Jump to content
IndiaDivine.org

Oxygen, Ozone, & Hydrogen Peroxide

Rate this topic


Guest guest

Recommended Posts

Guest guest

, surpriseshan2

wrote:

 

 

Oxygen, Ozone, & Hydrogen Peroxide

 

By Majid Ali, M.D.<majidalimd

_http://educate-yourself.org/cancer/ozonebymajidli17jul03.shtml_

(http://educate-yourself.org/cancer/ozonebymajidli17jul03.shtml)

July 17, 2003

 

(Abridgement from The Journal of Integrative Medicine article:

Oxidative

Regression To Primordial Cellular Ecology (ORPEC))

The author's clinical experience has led him to conclude that

oxygenative

antioxidant therapies such as nasal oxygen and intravenous

infusions of

ozone-oxygen gas mixture and hydrogen peroxide are among the most

beneficial

therapies for reversing the ORPEC state.

Since oxygen, ozone and hydrogen peroxide act as oxidants in a

laboratory

setting, therapies employing those agents are generally deemed

oxidative

therapies.191-193 Until recently, the author accepted that view

uncritically.

However, it is clear from studies presented in this article that

this is a gross

error. In reality, such therapies in the context of the ORPEC state

are

powerful oxygenative and antioxidant therapies. The reason for that

widespread

misconception is the failure to clearly understand the complex

biologic

consequences of adding oxygen, ozone, and hydrogen peroxide to

severely impaired

enzymatic and cellular ecosystems in patients with accelerated

oxidative injury.

A Burst of Thunderstorm, A Burst of Oxidants

 

An analogy of a burst of thunderstorm may be used to explain the

possible

mechanism action of ozone. The still air in a city on a hot, humid

summer

afternoon is thick with stagnant smog. The traffic on city streets

is snarled.

Tree leaves are dry and limp. Many persons are distressed by air

pollution.

Suddenly, dark clouds loom large and bring a heavy thunderstorm.

Strong winds

push out the polluted air. Tree leaves are bombarded by heavy

rains. The healthy

and robust leaves of trees withstand the storm well, while older

and

weakened leaves are severely damaged. Many withering leaves on tree

brances are

blown away. After the thunderstorm subsides, the air is clean and

crisp. The

trees looked washed, their leaves fresh and shiny. Bursts of

intravenously

injected ozone and hydrogen peroxide affect the blood elements the

same way. The

membranes of healthy erythrocytes withstand the oxidative stress of

ozone and

hydrogen peroxide well, recovering their normal morphology after

initial

membrane deformities. The senescent cells, by contrast, shrink and

undergo lysis.

Below, some theoretical, clinical and experimental considerations

are

presented that shed light on the apparent paradox of agents that

are oxidizing in

their essential roles, and yet provide the basis for oxygenative

antioxidant

therapies.

Intermittent Nasal Oxygen

 

The oxygenative role of nasal oxygen is self-evident. Oxygen is

also a

powerful oxidizer, as discussed earlier in the section devoted to

spontaneity of

oxidation in nature. The ORPEC hypothesis provides a clear

scientific basis

for oxygen's ability to also serve the opposing antioxidant role.

As discussed

earlier, anoxia increases oxidative stress directly by facilitating

the

generation of toxic reactive species as well as indirectly by

causing acidosis.

In this author's clinical experience, the use of intermittent nasal

administration of oxygen (2.5 to 3.5 L/min given for periods of one

hour two or three

times a day) benefits most patients in the ORPEC state. It is also

the

opinion of the author that oxygen therapy is very underutilized in

the care of

patients in the ORPEC state, such as those with fibromyalgia,

chronic fatigue

state, severe autoimmune disorders, and spreading malignant tumors.

Oxygen is

readily and inexpensively available to all patients. Also available

are

inexpensive portable rental units that may be used in travel as

well.

When used intermittently and in moderate doses as described here,

this

therapy has been found to be completely free of adverse effects.

The author also

has limited experience with oxygen therapy in patients with severe

pulmonary

emphysema and pulmonary interstitial fibrosis. Evidently, the use

of oxygen in

such patients must be monitored closely so that oxygen therapy does

not

cause further deterioration in the function of central sensors for

oxygen and

carbon dioxide.

Intravenous Ozone Therapy

 

Ozone is triatomic oxygen with a high electrovoltaic potential.

Ozone gas

infused intravenously at the Institute consists of a gaseous

mixture with

oxygen containing a very low concentration of ozone. It is prepared

by passing

pure oxygen through a high voltage field. The concentration of

ozone generated

depends on the rate of flow of oxygen as well as on the conditions

of voltage

and spacing of electrodes. The gaseous mixture used in our clinical

practice

is titrated to contain from 0.3 to 2.5% (30 to 50 ug O3/ml O2).

Thus,

intravenously administered " ozone " in reality represents 97 to

99.7% of pure

oxygen.

Practitioners who have never administered ozone gas mixture

intravenously

often express concern about the possibility of air embolism caused

by gas

infusion. Such concern is totally unwarranted. Pure oxygen and

ozone diffuse

immediately into the blood and do not persist as gases. The author

has tested for

that on numerous occasions by injecting 2 ml of the ozone mixture

into a

large vein, then immediately drawing the blood back. Except on

uncommon

occasions, the blood drawn back from the vein is pink (ozone turns

dark venous blood

into pink blood) and free of any gas bubbles. One can safely

presume that the

process of dissolution of the gas mixture would be complete by the

time it

reaches the large veins in the thorax.

