These episodes make great companion listening for a long drive.
A blueprint for choosing the right fish oil supplement — filled with specific recommendations, guidelines for interpreting testing data, and dosage protocols.
We’ve all experienced stress at some point in our lives. In fact, the term “stress” is pervasive in our everyday language. Although the word often has a negative connotation, stress is essential to our survival. It’s what kept us alive in the past as we made life or death – “fight or flight” – decisions when encountering saber-toothed cats, and, surprisingly, it’s what keeps us alive today when we eat fruits and vegetables, engage in exercise and other healthy lifestyle behaviors such as sauna use, or even take on that new project at work that is a little outside our comfort zone. These short-term “good” stressors provide hormetic benefits that switch on physiological processes that protect us from harm in the long-term.
In the modern world, however, myriad “bad” chronic stressors – such as debt, a cranky boss, or relationship problems – can become overwhelming, especially when we ruminate or dwell on them to excess. Rumination can set in motion a cascade of hormonal and physiological responses that harm our mental and physical health.
A key player in the body’s response to rumination is a biological pathway that starts with the release of corticotropin-releasing hormone. This brain-derived hormone drives the entire stress hormone system and has a direct effect on many parts of the body including the brain, gut, and DNA.
In the brain, corticotropin-releasing hormone increases the production of amyloid beta, which aggregates and forms plaques in the brain, disrupting the synapses that form between neurons and promoting neuronal cell death. This impairs energy metabolism in the brain’s cells, leading to the production of reactive oxygen species production and more amyloid plaque production – and a vicious cycle ensues.
In the gut, corticotropin-releasing hormone activates specialized immune cells called mast cells, initiating a kind of chemical warfare. The mast cells release proinflammatory cytokines and proteases that damage the gut, leading to intestinal permeability, a condition otherwise known as “leaky gut.” This leakiness allows bacteria and bacterial antigens to cross the gut’s inner layer, the epithelium, and activate even more immune cells, leading to more inflammation – a key driver in the aging process.
Stress-related inflammation also accelerates the shortening of telomeres – tiny end caps located at the end of a chromosome. Telomeres serve as protective buffers against DNA loss during DNA replication and DNA damage caused by inflammation, reactive oxygen species, and other chemical compounds. Telomere shortening is linked to biological aging because it promotes cell death, or, worse, it promotes alternative lengthening of telomeres – a harbinger of cancer.
Identifying strategies that buffer the negative effects of chronic stress is critical to our health. One highly effective strategy for buffering stress is meditation.
Research suggests that meditation, or mindfulness, may protect the brain from the negative effects of stress by decreasing ruminative thoughts and distraction. Reducing rumination may decrease distress and may even promote compassion and altruism.
One mechanism by which meditation protects the brain is through the production of gamma waves – a sign of neuroplasticity, which is linked to a capacity to learn new things and change synapses as a consequence of new behaviors. Neuroplasticity makes your brain more resilient and slows cognitive aging. While the young will always have a greater degree of neuroplasticity than the old, it is empowering to know that neural plasticity can be modulated through our lifestyles and behavior.
Meditation also increases the brain’s gray matter – the area of the brain associated with working memory and executive decision making. Gray matter is also where the omega-3 fatty acid DHA is enriched. DHA protects the brain against cognitive decline. As we age, our brains atrophy and we lose some of that gray matter. But meditation may increase brain volume in areas of the brain related to learning, memory, neurotransmitter production, empathy, compassion, attention, and self-relevance, while decreasing activity of the amygdala, the area of the brain involved in anxiety and fear.
Not only does meditation slow cognitive aging, but it also slows biological aging by slowing the shortening of telomeres, protecting your DNA. Studies by telomere experts Elizabeth Blackburn at UCSF and Elisa Epel show that meditation buffers the stress that shortens telomeres and activates the gene that encodes for the enzyme telomerase, which can extend the length of telomeres.
“Good” stress builds resilience, the body’s ability to adapt to stress and retard aging. The activation of stress resistance pathways through hormetic stress may be at the heart of many mechanisms of aging. However, chronic psychological stress can have negative effects on the brain and body and accelerates the aging process. Engaging in mindful meditation promotes healthy stress coping mechanisms, decreases rumination, and slows brain and biological aging.
Meditation can be practiced in many ways and venues, include yoga, transcendental meditation, nature walks, flotation tanks, and Headspace or Oak – app-based audio guides to meditation.
