Award details

Do hunger neuropeptides mediate the link between caloric restriction and lifespan extension?

Reference	BB/G009953/1
Principal Investigator / Supervisor	Professor John Speakman
Co-Investigators / Co-Supervisors
Institution	University of Aberdeen
Department	Inst of Biological and Environmental Sci
Funding type	Research
Value (£)	612,203
Status	Completed
Type	Research Grant
Start date	01/06/2009
End date	30/11/2012
Duration	42 months

Abstract

The mechanism by which caloric restriction (CR) induces cellular and molecular level events that lead to life extension remains obscure. One possibility is that eating less food generates signals directly to activate the CR programme. Alternatively reduced adiposity during CR may alter the adipokine profile, triggering the response. Normally reduced food intake and adiposity occur in parallel so separating between them is difficult. I will expose mice to altered ambient temperatures to dissociate changes in food intake from adiposity. I will monitor the extent to which the CR programme is initiated in animals that eat the same levels of food, but differ in their energy balance and body fatness. To further test the role of adipokines in switching on the CR programme I will place animals under CR so that they lose weight and switch the programme on. I will then replete levels of key adipokines (leptin and TNFalpha) using mini-osmotic pumps to their pre-restriction levels, to see if the CR programme can be switched off. Clearly whatever the peripheral trigger is, the CR programme is probably controlled by events in the brain. My recent work has implicated several neuropeptides in the hypothalamus (notably the hunger neuropeptides AgRP, NPY, POMC and CART) which are the immediate downstream targets of leptin in the hypothalamus. To experimentally confirm their role in CR, I will place animals under CR and then antagonise Y1 and Y5, or agonise MC4 and MC3 receptors which are the primary receptors of the relevant neuropeptides. If the neuropeptide profiles switch on the CR programme then these manipulations switch the CR programme off. If this experiment works the final experiment I will perform is to do the opposite. I will agonise Y1 and Y5 and antagonise MC4 and MC3 receptors while clamping intake. This should in theory turn on the CR programme without the animals eating less food.

Summary

Seventy years ago it was discovered that if rats are fed less than their normal ration of food they live longer. This treatment has since been found to extend the lives of many different species, including non-human primates. It is known that this process of restricting calorie intake (called caloric restriction - or CR) reduces the risk of developing age related diseases like cancer and it improves levels of many markers that alter with age - such as damage to DNA, fats and proteins, and circulating glucose and insulin levels. Exactly how CR exerts its effects remains uncertain. As a method for extending human life it is recognised that it would be extraordinarily difficult for people in modern society to restrict their intake of food voluntarily. A search has started therefore for drugs that will mimic the effects of CR, but without the need to eat less food. Another uncertainty concerns the mechanism that translates eating less food into switching on the cellular responses that ultimately lead to extended lifespan. There are two ideas about how this might work. When animals and people undergo CR they tend to lose body fat. The response to CR might be switched on by eating less food, alternatively it might be switched on by the reduction in body fatness. Normally these two things change together so it is difficult to separate which is of most importance. I have previously shown that when animals are taken off CR they over-eat until their fat stores are repleted. This suggests that it is probably signals from the fat that are important in signalling to the brain to switch on the 'CR programme' that ultimately extends life. The first part of this proposal aims to explore the roles of reduced fatness and fat signals (called adipokines) as opposed to simply eating less food in initiating the CR programme. To do this I will perform an experiment which dissociates the changes in food intake from the changes in body fatness using mice as a model organism. This can be achieved by exposing mice to different temperatures. For example if the temperature is made warm mice eat less food because their energy demands decrease, but they don't lose body fat because they remain in energy balance. Perhaps mice kept in the warm switch on the CR programme and live longer because they are eating less food. Alternatively if it is fat loss that is important as I suspect from my previous work I predict this manipulation will not switch on the CR programme. To further test the role of adipokines in switching on the CR programme I will perform another experiment where I place animals at normal room temperature under CR so that they lose weight and switch the programme on. I will then implant them with small devices that continuously deliver some of the compounds produced by fat so see if the CR programme can be switched off. Clearly whether reduced body fat, or eating less food switches, on the CR programme it is controlled by events in the animal's brains. My recent work has suggested that some neuropeptides in the hypothalamus are an important part of this process. These neuropeptides are known to interact with some of the signals generated by fat tissue. To experimentally test if they are indeed important I will place animals under CR and then interfere with these pathways by introducing compounds into their brains which disrupt the signalling. These compounds are commercially available and have very specific effects on receptor populations that the neuropeptides of interest interact with. If the neuropeptides that I suspect are important really do switch on the CR programme then interfering with them should switch the CR programme off. If this experiment works the final experiment I will perform is to do the opposite. Introduce compounds that have the opposite effects into the same brain regions. These should in theory turn on the CR programme but without the need for the animals concerned to eat less food.

Committee	Closed Committee - Agri-food (AF)
Research Topics	Ageing, Diet and Health, Neuroscience and Behaviour
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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