Another concern expressed by those unfamiliar with the clinical

uses of

ozone mixture is the toxicity of ozone as discussed by

environmentalists. It must

be recognized that those individuals are perturbed by the products

of

reaction of ozone with other ecopollutants such as oxides of

nitrogen. Ozone is a

highly reactive molecule. Indeed, ozone owes its many antiviral,

antibacterial, and antifungal properties to this aspect of this

specific aspect.

Microscopic Evidence for the Antioxidant Role of Intravenous Ozone

Therapy

In the concentration used our in clinical practice, ozone causes

temporary

and reversible erythrocyte membrane damage as evidenced by clumping

and red

cell membrane deformity. The evidence for the oxidative nature of

such

erythrocyte membrane deformities has been previously demonstrated

by the

reversibility of such changes with antioxidants such as ascorbic

acid, tocopherol, and

taurine.56,57

How may the observed overall invivo antioxidant effects of ozone, a

powerful

invitro oxidant, be explained? Ozone has well established effects

of

improving tissue perfusion and cellular oxygenation.67 Just as the

duality of oxygen

allows it to be a molecular Dr. Jekyll and Mr. Hyde, reactive

oxidant

species also play dual roles. Not only do they inflict oxidative

damage to enzymes,

induce mutations, and damage cell membranes, they also serve many

useful

functions such as modulation of cellular redox dynamics, activation

of gene

transcription, signal transduction, and apoptosis.93-95 It seems

that ozone

evokes an upregulatory response from cell membrane-associated

antioxidant enzyme

systems just as all oxidants do from all biologic antioxidant

systems. Though,

direct quantitative data for those effects are not yet forthcoming.

One may

also, with good reason, speculate that ozone elicits similar

responses from

other matrix- and cell organelle-related antioxidant systems. There

is yet an

other important mechanism by which ozone protects patients with

chronic

illnesses from accelerated oxidative stress. Viruses, bacteria,

fungi, PLFs and

parasite inflict cellular injury by causing oxidative stress. Ozone

also is a

well established antiviral, antibacterial, and antifungal agent.58-

63. Ozone

through its powerful antimicrobial effects reduces the overall

oxidative

stress on persons with chronic viral, bacterial, fungal and PLF

overgrowth

syndromes. Thus, the ORPEC hypothesis carries strong explanatory

power for the

empirically observed biologic antioxidant effects of ozone.

Intravenous Hydrogen Peroxide Therapy for the ORPEC State

 

The biologic antioxidant effects of hydrogen peroxide, a potent

oxidizer

like ozone, are mediated by all the mechanisms cited for ozone in

the preceding

section. The clinical benefits of hydrogen peroxide infusions

observed at the

Institute in patients with fibromyalgia and chronic fatigue

syndrome are the

subject of a separate report.72

Reference from the complete article in The Journal of Integrative

Medicine

1998;2:4-55

References

1. Ali M. Spontaneity of Oxidation in Nature and Aging. Monograph,

Teaneck,

New Jersey, 1983.

2. Ali M. The agony and death of cell. Syllabus of the Instruction

Course of

the American Academy of Environmental Medicine, Denver, Colorado,

1985.

3. Ali M. Molecular basis of cell membrane injury. In: Syllabus of

the

Instruction Course of the American Academy of Environmental

Medicine. Denver,

Colorado, 1990.

4. Ali M. Spontaneity of oxidation and chronic disease. In:

Syllabus of the

Instruction Course of the American Academy of Environmental

Medicine, Denver,

Colorado, 1992.

5. Ali M. Oxidative coagulopaty. In: Syllabus of the Capital

University of

Integrative Medicine, Washington, D.C., 1997.

6. Ali M. Spontaneity of oxidation in nature is the root cause of

all

illness. In: RDA: Rats, Drugs and Assumption. pp. 199-304. Life

Span, Denville, New

Jersey, 1995.

7. Ali M. Leaky cell membrane dysfunction. Monograph 1987. Teaneck,

New

Jersey.

8. Ali M. Oxidative plasma membrane injury and magnesium.

Environmental

Physician. Summer 1992. American Academy of Environmental Medicine,

Denver,

Colorado.

9. Ali M. Ascorbic acid reverses abnormal erythrocyte morphology in

chronic

fatigue syndrome. Am J Clin Pathol. 1990;94:515.

10. Ali M. Ascorbic acid prevents platelet aggregations by

norepinephrine,

collagen, ADP and ristocetin. Am J Clin Pathol. 1991;95:281.

11. Ali M. The basic equation of life. pp 225-236. In: The

Butterfly and

Life Span Nutrition. The Institute of Preventive Medicine Press,

Denville, New

Jersey. 1992.

12. Ali M. Spontaneity of oxidation and molecular basis of

environmental

illness. In: Syllabus of the 1991 Instruction Course of the

American Academy of

Environmental Medicine, Denver, Colorado, 1990.

13. Ali M. The Ghoraa and Limbic Exercise. The Institute of

Preventive

Medicine Press, Denville, New Jersey. 1993.

14. Ali M. What Do Lions Know About Stress? Life Span, Denville,

New Jersey.

1996.

15. Ali M. The Cortical Monkey and Healing. The Institute of

Preventive

Medicine, Bloomfield, New Jersey. 1989.

16. Ali M. Healing, Miracles and the Bite of the Gray Dog. Life

Span,

Denville, New Jersey. 1997.

17. Ali M. Hypothesis: Chronic fatigue is a state of accelerated

oxidative

molecular injury. J Advancement in Medicine. 1993;6:83-96.

18. Ali M. The Canary and Chronic Fatigue. 1994. Life Span,

Denville, New

Jersey.

19. Ali M, Ali O. AA Oxidopathy: the core pathogenetic mechanisms

of

ischemic heart disease. J Integrative Medicine 1997;1:1-112.

