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<h1>Blocking Tissue Destruction</h1>
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<div style="text-align: center;">
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<a href="/"><img class="epic" src="/icons/chads/chad.png"></a>
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<p class="nav"><span class="nav-left">Listed under <a href="/ray-peat.html">Ray Peat</a>.</span><span class="nav-right"><a href="/theme.html">Theme</a></span></p>
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<p>From the <a href="https://raypeat.com/articles/articles/tissue-destruction.shtml" target="_blank">original article</a> in 2006. Author: <a href="https://raypeat.com/" target="_blank">Ray Peat</a>.</p>
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<p>There
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always seems to be a rough balance between tissue regeneration and tissue
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degeneration, with growth and repair occurring when the equilibrium
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shifts in one direction,and with atrophy or degeneration occurring when
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the balance shifts in the other direction. If we can understand
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the mechanisms of atrophy, and how to retard or to block tissue destruction,
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then we can restore the balance to a degree which might allow regeneration
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to occur, even if we don't clearly understand the mechanisms of growth.
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</p>
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<p>Skin
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and bones are such different types of tissue that it will be useful
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to start with them, because if we can see similar processes of degeneration
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or regeneration in them, then the chances are good that the same processes
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will occur in other tissues too. Bone is a relatively stable tissue,
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while skin is a tissue whose cells divide rapidly.
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</p>
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<p>It
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is common medical knowledge that cortisone and realted glucocorticioid-type
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hormones cause skin to atrophy, becoming thinner. Using topical
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applications of a synthetic derivative of cortisione,CM Papa and A M.
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Kligman showed that the atrophy extended to the pigment cells,reducing
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theirr size and eliminating most of their dendritic branches. Some animal
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studies have found that estrogen caused the skin to become thinner.
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The other steroids they tested,progesterone, testosterone,and pregnenolone,
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acted in the opposite direction, making aged and atrophied skin thicker
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and more regular. They also made the pigment cells larger, and
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increased their branchinhg.l Since these hormones were already
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known to have protective actions against cortisone and estrogen, these
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results were not too surprising, though they did directly contradict
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the claims of people who made estrogen-containing cosmetics.
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</p>
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<p>Since
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progesterone and pregnenolone do not cause healthy, young skin to thicken,
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their effect in damaged skin is probably partly to replace the deficiency
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of that type of steroid which occurs with aging, and to offset the damaging
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effects of the catabolic hormones, whose influence does not decrease
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with age.</p>
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<p>Many
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years ago it was found that in old age a woman's estrogens were increasedd
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relative to the 17-keto steroids adrenal androgens. Later, it
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was found that the conversion of androgen to estrogen increases with
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age in both men and women, and that this occurs largely in fat cells.
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Several years ago, P. K. Siiteri found that low thyroid modified the
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enzymes of fat cells in a way that would tend to increase the conversion
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of androgen to estrogen. More recently, it was found that adding
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progesterone to the enzymes had the opposite effect of aging and hypothyroidism,
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protecting the androgen from conversion to estrogen. These researchers
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(C. J. Newton and colleagues, of London) concluded that the decreased
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output of progesterone after the menopause might account for the increased
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production of estrogen.3 Since progesterone declines in aging
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men, too, this could account for the same process in men.
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</p>
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<p>Vitamin
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A's effect on the skin opposes that of estrogen.4 There are several
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mechanisms that could account for this. Vitamin A is used in the
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formation of steroids, and since the skin is a major site of steroid
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metabolism, vitamin A might help to maintain the level of the anti-catabolic
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steroids. A deficiency of vitamin A causes excessive release of
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the lysosomal enzymes, acid hydrolases, resulting in tissue catabolism.5
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Also, vitamin A is necessary for the proper differentiation of cells
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in skin and other membranes. A deficiency tends to cause an increased
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rate of cell division, with the production of abnormal cells, and a
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substitution of keratinized cells for other types. Estrogen also
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promotes keratinization and speeds cell division. A deficiency
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of vitamin A can cause leukoplakia in the mouth and on the cervix of
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the uterus; although this is considered "pre-cancerous," I
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have found it to be very easily reversible, as I have discussed elsewhere.6
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I suspect that the intracellular fiber, keratin, is produced when a
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cell can't afford to do anything more complex. Adequate vitamin
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A speeds protein synthesis,7 and allows it to be used more efficiently.
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</p>
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<p>Prolactin
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(which is promoted by estrogen, and inhibited by progesterone) increases
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with stress and with age. It probably affects every tissue, but
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it seems to have its greatest efects on the secretory membranes.
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It is known to have strong effects on the kidney, gut and skin (sweat
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and oil glands, hair follicles, and feathers inbirds), and on the gills
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of fish. Its involvement with milk production suggests that it
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might mobilize calcium from bones, and inf fact it does contribute to
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osteoporosis. This was foreseen by G. Bourne, in his book on the
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metabolism of hard tissues, when he suggested that estrogen, acting
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through the pituitary, might be expected to promote osteoporosis.
