Caloric restriction or resveratrol supplementation and ageing in a non-human primate: first-year outcome of the RESTRIKAL study in Microcebus murinus
- First Online:
- Cite this article as:
- Dal-Pan, A., Terrien, J., Pifferi, F. et al. AGE (2011) 33: 15. doi:10.1007/s11357-010-9156-6
- 560 Views
A life-long follow-up of physiological and behavioural functions was initiated in 38-month-old mouse lemurs (Microcebus murinus) to test whether caloric restriction (CR) or a potential mimetic compound, resveratrol (RSV), can delay the ageing process and the onset of age-related diseases. Based on their potential survival of 12 years, mouse lemurs were assigned to three different groups: a control (CTL) group fed ad libitum, a CR group fed 70% of the CTL caloric intake and a RSV group (200 mg/kg.day–1) fed ad libitum. Since this prosimian primate exhibits a marked annual rhythm in body mass gain during winter, animals were tested throughout the year to assess body composition, daily energy expenditure (DEE), resting metabolic rate (RMR), physical activity and hormonal levels. After 1 year, all mouse lemurs seemed in good health. CR animals showed a significantly decreased body mass compared with the other groups during long day period only. CR or RSV treatments did not affect body composition. CR induced a decrease in DEE without changes in RMR, whereas RSV induced a concomitant increase in DEE and RMR without any obvious modification of locomotor activity in both groups. Hormonal levels remained similar in each group. In summary, after 1 year of treatment CR and RSV induced differential metabolic responses but animals successfully acclimated to their imposed diets. The RESTRIKAL study can now be safely undertaken on a long-term basis to determine whether age-associated alterations in mouse lemurs are delayed with CR and if RSV can mimic these effects.
KeywordsAgeingFood restrictionResveratrolEnergy balanceBiomarkersDoubly labelled water method
The main causes of mortality in western countries are chronic age-associated diseases such as cardiovascular diseases, cancers, type 2 diabetes, osteoporosis and kidney diseases. These diseases have a genetic background but environmental factors such as nutrition play a key role (Mokdad et al. 2004). Since the pioneering study of McCay et al. (1935), we know that caloric restriction (CR) without malnutrition can delay the onset of such age-associated pathologies, delay ageing and increase lifespan in rodents. Observational data suggest that the relationship between longevity, energy balance and caloric intake could exist in humans but further investigations are needed.
Several hypotheses have been proposed for the biological mechanism underlying the life-extending and anti-ageing actions of CR, such as slowing growth, reducing body fat, altering apoptosis, decreasing body temperature and increasing physical activity, attenuating oxidative damage, reducing glycemia and insulinemia and modifying immune function (Campbell and Richardson 1988; Gredilla et al. 2001; Gardner 2005). It is likely that all these and others actions might indeed play a role and a unifying hypothesis was needed. The concept of hormesis might well provide such a hypothesis. This refers to phenomena in which the response of an organism to a chemical or physical agent is qualitatively different when the agent is of high intensity than when it is of low intensity (Rattan 2004). A 30% CR that delays the ageing processes is a low intensity stressor, which enhances the ability of rats, mice and monkeys of all ages to cope with intense stressors (Masoro 2006). The pathway by which CR enhances protective and repair processes has not yet been well elucidated. Recently, a mechanism was proposed for CR-induced effects in yeast (Saccharomyces cerevisiae). Lin et al. (2000) demonstrated that the functional Sir2 gene is required for CR to increase replicative longevity in that species. More recently, an increasing amount of data has suggested that silent mating-type information regulation 2 homologous 1 (SIRT1), one of the seven mammalian orthologues of the yeast Sir2, regulates cell survival to a number of stressors and might be central to the effects of CR (Cohen et al. 2004; Picard et al. 2004; Rodgers et al. 2005; Bordone and Guarente 2005; Baur 2010).
Until the late 1980s, CR had not been tested in any animal model living longer than 4 years. Since then, studies in non-human primates, including rhesus and squirrel monkeys, have been in progress at the National Institute of Ageing (NIA) and the University of Wisconsin (UW) (Ingram et al. 1990; Lane et al. 1992; Kemnitz et al. 1993). The proportions of both rhesus and squirrel monkeys already dead in 2002 in the CR cohorts were about half of the controls (Lane et al. 2002). The most recent result from the UW primate study has indicated that adult-onset mild CR delays the onset of age-associated pathologies and promotes survival in rhesus monkeys (Colman et al. 2009) but this study has not yet shown any effect of CR on the maximum life expectancy of primates. Recently, a similar study was initiated on human subjects. Results at 6 months of CR are consistent to what has been observed in monkeys and rodents in terms of lower metabolic rate, body temperature and insulin and reduced DNA damage (Heilbronn et al. 2006).
