Product
Details
Integrated
Heart Health
Body Support™ Q-Plus™ dietary supplement
provides a generous serving of heart-healthy compounds—L-carnitine,
coenzyme Q10 (Co-Q10), and lecithin. L-carnitine and Co-Q10 are
natural substances found in all cells of the body and play an
important role in energy production. Both work in the mitochondria
of cells, the portion of a cell most actively dedicated to producing
cellular energy. More Co-Q10 and L-carnitine are found in the heart
tissue than in any other muscle while lecithin plays an important
role in cholesterol metabolism in the body. In addition, Co-Q10 is a
potent antioxidant. Q-Plus utilizes Eniva’s proprietary aqueous
delivery system to provide superior bio-availablity for maximum
effectiveness.*
|
Q-Plus Helps
to Support
|
| ·
Cardiovascular Health* |
| ·
Antioxidative Bioenergetic Balance* |
| ·
Energy Production* |
| ·
Fatty Acid Mitochondrial Transport* |
| ·
Immune Support* |
| ·
Oral Health* |
| ·
Mental and Nervous System Health* |
| ·
Transportation and Metabolism of Fats* |
|
Supplement Facts
|
| Serving
Size: 1 tbsp Servings Per
Container: 32 |
| |
Amount
Per
Serving
|
%
Daily
Value
|
|
Vitamin
C
|
15 mg
|
25
|
| Coenzyme
Q10 |
100 mg
|
†
|
| L-carnitine |
300 mg
|
†
|
| Lecithin |
500 mg
|
† |
† Daily Value not established.
Other
Ingredients: Purified Water, Sorbimacrogol, Glycerine,
Natural/Artificial Flavor, Stevia Leaf Extract, Ascorbic
Acid, Sorbic Acid (naturally preserves freshness), Sodium
Benzoate, (sodium salt of naturally occurring benzoic
acid).
As a dietary supplement:
Adults: 1 Tablespoon
It is recommended that before starting any new
supplementation program, you first consult your health
care professional.
Shake well before using.
Refrigerate after opening.
No sugars, artificial colors, or stimulants.
Do not use if tamper evident seal is either broken or
missing.
Keep
out of the reach of children.
|
Promoting
a Healthy Heart
Let’s face it, to stay alive our hearts need to beat 24 hours a
day, 7 days a week, 52 weeks a year. When you think about it,
maintaining a healthy heart and cardiovascular system is a lifelong
endeavor for all of us. Ideally, the quest for cardiovascular health
should include eating a healthy diet, exercising regularly, and
protecting our hearts with a variety of nutritional supplements.
Q-Plus is a generous blend of natural substances designed to promote
cardiovascular health.* Its contents - coenzyme Q10, L-carnitine,
and lecithin - have been specifically chosen for their demonstrated
and researched benefits.
How
Q-Plus Works
Q-Plus is a 100% vegetarian, liquid supplement formulated with a
lipid-soluble delivery system to provide superior bio-availability
for maximum absorption.
Co-Q10
Co-Q10 is a naturally occurring nutrient in each cell. It plays a
key role in the production of energy in the body and is also an
excellent antioxidant.* Co-Q10 is synthesized endogenously within
the body and distributed to bodily tissues where it is needed.
Within the body, it is located mostly in the skeletal and cardiac
muscle tissue, liver, kidney, brain, and reproductive organs—all
areas of high physiological activity.
Co-Q10 resides within the mitochondria of cells, where
life-sustaining, energy-producing processes take place. In the
mitochondria, the "power plants" of the cell, a series of
complex biochemical reactions take place. Co-Q10 is a vital
component of this energy-generating process at the cellular level;
it is a true coenzyme.
The body must continually generate energy within these minute,
cellular power plants, to support life. Hence, the presence of
Co-Q10 in the body is fundamental to sustaining life. The
relationship of Co-Q10 to the intricate mechanism of cellular energy
production brings about broader understanding of why Co-Q10
deficiencies may lead to serious malfunction of biochemical systems.
Deficiencies of Co-Q10, with respect to cardiovascular function,
have been documented since the 1970s. It is easy to grasp the
concept of altered heart function as a consequence of chronic Co-Q10
deficiency. The heart muscle is in constant need of an energy supply
to pump blood throughout the body. Muscle tissue, abundant in
mitochondria, is extremely vulnerable to Co-Q10 concentration. It
cannot perform without the energy-producing machinery intact.
Multiple double-blind clinical trials using Co-Q10 for
cardiovascular function have been performed.
As the body ages, its CoQ10 levels may drop and
its ability to absorb CoQ10 from food also decreases. Researchers
now recommend that even if older adults eat foods high in CoQ10,
like spinach, eggs and fish, they should still supplement with a
high quality CoQ10 product-one preferably in a body-ready design,
like Eniva's Q-Plus. Researcher's also note that for a "happy
heart," a minimum of 75 milligrams should be taken daily. Even
those who are younger can benefit with CoQ10-from heart concerns to
renewed energy and vitality-everyone wins with regular use of CoQ10.