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</p>
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<p>Since
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reading Bourne's book, I have doubted that it was rational to use estrogen
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to prevent osteoporosis, especially when it is known to be carcinogenic
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and when the ratio of estrogen to and androgens and progesterone increases
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after menopause. Now that several publications have appeared clearly
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showing that estrogen increases prolactin, that prolactin increases
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with cancellous bone; adrenal androgens.
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Thyroid. Rate of formation, overall metabolic rate. </p>
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<h2>Arthritis and natural hormones</h2>
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<p>A
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very healthy 71 year-old man was under his house repairing the foundation,
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when a support slipped and let the house fall far enough to break some
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facial bones. During his recovery, he developed arthritis in his hands.
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It is fairly common for arthritis to appear shortly after an accident,
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a shock, or surgery, and Han Selye's famous work with rats shows that
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when stress exhausts the adrenal glands (so they are unable to produce
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normal amounts of cortisone and related steroid hormones), arthritis
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and other "degenerative" diseases are likely to develop.
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</p>
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<p>But
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when this man went to his doctor to "get something for his arthritis,"
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he was annoyed that the doctor insisted on giving him a complete physical
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exam, and wouldn't give him a shot of cortisone. The examination showed
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low thyroid function, and the doctor prescribed a supplement of thyroid
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extract, explaining that arthritis is one of the many symptoms of hypothyroidism.
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The patient agreed to take the thyroid, but for several days he grumbled
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about the doctor 'fixing something that wasn't wrong' with him, and
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ignoring his arthritis. But in less than two weeks, the arthritis had
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entirely disappeared. He lived to be 89, without a recurrence of arthritis.
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(He died iatrogenically, while in good health.)</p>
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<p>Selye's
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work with the diseases of stress, and the anti-stress hormones of the
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adrenal cortex, helped many scientists to think more clearly about the
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interaction of the organism with its environment, but it has led others
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to focus too narrowly on hormones of the adrenal cortex (such as cortisol
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and cortisone), and to forget the older knowledge about natural resistance.
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There are probably only a few physicians now practicing who would remember
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to check for hypothyroidism in an arthritis patient, or in other stress-related
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conditions. Hypothyroidism is a common cause of adrenal insufficiency,
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but it also has some direct effects on joint tissues. In chronic hypothyroidism
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(myxedema and cretinism), knees and elbows are often bent abnormally.
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</p>
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<p>By
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the 1930's, it was well established that the resistance of the organism
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depended on the energy produced by respiration under the influence of
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the thyroid gland, as well as on the adrenal hormones, and that the
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hormones of pregnancy (especially progesterone) could substitute for
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the adrenal hormones. In a sense, the thyroid hormone is the basic anti-stress
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hormone, since it is required for the production of the adrenal and
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pregnancy hormones.</p>
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<p>A
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contemporary researcher, F. Z. Meerson, is putting together a picture
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of the biological processes involved in adapting to stress, including
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energy production, nutrition, hormones, and changes in cell structure.
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</p>
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<p>While
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one of Selye's earliest observations related gastrointestinal bleeding
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to stress, Meerson's work has revealed in a detailed way how the usually
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beneficial hormone of adaptation, cortisone, can cause so many other
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harmful effects when its action is too prolonged or too intense.
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</p>
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<p>Some
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of the harmful effects of the cortisone class of drugs (other than gastro-intestinal
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bleeding) are: Hypertension, osteoporosis, delayed healing, atrophy
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of the skin, convulsions, cataracts, glaucoma, protruding eyes, psychic
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derangements, menstrual irregularities, and loss of immunity allowing
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infections (or cancer) to spread.</p>
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<p>While
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normal thyroid function is required for the secretion of the adrenal
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hormones, the basic signal which causes cortisone to be formed is a
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drop in the blood glucose level. The increased energy requirement of
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any stress tends to cause the blood sugar to fall slightly, but hypothyroidism
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itself tends to depress blood sugar. </p>
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<p>The
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person with low thyroid function is more likely than a normal person
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to require cortisone to cope with a certain amount of stress.