Further studies are needed to test the validity of the CR paradigm in non-human primates to delineate the still debated mechanisms by which CR extends lifespan and ultimately test the molecules or interventions that will mimic the effects of CR and be relevant to humans. The present study “RESTRIKAL” aims to investigate the long-term effects of CR or supplementation with a mimetic compound (resveratrol; RSV) on the ageing process and lifespan of a non-human primate and highlight similar action pathways in both treatments. In that respect, the main originality of this study lies in the animal model, the grey mouse lemur (Microcebus murinus) whose size (60–110 g) and life expectancy (8–10 years) will allow obtaining longevity data in 5 years only. M. murinus is a nocturnal prosimian primate originating from Madagascar. The grey mouse lemur presents special characteristics that make it a unique model to investigate energy regulation and ageing processes. Firstly, it displays a strong seasonal rhythm linked to photoperiod that is associated with natural and massive winter obesity i.e. an important increase in body mass due to fat storage in only a few weeks (Génin and Perret 2000). Secondly, grey mouse lemurs exhibit very marked daily rhythms with periods of heterothermia during their diurnal resting phase (Perret and Aujard 2001). These phases of daily heterothermia, very rare in primates, are an efficient mechanism of energy saving in small mammals (Terrien et al. 2009a) and thereby a good response index to energy stresses. It is also a unique model to assess the importance of biological rhythms on the processes of ageing and longevity. For example, a weakened and fragmented locomotor activity rhythm during normal ageing has been demonstrated in this primate (Cayetanot et al. 2005). The longevity of this primate is adequate for performing longitudinal studies, and several biomarkers of ageing have already been validated in the mouse lemur colony, in particular decrease in sexual and aggressive behaviours (Aujard and Perret 1998; Nemoz-Bertholet et al. 2004), decrease in sexual hormones (Aujard and Perret 1998), melatonin (Aujard et al. 2001), DHEA-S (Perret and Aujard 2005) and insulin-like growth factor-1 (IGF-1) (Aujard et al. 2010), cognitive impairments (Picq 2007) and MRI-evaluated cerebral atrophy (Dhenain et al. 2003; Kraska et al. 2009). Moreover, it has recently been demonstrated that the energy balance of aged mouse lemurs is impaired in response to cold exposure (Terrien et al. 2009b). The first aim of this study is to determine whether CR can modify the physiological processes in the grey mouse lemur that lead to a delay in age-related diseases and an increase in lifespan.
The second aim of this study is to determine whether RSV, a natural polyphenolic compound that activates proteins implicated in energy metabolism homeostasis, could be used as a mimetic compound of CR. Indeed, CR will be very difficult to implement in humans because of social and practical constraints. In the past 5 years, numerous studies have focused on the development of “CR mimetic” compounds that would minimise many age-related diseases in humans without a reduction in caloric intake (Weindruch et al. 2001; Chen and Guarente 2007; Ingram et al. 2007; Wakeling et al. 2009). Among them, RSV seems to be a promising molecule (Howitz et al. 2003; Borra et al. 2005; Lagouge et al. 2006; Allard et al. 2009; Anderson and Prolla 2009). Trans-RSV, the most active form of RSV, has been the subject of many in vitro, ex vivo and in vivo studies to test its various and promising anti-inflammatory (Donnelly et al. 2004), anti-oxidant (Iannelli et al. 2007), anti-cancer (Baur et al. 2006), metabolic and cardiovascular (Shanmuganayagam et al. 2007) properties.
