Hostname: page-component-745bb68f8f-s22k5 Total loading time: 0 Render date: 2025-02-11T17:36:02.283Z Has data issue: false hasContentIssue false

Episodic memory as an explanation for the insurance hypothesis in obesity

Published online by Cambridge University Press:  11 May 2017

Kirsty Mary Davies
Affiliation:
Department of Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom. kmd34@cam.ac.uknsc22@cam.ac.uklgc23@cam.ac.ukhttp://www.psychol.cam.ac.uk/ccl/http://www.lucycheke.com/home
Lucy Gaia Cheke
Affiliation:
Department of Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom. kmd34@cam.ac.uknsc22@cam.ac.uklgc23@cam.ac.ukhttp://www.psychol.cam.ac.uk/ccl/http://www.lucycheke.com/home
Nicola Susan Clayton
Affiliation:
Department of Psychology, University of Cambridge, Cambridge CB2 3EB, United Kingdom. kmd34@cam.ac.uknsc22@cam.ac.uklgc23@cam.ac.ukhttp://www.psychol.cam.ac.uk/ccl/http://www.lucycheke.com/home

Abstract

In evaluating the insurance hypothesis as an explanation for obesity, we propose one missing piece of the puzzle. Our suggested explanation for why individuals report food insecurity is that an individual may have an impaired episodic ability to plan for the future.

Type
Open Peer Commentary
Copyright
Copyright © Cambridge University Press 2017 

According to the insurance hypothesis proposed by Nettle et al., “humans possess evolved mechanisms that respond to cues or experiences indicating that access to sufficient food is uncertain by increasing energy intake relative to expenditure, and hence storing more fat” (sect. 6, para. 1). However, given the current “obesogenic” environment of highly available energy-rich food, it is unclear why modern humans, at least in the Western world, might experience food insecurity. One possible explanation is that some individuals have a reduced ability to imagine and plan for the future, and that this may lead to feelings of insecurity regarding the future availability of food.

The ability to imagine and plan for the future is known as “episodic foresight” and is one half of an overarching ability to re-experience the personal past and imagine the personal future, known as “mental time travel” (Tulving Reference Tulving1993). There is now a general consensus that ability in episodic memory and episodic foresight are linked within the individual. They involve common mental processes (Schacter & Addis Reference Schacter and Addis2007), engage the same neural substrates (Buckner & Carroll Reference Buckner and Carroll2007), and are impaired in the same patients (Hassabis et al. Reference Hassabis, Kumaran, Vann and Maguire2007; Tulving Reference Tulving1985). They also develop at the same time in children (Suddendorf & Busby Reference Suddendorf and Busby2003; Reference Suddendorf and Busby2005) and decline in the same way in the elderly (Addis et al. Reference Addis, Wong and Schacter2008). These abilities appear also to be linked evolutionarily. Animals that exhibit behaviour suggestive of episodic memory have also been found to plan for the future (Cheke & Clayton Reference Cheke and Clayton2012; Clayton & Dickinson Reference Clayton and Dickinson1998; Correia et al. Reference Correia, Dickinson and Clayton2007; Raby et al. Reference Raby, Alexis, Dickinson and Clayton2007).

Growing evidence also suggests that mental time travel ability influences and is influenced by obesity. The decision to eat a given food is controlled not only by homeostatic signals, but also influenced by higher neural systems – for example, the hippocampus (Berthoud Reference Berthoud2011). The hippocampus is an integral brain region for mental time travel (Schacter et al. Reference Schacter, Addis and Buckner2008; Simons & Spiers Reference Simons and Spiers2003), and this ability has been demonstrated to play a key role in consumption regulation (Higgs Reference Higgs2002; Higgs et al. Reference Higgs, Williamson and Attwood2008). Patients with bilateral hippocampal damage producing episodic amnesia (a condition that produces severe deficits in both episodic memory and foresight) appear to consume several consecutive meals without reporting satiety (Hebben et al. Reference Hebben, Corkin, Eichenbaum and Shedlack1985; Rozin et al. Reference Rozin, Dow, Moscovitch and Rajaram1998). Furthermore, in rats, selective lesions to the hippocampus produce increased food intake and weight gain relative to intact and sham-operated controls (Davidson et al. Reference Davidson, Chan, Jarrard, Kanoski, Clegg and Benoit2009).

