Presently, about 12% of the population is 65 years or older and by the year 2030 that figure is expected to reach 21%. In order to promote the well-being of the elderly and to reduce the costs associated with health care demands, increased longevity should be accompanied by ageing attenuation. Energy restriction, which limits the amount of energy consumed to 60–70% of the daily intake, and intermittent fasting, which allows the food to be available ad libitum every other day, extend the life span of mammals and prevent or delay the onset of major age-related diseases, such as cancer, diabetes and cataracts. Recently, we have shown that well-being can be achieved by resetting of the circadian clock and induction of robust catabolic circadian rhythms via timed feeding. In addition, the clock mechanism regulates metabolism and major metabolic proteins are key factors in the core clock mechanism. Therefore, it is necessary to increase our understanding of circadian regulation over metabolism and longevity and to design new therapies based on this regulation. This review will explore the present data in the field of circadian rhythms, ageing and metabolism.

As obesity and metabolic diseases rise, there is need to investigate physiological and behavioural aspects associated with their development. Circadian rhythms have a profound influence on metabolic processes, as they prepare the body to optimise energy use and storage. Moreover, food-related signals confer temporal order to organs involved in metabolic regulation. Therefore food intake should be synchronised with the suprachiasmatic nucleus (SCN) to elaborate efficient responses to environmental challenges. Human studies suggest that a loss of synchrony between mealtime and the SCN promotes obesity and metabolic disturbances. Animal research using different paradigms has been performed to characterise the effects of timing of food intake on metabolic profiles. Therefore the purpose of the present review is to critically examine the evidence of animal studies, to provide a state of the art on metabolic findings and to assess whether the paradigms used in rodent models give the evidence to support a ‘best time’ for food intake. First we analyse and compare the current findings of studies where mealtime has been shifted out of phase from the light–dark cycle. Then, we analyse studies restricting meal times to different moments within the active period. So far animal studies correlate well with human studies, demonstrating that restricting food intake to the active phase limits metabolic disturbances produced by high-energy diets and that eating during the inactive/sleep phase leads to a worse metabolic outcome. Based on the latter we discuss the missing elements and possible mechanisms leading to the metabolic consequences, as these are still lacking.

The objective of this study was to determine whether rabbits fed in a restricted regimen (75%) showed increased competition for feeding, drinking and use of specific areas of the cages as compared with those provided feed ad libitum. This evaluation was carried out by measuring their space utilisation in the cage, the incidence of agonistic behaviour and rates of mortality. In total, 504 rabbits between 31 and 66 days of age were used in this study. A total of 200 heavy-weight rabbits and 56 light-weight rabbits were randomly housed in 32 cages, each cage containing eight rabbits: 25 cages housing heavy rabbits and seven cages housing the light-weight ones. They were all fed ad libitum (AD). In addition, a total of 208 heavy-weight rabbits and 40 light-weight rabbits were randomly housed in 31 cages, each of them containing eight rabbits: 26 cages housing heavy weight rabbits and five cages housing light-weight ones. They were all fed a restricted diet (R) regimen. The restriction was calculated to be 75% of the feed consumed by the AD group. The total space available in the cage was 3252 cm2, with a stocking density of 24.6 animals/m2. Animals between 32 and 60 days of age from 20 different cages were observed nine times per week (morning or afternoon) by means of scan and focal sampling by one observer. During each period, cages were assessed for 5 min, registering every minute the position of all the animals in relation to Area A (feeder), Area B (central part) or Area C (back and drinker area). The incidence of agonistic behaviour such as displacement, biting and jumping on each other was also assessed. Performance variables such as daily gain and feed conversion ratio, in addition to general health status and mortality rates, were recorded for all rabbits. When the rabbits were under restricted feeding, the competition for feed and drink increased with clear signs of agonistic behaviour such as biting, displacement and animals jumping on top of each other. Although this competition was maintained during the entire growing period, the BW homogeneity between animals in the same cage was similar in both cases, suggesting that all animals could consume similar quantities of feed. The possible advantages of a restricted diet, such as better feed conversion ratio, were observed in this study only in the last few weeks of the growing period.

