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1.
Cell Rep ; 8(6): 1781-1792, 2014 Sep 25.
Article in English | MEDLINE | ID: mdl-25220459

ABSTRACT

Diet composition is a critical determinant of lifespan, and nutrient imbalance is detrimental to health. However, how nutrients interact with genetic factors to modulate lifespan remains elusive. We investigated how diet composition influences mitochondrial ATP synthase subunit d (ATPsyn-d) in modulating lifespan in Drosophila. ATPsyn-d knockdown extended lifespan in females fed low carbohydrate-to-protein (C:P) diets but not the high C:P ratio diet. This extension was associated with increased resistance to oxidative stress; transcriptional changes in metabolism, proteostasis, and immune genes; reduced protein damage and aggregation, and reduced phosphorylation of S6K and ERK in TOR and mitogen-activated protein kinase (MAPK) signaling, respectively. ATPsyn-d knockdown did not extend lifespan in females with reduced TOR signaling induced genetically by Tsc2 overexpression or pharmacologically by rapamycin. Our data reveal a link among diet, mitochondria, and MAPK and TOR signaling in aging and stresses the importance of considering genetic background and diet composition in implementing interventions for promoting healthy aging.


Subject(s)
Drosophila Proteins/metabolism , Longevity/physiology , Mitochondria/metabolism , Mitochondrial Proton-Translocating ATPases/metabolism , TOR Serine-Threonine Kinases/metabolism , Animals , Cell Cycle Proteins/metabolism , Diet, Carbohydrate-Restricted , Drosophila , Drosophila Proteins/antagonists & inhibitors , Drosophila Proteins/genetics , Female , Gene Expression Regulation , Hormone Antagonists/pharmacology , Longevity/drug effects , Metabolic Networks and Pathways/drug effects , Mifepristone/pharmacology , Mitochondrial Proton-Translocating ATPases/antagonists & inhibitors , Mitochondrial Proton-Translocating ATPases/genetics , Oxidative Stress/drug effects , Phosphorylation/drug effects , RNA Interference , Signal Transduction/drug effects , Sirolimus/pharmacology
2.
J Gerontol A Biol Sci Med Sci ; 69(8): 945-54, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24149429

ABSTRACT

Botanicals possess numerous bioactivities, and some promote healthy aging. Dietary macronutrients are major determinants of life span. The interaction between botanicals and macronutrients that modulates life span is not well understood. Here, we investigated the effect of a cranberry-containing botanical on life span and the influence of macronutrients on the longevity-related effect of cranberry in Drosophila. Flies were supplemented with cranberry on three dietary conditions: standard, high sugar-low protein, and low sugar-high protein diets. We found that cranberry slightly extended life span in males fed with the low sugar-high protein diet but not with other diets. Cranberry extended life span in females fed with the standard diet and more prominently the high sugar-low protein diet but not with the low sugar-high protein diet. Life-span extension was associated with increased reproduction and higher expression of oxidative stress and heat shock response genes. Moreover, cranberry improved survival of sod1 knockdown and dfoxo mutant flies but did not increase wild-type fly's resistance to acute oxidative stress. Cranberry slightly extended life span in flies fed with a high-fat diet. These findings suggest that cranberry promotes healthy aging by increasing stress responsiveness. Our study reveals an interaction of cranberry with dietary macronutrients and stresses the importance of considering diet composition in designing interventions for promoting healthy aging.


Subject(s)
Aging/drug effects , Longevity/physiology , Plant Extracts/pharmacology , Vaccinium macrocarpon , Aging/physiology , Animals , Dietary Supplements , Drosophila , Energy Intake/physiology , Female , Humans , Longevity/drug effects , Male , Oxidative Stress , Superoxide Dismutase/physiology , Superoxide Dismutase-1
3.
Age (Dordr) ; 35(1): 69-81, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22083438

