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Caloric restriction (CR) reduces the pathological effects of aging and extends the lifespan in many species, including nonhuman primates, although the effect on the brain is less well characterized. We used two common indicators of aging, motor performance speed and brain iron deposition measured in vivo using MRI, to determine the potential effect of CR on elderly rhesus macaques eating restricted (n = 24, 13 males, 11 females) and standard diets (n= 17, 8 males, 9 females). Both the CR and control monkeys showed age-related increases in iron concentrations in globus pallidus (GP) and substantia nigra (SN), although the CR group had significantly less iron deposition in the GP, SN, red nucleus and temporal cortex. A Diet x Age interaction revealed that CR modified age-related brain changes, evidenced as attenuation in the rate of iron accumulation in basal ganglia and parietal, temporal, and perirhinal cortex. Additionally, control monkeys had significantly slower fine motor performance on the Movement Assessment Panel, which was negatively correlated with iron accumulation in left SN and parietal lobe, although CR animals did not show this relationship. Our observations suggest that the CR induced benefit of reduced iron deposition and preserved motor function may indicate neural protection similar to effects described previously in aging rodent and primate species.
Caloric restriction (CR), a reduction of calories without changes in essential nutrient intake, reduces the pathological effects of aging and extends the lifespan in many species, including yeast and nematodes (Weindruch and Walford, 1988), rodents (Masoro, 2005) and nonhuman primates (Mattison et al., 2007; Colman et al., 2009). CR diets started in middle-aged rhesus monkeys reduces overall mortality and morbidity, sarcopenia (Colman et al., 2008) and insulin resistance (Gresl et al., 2001)--possibly via decreases in oxidative stress (Forster et al., 2000; Wanagat et al., 1999) or alterations in internal metabolic and signaling pathways (Masoro, 2005; Masoro et al., 1992; Anson et al., 2003; Qin et al., 2006). Although less understood, the effects of CR on the brain are similarly protective: CR increases dendritic spine density (Stranahan et al.,2009), increases astrocytic functions including glutamate uptake (Ribeiro et al., 2009), reduces cortical amyloid deposition (Mouton et al., 2009) and attenuates iron accumulation (Xu et al., 2008) after CR diet both in young and old rodents.
One cross-species marker of aging in the brain is an increased concentration of non-heme iron (Peran et al., 2007; Zecca et al., 2004a; Dhenain et al., 1997; Zecca et al., 2001). The concentration and distribution of iron accumulation has been well established histologically, with the highest rates of deposition near striatal regions, globus pallidus (GP) and substantia nigra (SN), and moderate accumulation in cortical grey matter with relative sparing of white matter (Haacke et al., 2005; Koeppen, 2003; Hallgren and Sourander, 1958). Much of this non-heme brain iron is stored in ferritin, a spherical protein that sequesters crystallized iron in high local concentrations (Zecca et al., 2004a; Martin et al., 1998). Iron stored in ferritin causes magnetic field inhomogeneities, shortening the transverse relaxation time constant and increasing the relaxation rate (R2) of nearby protons, creating a signature signal hypointensity on T2-weighted MR images (House et al., 2007). Several histological investigations have demonstrated high correlations between iron concentration and iron deposition measured with MR (Hardy et al., 2005; Bizzi et al., 1990; Drayer et al., 1986; Gelman et al., 1999; Bartzokis et al., 1997), resulting in an acceptance of T2 or its inverse, R2, as abiomarker of brain aging (Schenck and Zimmerman, 2004). A second common measure of the progression of aging is motor performance, which decreases with age in humans and monkeys (Gash et al., 1999). Perhaps not coincidentally, iron is higher in brain regions associated with motor function such as GP and SN.
The primary aim of these analyses was to determine the potential effect of CR on brain iron and motor function in aged rhesus monkeys. We hypothesized that CR would attenuate the normal effects of age on brain iron deposition, as indexed by increased R2, in iron-rich regions including the nigro-striatal pathway. We also hypothesized that CR animals would exhibit better manual dexterity and faster fine motor performance and that motor speed would be related to iron load in subcortical areas, such as GP.
