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THE NUTRI-SPEC LETTER
Volume 10 Number 5
From:
Guy R. Schenker, D.C.
May, 1999
Dear Doctor,
Patients by the dozens drag themselves into your
office every day with the following complaints:
- chronic fatigue
- muscular weakness
- anemia
- postural dizziness
- decreased libido
- poor circulation
- deficient self assurance
- osteoporosis
- accelerated aging
You realize from reading the last several issues of
this Letter that many of these patients have an
electrolyte insufficiency (EI) imbalance. You know that
this imbalance is all about two things:
- poor mineral retention
- fluid dynamics out of control
Review the charts and diagrams from last month's
Letter to refresh your memory on the three primary body
fluid compartments. Fluid and electrolytes must be
maintained in proper quantity and proper pH in each of
these fluid compartments. These compartments represent
the three clinically testable levels of biological
organization -- the systemic, tissue, and cellular levels.
What must you do to put the wind back in the sails of
these flaccid patients? One of the first things you must
do is ...
PLEASE PASS THE SALT.
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Please pass it among your own family members at meal time
-- but by all means pass it to your electrolyte
insufficiency patients.
We have cited several studies in this letter over the
years highlighting the essentiality of sodium chloride.
Probably the most fascinating of these was the study done
at Johns Hopkins University and published in the September
1995 Journal of The American Medical Association. This
study demonstrated a treatment for chronic fatigue
syndrome that resulted in improved energy levels in 76% of
the patients. I have never seen another study that
achieved such dramatic symptomatic improvement in this
devastating clinical condition. What was the keystone of
this phenomenally successful treatment for chronic fatigue
syndrome? Sodium chloride. These patients virtually all
had low blood pressure accompanying their chronic fatigue
and responded dramatically to an increased intake of
common table salt. In NUTRI-SPEC terms, of course, these
patients had an electrolyte insufficiency imbalance.
Research done at Hartford Hospital in Connecticut and
reported at the American College of Cardiology Conference
in Anaheim in March of 1997 also studied chronic fatigue
syndrome. It was found that more than half the patients
achieved symptomatic improvement by increasing their salt
and water intake.
In the March 14, 1998 issue of The Lancet, a study
was published showing the harmful affects of restricting
salt intake. The data for this study was collected from
over 11,000 subjects over a period of over 25 years
beginning in 1971. There was an inverse relationship
discovered between salt intake and mortality. In other
words, the length of your life is directly proportional to
how much salt you eat.
I remember reading an interview with a medical
physician from India several years ago. As you might
expect the doctor bemoaned the still outrageously high
incidence of malnutrition and poor hygiene in his country.
To make matters worse there are many areas of the country
where medical care must be provided with deplorably
inadequate medical supplies.
At this point in the interview the doctor was asked,
"If you could choose just three therapeutic agents to use
exclusively in a clinic in a disease-ridden impoverished
area of India, which three would you most value?"
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He answered unhesitatingly, "Morphine to control the
pain of my terminal patients; a broad spectrum antibiotic
to deal with the rampant spread of bacterial disease; and
salt to administer to virtually every patient for its
favorable impact on adaptative capacity."
Never lose sight of the clinical importance of sodium
chloride. There is a small segment of your patient
population who have an electrolyte stress imbalance and
fall into the low renin category (refer to the ES (R-)
column of the Electrolyte Stress Chart provided in the
last Letter) who must restrict sodium intake. Most of the
rest of your electrolyte stress patients need to be
careful about salt intake because of its chloride (not its
sodium) content. All the rest of your patients must be
careful to obtain adequate salt. This is not a problem
for most, because our need for salt is accompanied by an
appetite that is almost certain to meet our needs. In
your EI patients, however, the taste for salt -- even a
craving for salt -- may not provide adequate intake, at
least until you have corrected the fundamental metabolic
imbalance.
The problem with your electrolyte insufficiency
patients is not just with sodium chloride but with poor
mineral retention in general. Once your EI patients have
lost the ability to retain electrolytes, they are left
without the strength to handle most any kind of stress
load -- either physical or emotional. These patients are
your hypo-volemic, hypo-tonic weaklings. They are a
deflated balloon begging for you to pump them up.
Why have these electrolyte insufficiency patients
lost their ability to retain minerals, and why are they
likely to suffer from one or more of the conditions listed
at the top of this Letter? The short answer is, they have
"weak kidneys." The complete answer is that the patient
has lost kidney control of electrolyte balance because of
a combination of metabolic and endocrine imbalances.
As illustrated in the electrolyte insufficiency chart
provided for you last month, there are two sub-categories
of endocrine dysfunctions. One represents a renin
insufficiency and one represents an aldosterone
insufficiency. These represent the two major sub-
categories of EI patients -- EI (R-) and EI (A-).
What is the association between renin and "weak
kidneys?" Via renin, the kidney works with the liver and
lung to form angiotensin, which has much to do with
vascular tone and with the retention of mineral salts.
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You also learned last month that the EI (R-) EI patient
typically has one or more of anaerobic, ketogenic,
parasympathetic, or respiratory alkalosis imbalances.
Your other basic category of EI patient consists of
those whose adrenal aldosterone output is generally in-
adequate. This results in further loss of sodium and
chloride, along with citrates, bicarbonates, and calcium.