ABSTRACT

Resveratrol, a polyphenolic compound, has been shown to extend lifespan in different organisms. Emerging evidence suggests that the prolongevity effect of resveratrol depends on dietary composition. However, the mechanisms underlying the interaction of resveratrol and dietary nutrients in modulating lifespan remain elusive. Here, we investigated the effect of resveratrol on lifespan of Drosophila melanogaster fed diets differing in the concentrations of sugar, yeast extract, and palmitic acid representing carbohydrate, protein, and fat, respectively. Resveratrol at up to 200 µM in diets did not affect lifespan of wild-type female flies fed a standard, restricted or high sugar-low protein diet, but extended lifespan of females fed a low sugar-high protein diet. Resveratrol at 400 µM extended lifespan of females fed a high-fat diet. Lifespan extension by resveratrol was associated with downregulation of genes in aging-related pathways, including antioxidant peroxiredoxins, insulin-like peptides involved in insulin-like signaling and several downstream genes in Jun-kinase signaling involved in oxidative stress response. Furthermore, resveratrol increased lifespan of superoxide dismutase 1 (sod1) knockdown mutant females fed a standard or high-fat diet. No lifespan extension by resveratrol was observed in wild-type and sod1 knockdown males under the culture conditions in this study. Our results suggest that the gender-specific prolongevity effect of resveratrol is influenced by dietary composition and resveratrol promotes the survival of flies by modulating genetic pathways that can reduce cellular damage. This study reveals the context-dependent effect of resveratrol on lifespan and suggests the importance of dietary nutrients in implementation of effective aging interventions using dietary supplements.


Subject(s)
Aging/drug effects , Caloric Restriction , Drosophila melanogaster/physiology , Longevity/drug effects , Oxidative Stress/physiology , Stilbenes/pharmacology , Aging/physiology , Animals , Antioxidants/pharmacology , Diet, High-Fat , Female , Male , Resveratrol , Ribonucleotide Reductases/antagonists & inhibitors , Signal Transduction
4.
Exp Gerontol ; 45(3): 243-51, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20080168

ABSTRACT

Reducing oxidative damage is thought to be an effective aging intervention. Açai, a fruit indigenous to the Amazon, is rich in phytochemicals that possesses high anti-oxidant activities, and has anti-inflammatory, anti-cancer and anti-cardiovascular disease properties. However, little is known about its potential anti-aging properties especially at the organismal level. Here we evaluated the effect of açai pulp on modulating lifespan in Drosophila melanogaster. We found that açai supplementation at 2% in the food increased the lifespan of female flies fed a high fat diet compared to the non-supplemented control. We measured transcript changes induced by açai for age-related genes. Although transcript levels of most genes tested were not altered, açai increased the transcript level of l(2)efl, a small heat-shock-related protein, and two detoxification genes, GstD1 and MtnA, while decreasing the transcript level of phosphoenolpyruvate carboxykinase (Pepck), a key gene involved in gluconeogenesis. Furthermore, açai increased the lifespan of oxidative stressed females caused by sod1 RNAi. This suggests that açai improves survival of flies fed a high fat diet through activation of stress response pathways and suppression of Pepck expression. Açai has the potential to antagonize the detrimental effect of fat in the diet and alleviate oxidative stress in aging.


Subject(s)
Arecaceae , Dietary Fats/administration & dosage , Drosophila melanogaster/physiology , Aging , Animals , Female , Fruit , Gene Expression Profiling , Male , Metallothionein/genetics , Oxidative Stress , Phosphoenolpyruvate Carboxykinase (GTP)/genetics
5.
Magn Reson Med ; 53(4): 858-65, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15799053

ABSTRACT

One can acquire high-resolution pulmonary and cardiac images in live rodents with MR microscopy by synchronizing the image acquisition to the breathing cycle across multiple breaths, and gating to the cardiac cycle. The precision with which one can synchronize image acquisition to the motion defines the ultimate resolution limit that can be attained in such studies. The present work was performed to evaluate how reliably the pulmonary and cardiac structures return to the same position from breath to breath and beat to beat across the prolonged period required for MR microscopy. Radiopaque beads were surgically glued to the abdominal surface of the diaphragm and on the cardiac ventricles of anesthetized, mechanically ventilated rats. We evaluated the range of motion for the beads (relative to a reference vertebral bead) using digital microradiography with two specific biological gating methods: 1) ventilation synchronous acquisition, and 2) both ventilation synchronous and cardiac-gated acquisitions. The standard deviation (SD) of the displacement was < or =100 microm, which is comparable to the resolution limit for in vivo MRI imposed by signal-to-noise ratio (SNR) constraints. With careful control of motion, its impact on resolution can be limited. This work provides the first quantitative measure of the motion-imposed resolution limits for in vivo imaging.