Although RSV effects share many metabolic similarities with CR (Barger et al. 2008) and although it seems to be a promising molecule to delay the incidence of age-associated chronic diseases (Athar et al. 2007), its metabolic effects in primates are still unknown. Indeed, relatively low concentrations can extend yeast, worm and Drosophila lifespan in a Sir2-dependent manner by mimicking CR (Wood et al. 2004). More interestingly, RSV can activate SIRT1, the most studied mammalian orthologue of Sir2, in humans (Borra et al. 2005). Most recently, several studies have also demonstrated RSV can stimulate AMPK activity in mice (Dasgupta and Milbrandt 2007; Canto et al. 2009). These results highlight that RSV could play an important part in energy regulation processes. RSV treatment also reduces the signs of ageing in mice but does not increase the longevity of ad libitum-fed animals when started at midlife (Pearson et al. 2008). However, non-human primates and humans present metabolic responses to a long-term CR and mimetic compound that might differ slightly from what was repeatedly observed in rodents and other lower organisms (Heilbronn et al. 2006; Colman et al. 2009; Witte et al. 2009). For example, CR in mice down-regulates genes involved in oxidative stress and reduces oxidative damage, lipid peroxidation and protein carbonyls (Sohal et al. 1994; Dubey et al. 1996; Lee et al. 1999; de Oliveira et al. 2003). In non-human primates, genes involved in protection against oxidative stress are not altered by CR, although protein carbonylation is reduced (Zainal et al. 2000). More data on primates are needed. Thus, the third goal of the study is to define whether CR and RSV act through similar pathways by stimulating sirtuins in the mouse lemur. This point will be developed in future years of the study.
Since the beginning of the RESTRIKAL study, a battery of tests has been performed on adult grey mouse lemurs at regular intervals until their natural death to assess the impact of both treatments on energy metabolism modification and the ageing process. These tests were selected to assess parameters changing with chronological ageing. They are minimally invasive and appropriate for a longitudinal study. Several indices of energy balance were measured such as body mass gain, food intake, body composition, resting metabolic rate (RMR) and physical activity. Concerning endocrine systems, IGF-1 levels were measured because this hormone is a modulator of energy balance and an ageing marker that declines with time (Aujard et al. 2010). Indeed, genetic alterations in the human IGF-1 receptor that result in an altered IGF signalling pathway seem to be linked to human longevity, suggesting a role of this pathway in the modulation of human lifespan (Suh et al. 2008). Testosterone levels are also measured to highlight possible effects on sexual behaviour and, notably, test if the balance between reproduction cost and survival of grey mouse lemurs is modified. The first-year outcome of this longitudinal follow-up demonstrates the validity of CR and RSV interventions for assessing whether they can delay ageing in a non-human primate. We expect that the present study will provide novel insights into the biology of ageing by testing the effect of CR or RSV treatment on a non-human primate model. We expect that CR will increase lifespan in the grey mouse lemurs and decrease markers of several chronic diseases. Lastly, we expect that RSV stimulation of the sirtuin pathway will mimic the effect of CR. In the long run, such a study might allow us to develop nutritional strategies to delay the effect of ageing.
Animals and animal care
The 42 male grey mouse lemurs (M. murinus, Cheirogaleidae, primates) used in this study were born in the laboratory breeding colony at Brunoy, France (agreement A91-114-1) from stock originally caught more than 40 years ago on the southwest coast of Madagascar. All animals were included in a single cohort at the age of 38 ± 1 months, which is considered an adult age in this species. The project began at the onset of the winter-like season in the lab. The general conditions of captivity were maintained with respect to ambient temperature (25°C) and relative humidity (55%). The grey mouse lemur is a nocturnal primate that shows high levels of locomotor activity and normothermic body temperature during the night. Just before the onset of the light phase, it enters a torpid state during which it decreases its body temperature and metabolic rate until 4 to 6 h after the beginning of the day when its body temperature returns to normothermic values. The mouse lemur exhibits photoperiod-dependent seasonal variations in most of its physiological functions. Another interesting particularity of this species is its body mass gain during winter. Indeed, at the beginning of winter the body mass of the grey mouse lemur increases by approximately 50% to 70% and only returns to basal levels in the summer. In the breeding colony, animals are exposed to an artificial photoperiodic regimen consisting of six months of summer-like long day length (14:10 h light-darkness, LD) and 6 months of winter-like short day length (10:14 h light-darkness, SD). These photoperiodic regimens are sufficiently discriminating to induce radically different physiological and behavioural responses, as observed in nature in Madagascar. The change of photoperiod occurred abruptly without any significant disturbance for the animals. To minimise social influences during the different experiments, animals were housed individually in 1 m3 cages, provided with a nest and supports and separated from each other by metallic partitions. Animals were weighed once a week to monitor body mass variations. All experiments were performed in accordance with the Principles of Laboratory Animal Care (National Institutes of Health publication 86-23, revised 1985) and French national laws.