20. Des Marais DJ, Strauss H, Summons RE et al. Carbon isotope

evidence for

the stepwise oxidation of the Proterozoic environment. Nature

1992;359:605-609.

21. Canfield DE, Teske A. Late proterozoic rise in atmospheric

oxygen

concentration inferred from phylogenetic and sulphur-isotope

studies. Nature

1996;382;127-132.

22. Miller SM. The origins of life on earth. 1974. Prentice-Hall,

Englewood

Cliffs, New Jersey.

23. Margulis L. Biodicersity: Molecular biologica; domains,

symbiosis and

kingdon origins. Biosystems 1992;27:39-51.

24. Carpendale MT, Griffis J. Is there a role for medical ozone in

the

treatment of HIV and associated infections. Monograph. Bay Medical

Research

Foundation 1991.

25. Carpendale MT, Freeberg JK. Ozone inactivates HIV at non-

cytotoxic

concentrations. Antiviral Research 1991; 16:281-292.

26. Matassi R, D'Angelo F, Franching A, et al. Ozone therapy in

Herpes

Simplex and Herpes Zoster diseases. In: Laraus J. ed. Medical

Applications of

Ozone. International Ozone Association. 1985 pp 134-139. Norwalk,

CT.

27. Botstein D, Chervitz SA, Cherry JM. Yeast as a model organism.

Science

1997;277:1259-1260.

28. BLASTP analysis were done between all yeast ORF translations

and all

unique protein sequences in the human, mouse, rat, cow, and sheep

sequences in

GenBank as of 22 July 1997. We used the BLOSUM62 substitution

mastrix and

low-complexity filters seg and xnu. " Unknown function " means that

the ORF had no

entry in either the Gene_Product or Description fields within its

SGD Locus

page as of 30 July 1997. For all ORFs, 3783 (60.8%) have unknown

function by

this definition. BLASTP, version 2.0a, W. Gish, unpublished data;

SF Altschul,

W Gish, W Miller, EW Myers, DJ Lipman. J Mol Biol 1990;215:403.

29. Beale LS. Observations upon the nature of the red blood

corpuscles.

Trans Microsc Soc. London 1864:12:37.

30. Magath TB. Spirochetes in the blood. Am J Clin Pathol.

1953;23:691-693.

31. Mattman LH. Cell Wall Deficient Forms: Stealth Pathogens. CRC,

Boca

Raton, 1992.

32. Ali M, Ali O, Bradford R. et al Immunostaining of candida

organisms in

peripheral smears. (Abstract). 1995. American Academy of

Otolaryngic Allergy,

Spring Meeting, Palm Desert, CA.

33. Ali M and Ramanarayanan MP: A computerized micro-ELISA assay

for

allergen-specific IgE antibodies. Am J Clin Pathol 1984;81:591.

34. Ali M, Ramanarayanan MP, Nalebuff DJ, et al: Serum

concentrations of

allergen-specific IgG antibodies in inhalant allergy: Effect of

specific

Immunotherapy. Am J Clin Pathol. 1983;80:290.

35. Ali M. Altered States of Bowel Ecology. Monograph. Life Span,

Denville,

New Jersey 1983.

36. Lorian V, Waluschka A. Blood cultures showing aberrant forms of

bacteria. Am J Clin Pathol 1972;57:406-409.

37. Lorian V, Atkinson B. Abnormal forms of bacteria produced by

antibiotics. Am J Clin Pathol 1975;64:678-688.

38. Komber KR, Boon RJ, Sutherland R. Comparative effects of

amoxycillin and

ampicillin on the morphology of Eschercia coli in vivo and

correlation with

activity. Antimicrob Agents Chemother 1977;12:736-744.

39. Nakao M, Nishi T, Tsuchiya K. In vitro and in vivo morphologic

response

of Klebsiella pneumoniae to cefotiam and cefazolin. Antimicrob

Agens

Chemother 1981;19:901-910.

40. Davis KJ, Vogel P, Fritz DL, et al. Bacterial filamentation of

Yersenia

pestis by B-lactam antibiotics in experimentally infected mice.

Arch Pathol

Lab med 1997;121:865-8. -induced

41. Dwyer JJ, Burnett LE. Acid based status of the oyster

Crassostrea

virginica in response to air exposure and to infections by

Perkinsus marinus. Biol

Bulletin 1996;190:139-147.

42. Knoll AH, in Origins and Early Evolution of the Metazoa (eds

Lipps, JH

Signor, D.W.53-84. (Plenum, New York, 1992).

43. Holland HD. The Chemistry of the Atmosphere and Oceans (Wiley,

New York,

1978).

44. Knoll AH. Breathing room for early animals. Nature 1996;382:111-

112.

45. Mattman LH. Cell Wall Deficient Forms: Stealth Pathogens. CRC

Press,

Boca Raton, Florida, 1993.

46. Henning W. Phylogenetic Systematics. University of Illinois

Press,

Urbana, Il.) 1966.

47. Margulis L. Symbiosis in Cell Evolution. 1992 2nd edn. WH

Freeman, New

York

48. Gross M. Life on the Edge:Amazing Creatures Thriving in Extreme

Environment. Plenum 1998. England.

49. Saccharomyces Genome Database (SGD) at

http://genome-www.stanford.edu/Saccharomyces/;Yeast Genome from

MIPS (Martinsried Institute for Protein

Sequences) at http://speedy.mips.biochem.mpg.de/mips/ yeast/

www.proteome.

com/YPDhome.html; A. Goffeau et al., Science 1996;274:546. The

Saccharomyces Genome

Database is suppported by an NIH research resources grant (HG

01315).