The low aldosterone output is also reflected in the
decreased pulse pressure, and an increased urinary
specific gravity. Your EI (A-) patients are typically
found to be either dysaerobic, glucogenic, or sympathetic
and will likely have a renal or potassium excess acidosis.
What else goes wrong with the kidneys of your EI
patients? Kidney dysfunction can be associated with
anemia. A normal kidney splits erythropoeitin from plasma
protein, thus stimulating bone marrow RBC production.
The kidney also produces the active form of vitamin
D. Renal endocrine insufficiency thus results in calcium
deficiency, osteomalacia, and osteoporosis.
The protein anabolism of testosterone and DHEA is
partially mediated by the kidney. There is a reciprocal
relationship between androgens and the kidney, as
androgens are renotrophic. They increase the size and
weight of the kidneys. Androgens are extremely anabolic.
This anabolic property is partly under renal control.
Your EI patient will often be emaciated in association
with poor protein metabolism.
Your Formula EI contains kidney, adrenal and heart,
along with vitamin D and calcium glycerophosphate to
support the osteoblastic role of the kidney, as well as
RNA to help with protein anabolism.
Your revised QRG protocol for this imbalance has
given you the first comprehensive and effective approach
to patients suffering the debilitating fatigue and stress
and hormonal imbalances associated with EI imbalance
The ability to retain electrolytes and the ability to
control electrolyte and water composition in the three
body fluid compartments is such a critical part of
maintaining health. A failure of this metabolic balance
system pulls the plug on a patient's personal power. The
list of possible symptoms is endless, but will in each of
your EI patients include one or more of those listed at
the top of this Letter. Only with NUTRI-SPEC can you find
and correct the fundamental cause of these symptoms.
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With your QRG analysis it takes no more than 10
seconds to determine if your patient has an electrolyte
insufficiency. The essential clinical signs are
orthostatic systolic failure, orthostatic diastolic
failure, and clinostatic pulse failure, plus a tendency to
bradycardia when recumbent. Nothing could be simpler.
Once found, the imbalance is easily and effectively
treated by working through the EI Supplements page of your
QRG. The EI supplement page does a nice job of
distinguishing for you between those patients who are
primarily EI (R-) and those who are EI (A-). You have a
powerful arsenal of supplements available for your EI
patients. Let us consider just a few:
Phenylalanine has a dramatic impact on many patients
with chronic fatigue -- and many patients with chronic
fatigue have an EI Imbalance. The only study I have ever
seen that rivals the success achieved by the Johns Hopkins
study with sodium chloride was a study that assessed the
levels of essential amino acids in chronic fatigue
sufferers. This study did nothing more complicated than
supplement chronic fatigue patients with the amino acids
in which they were low according to serum levels. More
than 75% of the test group showed either very good or
excellent improvement in symptoms with nothing more than
amino acid supplementation. Furthermore, of all the amino
acids studied, Phenylalanine was by far the most
clinically significant. Fully 72% of the chronic fatigue
sufferers were found to have low levels of phenylalanine.
Many of the patients in this study also suffered from
depression. Both the fatigue and depression resolved in
most of these patients with phenylalanine supplementation.
The amino acid glutamine is used for many of your EI
patients. Glutamine is more important than any other
amino acid in maintaining nitrogen balance. Glutamine
plays an anabolic role in that it stimulates muscle
glycogen synthesis following exercise, and reverses the
catabolic effect on muscles due to excess glucocorticoids
or to low levels of androgens. In other words, adequate
glutamine is essential to prevent protein wasting. In
this regard glutamine works with the RNA which is an
important ingredient in your Formula EI.
Glutamine is also essential for the acid/alkaline
component of many electrolyte insufficiency problems,
particularly those with the renal/adrenal/potassium
excess acidosis.
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Complex P is essential for many of your EI (R-)
patients. Giving these patients Complex P (assuming it
was indicated by your objective findings) will increase
the tone of their vascular system; it will increase their
blood pressure and pulse pressure; and it will strengthen
the heart and adrenals.
Perhaps the most important supplement for your EI
(A-) patients is Formula EW. It has a powerful impact on
the movement of electrolytes and water from one body fluid
compartment to another. It not only influences fluid
dynamics but influences membrane permeability as well. In
the October Letter we closed with a long list (which you
may want to review) of the clinical benefits of using
Formula EW. All the clinical benefits of Formula EW
(which consists of glycerol plus vitamin E) are
attributable to the two major actions of glycerol:
- It quickly permeates all three body fluid compartments,
carrying electrolyte buffers and other solutes, along with
biologically activated water to meet physiological demand.
- Glycerol also binds with and neutralizes the free fatty
acids that are the primary cause of the aging process that
results form free radical peroxidation -- particularly the
abnormal fatty acids with conjugated double bonds which
most accelerate the aging process.
Most of the rest of your EI supplement page consists
of sodium combined with various anions. The combination
of anions that each patient needs depends on whether they
are EI (A-) or EI (R-), and on what other NUTRI-SPEC
imbalances they may have. Notice that one of the
supplements is sodium combined with glycerophosphate,
which gives all the same benefits of glycerol with the
additional benefits of the minerals sodium and
phosphorous. You may also note that your Formula EI
contains calcium glycerophosphate.
Give the specific supplements indicated for your EI
patients, including their electrolyte tonic before
breakfast and perhaps another mix consumed throughout the
day, and you will empower them like no one else can.
Sincerely,
Guy R. Schenker, D.C.
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