Introduction
The difference between good and bad stress
Hormones that mediate stress in the body and brain
Stress increases leaky gut
Reducing stress and inflammation promotes longevity
Stress weakens the immune system
Meditation promotes mindfulness and compassion
How mediation shapes the brain through neuroplasticity
Stress accelerates telomere attrition and cellular senescence
Short telomeres promote cell death
Short telomeres promote cancer initiation
Meditation can reverse telomere attrition and aging
Different methods of meditation
A neuro-behavioral condition characterized by inattention and/or hyperactive or impulsive behavior that interferes with functioning, learning, or development.
Star-shaped cells found in the brain and spinal cord. Astrocytes facilitate neurotransmission, provide nutrients to neurons, maintain neuronal ion balance, and support the blood-brain barrier. Astrocytes also play a role in the repair and scarring process of the brain and spinal cord following traumatic injuries.
The shrinking or wasting away of cells, organs, or tissues that may occur as part of a disease process, trauma, or aging.
One of two types of fat, or adipose, tissue (the other being white adipose tissue, or white fat) found in mammals. The primary function of brown adipose tissue is to generate body heat. In contrast to white adipocytes (fat cells), which contain a single lipid droplet, brown adipocytes contain numerous smaller droplets and a much higher number of mitochondria, which make it brown. Brown fat also contains more capillaries than white fat, since it has a greater need for oxygen than most tissues.
Proteins that preserve cell viability at low temperatures by binding to nucleic acids and, subsequently, controlling gene expression. Cold shock proteins have what is known as a "cold-shock domain," a sequence of amino acids whose expression is associated with cold and is thought to help cells survive in lower than optimal temperatures.
A type of proteolytic enzyme that breaks down collagen. Collagenases are involved in both normal and pathological turnover of connective tissues. Their production is significantly increased at sites of inflammation due to the stimulation of pro-inflammatory cytokines.
Cooling of the body for therapeutic purposes. Cryotherapy can include the use of products such as ice packs on a localized portion of the body, such as a joint or muscle, or whole body exposure to extremely low temperatures in water or air. Cryotherapy has profound effects on many parts and functions of the body, including the brain, immune system, and metabolism, among others.
A broad category of small proteins (~5-20 kDa) that are important in cell signaling. Cytokines are short-lived proteins that are released by cells to regulate the function of other cells. Sources of cytokines include macrophages, B lymphocytes, mast cells, endothelial cells, fibroblasts, and various stromal cells. Types of cytokines include chemokines, interferons, interleukins, lymphokines, and tumor necrosis factor.
A neurotransmitter best known for its role in motor, motivation, and pleasure control. Dopamine also functions as a paracrine (cell-to-cell) hormone in other parts of the body. It is derived from tyrosine and is the precursor to norepinephrine and epinephrine. Some evidence suggests that dopamine may also be involved in pain modulation.
Beneficial stress that can be psychological, physical (e.g. exercise), or biochemical (hormesis) in nature.
An antioxidant produced within cells that enzymatically reduces hydrogen peroxide to water to limit its harmful effects. Glutathione peroxidase's primary role is to protect cells from oxidative damage, a key factor in many diseases.
An antioxidant produced within cells that converts oxidized glutathione to reduced glutathione. Glutathione reductase is essential for protection against oxidative damage. Oxidative damage is a key factor in many diseases.
A family of proteins produced by cells in response to exposure to stressful conditions. Heat shock proteins are expressed in response to heat as well as exposure to cold and UV light, and during wound healing and tissue remodeling. Many heat shock proteins function as chaperones by stabilizing new proteins to ensure correct folding or by helping to refold proteins that were damaged by cell stress. A 30-minute 73ºC sauna session in healthy young adults has been shown to cause a robust and sustained increase in the production of heat shock proteins for up to 48 hours afterward.[1]
A sustained period of winter dormancy in warm-blooded animals. Hibernation is characterized by prolonged periods of inactivity and low nutrient intake.
Biological responses to low-dose exposures to toxins or other stressors such as exercise, heat, cold, fasting, and xenohormetics. Hormetic responses are generally favorable and elicit a wide array of protective mechanisms. Examples of xenohormetic substances include plant polyphenols – molecules that plants produce in response to stress. Some evidence suggests plant polyphenols may have longevity-conferring effects when consumed in the diet.
A proinflammatory cytokine produced by macrophages. IL-1 beta is an important mediator of the body’s inflammatory response. It is involved in a variety of cellular activities, including cell proliferation, differentiation, and apoptosis.
A pro-inflammatory cytokine that plays an important role as a mediator of fever and the acute-phase response. IL-6 is rapidly induced in the context of infection, autoimmunity, or cancer and is produced by almost all stromal and immune cells. Many central homeostatic processes and immunological processes are influenced by IL-6, including the acute-phase response, glucose metabolism, hematopoiesis, regulation of the neuroendocrine system, hyperthermia, fatigue, and loss of appetite. IL-6 also plays a role as an anti-inflammatory cytokine through inhibition of TNF-alpha and IL-1 and activation of IL-1ra and IL-10.