50. Kataoka T. Cell 1985;40:19-22.

51. Miller RV. Bacterial gene swpping in nature. Scientific

American

1998;January; 67-71.

52. Ali M. Oxidant injury pokes holes in cell membranes. In: The

Canary and

Chronic Fatigue. pp 197-205. Life Span, 1995. Denville, New Jersey.

53. Ali M. Oxidative theory of cell membrane and plasma damage. In:

RDA:

Rats, Drugs and Assumption. Page 281-302. 1995 Life Span, Denville,

New Jersey.

54. Ali M, Ali O. Leaky cell membrane dysfunction. In: AA

oxidopathy: The

core pathogenetic mechanism of ischemic heart disease. pp 72-74. J

Integ

Medicine 1997;1:6-112.

55. Ali M. Experience with intravenous nutrient therapy for

allergic

patients with chronic fatigue. Am Acad Otolaryngic Allergy

Abstracts Summer 1992;p23.

56. Ali M. Intravenous Nutrient Protocols in Molecular Medicine.

Institute

of Preventive Medicine. 1989. Bloomfield, New Jersey.

57. Ali M. Leaky cell membrane dysfunction. Monograph 1987.

Teaneck, New

Jersey.

58. Yusuf, S. Calcium antagonists in coronary artery disease and

hypertension-Time for reevaluation? Circulation 1995;92:1079-1082.

59. Furberg CD, Psaty BM, Meyer JV. Nifedipine: Dose-related

increase in

mortality in patients with coronary heart disease.

Circulation;92:1326-1331.

60. Boden WE, Schelewaert R, Walters EG. Design of a placebo-

controlled

clinical trial of long-acting diltiazem and aspirin versus aspirin

alone in

patients receiving thrombolysis with a first acute myocardial

infarction. Am J

cardiol 1995;75:1120-1123.

61. Thadani U, Zellner S, Glasser S et al. Double-blind, dose-

response,

placebo-controlled multicenter study of nisoldipine: a new second-

generation

calcium channel blocker in angina pectoris. Circulation

1991;84:2398-2408.

62. Fisher A, Bogouslaviskt J. Further evolution toward effective

therapy

for acute ischemic stroke JAMA;279:1298-1303.

63. Woods, KL, Fletcher S. Long-term outcome after intravenous

magnesium

sulphate in suspected acute myocardial infaction: The second

Leicester

Intravenous Magnesium Intervention Trial (LIMIT-2). Lancet

1995;343:816-9.

64. Woods KL, Fletcher S, Roffe C, Haider Y. Intravenous magnesium

sulphate

in suspected acute myocardial infarction: Results of the second

Leicester

Intravenous Magnesium Intervention Trial (LIMIT-2). Lancet

1992;339:1553-8.

65. Ali M. Experience with intravenous nutrient therapy for

allergic

patients with chronic fatigue. Am Acad Otolaryngic Allergy

Abstracts Summer 1992;p23.

66. Seelig MS, Elin RJ. Reexamination of magnesium infusions in

myocardial

infarction. Am J cardiol 1995;76:172-173.

67. Halstead BW. The Scientific Basis of Chelation Therapy. Golden

Quill

Publishers, Inc. Box 1278, Colton, Ca

68. Baldridge CW, Gerald RW. The extra respiration of phagocytosis.

Am J

Physiol 1933;103:235.

69. Berendes H, Bridges RA, Good RA. A fatal granulomatosis of

childhood.

The clinical study of a new syndrome. Minn Med 1957;40:309.

70. Cohen MS, Metcalf JA, Root RK. Regulation of oxygen metabolism

in human

granulocytes: Relationship between stimulus binding and oxidative

response

using plant lectins as probes. Blood 1980;55:1003.

71. Curnutte JT, Babior BM. Biological defense mechanisms. The

effect of

bacteria and serum on superoxide production by granulocytes. J Clin

Invest

1974;53:1662.

72. Babior BM, Kipnes RS, Curnutte JT. Biological defense

mechanisms. The

production by leukocytes of superoxide, a potential bacterial

agent. J Clin

Invest 1973;52:741.

73. Ali M. Cell Membrane Stressors. Monograph 1987

74. Virchow R. Die Cellularpathologie in ihrer Bedeutung auf

physiologische

und pathologische Gewebslehre. Hirschwald, Berlin 1858

75. Bordue L. Recherches sur le tissu muqueux ou l'organ

cellulaire. Paris

1767, 1 and 2.

76. Reichert CB. Vergleichende Beobachtungen uber das Bindegewebe

und die

verwandten Gebilde. Dorpat 1845, S.168.

77. Rokitansky C. v., Handbuch der pathologischen Anatomie. Wein

1846.

78. Pischinger A. Matrix and Matrix Regulation. 1975 Haug

International,

Brussels.

79. Bradford R. Henry A. Oxidology. 1997. Bradford Research

Institute. San

Diego

80. Keidel W. Lehrbuch der Klimatologie. G. Thieme Verlag.

Stuttgart 1970.

81. Nimni ME. ed. Collagen 1-4. 1988 CRC, Boca raton, Florida.

82. Berg RA, Prockop DJ. Biochem. Biophys Res Commun 1973;52:115-

120.

83. Holmgren SK, Taylor KM, Bretscher LE, et al. Code of collagen's

stability deciphered. Nature 1998;392:666.

84. Shaw W. Role for certain yeast and bacteria byproducts

discovered by

organic acid testing in the etiology of a wide variety of human

diseases.

Bulletin of the Great 84.

