View CartMy Account / Order StatusHelp

Join our mailing list.


McAfee Secure sites help keep you safe from identity theft, credit card fraud, spyware, spam, viruses and online scams






 
 Click Here!
(Your shopping cart is empty)

  Home > Supplements >

  DHLA Nano-Plex with RESVERATROL, Premier Research Labs, 8 fl oz
  PRL-109
 
Our Price: CAD $154.99
Sale Price: CAD $147.00
You Save CAD $7.99


Stock Status: In Stock
Product Code: PRL-109
Qty:


Description
 

DHLA Nano-Plex (with Resveratrol) - 8oz


For the first time in history, Premier Research Labs have developed a stable, fully reduced form of lipoic acid (DHLA) derived from "once-living" sources and the not typical synthetic sources.  Now you can obtain the tremendous amounts of exquisitely bio-available DHLA, fully active and intracellularly potent.  DHLA Nano-Plex is vastly superior to alpha-lipoic acid (ALA) or R-lipoic acid in free radical reducing capacity.  Thus  DHLA Nano-Plex can deliver more comprehensive reduction of oxidative stress for literally every organ and gland, especially the brain and the nervous system.  For example, DHLA can reduce the superoxide anion free radical and the peroxyl radical whereas ALA and R-lipoic acid cannot.  In Premier Research Lab's patent-pending process,  DHLA Nano-Plex is produced by 12 strains of beneficial probiotic organisms that are micro-digested into particle sizes so tiny they become exceptionally bio-available.  Just ¼ teaspoon provides 50 mg of DHLA, 36 mg of R-lipoic and 5 mg of Resveratrol.  There is no other direct DHLA supplement available in the world!  The closest you might come is a product with 50 mg of alpha-lipoic or R-lipoic acid which usually derived from synthetic sources.*

Also available in 2oz size

DHLA Nano-Plex

Recommended Use:  ¼ teaspoon in water/juice 1-2 times/day. Shake gently before use.  
Container Size:  2 or 8 ounces
Ingredients: Proprietary blend 1.25ml - Stabilized DHLA (80mg), S-Lipoic Acid, Tumeric (rhizome), Bifidobbacterium Species, Enterococcus Species, Lactobacillus Species, Streptcoccus therm.
Other Ingredients:  Purified water, certified organic alcohol



* These statements have not been evaluated by the Food and Drug Administration.  This health product is not intended to diagnose, treat, cure or prevent disease. 


DHLA: The Spectacular Antioxidant

DHLA (dihydrolipoic acid) is unique as an antioxidant due to its spectacular effectiveness in quenching every known free radical that occurs in living tissue, including both fat and water soluble tissues.  No other antioxidant has this incredible capability.  DHLA is readily absorbed orally and has very low toxicity.  It has unequalled potential as a highly effective therapeutic agent in clinical conditions associated with free radical damage such as Parkinson's disease, Alzheimer's disease and other neurodegenerative illnesses. (1)

Until 2003, DHLA in a stabilized form was not available.  DHLA could only be obtained indirectly through consuming ALA (alpha lipoic acid) which in turn, was converted by the body into small amounts of DHLA.  However, this process did not deliver a significant or reliable supply of DHLA.  Research studies have attempted to measure the effect of DHLA on cellular tissue using indirect methods based on ALA consumption.  As a result, DHLA is known to be a powerful electron donor to other compounds.  Ascorbic acid and indirectly vitamin E are regenerated by DHLA. (2)  Busse et. al. found that the oxidized form of DHLA, ALA, increased intracellular glutathione. (3)  DHLA was shown to regenerate coenzyme QIO, glutathione and NADPH or NADH and by this mechanism, increase cellular ATP production.(4)  The oxidized form of DHLA, ALA, also assists in the conversion of pyruvate to acetyl-coenzyme A, the beginning point of the Krebs cycle which produces the high energy molecule ATP.


Radical Synthetic vs. "Once Living" Sources

ALA, R-lipoic acid or DHLA that are derived from synthetic sources can never match natural source counterparts in the ability to sustain and repair the DNA of the cell.  A natural ("once living") source is comprised of dynamic, complex processes where each molecule contains atoms that generate photons, or in other words, pure light.  The photonic field around each molecule creates a "body of light" which surrounds all living substances.  Only nutrients derived from a "once living" source are capable of upgrading cellular DNA, according to quantum physics researcher and expert, Dr. Fritz-Albert Popp. (33)

On the other hand, synthetic source nutrients may provide initial cellular benefits, but over time, they act to accelerate the degeneration of DNA, ending in earlier cell death.  Synthetic nutrients initially stimulate the cell to accomplish work which may appear to be beneficial, but long-term, the DNA and cellular degradation cannot justify the initial benefits.  Consequently, using ALA derived from a synthetic source can defeat the purpose of using an ALA supplement to live longer more healthfully.  Not only has a stable form of DHLA been badly needed, but also a DHLA source that has been derived from a "once living" source so it is capable of imparting significant, long-term DNA protection and cellular benefits.