Animals were fed with the same standard diet used in the laboratory breeding colony and in recent publications using the same animal model (Génin and Perret 2003; Giroud et al. 2008b; Giroud et al. 2010). They were fed with fresh fruit (banana and apple) and a daily mixture made up of cereals, milk and egg. This diet is composed of 61% carbohydrates, 23% proteins and 16% lipids. Water was always given ad libitum.
After a 2-week habituation phase, animals were randomised to the following groups. An ad libitum control (CTL) group of 14 animals was fed with the standard diet. The daily amount of food given to the animals (15 g of mixture and 6 g of fresh fruit per day, equivalent to 105 kJ/day on average) was estimated from preliminary internal studies of the Brunoy laboratory over a year of measuring spontaneous food intake in isolated control adult animals (unpublished data). During the first 2 weeks of the SD period, animals remained undisturbed and more food (169 kJ/day) was given to allow annual fattening. Then, the amount was progressively decreased (128 kJ/day in the third week, 116 kJ/day in the fourth week) until the fifth week when the amount of food was fixed for the rest of the year (102 kJ/day). A CR group of 14 animals was fed the same diet but received 30% less than the CTL group, which corresponded to an average of 71 kJ per day (i.e. 10 g of mixture and 4 g of fresh fruit per day). This restriction was based on several studies on different species (Lane et al. 2000; Blanc et al. 2003). It was applied throughout the year, except during the critical period of fattening. During the first 3 weeks of the SD period, CR animals received the same amount of food as the CTL group to allow them to fatten normally and, after these first 3 weeks, the 30% caloric restriction applied was the same during SD and LD periods. Finally, a third group (RSV group) of 14 animals was fed with the same quantity of food as CTL but supplemented with 200 mg of RSV per kilogram bodyweight per day (Sequoia Research Products, UK). This dosage was selected from the literature from studies in rodents, and was intermediate between the 40 mg/kg.d–1 of Baur et al. (2006) and the 400 mg/kg.d–1 of Lagouge et al. (2006). To know exactly the quantity of food really ingested by the animals, daily leftovers were measured and corrected for water evaporation.
Daily energy expenditure, body composition and water turnover
Water from serum and urine samples were extracted by cryo-distillation, as previously described (Gilbert et al. 2007). A 0.1 µL of water was reduced to hydrogen and carbon monoxide by reduction on a glassy carbon reactor held at 1,400°C in an elemental analyser (Flash HT, Thermofisher, Germany). Hydrogen and carbon monoxide gases were separated by a gas–liquid chromatography column held at 104°C coupled to a continuous flow Delta-V isotope ratio mass spectrometer. Isotopic abundances of deuterium and 18-oxygen in hydrogen and carbon monoxide gases were measured in quintuplicate and repeated if SD exceeded 2‰ and 0.5‰, respectively. All enrichments were expressed as International Atomic Energy Agency standards. CO2 production was calculated according to the single pool equation of Speakman (Blanc et al. 2000): rCO2 = (N/2.078) × (ko–kd) – 0.0062 × kd × N, where N represents the average isotope dilution space of oxygen-18 calculated from Coward (1990) by the plateau method using the 1 h post-dose sample. ko and kd represent the isotope constant elimination rates calculated by linear regression of the natural logarithm of isotope enrichment as a function of elapsed time from day 1 samples. DEE was calculated by Weir's equation (Weir 1949) using a food quotient of 0.86 estimated from the animal's diet. TBW was measured from the dilution space of 18-oxygen after correction for exchange by the factor 1.007 (Racette et al. 1994). Fat-free mass (FFM) was calculated from TBW by assuming a hydration coefficient of 73.2%, which was shown to be unchanged by chronic CR (Blanc et al. 2005). Fat mass (FM) was calculated as the difference of FFM from body mass. Water turnover was assessed by the multiplication of the average isotope dilution space of oxygen-18 (N) with the deuterium constant elimination rate (kd) and corrected for isotope fractionation (Blanc et al. 2000). FFM and FM were expressed in g, TBW was expressed in % and DEE was expressed in kJ/day.
