Oxidative stress and neurotrophic support decline seem to be crucially involved in brain aging. Emerging evidences indicate the pro-oxidant methylglyoxal (MG) as a key player in the age-related dicarbonyl stress and molecular damage within the central nervous system. Although exercise promotes the overproduction of reactive oxygen species, habitual exercise may retard cellular aging and reduce the age-dependent cognitive decline through hormetic adaptations, yet molecular mechanisms underlying beneficial effects of exercise are still largely unclear. In particular, whereas adaptive responses induced by exercise initiated in youth have been broadly investigated, the effects of chronic and moderate exercise begun in adult age on biochemical hallmarks of very early senescence in mammal brains have not been extensively studied. This research investigated whether a long-term, forced and moderate running initiated in adult age may affect the interplay between the redox-related profile and the oxidative-/MG-dependent molecular damage patterns in CD1 female mice cortices; as well, we investigated possible exercise-induced effects on the activity of the brain derived neurotrophic factor (BDNF)-dependent pathway. Our findings suggested that after a transient imbalance in almost all parameters investigated, the lately-initiated exercise regimen strongly reduced molecular damage profiles in brains of adult mice, by enhancing activities of the main ROS- and MG-targeting scavenging systems, as well as by preserving the BDNF-dependent signaling through the transition from adult to middle age.
Citation: Falone S, D'Alessandro A, Mirabilio A, Petruccelli G, Cacchio M, Di Ilio C, et al. (2012) Long Term Running Biphasically Improves Methylglyoxal-Related Metabolism, Redox Homeostasis and Neurotrophic Support within Adult Mouse Brain Cortex. PLoS ONE 7(2): e31401. https://doi.org/10.1371/journal.pone.0031401
Editor: Alejandro Lucia, Universidad Europea de Madrid, Spain
Received: November 17, 2011; Accepted: January 8, 2012; Published: February 8, 2012
Copyright: © 2012 Falone et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was funded by the Foundation of the Cassa di Risparmio dell'Aquila. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Aging is associated with the accumulation of reactive oxygen species (ROS)-damaged biomolecules and this phenomenon may be due to either an increased production of ROS or to a decreased efficiency of antioxidant defenses; this condition may facilitate the onset of oxidative stress, thus promoting structural and functional alterations –. The central nervous system (CNS) is highly susceptible to the oxidative stress and to senescence, mainly due to the high oxidative metabolism and to the poor self-repairing capacities of post-mitotic neuronal populations; in addition, high levels of redox-active metal ions, relatively low antioxidant defenses, and the presence of membranes highly prone to peroxidative attack also account for the high vulnerability of the brain towards oxidative damage , . Coherently, many studies have observed in aged brains increased levels of oxidatively-modified lipids and proteins, and these molecular alterations are thought to play major roles in the pathogenesis of several age-related neurodegenerations .
Brain senescence and many age-related diseases are also commonly associated with increased levels of glycative-modified macromolecules. Methylglyoxal (MG), a pro-apoptotic and pro-oxidant dicarbonyl compound, is one of the main responsible for glycating reactions towards proteins and lipids within aged tissues, where MG reacts predominantly with arginine residues to form, among other derivatives, hydroimidazolones and arg-pyrimidine –. As MG is endogenously formed mainly as a byproduct of carbohydrate and lipid metabolism, organisms have developed the glyoxalase system, an ubiquitous detoxification pathway protecting cells from MG-related cytotoxicity . Many researchers have reported age-dependent increases in the levels of proteins structurally and functionally modified by MG, and this is essentially due to either a reduced efficiency of the glyoxalase system or to an increase of its glycolytic precursors . MG impairs cell redox homeostasis by inhibiting glyoxalases and by depleting the intracellular pool of reduced glutathione (GSH), which is an essential co-factor for glyoxalase 1 and for crucial antioxidant enzymes, such as the glutathione peroxidase (GPX) , . As discussed by Kuhla and colleagues , MG cytotoxicity may play a very important role in brain aging. Our group has demonstrated that MG is strongly toxic to nervous cells, in which it triggers both a pro-oxidant shift in the cellular milieu and pro-inflammatory responses . In addition, our group has shown that MG alters the expression levels of both brain derived neurotrophic factor (BDNF) and its high affinity tyrosinekinase B receptor (TrkB), thus eventually affecting important neuronal functions .
Although physical exercise promotes ROS overproduction , a sedentary lifestyle is becoming increasingly known as an accelerating factor towards unhealthy aging . This apparent paradox could be explained by taking into account that the habitual exposure to exercise bouts triggers hormetic responses by inducing many biochemical and molecular adaptations, such as the enhancement of crucial neurotrophic support and antioxidant defenses, thus improving the resistance towards oxidative stress –. Several authors have also reported that a regular and moderate physical exercise reduces the age-dependent cognitive decline and preserves abilities in learning and memory tasks –. These findings encourage a growing number of sedentary individuals of adult and mature age to initiate physical exercise through which weight status, cardiovascular function, metabolic and brain health could be significantly controlled or preserved.
However, whereas hormetic responses induced by exercise initiated in youth have been broadly investigated, the effects of chronic and moderate exercise begun in adult and mature age on biochemical hallmarks of very early senescence in mammal brains have not been extensively studied, and only sporadic literature is available , . Moreover, despite the large research interest in this field, no scientific evidence has been provided so far about the role of physical exercise in regulating the accumulation of brain MG-related molecular damage. Hence, physiological changes and responses induced by exercise within CNS might be explored by conceiving an interplay among MG-related metabolism and damage, antioxidative pathways and neurotrophic support. Indeed, the BDNF-dependent signaling pathways, such as the phosphorilated cAMP response element binding (p-CREB) transcriptional activator and the phosphorilated TrkB have been suggested to be involved in positive adaptations triggered by exercise within brain , –.
On this basis, we performed a time-course analysis aimed at assessing whether a program of moderate and regular exercise could affect the interplay between redox-related profiles and oxidative-/MG-dependent molecular damage patterns in brain cortices of mice undergoing the transition from adult to middle age. Several age-dependent cognitive declines have been reported during this biological time period , which is roughly similar to the transition through the mature age in humans , therefore this age range may be adequate to investigate exercise-dependent central effects. In addition, we investigated the possible interactions of the BDNF-activated pathway with the above mentioned processes. Our experimental design involved non spontaneous physical activity since some preeminent authors have argued that forced exercise protocols are more similar to human exercise practise and less likely biased depending on genetic differences between good and poor runners , .
Effects of age and exercise on ponderal state and food intake
No significant main effect of age was detected on body weight or food consumption (not shown). Treadmill running induced no significant alterations in ponderal state or appetence behaviour (not shown).
Effects of age and exercise on oxidative damage and antioxidant/redox status
The colorimetric assay did not reveal any significant age-dependent change in cortical thiobarbituric acid reactive substances (TBARS) concentrations (Fig. 1a). On the contrary, the content of oxidized proteins increased in an age-dependent way (P<0.001, S4 vs S2) (Fig. 1b). Significant increases in TBARS (Fig. 1a) and protein carbonyl content (PCC) (Fig. 1b) were detected in brain cortices after two months of exercise, when compared to sedentary animals (P<0.001, E2 vs S2). Conversely, four months of exercise did not significantly elevate cortical TBARS levels (Fig. 1a), whereas PCC content was significantly reduced in E4, when compared to S4 (Fig. 1b, P<0.01).
Thiobarbituric acid-reactive substances (TBARS, panel a) levels and protein carbonyl content (PCC, panel b) in cortices of mice undergoing a two- or four-month moderate and regular treadmill-based exercise program (E2 or E4, respectively); age-matched sedentary animals (S2, S4) were used as controls (n = 6 per group). No significant age-dependent change was observed in cortical TBARS concentrations (S4 vs S2), while two months of exercise elevated significantly TBARS amounts (E2 vs S2). Four-month exercised and unexercised mice showed similar TBARS levels (E4 vs S4). The PCC increased in an age-dependent manner (S4 vs S2). Two months of exercise elevated PCC, in comparison to sedentary animals (E2 vs S2). Conversely, PCC content was significantly reduced in four-month-exercised mice, when compared to age-matched unexercised animals (E4 vs S4). Values were given as means ± std. dev. The level of statistical significance was computed by using two-way ANOVA and post-hoc Newman-Keuls test: *** P<0.001; ** P<0.01. Experiments were performed in triplicate.
