Wednesday, October 2, 2013

Shelly Fan - The Fat-Fueled Brain: Unnatural or Advantageous?


The current method of doing a ketogenic diet is not like the popular version in the press, a misrepresentation based on Dr. Atkins' original keto diet in the early 1970s. At that time, the medical establishment thought he was crazy for advocating a diet based primarily on protein (mostly from meat) and fat. The popular image was the steak and bacon diet, with a side of whole cream or a stick of butter.

But he persisted and the evidence and research began to accumulate. As this evidence mounted, Atkins responded to some of the criticisms of his diet by changing the emphasis from high-fat red meat to chicken, fish, and turkey. He also reduced the recommended amounts of saturated fats in the diet.

As of now, many experts suggest that saturated fats should be around 10-15% of all calories from fat, with the remained 85-90% divided between monounsaturated fats (almonds, olive oil) and polyunsaturated fats (omega-3, -6, and -9 from fish, flax seed, pumpkin seeds, walnuts, and other nuts).

By the early 2000s, low-carb diets were the fad, and like all fads, it faded away and Americans continued to get fatter, unhealthier, and more resigned to living that way. But in many circles, various versions of the keto diet live on - as the Paleo Diet of Loren Cordain, Ph.D., or as a general low-carb lifestyle adopted by many fitness enthusiasts and athletes.

The reason we can do a low-carb or even a no carb diet is because, of the four macronutrients (water, protein, fats, and carbohydrates), only three are essential to human life. Can you guess the one that isn't?

You got it - carbohydrates are not an essential macronutrient for human survival.

I have been eating a low-carb diet for the better part of 10 years. In the last 3-5 yrs it has become very low-carb. My energy is better, more level throughout the day, my brain is sharp, my mood is more steady, and despite everything you might read, it has not hurt my workouts. Granted, if I planned to ride my bike for 2-3 hours, I would probably ingest a couple of cans of pumpkin the night before so that I have some reserves of carbohydrate and pop a gell if I feel myself approaching a bonk. But I don't do that. I can ride hard for an hour on an empty stomach (well, on 12 grams of BCAAs) and feel great.

It's not really that hard to do this kind of a diet. Many days, my only carbohydrate source is 2 cups of mixed berries (mostly blueberries, raspberries, blackberries, and black cherries) with my cottage cheese for breakfast. Late morning or noonish I might have a couple of chicken sausages (120 calories each, 15 grams of protein, 5 grams of fat), a couple of sticks of lite string cheese (50 calories each, 7 grams of protein, 2.5 grams of fat) and a handful of walnuts or almonds. A few hours later it might be 6-8 oz. of deli chicken or turkey between two thick slices of part-skim mozzarella, or a chicken breast with some spinach or broccoli. Finally, I often have 2-4 squares of 90% dark chocolate with almond butter or sunflower seed butter. [During the day I might eat 2-5 additional tablespoons of almond butter, sunflower seed butter, or some other type of nut butter, though usually not peanut butter so much anymore.]

My version of this diet is what works for my body (trial and error). I generally eat more protein than the typical keto diet, which can be up to 75-90% fat. And I supplement a lot of my fats with fish oil (8-10 grams a day), pumpkin oil (4-5 grams a day), conjugated linoleic acid (CLA, 4-5 grams a day), and omega-3/6/9 (4-5 grams a day) - for a whopping total of 20-25 grams a day.

Anyway, here is an article from Scientific American Mind looking at the current research on ketogenic diets and the many health benefits we can reap from ditching carbohydrates.

The fat-fueled brain: Unnatural or advantageous?


By Shelly Fan | October 1, 2013

Disclaimer: First things first. Please note that I am in no way endorsing nutritional ketosis as a supplement to, or a replacement for medication. As you’ll see below, data exploring the potential neuroprotective effects of ketosis are still scarce, and we don’t yet know the side effects of a long-term ketogenic diet. This post talks about the SCIENCE behind ketosis, and is not meant in any way as medical advice.


It’s not bacon; it’s therapy! Source: Renée S. Suen on Flickr.