Benefits of Alpha Lipoic Acid

Many research studies show the spectacular benefits from the use of ALA, even ALA derived from synthetic sources.  Although these studies demonstrate many, short-term benefits of synthetic ALA, they do not test for or warn against the long-term problems encountered in consuming synthetically derived agents.

Unfortunately, most research studies using ALA have used the synthetic form which contains equal amounts of the R and the S racemic forms. The S form occurs only in synthetic source ALA, never in naturally-derived ALA, and has negative, pro-inflammatory effects.  In an attempt to enhance the effectiveness of synthetic ALA, some manufacturers have chemically removed the S-form, thus producing a new form, stand alone R-lipoic acid.  Because synthetically derived ALA contains both R and S forms, studies show that synthetic R-lipoic acid alone is superior to ALA (which contains both R and S forms).  However, new research since the year 2000 has shown the S-form of lipoic acid (which has pro-inflammatory effects) may well be the cause of this pro-oxidant study finding (rather than as an effect of DHLA).


Benefits of Stabilized DHLA

The above clinical research studies using synthetically-derived ALA had obviously spectacular physiological benefits. However, as has been emphasized earlier, these benefits are not without a price to pay, namely, the eventual degradation of the cellular DNA which occurs during long-term use of synthetic compounds.

Advantages of Natural-Source DHLA

Stabilized DHLA (natural-source) may prove to be one of the most significant antioxidant compounds ever created, since it can accomplish all the feats attributed to ALA and more, but without ALA's negative effects. In fact, some authors believe that the benefits ascribed to ALA are in fact, actually due to the internal generation of DHLA (after ALA consumption). For the very first time, stabilized DHLA is now available that can offer significant and reliable amounts of DHLA, without the need to consume synthetic precursors.


DNA and Nerve Protection

Stabilized DHLA can provide exquisite neuroprotection as well as superior DNA protection and repair, unmatchable by any other antioxidant. Studies show that DHLA increases cellular energy and efficiency by increasing ATP. At the same time, DHLA helps regenerate the production of vitamin E, CoQIO, glutathione, NADH and NADPH to provide unparalleled DNA protection. In addition, DHLA has the capacity to induce repair of DNA strand breaks.7 For long-term benefits of DHLA, only natural-source DHLA is recommended to avoid the long-term degradation of DNA from synthetically-derived sources.


Arterial and Heart Protection

Research has shown that DHLA can accelerate recovery of the aortic blood flow during reperfusion (resumption of blood flow) and increase ATP synthesis in the rat heart.27 ALA forms were not helpful only internally generated DHLA was able to reduce the infarct or necrotic tissue size in middle cerebral artery occlusion in mice.28 Wolz et. al. believe ALA must be reduced to the DHLA form in order to provide neuroprotection.29 Natural-source, stabilized DHLA (now available) can provide exquisite neuroprotection as well as superior DNA repair and protection without compromise.


DHLA: Safety and Effectiveness

Clinical research by Dr. Robert J. Marshall has shown that the newly available natural-source, stabilized DHLA is both safe and effective for general use, including those with chronic illness and neurodegenerative disease. If high dosages (over 300 mg/day) of stabilized DHLA are used, to get maximum benefits the concurrent use of additional nutrients such as nutritional yeast which contains natural-source B vitamins, sulphur-based amino acids and reduced glutathione, is an excellent adjunct.


Brief Clinical Observations

The discoverer and inventor of stabilized DHLA, Dr. Marshall, has observed various immediate, spectacular effects of oral administration of stabilized DHLA in his office.

One 44-year woman presented with a history of bilateral, maxillary sinus infection with extreme pain even to the touch. She had used oral antiobiotics for more than a year with no relief and was unable to breathe through her sinuses for at least 10 months. Further, she had begun to experience pain at her liver, chronic fatigue, loose stool and severe brain fog. After only one dose (30 drops) of natural-source, stabilized DHLA, within less than one minute, she remarked, "I can breathe through my nose! My head feels clear for the first time in 10 months."