Spectrophotometric analyses of the catalytic activities of the main antioxidant enzymes revealed no major age-dependent variations of total superoxide dismutase (tSOD) and catalase (CAT) specific activities (Fig. 2a and b), whereas a significant age-dependent increase in GPX activity was observed (P<0.001, S4 vs S2) (Fig. 2c). Significant age-related changes in glutathione reductase (GR) activity could not be detected (Fig. 3a). After two months of regular exercise, marked reductions in brain cortex enzymatic activities of tSOD, CAT and GPX (P<0.05, E2 vs S2) were revealed (Fig. 2a, b and c), together with a marked increase in GR activity (P<0.001, E2 vs S2) (Fig. 3a). On the contrary, four-month exercise caused a significant enhancement of specific activities of tSOD (P<0.05) and CAT (P<0.01), in comparison to the age-matched sedentary group (Fig. 2a and b). No statistical differences were found when comparing GPX and GR specific activities between E4 and S4 (Fig. 2c and 3a).
Specific activities of superoxide dismutase (SOD) (panel a), catalase (CAT) (panel b) and glutathione peroxidase (GPX) (panel c) in brain cortices of adult CD1 female mice undergoing a two- or four-month moderate and regular treadmill-based exercise program (E2 or E4, respectively); age-matched sedentary animals (S2, S4) were used as controls (n = 6 per group). No major age-dependent variation of tSOD and CAT specific activities was revealed; however, a significant increase in GPX activity was detected when comparing S4 and S2. Two-month physical activity reduced specific activities of tSOD, CAT and GPX catalytic capacities (E2 vs S2), whereas four-month exercise triggered a significant elevation of tSOD and CAT (E4 vs S4). Values were given as means ± std. dev. The level of statistical significance was computed by using two-way ANOVA and post-hoc Newman-Keuls test: * P<0.05; ** P<0.01; *** P<0.001. Experiments were performed in triplicate.
Specific activity of glutathione reductase (GR) (panel a) and balance of the glutathione redox couple (panel b) in brain cortices of adult CD1 female mice undergoing a two- or four-month moderate and regular treadmill-based exercise program (E2 or E4, respectively); age-matched sedentary animals (S2, S4) were used as controls (n = 6 per group). No significant age-dependent change in GR activity could be observed (S4 vs S2). Two-month physical activity caused a marked increase in GR activity (E2 vs S2), while no statistical differences were found when comparing GR specific activities between E4 and S4 groups. No significant age-dependent change was observed in the total vs oxidized GSH ratio (S4 vs S2). Both two and four months of exercise caused a marked decrease of the total vs disulfide glutathione ratio (E2 vs S2 and E4 vs S4). Values were given as means ± std. dev. The level of statistical significance was computed by using two-way ANOVA and post-hoc Newman-Keuls test: *** P<0.001. Experiments were performed in triplicate.
The colorimetric assessment of the status of the glutathione redox couple revealed no significant age-dependent changes in the cortical total vs oxidized glutathione ratios (Fig. 3b). After both two and four months of exercise, our analysis revealed a remarkable decrease of total vs disulfide glutathione ratios (P<0.001, E2 vs S2 and E4 vs S4) (Fig. 3b).
Effects of age and exercise on MG-related damage and detoxification system
The arg-pyrimidine-directed immunoblot analysis showed a very strong age-dependent elevation of the levels of MG-damaged proteins within mice brain cortices (P<0.001, S4 vs S2) (Fig. 4a). Marked age-dependent increases in glyoxalase 1 (GLO1) and glyoxalase 2 (GLO2) specific activities were also observed when comparing S4 to S2 (P<0.001) (Fig. 4b and c). Our analyses showed a slight, but not significant, increase in the levels of MG-damaged proteins within cortices of two-month-exercised mice, together with a striking decrease (P<0.001) of MG-dependent protein damage in brain cortices of four-month-trained mice (Fig. 4a). GLO1 specific activity resulted elevated after four months of running protocol (P<0.001, E4 vs S4), whereas GLO2 catalytic activity was higher as a result of two months of exercise (P<0.001, E2 vs S2) (Fig. 4b and c).
Immunoreactivity levels against arg-pyrimidine (arg-pyr, panel a) and specific activities of glyoxalase 1 (GLO1, panel b) and glyoxalase 2 (GLO2, panel c) in brain cortices of adult CD1 female mice undergoing a two- or four-month moderate and regular treadmill-based exercise program (E2 or E4, respectively); age-matched sedentary animals (S2, S4) were used as controls (n = 6 per group). Dot blot assays revelead an age-dependent increase in the levels of MG-damaged proteins (S4 vs S2). No significant variation of MG-damaged polypeptides was detected after two months of exercise (E2 vs S2), while immunoreactivity against MG-modified arginine residues decreased markedly after four-month physical activity, with respect to age-matched unexercised mice (E4 vs S4). Immunosignals were normalized against the Coomassie Brilliant Blue (CBB)-based total protein staining. In the panel a, right section, representative PVDF-dot immunoblots of three independent experiments are reported, together with analyses for total protein loading performed by the ImageJ software. Both GLO1 and GLO2 specific activities increased in an age-dependent manner (S4 vs S2). The exercise program elevated GLO2 activity exclusively after two months of regular exercise (E2 vs S2), whereas GLO1 specific activity was increased only after four months of physical activity (E4 vs S4). Values were given as means ± std. dev. The level of statistical significance was computed by using two-way ANOVA and post-hoc Newman-Keuls test: * P<0.05; *** P<0.001. Experiments were performed in triplicate.
Effects of age and exercise on BDNF-dependent neurotrophic support
Significant age-dependent reductions in the protein levels of BDNF, p-CREB (Fig. 5a and b) and p-TrkB (Fig. 6) could be immunodetected in sedentary animals (P<0.05 for BDNF and p-CREB; P<0.001 for p-TrkB). Two months of exercise caused a conspicuous decrease in the protein expression of BDNF (P<0.01), p-CREB (P<0.001) (Fig. 5a and b, respectively) and p-TrkB (P<0.001) (Fig. 6), in comparison with age-matched sedentary mice. In contrast, protein levels of BDNF, p-CREB (Fig. 5a and b) and its activated high affinity receptor (Fig. 6) were significantly elevated after four months of regular running, with respect to age-matched unexercised animals (P<0.001 for both BDNF and p-CREB; P<0.01 for p-TrkB).
Western immunoblot against the brain derived neurotrophic factor (BDNF) (panel a) and the phosphorilated cAMP response element binding (p-CREB) transcriptional activator (panel b) in brain cortices of adult CD1 female mice undergoing a two- or four-month moderate and regular treadmill-based exercise program (E2 or E4, respectively); age-matched sedentary animals (S2, S4) were used as controls (n = 6 per group). A significant age-dependent variation in BDNF protein expression was detected (S4 vs S2). BDNF levels were also significantly reduced in two-month exercised mice (E2 vs S2), yet strongly enhanced in four-month exercised mice (E4 vs S4), with respect to age-matched counterparts. Significant age-dependent reductions in the protein levels of p-CREB (S4 vs S2). Two months of exercise caused a conspicuous decrease in p-CREB protein levels (E2 vs S2), whereas p-CREB protein amounts increased after four months of regular running (E4 vs S4), with respect to age-matched unexercised mice. Immunosignals were normalized against the housekeeping β-actin. Representative PVDF-western immunoblots of three independent experiments are reported. Values were given as means ± std. dev. The level of statistical significance was computed by using two-way ANOVA and post-hoc Newman-Keuls test: * P<0.05; ** P<0.01; *** P<0.001. Experiments were performed in triplicate.
Western immunoblot against the activated high affinity tyrosinekinase B receptor (p-TrkB) in brain cortices of adult CD1 female mice undergoing a two- or four-month moderate and regular treadmill-based exercise program (E2 or E4, respectively); age-matched sedentary animals (S2, S4) were used as controls (n = 6 per group). Significant age-dependent reductions in the protein amounts of p-TrkB (S4 vs S2) were detected. Two months of exercise caused a conspicuous decrease in the expression levels of p-TrkB, with respect to age-matched unexercised mice (E2 vs S2), whereas protein levels of the activated receptor were significantly elevated after four-month physical activity, when compared to sedentary animals (E4 vs S4). Immunosignals were normalized against the housekeeping β-actin. In the lower sections, representative PVDF-western immunoblots of three independent experiments are reported. Values were given as means ± std. dev. The level of statistical significance was computed by using two-way ANOVA and post-hoc Newman-Keuls test: ** P<0.01; *** P<0.001. Experiments were performed in triplicate.
