Cortisol
262 sourcesRay Peat viewed cortisol as one of the key stress hormones whose chronic elevation drives aging and disease. While cortisol serves essential functions in acute stress (mobilizing fuel, suppressing inflammation), Peat emphasized that chronically elevated cortisol — driven by inadequate nutrition, thyroid deficiency, PUFA consumption, and other stressors — breaks down muscle and bone, promotes fat storage, suppresses immune function, and damages the brain.
Peat noted that cortisol and thyroid hormone have opposing actions: cortisol promotes gluconeogenesis (making glucose from protein), while thyroid supports efficient glucose oxidation. When thyroid function is low, the body relies more on cortisol to maintain blood sugar, creating a destructive cycle. He recommended addressing cortisol excess through frequent eating (sugar + protein), thyroid support, adequate sleep, and avoiding PUFAs.
Key Positions
- Chronic cortisol elevation breaks down muscle, bone, and brain tissue for gluconeogenesis
- Cortisol rises when blood sugar drops — frequent meals with sugar and protein prevent this
- Hypothyroidism forces greater reliance on cortisol for blood sugar maintenance
- Cortisol promotes fat storage (especially abdominal) while breaking down lean tissue
- Pregnenolone and progesterone oppose cortisol's catabolic effects
- Nighttime cortisol surges cause sleep disturbances and night waking
- DHEA and cortisol have an inverse relationship; the DHEA/cortisol ratio indicates stress status
Sources
262 items-
The transparency of life: Cataracts as a model of age-related disease.
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Thyroid
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Thyroid, insomnia, and the insanities: Commonalities in disease
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Thyroid: Therapies, Confusion, and Fraud.
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Tissue-bound estrogen in aging
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Tryptophan, serotonin, and aging.
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Unsaturated fatty acids: Nutritionally essential, or toxic?
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Using Sunlight to Sustain Life
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VV Fitness Blog - Vahdaneh Vahid
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Vashinvetala (formerly Pranarupa)
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Water: swelling, tension, pain, fatigue, aging
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When energy fails: Edema, heart failure, hypertension, sarcopenia, etc.