L-Carnitine
Among the most important of the supplements for maintaining a
healthy heart and cardiovascular system is L-carnitine.* Although we
are more familiar with L-carnitine as a safe and effective dietary
supplement for enhancing exercise performance and managing weight,
the scientific evidence that supports the beneficial role of L-carnitine
in cardiovascular well-being is so compelling that L-carnitine was
originally used as a prescription drug for the heart.*
L-carnitine is a naturally occurring vitamin-like nutrient that
plays an essential role in fat metabolism and energy production.*
This nutrient is naturally produced and stored within our bodies,
particularly in the skeletal and heart muscle, and is also a
component of our diets, mainly in foods of animal origin. The
metabolic function of L-carnitine is to transport fatty acids into
the mitochondria, the energy-producing organelles within our cells.
Inside the mitochondria, the fatty acids are burned and cellular
energy is produced.
Since L-carnitine is an essential component of the fat-burning
process, it is a critical nutrient for the heart, because cardiac
muscle obtains an amazing 70 percent of all its energy requirements
from the burning of fatty acids. Thus, it is not surprising that a
high concentration of L-carnitine is found in cardiac muscle and
that L-carnitine is considered to be vital for the proper mechanical
functioning of the heart.
Studies on the beneficial effects of L-carnitine on the
cardiovascular system began as early as 1937. L-carnitine benefits
the cardiovascular system in several ways. First, it is responsible
for clearing fatty acids (triglycerides) out of the blood and
transporting them into the mitochondria to be broken down.
Therefore, heart muscles are particularly vulnerable to L-carnitine
deficiency.
Lecithin
Lecithin is a lipid that is required by every cell in your body. The
cell membranes in the body are composed largely of lecithin. These
membranes handle the flow of nutrients in and out of the cell. The
protective sheaths around your brain are also made of lecithin. In
addition, muscles and nerve cells use lecithin.
Lecithin has an important role in the metabolism of dietary fats. It
aids in the transport and metabolism of dietary lipids.* Thus,
lecithin helps promote cardiovascular health.*
All
Natural Supplement
The all-natural state of this supplement also makes it unique.
Q-Plus attributes:
- No Fructose or Sugars
- No Artificial Colors or Flavorings
- No Calories or Caffeine
- No Animal By-products or Animal Testing
| *
This statement has not been evaluated by the Food and Drug
Administration. This product is not intended to diagnose,
treat, cure, or prevent any disease. |
Scientific
Reference
Bertilli, A. , Ronca, G. Carnitine and Coenzyme Q: Biochemical
Properties and Functions, Synergism and Complementary Action. Int
Jour Tiss Reac., 12 (3): 183-186, 1990.
Bliznakov, Emile G., Coenzyme Q, the Immune System and Aging.
Biomedical and Clinical Aspects of Coenzyme Q, 3: 311-323, 1981.
Conte, A. et al., Protection of Adenylate Pool and Energy Charge by
L-Carnitine and Coenzyme Q during Tissue Reac.,12(3): 187-191, 1990.
Folkers, Karl et al., Activities of Vitamin Q10 in Animal Models and
a Serious Deficiency in Patients with Cancer. Biochem. Biophys. Res.
Comm., 234(2): 296-299, 1997.
Folkers, Karl, Relationships between Coenzyme Q and Vitamin E. AJCN,
27: 1026-1034, 1974.
Folkers, Karl et al., A One Year Bioavailability Study of Coenzyme
Q10 with 3 Months Withdrawal Period. Molec. Aspects Med., 15:
S281-S285, 1994.
Folkers, Karl et al., Biochemical Deficiencies of Coenzyme Q10 in
HIV-Infection and Exploratory Treatment. Austin, Texas, 1988.
Folkers, Karl, Relevance of the Biosynthesis of Coenzyme Q10 and of
the Four Bases of DNA as a Rationale for the Molecular Causes of
Cancer and a Therapy. Biochem. Biophys. Res. Comm., 224: 358-361,
1996.
Folkers, Karl and Simonsen, Rodney, Two Successful Double-blind
Trials with Coenzyme Q10 (Vitamin Q10) on Muscular Dystrophies and
Neurogenic Atrophies. Biochimicha et Biophysica Acta, 1271: 281-286,
1995.
Folkers, K., and Langsjoen, Per H. et al., Pronounced Increase of
Survival of Patients with Cardiomyopathy when Treated with Coenzyme
Q10 and Conventional Therapy. Int. J. Tiss. Reac., 12(3):163-168,
1990.
Hogenauer, G. et al., The Macrophage Activating Potential of
Ubiquinones. Energy Depletion in Rat Heart Slices. Int. J.