Some authors demonstrated that early biomolecular and functional impairments occur in mice brains during the transition from adult to middle age , . Coherently, we found important alterations in mouse brain cortices within such time period. In fact, though no major sign of ongoing redox imbalance was detected (Figs. 1a, 2a and b, 3a and b), an age-dependent increase in GPX activity was observed (Fig. 2c). GPX-mediated adaptive responses towards age-related ROS overproduction were previously found by some of us in muscles, livers and lungs of aged rats , . Mammalian GPX is known to act as the first line of defence against H2O2 within cells, having greater affinity for H2O2 than CAT . Since the ratios of interconvertible forms of redox couples are linked to the cellular redox state, and given the fact that reduced glutathione is an essential co-factor for crucial antioxidant enzymes, the observed lack of age-dependent variations in the total vs oxidized glutathione ratio confirmed that no major redox imbalance occurred within the mouse cortex during the time period investigated. This may imply that antioxidant defense systems and the redox status are adequately efficient and responsive to manage the bland oxidative challenge occurring within brain cortex during the transition from adult to middle age. This could also explain why we did not detect any age-dependent elevation in the levels of lipid peroxidative damage within brain cortex (Fig. 1a), a region particularly prone to free radical attack . Conversely, we found major age-dependent changes in the MG-related protein damage profile, as well as in the specific activities of MG-targeting catabolic enzymes within brain cortices of sedentary animals (Fig. 4a, b and c). MG is one of the most important dicarbonyl precursor of stable advanced glycation end products (AGEs), which are thought to be detrimental factors in the aging process , . The formation of AGEs is often associated with the endogenous production of protein carbonyls , , and this may explain the observed age-dependent elevation of the cortical PCC in sedentary mice (Fig. 1b). Increased protein oxidation is thought to be linked to the age-dependent cerebral functional decline. Indeed, elevated protein carbonyls have been detected in hippocampi of aged rats with memory impairments . Our findings indicated that MG and AGEs may be strictly associated with the transition from adult to middle age within mouse brains, although we revealed an attempt to counteract MG-dependent damages through the activation of the glyoxalase system, which is the main cellular route by which MG is catabolized .
In the time period analyzed, significant age-dependent reductions in the protein expression of BDNF, p-CREB (Fig. 5a and b) and activated high affinity TrkB receptor (Fig. 6) were also found in sedentary mice. This enforces the notion that a decline in the activity of the BDNF signaling may be linked to the transition from adult to middle age within brains , . Our findings further confirmed the important link between elevated MG-induced molecular damages and the decline in neurotrophic support, as previously suggested by some of us .
As a first summary, our data confirmed that the transition from adult to middle age may be a critical biological period in which early hallmarks of tissue senescence can be detected within the mouse brain cortex. The intriguing link between such alterations and the initial age-related decline in cognitive abilities  remains to be investigated.
The regular running protocol did not impose excessive stress on the animals, neither did the treatment harm critical health parameters of the animals, as shown by the unchanged ponderal state and appetence behaviour.
Consistently with other reports , our findings suggested that one of the hormetic responses triggered in rodent brains by repeated exposures to moderate exercise may be the activation of the major ROS scavenging defense systems. In fact, the four-month exercise program initiated in adult age significantly enhanced the enzymatic activities of important ROS-scavenging systems (SOD and CAT) (Fig. 2a and b). A limited number of studies have investigated the effects of exercise on the major antioxidant enzymatic protection in rodent brains , ; results are often controversial due to the use of different animal species and exercise paradigms, as well as to the investigation of different biological time periods and CNS regions. Our results are in good accordance with findings reported by Devi and Kiran , who demonstrated a high responsivity of CAT and SOD in cortices of adult rats towards the oxidative challenge elicited by 12 weeks swimming training. Our results are not in accordance with data reported by Somani and co-workers , who showed unchanged SOD and GPX activities within brain cortices of rodents undergoing long-term running; however, the authors used a different biological model (male rat) and the age of the animals was not even mentioned; in addition, Somani and co-workers  used a progressively increasing angle of inclination of the treadmill belt, thus altering the actual work load of the training program, which is a very different type of exercise with respect to that used this study.
As extensively reviewed by Ji , most genes coding for antioxidant enzymes contain regulatory sequences in their promoter and intron regions that can interact with redox-sensitive transcription factors, such as the nuclear factor-κB (NF-κB) and activator protein 1 (AP-1). In coherence with the observed enhancement of the major ROS-scavenging systems, the long-term lifestyle intervention inhibited the age-dependent elevation of carbonylated proteins (Fig. 1b). Our findings are not in accordance with results provided by Toldy and co-workers . In their paper, the authors reported no significant changes in brain protein oxidation levels and nuclear factor-κB (NF-κB)/activated protein-1 (AP-1) DNA binding activities in rodents undergoing a training program, in disagreement with the idea of an exercise-induced decrease in SOD activity. However, the experimental design and procedures used were rather different than those we followed. First of all, Toldy and co-workers  used a different experimental model (rat). Furthermore, the authors used rodents much younger than our mice, thus exploring a very different time period. Moreover, the exercise protocol was based on a 6-week swimming activity; the last difference appears very important when considering what the authors stated in their discussion (“…running has a more powerful effect than swimming…”) .
In accordance with our findings, Radak and colleagues  observed that long-term swimming lowered the rat brain content of oxidized proteins through the possible upregulation of the proteasome activity; however, the role played by the proteasome in mediating the training-induced central effects is still largely unclear . The four-month exercise regimen did not cause any significant change in brain TBARS levels (Fig. 1a) and this could imply that, as already discussed, the mouse brain cortex is still adequately protected against the ROS-induced lipid peroxidative damage in the age range under investigation. Our study revealed a remarkable decrease in GSH levels within cortices of four-month exercised animals (Fig. 3b), probably as a consequence of the observed enhancement of the glyoxalase system activity (Fig. 4b), since the reduced form of glutathione is an essential cofactor of GLO1. In coherence with the observed improvement of MG-targeting enzymatic catabolism, we found a remarkable reduction in the levels of MG-modified proteins in cortices of four-month exercised mice (Fig. 4a). To the best of our knowledge, this is the first experimental evidence demonstrating the preventing effect elicited by a habitual and moderate exercise on the age-related accumulation of MG-damaged proteins in mammal CNS. The value of our observation may be worthy of note as elevated amounts of AGEs and MG-modified macromolecules seem to be common hallmarks in the progression of aging, as well as of many age-associated diseases , .
As already discussed, impaired neurotrophin signaling cascades are known to be linked to aging and to several age-related cognitive dysfunctions . Interestingly, the long-term running markedly improved the neurotrophic support profile within brain cortices. Indeed, we found substantially higher protein expression levels of BDNF, p-CREB (Fig. 5a and b), and p-TrkB (Fig. 6) in four-month treadmill-trained animals, with respect to age-matched sedentary rodents. Other authors suggested that the BDNF-activated pathway could be crucially involved in neuroactive effects of exercise , –. Our findings seem to indicate that the BDNF-dependent pathway can still be upregulated within brain cortex even when the long-term exercise is initiated lately in the adult age. Since BDNF is an important modulator of the molecular and enzymatic machinery which protects cells from oxidative stress , the upregulated BDNF-dependent signaling may be linked to the increased expression of antioxidant enzymes we observed in four-month-exercised mice, with respect to age-matched sedentary animals.
Taken together, these findings suggested that a four-month moderate exercise program, even when it is initiated in adult age, triggered multiple hormetic responses within the mouse brain cortex through, among others, the activation of molecular machinery aimed at repairing/removing MG-dependent biochemical damages.
