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on medicine and current thought, including CFS

by John Graham

Beginnings,metaphors, holons

Imaging fullfilment and healing

Chronic fatigue

 

 

 

 

 

 

 

 

 

 

 

 

 

CHAPTER 8

THE SCIENCE OF CHRONIC FATIGUE SYDROMES

 

We can now try to elaborate upon the science of these syndromes, realising that this is work in progress.

We will now proceed to look in some detail at elements that need understanding so that we can look at the patterns that connect them.

This is written with more technical data than I first intended.

From time to time I will try to summarize the crucial information.

 

IDENTIFYING ABNORMALITIES AND EXPLAINING MECHANISMS.

Here we are operating in medical models, drawing upon scientific methods.

This chapter is largely about genes and viruses.

The most likely explanations relate to the following factors:

Genetic vulnerability.
It would be difficult to adequately describe the range of gene research which is being undertaken in this early part of the 21st century, but I want to mention the following,

Genes, which shape gene products such as functional protein and enzyme activity levels.

These include genes, which for example shape lipid profiles.

Some specific genes shape immune responses.

(e.g.MHC genes commonly described as HLA, genes which code for cytokines and for their receptors and probably an array of genetic polymorphisms relating to substances in cascades of events along complex immune pathways.)

Genes have times of being activated such that their products come into action.

Germ cell DNA in the ovum and sperm carries information from one generation to the next.

In somatic cells the genes carry out their functions in every nucleated cell.

Somatic mutations in these cells can have minor or major, as well as short term or long term consequences for those cells and for the whole organism.

The ongoing work on the complete human genome is already bearing fruit in very many diseases.

Human beings have about 24,000 genes which code for protein synthesis.

These genes may have tens of thousands to hundreds of thousands of base sequences.

Through the existence of spliceosomes, genes can code for more than one protein.

Major Histocompatibility Complex

Study of HLA and major histocompatibility complex (MHC) molecules, is revealing intriguing links with specific disorders.

The term histocompatibility arose in the context of grafts (and acceptance or rejection) between members of a species.

By international agreement HLA is the logo for human MHC.

MHC can be used as a term to cover the genes and gene products.

The MHC genes are located on the short arm of chromosome 6.

Class I molecules are expressed on virtually all cell surfaces and are products of 3 reduplicated loci: HLA-A, HLA-B and HLA-C.

Class II molecules are restricted in expression to B-lymphocytes, dendritic cells, macrophages, monocytes, antigen-activated T lymphocytes, and to epithelial and endothelial cells that have been activated by interferon. They are products of closely linked genes in the HLA-D region.

Class III molecules are the C4, C2 and Bf components of complement.

Complement is a cascading series of plasma enzymes, regulatory proteins and proteins capable of cell lysis. Complement activity is involved in the opsonization of bacteria, and some fractions are potent mediators of immune cell activation (e.g. C5a is a potent chemo attractant for neutrophils and monocyte-macrophages.)

I will expand on the immunological mechanisms in later chapters..

One illustration is the discovery that four environmental exposures may increase the emergence of type1diabetes in people possessing certain HLA haplotypes.

These are exposures to

(1) Certain coxsackie B viruses,

(2) Beta casein A1 from cow’s milk,

(3) Exposure to cereals such as wheat (this latter at specific times of development such as before 4 months of age)

(4) Vitamin D deficiency during pregnancy

Environmental stress.
Chemicals including pesticides, industrial products, intoxicants and anaesthetics may cause severe, moderate or subtle effects on cellular chemistry especially contributing to cell membrane abnormalities in mitochondria. These changes may be evident quickly or may not emerge or be detected for months, years or even decades.

DNA itself is susceptible to injury, particularly in rapidly dividing cells.

Many experts suggest that injury to mitochondria is important.

Mitochondria are the cytoplasmic organelles, which provide 80% of the energy of eukaryotic cells.

The mitochondrial DNA is 10 times more susceptible to mutation than nuclear DNA, and mitochondrial membranes are susceptible to oxidative injury.

One thing that appears to be protective of nuclear DNA is the time it rests in a folded form in between times of cell replication.

There is some evidence that immune responses can be suboptimal in mammalian cells when pesticides and some industrial products are present in very low concentrations.

Yet other environmental chemicals appear to be hormone disrupters (eg oestrogen disrupters) or diverters of steroid hormones into unwanted pathways.

This is pertinent to recent and long-standing controversies such as hormone replacement therapies.

There are reasons to be alarmed about the extensive exposure of all living systems on the earth to these chemicals!

This requires us to ask all industries and their support systems, to act for all of the people on the earth, rather than just for their shareholders.

A transparency and honesty, which has been hitherto unknown on earth, is needed.

Scientists, who are beholden to multinational or national corporate organizations, could blaze a trail of friendship to knowledge and commitment to integrity to bring about a new and healing era of our earth.

David Suzuki has blazed a trail in creating and maintaining awareness of ecology.

PATHOGENS

At the beginning of the following material on micro-organisms, I remind the reader that we are looking at the earliest forms of life, including their evolution and genetics, and sometimes, living pieces which have emerged such as viruses.

The first forms of life are likely to be primitive bacteria, which emerged on the earth some 3.8 billion years ago.

All organisms which have arisen since, live in the presence of and interact with the organisms called prokaryotes.

In chapters to come, I will elaborate on prokaryotes.

Celera, the private team that completed the human genome project, describe the genome as a dynamic and vibrant ecosystem.

This lifestyle diversity owes itself to the ability to trade RNA and DNA.

Elisabet Sahtouris writes” To this day, every bacterium on this planet can trade bits of DNA with any other it can contact.”

What an amazing contribution to our understanding of evolution!

Although I refer to pathogens (disease causing agents), I am attentive to the potential for organisms to give rise to certain kinds of injury in the host, albeit as a survival mechanism for themselves, or to coexist in a non-damaging way.

Micro-organisms may evolve into complementary and benign roles and are probably essential to many ecological balances.

In a strange way, some organisms are pathogens for a time, or to some creature, or to particular people, but not to others.

In the chapters to follow I will discuss viruses, bacteria and other infective organisms.

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