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Episode
Top 10 Things You Do DAILY That Destroy Your Brain
~43 min
Episode Brief·YouTube

Top 10 Things You Do DAILY That Destroy Your Brain

Sten Ekberg
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TL;DR

The four things you'd lose by not watching

4 items

TL;DR

The four things you'd lose by not watching

4 items
1

Alzheimer's is a metabolic disease (type 3 diabetes) driven by insulin resistance from sugar and processed foods; the brain starves amid plenty while AGEs and inflammatory cytokines damage the hippocampus.

2

The brain's glymphatic cleanup system depends on fasting (autophagy inside cells) and deep sleep (CSF flushing outside cells); constant snacking and poor sleep allow amyloid beta and tau tangles to accumulate.

3

Movement provides 90% of the brain's stimulation and triggers BDNF and human growth hormone for synaptogenesis; a sedentary lifestyle leads to brain atrophy and increased dementia risk.

4

Screen time flattens 3D spatial navigation into 2D tunnel vision, shrinking the hippocampus and increasing baseline stress; the brain loses complexity because it isn't required to actively construct reality.

Protocols

Concrete recipes — what, when, how much, and why

11 items

Avoid Sugar and Processed Foods to Prevent Brain Insulin Resistance

WhatEliminate or drastically reduce sugar and processed foods to avoid insulin resistance, AGEs, and neuroinflammation that damage the hippocampus.
WhenAt all meals; replace with whole foods.
DoseNo specific dose; aim for minimal added sugar and processed food intake.
For whomEveryone, especially those with metabolic syndrome or family history of dementia.
WhySugar and processed foods drive insulin resistance, starving the brain of glucose despite high blood sugar, and fructose promotes fatty liver and inflammatory cytokines that cross the blood-brain barrier.
CaveatsNot about eliminating all carbohydrates; whole-food carbs in moderation may be acceptable for metabolically healthy individuals.

Ekberg frames Alzheimer's as 'type 3 diabetes,' a metabolic disease rooted in insulin resistance. When the brain becomes insulin resistant, it cannot use the abundant blood sugar, effectively starving in the midst of plenty. High sugar intake also generates AGEs—damaged proteins that harm brain tissue—and fructose specifically drives liver fat accumulation, leading to systemic inflammation that breaches the blood-brain barrier. The hippocampus, essential for converting short-term to long-term memory and for spatial navigation, suffers significant impairment. He notes that sugar and processed foods are addictive and nutrient-depleted, promoting overeating and perpetuating the cycle. The solution is to return to a whole-food diet that keeps insulin low and allows the brain to use ketones as an alternative fuel.

Mechanism

Insulin resistance prevents glucose uptake in brain cells; advanced glycation end products (AGEs) cross-link proteins and damage tissue; fructose drives non-alcoholic fatty liver, increasing cytokine production that triggers neuroinflammation; the hippocampus, critical for memory and spatial awareness, is particularly impaired.

When the brain becomes insulin resistant along with the rest of the body, then we can have a lot of blood sugar floating around in the bloodstream, but because the cells are insulin resistant, they don't receive that blood sugar. So, we're basically starving the brain in the midst of plenty.

Also said
“It's primarily the fructose in the sugar that drives this formation of liver fat.”— Specifies fructose as the key driver of fatty liver, not just glucose.
“What they have found is significant hippocampal impairment. And hippocampus is a structure in the brain that's part of the limbic system. And the hippocampus has a lot to do with memory.”— Links the metabolic damage directly to the brain region most affected in dementia.

Don't Follow a Low-Fat Diet; Prioritize Healthy Fats and Cholesterol

WhatAvoid low-fat and low-cholesterol diets; consume adequate healthy fats (grass-fed meats, fatty fish, eggs, etc.) to supply the brain with cholesterol and essential fatty acids.
WhenDaily dietary pattern.
DoseRoughly 60% of calories from fat, 20% from protein, 20% from carbohydrates as a baseline for metabolically healthy individuals; lower carb if reversing metabolic disease.
For whomEveryone, especially those following official low-fat dietary guidelines.
WhyThe brain is 60% fat by dry weight, and cholesterol is critical for cell membranes, myelin, and steroid/neurosteroid hormones. Low-fat diets typically lead to high-carb intake, fueling insulin resistance.
CaveatsFat quality matters; emphasize unprocessed fats from grass-fed and wild sources, not processed seed oils.

