Circadian rhythms and appetite

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The control of food intake is a flexible system whereby internal and external environmental cues can alter the timing of feeding and appetite. The suprachiasmatic nucleus in the hypothalamus is the vital coordinator of these stimuli that ultimately generates fluctuations in neuronal and hormonal activities that are known as circadian rhythms. Circadian rhythms are driven by the daily variations in ambient light, which, by alterating gene expression, elicit a host of physiological responses including fluctuations in the hormones involved in appetite and food intake. Various factors such as temperature and social cues influence circadian rhythms; indeed, food intake itself can regulate these rhythms, but the neural mechanisms by which this occurs remains elusive. It has recently been proposed that there is a ‘food entrainable oscillator’ that exists independently of the SCN, and which controls food anticipation activity. The importance of circadian rhythms for ensuring good health has been highlighted by our modern day lifestyle, as jet-lag and shift work have shown that disruption of these delicate balances can lead to pathologies such as metabolic syndrome.

The generation of Circadian Rhythms: the clock genes

Clock mechanisms are formed by the transcription and translation of clock genes, which rely on feedback loops. In mammals, Clock and Bmal1 genes are part of the positive loop and Per genes, the negative loop. The clock genes regulate a self-sustaining rhythm in cells that even without light will maintain a roughly 24 hour rhythm. An extreme example is of cave fish which have lived in complete darkness for millions of years and their clock genes are still present in their DNA.

The rhythmic output of organs can be influenced by metabolic, endocrine and homeostatic events, as well as by the circadian clock. For example, the SCN can change the rhythm of expression of liver genes and enzymes without using clock genes, but through second messenger systems induced by the autonomic nervous system instead. Other genes can also affect circadian clock genes; for example the ROR-alpha gene is a positive regulator of Bmal1, which regulates lipogenesis and lipid storage.

Genes which encode important proteins of core clock mechanism are circadian locomotor output cycles kaput (Clock), brain and muscle-Arnt-like 1(Bmal1), Period1 (Per1),Period2 (Per2), Period3 (Per3),Cryptochrome1(Cry1) and Cryptochrome2(Cry2). CLOCK (the protein product of Clock) is a transcription factor which dimerises with BMAL1 (the protein product of Bmal1) to activates transcription. CLOCK and BMAL1 are proteins which form basic helix-loop-helix transcription factor.Basic helix loop-helix is a structural motif.CLOCK and BMAL1 transcription factors form a heterodimeric complex. The above complex binds to E-box, which is a DNA sequence found in the promoter region of the gene and E-box like promoter sequences. The binding of CLOCK:BMAL1 complex to E-box located in the promoter region of ""Per"" and ""Cry"" genes and activates their transcription. PER and CRY proteins are able to undergo nuclear transformation and inhibit CLOCK:BMAL1 complex, which results in the decreased transcription of their owm genes. CLOCK:BMAL1 and PER-CRY transcription-translation loop is able to detect and self adjust to the changes. CLOCK:BMAL1 and PER-CRY constitute the core of the circadian clock and are able to generate 24 hour rhythms of gene expression.. Recent studies on the function and interaction of CLOCK:BMAL1 interaction have shown that it induces transcription in the following genes: RORɑ and REV-ERBɑ . RORɑ and REV-ERBɑ regulate lipid metabolism and adipogenesis. The complex is also involved in the regulation of ""Bmal1"" transciption, with RORɑ stimulating and REV-ERBɑ inhibiting the transcription. Another gene which is activated by CLOCK:BMAL1 heterodimer is Pparɑ, which codes for a nuclear receptor involved in glucose and lipid metabolism.

Studies on mice with impaired Clock function showed increased food intake and eradication of rhythmic expression of Cart and Orexin hormones . Experimental data reported by Bray et.al shows that CLOCK -/- mice exhibit obesity,altered feeding patterns,hyperphagia and hormonal abnormalities similar to those found in metabolic syndromes, such as hyperlipidemia(abnormally elevated levels of lipoproteins in the blood), hyperglycemia()high amount of glucose in blood plasma) and hyperinsulinemia (excess levels of circulating insulin in the bloodstream).

The SCN, circadian rhythms and feeding behaviour

A wide variety of organisms, from cyanobacteria to humans, all share common internal clock mechanisms that have been present for millions of years in evolutionary history. The circadian clock in mammals is responsible for setting specific temporal patterns within our bodily systems, including many physiological functions (body temperature, melatonin release, glucocorticoid secretion) and behavioural functions (alertness, working memory,) in order to keep us alive and running smoothly.