Another novel finding arising from this research was that the regular and moderate exercise program elicited a biphasic response in mouse brain cortices. In particular, in two-month exercised mice we found increased cortical levels of TBARS and PCC (Fig. 1a and b), as well as declines in the CAT, SOD and GPX specific activities (Fig. 2a, b and c) and in the levels of reduced GSH (Fig. 3b), with respect to age-matched sedentary mice. These results suggested a redox shift towards a more oxidized cellular environment, in which GSH, the major thiol-based intracellular antioxidant, was strongly challenged by ROS overproduction. This may explain the higher levels of oxidatively-damaged lipids and proteins we found in cortices of two-month-exercised mice (Fig. 1a and b). However, an early tissue responsiveness was observed; in particular, higher specific activities of GR (Fig. 3a) and GLO2 (Fig. 4c) were detected within cortices of two-month-exercised mice, when compared to age-matched unexercised animals. This might indicate the activation of the GSH recycling pathway, which could be most likely triggered by the higher utilization rate of the reduced form of glutathione by the glyoxalase system. The early stimulation of MG-removal system suggested that the increased MG formation may be one of the earliest molecular events occurring in the brain cortex as a result of treadmill running. This, in turn, could contribute to the redox-related biochemical changes we observed, as MG is known to deplete intracellular GSH pool and to facilitate ROS-dependent chemical damage , , . As a consequence of the induced oxidative stress, the first two months of exercise lowered the cortical protein levels of both BDNF (Fig. 5a) and p-TrkB (Fig. 6), with respect to age-matched sedentary controls. Several mechanisms by which oxidative stress may decrease BDNF have been suggested, including decreased CREB, increased NF-κB DNA-binding activity or energy depletion , . Coherently, we found decreased cortical levels of p-CREB in 2-mo exercised animals, with respect to age-matched unexercised controls (Fig. 5b).To the best of our knowledge, this study provides the first experimental evidence of a double-step effect on antioxidative, antiglycative and neurotrophic molecular networks in the cortex of mammals undergoing a long-term, forced and moderate running exercise regimen initiated in adult age. It is not uncommon to observe reduced resistance and resilience in organisms which are already challenged by endogenous processes (e.g., aging, infections, diseases etc) . However, we cannot exclude that transient imbalances in biomolecular networks we investigated in our experimental model might act as stressors required by physical exercise to trigger physiological adaptations and hormetic responses within brains of exercised animals.
In conclusion, our results suggested that a long-term, enforced and moderate exercise initiated in adult age positively affects the major ROS- and MG-targeting scavenging systems and the molecular damage profiles in adult mice brain cortices, preserving as well the BDNF-related neurotrophic support during the physiological transition from adult to middle age.
On the other hand, our findings showed that moderate treadmill running required a time lag in order to activate efficient adaptive mechanisms and compensative adjustments aimed at improving biomolecular redox and neurotrophic patterns within the mouse cortex. Given the multiple systems recruited to modulate the action of physical activity, the understanding of molecular targets underlying exercise-induced physiological adaptations could lead to the development of new therapeutic approaches aimed at retarding cellular senescence and at preventing age-related neurodegenerative diseases. Although many biochemical and molecular aspects still remain to be investigated, this study sheds new interesting lights on the physiological responses and molecular targets activated by regular and moderate physical exercise during the adult and middle ages, thus strengthening the importance of conceiving and developing non-pharmacological approaches aimed at modulating and retarding the brain senescence process.
Materials and Methods
Chemicals and antibodies
The monoclonal antibody against arg-pyrimidine was purchased from Cosmo Bio Co., LTD (cat. NOF-N213430-EX; Tokyo, Japan). Rabbit anti-BDNF (cat. sc-20981) and anti-p-CREB (sc-101662) antibodies were supplied by Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA). Rabbit anti-TrkB phospho Y705 (cat. ab52191) and anti-β-actin (cat. ab8227) antibodies were purchased from Abcam (Cambridge, UK). The anti-rabbit peroxidase-conjugate secondary antibody (cat. PI-1000) was provided by Vector Laboratories, Inc. (Burlingame, CA, USA). Sigma Aldrich (St. Louis, MO, USA) supplied the anti-mouse secondary antibody (cat. A9044) and all the chemicals, substrates and reagents which are not listed elsewhere. Acrylamide/bis acrylamide (cat. 1610125), premixed Laemmli sample buffer (cat. 1610737), Kaleidoscope prestained standards (cat. 1610324) and Immun-Blot PVDF Sandwiches (cat. 1620239) were purchased from Bio-Rad Laboratories (Hercules, CA, USA). Thermo Fisher Scientific (Rockford, IL, USA) provided metal-enhanced 3′,3-diaminobenzidine (DAB) substrate kit (cat. 34065) and bicinchoninic acid (BCA) protein assay kit (cat. 23225). Cayman Chemical (Ann Arbor, MI,USA) supplied the total/oxidized glutathione (cat. 703002) and the protein carbonyl (cat. 10005020) assay kits. Oxis International (Foster City, CA, USA) provided the colorimetric assay for lipid peroxidation (cat. 21012).
Animals and running protocol
9-month old CD1 female mice (45–50 grams; N = 48; Harlan Laboratories, Inc., Frederick, MD, USA) were acclimatized for 10 days in the laboratories of the Excellence Research Center on Aging of the University Foundation “G. d'Annunzio” of Chieti (Italy), to housing conditions (22±2°C, 12–12 h light-dark cycle with lights on from 8 a.m. to 8 p.m., free access to water and food, 6 mice per cage). Animals were familiarized to the Exer 3/6 motorized low-noise treadmill (Columbus Instruments, Columbus, OH, USA) for 2 weeks (9 m/min for 10 min, 5 days/week). Rodents were then randomly assigned to four groups (12 mice each) and divided as follows: animals committed to be sacrificed 2 or 4 months later, in presence (E2, E4) or absence (S2, S4) of physical activity protocol.
Exercised groups started the training program (warm-up at 5 m/min for 3 min, running at 13 m/min for 20 min, cool-down at 5 m/min for 3 min, zero inclination, 5 days/week). The final running work load was reached by incrementing 1 minute every day, starting from 10 min/day. Mice were motivated to run by gentle hand prodding, without electric shocks in order to minimize stress. Mice were observed while exercising to ensure continuous running and to monitor signs of undue stress. Sedentary groups were exposed to the same environmental conditions (handling, treadmill motor noise, vibration and deprivation of food and water) while exercising mice performed their running sessions. Food consumption and animal weight were daily monitored throughout the experiment. 24 h after the last training session, mice were rapidly sacrificed by decapitation and cortices were surgically removed and stored at −80°C until further analyses. Every possible effort was taken in order to minimize both the number and the suffering of used animals, according to the principles of the Declaration of Helsinki and to the European Community Council (86/609/CEE). Formal approval for experimental procedures was provided by Health Minister (protocol 13/97-A).
Sample preparation for enzymatic activity
Brain cortices were homogenized and sonicated (cycle 0.5 – amplitude 50%) in 5 vol of 0.1 M phosphate buffer (pH 7) containing 1 mM ethylenediaminetetraacetic acid (EDTA) and 1.5 mM dithiothreitol (DTT), for subsequent enzymatic analyses of GPX, GLO1, GLO2 and GR, or 0.1% Triton X-100, to assess activities of tSOD and CAT. Then, samples were centrifuged at 15000 g for 30 min at 4°C and supernatants were used for assessments of enzymatic activities and of total protein content , by using a Lamba25 spectrophotometer (PerkinElmer Inc., Waltham, MA, USA). Every assay was performed in triplicate.
The tSOD (EC 22.214.171.124) activity was assayed by measuring its ability to inhibit the autoxidation of epinephrine, which was spectrophotometrically monitored at 480 nm at 30°C, according to Sun and Zigman . One unit of tSOD activity was assumed to provide 50% of inhibition.
The CAT (EC 126.96.36.199) activity was assayed by monitoring the decomposition of 10 mM H2O2 at 240 nm, as described by Aebi . One unit of enzyme activity was defined as 1 µmol of H2O2 reduced/min at 25°C.
The selenium-dependent GPX (EC 188.8.131.52) activity was determined by following the oxidation of nicotinamide adenine dinucleotide phosphate (NADPH) at 340 nm in a glutathione reductase-coupled reaction, using H2O2 as substrate . One unit of enzyme activity was defined as 1 µmol of GSH-conjugated/min at 25°C.