Ekberg challenges the fat phobia that led to official recommendations of low-fat, high-carb diets. He explains that the brain's dry weight is 60% fat, a significant portion of which is cholesterol. This cholesterol is non-negotiable for building cell membranes and myelin, the insulating coating that allows precise electrical signaling. It also serves as the raw material for all steroid hormones and neurosteroids. When people cut fat, they replace it with carbohydrates, flipping the ancestral macronutrient ratio from roughly 60% fat/20% carb to 20% fat/60% carb. This high-carb intake drives the epidemic of obesity, type 2 diabetes, and metabolic disease, which in turn damages the brain. He suggests that a whole-food diet naturally lands around 60% fat, 20% protein, and 20% carbs, with lower carbs for those needing to reverse metabolic damage.

Mechanism

Cholesterol forms the structural backbone of all cell membranes and the myelin sheath that insulates nerves for rapid signal transmission. It is also the precursor for cortisol, testosterone, estrogen, and neurosteroids used for internal brain communication. When dietary fat and cholesterol are restricted, the body may not produce enough, compromising membrane integrity and hormone synthesis. Additionally, low-fat diets are inevitably high in carbohydrates, which spike blood sugar and insulin, promoting the very metabolic disease that damages the brain.

The brain is 60% fat by dry weight. If we take out the water, 60% of the rest of it is fat. And a very significant portion of that is cholesterol.

Also said
“When people try to go low fat, they usually turn it the other way around and they end up with 20% of calories from fat and 60% from carbohydrate, which is pretty much what is officially recommended and which is part of why we have this epidemic of obesity, type 2 diabetes, and metabolic disease.”— Directly blames official low-fat guidelines for the metabolic disease epidemic.

Reduce Grain Consumption to Protect Gut and Brain Barriers

WhatMinimize or eliminate grains, especially wheat, to prevent gluten and lectin-induced leaky gut and subsequent neuroinflammation.
WhenReplace grains with vegetables, tubers, or other whole-food carbohydrate sources.
DoseNo specific dose; ideally avoid wheat and other gluten-containing grains.
For whomEveryone, particularly those with gut issues, autoimmune conditions, or brain fog.
WhyGluten and lectins in grains degrade tight junctions in the gut lining, causing leaky gut. This allows bacterial lipopolysaccharides (LPS) into the bloodstream, which cross the blood-brain barrier and trigger neuroinflammation.
CaveatsSome people may tolerate properly prepared grains, but the speaker implies they are generally problematic.

Ekberg explains that grains not only spike blood sugar (contributing to habit #1) but also contain gluten and lectins that physically break down the gut's selective barrier. Once the gut becomes leaky, bacterial endotoxins like LPS leak into the blood and reach the brain, where they provoke an immune response and chronic neuroinflammation. This mechanism is separate from the insulin resistance pathway and adds another layer of damage. He emphasizes that the gut-brain axis is bidirectional and that a compromised gut lining inevitably compromises the brain's protective barriers.

Mechanism

Wheat gluten and lectins bind to and disrupt the tight junction proteins that seal the intestinal lining. The resulting intestinal permeability ('leaky gut') allows LPS—fragments of gut bacteria—to enter circulation. LPS are small enough to cross the blood-brain barrier and activate the brain's immune cells, causing neuroinflammation. Ekberg summarizes this as 'leaky gut equals leaky brain,' indicating that gut barrier dysfunction directly translates to brain barrier dysfunction and inflammation.

Leaky gut equals leaky brain.

Also said
“Grains contain gluten and lectin especially wheat and those two molecules will degrade they'll break down the tight junctions in your gut.”— Specifies the exact molecules and their action on gut integrity.
“These LPS's they're very irritating they stimulate our immune system to respond and produce inflammation. So now in the brain of course we end up with neuroinflammation.”— Traces the pathway from gut to brain inflammation.

Lower Omega-6 Intake to Restore Membrane Fluidity

WhatDrastically reduce consumption of seed oils (soybean, canola, corn, safflower) and grain-fed animal products to lower the omega-6 to omega-3 ratio toward ancestral levels (1:1 to 4:1).
WhenAt all meals; replace seed oils with olive oil, coconut oil, butter, or animal fats from grass-fed sources.
DoseNo specific dose; aim to eliminate seed oils and choose grass-fed meat/dairy.
For whomEveryone, especially those consuming standard Western diets high in processed foods and restaurant meals.
WhyExcess omega-6 fatty acids compete with DHA for incorporation into brain cell membranes, making them rigid and stiff, impairing signaling and increasing neuroinflammation.
CaveatsOmega-6 fats are essential in small amounts; the problem is the extreme imbalance, not their presence.

