Physiological adaptation to prolonged starvation
Deranged Physiology
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?Endocrinology, Metabolism and Nutrition
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Physiological adaptation to prolonged starvation
By?Alex Yartsev?- 25/06/2015Last updated 03/11/2018 - 00:28
Topic:?Endocrinology Metabolism and Nutrition
Previous chapter: Refeeding syndrome
Next chapter: Summary of guidelines for nutritional support in ICU
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This is a summary of the physiological responses to the total or near-total absence of nutrition.
The metabolic response to starvation is characterised by a switch from carbohydrate metabolism to fat cmetabolism, in the context of a hypometabolic state, with minimised catabolism.
Initially, stores of carbohydrate precursors (eg. glycogen) are depleted.
Then, in the first 24-48 hours there is increased gluconeogenesis from amino acids and glycerol.
Subsequently, ketogenesis takes over, and much of the body metabolic needs are met by ketone bodies and free fatty acids.
This is the consequence of decreasing insulin levels, and relatively increased influence from catecholamines and cortisol.
Over prolonged starvation, protein catabolism begins, resulting in degradation of structurally important proteins, and organ system dysfunction.
The physiological adaptation to starvation has been asked about in?Question 27?from the second paper of 2013. Specifically, the college wanted to know about the metabolic changes of starvation and the stress response.
Composition and quantity of nutrients stored in the human body
George F Cahill is the guru of food deprivation physiology. His 1970 article?"Starvation in Man"?remains a masterpiece of scientific writing. Therein one may find a table entitled "Fuel Composition Of Normal Man" which I have uselessly interpreted into another weird cylinder diagram.
Whatever the value of that may be.
Anyway, each of us has about 20-25g of circulating fuel (of which the majority is glucose), worth about 113 calories. If we take this?Homo vulgaris?to be a 20 year old specimen measuring 70kg and 170cm, we can calculate that at their?basal metabolic rate?of 1800kcal/day they go through one blood volume worth of calories every 90 minutes.
Thus, the circulating nutrient volume is constantly being consumed and replenished.
Then, we have a rapidly available glycogen storehouse, of which two thirds resides in the muscle. There is a total 900kcal of this stuff, and it is also constantly being consumed and replenished. It is replenished after meals (when insulin drives glucose into cells and promotes glyconeogenesis) and it is consumed between meals (when glucagon activated glycogenolysis, releasing glucose out of cells).
Glycogen is a poor means of storing energy. It is a?starch-like branching molecule, has a low calorie density, only about 4 kcal per gram.?Cahill?reminds us that this density is actually measured in dried glycogen - in reality, 2g of water is stored together with each 1g of glycogen (in order to maintain intracellular isotonicity) and this dilutes its energy density even further.
Fat, on the other hand, is stored in blobs which are essentially free of water. It is a much more efficient energy storage system. And the vast majority of the fat in the body is available as a metabolic fuel, if push comes to shove. Those blobs are cushioning, they serve a purely cosmetic role and if you need to burn them to survive, so be it- they will not be missed. Not only that, but fat has a far higher energy density - something like 9.4 kcal per gram.
Protein does not come in a fuel storage form. It is structurally important; all of your protein has some function, and to burn it as fuel would be a gesture of desperation. An organism which is consuming its own protein is truly struggling. That said, if your organism is struggling it has some 6kg or so of protein to get through before it dies.
Metabolic adaptation to a brief period of fasting
The main change from the normal pattern is the refusal of the myocardium and skeletal muscle to use glucose. Instead, they switch over exclusively to free fatty acid and ketone metabolism.
The glycogen reserves in humans never get completely depleted. There is at all times a hepatic reserve, waiting to mobilise and rescue the organism from some sort of horrible situation.
The diagram below is again a paraphrase of Cahill; the mass of nutrients given in it is the amount consumed in a 24 hour period.
Furthermore, the Cori cycle plays a more important role. 36g of the daily glucose is converted into lactate, which shuttles back to the liver.
The liver uses free fatty acids to power the process of gluconeogenesis.
Thus, any lactate converted back to glucose is really free fatty acid energy converted to glucose. In essence, all these Cori-cycling anaerobic glycolysis tissues are running on free fatty acid energy, and glucose and lactate merely act as vessels which contain that energy.
Hormones responsible for the metabolic adaptation to brief fasting
Well, its all about increasing the rate of lipolysis, is it not. And the rate of lipolysis in fatty tissues is governed by the intracellular content of cAMP, which responds to both insulin and noradrenaline.
The major hormonal player in this adaptation is insulin, or rather, its lack. With the absence of regular glucose peaks (given the lack of eating) insulin levels drop. Insulin is the primary inhibitor of lipolysis, because the tyrosine kinase activity of its intracellular domain activates a phosphodiesterase, which keeps intracellular cAMP levels low. As insulin levels drop, the background sympathetic activity becomes unopposed, and the hormone sensitive lipase begins to dismantle their triglyceride stores, releasing delicious fatty acids into the bloodstream.
(Yes, there are three lipases in the pathway, because there are three fatty acid molecules attached to the glycerol. Only the first lipase is hormone-sensitive.)
So, noradrenaline increases the rate of lipolysis (by affecting the bored and lonely beta-3 receptor, which doesn't seem to have much of a function outside of lipolysis), and insulin decreases the rate of lipolysis. Which effect is dominant in ICU patients who are frequently marinading in infusions of both noradrenaline and insulin? Hard to say. The catecholamine excess associated with critical illness definitely?causes lipolysis, even in absence of exogenous catecholamines.