The "master" circadian clock of mammals is in the suprachiasmatic nucleus (SCN) of the hypothalamus. The main input to the SCN consists of signals encoding light; these are carried from the retina to the SCN by the retinohypothalamic tract. Vasoactive intestinal polypeptide, released from a subpopulation of neurones in the SCN, activates and synchronises other SCN neurons, the output of which coordinates behavioural rhythms. One way in which the SCN may regulate food intake is by directing the sleep/wake cycle.

The role of the SCN in feeding patterns has been determined using rodents, as their food intake is less influenced by cognition and social behaviour as found in humans. The sleep/wake cycle is driven by fluctuations in two main hormones: corticosterone (cortisol in humans) and melatonin. In rats, corticosterone secretion increases during the night when these nocturnal animals are active. This rise is followed by an increase in locomotor activity, in which rats forage for food and subsequently begin to feed. Melatonin is an important hormone that is released from the pineal gland during the night which, amongst its many actions affects sleep and appetite.

.SCN regulation of the sleep/wake cycle; The SCN innervates multiple regions of the brain that regulate the sleep-wake cycle. a) The most intense output from the SCN is to the ventral sub-paraventricular zone (SPZ); this projects to the dorsomedial hypothalamus (DMH) which controls a wide range of circadian responses including corticosteroid secretion. The DMH innervates the medial parvicellular paraventricular nucleus (PVHm) and regulates the CRH neurons which control pituitary regulation of corticosteroid production. The SCN is also involved in regulating the release of melatonin from the pineal gland. The SCN projects to the dorsal parvicellular paraventricular nucleus, (PVHd) which projects to sympathetic preganglionic neurons in the spinal cord which regulate melatonin output by the release of noradrenaline into the pineal gland. b) The DMH also has GABAergic projections to the ventrolateral preoptic nucleus VLPO (the sleep promoting region) and glutamatergic projections to the orexin producing neurons and the melanin-concentrating hormone (MCH)neurons in the lateral hypothalamus (LHA) which together regulate sleep and wakefulness and ultimately feeding. Hormones involved in appetite regulation such as ghrelin and leptin can influence these areas of the brain thus may have a role in resetting the circadian rhythms generated by the SCN. (Adapted from figure 2c&d Saper et al. (2005).)

However, it is important to note that these hormones have different physiological roles in different species. For example, melatonin is released during the night in both humans and rodents, and yet latter are nocturnal and therefore most active at night. This indicates that melatonin has the opposite effects in rodents as it does in humans in that it appears to drive the awake period in rats and induce the sleep period in humans. Thus it is appearent that whilst the SCN may regulate the sleep-wake cycle, this regulation is species-specific which suggests that the role the SCN has in feeding behaviours is equally complex due to the diverse actions of the hormones involved.

Nevertheless, it is possible that that the SCN may drive feeding patterns directly as the SCN appears to have reciprocal interactions with the orexigenic regions of the brain namely the lateral hypothalamus.

The SCN and orexigneic regions of the brain. SCN fibres terminate in and around the arcuate nucleus (ARC) and the ventral part of the lateral hypothalamus . Activation of the arcuate nucleus releases NYP and AgRP (two potent orexigenic peptides) into the PVN which ultimately stimulates feeding and slows metabolism . Adapted from Fig 3. Froy 2010

Alternatively, it is possible that the SCN initiates feeding by conducting circadian rhythmic oscillations in the hormones involved in appetite. Indeed, a number of hormones involved in feeding behaviour and appetite, including leptin and ghrelin, show circadian oscillations. . Leptin has been shown to exhibit circadian patterns in both gene expression and protein secretion in humans, with a peak during the sleep phase in humans . Furthermore, rodent studies have shown that ablation of the SCN eliminates leptin circadian rhythmicity and yet the role of the SCN in conducting this pattern is unclear. As leptin binds to receptors in the hypothalamus to suppress of appetite and an increase metabolism it seems plausible to suggest that the SCN can alter appetite indirectly via hormone regulation.

Whilst the role the SCN has in driving feeding behaviour remains elusive the latest research indicates that in addition to this central circadian clock there exists peripheral oscillators in other areas of the brain and other organs that produce rhythmic patterns in feeding time. Furthermore, it has been shown that rodents show food anticipatory behaviour indicating that these peripheral oscillators can be reset by feeding time itself thus have been named food entrainable oscillators. Moreover, it has been suggested that the SCN can signal to peripheral oscillators using signalling molecules such as TGF-alpha and prokinecticin 2 that prevent dampening of circadian rhythms in the tissues . The recent study by Gilbert et al. (2009) have shown that transforming growth factor alpha is an important SCN peptide that regulates activity and feeding behaviour. Indeed intraperitoneal infusions of TGF-alpha was found to not only reduce locomotor activity but also to cause reduced food consumption and weight loss in Syrian hamsters Whilst the site of action of TGF alpha in this experiment was found to be the brain it is also possible that they act outside the central nervous system.