Ekberg traces the modern omega-6 overload to the explosion of seed oils in processed foods and restaurant cooking over the last 50 years, combined with grain-fed livestock whose meat and dairy reflect the same imbalanced fatty acid profile. He contrasts this with ancestral diets that maintained a ratio close to 1:1. The consequence for the brain is that cell membranes lose their delicate balance of fluidity and rigidity, compromising everything from nutrient transport to electrical signaling. The result is degraded neuronal membranes, impaired communication, and heightened neuroinflammation. The fix is to avoid seed oils and prioritize grass-fed animal products and wild-caught fish.

Mechanism

DHA (docosahexaenoic acid) is the most important fatty acid for brain cell membrane structure. Omega-6 fatty acids are structurally similar and compete for the same membrane slots. When the dietary ratio of omega-6 to omega-3 is high (modern 20:1–40:1 vs. ancestral 1:1–4:1), omega-6 displaces DHA, producing rigid, less fluid membranes. This rigidity degrades neuronal communication, receptor function, and signal transduction, while also promoting a pro-inflammatory state in the brain.

When the brain makes a new cell membrane, if there's too much omega6 around, then it's going to be included in that cell membrane instead of the DHA.

Also said
“With a really high ratio, what happens is we get an increase in neuroinflammation and we also get degraded neuronal membranes and communication.”— States the dual consequence of membrane rigidity.
“Today when we look around the world what we see is a 20 to one. People have 20 times more omega6 or as high as 40 times as much omega6 as omega 3 and DHA.”— Quantifies the modern imbalance.

Practice Intermittent Fasting to Activate Brain Autophagy

WhatAvoid constant eating and snacking; compress eating into 1–2 meals per day without snacks to allow prolonged fasting periods that trigger autophagy in brain cells.
WhenDaily; aim for at least a 12–16 hour fasting window, ideally longer.
Dose1–2 meals per day, no snacks; fasting window of 12+ hours.
For whomMost adults; those with medical conditions should consult a doctor.
WhyFasting activates autophagy, the intracellular cleanup process that clears misfolded proteins like amyloid beta and tau; constant insulin spikes from snacking shut this down completely.
CaveatsNot for pregnant women, those with eating disorders, or certain medical conditions without supervision.

Ekberg emphasizes that the brain's glymphatic system has two steps: intracellular autophagy (triggered by fasting) and extracellular CSF flushing (triggered by deep sleep). Constant eating—even healthy snacks—keeps insulin spiked and autophagy suppressed. He contrasts ancestral patterns of 1–2 insulin spikes per day with modern habits of 6–15 spikes from meals, snacks, and sipping sweet beverages. This chronic suppression of autophagy allows neurotoxic waste to build up. He recommends returning to a pattern of fewer meals, no snacks, and no caloric beverages between meals to restore the brain's nightly cleaning cycle.

Mechanism

Autophagy ('self-eating') is the process by which cells degrade and recycle damaged components, including misfolded proteins. Insulin is a potent inhibitor of autophagy. Every time we eat, insulin rises, halting the cleanup. Ancestral eating patterns involved 1–2 meals daily with long fasting gaps, allowing autophagy to run. Modern snacking keeps insulin elevated, preventing the brain from clearing amyloid beta and tau proteins, which then accumulate into plaques and tangles associated with Alzheimer's.

During fasting, we clean up inside the cells with a process called autophagy or self-eating. But with snacking and with constant insulin spikes, that shuts down that autophagy completely.

Also said
“Our ancestors might have had one or two insulin spikes, one or two meals per day. Today, with snacks and meals, we might have six or up to 15 with people eating nuts and candy out of bowls.”— Quantifies the modern deviation from the fasting pattern the brain evolved with.
“If we don't get the proper cleanup inside the cells, now we have buildup of certain waste products called amyloid beta which is a waste protein. It's a misfolded protein that forms plaques and is associated with dementia and Alzheimer's.”— Names the specific waste products that accumulate without autophagy.

Prioritize Deep Sleep for Glymphatic Brain Cleaning

WhatEnsure sufficient high-quality sleep, especially deep slow-wave sleep, to activate the glymphatic system's extracellular cleaning; avoid blue light before bed to prevent cortisol spikes.
WhenNightly; aim for consistent sleep schedule and dark, cool sleeping environment.
Dose7–9 hours of sleep with adequate deep sleep stages; avoid screens 1–2 hours before bed.
For whomEveryone; especially those with sleep disorders or high dementia risk.
WhyDuring deep sleep (1–4 Hz brainwaves), astrocytes shrink by 60%, dramatically increasing CSF flow to wash away extracellular amyloid beta, tau tangles, and metabolic waste.
CaveatsSleep apnea and other disorders must be addressed; blue light from screens is a major disruptor.

