|

(253) 460-4244


|
|
| |
| |
 |
 |
|
GlucoBalance
180 Capsules -
$34.01 plus tax
-
Formulated for
Biotics Research by Jonathan V. Wright, M.D. and
Alan R. Gaby, M.D., leaders in the field of
nutritional science.
-
Wide clinical use
in the U.S.A. 1000 mcg chromium (as aspartate).
Chromium is essential for glucose metabolism.
-
Contains both
Niacin, a vital component of GTF (Glucose
Tolerance Factor) and Niacinamide, necessary for
producing NAD (Nicotinamide Adenine Dinucleotide)
in insulin secreting pancreatic B cells.
-
Formulated with a
uniquely high amount of biotin - 3000 mcg.
Biotin is essential for glucose phosphorylation
by hepatic glucokinase, the first step in
glucose utilization
Effective
regulation of blood glucose has important
implications for health. Even mild disruptions
of glucose homeostasis can have adverse
consequences. Chronic diabetes may result in
cardiovascular disease, neuropathy, blindness,
or renal failure. Hypoglycemia (also called
reactive hypoglycemia or dysinsulinism), though
not general associated with the organ damage
seen in diabetes, can be responsible for a
number of troublesome physical and psychological
symptoms.
-
The human body
possesses a complex set of checks and balances
to maintain blood glucose concentrations within
a narrow range. Blood sugar control is
influenced by the pituitary, thyroid, and
adrenal glands, as well as by the pancreas,
liver, kidney, and even skeletal muscle.
-
Glucose
homeostasis also depends on the presence of a
wide range of micronutrients. In the typical
American diet, high in refined and processed
foods, many of these micronutrients are in short
supply. In addition, some individuals with blood
sugar disorders may have a special dietary need
for higher amounts of one or more
micronutrients.
RECOMMENDATION: Two (2) capsules, three (3)
times per day.
Warning: If you are taking diabetes medication,
do not use GlucoBalance without professional
supervision.
|
Function and
Contents
GlucoBalance contains
all of the nutrients that are essential for proper
glucose metabolism.
Serving Size 6 Capsules Amount % Daily
-
Vitamin A (as
retinyl acetate) 5000 IU 100%
-
Vitamin C (as
calcium ascorbate and ascorbic acid) 500 mg 833%
-
Vitamin D (as
cholecalciferol) 100 IU 25%
-
Vitamin E (as
d-alpha tocopheryl acetate) 400 IU 1333%
-
Thiamin (B1) (as
thiamin mononitrate) 50 mg 3333%
-
Vitamin (B2) (as
riboflavin) 25 mg 1470%
-
Niacin (as
niacinamide and niacin) 150 mg 750%
-
Vitamin B6 (as
pyridoxine hydrochloride) 30 mg 1500%
-
Folic Acid 800
mcg 200%
-
Vitamin B12 (as
cobalamin) 50 mcg 833%
-
Biotin 3000 mcg
1000%
-
Pantothenic Acid
(as calcium pantothenate) 100 mg 1000%
-
Calcium (as
ascorbate, citrate and carbonate) 200 mg 20%
-
Magnesium (as
aspartate, citrate and oxide) 400 mg 100%
-
Zinc (as zinc
picolinate and zinc citrate) 30 mg 200%
-
Selenium (as
selenomethionine) 150 mcg 214%
-
Copper (as copper
gluconate) 2 mg 100%
-
Manganese (as
manganese aspartate) 20 mg 1000%
-
Chromium (as
chromium aspartate) 1000 mcg 833%
-
Potassium (as
potassium aspartate) 99 mg 3%
-
Vanadium
(as vanadium aspartate) 20 mcg *
These statements have not been evaluated by the US
Food and Drug Administration. This product is not
claimed to diagnose, treat, cure, or prevent any
disease.