Forty-one rhesus monkeys (Macaca mulatta) between the ages of 18 and 31 were scanned and included in the analyses (see Table 1). The animals were all from the Dietary Restriction and Aging Study at the Wisconsin National Primate Research Center (WNPRC). Length of the CR diet ranged from 12 to 17 years, and was initiated when animals were in middle age. Details of the protocol have been reported previously (Kemnitz et al., 1993). CR animals (n = 17; 8 males, 9 females) were fed 30% less chow than control animals (n = 24; 13 males, 11 females) of a similarly formulated diet supplemented to achieve comparable vitamin and mineral content between CR and controls. Ferric Citrate within the mineral mix was the only source of iron in the diet (0.12% of total chow composition). The CR and control diets respectively contained 294 mg/kg and 206 mg/kg of iron. The rooms were maintained on a 12:12 light/dark cycle, and scans were typically conducted during the morning hours. The MRI scans of 7 additional monkeys were excluded from analysis due to poor quality images caused by head movement despite the anesthesia. The research protocol was approved by the Institutional Animal Care and Use Committee (IACUC) and the WNPRC is fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care(AAALAC).
Food intake for each animal was calculated daily, and the average amount of iron consumed from a chow ration per week was calculated for each animal over a two year period around the time of scan to achieve a complete view of iron intake during the study. To characterize iron uptake and assess whether circulating iron is related to ferritin-bound brain iron, serum levels iron were assayed. Whole blood was centrifuged to derive serum and a standard chemistry panel was then run on a COBAS INTEGRA analyzer (Meriter Laboratories, Madison, WI). Relevant hematology measures such as hematocrit (Hct), hemoglobin (Hgb), and mean corpuscular volume (MCV) were examined near the time of scan to determine whether monkeys exhibited characteristics of anemia or iron overload (Kemnitz et al., 1993).
The monkeys were scanned on a GE 3T Signa scanner using a quadrature transmit-receive volume coil with 18 cm diameter. The axial T2 relaxation scan was a multiple-slice, four-echo, spin-echo pulse sequence with four echoes at TE = 15, 30, 45 and 60 milliseconds. Other parameters included: repetition time = 2000 ms, flip angle = 90°, field of view = 160 millimeters, matrix = 256 × 256, slice thickness = 1.7mm. This sequence resulted in a voxel size of 0.625×0.625×1.7mm across 24 slices. The slice prescription was such that there was full coverage of deep grey structures and temporal lobes. A whole brain T2-weighted Fast Spin Echo (FSE) (TE=88.5ms, TR=4500ms, FA=90°, FOV=160mm, matrix=512×512, slice thickness=1.7mm) or a T2-weighted 3D FSE (TE=81.556, TR=2300ms, FA=55°, FOV=140mm, matrix=512×512) was also acquired and used during processing to achieve accurate normalization to a T2-weighted atlas (McLaren et al., 2009b). Additionally, a whole-brain T1-weighted scan (parameters reported in McLaren et al., 2009a) was acquired to aid in skull-stripping the brains. Animals were anesthetized before the scan with ketamine (up to 15 mg/kg) and xylaxine (up to 0.6 mg/kg).
Absolute and accurate T2 measurements with multiple-echo pulse sequences can be optimized using slice-selective refocusing pulses and crushers for removing stimulated echoes (see Poon and Henkelman, 1992 for a review of T2 mapping issues) and stimulated echoes can cause the T2 to be overestimated. However, thesignal obtained in this study is modulated primarily by T2, and based on previous studies is known to correlate highly with absolute T2 measurements.
The transverse relaxation rate, R2, was calculated by first performing log transformations of the voxel signal intensity data for all 4 TEs and then linear-fitting the slope according to the monoexponential Spin Echo signal intensity equation (Poon and Henkelman, 1992).