A 60 year-old male complaining of brain fog, diminished short-term memory and a general sense of malaise remarked that within one day of taking natural-source, stablilized DHLA, literally all his symptoms were gone. He had a renewed sense of mental acuity and a significant improvement in short-term memory.

A medical doctor has remarked that in many clinical cases, natural-source, stabilized DHLA reduced the amount of time and number of nutritional supplements needed to restore healthy nerve function in his patients. It has become one of his most used supplement "aces", especially in neurodegenerative cases.

References

1. Packer L, Witt EH, Tritschler HJ. Alpha-lipoic acid as biological antioxidant. Free RadBiolMed 1995;19:227-250.

2. Scholich H, Murphy ME, Sies H. Antioxidant activity of dihydrolipoatc against microsomal lipid peroxidation and its dependence on a-locophcro}. Biochem Biophys Acta 1989; 1001:256-261.

3. Busse E, Zimmer G, Schopohl B, etal. Influence of alpha-lipoic acid on intracellular glutathione in vitro and in vivo. Arzneimittel-Forschung 1992:42:829-831.

4. Kagan v, Serbinova E, Parker L. Antioxidant effects of ubiquinones in microsomes and mitochondria are mediated by locopherol recycling. Biochem Biophys Res Comm 1990; 169:85 1-857.

5. Passwaier RA. Lipoic Acid: The Metabolic Antioxidant. New Canaan, CT: Keats Publishing, Inc; 1995: 1-47.

6. Scott BC, Arouma OI, Evans PJ, et al. Lipoic and dihydrolipoic acid as antioxidants: a critical evaluation. Free Rad Res 1994;20;119-133.

7. Suzuki Yj, Tsuchiya M, Packer L. Thioctic acid and dihydrolipoic acid are novel antioxidants which interact with reactive oxygen species. Free Rad Res Comms 1991; 15:255-263.

8. Sandhya P, Mohandass S, Varalakshnii P. Role of DL alpha-lipoic acid in genlamicin induced nephrotoxicity. Mot CellBiochem 1995;145:11-17.

9. MGrunert RR. The effect of DL Alpha-lipoic acid on heavy-metal intoxication in mice and dogs. Arch Biochem Biophys 1960;86: 190-194.

10. Ou P, Tritschler Hj, Wolff SP. Thioctic (lipoic) acid: a therapeutic metal-chelating antioxidant. Biochem Pharmacol 1995;50:123-126.

11. MullerL, Menzel H. Studies on the efficacy of lipoate and dihydrolipoate in the alteration of cadmium toxicity in isolated hepatocyles. Biochem Biophys Acta 1990; 10523 :386-39 1 .

12. Sumathi R, Baskaran G, Varalakshmi P. Relationship between glutathione and DL alpha-lipoic acid against cadmium-induced hepatoloxicity. Jpn 3 Med Sci Biol 1996;49:39-48.

13. Sumathi R, Devi VK, Varalakshmi P. DL alpha-lipoic acid protection against cadmium-induced tissue lipid peroxidation. Med Sci Res 1994:22:23-25.

14. Keith RL, Sctiarahardjo I, Fernando Q, et al. Utilization of renal slices to evaluate the efficacy of chelating agents for removing mercury from the kidney. Toxicology 1997;116:67-75.

15. Gregus Z, Stein AF, Varga F. Effect of lipoic acid on biliary excretion of glutathione and metals. ToxicolAppl Pharmacol 1992;114:88-96.

16. Lykkesfeldt J, Hagen TM, Vinarsky V, Ames BN. Age-associated decline in ascorbic acid concentration, recycling, and biosynthesis in rat hepatocytes reversal with (R)-alpha-lipoic acid supplementation. FASEB J 1998 Sep;12(12):1183-9.

17. Hagen TM, Ingersoll RT, Lykkesfeldt J, Liu J, Wchr CM, Vinarsky V, Bartholomew JC, Ames AB. (R)-alpha-lipoic acid-supplemented old rats have improved mitochondrial function, decreased oxidative damage, and increased metabolic rate. FASEB J 1999 Feb;l3(2):41 1-8.

18. Hagen TM, Vinarsky V, Wehr CM. Ames BN. (R)-alpha-lipoic acid reverses the age-associated increase in susceptibility of hepatocytes to tert-butylhydroperoxide both in vitro and in vivo. Antioxid Redox Signal 2000 Fall;2{3):473-83.

