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Yield tables are used to identify trends in growing space efficiency (GSE) and to relate GSE to self-tolerance and intraspecific competition. The method is useful when data specifically collected for this purpose are not available. Plonski's normal yield tables for jack pine (Pinus banksiana Lamb.), paper birch (Betula papyrifera Marshall), trembling aspen (Populus tremuloides Michx.), and black spruce (Picea mariana (Mill.) B.S.P.) are used. An exponential volume-age function was partitioned into volume-area and area-age functions. The exponents of these two components form the B/D ratio, which is used to determine the mode of the stand at a given time, e.g., if B/D is <3/2, then the stand is in area occupation mode, and if B/D is >3/2, then the stand is in area exploitation mode. The dominant mode is the one most responsive to availability of growth resources, showing greater acceleration when resources are plentiful and more rapid deceleration when resources are scarce. Jack pine and paper birch are identified as area occupiers, whereas trembling aspen and black spruce are area exploiters and are therfore self-tolerant. Asymmetric competition was deemed to be present for paper birch throughout the life of the stand on site class I and for trembling aspen on all sites prior to senescence. Les tables de production sont utilisées pour identifier les tendances de l'efficacité à utiliser l'espace de croissance (EEC) et pour relier l'EEC à l'auto-tolérance et à la compétition intraspécifique. La méthode est utile lorsque des données spécifiquement récoltées à cette fin ne sont pas disponibles. Les tables normales de production de Plonski pour le pin gris (Pinus banksiana Lamb.), le bouleau à papier (Betula papyrifera Marshall), le peuplier faux-tremble (Populus tremuloides Michx.) et l'épinette noire (Picea mariana (Mill.) B.S.P.) ont été utilisées. Une fonction exponentielle reliant le volume à l'âge a été séparée en fonctions reliant le volume à la surface et la surface à l'âge. Les exposants de ces deux composantes forment le rapport entre B et D qui est utilisé pour déterminer le mode du peuplement à un temps donné; p. ex. si B/D est plus petit que 3/2, le peuplement est dans un mode d'occupation de la surface et, si B/D est plus grand que 3/2, le peuplement est dans un mode d'exploitation de la surface. Le mode dominant est celui qui réagit le plus à la disponibilité des ressources qui supportent la croissance; il est associé à une plus forte accélération quand les ressources sont abondantes et à une plus forte décélération lorsque les ressources sont rares. Le pin gris et le bouleau à papier sont identifiés comme des occupants de la surface alors que le peuplier faux-tremble et l'épinette noire sont des exploitants et sont, par conséquent, auto-tolérants. Nous avons jugé qu'une compétition asymétrique était présente dans le cas du bouleau à papier tout au long de la vie d'un peuplement établi sur une station de qualité I et, dans le cas du peuplier, sur toutes les stations avant la période de sénescence. [ABSTRACT FROM AUTHOR]

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Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Age estimates are essential for fisheries assessment and management, but deepwater (>200 m) fishes are often difficult to age using traditional techniques. Therefore, age-predictive epigenetic clocks were developed for a model deepwater reef fish, blackbelly rosefish Helicolenus dactylopterus, using two tissue types (fin clips and muscle; n = 61 individuals; 9−60 years) and Δ14C-validated consensus age estimates. The influence of biological information (length and sex) on epigenetic clock accuracy, and the potential for developing a multi-tissue clock, were also assessed. Bisulfite-converted restriction site-associated DNA sequencing (bsRADseq) was used to identify CpG sites (cytosines followed by guanines) exhibiting age-correlated DNA methylation, and epigenetic clocks showed strong agreement (R2 > 0.98) between predicted and consensus ages. Including length and sex data enhanced accuracy and precision (R2 > 0.99; mean absolute error < 1 year). Age-associated CpG sites were identified across tissues, but a multi-tissue clock performed poorly relative to single-tissue clocks. Overall, results demonstrate that accurate and precise epigenetic clocks can be developed for deepwater fishes, and the inclusion of biological information may enhance clock accuracy and precision. [ABSTRACT FROM AUTHOR]

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Epigenetics is revealing how "nature is nurtured", with environmental factors such as nutrition, environmental neurotoxicants, and psychological stress influencing DNA expression. In this current opinion paper, we argue that understanding the dynamic interplay between the genome acquired at conception and environmental exposures throughout life requires pregnancy and birth cohorts, and that greater Canadian national commitment to the infrastructure needed for sustaining such cohorts is warranted. We present a framework that is now being implemented in Alberta.