Research in rodents has shown that both diet-induced and genetic models of obesity are associated with impaired memory function and hippocampal damage. For example, rats maintained on a high-fat, high-sugar diet display spatial memory deficits after only 72 hours, and non-spatial memory deficits after 60 days (Kanoski & Davidson Reference Kanoski and Davidson2010). In addition, rats fed a sucrose or fructose solution for four weeks showed a 40% reduction in hippocampal neurogenesis and increased hippocampal apoptosis compared to the water solution control group (van der Borght et al. Reference van der Borght, Kohnke, Goransson, Deierborg, Brundin, Erlanson-Albertsson and Lindqvist2011). Genetic models of obesity demonstrate similar memory deficits (Li et al. Reference Li, Aou, Oomura, Hori, Fukunaga and Hori2002; Winocur et al. Reference Winocur, Greenwood, Piroli, Grillo, Reznikov, Reagan and McEwen2005) often accompanied by hippocampal dysfunction (Li et al. Reference Li, Aou, Oomura, Hori, Fukunaga and Hori2002). Hippocampal dysfunction has also been shown in overweight humans (Jagust et al. Reference Jagust, Harvey, Mungas and Haan2005; Raji et al. Reference Raji, Ho, Parikshak, Becker, Lopez, Kuller, Hua, Leow, Toga and Thompson2010), and there is evidence to suggest this is associated with episodic memory deficits (Cheke et al. Reference Cheke, Simons and Clayton2016; Cournot et al. Reference Cournot, Marquie, Ansiau, Martinaud, Fonds, Ferrieres and Ruidavets2006; Gunstad et al. Reference Gunstad, Paul, Cohen, Tate and Gordon2006a). Although there is, to date, little research investigating episodic foresight in obesity, overweight/obese individuals have been shown to have problems with planning tasks, including the Tower of London task (Gunstad et al. Reference Gunstad, Paul, Cohen, Tate, Spitznagel and Gordon2007; Sweat et al. Reference Sweat, Starr, Bruehl, Arentoft, Tirsi, Javier and Convit2008).

This evidence suggests that obesity is associated with neural and psychological deficits consistent with impaired mental time travel. Such a reduction in the ability to learn from personal experience, and to extrapolate that experience to imagine the personal future, may lead to feelings of uncertainty and insecurity about the environment, and the availability of resources. As such, it may be that, although high-energy food is more available than ever before, psychological uncertainty may give the impression of uncertain resources, which the insurance hypothesis suggests may lead to increased energy storage and consequent body fat.

In summary, we suggest that impaired hippocampal function and mental time travel may be a key mechanism underpinning the insurance hypothesis, creating the perception of limited resources even in a plentiful environment. Furthermore, given evidence that deficits in mental time travel can both precede and follow the development of obesity, it may be that this forms part of a vicious cycle in which memory and planning deficits promote obesity, which itself reduces the ability to remember and plan.