The GR (EC 184.108.40.206) activity was monitored by following the conversion of NADPH into NADP+ at 340 nm, by using GSSG as substrate . One unit of enzyme activity was defined as 1 µmol of NADPH oxidized/min at 25°C.
The GLO1 (EC 220.127.116.11) activity was assayed as described by Mannervik and colleagues , by following the production of (R)-S-lactoylglutathione at 240 nm. One unit activity was defined as 1 µmol of lactoylglutathione produced/min at 25°C.
The GLO2 (EC 18.104.22.168) activity was assayed by recording the decrease of absorbance at 240 nm . One unit of enzyme activity was defined as 1 µmol of (R)-S-lactoylglutathione hydrolyzed/min at 25°C.
Brain cortices were homogenized and sonicated (cycle 0.5-amplitude 50%) in 5 vol of radio immunoprecipitation assay (RIPA) buffer containing 1% protease inhibitor cocktail and 2% phosphatase inhibitor cocktails I and II. Extracts were centrifuged at 15000 g for 30 min at 4°C and total protein content was assessed by using the BCA method, with bovine serum albumin (BSA) as the standard . Twenty-five micrograms of denatured proteins from each sample were run through polyacrylamide denaturing gels (12–15%) and bands were transferred onto methanol-activated polyvinylidene fluoride (PVDF) sheets by wet electrophoretic transfer , . Non-specific binding sites were blocked with 5% (w/v) BSA in Tris-buffered saline containing 0.05% (v/v) Tween 20 (TBS–T) for 1 h. Membranes were then incubated overnight at 4°C with TBS-T containing primary antibodies, by using the following dilution conditions: anti-BDNF (1∶100), anti-p-TrkB (1∶400), anti-p-CREB (1∶75), anti-β-actin (1∶1000). PVDF sheets were washed 3 times with TBS-T (5 min each) and incubated with TBS-T containing the horseradish peroxidase-conjugated secondary antibody (dil. 1∶2000) for 2 h. Membranes were washed 3 times with TBS (5 min each) and the specific immune complexes were detected by using metal-enhanced DAB substrate kit, as suggested by the supplier. Bands were digitally acquired and processed by using the Nonlinear Dynamics TotalLab software. Results were normalized to the signals corresponding to the β-actin housekeeping protein, and given as relative units (RU). The experiments were performed in triplicate.
Arg-pyrimidine-directed dot immunoblot
Twenty-five micrograms of RIPA-extracted native proteins (see Western immunoblot, sub-section 2.10) were spotted onto methanol-activated PVDF sheets and air dried for 10 min. Membranes were blocked with non-fat dry milk for 1 h and incubated overnight at 4°C with TBS-T containing the monoclonal antibody anti-arg-pyrimidine (dil. 1∶100). Sheets were washed 3 times with TBS-T (5 min each) and incubated with TBS-T containing the horseradish peroxidase-conjugated secondary antibody (dil. 1∶8000) for 2 h. Membranes were washed 3 times with TBS (5 min each) and immune complexes were detected by using the metal-enhanced DAB substrate kit, as recommended by the supplier. Membranes were digitally acquired and data analysis was performed after normalization versus Brilliant Blue Coomassie-R-stained total proteins, by using ImageJ and Nonlinear Dynamics TotalLab softwares . Results were given as relative units (RU). The experiments were performed in triplicate.
Thiobarbituric acid-reactive substances (TBARS)
The measurement of TBARS is a well-established method used to detect lipid peroxidative damage through the photometric detection of the thiobarbituric acid-conjugated adduct . The final complex was extracted into n-butanol and the absorbance was read at 532 nm by a PerkinElmer Lamba25 spectrophotometer. A linear calibration curve was prepared from pure malondialdehyde (MDA)-containing reactions.
The 2,4-dinitrophenylhydrazine (DNPH)-based assay was used in order to measure the amounts of colorimetrically oxidatively-modified proteins. Extracts obtained as described in sub-section 2.3 were treated to remove nucleic acids by adding 0.1 vol of streptomycin sulphate 10% (w/v), and centrifuged at 6000 g for 10 min at 4°C. 100 µl of supernatants were processed as described by Levine and co-workers . Photometric data at 370 nm were obtained by using a Victor3 microplate reader (PerkinElmer), and normalized to the total protein concentration in the final pellets (absorbance reading at 280 nm; BSA-based linear calibration in the range 0–2.8 mg/ml) in order to consider protein loss during the washing steps, as suggested in the kit's user manual.
Glutathione redox couple ratio
Total (tGSH) and oxidized glutathione (GSSG) concentrations were measured through a 5,5′-dithiobis-2-nitrobenzoic acid (DTNB)-based enzymatic recycling method . The quantification of GSSG was accomplished by first derivatizing the reduced form of glutathione with 2-vinylpyridine, as recommended by the kit's manufacturer. The absorbance at 405 nm was followed for 30 min by using a Victor3 microplate reader (PerkinElmer). A linear calibration curve was computed from pure GSSG-containing reactions (ranges: 0–8 µM GSSG, 0–16 µM tGSH equivalents).
Statistical analyses were performed by using Statsoft Statistica 7 and SyStat SigmaStat v3.5. Results were given as means ± standard deviations. Ponderal and food uptake profiles were analyzed by 2-way ANOVA for repeated measures. All other dependent variables were processed by 2-way ANOVA analysis, in order to detect main effects due to time, life style and interactions. Post-hoc Newman-Keuls tests were used when appropriate. The null hypothesis was rejected with P<0.05.
We wish to thank Dr. Ilenia Taddei for her valuable assistance in the technical editing of this manuscript.
Conceived and designed the experiments: FA. Performed the experiments: SF AD AM GP SDL. Analyzed the data: SF. Contributed reagents/materials/analysis tools: SF MC CDI. Wrote the paper: SF FA.
- 1. Sohal RS, Weindruch R (1996) Oxidative stress, caloric restriction, and aging. Science 273: 59–63.RS SohalR. Weindruch1996Oxidative stress, caloric restriction, and aging.Science2735963
- 2. Fulle S, Di Donna S, Puglielli C, Pietrangelo T, Beccafico S, et al. (2005) Age-dependent imbalance of the antioxidative system in human satellite cells. Exp Gerontol 40(3): 189–197.S. FulleS. Di DonnaC. PuglielliT. PietrangeloS. Beccafico2005Age-dependent imbalance of the antioxidative system in human satellite cells.Exp Gerontol403189197
- 3. Fanò G, Mecocci P, Vecchiet J, Belia S, Fulle S, et al. (2001) Age and sex influence on oxidative damage and functional status in human skeletal muscle. J Muscle Res Cell Motil 22(4): 345–351.G. FanòP. MecocciJ. VecchietS. BeliaS. Fulle2001Age and sex influence on oxidative damage and functional status in human skeletal muscle.J Muscle Res Cell Motil224345351
- 4. Frazzini V, Rockabrand E, Mocchegiani E, Sensi SL (2006) Oxidative stress and brain aging: is zinc the link? Biogerontology 7: 307–314.V. FrazziniE. RockabrandE. MocchegianiSL Sensi2006Oxidative stress and brain aging: is zinc the link?Biogerontology7307314
- 5. Sayre LM, Perry G, Smith MA (2008) Oxidative stress and neurotoxicity. Chem Res Toxicol 21: 172–188.LM SayreG. PerryMA Smith2008Oxidative stress and neurotoxicity.Chem Res Toxicol21172188
- 6. Amicarelli F, Colafarina S, Cesare P, Aimola P, Di Ilio C, et al. (2001) Morphofunctional mitochondrial response to methylglyoxal toxicity in Bufo bufo embryos. Int J Biochem Cell Biol 33: 1129–1139.F. AmicarelliS. ColafarinaP. CesareP. AimolaC. Di Ilio2001Morphofunctional mitochondrial response to methylglyoxal toxicity in Bufo bufo embryos.Int J Biochem Cell Biol3311291139