Ekberg recalls that 40 years ago, science didn't know why we sleep. Now, he says, the primary function is this clean-and-rinse cycle. He stresses that deep sleep is not a luxury or unproductive time; it is when the brain physically washes away the waste products that cause dementia. He warns that artificial light from screens is a potent sleep disruptor because it increases cortisol. He urges listeners to treat sleep as 'precious and even sacred,' and to structure their evenings to protect the early-night deep sleep periods when glymphatic activity peaks.

Mechanism

Deep sleep is characterized by slow brainwave frequencies (1–4 Hz). This state triggers astrocytes—a type of glial cell—to shrink by up to 60%, creating expanded interstitial space. This allows cerebrospinal fluid to flow rapidly through the brain, flushing out extracellular debris including amyloid beta and tau proteins. Without this nightly rinse cycle, waste accumulates and contributes to neurodegeneration. Blue light from screens suppresses melatonin and raises cortisol, directly interfering with the ability to enter deep sleep.

Personal experience

I remember back in college which was about 40 years ago now that they didn't really know why we slept. There was very little evidence and actual knowledge. They knew that you didn't feel good. You got really tired. You could get schizophrenic after so many days without sleep. But they really didn't have an idea of why we sleep. What's the function? And now we know that yes, we needed to consolidate our memories. But the biggest thing is probably what I just went over that if we can't sleep properly, if we can't get into that deep sleep stage, we can't clean our brains properly.

Sleep is not just about the rest. It is basically a clean and rinse cycle.

Also said
“During deep sleep... astrocytes... get up to 60% smaller... and what happens now when these astrocytes shrink and there's all this room between the cells is that we get a dramatic increase in the flow of CSF of cerebral spinal fluid... it can wash away the debris that has accumulated.”— Details the physical mechanism of the glymphatic flush.
“Blue light artificial light from screens will increase cortisol which will interfere with sleep very effectively.”— Identifies a key modern disruptor of the cleaning cycle.

Manage Chronic Stress to Protect the Hippocampus and Cortex

WhatActively work to change perception of threats and reduce chronic stress through awareness, choosing to feel better, and gradually shifting responses over time.
WhenOngoing daily practice; no quick fix.
DoseIncremental progress over months to years; start by noticing negative feelings and deciding to change them a little each day.
For whomEveryone experiencing chronic stress, overwhelm, fear, or social isolation.
WhyChronic stress elevates cortisol (directly toxic to hippocampus), increases inflammation, and shifts blood flow from the cortex to the brain stem, starving the thinking brain and causing cortical thinning.
CaveatsNot about eliminating all stress; acute eustress is beneficial. The goal is to prevent stress from becoming chronic and to change perception.

Ekberg explains that all negative emotions—fear, overwhelm, uncertainty, social isolation—are perceived by the brain as threats, triggering the same stress response. He emphasizes that there are really only two categories of feeling: good and bad. By paying attention to how you feel, you can begin to choose differently. He acknowledges there is no quick fix; it's about noticing when you feel bad and deciding to feel a little better today, a little more tomorrow. Over a year, your life circumstances may not change, but your response to them can be completely different. He warns against resignation ('that's just my life') and stresses that perception is malleable.

Mechanism

Perceived threats activate the HPA axis, releasing cortisol and adrenaline. Cortisol raises blood sugar for energy but is directly neurotoxic, and the hippocampus—dense with cortisol receptors—is especially vulnerable. Simultaneously, the sympathetic nervous system redirects blood flow from the prefrontal cortex to the brain stem, prioritizing reflexive survival over conscious thought. Chronic activation leads to hippocampal damage, cortical thinning, and a depressed cell-based immune response while increasing systemic inflammation.

Cortisol is directly destructive to brain tissue. And when we go through these, we have to realize and remember that chronic stress is not supposed to be there.

Also said
“With a stress response, we change our focus and we shift our blood flow, our blood supply from the cortex to the brain stem.”— Explains the blood flow redistribution that starves the thinking brain.
“There's no quick fix for chronic stress. But you also don't want to just say, 'Oh well that's my life. There's nothing I can do about it.' because it's more about your perception and you can change that.”— Offers hope and a long-term strategy rather than a quick hack.

Engage in Regular Intense Exercise for BDNF and Brain Regeneration

WhatIncorporate short, intense bursts of exercise followed by full recovery to produce human growth hormone and BDNF, which drive synaptogenesis and brain repair.
WhenSeveral times per week; any movement is good, but intensity provides the hormonal benefits.
DoseShort, intense, acute bouts with full recovery; no specific duration given, but modeled on ancestral patterns of brief exertion followed by rest.
For whomEveryone; especially sedentary individuals.
WhyExercise is eustress—a positive, constructive stress that challenges the body and triggers the release of BDNF ('miracle growth for the brain') and human growth hormone, both required for making new synapses and regenerating brain tissue.
CaveatsMust allow full recovery; chronic intense training without recovery becomes distress. Start at appropriate fitness level.