Resting metabolic rate
Oxygen consumption was measured with a closed circuit respirometer. This protocol was applied four times per year, in the first and last third of each photoperiod (SD1, SD2, LD1 and LD2) (Fig. 1). All the animals were experimented with this procedure (13 CTL, 14 CR and 14 RSV). For this nocturnal species, RMR measurements on post-absorptive animals were performed during their daily resting period, 4–6 h after the beginning of the light period to avoid torpor metabolism. Animals were trained to nest in the respiratory chamber that consisted of an opaque chamber of 2.5 l with a woven floor to absorb any urine. During the experiment, the respiratory chamber was placed in a cabinet at a controlled ambient temperature of 25.0 ± 0.5°C, a value within the thermoneutral zone defined for the mouse lemur (Aujard and Perret 1998). After a 20 min habituation phase under constant air-flow ventilation (2 l.min−1) drawn through the respirometry chamber from bottom to top, the chamber was closed for a 40 min period. VO2 consumed by the animal was calculated from initial and final concentrations of O2 in the chamber that were measured on dried gas using a Servomex 570 A paramagnetic gas analyser (accuracy 0.01% O2). The analyser was routinely calibrated with N2 and atmospheric air. O2 consumption was expressed as ml O2 h−1. O2 consumption was adjusted for the body weight of the animal (Blanc et al. 2003). Body temperatures were not measured before the experiment to avoid disturbance of the sleeping animal but males never entered deep torpor at an ambient temperature of 25°C.
Spontaneous locomotor activity
Spontaneous locomotor activity was estimated once a year at the end of the LD period, during their breeding season, when the animals are more active (Aujard et al. 2007) (Fig. 1). For technical reasons, only five CTL, nine CR and seven RSV followed this protocol. Spontaneous locomotor activity was estimated using a device with presence and motion sensors adapted to the mouse lemur (homemade system developed in the laboratory). The apparatus was placed in an ambient temperature controlled room (25°C). Animals were housed individually in a cage with a capacity of 1 m3 each provided with nest and supports. Each animal was placed in a totally closed wooden nest, except for both sides of the nest on which were placed eight presence sensors (Honeywell, transmitter: SEP8705003, receiver: SDP8405014) to know when the animal was in the nest. These presence sensors were continuously recording. Moreover, two motion sensors (Gardtec, Gardscan ‘M’ series infrared detectors) were placed in the corners of the cage to detect the spontaneous movements of the animal during its activity period. If the animal was in movement, the motion sensors recorded data every two seconds. Thus, data were expressed in arbitrary units (a.u.). Data were stored in a computerised system (developed in the laboratory). They were then computed to represent the time course of these movement patterns using a software filtering “Actocebe 3.0” developed in language G from National Instruments. Total movements were averaged at 5-min intervals for further analysis.
Blood collections were taken via the saphenous vein of the animals, without anaesthesia, at the end of their resting phase before the food allotment became available. Blood was collected in capillary tubes containing EDTA and immediately centrifuged (7,000 rpm at 4°C for 30 min) after collection. One hundred microlitres was collected per sampling and represented less than 2% of the blood volume of the animal. Plasma was stored at –80°C.
Blood sampling for IGF-1 level analysis was performed four times a year, in the first and last third of each photoperiod (SD1, SD2, LD1 and LD2) (Fig. 1). IGF-1 level was measured for 11 animals by group, using an IGF-1 IRMA kit (Immunotech SA, Marseille Cedex, France). A dilution step was performed before the assay to dissociate IGF-1 from its binding proteins. The antibodies used in this immunoassay are highly specific for IGF-1 (extremely low cross-reactivity against insulin, pro-insulin, IGF-2 and growth hormone). The intra-assay coefficient of variation was 6.3% and inter-assay coefficient of variation was 6.8%. Assay sensitivity was 2 ng/ml. Values were expressed in ng/ml.
Blood sampling for testosterone level analysis was performed three times a year, in the middle of the SD period and twice during the LD period, which is the activity period of grey mouse lemur (SD, LD1 and LD2) (Fig. 1). Testosterone was analysed for 12 CTL, 11 CR and 11 RSV. Testosterone was assayed using the testosterone ELISA kit DE1559 (Demeditec, Kiel, Germany), which measures the total testosterone in plasma (expressed in ng/ml). After two distinct periods of incubation of 60 and 15 min with the different reagents, the optical density was read with a spectrophotometer at 450 nm (Bio-Tek Instruments Inc., Winooski, USA). Assay sensitivity was 0.083 ng/ml. The intra-assay coefficient of variation was 6.7% and inter-assay coefficient of variation was 9.7%. Values were expressed in ng/ml.
Testis size variations of each animal, expressed as a scale in a.u., was assessed once a week by the same person to complete the testosterone level analysis by estimating visually their sexual status (if there was no testis, a score of zero was given, if the testis began to appear, a score of one and when the testis were well developed, a score of two).