A proinflammatory cytokine produced by macrophages. MIP-1 alpha induces the body’s inflammatory response and is associated with cell adhesion and migration.
The process by which new mitochondria are made inside cells. Many factors can activate mitochondrial biogenesis including exercise, cold shock, heat shock, fasting, and ketones. Mitochondrial biogenesis is regulated by the transcription factor peroxisome proliferator-activated receptor gamma coactivator 1-alpha, or PGC-1α.
An increase in the size of muscle cells that occurs with exercise and physical activity.
The process of forming new neurons. Neurogenesis is essential during embryonic development, but also continues in certain brain regions throughout human lifespan.
A substance produced in the brain. Norepinephrine acts as a hormone and neurotransmitter and is best known for its role in the body’s “fight or flight” response to stress. Its role as a neurotransmitter has been exploited as a molecular target for a class of drugs known as norepinephrine reuptake inhibitors, which were developed for the purpose of treating disorders ranging from ADHD to narcolepsy and depression. Norepinephrine also plays a role in converting white adipose tissue into brown adipose tissue via an uncoupling protein 1 (UCP-1) mediated mechanism.
The master regulator of mitochondrial biogenesis. PGC-1α is activated in human skeletal muscle in response to endurance exercise. It is strongly induced by cold exposure, linking this environmental stimulus to adaptive thermogenesis. PGC-1a has been implicated as a potential therapy for Parkinson's disease by conferring protective effects on mitochondrial metabolism.
A group of lipid-signaling molecules that have diverse hormone-like effects. Prostaglandins play roles in inflammation, vasoconstriction or vasodilation, aggregation or disaggregation of platelets, calcium movement, cell growth, and thermoregulation. Prostaglandins are produced in many places throughout the human body.
A cold-shock protein that is induced by exposure to low temperatures, such as those that encountered during hibernation. In a cell model of Parkinson's disease, RBM3 provided neuroprotection, suggesting that RBM3 induction may be a suitable strategy for Parkinson's disease therapy.[1]
The loss of skeletal muscle tissue with age. Sarcopenia is one of the most important causes of functional decline and loss of independence in older adults.
Skeletal muscle stem cells. Satellite cells are typically dormant, but if the muscle is stressed or injured, they play essential roles in the regenerative growth of new muscle fibers. They have chemotactic properties, which means they can migrate from one location within a muscle fiber to another, where they can participate in the process of developing a new muscle fiber.
A class of powerful antioxidant enzymes produced in cells. Superoxide dismutases convert harmful superoxide radicals to harmless molecular oxygen and hydrogen peroxide, providing cellular defense against reactive oxygen species.
The junction between one neuron and another or a gland or muscle cell. Synapses are critical elements in the transmission of nerve signals. Their formation is necessary for the establishment and maintenance of the brain’s neuronal network and the precision of its circuitry.
A physiological process that results in the production of heat. There are two types of thermogenesis: shivering and nonshivering. Shivering thermogenesis, as its name implies, involves shivering to produce heat. During shivering, skeletal muscles undergo repeated, rapid contractions that produce little net movement and instead, produce heat. Nonshivering thermogenesis generates heat in the absence of shivering by unique mechanisms in both skeletal muscle and adipose (fat) tissue depots. These processes involve uncoupling electron transport from ATP synthesis and repetitive, non-productive transport of ions across the adipose cell membrane.
A proinflammatory cytokine. TNF-alpha is produced by a wide range of cells, including macrophages, lymphocytes, glial cells, and others. TNF-alpha signaling inhibits tumorigenesis, prevents viral replication, and induces fever and apoptosis. Dysregulation of the TNF-alpha signaling pathway has been implicated in a variety of disorders including cancer, autoimmune diseases, Alzheimer’s disease, and depression.
Muscle fibers used primarily during aerobic activities requiring low-level force and endurance. Type 1 fibers typically exhibit slow contraction times and high fatigue resistance. Also known as “slow twitch” fibers.
Muscle fibers used primarily during activities requiring high-level force, speed production, and low endurance. Type 2 fibers typically exhibit rapid contraction times and low fatigue resistance. Also known as “fast twitch” fibers.
A protein found in the mitochondria of brown adipose tissue, previously known as thermogenin. UCP1 is expressed only in brown adipose tissue, a specialized tissue which functions to produce heat via non-shivering thermogenesis.
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