Absence of meal-induced insulin sensitization (AMIS) results in a predictable progression of dysfunctions, including postprandial hyperglycemia, compensatory hyperinsulinemia, resultant hyperlipidemia, increased oxidative stress, and obesity, progressing to syndrome X and diabetes. To one year of age, rats show a slow development of AMIS, but this can be potentiated by addition of a low-dose sucrose supplement to the diet. Provision of a synergistic antioxidant cocktail consisting of S-adenosylmethionine, vitamin E, and vitamin C (Samec) attenuates the rate and extent of development of AMIS in both normal aging animals and in aging animals on the sucrose diet. Adiposity, assessed from weighed regional fat masses and from bioelectrical impedance to estimate whole-body adiposity, correlated strongly with AMIS (r2 = 0.7-0.8). Rats given the sucrose supplement had accelerated AMIS and developed fasting hyperinsulinemia and postprandial hyperglycemia, hyperlipidemia, hyperinsulinemia, and adiposity. Samec completely compensated for the negative impact of this sucrose supplement and attenuated development of the associated dysfunctions. AMIS is explained by the HISS (hepatic insulin-sensitizing substance) hypothesis, which is outlined in the paper.

Little is know about forskolin binding in the rat brain during ontogenetic development. For this paper, we have characterized specific binding sites for [3H]-forskolin in cerebrocortical membranes from young (12-day-old) and adult (90-day-old) rats. High-affinity, as well as super-high-affinity, [3H]-forskolin binding sites were detected in samples from both age groups tested, and the binding parameters of these sites differed significantly. Whereas the number of high-affinity [3H]-forskolin binding sites was higher by about 50% in adult than in young rats, their affinity was markedly (about 4 times) lower. In the presence of AlF4-, the number high-affinity [3H]-forskolin binding sites in samples from young rats rose to the level determined in samples from adult animals, and the number of super-high-affinity sites considerably increased in both age groups. The different characteristics of [3H]-forskolin binding found in cerebrocortical membranes from young and adult rats may be closely related to markedly diminished adenyl cyclase activity in preparations from adult animals. Results of our experiments with suramin indicated that this drug may act as a competitive inhibitor of [3H]-forskolin binding.

Although changes in the soleus H-reflex (an electrical analog of the tendon jerk) with age have been examined in a number of studies, some controversy remains. Also, the effect of age on inhibitory reflexes has received little attention. The purpose of this paper was to examine some excitatory and inhibitory reflexes systematically in healthy human subjects having a wide range of ages. We confirmed that both the maximum H-reflex (Hmax) and the maximum M-wave (Mmax) (from direct stimulation of motor axons) decrease gradually with age. The decrease in Hmax was larger so the Hmax/Mmax ratio decreased dramatically with age. Interestingly, the modulation of the H-reflex during walking was essentially the same at all ages, suggesting that the pathways that modulate the H-reflex amplitude during walking are relatively well preserved during the aging process. We showed for the first time that the short-latency, reciprocal inhibitory pathways from the common peroneal nerve to soleus muscle and from the tibial nerve to the tibialis anterior muscle also decreased with age, when measured as a depression of ongoing voluntary activity. These results suggest that there may be a general decrease in excitability of spinal pathways with age. Thus, the use of age-matched controls is particularly important in assessing abnormalities resulting from disorders that occur primarily in the elderly.