Animals are followed until their spontaneous death. All animals that will die during the study undergo a complete autopsy by a veterinarian. Based on specific criteria (rapid body mass loss, anaemia, difficulty breathing), dying animals will be deeply anaesthetised. After autopsy will be completed, all organs will be harvested and kept for future analysis. Special attention will be give to the mouse lemur's brain to check it for Alzheimer-like pathology.
For calculation, we chose the increase in the mean lifespan as the primary outcome. In the breeding colony of the Brunoy laboratory, analysis of survival from 254 male mouse lemurs allowed us to determine the mean lifespan (mean ± SEM: 6.0 ± 0.2 years), the mean lifespan of the 10% longest living animals (10.0 ± 0.2 years) and the observed maximal survival duration (12.0 years). Based on literature (Lin et al. 2000; Tissenbaum and Guarente 2001, Anderson et al. 2003; Howitz et al. 2003; Ingram et al. 2006; Valenzano et al. 2006), we expected that the mean lifespan of the restricted and the RSV-supplemented groups would increase by a minimum of 30%. With this parameter, assuming a common standard deviation of 5% and a power analysis of 80%, a sample size of 12 individuals per group was required. We chose to increase the groups size (n = 14) to compensate the effect of early hazardous deaths in reducing statistical powers of metabolic and behavioural variables measured throughout the time course of the study during the project. The actual total power will be recalculated a posteriori.
Because of the large amount of data gathered during this longitudinal study, an Access database was created to comprehensively analyse all the results. For technical and setup reasons, the number of animals used for each experiment varied, especially for the locomotor activity monitoring, which was planned after the beginning of the project. Moreover, one animal of the CTL group suffering from a urinary tract infection died during the first year of this study and was removed from the analysis. All values are expressed as mean ± SEM. After checking for the normality of the distribution, ANOVA or repeated ANOVA for related samples was used to assert significant variations in all studied parameters. Data from average seasonal body mass plateaus and IGF-1 levels were log-transformed to obtain data with a normalised distribution. Adjustments of FFM, RMR and TEE for body size were performed by analysis of covariance with a fluctuating slope model. Comparisons were considered to differ significantly when p < 0.05. All statistics were performed by SYSTAT for Windows (V9, SPSS Inc., USA).
As shown in Fig. 2b, the animals presented an initial average body mass of 90 ± 5 g. All animals fattened during the first 12 weeks of the SD period to reach a plateau of 131 ± 8 g about 8–9 weeks before decreasing their body mass until another plateau of 83 ± 9 g in the middle of the LD period (Fig. 2b, p < 0.001). Across the first year of the study, body mass did not significantly differ between the three groups even though a trend effect of treatment was observed (p = 0.072). However, when the data were split by seasons, CR animals presented a lower body mass compared with CTL and RSV groups during the second half of the LD period (74 ± 2 vs. 87 ± 4 and 90 ± 3 g, respectively, p = 0.021, Fig. 2c).
The RESTRIKAL project aimed to compare for the first time the effects of a long-term CR or a mimetic compound supplementation on multiple ageing processes in a heterothermic primate. After 1 year, all mouse lemurs appeared in excellent health, suggesting no detrimental effect of both diets. Expected variations because of photoperiodic entrainment were present in all groups. Neither CR nor RSV supplementation affected photoperiodic variations in FFM, FM, TBW, water turnover, IGF-1 levels or testosterone levels. However, the evolution of FFM and water turnover in RSV-supplemented animals presented several differences compared with controls. Indeed, FFM and water turnover values in the RSV group varied in an opposite manner to the CTL group. Moreover, the RSV group exhibited higher values of DEE at the beginning of the LD period and a strong increase in RMR without any increase in spontaneous daily locomotor activity at the end of the LD period. Lastly, although body mass values did not differ between groups during the SD photoperiod, CR animals presented with a significant decrease of their body masses at the end of the LD period.
Exposed to a SD photoperiod, mouse lemurs fattened quickly and, after 2–3 months, exhibited a spontaneous reduction of their caloric intake (Génin and Perret 2000). Consequently, CR was proportionally less severe in SD than LD (21% vs. 30%, respectively). Therefore, the body mass of CR animals did not differ from those of controls during the first 6 months of this study i.e. the SD period. Accordingly, IGF-1 levels were not modified. However, at the end of the LD photoperiod, restricted animals exhibited a lower body mass than controls and, although not significantly different, their IGF-1 levels were reduced. A similar decrease in IGF-1 levels has been demonstrated in mice exposed to moderate CR after 24 weeks of treatment (Huffman et al. 2008).