SPM5 was used for all coregistration and normalization steps (Ashburner and Friston, 2000; Mechelli et al., 2005; Ridgway et al., 2008). R2 Relaxation maps for each animal were normalized to our T2-weighted Rhesus Macaque atlas (McLaren et al., 2009b) to obtain a common space for voxel-wise analysis using a three-stage process. First, we estimated the transformation matrix needed to coregister the TE45 volume of the multi-echo relaxation image to the T2-weighted image from the same individual using a 6-parameter transformation. Next, we estimated the transformation matrix needed to spatially normalize that individual’s T2-weighted image to a previously published T2-weighted atlas using a 12-parameter affine transformation. The T2-weighted atlas template (McLaren et al., 2009b) was created from nine monkeys (none of which overlapped with the current analysis) and is registered with the histological atlas of Saleem & Logothetis (Saleem and Logothetis, 2007). No non-linear transforms were performed because the reduced variability of the rhesus brainsfit the atlas space within approximately a millimeter without them. Finally, the two transformation matrices were combined (i.e. TE45→T2 and T2→T2 atlas) to warp the R2 relaxation maps to 112RM-SL atlas space and were resliced to 0.5mm isotropic voxels. T2-weighted images were manually deskulled using a brain mask traced from high resolution T1 images acquired during the same scan session prior to normalization to reduce the impact of skull information on the registration between brains.
Full factorial Analyses of Covariance (ANCOVA) of the R2 images were conducted in SPM5 to examine the main effects of Age and Diet Group, as well as the Age x Diet Group interaction(Ashburner and Friston, 2000). Sex and Total Brain Volume (TBV) were included as covariates. The effect of sex was controlled for because some studies suggest females have less brain iron accumulation (Bartzokis et al., 2007). In order to minimize false positive results, an omnibus F-contrast for Age, Diet Group and Age x Diet Group at a liberal voxel-wise threshold of alpha = .05 (uncorrected) was used to mask all further contrasts. Separate one-tailed t-tests were then conducted to examine: 1) the negative association of Age, based on the prediction that R2 should decrease with age (i.e. increased iron accumulation); 2) whether the CR group had increased R2, based on the prediction that CR should attenuate iron accumulation; 3) the Age x Diet Group interaction, where control animals would show the expected decrease in R2 signal per year of age versus no such relationship for CR monkeys. TBV was calculated from automated segmentation of the T2-weighted images using FAST in FSL (Zhang et al., 2001) and entered in the model to account for any possible confounding influence of global volume on relaxation signal.
A voxel threshold of alpha = .005 (uncorrected) was used for all contrasts based on a priori regional hypotheses involving specific sub-cortical structures and R2. Multiple-comparison correction was performed using estimates from a Monte Carlo simulation with AlphaSim (http://afni.nimh.nih.gov/pub/dist/doc/manual/AlphaSim.pdf) to achieve a corrected cluster-level alpha = .05 (Forman et al., 1995). The Monte Carlo simulation estimates the probability of generating a cluster with 680 voxels based on randomly computed images with the same dimensions, voxel probability threshold, and smoothness parameters as MRI images inputted for analysis, which can be used as a threshold to remove small clusters likely to be significant only by chance. Although violation of non-stationarity is a concern for cluster correction of imaging data, our use of a 4mm FWHM kernel does not appreciably bias the true alpha when using this permutational estimate of cluster size (Hayasaka et al., 2004).
We used an automated monkey Movement Assessment Panel (mMAP) testing system (Gash et al., 1999) to test the motor performance times of the animals retrieving small food items from a receptacle chamber. A day’s testing session consisted of 12 trials, with equal trials between the right and left hand. The trial was initiated when the tester placed a small food item (e.g., a piece of cereal) into the center of the food receptacle. The trial was completed when the monkey removed the food from the receptacle and withdrew its hand back into the home cage. There was a 30-sec delay before the next trial was initiated. The process was repeated until six trials had been completed with each hand. Monkeys were given 45 sec to retrieve food before the trial was aborted.