Proteolysis in fasting is not studied as well as lipolysis, but it is clear that an insulin deficit also activates proteolytic pathways (because the administration of small amounts of intravenous dextrose seems to inhibit proteolysis)
Which brings up an interesting question. Nobody ever just lies there and starves quietly for their first few days in the ICU. What happens to these patients?
They still starve.
But, if 150g (600kcal) or so of simple carbohydrate is delivered every day (which is 3 litres of?5% dextrose, or around 600ml of Jevity), the proteolytic pathway is switched off. Lipolysis continues, but the exogenous glucose results in enough insulin release to abort the ketogenesis.
In short, feeding your patient even a tiny amount of carbohydrate will prevent ketosis and protein catabolism.
Sneakily, one can achieve the same effect by administering insulin as a part of an insulin-dextrose infusion. At protocol rate (80ml/hr) one ends up giving only 1920ml of 5% dextrose in 24 hours, which is just short of 100g (or 400kCal); but the exogenous insulin switches off the ketogenesis and proteolysis anyway.
Adaptation to prolonged fasting
Proteolysis cannot continue at a rate of 75 grams per day. This would be insane, and all of the protein would be depleted very quickly.
Thus, with prolonged starvation, the rate of protein catabolism reduces. This can be seen from experiments, as a decreased rate of urinary nitrogen (urea) excretion. Because the rate if urea production is so low, the obligatory rate of urine production is also lower.
A fasting person requires much less fluid this way, which must have been an evolutionary advantage.
The adaptation to prolonged starvation is primarily a change in the pattern of ketone use. The brain gives up its addiction to glucose, and survives on a diet of ketones. At this stage, nothing else uses glucose- every tissue in the body either burns fatty acids, burns ketones, or uses the Cori cycle. Because there is a decreased need for glucose, there is a decreased need for gluconeogenesis, and thus a decreased need for protein catabolism.
in summary, there are 3 phases of fasting:
Weight loss due to fasting
With total acaloric fasting, a certain?healthy 41 yr old member of a cloistered religious community?lost 0.9kg per day for the first few days of the fast, a rate which decreased to a stable 0.3kg/day towards the third week of fasting.
This rate seems consistent among various experimentally fasted subjects. Most seem to lose about 20% of their body weight during a 30 day fast.
The total amount of weight lost in the course of a fasting experiment is not representative of the critical care population. Our patients are infrequently monastic ovolactovegetarians with a normal BMI. Additionally, in a critical care setting the metabo
lic demands are greatly increased. One can only estimate that the ICU patient loses weight at a much faster rate, especially if burns, trauma or sepsis are involved.
Electrolyte changes during prolonged starvation
The 41 yr old monk lost 0.9kg per day for the first few days of the fast. This initial rapid weight loss is not totally due to the loss of dry nutrient mass. Think about it: the burning of 0.9kg of fat protein and carbohydrate in one day day would yield 3150 kcal in total, which is insane (given that a basal metabolic rate we agreed on is 1800 kcal/day).
The extra weight loss is actually due to diuresis and natriuresis. The urinary loss of the sodium cation is obligatory loss. As ketone anions are lost in the urine, they require a cation to accompany them; initially this is sodium, and later in the fast it is ammonium.
Potassium decreases initially,?and remains stable at around 3.0 mmol/L. There is a constant rate of urinary potassium loss, which is thought to be the result of lean tissue dissolving. It seems to parallel the rate of proteolysis, and it seems related to lean body mass.
Magnesium remains surprisingly stable.
Calcium remains stable
Phosphate remains stable
Uric acid levels increase, perhaps as a product of protein catabolism; not only that but urate seems to compete with ketoacids for renal tubular transport sites.
Cardiovascular effects of prolonged starvation
Heart rate decreases,?and healthy fasted volunteers may get as bradycardic as 35 BPM.
The heart rate increases again (slightly ) after the 4th week.Blood pressure decreases,?and in the 1982 study by Kerndt et al the subject terminated his fast because the postural hypotension was interfering with his monastic duties.
ECG changes occur:?most commonly, a right axis deviation and a decrease in T wave and QRS amplitude. Extreme starvation and malnutrition (eg. in?long term prisoners of war)?also results in QT interval prolongation, T wave inversion and ST depression.
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Previous chapter: Refeeding syndrome
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Next chapter: Summary of guidelines for nutritional support in ICU
References
The best source of information regarding the body content of fuel and the metabolic adaptation to starvation can be found in?Dr Cahill's article from 1970.
My main reference for the electrolyte disturbances and other physiological changes with starvation come from the Kerndt experiments.
Finally, I have managed to find a monograph of the original 1915 study by F G Benedict, performed upon Mr L., a Maltese gentleman with an interest in prolonged fasting. The entire monograph is a bizarre and beautiful read, a day-by-day chronicle of voluntary starvation, documented with amazing attention to every miniscule scatological detail. My hat is off to these early pioneers.
Peter R. Kerndt, MD, James L. Naughton, MD, Charles E. Driscoll, MD, and David A. Loxterkamp, MD?Fasting: The History, Pathophysiology and Complications?West J Med. 1982 November; 137(5): 379–399.
Cahill GF; Parris, Edith E.; Cahill, George F. (1970).?"Starvation in man". N Engl J Med 282 (12): 668–675.
Benedict, FG:?A study of prolonged fasting.?Washington DC Carnegie Institute, 1915 (Publication No. 203)
Klein S, Peters EJ, Shangraw RE, Wolfe RR.?Lipolytic response to metabolic stress in critically ill patients. Crit Care Med. 1991 Jun;19(6):776-9.
Laurence B. Ellis?ELECTROCARDIOGRAPHIC ABNORMALITIES IN SEVERE MALNUTRITION?Br Heart J. 1946 April; 8(2): 53–61. PMCID: PMC480993
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