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This commentary represents a dialogue on key aspects of disease-related malnutrition (DRM) from leaders and experts from academia, health across disciplines, and several countries across the world. The dialogue illuminates the problem of DRM, what impact it has on outcomes, nutrition care as a human right, and practice, implementation, and policy approaches to address DRM. The dialogue allowed the germination of an idea to register a commitment through the Canadian Nutrition Society and the Canadian Malnutrition Task Force in the UN/WHO Decade of Action on Nutrition to advance policy-based approaches for DRM. This commitment was successfully registered in October 2022 and is entitled CAN DReaM (Creating Alliances Nationally for Policy in Disease-Related Malnutrition). This commitment details five goals that will be pursued in the Decade of Action on Nutrition. The intent of this commentary is to record the proceedings of the workshop as a stepping stone to establishing a policy-based approach to DRM that is relevant in Canada and abroad. [ABSTRACT FROM AUTHOR]

The lack of estrogen in postmenopausal women not using hormone replacement therapy (HRT), compared with those using HRT, may reduce submaximal blood flow during exercise and result in an oxygen delivery limitation constraining oxygen uptake (VO2s have been changed to V in the abstract, but will appear correctly in the body of the paper.) kinetics. The adaptation of pulmonary VO2 (VO2p) during the transition to exercise in older women was examined in this study. Thirty-one healthy postmenopausal women (mean age, 61 ± 6 years), 15 not using HRT and 16 using HRT, performed repeated exercise transitions (6 min) on a cycle, to work rates corresponding to 80% of estimated ventilatory threshold (moderate-intensity exercise) and to Δ50 (heavy-intensity exercise). There was no difference in moderate-intensity VO2p between non-HRT (40 ± 9 s) and HRT (41 ± 9 s) women. Similarly, there was no difference in heavy-intensity VO2p between non-HRT (44 ± 8 s) and HRT (45 ± 8 s) women. Thus, HRT did not affect the slowing of VO2 kinetics of older women. [ABSTRACT FROM AUTHOR]

The article exploring the impact of COVID-19 on the willingness of older adults to participate in physiology research. Topics discussed include the coronavirus disease (COVID-19) pandemic was announced in March 2020 2020) and by June 2021; and the risk of serious illness or death from COVID-19 increases with chronological ageing, thus posing a significant threat to the health and well-being of older adults.

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Skeletal muscle is highly vascularized, with perfusion being tightly regulated to meet wide-ranging metabolic demands. For decades, the capillary supply has been explored mainly in terms of evaluating the capillary numbers and their function in the supply of oxygen and substrates and the removal of metabolic byproducts. This review will focus on recent discoveries concerning the role played by capillaries in facilitating other aspects of cell regulation and maintenance, in health and disease, as well as alterations during the aging process. [ABSTRACT FROM AUTHOR]

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Copyright of Canadian Journal of Civil Engineering is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Physiology & Pharmacology is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Physiology & Pharmacology is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Physiology & Pharmacology is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Animal Science is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Civil Engineering is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

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Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Zoology is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Botany is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Physiology & Pharmacology is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Dredging operations in European harbors for maintenance of navigable water depth produce vast amounts of harbor mud. Between 2005 and 2007, the second largest harbor construction project in Germany was designed as a pilot study, using dredged harbor mud as backfill material to avoid expensive deposition or ex situ treatment. During this project, strong surface deformations of the backfill highlighted the need for an improved assessment of undrained shear strength of naturally liquid harbor mud. The strength of harbor mud cannot be measured accurately under corresponding low in situ effective stress levels by standard laboratory tests. Therefore, a large-scale oedometer cell with a diameter of 22 cm was designed, providing the opportunity to perform vane shear measurements during consolidation. This study shows that East Harbor mud is a very sensitive, organogenic clay of extremely high plasticity, exhibiting very small undrained shear strength when compared with other cohesive soils. Both the peak and residual undrained shear strengths are shown to increase about 3%-4% per log-cycle increase in secondary compression time (days). Les opérations de dragage dans les ports européens, effectuées pour maintenir la profondeur nécessaire à la navigation, produisent de grandes quantités de boues de port. Entre 2005 et 2007, la construction du deuxième plus grand projet portuaire en Allemagne a été conçu comme une étude pilote sur l'utilisation de boues de dragage comme matériau de remblayage afin d'éviter la déposition coûteuse ou le traitement ex-situ. Durant ce projet, des fortes déformations de la surface du remblai ont fait remarquer le besoin d'une meilleure évaluation de la résistance au cisaillement non drainé des boues, qui sont naturellement liquides. La résistance des boues ne peut pas être mesurée précisément à des faibles niveaux de contrainte effective correspondant aux conditions in situ par des essais de laboratoire standards. Ainsi, une cellule odométrique de grande échelle, avec un diamètre de 22 cm, a été conçue afin d'obtenir des mesures scissométriques pendant la consolidation. Cette étude montre que la boue du port Est est une argile organogénique très sensible avec une plasticité extrêmement élevée, et qui présente une résistance au cisaillement non drainé très faible comparativement aux autres sols fins. Les résistances au cisaillement non drainé maximum et résiduelles ont augmenté de 3-4 % par log-cycle en temps de compression secondaire (jours). [ABSTRACT FROM AUTHOR]