From 74 to 180 days of age, a complete diet was offered either ad libitum (AL) or at proportionately 0·8 of the observed consumption (R) to two groups of purebred Yorkshire gilts, comprising 128 and 127 animals, respectively. Half of the animals in each group was served at the first detected oestrus, and the other half at the third detected oestrus, according to a plan defined at the start of the experiment. Animals which failed to show oestrus before 240 days of age were culled.

At 100 kg live weight (LW), AL gilts were younger (-20 days) and had thicker backfat (+2.3 mm) than R gilts. At the first detected oestrus, AL females were also younger (198 v. 203 days), heavier (127 v. 117 kg LW) and fatter (17·8 v. 14·7 mm backfat thickness) than R gilts. No difference between feeding treatments during rearing was observed in the percentage of females detected on heat before day 240. Seventy-three animals were culled from the start of the experiment until service, half of them (54%) failing to show oestrus. At service, LW and backfat thickness in the four treatments ranged from 117 to 148 kg LW and 14·9 to 19·7 mm, respectively. The body fatness, estimated from the ratio of backfat to LW, was higher in AL than in R gilts (0·14 and 0·12 , respectively), whereas no difference was observed between E1 and E3 gilts (0·13 on average). After the first service 15% of the gilts came back into heat but the conception rate was not affected by feeding treatment during rearing.

Seventy-two crossbred barrows (28.7 ± 0.3 kg live weight (LW)) were used to examine whether there is a relation between eating traits, and performance and carcass traits in ad libitum and restrictedly fed group-housed pigs. The experiment included two replicates, each consisting of 36 pigs. From day 1 to 42, all pigs were maintained with free access to a starter diet containing 12.7 MJ metabolizable energy (ME) and 8.2 g ileal apparent digestible lysine per kg. The experimental period was from day 42 (55.9 kg LW) to the end of the experiment (110.2 kg LW). The pigs in treatment 1 were maintained with free access to a high (H) energy diet (13.1 MJ ME and 7.1 g ileal apparent digestible lysine per kg). For pigs in treatments 2 and 3 the daily energy allowance per pig was restricted to 18 MJ ME above the daily energy requirement for maintenance using diet H, and a low (L) energy diet (12.5 MJ ME and 6.7 g ileal apparent digestible lysine per kg), respectively. The weekly measured LW was used to compute the energy requirements for maintenance (M = 0·719 MJ ME × LW (kg)0.63). Daily food intake and eating traits per pig were determined using transponders and an electronic feeding station equipped with an antenna.

Daily energy intake of the ad libitum and restrictedly fed pigs was correlated with growth and lean meat tissue content of the carcass. In the pigs given food ad libitum, daily energy intake was correlated with daily feeder visiting time, time per meal and food intake per meal, but not with number of meals per day and rate of food intake. In the restricted treatments, number of meals per day was correlated with energy intake, but not with lean tissue content of the carcass. In conclusion, number of meals per day explained part of the variation of lean tissue content of the carcass in ad libitum, but not in restrictedly fed group-housed pigs.

Two experiments were carried out with Scottish Blackface lambs to investigate the effects of restricted nutrition during pregnancy and lactation on voluntary food intakes (VFI) between weaning and 2 years of age. Ewes were given diets providing 0·7 (LP) or 10 (HP) of their estimated metabolizable energy requirements during the last 6 weeks of pregnancy and subsequently grazed swards with mean sward surface heights of approximately 3 cm (LL) or 6 cm (HL) during lactation. All lambs were weaned at 17 weeks of age. In experiment 1, four treatment combinations (LP-LL, LP-HL, HP-LL and HP-HL) were applied and female lambs were studied. In experiment 2, two treatment combinations (LP-LL and HP-HL) were applied and male lambs were studied. In both experiments the lambs received a common level of nutrition between weaning and 2 years of age.