|
|
Research and
additional information:
The following
nutrients are particularly important when
considering blood sugar disorders:
Chromium
The effect of chromium on glucose metabolism
apparently requires its conversion to glucose
tolerance factor (GTF), a low-molecular-weight
compound that contains chromium, niacin (nicotinic
acid), glycine, glutamic acid, and cysteine. GTF,
has been shown to potentiate the action of insulin
at the cellular level. (1,4)
Tissue chromium levels were found to decline with
age in Americans. (2) In other studies, including
one by the U.S. Department of Agriculture, more than
50% of people consumed less than the lower level of
chromium recommended by the National Academy of
Sciences, Nutritional Research Council. (3, 37)
Chromium aspartate is a well-utilized form of
supplemental chromium being solubilized at a wide
range of ph. The amounts of chromium used in most
clinical trials (*150 to 200 ug/day) are apparently
inadequate for some patients, even when more
efficient Chromium compounds are used. Larger
amounts of chromium, such as 500 to 1,000 ug/day,
have often had a greater benefit. (4)
Niacin and
Niacinamide
As a component of glucose tolerance factor, niacin
plays an important role in carbohydrate metabolism.
Many refined foods consumed by Americans are
depleted of niacin. Grains and other foods that are
“enriched” usually contain added niacinamide, which
apparently cannot be converted by the human body
into niacin. In addition, many vitamin supplements
contain niacinamide, rather than niacin. Although
niacinamide is capable of performing most of the
functions of vitamin B3, a small amount of niacin
seems to be necessary for the synthesis of GTF. (5)
Both niacin and niacinamide may also be important
for blood sugar control through a mechanism
unrelated to GTF. As precursors to NAD, which is an
important metabolite concerned with intracellular
energy production, niacin and niacinamide may
prevent the depletion of NAD in pancreatic B cells.
Biotin
The initial step in glucose utilization by the cell
is its phosphorylation, mediated by the
biotin-dependent enzyme hepatic glucokinase. Thus
adequate biotin intake is required to initiate
intracellular glucose into the cell. (6)
Biotin may also play a role in stabilizing blood
sugar levels through biotin-dependent enzymes acetyl
Co A carboxylase and pyruvate
carboxylase. (37) Thus biotin deficiency should be
avoided in those
with blood sugar disorders.
Pyridoxine (vitamin B6)
Serum vitamin B6 levels were below normal in 25% of
518 diabetics. (7) Particularly where peripheral
neuropathy is present, the inadequate B6 intake
should be contemplated.(8)
Copper
Because the typical American diet contains only
about half of the RDA (2 mg/day) for copper (9,36),
deficiency of this mineral may be common. Copper is
involved with insulin binding, and copper deficiency
in mammals may be reflected in increased
glucosylated hemoglobin, indicative of chronically
raised blood sugar levels. (10)
Magnesium
The American diet is often low in magnesium. Dietary
surveys have
shown that 80-85% of American women consume less
than the RDA for the mineral. (11) Daily magnesium
intake in two other studies was only about
two-thirds of the RDA. (12,13,36) This may be
particularly relevant in diabetics, where magnesium
deficiency is thought to play a role in the
development of insulin resistance. (14) Serum
magnesium has been found to be significantly lower
in many diabetics (15), therefore, it is reasonable
to make sure that diabetics have adequate dietary
intake of magnesium. Low magnesium levels may also
be associated with hypoglycemia. (16)
Zinc
Zinc is involved both with insulin synthesis by
pancreatic B cells (17) and insulin binding to liver
and adipose tissue cells. (18,19) People with zinc
deficiency may have significantly higher glucose
levels and lower insulin levels than similar
patients without zinc deficiency. (20)
Vitamin C (ascorbic acid)
Ascorbic acid levels may be lower in diabetics than
controls (22) and patients with inadequate ascorbic
acid levels may be found to have abnormal blood
sugar curves. (23) In addition, ascorbic acid may
compete with glucose for transport across cell
membranes, (24) so that in hyperglycemia, ascorbic
acid transport into the cell may be inhibited. (25)
Ascorbic acid deficiency may allow sorbitol to
accumulate in
erythrocytes, which may pre-dispose diabetics to
certain types of end-organ damage. (26) Care should
be taken to ensure that those with blood sugar
abnormalities have adequate ascorbic acid intake.