Ekberg distinguishes between distress (chronic, unrelenting) and eustress (short, intense, with recovery). He argues that all animals live with bursts of activity followed by rest, and this pattern is essential for brain health. Exercise provides the mechanical and proprioceptive signals that constitute the majority of the brain's work. When exercise is intense enough to be a challenge, it triggers a regenerative response mediated by BDNF and growth hormone. Without this stimulus, the brain lacks the biochemical tools to maintain its circuitry, leading to degeneration. He notes that even non-exercise movement is beneficial, but intensity amplifies the neuroprotective effect.

Mechanism

Intense physical activity is a hormetic stressor that signals the body to adapt and grow stronger. It stimulates the release of human growth hormone and brain-derived neurotrophic factor (BDNF). BDNF promotes the survival and growth of neurons and is essential for synaptogenesis—the formation of new synaptic connections. Without these hormones, the brain cannot effectively repair or rewire itself, leading to atrophy. Movement also provides the sensory input that drives 90% of brain activity.

BDNF is basically miracle growth for the brain. It's a hormone that makes it possible... to make new synapses.

Also said
“Movement provides 90% of the brain's work of the stimulation that gives the brain a reason to do something.”— Frames movement as the primary driver of brain activity.
“Without enough movement, without enough exercise, then your brain is going to have a lack of regeneration. It's not going to be able to repair itself as well. And that's the same thing as atrophy, shrinkage, and an increased risk of dementia.”— Directly links sedentary behavior to brain atrophy and dementia.

Avoid Smoking and Alcohol to Prevent Brain Hypoxia and Neurotoxicity

WhatEliminate smoking and minimize or eliminate alcohol consumption to protect cerebral blood flow, oxygen delivery, and myelin integrity.
WhenLifestyle choice; cessation is critical.
DoseZero smoking; alcohol as little as possible (none for brain health).
For whomSmokers and drinkers; anyone concerned with brain health.
WhySmoking causes chronic vasoconstriction and carbon monoxide-induced hypoxia, reducing brain oxygen by ~1/3. Alcohol is directly neurotoxic to white matter, depletes B vitamins needed for myelin repair, and shrinks the prefrontal cortex.
CaveatsThe damage is dose-dependent; even moderate drinking may have neurotoxic effects.

Ekberg details the synergistic damage of smoking and alcohol. He explains that the brain is a 'greedy master' that will sacrifice other organs to preserve itself, yet smokers voluntarily reduce oxygen delivery by a third. He notes the brain's extreme sensitivity: just 4 seconds without blood flow causes unconsciousness. Alcohol compounds the problem by directly attacking the brain's insulation and the vitamins needed to rebuild it. He points out that the prefrontal cortex isn't fully myelinated until age 25, which is why teenagers have poor impulse control—alcohol accelerates the degradation of this critical region.

Mechanism

Nicotine constricts blood vessels, reducing cerebral blood flow. Carbon monoxide from smoke binds hemoglobin with 200–250x the affinity of oxygen, permanently occupying binding sites and slashing oxygen-carrying capacity. The brain, consuming 20–25% of the body's oxygen, is highly vulnerable to this chronic hypoxia. Alcohol directly damages white matter (myelin) and shrinks the prefrontal cortex, impairing judgment and impulse control. Its metabolism depletes B1 and B12, which are essential for myelin synthesis, creating a dual hit: destruction plus impaired repair.

If you're a heavy smoker, the combined effect of those could mean that you reduce your oxygen delivery by about one-third.

Also said
“Carbon monoxide binds 200 to 250 times harder with hemoglobin. So it gets like totally stuck.”— Explains the irreversible binding that makes even small amounts of carbon monoxide significant.
“Alcohol is directly neurotoxic to brain tissue and it especially primarily targets the white matter, the insulating matter.”— Specifies the brain tissue most vulnerable to alcohol.

Limit Screen Time and Re-engage with 3D Movement

WhatReduce daily screen time, take frequent breaks to move in three-dimensional space, and ensure that visual motion is paired with physical movement to activate spatial navigation circuits.
WhenDaily; avoid prolonged uninterrupted screen sessions. Replace some screen leisure with outdoor or physical activities.
DoseNo more than several hours per day; avoid 16-hour screen days. Incorporate movement breaks every 30–60 minutes.
For whomEveryone, especially those with desk jobs or heavy recreational screen use.
WhyScreens force 2D tunnel vision without corresponding body movement, starving spatial navigation circuits, shrinking the hippocampus, and raising baseline stress from lost peripheral awareness.
CaveatsScreens are not inherently evil; the brain can handle several hours. The danger is extreme imbalance where movement is near zero.