In both experiments, mean live weights were proportionately 0·2 higher for HP-HL than for LP-LL lambs at weaning (P < 0·001) and in experiment 2 mean live weights and body condition scores were still higher in HP-HL than in LP-LL lambs at 2 years of age (P < 0·05). Abomasum weights were higher in HP than in LP lambs at birth and higher in HP-HL than in LP-LL lambs at weaning in experiment 1 and the weights of the rumen and dimensions of the rumen villi were greater in HP-HL than in LP-LL lambs at weaning in both experiments (P < 0·05). The treatments had no effect on lipid content or mean adipocyte diameter in the main fat depots at birth or weaning. There were no treatment effects on VFI in either experiment. It was concluded that restricted nutrition during late pregnancy and early lactation does not affect VFI between weaning and 2 years of age in sheep, even though there are differences in live weight and the development of the gastrointestinal tract at weaning and there may be long-term effects on live weight and body condition, particularly in male animals.

Responses to four generations of divergent selection in pigs for lean growth rate (LGS) with restricted feeding were studied. The selection criterion was designed to obtain equal correlated responses in growth rate and carcass lean content, measured in phenotypic s.d. Animals were to be performance tested in individual pens with a mean starting weight of 30 kg for a period of 84 days. Daily food intake was equal to 0·75 gig of the daily food intake for pigs offered food ad-libitum. In the high, low and control lines, there ivere 1250 Large White-Edinburgh (LW) pigs and 875 British Landrace-Wye (LR) pigs. Each selection line consisted of 10 sires and 20 dams, with a generation interval ofl year.

After four generations of selection, cumulative selection differentials were 5·9 and 4·8 phenotypic s.d. for LW and LR populations, with similar responses, 1·8 (s.e. 0·17) phenotypic s.d. Mean weight at the end of test, growth rate and backfat depths at the shoulder, mid back and loin were 89 kg, 712 g/day, 26,13 and 13 mm for LW and for LR pigs were 87 kg, 683 g/day, 28,10 and 10 mm. High line pigs were heavier at the end of test (4·3 (s.e.d. 1·4) kg and 4·0 (s.e.d. 1·6) kg) for LW and LR populations, with corresponding responses in growth rate (54 (s.e.d. 16) g/day and 47 (s.e.d. 18) g/day). Responses in the three backfat depths were −4·1 (s.e.d. 1·2) mm, −2·6 (s.e.d. 0·7) mm and −2·9 (s.e.d. 0·7) mm for LW and −2·2 (s.e.d. 0·05) mm, −2·2 (s.e.d. 0·4) mm and −2·4 (s.e.d. 0·5) mm for LR populations. Responses in weight off test and backfat depths were symmetric about the control lines.

Heritabilities for LGS were 0·34 and 0·28 (s.e.d. 0·5) for the LW and LR populations, when estimated by residual maximum likelihood. Common environmental effects for LGS were 0·11 (s.e. 0·03) for LW and 0·17 (s.e. 0·04) for LR. Heritabilities for growth rate and average backfat depth were similar for LW and LR populations (0·17 and 0·29, s.e. 0·05), as were common environmental effects (0·10 s.e. 0·04). Average phenotypic and genetic correlations between growth rate and backfat, for LW and LR populations, were small (0·15 (s.e. 0·03) and −0·06 (s.e. 0·16), respectively).

Responses to selection and genetic parameter estimates demonstrate that there is substantial genetic variation in growth and fat deposition when pigs are performance tested on restricted feeding.

The mean retention time (MRT) of stained hay through the whole digestive tract and its digestibility were measured in Japanese sika deer (Cervus nippon) and were compared with those in sheep when lucerne (Medicago sativa) hay was fed at 10, 20 and 30 g/kg body-weight. The recoveries in faeces of plastic particles with five specific gravities were also measured in deer. MRT for deer was significantly shorter than that for sheep at 10 and 20 g/kg feeding levels. The digestibilities of dry matter, organic matter, and neutral-detergent fibre were significantly lower for deer than for sheep at 30, 30 and 10 g/kg feeding levels respectively. The recovery rates of plastic particles were increased, but the ruminated rates were decreased, with increasing specific gravity in deer. These results suggest that the lower digestibility of lucerne hay in Japanese deer may be due to a shorter MRT compared with sheep.