85. Sell D, Monnier V. Structure elucidation of a senescence cross-

link from

human extracellular matrix. Implications of pentoses in the aging

process. J

Biol Chem 1989;264:21597-21602.Plains laboratory. Overland Park, KS

66204

86. Shaw W. Role for certain yeast and bacteria byproducts

discovered by

organic acid testing in the etiology of a wide variety of human

diseases.

Bulletin of The Great Plains Laboratory. Overland park, KS 66204

(913) 341-8949.

87. Gupta S. Aggarawal and Heads C. Dysregulated immune system in

children

with autism. Beneficial effects of intravenous immune globulin on

autistic

characteristics. Autism Develop Dis 1996;26:439-452.

88. Nagaraj RH et al. Suppression of pentosidine formation in

galactosemic

rat lens by an inhibitor of aldose reductase. Diabetes 1994;43:580-

6.

89. Cuatrecases P, Tell GPE. Insulin-like activity of

coconcanavalin A and

wheat agerm agglutinin-direct interactions with insulin receptors.

Proc Natl

Acad Sci USA 1973;70:485-9.

90. Erickson RH, Kim YS. Interaction of purified brush-border

membrane

amniopeptidase N and dipeptidase IV with lectin-Sepharose

derivatives. Biochim

Biophys Acta 1983;743:37-42.

91. Pischinger A. Matrix and Matrix Regulation. Haug International.

1975,

Brussels, pages 69-78

92. Klotz SA. A fibronectin receptor on Candida albicans mediates

adherence

of the fungus to extracellular matrix. J Infectious Dis

1991;163:604-6.

93. M. Kolarova. Host-tumor relationship XXXIV. Hyaluronidase

activity and

hyaluronidase inhibitor in the serum of patients with malignant

tumors.

Neoplasma 1977;24:285.

94. Savolainen ER. Enzymes of collagen biosynthesis in diseases of

the liver

and connective tissues. Changes in prolyl hydroxylase and

galactosylhydroxylsyl glucosyltransferase in serum and tissues.

Chem Absts 1979 91:1729Ilt.

95. Alitalo K, et al. Extracellular matrix proteins characterize

human tumor

cell lines. International Journal of Cancer 1981;27:755.

96 Harris DA. Bioenergetics at a glance. 1995. pp84-85. Blackwell

Science.

97. De Stefano N, Argov Z, Matthews PM, Karpati G, Arnold DL.

Impairment of

muscle mitochondrial oxidative metabolism in McArdle's disease.

Muscle &

Nerve 1996;19(6):764-9.Harris

98. Sjostrand FS. Electron microscopy of mitochondria and

cytoplasmic double

membranes. Nature (London) 1953;171:30.

99. Lindane AW, Marzuki S, Ozawa T, et al. Mitochondrial DNA

mutations as an

important contributor to aging and degenerative diseases. Lancet

1985;1:642-5.

100. Babcock GT, Wickstrom M. Oxygen activation and the

conservation of

energy in cell respiration. Nature 1992;356:301-309.harris

101. Cui L, Schinazi RF, Gosselin G, et al. Effect of beta-

enantriomeric and

racemic nucleoside analogues on mitochondrial functions in HepG2

cells.

Implication for predicting drug hepatotoxicity. Biochemical

Pharmacology.

1996;52(10):1577-84.

102. Cui L, Yoon S, Schinazi RF, et al. Cellular and molecular

events

leading to mitochondrial toxicity of

1-(2-deoxy-2-fluoro-1-beta-D-arabinofuranosyl)-5-iodouracil in human

liver cells. J Clin Invest 1995;95(2):555-63.

103. Hickman PF, Kemp GJ, Thompson CH, Salisbury AJ, Wade K, Harris

AL,

Radda GK. Bryostatin 1, a novel antineoplastic agent and protein

kinase C

activator, induces human myalgia and muscle metabolic defects: a

31P magnetic

resonance spectroscopic study. British Journal of Cancer 1995;72

(4):998-1003.

104. Altschuld RA, Jung DW, Phillips RM, et al. Evidence against

norepinephrine-stimulated efflux of mitochondrial Mg2+ from intact

cardiac myocytes. Am

J Physiol. 1994;266:H1103-11.

105. McCully KK, Sisto SA, Natelson BH. Use of exercise for

treatment of

chronic fatigue syndrome. Sports Medicine 1996;21(1):35-48.

106. Eisenger J, Plantamura A, Ayavou T. Glycolysis Abnormalities

in

Fibromyalgia. J Amr Coll Nutr 1994;13(2):144-148.

107. Wysenbeck AJ, Shapira Y, Leibovici L. Primary fibromyalgia and

the

chroanic fatigue syndrome. Rheumatol Int 1991;10:227-229.

108. Plioplys AV, Plioplys S. Electron-microscopic investigation of

muscle

mitochondria in chronic fatigue syndrome. Neuropsychobiology.

1995;32(4):175-81.

109. Vecchiet L, Montanari G, Pizzigallo E, Iezzi S, deBigontina P,

Dragani

L, Vecchiet J, Giamberardino MA. Sensory characterization of

somatic parietal

tissues in humans with chronic fatigue syndrome. Neuroscience

Letters

1996;208(2);117-20.

110. Cheney PR, Davidson M, Voyles CS, Wilson S. Bicycle Ergometry

with gas

analysis and neuroendoctrine responses to exercise in chronic

fatigue

syndrome. Albany, NY 1992.

111. Mengshoel AM, Forre O, Komnaes HB. Muscle strength and aerobic

capacity

in primary fibromyalgia. Clin Exp Rheumatol 1990;8:475-479.

