What is intermittent fasting
Fasting is an ancient practice that involves avoiding calories for a period of time. Itย is a simple way to control your weight that doesnโt require you to follow a specific diet, count calories or measure food.
Intermittent fasting schedules
There are many ways to practice intermittent fasting for weight loss. The following are some of the most popular schedules:
Time-restricted eating ย
This involves consuming all of your meals within a period of 4-12 hours in a day. For example, you could choose to have your meals and calories between 8 am and 6 pm.ย Limiting your calorie intake to daylight hours is called โeating with the sunโ.ย Time-restricted eating is particularly beneficial if you eat your meals before sunset. Not only does this help you eliminate bad habits like late-night snacking, but it improves your sleep and blood sugar control. Over time,ย time-restricted eatingย canย lower your blood sugar levels, make you more sensitive to insulin, and reduce your blood pressure.
One-meal-a-day (OMAD)
This involves packing all of your dayโs calories in a single meal that you consume within 1-2 hours. A smallย studyย showed that fasting for 24 hours 3 times a week and eating only dinner on fasting days, eliminated the need for insulin in type-2 diabetic patients. This fasting approach also resulted in improved HbA1C, lower body mass index, and reduced waist circumference.
Alternate-day Fasting
This involves alternating between days in which you consume no calories and days in which you eat normally. Another way of looking at ADF is as three 36-hour fasts per week. ย For example, eat normally on Monday until 6pm. Donโt eat until breakfast on Wednesday morning. Finish dinner by around 6pm Wednesday night. Now donโt eat again until breakfast on Friday. Eat normally the rest of the day and finish dinner by 6pm or so Friday night. Now donโt eat again until breakfast on Sunday. This way of fastingย increases life span in rodents by 80%, possibly by decreasing glucose levels and regulating insulin. It alsoย reduces the incidence of cancerย in lab animals genetically predisposed to it.ย Alternate-day fastingย is the most studied method of intermittent fasting in humans, and itโs been shown to lead to weight loss and to improve heart health, as it reduces circulating levels of LDL or โbadโ cholesterol.
The 5:2 โdietโ
ย Theย 5:2 planย involves eating normally for five days each week and then fasting for the last two. For example, you might decide to fast Monday and Tuesday and then eat normally the rest of the week. You can also look at it as one 60-hour fast per week. Finish dinner at 6pm on Sunday night and donโt eat again until breakfast on Wednesday morning, for example.
How to do intermittent fasting
If you are just getting started with intermittent fasting, we recommend slowly working up to your target fasting schedule over the course of several weeks or months. Start by reflecting on your eating habits. Do you snack in between meals or after dinner? If so, try a 12-hour fast overnight. This means you finish dinner by 7 pm, for example, and donโt eat anything else until 7 am the next day. If you usually donโt feel the need to eat after dinner or between meals, try a 14-16 hour fast (For example, finish dinner by 6 pm and donโt eat again until 10 am the next day). ย If youโd like to fast longer, add 1-hour increments every 5 days or so. Drink water to keep you both hydrated and distracted from hunger. If you need caffeine, drink unsweetened black coffee and tea.
What happens to your body during intermittent fasting?
There are many things that happen during intermittent fasting that either donโt happen or that happen very slowly when we are always eating.
When you eat, your cells enter growth mode
In a well-fed state, the individual cell in your body is in โgrowthโ mode. Itsย insulinย signaling andย mTORย pathways that tell the cell to grow, divide and synthesize proteins are active. By the way, these pathways, when overactive,ย have implications in cancer growth.
The โmammalian target of rapamycinโ or mTOR loves having plentiful nutrients around, especially carbohydrates and proteins. When active, mTOR tells the cell not to bother withย autophagyย (literally cellular โself-eatingโ), a recycling and cleanup process that rids your body of damaged and misfolded proteins, for example. The well-fed cell isnโt worried about being efficient and recycling its components โ itโs too busy growing and dividing.
In a well-fed state, your cells and their components are also highlyย acetylated. This means that various molecules in your cells, including the โpackagingโ proteins called histones that wrap your DNA up nicely within the core of your cells, are โdecoratedโ with acetyl groups on their lysine (amino acid) residues. Donโt worry if you donโt understand the jargon in that last sentence. What you really need to know is that the well-fed cell has manyย genes, including those associated with cellular survival and proliferation, turnedย on. This is because acetylation tends to loosen the packaging proteins that normally keep your DNA wrapped up, and lets your DNA be read for protein production.
While your cells turnย onย cellular growth and proliferation genes when you arenโt fasting, they also turn other genesย off. These include genes related toย fat metabolism, stress resistance and damage repair. Actually, with intermittent fasting some of your fat gets turned intoย ketone bodiesย that appear to reactivate these genes, leading toย lowered inflammation and stress resistance in the brain, for example.