Subject(s)
Cardiovascular Physiological Phenomena , Diaphragm/physiology , Magnetic Resonance Imaging/methods , Myocardial Contraction/physiology , Animals , Diaphragm/diagnostic imaging , Male , Radiography , Rats , Rats, Inbred F344 , Reproducibility of Results , Tungsten
6.
Int J Radiat Oncol Biol Phys ; 58(5): 1562-9, 2004 Apr 01.
Article in English | MEDLINE | ID: mdl-15050337

ABSTRACT

PURPOSE: To assess the usefulness of hyperpolarized helium (3He) MRI, including apparent diffusion coefficient measurements, in the detection and evaluation of radiation-induced lung injury in rats. METHODS AND MATERIALS: Female Fischer-344 rats were treated to the right lung with fractionated dose of 40 Gy (5 x 8 Gy) using 4-MV photons. Conventional proton (1H) and hyperpolarized (3He) MRI were used to image the lungs 3-6 months after radiation treatment. Apparent diffusion coefficient (ADC) maps of hyperpolarized 3He in the lungs were calculated using a nonlinear, least-squares fitting routine on a pixel-by-pixel basis. After imaging, lungs were processed for histologic assessment of damage. RESULTS: The effect of radiation was time dependent with progressive right lung damage ranging from mild to moderate at 3 months to severe fibrosis with structural deformation at 6 months after radiation. There was a significant decrease in the apparent diffusion coefficient of hyperpolarized 3He gas in radiation-treated lungs. Areas of decreased ADC in the lungs correlated with fibrosis shown by histology. CONCLUSION: This is the first study to show that hyperpolarized 3He MRI can detect radiation-induced lung injury noninvasively. Reduced hyperpolarized 3He ADC values postradiation likely reflect reduced alveolar volumes associated with fibrosis of the interstitium. Future studies at earlier time points may determine whether this noninvasive imaging technique can detect lung damage before clinical symptoms. Development of this new approach of magnetic resonance lung imaging in the rat model of radiation-induced lung injury will increase the ability to develop appropriate algorithms and more accurate models of the normal tissue complication probability.


Subject(s)
Helium , Lung/radiation effects , Magnetic Resonance Imaging/methods , Protons , Radiation Injuries, Experimental/diagnosis , Radiation Injuries/diagnosis , Animals , Female , Least-Squares Analysis , Lung/pathology , Radiation Injuries/pathology , Radiation Injuries, Experimental/pathology , Rats , Rats, Inbred F344
7.
Magn Reson Med ; 47(2): 314-21, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11810675

ABSTRACT

A fundamental problem associated with using the conventional electrocardiograph (ECG) to monitor a subject's cardiac activity during magnetic resonance imaging (MRI) is the distortion of the ECG due to electromagnetic interference. This problem is particularly pronounced in MR microscopy (MRI of small animals at microscopic resolutions (< 0.03 mm(3))) because the strong, rapidly-switching magnetic field gradients induce artifacts in the animal's ECG that often mimic electrophysiologic activity, impairing the use of the ECG for cardiac monitoring and gating purposes. The fiber-optic stethoscope system offers a novel approach to measuring cardiac activity that, unlike the ECG, is immune to electromagnetic effects. The fiber-optic stethoscope is perorally inserted into the esophagus of small animals to optically detect pulsatile compression of the esophageal wall. The optical system is shown to provide a robust cardiac monitoring and gating signal in rats and mice during routine cardiac MR microscopy.


Subject(s)
Electrocardiography/instrumentation , Esophagoscopy , Fiber Optic Technology , Heart Atria/anatomy & histology , Heart Ventricles/anatomy & histology , Magnetic Resonance Imaging/instrumentation , Microscopy/instrumentation , Stethoscopes , Animals , Heart Rate/physiology , Hemodynamics/physiology , Mice , Mice, Inbred C57BL , Myocardial Contraction/physiology , Optical Fibers , Rats
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