In 1989 David Hood found chronic (35+ days) 10 Hz stimulation at 10 hours per day increased two critical enzymes of cell respiration by a factor of 3x! Citrate synthase, the "pacer" of the Krebs cycle & cytochrome c oxidase the last enzyme in the electron transport chain. UNBELIEVABLE! This is consistent with improved oxygen use in every one of our satisfied clients.
Testing systemic oxygen consumption / cell respiration in clients since 2005 with a test free-diver's call the static-breath-hold, that we call theresting-breath-hold (RBH) test; clients find routine improvements of 10-20% in as little as 7 days and up to 100% in 90 days. Cell's burn oxygen more efficiently, drawing oxygen from blood slower, producing more energy and less waste from every breath. Success rate 96%+. RBH-test gradually improves for years with cumulative nighttime use; up to DOUBLE the original time! That can mean nothing but 2x more efficient rate of oxygen burn & fractions of reactive oxygen species (ROS) creation, subsequently lowering requirement of anti-oxidant protection substantially.
In 2003 NASA-Goodwin found (2 years AFTER Pulsed electromagnetic therapy device called Earthpulse began commercial sales utilizing DC pulsed electromagnetic field @ 9.6 Hz) that 10 Hz pulsed electromagnetic field caused neural tissue regeneration @ 4x baseline with improved 3-D orientation (pg 17); while causing DNA to revert from maturation to developmental! (more than 175 maturation genes and 150 developmental genes pgs. 15-26)
The implications on longevity are staggering! Prior to NASA sanitizing this study, it contained data on 5 and 15 Hz stimulation. What was shown was both 5 and 15 Hz provided 2x neural tissue regeneration and NO genetic effects. A perfect bell-shaped curve around 10 Hz. Then why are pulsed electromagnetic therapy systems using frequencies higher???It makes no sense at all.
Developmental gene signature delays appoptosis / mitosis perhaps indefinitely in the absence of oxidative stress.
By now you should realize a conspiracy to keep this information from the public. See Gizmo the remarkable 16 y.o. (Sept 2010) Yorkie-Maltese on Sleep on Command™ 9.6Hz since 8 y.o., 10 hours per day (1/2 her life). Plays with food and toys like a puppy with eye's still clear.
In 2007 James Tong TRIPLED nerve synapse energy (ATP the fuel that fires all cellular processes) & nearly tripled mitochondrial density at nerve synapse junctions in minutes.
In Tong chart linked above, compare DENSITY of unstimulated mitochondria (white circles) with 10 Hz stimulated (black circles); and in lower chart compare ENERGY at synapse junction unstimulated (white circles) with 10 Hz stimulated (black circles). Change nearly 2x & 3x respectively! EarthPulse™ effects last all day!
IThat oxidative stress (damage) causes the breaks in the mitochondrial DNA (the mtDNA). The damage is at the mitochondrial DNA level. OXIDATIVE ELECTRONS ARE CREATED at the MITOCHONDRIAL LEVEL!!!....and that kicks in oxidative stress, reduced energy production, mitosis and/or appoptosis (programmed cell death). It is same regardless of tissue type. This is the crux of the mitochondrial theory (formerly known as the Free-Radical theory) of aging.
When sufficient mitochondrial DNA strand breaks occur and are left unchecked, subsequently the overall energy output of each individual mitochondrion drops. At the cellular level energy drops sufficiently and the mitosis / appoptosis (cell death) switch is thrown.
The mitochondria never sleep! Mitochondria under stimulation by pulsed electromagnetic fields (PEMF) at this very narrow frequency range synthesize more ATP from the oxygen you breath (purely shown through our RBH testing).
This extra energy is available at night for repair, hormone synthesis, memory consolidation and immune support; and during the day for physical and mental performance enhancement (ergogenic effects). More energy out of every breath you take! Now, relate the study below to just about any degenerative disease not mentioned...
J Neurol Sci. 2005 Jun 15;233(1-2):145-62.
Oxidative stress, mitochondrial dysfunction and cellular stress response....
There is significant evidence that the pathogenesis of several neurodegenerative diseases, including Parkinson's disease, Alzheimer's disease, Friedreich's ataxia (FRDA), multiple sclerosis and amyotrophic lateral sclerosis, may involve the generation of reactive oxygen species (ROS) and/or reactive nitrogen species (RNS) associated with mitochondrial dysfunction. The mitochondrial genome may play an essential role in the pathogenesis of these diseases, and evidence for mitochondria being a site of damage in neurodegenerative disorders is based in part on observed decreases in the respiratory chain complex activities in Parkinson's, Alzheimer's, and Huntington's disease. Such defects in respiratory complex activities, possibly associated with oxidant/antioxidant imbalance, are thought to underlie defects in energy metabolism and induce cellular degeneration. The impaired intramitochondrial metabolism with increased free iron levels and a defective mitochondrial respiratory chain, associated with increased free radical generation and oxidative damage, may be considered possible mechanisms that compromise cell viability.
