Description
This section lists the nutrients, hormones and other compounds,
naturally present within the human body, whose levels inevitably decline
in tandem with the progression of the Aging Process. It is becoming
increasingly common to attempt to restore levels of these compounds to
youthful levels, either by directly supplementing with these compounds
or by using their precursors in order to counteract their inevitable
decline with Aging.
The Body's Levels of these Substances Naturally Decline with Age
Amino Acids
The body's (especially the Brain's) levels of Acetyl-L-Carnitine (ALC)
decline in tandem with the Aging Process.
Carnitine levels in the Brain, Blood, Heart and Muscles decrease in
tandem with the progression of the Aging Process, while Carnitine levels
in the Liver increase in tandem with the Aging Process, indicating that
the transportation of Carnitine from the Liver to the Blood declines in
tandem with the Aging Process. references
The body’s ability to synthesize Creatine declines in tandem with the
progression of the Aging Process:
- Muscle Creatine Phosphate levels decline in tandem with the
progression of the Aging Process and the body’s ability to resynthesize
Creatine Phosphate after intensive Exercise declines in tandem with the
progression of the Aging Process. references
Older cells contain 20% - 30% less Glutathione than young Cells.
references
Phenylalanine absorption decreases significantly in tandem with the
Aging Process.
The body’s levels of S-Adenosylmethionine (SAM) decline in tandem with
the progression of the Aging Process. references
Carbohydrates
The content of Chondroitin Sulfate (CSA-B form) in the Dermis of the
Skin declines in tandem with the progression of the Aging Process.
references
The ratio of Chondroitin Sulfate-A (CSA-A) to Chondroitin Sulfate-C
(CSA-C) declines in tandem with the progression of the Aging Process and
this form of CSA should therefore be the major supplemental form of CSA.
references
The body's production of Hyaluronic Acid declines in tandem with the
Aging Process and the body’s excretion of Hyaluronic Acid increases in
tandem with the Aging Process: references
- The content of Hyaluronic Acid in the Dermis of the Skin declines in
tandem with the progression of the Aging Process (the Dermis of people
aged 60 and over often contain zero Hyaluronic Acid).
Carotenoids
The Lutein content of the Eyes declines in tandem with the progression
of the Aging Process. references
Digestive System Chemicals
The body's production of Hydrochloric Acid declines in tandem with the
Aging Process. references
Enzymes
Cytochrome C Oxidase activity declines in tandem with the progression of
the Aging Process. references
The body's production of Delta-6 Desaturase declines in tandem with the
Aging Process. references
The body’s production of Digestive Enzymes declines in tandem with the
progression of the Aging Process. references
The body’s Glutathione Peroxidase content declines in tandem with the
progression of the Aging Process. references
The body's production of Superoxide Dismutase (SOD) declines in tandem
with the Aging Process.
Growth Factors
Insulin-like Growth Factor-1 (IGF-1) levels decline in tandem with the
progression of the Aging Process. references
Nerve Growth Factor (NGF) production declines in tandem with the Aging
Process (the body’s production of NGF peaks at the age of two and then
steadily declines thereafter). references
Hormones
The body’s production and levels of Androstenediol declines in tandem
with the progression of the Aging Process - 80 year olds have 54% less
Androstenediol compared to 35 year olds. references
The body’s production and levels of Androstenedione declines in tandem
with the progression of the Aging Process - 80 year olds have 40% less
Androstenedione compared to 35 year olds. references
Dehydroepiandrosterone (DHEA) production declines in tandem with the
Aging Process (from 30 mg per day at age 20 to 6 mg at age 80):
references
- Cerebrospinal Fluid (CSF) DHEA levels decline in tandem with the
progression of the Aging Process.
The body’s levels of Dehydroepiandrosterone Sulfate (DHEAS) decline in
tandem with the progression of the Aging Process - by the age of 70,
DHEAS levels in most people have declined to approximately 20% of their
peak levels. references
The body’s production of Follicle Stimulating Hormone (FSH) declines in
tandem with the progression of the Aging Process. references
The production/release of Growth Hormone-Releasing Hormone (GHRH) from
the Hypothalamus declines in tandem with the progression of the Aging
Process.
Human Growth Hormone (hGH) production declines in tandem with the Aging
Process: references
- hGH production begins to decline at age 30 and by age 60 has tapered
off quite substantially. Exogenous, supplemental hGH administered by
injection has produced dramatic anti-Aging effects in older people
(although there are numerous side effects associated with the use of
exogenous hGH).