112. Plioplys AV. High dose L-Carnitine improves the chronic

fatigue

syndrome in a prospective cross-over study. Neuropsychobiology

1997;35:16-23.

113. Is fibromyalgia caused by a glycolysis impairment. Nutr Rev

1994;52(7):248-250.

114. Kramer TR, Burri BJ. Modulated mitogenic proliferative

responsiveness

of lymphocytes in whole blood cultures after low carotene diet and

mixed

carotenoid supplementation in women. Am J Clin Nutr 1997;65:871-5.

115. Kuratsune H, Yamaguti K, Takahashi M, Misaki H, Tagawa S,

Kitani T.

Acycarnitine deficiency in chronic fatigue syndrome. Clin Inf Dis

1994; Volume

18, Suppl 1:562-67.

116. Rengisson A, Henriksson KG. The muscle in fibromyalgia - a

review of

Swedish studies. J Rheumatol 1989;16:144-149.

117. Schwartz, et al. SPECT imaging of the brain: Comparison of

findings in

patients with chronic fatigue syndrome, AIDS dementia complex and

major

unipolar depression. American Journal of Radiology. 1994 April;162.

118. Stevens SR. Using exercise testing to document functional

disability in

CFS. Journal of Chronic Fatigue Sundrome 1995;1 Numbers 3/4:127-129.

119. Trounce I, Byrne E, Marzuki S. Decline in skeletal muscle

mitochondrial

respiratory chain function: a possible factor in ageing. Lancet

1989;I(8639):637-638.

120. Wong R, Lepaschuk G, Zhu G, Walker D, Catelliger D, Burton D,

Teo K,

Collins-Nakaj R, Motague T. Low levels of cellular ATP following

muscle

exhaustion in vivo by phosphorus NMR in chronic fatigue syndrome.

Chest

1992;102:1716-1722.

121. Ali M. Fibromyalgia: On The Moustache of a Mouse, (Work in

progress).

Life Span, Denville, New Jersey

122. Ali M. Oxidative coagulpathy and oxidative oxidopathy: Two

core

pathogenetic mechanisms of fibromyalgia. J Integrative Medicine.

(in press).

123. Bradford coagulative and complement.

124. Rudel T, Bokoch G. Membrane and morphological changes in

apoptotic

cells regulated by caspase-mediated activation of PAK2. Science

1997;276:1571.

125. Xu DG, et al. Elevation of neuronal expression of NAIP reduced

ischemic

damage in the rat hippocampus. Nature Medicine 1997;3:997.

126. Vander Heiden MG, et al. Bci-xL regulates the membrane

potential and

volume homeostasis of mitochondria. Cell 1997;91:627.

127. Kothakota S, et al. Caspase-3-generated fragment of gelsolin:

Effector

of morphological change in apoptosis. Science 1997;278:294.

128. Research News. Death by Dozens of Cuts. Science 1995;280:32-34.

129. McGregor NR, Dunstan RH, Zerbes M, Butt HL, Roberts TK,

Klineberg IJ.

Preliminary determination of a molecular basis to chronic fatigue

syndrome.

Biochemical and Molecular Medicine 1996;1-9.

130. Freed DLJ. Dietary lectins and disease. In: Food Allergy and

Intolerance. Eds: Brostoff J, Challacombe SJ. 1987 Bailliere

Tindall, East Sussex,

England.

131. Cuatrecases P, Tell GPE. Insulin-like activity of

coconcanavalin A and

wheat agerm agglutinin-direct interactions with insulin receptors.

Proc Natl

Acad Sci USA 1973;70:485-9.

132. Erickson RH, Kim YS. Interaction of purified brush-border

membrane

amniopeptidase N and dipeptidase IV with lectin-Sepharose

derivatives. Biochim

Biophys Acta 1983;743:37-42.

133. Freed DLJ. Non-Allergic Effects of Food. In Brostoff J,

Challacombe SJ

(eds.): Food Allergy and Intolerance. London, Bailliere Tindall

1987,375-400.

134. Ganguly P, Fossett NG. Evidence for multiple mechanisms of

interaction

between wheat gern agglutinin and human platelets. Biochim Biophys

Acta

1980;627:256-261.

135. Hedo JA, Harrison LC, Roth J. Binding of insulin receptors to

lictins:

evidence for common carbohydrate determinants on several membrane

receptors.

Biochemistry 1981;20:3385-3393.

136. Hilgert I, Horejsi VA, Angelisova P, Kristofova H. Lentil

lectin

effectively induces allotransplantation tolerance in mice. Nature

1980;284:273-5.

137. Livingston JN, Purvis BJ. Effects of wheat germ agglutinin on

insulin

binding and insulin sensitivity of fat cells. Am J Physiol

1980;238:E267-75.

138. Nirmul G, Severin C, Taub RN. In vivo effects of con A. I.

Immunosuppressive effects. Transplantation 1972;14:91-5.

139. Oppenheim JJ, Rostenstreich DL, eds: Mitogens in immunology.

New York:

Academic Press, 1976.

140. Shier WT. Concanavalin A as in inflammogen. In: Bittiger H,

Schnebli

HP, eds. Concavalin A as a tool. London: John Wiley and Sons.

1976;573-9.

141. Stillmark H. Uber rizin, ein giftiges ferment aus Samen von

Ricinis

communis L., und ainigen anderen Euphorbiaceen. Dorpat (Tartu),

1888. Inaugural

dissertation.

142. Landsteiner K, Raubitschek H. Boebachtungen uber Hamolyse and

hamagglutination. Zenbralbl Bakteriol 1907;45:660-7.