Testing systemic oxygen consumption / cell respiration in clients since 2005 with a test free-diver's call the static-breath-hold, that we call theresting-breath-hold (RBH) test; clients find routine improvements of 10-20% in as little as 7 days and up to 100% in 90 days. Cell's burn oxygen more efficiently, drawing oxygen from blood slower, producing more energy and less waste from every breath. Success rate 96%+. RBH-test gradually improves for years with cumulative nighttime use; up to DOUBLE the original time! That can mean nothing but 2x more efficient rate of oxygen burn & fractions of reactive oxygen species (ROS) creation, subsequently lowering requirement of anti-oxidant protection substantially.
In 2003 NASA-Goodwin found (2 years AFTER Pulsed electromagnetic therapy device called Earthpulse began commercial sales utilizing DC pulsed electromagnetic field @ 9.6 Hz) that 10 Hz pulsed electromagnetic field caused neural tissue regeneration @ 4x baseline with improved 3-D orientation (pg 17); while causing DNA to revert from maturation to developmental! (more than 175 maturation genes and 150 developmental genes pgs. 15-26)
The implications on longevity are staggering! Prior to NASA sanitizing this study, it contained data on 5 and 15 Hz stimulation. What was shown was both 5 and 15 Hz provided 2x neural tissue regeneration and NO genetic effects. A perfect bell-shaped curve around 10 Hz. Then why are pulsed electromagnetic therapy systems using frequencies higher???It makes no sense at all.
Developmental gene signature delays appoptosis / mitosis perhaps indefinitely in the absence of oxidative stress.
By now you should realize a conspiracy to keep this information from the public. See Gizmo the remarkable 16 y.o. (Sept 2010) Yorkie-Maltese on Sleep on Command™ 9.6Hz since 8 y.o., 10 hours per day (1/2 her life). Plays with food and toys like a puppy with eye's still clear.
In 2007 James Tong TRIPLED nerve synapse energy (ATP the fuel that fires all cellular processes) & nearly tripled mitochondrial density at nerve synapse junctions in minutes.
In Tong chart linked above, compare DENSITY of unstimulated mitochondria (white circles) with 10 Hz stimulated (black circles); and in lower chart compare ENERGY at synapse junction unstimulated (white circles) with 10 Hz stimulated (black circles). Change nearly 2x & 3x respectively! EarthPulse™ effects last all day!
IThat oxidative stress (damage) causes the breaks in the mitochondrial DNA (the mtDNA). The damage is at the mitochondrial DNA level. OXIDATIVE ELECTRONS ARE CREATED at the MITOCHONDRIAL LEVEL!!!....and that kicks in oxidative stress, reduced energy production, mitosis and/or appoptosis (programmed cell death). It is same regardless of tissue type. This is the crux of the mitochondrial theory (formerly known as the Free-Radical theory) of aging.
When sufficient mitochondrial DNA strand breaks occur and are left unchecked, subsequently the overall energy output of each individual mitochondrion drops. At the cellular level energy drops sufficiently and the mitosis / appoptosis (cell death) switch is thrown.
The mitochondria never sleep! Mitochondria under stimulation by pulsed electromagnetic fields (PEMF) at this very narrow frequency range synthesize more ATP from the oxygen you breath (purely shown through our RBH testing).
This extra energy is available at night for repair, hormone synthesis, memory consolidation and immune support; and during the day for physical and mental performance enhancement (ergogenic effects). More energy out of every breath you take! Now, relate the study below to just about any degenerative disease not mentioned...
J Neurol Sci. 2005 Jun 15;233(1-2):145-62.
Oxidative stress, mitochondrial dysfunction and cellular stress response....
There is significant evidence that the pathogenesis of several neurodegenerative diseases, including Parkinson's disease, Alzheimer's disease, Friedreich's ataxia (FRDA), multiple sclerosis and amyotrophic lateral sclerosis, may involve the generation of reactive oxygen species (ROS) and/or reactive nitrogen species (RNS) associated with mitochondrial dysfunction. The mitochondrial genome may play an essential role in the pathogenesis of these diseases, and evidence for mitochondria being a site of damage in neurodegenerative disorders is based in part on observed decreases in the respiratory chain complex activities in Parkinson's, Alzheimer's, and Huntington's disease. Such defects in respiratory complex activities, possibly associated with oxidant/antioxidant imbalance, are thought to underlie defects in energy metabolism and induce cellular degeneration. The impaired intramitochondrial metabolism with increased free iron levels and a defective mitochondrial respiratory chain, associated with increased free radical generation and oxidative damage, may be considered possible mechanisms that compromise cell viability.
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