Peripheral Clocks and Food Entrainable Oscillators

Peripheral clocks

The SCN and peripheral clocks are not affected by meal timings, but restriction of food is the dominant synchroniser for peripheral clocks. When rats are restricted of food, metabolic and hormonal factors used by the SCN to drive peripheral oscillators are uncoupled, to shift to food time. Normally, the SCN and peripheral oscillators will work together as one unit, but a change in food availability can uncouple them in order for survival, when feeding is low and shifted from their normal place in the light-dark cycle..

© Image
SCN and Peripheral Oscillator Interaction.

The Food Entrained Oscillator

The FEO is a mysterious circadian clock, which is independent of the SCN. It ensures that when food is scarce, the body is still ready to digest and extract nutrients from the food that has been found, the FEO is responsible for anticipation of meal-time (FAA) .

Clock genes may contribute to the FAA but are not essential – Pendergast et al (2009) showed that animals without essential clock genes Bmal1 or per1 or2 were arrhythmic in constant darkness but still could express FAA. The FEO’s existence is putative, and its network is believed to be scattered over several brain regions. For example, the dorsomedial hypothalamic nucleus has been reported for FAA expression and the possible site of the FEO. The circadian mechanism for the FEO is unknown, but it does present clear circadian features.

Laura Sheldon 19:09, 24 October 2010 (UTC)Laura

Sleep deprivation, shift-work and appetite

PD Diagram
The relationship between sleep duration and changes in serum leptin and ghrelin levels. (a) Mean leptin levels against average nightly sleep duration. As the number of hours sleep increases, the levels of serum leptin also increase. Standard errors for half-hour increments of average nightly sleep. (b) Mean ghrelin levels against total number of hours sleep. As the total number of hours sleep decreases, the mean levels of ghrelin increase. Standard errors for half-hour increments of total sleep time. Adapted from Taheri et. al (2004)

In modern society, where shopping, eating, working and drinking are widely available 24hours a day,major health implications have been linked as a result. This availability of around the clock activities has defied our bodies internal clock of the vital hours of sleep it requires . Over the last few decades where technology and social activities has dramatically advanced, the number of hours of sleep young adults get has decreased within the range of 1-2hours . This is strongly correlated with the prevalence of obesity within the U.K which has shown to have trebled over the last 3 decades . Although the rise in this obesity epidemic has been shown to be multi-factorial, sleep deprivation is just another factor to add to the list needing to be addressed in this ever rising health problem.

Several epidemiologic studies have shown that sleep deprivation elevates the levels of the appetite stimulating hormone ghrelin and decreases circulating leptin levels [Fig. 5.1] . These changes could be the causes of increased food intake in these sleep- deprived adults where a rise in body weight is also observed [Fig. 5.2] . It is therefore important to fully understand the health implications that sleep-deprivation, associated with jetlag and night shift workers, has on the body in order to develop future therapeutic schemes against such related disorders as obesity.

The relationship between average nightly sleep and changes in body mass index (BMI). As the average nightly hours of sleep decreases below 7 hours, the mean BMI increases. Furthermore, more than an average of 8 hours sleep also causes a rise in mean BMI. Standard errors for 45-min intervals of average nightly sleep. Adapted from Taheri et. al (2004)

Conclusion

Over the last decade, significant progress has been made in our understanding of the inter-relationship between circadian biology, sleep and metabolism in the context of obesity. The SCN which is a vital coordinator of circadian rhythms may have a possible role for driving feeding patterns, along with other peripheral oscillators in the brain and organs that produce rhythmic patterns in feeding time.

As a result of this newly industrialized world, sleep deprivation is a growing issue of concern and the serious health implications it has on the population need to be acknowledged. An adequate number of hours sleep each night is vital in ensuring a healthy lifestyle. Disruptions of the circadian variations in such appetite-regulating hormones as leptin and ghrelin may contribute to the development of obesity in sleep deprived patients.

Gaps still remain in our knowledge of the underlying biological rhythms and its association with the pathogenesis of obesity. So far previous therapeutic strategies have failed to curb the rising incidence of obesity, but if, through a greater understanding of these complex systems we are able to manipulate and control appetite the benefits will be a healthier population and less strain on the health services caused by obesity.