- 7. Lüth HJ, Ogunlade V, Kuhla B, Kientsch-Engel R, Stahl P, et al. (2005) Age- and stage-dependent accumulation of advanced glycation end products in intracellular deposits in normal and Alzheimer's disease brains. Cereb Cortex 15: 211–220.HJ LüthV. OgunladeB. KuhlaR. Kientsch-EngelP. Stahl2005Age- and stage-dependent accumulation of advanced glycation end products in intracellular deposits in normal and Alzheimer's disease brains.Cereb Cortex15211220
- 8. Hipkiss AR (2006) On the mechanisms of ageing suppression by dietary restriction-is persistent glycolysis the problem? Mech Ageing Dev 127: 8–15.AR Hipkiss2006On the mechanisms of ageing suppression by dietary restriction-is persistent glycolysis the problem?Mech Ageing Dev127815
- 9. Thornalley PJ (2008) Protein and nucleotide damage by glyoxal and methylglyoxal in physiological systems–role in ageing and disease. Drug Metabol Drug Interact 23: 125–150.PJ Thornalley2008Protein and nucleotide damage by glyoxal and methylglyoxal in physiological systems–role in ageing and disease.Drug Metabol Drug Interact23125150
- 10. Rabbani N, Thornalley PJ (2008) The dicarbonyl proteome: proteins susceptible to dicarbonyl glycation at functional sites in health, aging, and disease. Ann N Y Acad Sci 1126: 124–127.N. RabbaniPJ Thornalley2008The dicarbonyl proteome: proteins susceptible to dicarbonyl glycation at functional sites in health, aging, and disease.Ann N Y Acad Sci1126124127
- 11. Amicarelli F, Colafarina S, Cattani F, Cimini A, Di Ilio C, et al. (2003) Scavenging system efficiency is crucial for cell resistance to ROS-mediated methylglyoxal injury. Free Radic Biol Med 35: 856–871.F. AmicarelliS. ColafarinaF. CattaniA. CiminiC. Di Ilio2003Scavenging system efficiency is crucial for cell resistance to ROS-mediated methylglyoxal injury.Free Radic Biol Med35856871
- 12. Desai KM, Wu L (2008) Free radical generation by methylglyoxal in tissues. Drug Metabol Drug Interact 23: 151–173.KM DesaiL. Wu2008Free radical generation by methylglyoxal in tissues.Drug Metabol Drug Interact23151173
- 13. Kuhla B, Lüth HJ, Haferburg D, Weick M, Reichenbach A, et al. (2006) Pathological effects of glyoxalase I inhibition in SH-SY5Y neuroblastoma cells. J Neurosci Res 83: 1591–1600.B. KuhlaHJ LüthD. HaferburgM. WeickA. Reichenbach2006Pathological effects of glyoxalase I inhibition in SH-SY5Y neuroblastoma cells.J Neurosci Res8315911600
- 14. Di Loreto S, Caracciolo V, Colafarina S, Sebastiani P, Gasbarri A, et al. (2004) Methylglyoxal induces oxidative stress-dependent cell injury and up-regulation of interleukin-1beta and nerve growth factor in cultured hippocampal neuronal cells. Brain Res 1006: 157–167.S. Di LoretoV. CaraccioloS. ColafarinaP. SebastianiA. Gasbarri2004Methylglyoxal induces oxidative stress-dependent cell injury and up-regulation of interleukin-1beta and nerve growth factor in cultured hippocampal neuronal cells.Brain Res1006157167
- 15. Di Loreto S, Zimmitti V, Sebastiani P, Cervelli C, Falone S, et al. (2008) Methylglyoxal causes strong weakening of detoxifying capacity and apoptotic cell death in rat hippocampal neurons. Int J Biochem Cell Biol 40: 245–257.S. Di LoretoV. ZimmittiP. SebastianiC. CervelliS. Falone2008Methylglyoxal causes strong weakening of detoxifying capacity and apoptotic cell death in rat hippocampal neurons.Int J Biochem Cell Biol40245257
- 16. Viña J, Gomez-Cabrera MC, Lloret A, Marquez R, Miñana JB, et al. (2000) Free radicals in exhaustive physical exercise: mechanism of production, and protection by antioxidants. IUBMB Life 50: 271–277.J. ViñaMC Gomez-CabreraA. LloretR. MarquezJB Miñana2000Free radicals in exhaustive physical exercise: mechanism of production, and protection by antioxidants.IUBMB Life50271277
- 17. Williamson J, Pahor M (2010) Evidence Regarding the Benefits of Physical Exercise. Arch Intern Med 170: 124–125.J. WilliamsonM. Pahor2010Evidence Regarding the Benefits of Physical Exercise.Arch Intern Med170124125
- 18. Gomez-Cabrera MC, Domenech E, Viña J (2008) Moderate exercise is an antioxidant: upregulation of antioxidant genes by training. Free Radic Biol Med 44: 126–131.MC Gomez-CabreraE. DomenechJ. Viña2008Moderate exercise is an antioxidant: upregulation of antioxidant genes by training.Free Radic Biol Med44126131
- 19. Berchtold NC, Castello N, Cotman CW (2010) Exercise and time-dependent benefits to learning and memory. Neuroscience 167: 588–597.NC BerchtoldN. CastelloCW Cotman2010Exercise and time-dependent benefits to learning and memory.Neuroscience167588597
- 20. Falone S, Mirabilio A, Pennelli A, Cacchio M, Di Baldassarre A, et al. (2010) Differential impact of acute bout of exercise on redox- and oxidative damage-related profiles between untrained subjects and amateur runners. Physiol Res 59: 953–961.S. FaloneA. MirabilioA. PennelliM. CacchioA. Di Baldassarre2010Differential impact of acute bout of exercise on redox- and oxidative damage-related profiles between untrained subjects and amateur runners.Physiol Res59953961
- 21. O'Callaghan RM, Griffin EW, Kelly AM (2009) Long-term treadmill exposure protects against age-related neurodegenerative change in the rat hippocampus. Hippocampus 19: 1019–1029.RM O'CallaghanEW GriffinAM Kelly2009Long-term treadmill exposure protects against age-related neurodegenerative change in the rat hippocampus.Hippocampus1910191029
- 22. Muscari A, Giannoni C, Pierpaoli L, Berzigotti A, Maietta P, et al. (2010) Chronic endurance exercise training prevents aging-related cognitive decline in healthy older adults: a randomized controlled trial. Int J Geriatr Psychiatry 25: 1055–1064.A. MuscariC. GiannoniL. PierpaoliA. BerzigottiP. Maietta2010Chronic endurance exercise training prevents aging-related cognitive decline in healthy older adults: a randomized controlled trial.Int J Geriatr Psychiatry2510551064
- 23. Rolland Y, Abellan van Kan G, Vellas B (2010) Healthy brain aging: role of exercise and physical activity. Clin Geriatr Med 26: 75–87.Y. RollandG. Abellan van KanB. Vellas2010Healthy brain aging: role of exercise and physical activity.Clin Geriatr Med267587
- 24. van Praag H, Shubert T, Zhao C, Gage FH (2005) Exercise enhances learning and hippocampal neurogenesis in aged mice. J Neurosci 25: 8680–8685.H. van PraagT. ShubertC. ZhaoFH Gage2005Exercise enhances learning and hippocampal neurogenesis in aged mice.J Neurosci2586808685
- 25. Vaynman SS, Ying Z, Yin D, Gomez-Pinilla F (2006) Exercise differentially regulates synaptic proteins associated to the function of BDNF. Brain Res 1070: 124–130.SS VaynmanZ. YingD. YinF. Gomez-Pinilla2006Exercise differentially regulates synaptic proteins associated to the function of BDNF.Brain Res1070124130
- 26. Griffin EW, Bechara RG, Birch AM, Kelly AM (2009) Exercise enhances hippocampal-dependent learning in the rat: evidence for a BDNF-related mechanism. Hippocampus 19: 973–980.EW GriffinRG BecharaAM BirchAM Kelly2009Exercise enhances hippocampal-dependent learning in the rat: evidence for a BDNF-related mechanism.Hippocampus19973980
- 27. Aguiar AS Jr, Castro AA, Moreira EL, Glaser V, Santos AR, et al. (2011) Short bouts of mild-intensity physical exercise improve spatial learning and memory in aging rats: Involvement of hippocampal plasticity via AKT, CREB and BDNF signaling. Mech Ageing Dev. AS Aguiar JrAA CastroEL MoreiraV. GlaserAR Santos2011Short bouts of mild-intensity physical exercise improve spatial learning and memory in aging rats: Involvement of hippocampal plasticity via AKT, CREB and BDNF signaling.Mech Ageing DevIn press. In press.