The neuroendocrine system involving GH and IGF-1 mediates some of the metabolic consequences of caloric excess or restriction (Smith 1996). Obesity is associated with increases in levels of free IGF-1 (Nam et al. 1997) and free fatty acids, both of which are known to decrease GH secretion through a negative feedback mechanism (Lee et al. 1995). Endocrine changes under CR have been extensively studied in rodents (Shimokawa and Higami 2001). Weight loss, as observed with a restricted diet, is accompanied by a decrease in both free fatty acids and free IGF-1 levels, leading to a potential increase in GH secretion (Smith 1996). However, IGF-1 and GH levels were unaffected in humans after a 6 month-period of CR (Redman and Ravussin 2009).
Human ageing is marked by a reduction in both GH and IGF-1 concentrations in healthy adults (Veldhuis et al. 2005). Some of the anti-ageing actions of CR involve the modification of several neuroendocrine pathways but they remain to be studied (Berner and Stern 2004; Meites 1989). In some mammalian species, CR can reduce the age-related IGF-1 decline (Berryman et al. 2008). However, the observed decrease in IGF-1 levels after 1 year of CR in mouse lemurs cannot be attributed to ageing alone. Indeed, in this primate age-related changes in IGF-1 levels are characterised by a progressive decrease during the SD photoperiod, whereas levels remain high during the LD photoperiod even in old age (Terrien et al. 2009a; Aujard et al. 2010). It is most likely that changes in metabolism account for the decrease in IGF-1 in mouse lemurs at the end of the LD period.
Animals under moderate CR adapted quickly to the protocol. Indeed, body composition as reflected by FM, FFM and TBW was not modified by CR. However, during the SD photoperiod DEE was lower in restricted animals compared with control ones. Similar results were found in rhesus monkeys subjected to a 30% reduction in caloric intake after several years of treatment (Raman et al. 2007). The reduction in DEE in the grey mouse lemurs has to be related to its ability to enter daily torpor to conserve energy in the face of environmental constraints (Terrien et al. 2009a). Mouse lemurs exposed to moderate food shortage (Giroud et al. 2008a) exhibited an increasing frequency of daily torpor. Therefore, animals likely minimise energy expenditure and compensate for the effects of CR on body composition by entering deep torpor. Further studies should investigate the length and duration of torpor bouts in CR animals.
RMR, recorded after the daily torpor bout of each animal, was not different between control and CR animals. By contrast, the RMR of human subjects placed under a 25% CR decreases after three months compared with controls (Martin et al. 2007). In our experiments, the percentage of CR applied in the mouse lemur might not be sufficient to induce RMR variations or the duration of treatment (1 year) might not be long enough to induce significant modifications. At any rate, this lack of change in RMR also suggests that the animals do not save energy during their resting periods but probably during deeper torpor. Moreover, the CR group presented with lower values of water turnover compared with control animals, indicating greater water retention. This is probably because of the increased frequency of torpor bouts, an important mechanism in this species during SD photoperiods.
From the beginning of the LD photoperiod, all animals lost body mass. Body composition and related body mass did not differ between groups. The LD photoperiod corresponded to the breeding season with a general activation of physiological and behavioural parameters (Perret 1985). In particular, an increase of reproductive functions was expected. As reflected in this study, higher values of testosterone levels were observed for the CTL and CR groups in the LD period but we noticed no difference between the two groups. Interestingly, the expected increase in LD period-related water turnover was not observed for any group. Moreover, DEE did not differ between control and restricted animals. One possible explanation might be the period when these parameters were measured. Indeed, when the experimental design of this study was established, it was anticipated that animals would exhibit their most significant metabolic changes just after the photoperiodic shifts. However, changes in body mass and DEE as well as IGF-1 levels were more affected by dietary restriction in the second part of the LD period. Therefore, for the remaining years of the study, measurements will be made in the second part of the LD period.