Manganese
Manganese is a cofactor for certain enzymes involved
in the inter-mediary metabolism of carbohydrates. In
addition, the concentration of manganese in the
pancreas is approximately ten times higher than in
other organs. (27)
The optimal intake of manganese is not known but at
least half of the manganese is lost when whole
grains are replaced by refined flour. (29) The
American diet may be low in manganese. (36)
Both B12 and folate are involved in a number of
different steps in
carbohydrate metabolism and the incidence of B12
deficiency was
significantly greater in a series of diabetics than
in the general
population. (30) Folate is involved with
gluconeogenesis as a cofactor with key enzymes in
the liver and small intestine. (31) Deficiency of
either B12 or folate is to be avoided in those with
blood sugar abnormalities.
Vitamin B1 (thiamin)
Central to carbohydrate metabolism and Krebs Cycle
function is
adequate thiamin levels, and diabetics are more
often deficient in
thiamin. (32) Care should be taken to ensure that
thiamin intake is adequate in those with diabetes
and hypoglycemia.
Carnitine
Carnitine is involved as part of a vital transport
mechanism of fat metabolism in which fat enters
energy production pathway. Carnitine supplementation
may be considered in those with blood sugar
abnormalities.
Vanadium
Vanadate is an oxidized form of vanadium. Due to
possible insulinotropic effects of vanadate (33),
inadequate amounts of this trace mineral is
undesirable in those with blood sugar abnormalities.
Vitamin E and Selenium
Vitamin E and selenium are essential nutritional
factors which act as antioxidants and may be
involved in glucose balance. (34, 35) As many
complications associated with diabetes may be
related to excess free radical activity, prudence
demands that adequate selenium and vitamin E be
supplied in the diabetic diet.
References:
- Toepfer EW, Mertz W. Polansky MM, Roginski EE,
Wolf WR. Preparation of chromium-containing
material of glucose tolerance factor activity
from brewer’s yeast extracts and by synthesis. J
Agric Food Chem 1977;25:162-166.
- Schroeder HA,
Nason AP, Tipton IH. Chromium deficiency as a
factor in atherosclerosis. J Chronic Dis
1970;23:123-142.
- Anderson RA,
Kozlovsky AS. Chromium intake, absorption and
excretion of subjects consuming self-selected
diets. Am J Clin Nutri 1985;41:1177-1183.
- Glinsmann WH,
Mertz W. Effect of trivalent chromium on glucose
tolerance. Metabolism 1966;15:510-502.
- Urberg, M.
Zemel MB. Evidence for synergism between
chromium and nicotinic acid in the control of
glucose tolerance in elderly humans. Metabolism
1987;36:896-899.
- Anonymous.
Biotin and glucokinase in the diabetic rat. Nutr.
Rev 1970;28:242-244.
- Davis RE,
Calder JS, Curnow DH. Serum pyridoxal and folate
concentrations in diabetics. Pathology
1976;8:151-156.
- Jone CL,
Gonzalex V. Pyridoxine deficiency: a new factor
in diabetic neuropathy. J. Am Podiatry Assoc
1978;68:646-653.
- Wolf WR,
Holden J, Greene FE. Daily intake of zinc and
copper from self selected diets. Fed Proc
1977;36:1175.
- Klevay LM,
Canfiedl WK, Gallagher SK, Henrickson LK,
Bolonchuk W, et al. Diminished glucose tolerance
in two men due to a diet low in ic acid in the
control of glucose tolerance in elderly humans.
Metabolism 1987;36:896-899.
- Morgan KJ,
Stampley GL, Zabik ME, Fischer DR. Magnesium and
calcium dietary intakes of the Ul.S. population.
J Am Coll Nutr 1985;4:195-206.