The body’s production of Luteinizing Hormone (LH) declines in tandem
with the progression of the Aging Process. references
Melatonin secretion declines in tandem with the Aging Process:
references
The body’s endogenous production of Pregnenolone declines in tandem with
the progression of the Aging Process (production of endogenous
Pregnenolone declines by 60% between the ages of 35 and 75). references
The body’s production of Relaxin declines in tandem with the progression
of the Aging Process (especially after Menopause). references
(Female and male) Testosterone production declines in tandem with the
Aging Process - male Testosterone production declines only very slightly
after age 40 and males continue to produce Testosterone until their late
70's. references
The body’s production of Thymic Hormones declines in tandem with the
progression of the Aging Process.
Thymosin levels decline in tandem with the progression of the Aging
Process (especially between the ages of 20 and 40). references
Plasma Thymulin levels progressively and significantly decline in tandem
with the Aging Process. references
The body’s production of Thyroid Hormones declines in tandem with the
progression of the Aging Process. references
Krebs Cycle Chemicals
Adenosine Triphosphate (ATP) production declines in tandem with the
Aging Process.
Lipids
Cardiolipin levels decline in tandem with the progression of the Aging
Process. references
The Brain’s content of Docosahexaenoic Acid (DHA) declines in tandem
with the progression of the Aging Process (supplemental DHA may retard
this decline). references
The Phospholipids content of Cell Membranes declines in tandem with the
progression of the Aging Process: references
- The body's endogenous Phosphatidylcholine levels decline in tandem
with the Aging Process and Phosphatidylcholine (especially when
administered via intravenous infusion) can reverse the deterioration of
Cell Membranes that ocurs in tandem with the progression of the Aging
Process. references
- The body’s Phosphatidylserine (PS) content declines in tandem with the
progression of the Aging Process (after the age of 25).
Microorganisms
The number of Beneficial Bacteria (probiotics) in the Gastrointestinal
Tract declines in tandem with the progression of the Aging Process:
references
- The number of Bifidobacteria in the Large Intestine declines in tandem
with the progression of the Aging Process. references
Minerals
The body's Bromine content declines in tandem with the Aging Process to
the extent that by the age of 75 there is zero left in the body.
Calcium absorption decreases in tandem with the Aging Process.
The body’s Chromium content declines in tandem with the progression of
the Aging Process. references
The body’s concentration of Copper declines in tandem with the
progression of the Aging Process. references
Iron absorption decreases in tandem with the Aging Process.
The intestinal absorption of Magnesium declines in tandem with the
progression of the Aging Process. references
Neurotransmitters
Acetylcholine production declines in tandem with the progression of the
Aging Process. references
Dopamine production declines in tandem with the Aging Process:
references
- Up to the age of 45, Dopamine levels remain relatively stable.
- After the age of 45, the average Dopamine level of healthy people
declines in a linear fashion by approximately 13% per decade.
- When the Brain’s Dopamine level falls to 30% of youthful levels, the
progression of Parkinson’s Disease commences.
- When the Brain’s Dopamine level falls to 10% of youthful levels, death
occurs.
The body’s production of Nitric Oxide declines in tandem with the
progression of the Aging Process. references
Norepinephrine production declines in tandem with the Aging Process.
Nucleic Acids
The quantity of Ribonucleic Acid (RNA) that is stored in the Brain’s
Neurons and Glial Cells decreases in tandem with the Aging Process
(especially after age 40). references
Peptides
The body’s Carnosine levels decline in tandem with the progression of
the Aging Process. references
Proteins
The body’s endogenous production of Elastin declines in tandem with the
progression of the Aging Process - Elastin production begins to decline
after the age of approximately 25.
Quinones
The body's ability to absorb dietary Coenzyme Q10 declines in tandem
with the Aging Process, the body's ability to convert Coenzymes Q1 - Q9
into Coenzyme Q10 deteriorates in tandem with the Aging Process and the
body’s ability to produce endogenous Coenzyme Q10 from its nutritional
precursors declines in tandem with the Aging Process: references
- Endogenous Coenzyme Q10 synthesis begin to decline after the age of
20.
- Brain levels of Coenzyme Q10 decline markedly after the age of 50.
- Elderly people have only 50% of the levels of Coenzyme Q10 as those of
young people.
Skin Chemicals
The body's production of its endogenous moisturizer Na-PCA declines in
tandem with the Aging Process (note that supplemental Na-PCA should only
be applied topically):
- The Skin of older people contains up to 50% less Na-PCA than the Skin
of younger persons.
Sulfuric Compounds
The body’s content of Methylsulfonylmethane (MSM) declines in tandem
with the progression of the Aging Process.