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Aging is a multifactorial process that involves changes at the cellular, tissue, organ and the whole body levels resulting in decreased functioning, development of diseases, and ultimately death. Oxidative stress is believed to be a very important factor in causing aging and age-related diseases. Oxidative stress is caused by an imbalance between oxidants such as reactive oxygen species (ROS) and antioxidants. ROS are produced from the mitochondrial electron transport chain and many oxidative reactions. Methylglyoxal (MG) is a highly reactive dicarbonyl metabolite formed during glucose, protein and fatty acid metabolism. MG levels are elevated in hyperglycemia and other conditions. An excess of MG formation can increase ROS production and cause oxidative stress. MG reacts with proteins, DNA and other biomolecules, and is a major precursor of advanced glycation end products (AGEs). AGEs are also associated with the aging process and age-related diseases such as cardiovascular complications of diabetes, neurodegenerative diseases and connective tissue disorders. AGEs also increase oxidative stress. In this review we discuss the potential role of MG in the aging process through increasing oxidative stress besides causing AGEs formation. Specific and effective scavengers and crosslink breakers of MG and AGEs are being developed and can become potential treatments to slow the aging process and prevent many diseases. Le vieillissement est un processus multifactoriel qui implique des modifications au niveau des cellules, des tissus, des organes et du corps entier; ces modifications entraînent une diminution des fonctions, le développement de maladies, et ultimement la mort. Le stress oxydatif jouerait un rôle très important dans le vieillissement et les maladies liées à l’âge. Le stress oxydatif est causé par un déséquilibre entre des oxydants tels que les espèces réactives de l’oxygène (ROS) et les antioxydants. Les ROS sont produites par la chaîne de transport des électrons dans la mitochondrie ainsi que par de nombreuses réactions oxydantes. Le méthylglyoxal (MG) est un métabolite dicarbonyl hautement réactif formé durant le métabolisme du glucose, des protéines et des acides gras. Les taux de MG augmentent durant divers conditions, dont l’hypoglycémie. Une formation excessive de MG peut augmenter la production de ROS et causer un stress oxydatif. Le MG réagit avec les protéines, l’ADN et d’autres biomolécules, et est un précurseur important des produits terminaux avancés de glycation (AGE). Les AGE sont aussi associés au processus de vieillissement et aux maladies liées à l’âge, comme les complications cardiovasculaires du diabète, les maladies neurodégénératives et les maladies du tissu conjonctif. De plus, les AGE augmentent le stress oxydatif. Dans cette synthèse, nous discuterons du rôle potentiel du MG dans le processus de vieillissement, par l’augmentation de stress oxydatif et la formation d’AGE. Des piégeurs et des briseurs spécifiques et efficaces des liaisons croisées du MG et des AGE sont en développement, et pourraient devenir des traitements potentiels pour ralentir le processus de vieillissement et prévenir de nombreuses maladies. [ABSTRACT FROM AUTHOR]

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Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Applied Physiology, Nutrition & Metabolism is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)