References

Addis, D. R., Wong, A. T. & Schacter, D. L. (2008) Age-related changes in the episodic simulation of future events. Psychological Science 19(1):3341.CrossRefGoogle ScholarPubMed
Berthoud, H. R. (2011) Metabolic and hedonic drives in the neural control of appetite: Who is the boss? Current Opinion in Neurobiology 21(6):888–96. doi: 10.1016/j.conb.2011.09.004.CrossRefGoogle ScholarPubMed
Buckner, R. L. & Carroll, D. C. (2007) Self-projection and the brain. Trends in Cognitive Sciences 11(2):4957.CrossRefGoogle ScholarPubMed
Cheke, L. G. & Clayton, N. S. (2012) Eurasian jays (Garrulus glandarius) overcome their current desires to anticipate two distinct future needs and plan for them appropriately. Biology Letters 8(2):171–75. doi: 10.1098/rsbl.2011.0909.CrossRefGoogle ScholarPubMed
Cheke, L. G., Simons, J. S. & Clayton, N. S. (2016) Higher body mass index is associated with episodic memory deficits in young adults. Quarterly Journal of Experimental Psychology 69:2305–16. doi: 10.1080/17470218.2015.1099163.CrossRefGoogle ScholarPubMed
Clayton, N. S. & Dickinson, A. (1998) Episodic-like memory during cache recovery by scrub jays. Nature 395(6699):272–74. doi: 10.1038/26216.CrossRefGoogle ScholarPubMed
Correia, S. P. C., Dickinson, A. & Clayton, N. S. (2007) Western scrub-jays anticipate future needs independently of their current motivational state. Current Biology 17(10):856–61. doi: 10.1016/j.cub.2007.03.063.CrossRefGoogle ScholarPubMed
Cournot, M., Marquie, J. C., Ansiau, D., Martinaud, C., Fonds, H., Ferrieres, J. & Ruidavets, J. B. (2006) Relation between body mass index and cognitive function in healthy middle-aged men and women. Neurology 67(7):1208–14. doi: 10.1212/01.wnl.0000238082.13860.50.CrossRefGoogle ScholarPubMed
Davidson, T. L., Chan, K., Jarrard, L. E., Kanoski, S. E., Clegg, D. J. & Benoit, S. C. (2009) Contributions of the hippocampus and medial prefrontal cortex to energy and body weight regulation. Hippocampus 19(3):235–52. doi: 10.1002/hipo.20499.CrossRefGoogle ScholarPubMed
Gunstad, J., Paul, R. H., Cohen, R. A., Tate, D. F. & Gordon, E. (2006a) Obesity is associated with memory deficits in young and middle-aged adults. Eating and Weight Disorders 11(1):e1519. Available at: http://www.ncbi.nlm.nih.gov/pubmed/16801734.CrossRefGoogle Scholar
Gunstad, J., Paul, R. H., Cohen, R. A., Tate, D. F., Spitznagel, M. B. & Gordon, E. (2007) Elevated body mass index is associated with executive dysfunction in otherwise healthy adults. Comprehensive Psychiatry 48(1):5761.CrossRefGoogle ScholarPubMed
Hassabis, D., Kumaran, D., Vann, S. D. & Maguire, E. A. (2007) Patients with hippocampal amnesia cannot imagine new experiences. Proceedings of the National Academy of Sciences of the United States of America 104(5):1726–31.CrossRefGoogle ScholarPubMed
Hebben, N., Corkin, S., Eichenbaum, H. & Shedlack, K. (1985) Diminished ability to interpret and report internal states after bilateral medial temporal resection: Case H.M. Behavioral Neuroscience 99(6):1031–39. Available at: http://www.ncbi.nlm.nih.gov/pubmed/3843537.CrossRefGoogle ScholarPubMed
Higgs, S. (2002) Memory for recent eating and its influence on subsequent food intake. Appetite 39(2):159–66. Available at: http://www.ncbi.nlm.nih.gov/pubmed/12354684.CrossRefGoogle ScholarPubMed
Higgs, S., Williamson, A. C. & Attwood, A. S. (2008) Recall of recent lunch and its effect on subsequent snack intake. Physiology and Behaviour 94(3):454–62. doi: 10.1016/j.physbeh.2008.02.011.CrossRefGoogle ScholarPubMed