143. Boyd WC. Lectins. Ann NY Acad Sci 1970;169:168-90.

144. Renkonen KO. Studies on hemagglutinins present in seeds of

some

representatives of family of leguminoseae. Ann Med Exp Biol Fenniae

1948;26:66-72

145. Boyd WC, Shapleigh E. Diagnosis of subgroups of blood groups A

and B by

use of plant agglutinins (lectins). J Lab Clin Med 1954;44:235-7.

146. Hedo JA, Harrison LC, Roth J. Binding of insulin receptors to

lictins:

evidence for common carbohydrate determinants on several membrane

receptors.

Biochemistry 1981;20:3385-3393.

147. Hilgert I, Horejsi VA, Angelisova P, Kristofova H. Lentil

lectin

effectively induces allotransplantation tolerance in mice. Nature

1980;284:273-5.

148. Livingston JN, Purvis BJ. Effects of wheat germ agglutinin on

insulin

binding and insulin sensitivity of fat cells. Am J Physiol

1980;238:E267-75.

149. Nirmul G, Severin C, Taub RN. In vivo effects of con A. I.

Immunosuppressive effects. Transplantation 1972;14:91-5.

150. Oppenheim JJ, Rostenstreich DL, eds: Mitogens in immunology.

New York:

Academic Press, 1976.

151. Edwards JE, Jr. Invasive candida infections: Evolution of a

fungal

pathogen. N Eng J Med 1991;324:1060-1062.

152. Ali M, Ali O, Bradford R. et al Immunostaining of candida

organisms in

peripheral smears. (Abstract). 1995. American Academy of

Otolaryngic Allergy,

Spring Meeting, Palm Desert, CA.

153. Ali M and Ramanarayanan MP: A computerized micro-ELISA assay

for

allergen-specific IgE antibodies. Am J Clin Pathol 1984;81:591.

154. Ali M, Ramanarayanan MP, Nalebuff DJ, et al: Serum

concentrations of

allergen-specific IgG antibodies in inhalant allergy: Effect of

specific

Immunotherapy. Am J Clin Pathol. 1983;80:290.

155. Ali M. The bloodstream: An Open Ecosystem. In RDA: Rats, Drugs

and

Assumption. Page 424-435. 1995 Life Span, Denville, New Jersey.

156. Ali M. Naked bacteria, naked yeast. In RDA: Rats, Drugs and

Assumptions. Pages 455-457. 1995 Life Span, Denville, New Jersey.

157. Walsh TJ et al. Detection of circulating Candida enolase by

immunoassay

i patients with cancer and invasive candidiasis. N Eng J Med

1991;324:1026.

158. Roberts GD. Detetction of fungi in clinical specimens by phase-

contrast

microscopy. J Clin Micrbiol 1975;2:261-265.

159. Taschdjian CL, et al. Post Mortem Studies of Systemic

Candidiasis I.

Diagnostic Validity of Precipitin Reaction and Probable Origin of

Sensitization to Dytoplasmic Candidal Antigens. Sabouraudia

1969;7:110.

160. Jarvis WR. and the National Nosocomial Infections Surveillance

System.

Centers for Disease Control. Nosocomial Fungal Infections. January

1980-April

1990. Presented at the Third International Conference on Nosocomial

Infections. Atlanta July 31-August 3, 1990.

161. Mattman LH. L forms isolated from infections, in Microbial

Protoplasts,

Spheroplasts, and L Forms. Guze L.B., Ed., Williams & Wilkins,

Baltimore,

1968, 472-483.

162. Mattman LH, Tunstall LH, Kispert WG. A survey of L variation

in the

salmonellae, Zentralbl, Bakteriol, Parasitekd, Infektionskr, Hyg.

Abt. 1 Orig.

1969;210:65-74.

163. Mattman LH, Tunstall LH, Rossmoore HW. Induction and

characteristics of

staphylococcal L forms. Can J Microbiol 1961;7:705-713.

164. Almquist E. Studien uber das Verhalten einiger pathogenen

mikroorganismen bei niedriger temperatur. Zbl. Bakt. I Abt Orig.

1908;48:175-186.

165. Almquist E. Variation and life cycles of pathogenic bacteria.

J Infect

Dis 1922;31:483-493.

166. Metchnikoff E. Untersuchungen uber die intracellular verdauung

berwirbellosen thieren. Arb Zoologischem Inst Univ Wien 1883;5:141

167. Svoboda A. Regeneration of yeast protoplasts in agar gels. Exp

Cell Res

1966;44:640-642.

168. Svoboda A, Necas O. Mechanisms of regeneration of yeast

protoplasts.

VI. An experimental blocking of regeneration of protoplasts. Folia

Biol

(Prague) 1968;14:390-397.

169. Mattman LH. Cell Wall Deficient Forms: Stealth Pathogens. CRC

Press,

Boca Raton, Florida, 1993.

170 Mattman LH. Cell Wall Deficient Forms: Stealth Pathogens. CRC

Press,

Boca Raton, Florida, 1993.

171. Prasad I, Bradley SG. Cell wall defective variant of Nocardia

rubra. J

Gen Microbiol 1972;70:571-572.

172. Emmons CW, Binford CH, Utz JP, Kwon-Chung KJ. Medical

mycology. Lea and

Febiger, Philadelphia. 3rd edition. 1976;192-196.

173. Rippon JW. Medical Mycology: The pathogenic fungi and the

pathogenic

actinomycetes. W. B. Saunders Co., Philadelphia. 1974;191-195.

174. Klotz SA. A fibronectin receptor on Candida albicansmediates

adherence

of the fungus to extracellular matrix. J Infectious Dis

1991;163:604-6

175. Louria DB, Stiff DP, Bennett B. Disseminated moniliasis in the

adult.