During exposure to the LD photoperiod, CR impacted heavily on body mass variations of grey mouse lemurs (Génin and Perret 2003; Séguy and Perret 2005; Giroud et al. 2008a, b). In the LD photoperiod, mouse lemurs did not use daily torpor to avoid body mass loss even under a 40% CR (Giroud et al. 2008a). Moreover, this decrease of body mass could not be explained by changes in RMR or locomotor activity. Contrary to expectations, despite having less energy reserves, no increase in exploratory behaviour, as reflected by spontaneous daily locomotor activity, was observed in CR animals. Similar results were observed after several weeks of 40% CR in mouse lemurs in the LD photoperiod (Giroud et al. 2008a). However, when CR was higher, for example 80% (Génin and Perret 2003), a strong increase in locomotor activity was recorded, suggesting the active search of required food. In the rhesus monkey (Macaca mulatta), an increase in activity levels has been observed for animals under a 30% CR (Weed et al. 1997). However, these results were only valid for the older male group followed in the NIA study. In monkeys, the literature in this domain was well developed, but the results obtained in the different studies did not allow to conclude about caloric restriction effects on locomotor activity (Kemnitz et al. 1993; Ramsey et al. 1996; Delany et al. 1999; Moscrip et al. 2000). Presently, how CR affects locomotor activity is unclear. As stressed by Ingram et al. (2001), the large variability of the results could be attributed to various factors such as the age and sex of the animals and different CR intensities and durations. Further studies will be necessary to highlight the reality of CR effects on the locomotor activity of primates.
Animals supplemented with RSV ate approximately the same amount of food as controls during both photoperiods and exhibited similar photoperiodic variations in their body mass and FM. In the SD photoperiod, their body composition, energy expenditure, RMR and hormonal level were similar to those recorded in the control group. Interestingly, the RSV group did not present any difference in body mass compared with the control group, suggesting that RSV does not mimic CR for this parameter, at least after a year of treatment.
However, the FFM of the RSV group was higher in LD period compared with the control group, with a high inter-individual variability. Animals might have developed a larger muscle mass as demonstrated in RSV-supplemented mice that displayed increased muscle strength in locomotor tests after several weeks of treatment (Baur et al. 2006; Lagouge et al. 2006). Moreover, RSV can stimulate in vivo muscle cell glucose uptake through sirtuins and AMPK (Breen et al. 2008), an effect possibly involved in the muscle mass increase of RSV-supplemented mouse lemurs. DEE was also modified by RSV treatment in mouse lemurs with higher values compared with controls at the beginning of the LD period. A similar trend was observed for water turnover. Lastly, contrary to the CR group, the RMR of RSV-supplemented animals was noticeably increased in the early and late stages of the LD period. This RSV effect on the RMR was already seen in a previous study where a 4-week supplementation with RSV was sufficient to induce an increase of the grey mouse lemurs' RMR (Dal-Pan et al. 2010). Moreover, as for high-fat mice after several weeks of RSV supplementation (Lagouge et al. 2006), RSV seemed to activate significant energy metabolism of grey mouse lemurs, in particular their RMR.
In summary, a moderate CR or a mimetic compound supplementation was safely initiated in an adult heterothermic primate. First-year results of the study suggest a good adaptation of the animals to their diet. Preliminary results after 1 year of treatment suggest that RSV produces an activation of energy metabolism without body mass loss in contrast to CR, which produces a decrease of energy expenditure. Taken together, the effects of CR or RSV supplementation in grey mouse lemurs seemed more important during LD than during SD periods. Physiological and behavioural parameters are highly photoperiod-dependent in this primate, and it is likely that during LD photoperiods energy constraints are more important than during SD photoperiods, thereby leading to a more pronounced effect of the diet treatment. However, changes observed at the end of the LD period might also reflect the chronic effects of treatment after 1 year. The respective roles of this photoperiodic dependency and duration of treatment should be resolved in forthcoming years along with the evolution of validated biomarkers of ageing.
In conclusion, after only 1 year of treatment, it cannot be proposed that the hormesis theory is the most appropriate hypothesis to explain the effects observed in a non-human primate exposed to CR or RSV supplementation. CR and RSV might be two different stressors taking a different path to produce the same effects. Indeed, several differences were observed between CR and RSV supplementation, questioning the similarity of the pathways involved. If similar pathways between CR and RSV supplementation exist, as for example through sirtuins (especially SIRT1), it will be necessary to investigate the evolution of the levels of such molecules in future years of the RESTRIKAL project.
The authors acknowledge the continuing assistance provided by Eric Gueton for daily feeding and care provided to animals. Laurine Haro is recognised for expert technical assistance. This work was carried out with the financial support of the French National Research Agency (project ANR-06-PNRA-010-01) and the Foundation for French Medical Research.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.