Jagust, W., Harvey, D., Mungas, D. & Haan, M. (2005) Central obesity and the aging brain. Archives of Neurology 62(10):1545–48. doi: 10.1001/archneur.62.10.1545.CrossRefGoogle ScholarPubMed
Kanoski, S. E. & Davidson, T. L. (2010) Different patterns of memory impairments accompany short- and longer-term maintenance on a high-energy diet. Journal of Experimental Psychology: Animal Behavior Processes 36(2):313–19. doi: 10.1037/a0017228.Google Scholar
Li, X. L., Aou, S., Oomura, Y., Hori, N., Fukunaga, K. & Hori, T. (2002) Impairment of long-term potentiation and spatial memory in leptin receptor-deficient rodents. Neuroscience 113(3):607–15. doi: S0306452202001628 [pii].CrossRefGoogle ScholarPubMed
Raby, C. R., Alexis, D. M., Dickinson, A. & Clayton, N. S. (2007) Planning for the future by western scrub-jays. Nature 445(7130):919–21. doi: 10.1038/nature05575.CrossRefGoogle ScholarPubMed
Raji, C. A., Ho, A. J., Parikshak, N. N., Becker, J. T., Lopez, O. L., Kuller, L. H., Hua, X., Leow, A. D., Toga, A. W. & Thompson, P. M. (2010) Brain structure and obesity. Human Brain Mapping 31(3):353–64. doi: 10.1002/hbm.20870.CrossRefGoogle ScholarPubMed
Rozin, P., Dow, S. W., Moscovitch, M. & Rajaram, S. (1998) What causes humans to begin and end a meal? a role for memory for what has been eaten, as evidenced by a study of multiple meal eating in amnesic patients. Psychological Science 9:392–96.CrossRefGoogle Scholar
Schacter, D. L. & Addis, D. R. (2007) Constructive memory: The ghosts of past and future. Nature 445(7123):27. doi: 10.1038/445027a.CrossRefGoogle ScholarPubMed
Schacter, D. L., Addis, D. R. & Buckner, R. L. (2008) Episodic simulation of future events: Concepts, data, and applications. Annals of the New York Academy of Science 1124:3960. doi: 10.1196/annals.1440.001.CrossRefGoogle ScholarPubMed
Simons, J. S. & Spiers, H. J. (2003) Prefrontal and medial temporal lobe interactions in long-term memory. Nature Reviews Neuroscience 4(8):637–48. doi: 10.1038/nrn1178.CrossRefGoogle ScholarPubMed
Suddendorf, T. & Busby, J. (2003) Mental time travel in animals? Trends in Cognitive Sciences 7(9):391–96.CrossRefGoogle ScholarPubMed
Suddendorf, T. & Busby, J. (2005) Making decisions with the future in mind: Developmental and comparative identification of mental time travel. Learning and Motivation 36(2):110–25.CrossRefGoogle Scholar
Sweat, V., Starr, V., Bruehl, H., Arentoft, A., Tirsi, A., Javier, E. & Convit, A. (2008) C-reactive protein is linked to lower cognitive performance in overweight and obese women. Inflammation 31(3):198207.CrossRefGoogle ScholarPubMed
Tulving, E. (1985) Elements of episodic memory. Oxford University Press.Google Scholar
Tulving, E. (1993) What is episodic memory? Current Directions in Psychological Science 2(3):6770.CrossRefGoogle Scholar
van der Borght, K., Kohnke, R., Goransson, N., Deierborg, T., Brundin, P., Erlanson-Albertsson, C. & Lindqvist, A. (2011) Reduced neurogenesis in the rat hippocampus following high fructose consumption. Regulatory Peptides 167(1):2630. doi: 10.1016/j.regpep.2010.11.002.CrossRefGoogle ScholarPubMed
Winocur, G., Greenwood, C. E., Piroli, G. G., Grillo, C. A., Reznikov, L. R., Reagan, L. P. & McEwen, B. S. (2005) Memory impairment in obese Zucker rats: An investigation of cognitive function in an animal model of insulin resistance and obesity. Behavioral Neuroscience 119(5):1389–95. doi: 2005-13804-025 [pii].CrossRefGoogle Scholar