Medicine (Baltimore) 1962;41:307-337.

176. Lehrer RI. Measurement of candidiacidal activity of specific

leukocyte

types in mixed cell populations. I. Normal, myeloperoxidase-

deficient, and

chronic granulomatous disease neutrophils. Infect Immun

1970;130:241-245.

177. Lehrer RI, Cline MJ. Leukocyte candidacidal activity and

resistance to

systemic candidiasis in patients with cancer. Cancer (Phila)

1971;27:1211-1217.

178. Ali M. Oxidant injury damages energy enzymes. The Canary and

Chronic

Fatigue. 1994. Life Span, Denville, New Jersey.

179. Thompsen AM. The oxidizing capacity of the earth's atmosphere:

probable

past and future changes. Science 1992;256:1157-1165.

180. Tytgat J, Hess P. Evidence for cooperative interactions in

potassium

channel gating. Nature 1992;359:420-423.

181. Ism LL, De Jongh KS, Patton DE, et al. Primary structure and

functional

expression of the B1 subunit of the rat brain sodium channel.

Science

1992;256:839-842.

182. Caliguiri M, Murray C, Buchwald D, et al. Phenotypic and

functional

deficiency of natural killer cells in patients with CFID. J Immunol

1987;139:3306-3313.

183. Targan S, Stebbing N. In vitro interactions of purified cloned

human

interferons on NK cells: enhanced activation. J Immunol

1982;120:934-935.

184. Suhadolanik RJ, Reichenbach NL, Sobol RW, et al. Biochemical

defects in

2-5A synthetase/RNAase pathway associated with chronic fatigue

syndrome with

encephalopathy. In: The clinical and scientific basis of myalgic

enceplalomyeltitis/chronic fatigue syndrome. Byron Hyde, ed.

Ottawa, Canada. The

Nightingale Research Foundation. (Chapter 67) 1992;613-7.

185. Linde A, Anderson B, Svenson SB, et al. Serum levels of

lymphokines and

soluble cellular receptors in primary Epstein-Barr virus infection

and in

patients with chronic fatigue syndrome. The J Inf Dis 1992;165-994-

1000.

186. Buchwald D, Cheney PR, Peterson DL, et al. A chronic illness

characterized by fatigue, neurologic and immunologic disorders, and

active human

herpesvirus-6. Ann Int Medicine 1992;116:103-131.

187. Teresaki P. In: Chronic fatigue syndrome. Goldstein J, ed.

Chronic

Fatigue Syndrome Institute, Beverly Hills, CA, 1990.

188. Gupta S, Vayuvegula B. A comprehensive immunological analysis

in

chronic fatigue syndrome. Scan. J Immunol 1991;33:319-327.

189. Handbook of Toxicology Vol 1. Spector WS. ed. W.B. Saunders,

Philadelphia, 1956. Pages 184-5.

190. El-Ebiary M, Torres A, Fabregas N, at al. Significance of the

isolation

of Candida species from respiratory samples in critically ill,

non-neutropenic patients: an immediate postmortem histologic study.

Am J Respir Crit Care

Med. 1997;156:583-590.

191. Aubourg P. L'Ozone medical: Production, posologie, modes

d'applications

cliniques. Bull Med, Paris 1938;52:745-749.

192. Payr E. Uber Ozone Behandlung in der Chirurgie. Munch Med

Wschr

1936;82:220-291.

193. Hydrogen peroxide farr

194. Vosmaer A. Ozone: Its manufacture, properties and uses. Van

Nostrand

Publisher, New York 1916.

195. Roy D, Wong PKY, Englebrecht RS, Chian SK. Mechanism of

enteroviral

inactivation by ozone. Appl Environ Microbiol 1981;41:718-723.

196. Bolton DC, Tarkington BK, Zee YC, Osebold JW. An in vitro

system for

studying the effects of ozone on mammalian cell cultures and

viruses. Environ

Res 1982a;27:466-475.

197. Sleigh J, Linter SPK. Hazards of hydrogen peroxide. British

Med J

1985;291:1706.

198. Shenep JL, Stokes DC, Hughes WT. Lack of antibacterial

activity after

intravenous hydrogen peroxide infusion in experimental escherichia

coli

sepses. Infect Immun 1985;48:607-610.

199. Dockrell HM, Playfair JH. Killing of blood-state murine

malaria

parasites by hydrogen peroxide. Infect Immun 1983;39:456-459.

200. Weiss SJ, Young J, LoBuglio A, et al. Role of hydrogen

peroxide in

neutrophil-mediated destruction of cultured endothelial cells. J

Clin Invest

1981;68:714-721.

201. Root RK, Metcalf J, Oshino N, et al. H2O2 release from human

granulocytes during phagocytosis. J Clin Invest 1977;60:1266-1279.

202. Farr CH. Possible therapeutic value of intravenous hydrogen

peroxide.

Second International Symposium; Chelating Agents in Pharmacology,

toxicology

and Therapeutics 1987; Charles University, Pilsen, Czechoslovak (In

press).

203. Farr CH. Physiological and biochemical responses to

intravenous

hydrogen peroxide in man. J ACAM 1987; (In Press).

204. Ali M. Star Wars Medicine. In: The Cortical Monkey and

Healing. pp

101-160. Institute of Preventive Medicine, Denville, New Jersey

1990. Bloomfield,

New Jersey

205. Ali M. Enegetic- Molecular Medicine. In: RDA: Rats, Drugs and

Assumptions. pp 1995. Life Span, Denville, New Jersey.

 

 

 

 

 

 

 

 

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...