Vitamins
The ability of Choline to cross the Blood-Brain Barrier declines by up
to 80% in tandem with the Aging Process. references
Many elderly people are found to exhibit Folic Acid deficiency.
references
The body’s content of Lipoic Acid declines in tandem with the
progression of the Aging Process. references
The Brain’s Vitamin B1 content declines in tandem with the progression
of the Aging Process. references
The body's requirement for Vitamin C increases with the progression of
the Aging Process. references
The body's ability to absorb dietary Vitamin B6 declines in tandem with
the Aging Process (after the age of 40) and many elderly people are
found to exhibit Vitamin B6 deficiency. references
The body’s ability to absorb dietary Vitamin B12 declines in tandem with
the progression of the Aging Process (and daily supplements of 500 -
1,000 mcg per day are recommended in order to counteract this impaired
absorption in persons over the age of 60). references
The body’s ability to absorb Vitamin D declines in tandem with the
progression of the Aging Process. The body’s ability to produce Vitamin
D from 7-Dehydrocholesterol in the Skin after stimulation from UV-B also
declines in tandem with the progression of the Aging Process. Serum
Vitamin D levels decline by up to 50% in tandem with the progression
Aging Process. references
Plasma levels of the Gamma-Tocopherol form of Vitamin E decline in
tandem with the progression of the Aging Process. references
--------------------------------------------------------------------------------
Aging Process
Description
The Aging Process is the general decline in the structure and function
of the human body associated with the progression of time.
Other Factors that Retard the Aging Process
Cells
Proteasomes play a role in retarding the Aging Process (due to their
role in destroying and removing damaged, oxidized and cross-linked
Endogenous Proteins from the body via the process of Proteolysis).
references
Metabolism
Diet Restriction may retard the progression of the Aging Process:
references
- Diet Restriction may retard the Aging Process of the Pineal Gland.
- Diet Restriction may prevent the impairment of Coordination ability
that normally occurs in tandem with the progression of the Aging
Process.
- Diet Restriction may prevent the impairment of Learning ability that
normally occurs in tandem with the progression of the Aging Process.
Physical Therapies
Isotonic Exercise (weight lifting) may retard the increase in Muscle
Weakness and Muscular Atrophy (Sarcopenia) that occurs as a consequence
of the Aging Process. references
These Substances/Factors/Ailments may Accelerate the Aging Process
Aldehydes
Malondialdehyde may accelerate various aspects of the Aging Process.
Amino Acids
Homocysteine may accelerate the shortening of Telomeres and may
therefore accelerate the progression of the Aging Process. references
Carbohydrates
Excessive consumption of Simple Sugars may accelerate the Aging Process
by causing Cross-Linking (glycosylation) of the body's endogenous
Proteins:
- Excessive consumption of Fructose may accelerate the Aging Process
(due to it accelerating the process of Cross-Linking in the body’s
Tissues). references
- Sucrose may accelerate the Aging Process (the Fructose component of
the Sucrose molecule appears to play a larger role in accelerated Aging
than does the Glucose component of Sucrose). references
When Sucrose is removed from the diets of rats they live for twice as
long as when their diets contain Sucrose.
Electromagnetic Radiation
Excessive exposure to Sunlight (especially its Ultra-Violet Radiation
component, particularly UV-A) may accelerate the Aging Process in the
Skin (by causing the Skin's connective tissues to lose their elasticity)
- accelerated Aging of the Skin caused by Sunlight/Ultra-Violet
Radiation is usually known as Photoaging. references
Hormones
Excessive production of Insulin may accelerate the Aging Process.
references
Lipopigments
Lipopigments may accelerate the Aging Process by eliminating and
replacing endogenous Ribonucleic Acid (RNA) in the body's Cells and by
inhibiting the ability of Proteolytic Enzymes and Lipases to degrade
damaged Endogenous Proteins in Cells and thereby facilitating the
accumulation of damaged Endogenous Proteins in Cells: references
- Ceroid may accelerate the Aging Process. references
- Lipofuscin accelerates the Aging Process. references
Hormones
Excessive production of Cortisol may accelerate many aspectsof the Aging
Process (including Skin Aging). references
Immune System
Inflammation may play a central role in the Aging Process (including the
Aging Process of the Skin). references
Metabolism
Cross-Linking of the body's endogenous Proteins may accelerate the Aging
Process and the process of Cross-
Linking increases in tandem with the progression of the Aging Process.
references
Free Radicals, especially Oxygen Free Radicals and Hydroxyl Free
Radicals may cause Cross-Linking (especially within the body's
Connective Tissues) and are one of the main factors in the Aging
Process: references
- One of the means via which Free Radicals may accelerate the Aging
Process is by accelerating the shortening of Telomeres.
- Singlet Oxygen Free Radicals may accelerate the progression of the
Aging Process (including the Aging Process in the Skin). references
Insulin Resistance may accelerate the Aging Process (implying that
increased Insulin sensitivity could retard the progression of the Aging
Process).