The ketogenic diet is a nutritionist’s nightmare. High in saturated fat and VERY low in carbohydrates, “keto” is adopted by a growing population to paradoxically promote weight loss and mental well-being. Drinking coffee with butter? Eating a block of cream cheese? Little to no fruit? To the uninitiated, keto defies all common sense, inviting skeptics to wave it off as an unnatural “bacon-and-steak” fad diet.

Yet versions of the ketogenic diet have been used to successfully treat drug-resistant epilepsy in children since the 1920s – potentially even back in the biblical ages. Emerging evidence from animal models and clinical trials suggest keto may be therapeutically used in many other neurological disorders, including head ache, neurodegenerative diseases, sleep disorders, bipolar disorder, autism and brain cancer. With no apparent side effects.

Sound too good to be true? I feel ya! Where are these neuroprotective effects coming from? What’s going on in the brain on a ketogenic diet?


Ketosis in a nutshell


In essence, a ketogenic diet mimics starvation, allowing the body to go into a metabolic state called ketosis (key-tow-sis). Normally, human bodies are sugar-driven machines: ingested carbohydrates are broken down into glucose, which is mainly transported and used as energy or stored as glycogen in liver and muscle tissue. When deprived of dietary carbohydrates (usually below 50g/day), the liver becomes the sole provider of glucose to feed your hungry organs – especially the brain, a particularly greedy entity accounting for ~20% of total energy expenditure. The brain cannot DIRECTLY use fat for energy. Once liver glycogen is depleted, without a backup energy source, humanity would’ve long disappeared in the eons of evolution.

The backup is ketone bodies that the liver derives primarily from fatty acids in your diet or body fat. These ketones – β-hydroxybutyrate (BHB), acetoacetate and acetone – are released into the bloodstream, taken up by the brain and other organs, shuttled into the “energy factory” mitochondria and used up as fuel. Excess BHB and acetoacetate are excreted from urine, while acetone, due to its volatile nature, is breathed out (hence the characteristically sweet “keto breath”). Meanwhile, blood glucose remains physiologically normal due to glucose derived from certain amino acids and the breakdown of fatty acids – voila, low blood sugar avoided!


Carbohydrate restriction induces the pancreas to "tell" fat cells to release fatty acids, which get taken up by the liver and converted into ketones and released into blood. Once taken up by the brain, ketones enter the TCA cycle to generate energy. Source: Shelly Fan. (click to see large)


Brain on ketones: Energetics, Oxidation and Inflammation


So the brain is happily deriving energy from ketones – sure, but why would this be protective against such a variety of brain diseases?

One answer may be energy. Despite their superficial differences, many neurological diseases share one major problem – deficient energy production. During metabolic stress, ketones serve as an alternative energy source to maintain normal brain cell metabolism. In fact, BHB (a major ketone) may be an even more efficient fuel than glucose, providing more energy per unit oxygen used. A ketogenic diet also increases the number of mitochondria, so called “energy factories” in brain cells. A recent study found enhanced expression of genes encoding for mitochondrial enzymes and energy metabolism in the hippocampus, a part of the brain important for learning and memory. Hippocampal cells often degenerate in age-related brain diseases, leading to cognitive dysfunction and memory loss. With increased energy reserve, neurons may be able to ward off disease stressors that would usually exhaust and kill the cell.

A ketogenic diet may also DIRECTLY inhibit a major source of neuronal stress, by –well- acting like a blueberry. Reactive oxygen species are unfortunate byproducts of cellular metabolism. Unlike the gas Oxygen, these “oxidants” have a single electron that makes them highly reactive, bombarding into proteins and membranes and wrecking their structure. Increased oxidants are a hallmark of aging, stroke and neurodegeneration.

Ketones directly inhibit the production of these violent molecules, and enhance their breakdown through increasing the activity of glutathione peroxidase, a part of our innate anti-oxidant system. The low intake of carbohydrates also directly reduces glucose oxidation (something called “glycolysis”). Using a glucose-like non-metabolized analogue, one study found that neurons activate stress proteins to lower oxidant levels and stabilize mitochondria.

Due to its high fat nature, keto increases poly-unsaturated fatty acids (PUFAs, such as DHA and EPA, both sold over-the-counter as “brain healthy” supplements), which in turn reduces oxidant production and inflammation. Inflammatory stress is another “root of all evil”, which PUFAs target by inhibiting the expression of genes encoding for pro-inflammatory factors.


