyster shell after 30 days of P solution application was bound to Ca, followed by water soluble-P, Al--P, and Fe--P. Therefore, it was concluded that the adsorption amount of the phosphorus could be increased by adding the oyster shell to the filter medium. Also, it was concluded that adding the oyster shell to the filter medium in the constructed wetland was the scheme to extend the longevity of the constructed wetland by the phosphorus saturation, and using the oyster shell would be useful in aspect of economical efficiency and easiness. Especially, it would be the alternative proposal to reduce the environmental pollution in aspect of recycling wastes.

Adsorption↗