Three tests of increasing level of difficulty were evaluated for each animal. The platform task (level I difficulty) required the removal of a small food item from a level platform in the food receptacle. The straight rod task (level II) involved maneuvering the food item up a straight rod. The q-mark task (level III) required the animal to thread the food item over a question mark-shaped rod in the receptacle. Each task was tested for 10 days before progressing to the next level of difficulty. Mean manual performance speed was computed for each session for: 1) the amount of time it took a subject to initially move its hand into the outer testing chamber (“reaction time”, or RT); 2) the time spent in the outer chamber (“coarse” movement); and 3) the time spent removing the object from the inner chamber and withdrawing the hand (“fine” movement). Motor performance of a given animal, for each task, was divided into an “acquisition” phase during which the animals learned the task and improved their performance with each trial and a subsequent “proficiency” phase during which the animals’ performance reached an asymptote. Task proficiency was determined by examining when a subject-specific asymptote in performance occurred throughout the consecutive series of 12 trials per session; a scree test was used for this determination (Cattell, 1966).
Multivariate repeated measures analyses of covariance (MANCOVA) were used as omnibus analyses to test RT, coarse, and fine motor performance for each of the tasks (platform, rod, q-mark). ANCOVA was used for post-hoc testing between controls and CR monkeys. ANOVA tested differences in dietary iron intake, peripheral serum iron, and hematology variables. In order to explore whether CR-induced changes in central iron and motor performance were related, one-tailed split-level correlations were conducted between motor performance indices and regional R2 signal changes that were statistically different between CR and control monkeys. Maximal values of clusters generated from the Diet Group or Age x Diet Group analyses were used as regressors to test for associations between regional iron deposition and behavior. We predicted that controls would show slower motor performance as central iron increased in these maximal cluster values, whereas CR animals would not show this relationship. All behavioral analyses included Age and Sex as covariates. Alpha was set at 0.05. Analyses were conducted using SPSS 16.0 (Chicago, IL).
There was no significant Age, TBV, or difference in percentages of males and females between the two dietary groups (Table 1). There were no differences in hematology characteristics (Hgb, Hct, MCV) between the two groups as assessed with the blood panel after an initial year of CR (Kemnitz et al., 1993) and proximal to the time of scan.
Based on mineral composition of the chow and the average amount of chow eaten per week, CR monkeys consumed significantly more iron per week than control monkeys (CR: 34.37 ± 1.31 mg/week; Control: 29.52 ± 1.48 mg/week) [F(1,39) = 5.45, p < .05]. However, monkeys on CR (152.4 ± 5.81 μg/dl) and control (167.7 ± 10.4 μg/dl) diets had similar levels of circulating serum transferrin-boundiron [F(1,39) = 1.48, p = .231]. This result suggests that despite greater iron consumption there were no overt differences in iron uptake from the diet and peripheral partitioning of iron between tissue and the blood compartment.
Across all subjects, dietary iron intake was not significantly associated with peripheral serum iron, or central iron accumulation that differed as a function of dietary condition (see below). Yet, higher levels of circulating serum iron were associated with higher R2 signal in SN within the left [r(41) = .34, p<.05] and right [r(41) = .36, p < .05] hemispheres. The relationship was not significant with other ROIs that differed due to dietary condition (see below).
In a combined analysis of CR and control monkeys, we found a significant negative correlation between Age and R2, indicating an increase in iron deposition in older animals, in several deep grey matter structures including the GP and SN bilaterally (Table 2, Figure 1). The opposite contrast, where Age was positively correlated with R2, revealed clusters predominantly within cerebrospinal fluid spaces (CSF) adjacent to the midbrain and the parietal lobes. One possible explanation for this finding is that CSF has a shorter relaxation time than brain tissue and that the results suggest age-related atrophy in these areas.
We next investigated the effect of the two dietary conditions on R2. Brain regions where CR monkeys had higher R2 values than controls (i.e., less iron accumulation) included the GP, upper brainstem near red nucleus (RN), SN, and temporal cortex (see Figure 2). The significance and extent of each cluster can be found in Table 3 where the coordinates are reported in 112RM-SL space. There were no significant regions where controls had higher R2 than CR monkeys.