19. Suh JH, Shigeno ET, Morrow JD, Cox B, Rocha AE, Frei B, Hagen TM. Oxidative stress in the aging rat heart is reversed by dietary supplementation with (R)-(alpha)-lipoic acid. FASEB J 2001 Mar; 15(3):700-6.

20. Kawabata T, Packer L. Alpha-lipoale can protect against glycation of serum albumin, but not low density lipoprotein. Biochem Biophys Res Comms 1994;203:99-104.

21. Jacob S, Henriksen EJ, Schiemann AL, et al. Enhancement of glucose disposal in patients with type 2 diabetes by alpha-lipoic acid. Arzneimittel-Forschung 1995;45:872-874.

22. Jacob S. Henriksen EJ, Tritschler HJ, el al. Improvement of insulin-stimulated glucose-disposal in type 2 diabetes after repeated parenteral administration of thioctic acid. Exp Clin Endocrinol Diabetes 1996; 104:284-288.

23. Kchler W, Kuklinski B, Ruhlmann C, Plotz C. Diabetes mellitus-a free radical associated disease: Effects of adjuvant supplementation of antioxidants. In: Gries FA, Wessel K, eds. The role of antioxidants in diabetes mellitus: Oxygen radicals and antioxidants in diabetes. Frankfurt am Maine: pmi. Verl-Gruppe', 1993: 33-35.

24. Garrett NE, Malcangio M, Dewhurst M, Tomlinson DR. Alpha-lipoic acid corrects neuropeptide deficits in diabetic rats via induction of trophic support. Neurosct Lett 1997;222:191-194.

25. Nagamatsu M, Nickander KK, Schmelzer JD. Lipoic acid improves nerve blood flow, reduces oxidative stress, and improves distal nerve conduction in experimental diabetic neuropathy. Diabetic Care 1995; 18: 1160-1 166.

26. Ziegler D, Hanefield M, Ruhnau KJ, et al. Treatment of symptomatic diabetic peripheral neuropathy with the anli-oxidant alpha-lipoic acid. A 3-week mullicenter randomized controlled trial (ALADIN Study). Diabetologia 1995;38:1425-1433.

27. Assadnazari H, Zimmer G Freisleben HJ, et al. Cardioprotective efficiency of dihydrolipoic acid in working rat hearts during hypoxia and reoxygcnation. P nuclear magnetic resonance investigations. Arzneimittel-Forschung 1993:43:425-432.

28. Prehn JH, Karkoutly C, Nuglisch J, et al. Dihydrolipoale reduces neuronal injury after cerebral ischemia. J Cereb Blood Flow Metab 1992;12:78-87.

29. Wolz P, Krieglstein J. Neuroprotective effects of alpha-lipoic acid and its enantiomers demonstrated in rodent models of focal cerebral ischemia. Nettropharmacology 1996:35:369-375.

30. Filina AA, Davydova NG, Endrikhovskii SN, et al. Lipoic Acid as a means of metabolic therapy of open-angle glaucoma. Vestn Oftalmol 1995;lll:6-8.

31. Ou P, Nourooz-Zadeh J, Tritschler HJ, Wolff SP. Activation of aldose reductase in rat lens and metal-ion chelation by aldose reductase inhibitors and lipoic acid. Free Radic Res 1996;25:337-346.

32. Maitra I, Serbinova E, Tritschler HJ, Packer L. Alpha-lipoic acid prevents buthionine sulfoximine-induced cataract formation in newborn rats. Free Radic Biol Med 1995;l8:823-829.

33. Durr HP, Popp FA, Schommers W, eds. What Is Life: Scientific Approaches and Philophical Positions. World Scientific CO USA River Edge NJ 2002:307-328


 

Related Products/Accessories....
DHLA Nano-Plex with RESVERATROL, Premier Research
Sale Price: CAD $44.99
Add
PRL-109a



 Share your knowledge of this product with other customers... Be the first to write a review.



Browse for more products in the same category as this item:

Supplements
Detox / Cleansing
SPECIALS - SALE ITEMS!


Macadamia Cashew Butter (Raw, Certified Organic) 8 oz CAD $14.79
Greener Grasses - (10 oz) Nutritional Grass Complex CAD $34.99
Amazing Grace - by David Wolfe and Nick Good CAD $17.99
Upaya Naturals
CANADA
 About Us
 Become an Affiliate
 Privacy Policy
 Send Us Feedback
 
Company Info | Wholesale | Advertising | Product Index | Category Index | Help | Terms of Use
Copyright © 2004 Upaya Naturals. All Rights Reserved.
Shopping Cart Software by Volusion