Ekberg calls this his favorite topic. He contrasts the active, constructive brain in a 3D world—constantly integrating depth, texture, shading, gravity, and self-motion—with the passive consumption of pre-packaged 2D content. In the real world, the brain is an active participant creating a complex, multi-sensory model. On a screen, it is highly stimulated but does no constructive work, leading to simplification and reduced neural density. He emphasizes that BDNF, required for synaptogenesis, is produced by movement, so screen time without movement is a double hit: circuits aren't used, and the hormone needed to rebuild them isn't present. He reassures that computers are wonderful in moderation, but 16-hour days with only bathroom breaks will cause critical wiring loss.

Mechanism

The brain evolved to integrate visual input with proprioceptive and vestibular signals from physical movement through 3D space. A screen presents motion without body movement, creating a disconnect that fails to activate hippocampal spatial circuits, leading to measurable volume loss. Tunnel vision on a screen suppresses peripheral vision, which normally detects threats; the brain compensates with increased sympathetic tone (stress). The overall effect is decreased neural complexity—fewer circuits are used, so they are pruned, weakening the brain.

The eyes see motion, but there is no movement. There's no body movement to match it. There's no body movement to integrate with what you're seeing.

Also said
“What they have found with people who spend a lot of time in front of screens for a long period of time is that there's a measurable decrease in the volume of the hippocampus.”— Directly states the structural brain change associated with screen time.
“The result of that... is decreased complexity. We're getting fewer circuits involved. So we're reducing the neural density. The brain doesn't have as much to do. So it gets simplified. It gets weaker.”— Summarizes the overarching effect of screen time on brain architecture.

Leverage Neuroplasticity to Rewire Habits

WhatUnderstand that you are not fixed; you are constantly recreating yourself through daily habits. Change one small thing at a time to build momentum toward the brain you want.
WhenOngoing; start with awareness and incremental changes.
DoseOne small change at a time, consistently.
For whomAnyone who feels stuck or believes they cannot change.
WhyThe brain is continuously rewiring based on what you do. 'I am who I am' is false; you are who you have recreated since last week. This empowers deliberate change.
CaveatsRequires consistency; old pathways are strong, but new ones can be built with repetition.

Ekberg closes with a motivational message countering the fixed mindset. He argues that from a neuroplasticity perspective, the statement 'I am who I am' is completely wrong. You are not who you were last week; you are the sum of the habits you've repeated since then. This means that by changing one small habit at a time, you can gradually recreate yourself. He ties this to the earlier protocols: the brain will adapt to whatever you consistently do, so choose habits that build rather than destroy.

Mechanism

Synaptogenesis and synaptic pruning are ongoing processes. Circuits that are used are strengthened; unused ones are eliminated. By repeating new behaviors, you physically rewire the brain. BDNF and growth hormone support this plasticity, but the primary driver is consistent, intentional action.

You are not who you are. You are not who you were last week. You are who you have recreated since last week.

Also said
“If you keep changing one little thing at a time and you create a little bit momentum in the direction that you want, now you can recreate pretty much whatever you like.”— Provides the actionable strategy for leveraging neuroplasticity.

What's new

Personal practice updates, fresh positions, predictions

5 items

glymphatic-system-dual-cleanup

The brain has a unique waste-clearance system—the glymphatic system—that requires both fasting (intracellular autophagy) and deep sleep (extracellular CSF flushing) to remove amyloid beta and tau proteins.

Why this matters: Most people know sleep is important, but the specific two-step cleaning cycle and its absolute dependence on avoiding constant insulin spikes is rarely explained.

Background

Previously, the brain's waste removal was poorly understood; the lymphatic system doesn't extend into the brain. The discovery of the glymphatic system revealed that glial cells and cerebrospinal fluid work together during specific states.

Sten Ekberg explains that the brain lacks the body's lymphatic system and instead relies on cerebral spinal fluid (CSF) circulated by glial cells. This system operates in two phases. First, during fasting, autophagy cleans out misfolded proteins and metabolic waste inside neurons. Constant eating and insulin spikes shut down autophagy completely. Second, during deep sleep—specifically the slow-wave stage with brain frequencies of 1–4 Hz—astrocytes shrink by up to 60%, dramatically increasing CSF flow to wash away extracellular debris, including amyloid beta plaques and tau tangles. Without both fasting and deep sleep, these waste products accumulate, directly contributing to dementia. He contrasts ancestral eating patterns (1–2 meals/day) with modern snacking (6–15 insulin spikes/day) and emphasizes that blue light from screens raises cortisol, further disrupting deep sleep.