But during starvation, things are very different
When you practice intermittent fasting, your body reacts to what it sees as an environmental stress (low food availability) by changing the expression of genes that are important in protecting you from, well, stress.
We have a well-preserved starvation โprogramโ that kicks our cell into a completely different state when food, particularly glucose or sugar, isnโt around. With intermittent fasting and exercise, you activate theย AMPKย signaling pathway. AMPK or 5โฒ AMP-activated protein kinase is the brake to mTORโs gas pedal. AMPK signals the cell to go into self-protective mode, activatingย autophagyย and fat breakdown. It inhibits mTOR. At the same time, while you are fasting the levels of a molecule calledย NAD+ย begin to rise because you donโt have the dietary proteins and sugars around that normally convert NAD+ to NADH through theย Krebs cycle. NAD+, a molecule whose precursor is Vitamin B3,ย activates the sirtuins, SIRT1 and SIRT3. (Have you heard of the โlongevityโ molecule in wine called resveratrol? Yep, it became famous as being a potential activator of theย sirtuins). These sirtuins are proteins that remove the acetyl groups we talked about above from histones and other proteins. In this process, the sirtuins silence genes related to cell proliferation and activate proteins involved in creating new mitochondria (the power-generating factories of your cells) and cleaning upย reactive oxygen species.
Ketones, also produced during fasting, work asย deacetylase inhibitorsย (in other words, keeping acetyl groups in place). This turns on genes related to antioxidant processes and damage repair.
Whew, thatโs a lot happening while your body isnโt taking in any calories. Butย when exactly do these things happen? Weโve helped you visualize the timeline below and in the LIFE Fasting Tracker app, with a series of icons on the LIFE Fasting arc that represent the five stages of ย intermittent fasting!
The Five Stages of Intermittent (and Prolonged) Fasting

Some of this fat is used by the liver to produce ketone bodies (ketones). The two main ketones, acetoacetate and ฮฒ-hydroxybutyrate (BHB), serve as an alternative energy source for the cells of your ย heart, skeletal muscle, and brain, when glucose isnโt readily available. Did you know thatย your brain uses up some 60% of your glucose when your body is in the resting state? During intermittent fasting, ketone bodies generated by your liver partly replace glucose as fuel for your brain as well as other organs. This ketone usage by your brain is one of the reasons that intermittent fasting is often claimed to promote mental clarity and positive mood โ ketones produce less inflammatory products as they are being metabolized than does glucose, and they can even kick-start production of the brain growth factorย BDNF!ย Ketones have also been shown to reduce cellular damage and cell death in neurons and can also reduce inflammation in other cell types.

As their level in your bloodstream rises, ketones can act as signaling molecules, similar to hormones, to tell your body to ramp up stress-busting pathways that reduce inflammation and repair damaged DNA for example.