Biomedical and Clinical Aspects of Coenzyme Q, 3: 325-334, 1981.
Iwamoto, Y., Folkers, K., Deficiency of Co-Q10 in Hypertensive Rats
and Reduction of Deficiency by Treatment with Coenzyme Q10. Biochem
Biophys Res Comm v58 n3: 743-748, 1974.
Judy, W.V. et al., Regression of Prostate Cancer and Plasma Specific
Antigens (PSA) in Patients on Treatment with Co-Q10. Conference of
the International Coenzyme Q10 Association, Abstr 143, 1998.
Judy, W.V. et al., Dose Related Effectiveness of Coenzyme Q10 in the
Treatment of Chronic Fatigue. Conference of the International
Coenzyme Q10 Association, Abstr 86, 1998.
Kaikkonen, Jari et al., Effect of Oral Coenzyme Q10 Supplementation
on the Oxidation and Resistance of Human VLDL+LDL Fraction:
Absorption and Antioxidative Properties of Oil and Granule-Based
Preparations. Free Radical Biology & Medicine, 22(7): 1195-1202,
1997.
Kamikawa, Tadashi et al., Effects of Coenzyme Q10 on Exercise
Tolerance in Chronic Stable Angina Pectoris. Am. J. Cardiol., 56(4):
247-251, 1985.
Langsjoen, Per H. et al., A Six-Year Clinical Study of Therapy of
Cardiomyopathy with Coenzyme Q10. Int. J. Tiss. Reac., 12(3):
169-171, 1990.
Manzoli, U. et al., Coenzyme Q10 in Dilated Cardiomyopathy. Int. J.
Tiss. Reac., 12(3): 173-178, 1990.
Morisco, C. et al., Effect of Coenzyme Q10 Therapy in Patients with
Congestive Heart Failure: A Long-term Multicenter Randomized Study.
Clin. Invest., 71: S134-S136, 1993.
Poggesi, Loredana et al., Effect of Coenzyme Q10 on Left Ventricular
Function in Patients with Dilative Cardiomyopathy. Current
Therapeutic Research, 49(5): 878-886, 1991.
Ronca, G., Conte A. et al., Synergic and Complementary Effects of L-Carnitine
and Coenzyme Q on Long-Chain Fatty Acid Metabolism and on Protection
against Anthracycline Damage. Int. J. Tiss. Reac., 12(3):197-201,
1990.
Scaglione, F. et al., Coenzyme Q10 as an Immunoenhancer. A Single
Blind Placebo-Controlled and Randomized Clinical Study. Conference
of the International Coenzyme Q10 Association, Abstr 89, 1998.
Shults, Clifford W. et al., Absorption, Tolerability, and Effect on
Mitochondrial Activity of Oral Coenzyme Q10 in Parkinson's Patients.
Neurology, 50(3): 793-795, 1998.
Shults, Clifford W., Haas, Richard H. et al., A Possible Role of
CoEnzyme Q10 in the Etiology and Treatment of Parkinson's Disease.
Conference of the International Coenzyme Q10 Association, Abstr 54,
1998.
Stocker, Roland et al., Cosupplementation with Coenzyme Q Prevents
the Prooxidant Effect of (-Tocopherol and Increases the Resistance
of LDL to Transition Metal-Dependent Oxidation Initiation.
Arteriosclerosis, Thrombosis, and Vascular Biology, 16(5): 687-696,
1996.
Stocker, Roland et al., Ubiquinol-10 Protects Human Low Density
Lipoprotein more Efficiently against Lipid Peroxidation than does -Tocopherol.
Proc. Natl. Acad. Sci., 88: 1646-1650, 1991.
Syburra, C.A. Oxidative Stress in Patients with Multiple Sclerosis.
Conference of the International Coenzyme Co-Q10 Association, Abstr
125, 1998.
Wahlqvist, M.L. et al., Bioavailability of Two Different
Formulations of Coenzyme Q10 in Healthy Subjects. Asia Pacific J
Clin Nutr, 7(1): 37-40, 1998.
Weber, Christine et al., Intestinal Absorption of Coenzyme Q10
Administered in a Meal or as Capsules to Healthy Subjects. Nutrition
Research, 17(6): 941-945, 1997.
Weis, M. et al., Bioavailability of Four Oral Coenzyme Q10
Formulations in Healthy Volunteers. Molec. Aspects Med., 15:
S273-S280, 1994. Wilkinson, Edward G. et al., Bioenergetics in
Clinical Medicine II. Adjunctive Treatment with Coenzyme Q in
Periodontal Therapy. Research Communications in Chemical Pathology
and Pharmacology, 12(1): 111-124, 1975.
Williams, K.D., Manueke, J.D. et al., 52-Week Oral Gavage Chronic
Toxicity Study with Ubiquinone in Rats with a 4-Week Recovery.
Conference of the International Coenzyme Q10 Association, Abstr 73,
1998.
|