- 28. Fouquet C, Petit GH, Auffret A, Gaillard E, Rovira C, et al. (2011) Early detection of age-related memory deficits in individual mice. Neurobiol Aging 32: 1881–1895.C. FouquetGH PetitA. AuffretE. GaillardC. Rovira2011Early detection of age-related memory deficits in individual mice.Neurobiol Aging3218811895
- 29. Flurkey K, Currer JM, Harrison DE (2007) The Mouse in Aging Research. In: Fox JG, Barthold SW, Davisson MT, Newcomer CE, Quimby FW, Smith AL, editors. The Mouse in Biomedical Research 2nd Edition. Burlington: American College Laboratory Animal Medicine (Elsevier). pp. 637–672.K. FlurkeyJM CurrerDE Harrison2007The Mouse in Aging Research.JG FoxSW BartholdMT DavissonCE NewcomerFW QuimbyAL SmithThe Mouse in Biomedical Research 2nd EditionBurlingtonAmerican College Laboratory Animal Medicine (Elsevier)637672
- 30. Radak Z, Toldy A, Szabo Z, Siamilis S, Nyakas C, et al. (2006) The effects of training and detraining on memory, neurotrophins and oxidative stress markers in rat brain. Neurochem Int 49: 387–392.Z. RadakA. ToldyZ. SzaboS. SiamilisC. Nyakas2006The effects of training and detraining on memory, neurotrophins and oxidative stress markers in rat brain.Neurochem Int49387392
- 31. Liu YF, Chen HI, Yu L, Kuo YM, Wu FS, et al. (2008) Upregulation of hippocampal TrkB and synaptotagmin is involved in treadmill exercise-enhanced aversive memory in mice. Neurobiol Learn Mem 90: 81–89.YF LiuHI ChenL. YuYM KuoFS Wu2008Upregulation of hippocampal TrkB and synaptotagmin is involved in treadmill exercise-enhanced aversive memory in mice.Neurobiol Learn Mem908189
- 32. Amicarelli F, Di Ilio C, Masciocco L, Bonfigli A, Zarivi O, et al. (1997) Aging and detoxifying enzymes responses to hypoxic or hyperoxic treatment. Mech Ageing Dev 97: 215–226.F. AmicarelliC. Di IlioL. MascioccoA. BonfigliO. Zarivi1997Aging and detoxifying enzymes responses to hypoxic or hyperoxic treatment.Mech Ageing Dev97215226
- 33. Amicarelli F, Ragnelli AM, Aimola P, Bonfigli A, Colafarina S, et al. (1999) Age-dependent ultrastructural alterations and biochemical response of rat skeletal muscle after hypoxic or hyperoxic treatments. Biochim Biophys Acta 1453: 105–114.F. AmicarelliAM RagnelliP. AimolaA. BonfigliS. Colafarina1999Age-dependent ultrastructural alterations and biochemical response of rat skeletal muscle after hypoxic or hyperoxic treatments.Biochim Biophys Acta1453105114
- 34. Powers SK, Sen CK (2000) Physiological antioxidants and exercise training. In: Sen CK, Packer L, Hanninen O, editors. Handbook of oxidants and antioxidants in exercise. Amsterdam: Elsevier Science B.V.. 225 p.SK PowersCK Sen2000Physiological antioxidants and exercise training.CK SenL. PackerO. HanninenHandbook of oxidants and antioxidants in exerciseAmsterdamElsevier Science B.V.225
- 35. Desai KM, Chang T, Wang H, Banigesh A, Dhar A, et al. (2010) Oxidative stress and aging: is methylglyoxal the hidden enemy? Can J Physiol Pharmacol 88: 273–284.KM DesaiT. ChangH. WangA. BanigeshA. Dhar2010Oxidative stress and aging: is methylglyoxal the hidden enemy?Can J Physiol Pharmacol88273284
- 36. Brownlee M, Vlassara H, Kooney A, Ulrich P, Cerami A (1986) Aminoguanidine prevents diabetes-induced arterial wall protein cross-linking. Science 232: 1629–1632.M. BrownleeH. VlassaraA. KooneyP. UlrichA. Cerami1986Aminoguanidine prevents diabetes-induced arterial wall protein cross-linking.Science23216291632
- 37. Miyata T, Inagi R, Asahi K, Yamada Y, Horie K, et al. (1998) Generation of protein carbonyls by glycoxidation and lipoxidation reactions with autoxidation products of ascorbic acid and polyunsaturated fatty acids. FEBS Lett 437: 24–28.T. MiyataR. InagiK. AsahiY. YamadaK. Horie1998Generation of protein carbonyls by glycoxidation and lipoxidation reactions with autoxidation products of ascorbic acid and polyunsaturated fatty acids.FEBS Lett4372428
- 38. Nicolle MM, Gonzalez J, Sugaya K, Baskerville KA, Bryan D, et al. (2001) Signatures of hippocampal oxidative stress in aged spatial learning-impaired rodents. Neuroscience 107: 415–431.MM NicolleJ. GonzalezK. SugayaKA BaskervilleD. Bryan2001Signatures of hippocampal oxidative stress in aged spatial learning-impaired rodents.Neuroscience107415431
- 39. Tongiorgi E, Righi M, Cattaneo A (1997) Activity-dependent dendritic targeting of BDNF and TrkB mRNAs in hippocampal neurons. J Neurosci 17: 9492–9505.E. TongiorgiM. RighiA. Cattaneo1997Activity-dependent dendritic targeting of BDNF and TrkB mRNAs in hippocampal neurons.J Neurosci1794929505
- 40. Hof PR, Morrison JH (2004) The aging brain: morphomolecular senescence of cortical circuits. Trends Neurosci 27: 607–613.PR HofJH Morrison2004The aging brain: morphomolecular senescence of cortical circuits.Trends Neurosci27607613
- 41. Radak Z, Chung HY, Goto S (2008) Systemic adaptation to oxidative challenge induced by regular exercise. Free Radic Biol Med 44: 153–159.Z. RadakHY ChungS. Goto2008Systemic adaptation to oxidative challenge induced by regular exercise.Free Radic Biol Med44153159
- 42. Somani SM, Ravi R, Rybak LP (1995) Effect of exercise training on antioxidant system in brain regions of rat. Pharmacol Biochem Behav 50: 635–639.SM SomaniR. RaviLP Rybak1995Effect of exercise training on antioxidant system in brain regions of rat.Pharmacol Biochem Behav50635639
- 43. Devi SA, Kiran TR (2004) Regional responses in antioxidant system to exercise training and dietary vitamin E in aging rat brain. Neurobiol Aging 25: 501–508.SA DeviTR Kiran2004Regional responses in antioxidant system to exercise training and dietary vitamin E in aging rat brain.Neurobiol Aging25501508
- 44. Ji LL (2008) Modulation of skeletal muscle antioxidant defense by exercise: Role of redox signaling. Free Radic Biol Med 44: 142–152.LL Ji2008Modulation of skeletal muscle antioxidant defense by exercise: Role of redox signaling.Free Radic Biol Med44142152
- 45. Toldy A, Stadler K, Sasvári M, Jakus J, Jung KJ, et al. (2005) The effect of exercise and nettle supplementation on oxidative stress markers in the rat brain. Brain Res Bull 65: 487–493.A. ToldyK. StadlerM. SasváriJ. JakusKJ Jung2005The effect of exercise and nettle supplementation on oxidative stress markers in the rat brain.Brain Res Bull65487493
- 46. Radak Z, Kaneko T, Tahara S, Nakamoto H, Pucsok J, et al. (2001) Regular exercise improves cognitive function and decreases oxidative damage in rat brain. Neurochem Int 38: 17–23.Z. RadakT. KanekoS. TaharaH. NakamotoJ. Pucsok2001Regular exercise improves cognitive function and decreases oxidative damage in rat brain.Neurochem Int381723
- 47. Chao MV, Rajagopal R, Lee FS (2006) Neurotrophin signaling in health and disease. Clin Sci (Lond) 110: 167–173.MV ChaoR. RajagopalFS Lee2006Neurotrophin signaling in health and disease.Clin Sci (Lond)110167173
- 48. Gomez-Pinilla F (2008) The influences of diet and exercise on mental health through hormesis. Ageing Res Rev 7: 49–62.F. Gomez-Pinilla2008The influences of diet and exercise on mental health through hormesis.Ageing Res Rev74962
- 49. Greenwood BN, Strong PV, Foley TE, Fleshner M (2009) A behavioral analysis of the impact of voluntary physical activity on hippocampus-dependent contextual conditioning. Hippocampus 19: 988–1001.BN GreenwoodPV StrongTE FoleyM. Fleshner2009A behavioral analysis of the impact of voluntary physical activity on hippocampus-dependent contextual conditioning.Hippocampus199881001