During fasting, we clean up inside the cells with a process called autophagy or self-eating. But with snacking and with constant insulin spikes, that shuts down that autophagy completely.

Also said
“During deep sleep... astrocytes... get up to 60% smaller... and what happens now when these astrocytes shrink and there's all this room between the cells is that we get a dramatic increase in the flow of CSF of cerebral spinal fluid... it can wash away the debris that has accumulated.”— Details the second step of the glymphatic system and the magnitude of astrocyte shrinkage.
“Our ancestors might have had one or two insulin spikes, one or two meals per day. Today, with snacks and meals, we might have six or up to 15 with people eating nuts and candy out of bowls.”— Quantifies the modern deviation from the fasting pattern the brain evolved with.

movement-90-percent-brain-stimulation

Movement, posture, and position in gravity provide 90% of the brain's incoming stimulation; without it, the brain loses its primary reason to process information and atrophies.

Why this matters: The claim that 90% of the brain's work is movement-related is a striking, specific figure that reframes exercise as fundamental to cognition, not just physical health.

Background

Conventional wisdom treats exercise as beneficial for brain health via increased blood flow or endorphins, but rarely as the dominant source of neural input.

Ekberg argues that the brain's evolutionary purpose is to process movement through a three-dimensional world. Sensory inputs from proprioception, balance, and spatial navigation constitute the vast majority of the signals the brain integrates. He states that 90% of the brain's work comes from movement, posture, and gravity. Intense, short bursts of exercise (eustress) followed by recovery trigger the release of human growth hormone and brain-derived neurotrophic factor (BDNF), which he calls 'miracle growth for the brain.' These hormones are essential for synaptogenesis—the creation of new neural connections. Without sufficient movement, the brain lacks the stimulation to maintain its circuits, leading to a lack of regeneration, atrophy, shrinkage, and increased dementia risk. He contrasts this with chronic distress, which breaks the body down, while eustress builds it up.

Movement provides 90% of the brain's work of the stimulation that gives the brain a reason to do something. 90% of it has to do with movement, with posture, with position in a field of gravity.

Also said
“BDNF is basically miracle growth for the brain. It's a hormone that makes it possible... to make new synapses.”— Links movement-induced BDNF directly to the physical substrate of learning and memory.
“Without enough movement, without enough exercise, then your brain is going to have a lack of regeneration. It's not going to be able to repair itself as well. And that's the same thing as atrophy, shrinkage, and an increased risk of dementia.”— Spells out the consequence of a sedentary lifestyle in stark terms.

smoking-carbon-monoxide-brain-hypoxia

Smoking causes chronic cerebral hypoxia not just from vasoconstriction but because carbon monoxide binds hemoglobin 200–250 times more tightly than oxygen, reducing oxygen delivery by about one-third in heavy smokers.

Why this matters: The carbon monoxide mechanism is rarely discussed in the context of brain health; the specific binding affinity and the one-third reduction figure make the damage tangible.

Background

Most anti-smoking messages focus on lung damage and cardiovascular disease; the direct brain oxygen starvation is less emphasized.

Ekberg details two synergistic effects of smoking on the brain. Nicotine causes chronic vasoconstriction, reducing blood flow to peripheral areas including the brain. Simultaneously, cigarette smoke contains carbon monoxide, which binds to hemoglobin with an affinity 200–250 times greater than oxygen. This permanently occupies hemoglobin, reducing the blood's oxygen-carrying capacity. For a heavy smoker, the combined effect can slash oxygen delivery to the brain by roughly one-third. Since the brain consumes 20–25% of the body's oxygen despite being only 2% of body weight, it is exquisitely sensitive to hypoxia. He notes the brain's selfishness: it will sacrifice other organs to preserve itself, yet smokers voluntarily impose chronic brain starvation. He also points out that the brain's 'passing out' mechanism exists solely to get the head level with the heart when blood flow drops.

If you're a heavy smoker, the combined effect of those could mean that you reduce your oxygen delivery by about one-third.

Also said
“Carbon monoxide binds 200 to 250 times harder with hemoglobin. So it gets like totally stuck. And therefore, when you smoke, even a tiny tiny tiny little bit of carbon monoxide is going to stick to that hemoglobin and stay there.”— Explains the irreversible binding that makes even small amounts of carbon monoxide significant.
“The brain is 2% of your body weight uses 20 to 25% of all your energy, of all your calories, of all your oxygen and all your blood flow. So it's not very tolerant for a lack of oxygen and blood.”— Quantifies the brain's extreme metabolic demand, underscoring the impact of oxygen deprivation.

screen-time-hippocampus-shrinkage-spatial-disconnect

Excessive screen time shrinks the hippocampus not just because of blue light, but because the eyes see motion without corresponding body movement, starving the spatial navigation circuits and forcing tunnel vision that raises baseline stress.