Finally, we investigated the direct effect of diet on the age gradient decline in R2 to examine the protective effect of CR, which would emerge as a significant interaction between Age and Diet Group. Regions where Age and R2 correlations had a significantly steeper slope for controls as compared to CR monkeys were the parietal and temporal cortices, striatal regions, SN, RN and hippocampus (Figure 3, Table 4).
The motor performance of all 41 monkeys was evaluated. However, a sub-set of animals did not finish the full set of tasks: 33 animals completed the platform and rod tasks, and 28 completed the q-mark task. Those subjects unable or unwilling to perform did not differ by dietary group (Controls = 7; CR = 6). All animals that completed tasks were included in the analyses.
A repeated measures MANCOVA first examined all motor indices for a given task (platform, rod, q-mark) during both initial acquisition and asymptotic proficiency. A Motor Task by Dietary Group interaction indicated that CR monkeys performed the q-mark tasks more quickly overall than controls [F(5, 125) = 4.26, p < .05], but not the platform or rod tasks (data not shown). A subsequent omnibus tested whether or not groups exhibited differing motor performance for any of the motor indices (RT, coarse, fine) during acquisition and proficiency phases across the three mMAP tasks. For fine motor movement, a Motor Index by Dietary Group interaction requiring Huynh-Feldt correction indicated that CR monkeys were faster overall for the motor components of each task [F(2.02,125) = 3.68, p < .05]. Post hoc analyses across motor indices and tasks were then conducted. Subjects had similar RT, coarse, and fine motor times for the platform and rod tasks (see Figure 4). In order to account for the influence of sustained motivation and attention during the q-mark task for RT, coarse or fine motor movement, acquisition or proficiency performance during the platform and rod tasks were included as covariates. RT and coarse movement did not differ between groups in the q-mark task. CR monkeys performed fine motor movements in the inner chamber faster during the acquisition [F(1,22) = 4.72, p < .05] and proficiency [F(1,22) = 5.42, p < .05] phases of the task.
Given that only fine motor performance for the q-mark task differed between groups, exploratory split-level correlations were conducted to assess the extent to which lower R2 among Dietary Group or Age x Dietary Group ROIs were associated with this change. For ROIs related to the main effect of Dietary Group, controls with lower R2 in the left SN took longer to perform the task during the acquisition phase [r(10) = −0.59, p < 0.05]; CR monkeys did not show this relationship [r(18) = 0.30, p = 0.11]. A similar pattern of associations was seen in an Age x Dietary Group cluster encompassing right dorsal superior temporal sulcus, where controls with lower R2 values also had slower fine motor acquisition performance [r(10) = −0.56, p < .05]. This effect was not seen in CR monkeys [r(18) = −0.20, p = 0.31].
Several measures of aging in old monkeys, including sarcopenia, poor glucoregulation, and atrophy of grey matter in the CNS are favorably affected by a CR diet (Colman et al., 2008, 2009; Anderson et al., 2009; Gresl et al., 2003). Less is known, however, about CR’s protective effect on two other markers of brain aging: the accumulation of iron and deteriorating motor performance. Iron concentrations increase naturally with age in deep nuclei (striatum, GP, SN and RN) in both humans (Peran et al., 2007; Bartzokis et al., 2007; Xu et al., 2008) and monkeys (Hardy et al., 2005; Cass et al., 2007). Motor deficits also increase with age, and can progress clinically to age-related disorders (Nagahara et al., in press; Lacreuse et al., 1999; Herndon et al., 1997). In the present study, we confirmed the age-associated increase of iron in a number of brain regions that typically show the most accumulation with age, as indexed by robust negative correlations between Age and R2 in GP and SN (Haacke et al., 2005; Koeppen, 2003; Hallgren and Sourander, 1958).