Excessive Oxidation may accelerate the Aging Process: references
- One of the means via which excessive Oxidation may accelerate the
Aging Process is by accelerating the shortening of Telomeres.
Minerals
Excessive consumption of Calcium may accelerate the Aging of Cells
unless ample Zinc is available to counteract Calcium.
Excessive Iron may accelerate the Aging Process (due to Iron’s role in
the generation of Hydroxyl Free Radicals). references
Neurotransmitters
Low Norepinephrine/Serotonin ratio may be linked to an acceleration of
the Aging Process:
- The Aging Process in rats was almost halted for 10 months by
eliminating Tryptophan (the primary precursor for Serotonin) from their
diet.
Proteins
Glycosylated Hemoglobin levels are recognized as a biomarker of the
Aging Process (or as an indication of biological age). Glycosylated
Hemoglobin levels increase in tandem with the progression of the Aging
Process.
Nuclear Factor-Kappa B (NF-Kappa B) may contribute to the Aging Process
of the Skin: references
- NF-Kappa B may initiats the degradation of the Collagen and Elastin
content of the Skin that occurs during the progression of the Aging
Process (it “switches on” the Genes for the enzyme that degrades
Collagen and Elastin).
Recreational Drugs
Tobacco smoking may accelerate the Aging Process in the Skin (by
increasing the degradation of Collagen by the Collagenase enzyme).
references
Theories of Aging
The Neuroendocrine Theory of Aging (also known as the Hypothalamic
Theory of Aging; Ontogenetic Theory of Aging) links the Aging Process to
the Hypothalamus and related structures of the Brain. It proposes that
Aging is caused by a progressive loss of sensitivity to the body’s
negative feedback mechanism which causes a continual shift in
homeostasisduring the life span: references
- The Immunological Theory of Aging (also known as the Immune Theory of
Aging) links the Aging Process to the gradual decline of the Immune
System. Declining quality and quantity of T-Lymphocytes is a key aspect
to this theory. This decline is linked to atrophy of the Thymus Gland.
The Immunological Theory of Aging is a subset of the Neuroendocrine
Theory of Aging as there is a close interaction between the Thymus Gland
and the Neuroendocrine system. references
The Genetic Theory of Aging (also known as the Molecular Clock Theory
of Aging) links the Aging Process to genetic predispositions to develop
various degenerative diseases such as Atherosclerosis:
- The ERC Theory of Aging (also known as the Extrachromasomal rDNA
Circles theory of Aging) is a subset of the Genetic Theory of Aging that
attributes the so-called “aging clock” to the damaging (mutating)
effects of Extrachromasomal rDNA Circles on the body’s Deoxyribonucleic
Acid (DNA). references
- Telomeres (structures on Chromosomes) are strongly speculated to be
the mechanisms via which the Genetic Theory of Aging operates:
references
- Telomere shortening at the end of chromosomes is the major mechanism
of cellular senescence in Skin Aging.
The Environmental Theory of Aging links the Aging Process to poor
diet, inadequate Exercise and exposure to Toxins.
The Free Radical Theory of Aging (also known as the Cumulative Theory of
Aging, or the Oxidative Stress Theory of Aging) links the cumulative
effects of Free Radical generation to the progression of the Aging
Process: references
- The Cross-Linking Theory of Aging (also known as the Glycosylation
Theory of Aging) is a subset of the Free Radical Theory of Aging that
specifically links increased Cross-Linking (Glycosylation) to the
progression of the Aging Process.
- The Lysosomal Membrane Theory of Aging is a subset of the Free Radical
Theory of Aging. This theory proposes that the Aging Process is caused
by increased activity in Lysosomes due to instability of Lysosomal
Membranes
- The Membrane Theory of Aging is a subset of the Free Radical Theory of
Aging and attributes changes in Mitochondrial Cell Membranes to the
Aging Process. These changes are believed to cause increased rigidity
and altered permeability of Cell Membranes.
- The Mitochondrial DNA Theory of Aging (also known as the Mitochondrial
Clock Theory of Aging; Membrane Hypothesis of Aging; or Oxygen
Radical-Mitochondrial Injury Theory of Aging) is a subset of the Free
Radical Theory of Aging and specifically links Free Radicals-induced
damage to the Mitochondria (particularly Mitochondrial DNA) of Cells to
the progression of the Aging Process. references
The Pineal Theory of Aging links the decline and atrophy of the
Pineal Gland that occurs in tandem with the Aging Process with reduced
life span: references
- When the Pineal Glands of old mice were transplanted into younger
mice, the younger mice experienced a shortened life span - to 17 months;
when the Pineal Glands of young mice were transplanted into older mice,
the older mice experienced an increased lifespan - to 34 months. |