Why this matters: Goes far beyond the usual 'blue light disrupts sleep' warning to explain a structural brain change from the mismatch between visual motion and physical stillness.

Background

Common advice about screen time focuses on sleep disruption via blue light; the spatial navigation and hippocampal volume angle is rarely mentioned in popular health content.

Ekberg explains that the brain evolved to process a three-dimensional world where visual input is always paired with physical movement, proprioception, and spatial navigation. A screen presents a flat, two-dimensional image that compresses depth, texture, and gravity cues. When watching motion on a screen, the eyes detect movement but the body remains still, creating a disconnect. This fails to activate the spatial circuits, leading to measurable decreases in hippocampal volume over time. Additionally, screen use forces a form of tunnel vision that suppresses peripheral vision—the system normally used to detect threats. Losing peripheral awareness causes the brain to compensate with increased sympathetic tone, raising baseline stress. The result is decreased neural complexity: fewer circuits are involved, so the brain simplifies and weakens. He emphasizes moderation, noting the brain can handle several hours but not 16-hour days.

The eyes see motion, but there is no movement. There's no body movement to match it. There's no body movement to integrate with what you're seeing.

Also said
“What they have found with people who spend a lot of time in front of screens for a long period of time is that there's a measurable decrease in the volume of the hippocampus.”— Directly states the structural brain change associated with screen time.
“The result of that... is decreased complexity. We're getting fewer circuits involved. So we're reducing the neural density. The brain doesn't have as much to do. So it gets simplified. It gets weaker.”— Summarizes the overarching effect of screen time on brain architecture.

chronic-stress-cortex-blood-flow-shift

Chronic stress shifts blood flow from the cortex (thinking brain) to the brain stem (reflexive survival brain), effectively starving the cortex and contributing to cortical thinning.

Why this matters: The blood flow redistribution is a concrete physiological mechanism that explains why chronic stress impairs cognition and shrinks the brain, beyond the usual cortisol narrative.

Background

Stress is commonly linked to cortisol and inflammation, but the acute shift in cerebral blood flow from higher-order regions to primitive survival centers is less widely known.

Ekberg describes the stress response as an emergency system designed for short-term threats. When a threat is perceived, the HPA axis activates, releasing cortisol and adrenaline. Cortisol raises blood sugar for energy but is directly destructive to brain tissue, and the hippocampus—rich in cortisol receptors—takes the most damage. Simultaneously, the body shifts blood flow from the cortex, where conscious thought, learning, and evaluation occur, down to the brain stem, which handles reflexes and instinctive reactions. This makes sense for an acute physical threat where thinking is too slow, but under chronic stress, the cortex is repeatedly deprived of blood and oxygen, leading to thinning and shrinkage. He stresses that the solution is not to accept stress as unchangeable but to gradually shift perception, because the brain interprets all negative feelings—fear, overwhelm, isolation—as threats.

With a stress response, we change our focus and we shift our blood flow, our blood supply from the cortex to the brain stem.

Also said
“Cortisol is directly destructive to brain tissue. And when we go through these, we have to realize and remember that chronic stress is not supposed to be there.”— Highlights the direct tissue damage from cortisol, reinforcing the urgency.
“If you have chronic stress then you're basically a lot of times you're taking your cortex offline and you're starving the cortex and it shrinks.”— Bluntly states the consequence of the blood flow shift.
Disclosed sponsorships1speaker disclosed

Uvexia

Supplement Sponsored · disclosed

While explaining the concept of eustress (good stress), Ekberg notes that the Greek prefix 'eu' means true or good, and by coincidence his supplement brand is called Uvexia, meaning 'true wellness.' He does not elaborate on the products or make a direct pitch.

DisclosureSten Ekberg's own supplement brand; mentioned in passing during the eustress discussion.

Personal experience

Speaker owns the brand and mentions it as an aside.

By some coincidence, my supplement brand is called Uvexia, which means true wellness, but that's another story.

Find Uvexia

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Topics covered

type-3-diabetesinsulin-resistanceadvanced-glycation-end-productshippocampuslow-fat-dietscholesterolmyelingrainsglutenlectinsleaky-gutlipopolysaccharidesneuroinflammationomega-6omega-3dhaseed-oilscell-membrane-fluidityglymphatic-systemautophagy
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Educational summary of the cited expert source — not medical advice. Open the source recording linked above and consult a qualified physician before acting on any protocol.