Autophagyย is an important process for cellular and tissue rejuvenation โ it removes damaged cellular components including misfolded proteins. When your cells canโt or donโt initiate autophagy, bad things happen,ย including neurodegenerative diseases, which seem to come about asย a result of theย reduced autophagy that occurs during aging. ย Intermittent fasting activates the AMPK signaling pathway and inhibits mTOR activity, which in turn activates autophagy. This only begins to happen, however, when you substantially deplete your glucose stores and your insulin levels begin to drop.
Intermittent fastingย is one way in which you can increase autophagy in your cells and possibly reduce the effects of aging. A 2019ย studyย with 11 overweight adults who only ate between 8 am and 2 pm showed increased markers of autophagy in their blood after fasting for around 18 hours, compared to control participants who only fasted for 12 hours. A second study detectedย ย autophagyย ย in human neutrophils starting at 24 hours of fasting. ย In a thirdย study, skeletal muscle biopsies of healthy male volunteers who fasted for 72 hours showed reduced mTOR and increased autophagy.ย In mice deprived of food, autophagy increases after 24 hours and this effect is magnified in cells of the liver and brain after 48 hours.
But intermittent fasting is not the only way to enhance the ability of your cells to recycle old components.ย Some of the known benefits of exercise for overall health have to do with increased autophagy. For example, autophagy induced by exerciseย delays the progression of heart diseaseย by giving the heart better quality cell parts and reducing oxidative damage.
Exercise, just like intermittent fasting, inactivates mTOR, which increases autophagy in many tissues. Exercise mimics the effects of going without food for an extended period:ย It activates AMPKย as well as autophagy-related genes and proteins.
In mice, endurance exerciseย increases autophagy in the heart, liver, pancreas, fat tissue, and brain. In humans, autophagy increases duringย high intensity exercise, includingย marathon running and cycling.

Part of the reason for this is that ketone bodies produced during fasting promote growth hormone secretion, for example in the brain.ย Ghrelin, the hunger hormone, also promotes growth hormone secretion. Growth hormone helps preserve lean muscle mass and reduces fat tissue accumulation,ย particularly as we age. It also appears to play a role inย mammalian longevityย and can promoteย wound healing and cardiovascular health.

Lowering your insulin levels through Intermittent fasting has a range of health benefitsย both short term and long term. Lowered insulin levels put a brake on the insulin and mTOR signaling pathways, activating autophagy. Lowered insulin levels can reduce inflammation, make you more insulin sensitive (and/or lessย insulin resistant, which is especially a good thing if you have a high risk of developing diabetes) and protect you from chronic diseases of aging includingย cancer.

Prolonged fasting reduces circulating IGF-1 levels and PKA activity in various cell populations. IGF-1, or insulin-like growth factor 1, looks a lot like insulin and has growth-promoting effects on almost every cell in the body. IGF-1 activates signaling pathways including the PI3K-Akt pathway that promotes cell survival and growth. PKA can also activate the mTOR pathway (and, of interest, too much caffeine during a fast may promote activation of PKA).
You might see where this is leading โ pressing the brakes on IGF-1 and PKA through nutrient restriction and fasting can turn down cellular survival pathways and lead to breakdown and recycling of old cells and proteins. Studies in mice have shown that prolonged fasting (greater than 48 hours), by reducing IGF-1 and PKA, leads toย stress resistance, self-renewal and regeneration of hematopoietic or blood cell stem cells. Through this same mechanism, prolonged fasting for 72 hours has been shown toย preserve healthy white blood cell or lymphocyte counts in patients undergoing chemotherapy.
How to break a fast
We almost forgot about the last and perhaps most important stage of intermittent fasting โ the refeeding stage! Itโs important to break your fast with a nutritious, balanced meal that will further improve the function of cells and tissues that went through cleanup while you were fasting. Fromย Mark Mattson and colleagues at the National Institute on Aging:
โUpon refeeding, ingested carbohydrates* and glucose stimulate release into the blood of the incretin hormone glucagon-like peptide 1 (GLP1) from enteroendocrine cells in the gut. GLP1 enhances clearance of glucose from the blood by stimulating insulin release from the pancreas and increases the insulin sensitivity of cells. GLP1 crosses the bloodโbrain barrier and can act directly on neurons to promote synaptic plasticity, enhance cognition and bolster cellular stress resistance.โ
*Update: This isnโt a recommendation to break your fast with lots of carbs and sugars, which may in fact lead to problematic blood sugar spikes. A few carbs can go a long way. Itโs best toย break your fast with a balanced mealย including plenty of vegetables, plant fibers and plant fats, with healthy proteins and some whole grains or legumes if you choose. Avoid simple sugars and processed/packaged foods. Learn what works best for your body, and whatย youย feel best eating following your fasts.
CITED FROM LIFEAPPS