Neurons on Ketones: Dampen that enthusiasm!


Excited neurons transmit signals, process information and form the basis of a functioning brain. OVER-excited neurons tend to die.

The brain teeters on a balance between excitation and inhibition through two main neurotransmitters, the excitatory glutamate and the inhibitory GABA. Tilt the scale towards glutamate, which occurs in stroke, seizures and neurodegeneration, and you get excitotoxicity. In other words, hyper-activity is toxic.

Back in the 1930s, researchers found that direct injection of various ketone bodies into rabbits prevented chemically-induced seizures through inhibiting glutamate release, but the precise mechanism was unclear. A recent study in hippocampal neurons showed that ketones directly inhibited the neuron’s ability to “load up” on glutamate – that is, the transmitter can’t be packaged into vesicles and released – and thus decreased excitatory transmission. In a model of epilepsy that used a chemical similar to glutamate to induce damage, the diet protected mice against cell death in the hippocampus by inhibiting pro-death signaling molecules. On the other end of the excitation-inhibition balance, ketones increase GABA in the synapses (where neurotransmitters are released) of rats and in the brains of some (but not all) epileptic humans subjects. This increase in inhibition may confer both anti-seizure effects and neuroprotection, though data is still scant.

Then there are some fringe hypotheses. The acidity of ketones may decrease the pH of certain brain microdomains, which might be the mechanism of keto’s positive effect on Type II Bipolar disorder (lots of mays and mights, I know). As keto affects the whole body, global changes due to calorie restriction and regulation of the satiety hormone Leptin are bound to alter brain function, and play a circumstantial role.


Neuroprotection? Show me the evidence!


All these molecular changes suggest that a ketogenic diet is protective against brain injury. But is there any REAL evidence?

A study with 23 elderly with mild cognitive impairment showed that a ketogenic diet improved verbal memory performance after 6 weeks compared to a standard high carbohydrate diet. In a double-blind, placebo-controlled study, 152 patients with mild- to moderate Alzheimer’s disease were given either a ketogenic agent or a placebo, while maintaining a normal diet. 90 days later, those receiving the drug showed marked cognitive improvement compared to placebo, which was correlated with the level of ketones in the blood.

In a pilot study in 7 patients with Parkinson’s disease, 5 were able to stick to the diet for 28 days and showed marked reduction in their physical symptoms. In an animal model of Amytrophic Lateral Sclerosis (ALS), a ketogenic diet also led to delayed motor neuron death and histological and functional improvements, although it did not increase life span; clinical trials are on the way.

Remarkably, a long-term ketogenic diet does not seem to be associated with significant side effects, although constipation, dehydration and electrolyte and micronutrient deficiencies are common complaints. More serious complications include increased chance of kidney stones, gallbladder problems and bone fractures, especially in children. Menstrual irregularities often occur in women, with potential impact on fertlity. Although ketoacidosis – acidification of the blood due to pathological levels of ketones – was historically proposed as a side effect, nutritional ketosis simply cannot achieve the level of ketones required to induce this life-threatening state. Nevertheless, there are no studies directly monitoring the side effects of ketosis yet, hence it’s too early to conclude that the diet is completely safe for everyone.


Brain [hearts] Bacon

While promising, large-scale placebo-controlled clinical trials in patients with neurological disorders are still lacking. The existing data needs to be interpreted carefully to avoid generating false hope or encourage patients to “ditch drugs for diet”. Nevertheless, the possibility that we can reduce symptoms of untreatable neurological disorders through modifying dietary composition is quite incredible; that a ketogenic diet may benefit physical and cognitive performance in healthy individuals is an even more tantalizing idea.

As the science behind this age-old dietary therapy gradually comes to light, social issues such as low adherence and public prejudice will need to be resolved. In the meantime, to those neuroscientists interested in studying keto: pass the bacon and I VOLUNTEER!

Final note: Before I let you go, I’d like to stress again that keto is NOT something to try out without talking to your doctor first, nor is it a replacement for pharmaceuticals. There’s simply not enough evidence, on either its effectiveness or side effects. Nevertheless, it’s a cool area of research to keep an eye on!

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