- 50. Hopkins ME, Bucci DJ (2010) BDNF expression in perirhinal cortex is associated with exercise-induced improvement in object recognition memory. Neurobiol Learn Mem 94: 278–284.ME HopkinsDJ Bucci2010BDNF expression in perirhinal cortex is associated with exercise-induced improvement in object recognition memory.Neurobiol Learn Mem94278284
- 51. Erickson KI, Voss MW, Prakash RS, Basak C, Szabo A, et al. (2011) Exercise training increases size of hippocampus and improves memory. Proc Natl Acad Sci U S A; 108: 3017–3022.KI EricksonMW VossRS PrakashC. BasakA. Szabo2011Exercise training increases size of hippocampus and improves memory.Proc Natl Acad Sci U S A;10830173022
- 52. Mattson MP, Lovell MA, Furukawa K, Markesbery WR (1995) Neurotrophic factors attenuate glutamate-induced accumulation of peroxides, elevation of intracellular Ca2+ concentration, and neurotoxicity and increase antioxidant enzyme activities in hippocampal neurons. J Neurochem 65: 1740–1751.MP MattsonMA LovellK. FurukawaWR Markesbery1995Neurotrophic factors attenuate glutamate-induced accumulation of peroxides, elevation of intracellular Ca2+ concentration, and neurotoxicity and increase antioxidant enzyme activities in hippocampal neurons.J Neurochem6517401751
- 53. Tatone C, Amicarelli F, Carbone MC, Monteleone P, Caserta D, et al. (2008) Cellular and molecular aspects of ovarian follicle ageing. Hum Reprod Update 14: 131–142.C. TatoneF. AmicarelliMC CarboneP. MonteleoneD. Caserta2008Cellular and molecular aspects of ovarian follicle ageing.Hum Reprod Update14131142
- 54. Iwata E, Asanuma M, Nishibayashi S, Kondo Y, Ogawa N (1997) Different effects of oxidative stress on activation of transcription factors in primary cultured rat neuronal and glial cells. Brain Res Mol Brain Res 50: 213–220.E. IwataM. AsanumaS. NishibayashiY. KondoN. Ogawa1997Different effects of oxidative stress on activation of transcription factors in primary cultured rat neuronal and glial cells.Brain Res Mol Brain Res50213220
- 55. Zou J, Crews F (2006) CREB and NF-kappaB transcription factors regulate sensitivity to excitotoxic and oxidative stress induced neuronal cell death. Cell Mol Neurobiol 26: 385–405.J. ZouF. Crews2006CREB and NF-kappaB transcription factors regulate sensitivity to excitotoxic and oxidative stress induced neuronal cell death.Cell Mol Neurobiol26385405
- 56. Macri MA, D'Alessandro N, Di Giulio C, Di Iorio P, Di Luzio S, et al. (2010) Region-specific effects on brain metabolites of hypoxia and hyperoxia overlaid on cerebral ischemia in young and old rats: a quantitative proton magnetic resonance spectroscopy study. J Biomed Sci 17: 14.MA MacriN. D'AlessandroC. Di GiulioP. Di IorioS. Di Luzio2010Region-specific effects on brain metabolites of hypoxia and hyperoxia overlaid on cerebral ischemia in young and old rats: a quantitative proton magnetic resonance spectroscopy study.J Biomed Sci1714
- 57. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254.MM Bradford1976A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.Anal Biochem72248254
- 58. Sun M, Zigman S (1978) An improved spectrophotometric assay for superoxide dismutase based on epinephrine autoxidation. Anal Biochem 90: 81–89.M. SunS. Zigman1978An improved spectrophotometric assay for superoxide dismutase based on epinephrine autoxidation.Anal Biochem908189
- 59. Aebi H (1984) Catalase in vitro. Methods Enzymol 105: 121–126.H. Aebi1984Catalase in vitro.Methods Enzymol105121126
- 60. Paglia DE, Valentine WN (1967) Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 70: 158–169.DE PagliaWN Valentine1967Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase.J Lab Clin Med70158169
- 61. Di Ilio C, Polidoro G, Arduini A, Muccini A, Federici G (1983) Glutathione peroxidase, glutathione reductase, glutathione S-transferase, and gamma-glutamyltranspeptidase activities in the human early pregnancy placenta. Biochem Med 29: 143–148.C. Di IlioG. PolidoroA. ArduiniA. MucciniG. Federici1983Glutathione peroxidase, glutathione reductase, glutathione S-transferase, and gamma-glutamyltranspeptidase activities in the human early pregnancy placenta.Biochem Med29143148
- 62. Mannervik B, Aronsson AC, Marmstål E, Tibbelin G (1981) Glyoxalase I (rat liver). Methods Enzymol 77: 297–301.B. MannervikAC AronssonE. MarmstålG. Tibbelin1981Glyoxalase I (rat liver).Methods Enzymol77297301
- 63. Guha MK, Vander Jagt DL, Creighton DJ (1988) Diffusion-dependent rates for the hydrolysis reaction catalyzed by glyoxalase II from rat erythrocytes. Biochemistry 27: 8818–8822.MK GuhaDL Vander JagtDJ Creighton1988Diffusion-dependent rates for the hydrolysis reaction catalyzed by glyoxalase II from rat erythrocytes.Biochemistry2788188822
- 64. Smith PK, Krohn RI, Hermanson GT, Mallia AK, Gartner FH, et al. (1985) Measurement of protein using bicinchoninic acid. Anal Biochem 150: 76–85.PK SmithRI KrohnGT HermansonAK MalliaFH Gartner1985Measurement of protein using bicinchoninic acid.Anal Biochem1507685
- 65. Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680–685.UK Laemmli1970Cleavage of structural proteins during the assembly of the head of bacteriophage T4.Nature227680685
- 66. Towbin H, Staehelin T, Gordon J (1979) Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci USA 76: 4350–4354.H. TowbinT. StaehelinJ. Gordon1979Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proc Natl Acad Sci USA7643504354
- 67. Aldridge GM, Podrebarac DM, Greenough WT, Weiler IJ (2008) The use of total protein stains as loading controls: an alternative to high-abundance single-protein controls in semi-quantitative immunoblotting. J Neurosci Methods 172: 250–254.GM AldridgeDM PodrebaracWT GreenoughIJ Weiler2008The use of total protein stains as loading controls: an alternative to high-abundance single-protein controls in semi-quantitative immunoblotting.J Neurosci Methods172250254
- 68. Silva-Adaya D, Pérez-De La Cruz V, Herrera-Mundo MN, Mendoza-Macedo K, Villeda-Hernández J, et al. (2008) Excitotoxic damage, disrupted energy metabolism, and oxidative stress in the rat brain: antioxidant and neuroprotective effects of L-carnitine. J Neurochem 105: 677–689.D. Silva-AdayaV. Pérez-De La CruzMN Herrera-MundoK. Mendoza-MacedoJ. Villeda-Hernández2008Excitotoxic damage, disrupted energy metabolism, and oxidative stress in the rat brain: antioxidant and neuroprotective effects of L-carnitine.J Neurochem105677689
- 69. Levine RL, Williams JA, Stadtman ER, Shacter E (1994) Carbonyl assays for determination of oxidatively modified proteins. Methods Enzymol 233: 346–357.RL LevineJA WilliamsER StadtmanE. Shacter1994Carbonyl assays for determination of oxidatively modified proteins.Methods Enzymol233346357
- 70. Baker MA, Cerniglia GJ, Zaman A (1990) Microtiter plate assay for the measurement of glutathione and glutathione disulfide in large numbers of biological samples. Anal Biochem 190: 360–365.MA BakerGJ CernigliaA. Zaman1990Microtiter plate assay for the measurement of glutathione and glutathione disulfide in large numbers of biological samples.Anal Biochem190360365