- Lakshmanan
FL, Rao RB, Kim WW, Kelsay JL. Magnesium
intakes, balances and blood levels of adults
consuming self-selected diets. Am J Clin Nutri
1984;40:1380-1389.
- Srivastava
US, Nadeau MH, Gueneau L. Mineral intakes of
university students; magnesium content. Nutr Rep
Int 1978;18:235-242.
- Yajnik CS,
Smith RF, Hockaday TDR, Ward NI. Fasting plasma
magnesium concentrations and glucose disposal in
diabetes. Br Med J 1984;288:1027-1028.
- Ceriello A, Guigliano D, Dello Russo P,
Passariello N. Hypomagnesemia in relation to
diabetic retinopathy. Diabetes Care
1982;5:558-559.
|
|
Additional
references: |
A scientific review: the role
of chromium in insulin resistance.
Diabetes Educ. 2004;Suppl:2-14.
Cheng HH, Lai
MH, Hou WC, Huang CL.J
Antioxidant effects of chromium supplementation
with type 2 diabetes mellitus and euglycemic
subjects. J Agric Food Chem. 2004 Mar
10;52(5):1385-9
Fox CH,
Ramsoomair D, Mahoney MC, Carter C, Young B,
Graham R.
An investigation of hypomagnesemia among
ambulatory urban African Americans. J Fam
Pract. 1999 Aug;48(8):636-9
Shamberger RJ.
Calcium, magnesium, and other elements in the
red blood cells and hair of normals and patients
with premenstrual syndrome. Biol Trace Elem
Res. 2003 Aug;94(2):123-9
Iketani T,
Kiriike N, Murray, Stein B, Nagao K, Nagata T,
Minamikawa N, Shidao A, Fukuhara H.
Effect of menatetrenone (vitamin K2) treatment
on bone loss in patients with anorexia nervosa.
Psychiatry Res. 2003 Mar 25;117(3):259-69
McLean RR,
Jacques PF, Selhub J, Tucker KL, Samelson EJ,
Broe KE, Hannan MT, Cupples LA, Kiel DP.
Homocysteine as a predictive factor for hip
fracture in older persons. N Engl J Med.
2004 May 13;350(20):2042-9
Eisinger J,
Clairet D.
Effects of silicon, fluoride, etidronate and
magnesium on bone mineral density: a
retrospective study. Magnes Res. 1993
Sep;6(3):247-9
Schiano A,
Eisinger F, Detolle P, Laponche AM, Brisou B,
Eisinger J. [Silicon,
bone tissue and immunity] [Article in French]
Rev Rhum Mal Osteoartic. 1979
Jul-Sep;46(7-9):483-6
Schaafsma A,
de Vries PJ, Saris WH.
Delay of natural bone loss by higher intakes of
specific minerals and vitamins. Crit Rev
Food Sci Nutr. 2001 May;41(4):225-49
Volpe SL,
Taper LJ, Meacham S.
The relationship between boron and magnesium
status and bone mineral density in the human: a
review. Magnes Res. 1993 Sep;6(3):291-6
Nielsen FH.
Studies on the relationship between boron and
magnesium which possibly affects the formation
and maintenance of bones. Magnes Trace Elem.
1990;9(2):61-9
Fletcher RH,
Fairfield KM.
Vitamins for chronic disease prevention in
adults: clinical applications. JAMA.
2002 Jun 19; 287(23): 3127-9
Ames BN,
Elson-Schwab I, Silver EA.
High-dose vitamin therapy stimulates variant
enzymes with decreased coenzyme binding affinity
(increased K(m)): relevance to genetic disease
and polymorphisms. Am J Clin Nutr. 2002
Apr;75(4):616-58
FULL-TEXT

|
|
|
|
 |
 |
 |
 |
 |
|
|
| |
home |
new patient |
massage therapy |
great stuff |
case
studies | laser therapy |
products | links
search | directions |
about us |
contact |
privacy
Dr. Darryl Roundy
‡ Copyright ©1996-2008
‡ All Rights Reserved
‡ Updated
08/05/2008
|
|
|
|