We also observed a main effect of diet on motor performance and brain iron accumulation in deep brain nuclei. Levels of iron concentration were lower in CR monkeys than controls in GP and SN bilaterally, and left RN. In association with these neural effects, the CR group performed significantly faster than controls on the q-mark task (3.08 vs. 3.75 sec). These task performance speeds are comparable to the values reported by Cass and colleagues (Cass et al., 2007), who used the same motor battery in assessments of middle-aged (15–17 years) and elderly monkeys (21–32 years). The CR animals in our cohort performed the task at the same level as Cass’ middle-aged monkeys (3.08 and ~3.25 sec, respectively) despite being nearly 10 years older on average. Although these changes in fine motor movement may be influenced by differences in food motivation among CR monkeys (Raman et al., 2007) or attentional processes, these possibilities were controlled for by covarying their performance on both of the simpler platform and rod tasks. Additionally, because we covaried for the effects of age and sex, related variables such as arm strength or sex-specific fine motor differences would not have influenced the results. CR in monkeys and rodents confers protection from age-or substance-related decline in several motor domains beside fine motor movement, including hand-eye coordination and balance (Duan and Mattson, 1999; Ramsey et al., 2000; Maswood et al., 2004). In humans, comparable deposition in SN pars compacta and changes in motor performance are observed in connection with neurodegenerative diseases, including Parkinson’s disease (Gorell et al., 1995) and Alzheimer’s disease by itself (Zhu et al., 2009) or with parkinsonism (Brar et al., 2009).
Indeed, our findings complement studies examining several Parkinson’s disease-like motor and neural deficits in rodents and rhesus monkeys caused by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), which induces oxidative and metabolic stress akin to the accumulation of more reactive oxyhydroxy forms of intracellular iron (Tipton and Singer, 1993). Mice or monkeys given MPTP exhibited deficits in motor speed, coordination, and locomotion compared to baseline, but animals on long-term CR recovered more quickly than dietary controls (Duan and Mattson, 1999; Maswood et al., 2004). This improvement corresponded to reduced depletion of dopamine in striatum and more tyrosine hydroxylase positive neurons in SN and striatum, indicating preservation of dopamine-rich neurons. CR therefore broadly reduces oxidative stress in basal ganglia across species with corresponding benefits in a variety of motor tasks.
Finally, the influence of age on iron accumulation was positively modulated by CR in caudate, SN, red nucleus, hippocampus, parietal and temporal cortices. This iron homeostasis suggests that CR slowed the aging process in these regions. A flattening of the aging slope concurs with previous findings suggesting a protective effect of CR, including grey matter volume preservation in CR monkeys (Colman et al., 2009). Improved motor performance and manual dexterity in the CR animals further underscores the functional significance of these findings. Fine motor deficits in the q-mark task were evident in the split-level correlations with iron accumulation. Increased iron was associated with slower food retrieval time in left SN and left parietal cortex for control but not CR monkeys. However, discerning if there is high specificity for these neural associations with only motor performance will require further study and is beyond the scope of this report.
Iron homeostasis in the gut and brain are tightly regulated to minimize oxidative damage (Bishop et al., 2007). It is likely that changes in these regulatory systems mediate linear age-related increases in ferritin and perhaps neuromelanin iron sequestration in BG among microglia and to a much lesser extent dopaminergic neurons (Zecca et al., 2004a,b). As animals age, the rate of non-enzymatic glycation between proteins and sugars increases, leading to the production of advanced glycation end products (AGEs) and subsequent free radical production (Yan et al., 1996). Mitochondrial dysfunction in electron exchange transport systems also produces free radicals as a function of age (Parker et al., 1994). The generation of reactive oxygen species causes a strong compensatory response of the cell to increase antioxidant activity by upregulating ferritin production to bind excess redox-ready iron and reduce related toxicity (Lovell et al., 1995; Ansari and Scheff, 2010; Young and Woodside, 2001; Grosser et al., 2004; Recalcati et al., 2008; Halliwell and Gutteridge, 1990).