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However, if large amounts of cortisone are produced for a long time,
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the toxic effects of the hormone begin to appear. According to Meerson,
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heart attacks are provoked and aggravated by the cortisone produced
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during stress. (Meerson and his colleagues have demonstrated that the
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progress of a heart attack can be halted by a treatment including natural
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substances such as vitamin E and magnesium.)</p>
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<p>While
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hypothyroidism makes the body require more cortisone to sustain blood
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sugar and energy production, it also limits the ability to produce cortisone,
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so in some cases stress produces symptoms resulting from a deficiency
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of cortisone, including various forms of arthritis and more generalized
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types of chronic inflammation. </p>
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<p>Often,
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a small physiological dose of natural hydrocortisone can help the patient
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meet the stress, without causing harmful side-effects. While treating
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the symptoms with cortisone for a short time, it is important to try
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to learn the basic cause of the problem, by checking for hypothyroidism,
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vitamin A deficiency, protein deficiency, a lack of sunlight, etc. (I
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suspect that light on the skin directly increases the skin's production
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of steroids, without depending on other organs. Different steroids
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probably involve different frequencies of light, but orange and red
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light seem to be important frequencies.) Using cortisone in this
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way, physiologically rather than pharmacologically, it is not likely
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to cause the serious problems mentioned above.</p>
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<p>Stress-induced
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cortisone deficiency is thought to be a factor in a great variety of
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unpleasant conditions, from allergies to ulcerative colitis, and in
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many forms of arthritis. The stress which can cause a cortisone
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deficiency is even more likely to disturb formation of progesterone
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and thyroid hormone, so the fact that cortisone can relieve symptoms
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does not mean that it has corrected the problem.</p>
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<p>According
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to the Physicians' Desk Referenc, hormones similar to cortisone are
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useful for treating rheumatoid arthritis, post-traumatic osteoarthritis,
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synovitis of osteoarthritis, acute gouty arthritis, acute nonspecific
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tenosynovitis, psoriatic arthritis, ankylosing spondylitis, acute and
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subacute bursitis, and epicondylitis. </p>
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<p>Although
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cortisone supplementation can help in a great variety of stress-related
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diseases, no curewill take place unless the basic cause is discovered.
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Besides the thyroid, the other class of adaptive hormones which are
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often out of balance in the diseases of stress, is the group of hormones
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produced mainly by the gonads: the "reproductive hormones."
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During pregnancy these hormones serve to protect the developing baby
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from the stresses suffered by the mother, but the same hormones function
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as part to the protective anti-stress system in the non-pregnant individual,
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though at a lower level.</p>
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<p>Some
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forms of arthritis are known to improve or even to disappear during
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pregnancy. As mentioned above, the hormones of pregnancy can make up
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for a lack of adrenal cortex hormones. During a healthy pregnancy, many
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hormones are present in increased amounts, including the thyroid hormones.
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Progesterone, which is the most abundant hormone of pregnancy, has both
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anti-inflammatory and anesthetic actions, which would be of obvious
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benefit in arthritis. </p>
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<p>There
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are other naturally anesthetic hormones which are increased during pregnancy,
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including DHEA, which is being studied for its anti-aging, anti-cancer,
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and anti-obesity effects. (One of the reasons that is frequently given
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for the fact that this hormone hasn't been studied more widely is that,
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as a natural substance, it has not been monopolized by a drug patent,
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and so no drug company has been willing to invest money in studying
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its medical uses.) These hormones also have the ability to control cell
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division, which would be important in forms of arthritis that involve
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invasive tissue growth.</p>
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<p>While
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these substances, so abundant in pregnancy, have the ability to substitute
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for cortisone, they can also be used by the adrenal glands to produce
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cortisol and related hormones. But probably the most surprising property
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of these natural steroids is that they protect against the toxic side-effects
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of excessive adrenal hormones. And they seem to have no side-effects
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of their own; after about fifty years of medical use, no toxic side
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effects have been found for progesterone or pregnenolone.
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</p>
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<p>Pregnenolone
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is the material the body uses to form either progesterone or DHEA. Others,
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including DHEA, haven't been studied for so long, but the high levels
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which are normally present in healthy people would suggest that replacement
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doses, to restore those normal levels, would not be likely to produce
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toxic side effects. And, considering the terrible side effects of the
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drugs that are now widely used, these drugs would be justifiable simply
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to prevent some of the toxic effects of conventional
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treatment. </p>
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<p>It
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takes a new way of thinking to understand that these protective substances
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protect against an excess of the adrenal steroids, as well as making
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up for a deficiency. Several of these natural hormones also have a protective
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action against various poisons; Selye called this their "catatoxic"
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effect.</p>
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<p>Besides
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many people whose arthritis improved with only thyroid supplementation,
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I have seen 30 people use one or more of these other natural hormones
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for various types of arthritis, usually with a topical application.
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Often the pain is relieved within a few minutes. I know of several other
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people who used progesterone topically for inflamed tendons, damaged
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cartilage, or other inflammations. Only one of these, a woman with rheumatoid
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arthritis in many joints, had no significant improvement. An hour after
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she had applied it to her hands and feet, she enthusiastically reported
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that her ankle had stopped hurting, but after this she said she had no noticeable improvement.
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</p>
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<p>We
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often hear that "there is no cure for arthritis, because the causes
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are not known." If the cause is an imbalance in the normal hormones
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of adaptation and resistance, then eliminating the cause by restoring
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balance will produce a true cure. But if it is more profitable
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to sell powerful drugs than to sell the nutrients needed to form natural
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hormones (or to supplement those natural hormones) we can't expect the
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drug companies to spend any money investigating that sort of cure. And
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at present the arthritis market amounts to billions of dollars in drug
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sales each year. </p>
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<hr>
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