Despite this tightly managed homeostasis, excess iron in the cytosol increasingly becomes integrated with unstable complexes such as haemosiderin and induces oxidative stress—which may occur due to dysregulated mitochondria-bound transport complexes releasing bound iron (Mastroberardino et al., 2009). Microglia could additionally release proinflammatory cytokines such as interleukin-6 that can act in a paracrine manner on neurons, mediating induction of oxidative stress and diffuse atrophy (Willette et al., 2010). By contrast, there are many more neuromelanin cells in the locus coeruleus, which appear to buffer against excess iron accumulation through chelation (Zecca et al., 2004b). There is also much less iron that accumulates in this area compared to BG, perhaps due to the lack of dopamine-rich neurons that require relatively more iron to drive mitochondrial electron transfer (Mastroberardino et al., 2009).
Although the CR group had slightly higher levels of dietary iron intake, both groups had similar levels of peripheral non-heme iron, suggesting that peripheral uptake did not mediate CR induced decreases in central iron accumulation. Further, the negative correlation of serum iron and R2 signal in SN points to compensatory changes in central transport or uptake mechanisms. Higher peripheral transferrin induces epithelial cells of the blood-brain barrier to have a reduced capacity both for binding transferrin and transferring iron ions into the interstitium of brain (Moos, 2002), downregulating central accumulation and potential neurotoxic effects in areas such as SN (Zecca et al., 2004a; Gorell et al., 1995; Unger et al., 2007). CR has been shown tomaintain the hypothalamic-pituitary-gonadal (HPG) axis, which in turn maintains perfusion (Wilson et al., 2008). Lifelong 40% CR in mice improves blood-brain vascular integrity and reduces neuronal loss after induction of thiamine deficiency, which upregulates reactive iron, iron sequestration proteins, and oxidative stress in microglia (Calingasan and Gibson, 2000). CR may likewise reduce age-related BBB permeability andparenchymal iron influx.
Other possible mechanisms by which CR could regulate iron accumulation include changes in transferrin receptor binding potentials on neurons (Roskams and Connor, 1990) or alterations in the amount of soluble intracellular iron sequestered into ferritin versus ion use in protein synthesis or efflux into interstitial CSF (Bradbury, 1997). Finally, CR may also act intracellularly by lowering energy metabolism (Fontana, 2009; Masoro et al., 1992), subsequently down regulating AGEs, oxidative stress (Zainal et al., 2000; Kayo et al., 2001), and possibly a compensatory increase in L-ferritin binding. It was not feasible to directly examine histological tissue to test these hypotheses in this ongoing, longitudinal study. Such samples will be collected at time of death to examine ferritin binding potential and other intracellular mechanisms.
Monkeys on a CR diet show reduced iron accumulation in the GP, SN and temporal cortex compared to controls in addition to showing less correlation between iron concentration and Age in GP and SN. Consumption of a CR diet from middle age slows the rate of iron accumulation in parietal and temporal cortices, GP, SN and RN. CR monkeys showed preservation of motor performance, appearing similar to published reports of monkeys 10 years younger, which were associated with the iron determination in brain areas associated motor function. Our observations suggest that the CR benefit of reduced iron deposition and preserved motor function may indicate neural protection similar to effects described previously in aging rodent and primate species.
The authors gratefully acknowledge the excellent technical assistance provided by R. Fisher, S. Baum, J. Smith, J. Adriansjach, C. Armstrong, the Waisman Center, the Animal Care, Veterinary and Pathology Staffof the WNPRC, EVP, and thank Dr. Craig Atwood, Ph.D. for critical comments on the manuscript. This work was supported by funding from the NIH to the WNPRC grants (P01 AG11915 and P51 RR000167) and Institute of Aging grant AG000213. This research was conducted in part at a facility constructed with support from Research Facilities Improvement Program grant numbers RR15459-01 and RR020141-01. The project also benefited from resources and facilities at the Wm. S. Middleton Memorial Veterans Hospital.