NUTRITIONAL SUPPLEMENT FOR INCREASING COGNITIVE FUNCTIONS

Abstract

The invention provides compositions and methods that are effective to improve NO production in vivo and/or to increase NO levels in blood. Such compositions and methods are useful to increase oxygenation of the brain and to improve cognitive function.

Description

BACKGROUND OF THE INVENTION

Nitric Oxide Synthase (NOS) in endothelial cells converts L-arginine to L-hydroxyarginine and subsequently to nitric oxide (NO) and L-citrulline (FIG. 1 and FIG. 2). NO exherts its biological action on smooth muscle by increasing cGMP, which leads to vasodialation and increased blood flow in the brain. Two L-citrulline molecules combine to generate L-arginine to boost the NO generation cycle. NO acts as a neurotransmitter for the autonomic nervous system, increases cerebral blood flow and oxygenation of the brain, and improves cognitive functions.

A previous dietary supplement was designed and sold to maximize the benefits of NO. It contained the amino acids L-citruline and L-arginine, as well as BioPerine® (extract, FIG. 3) that helps the body absorb the amino acids (see U.S. Pat. No. 5,536,506 and European Patent EP0810868B1). BioPerine® (extract) inhibits human CYP3A4 and P-glycoprotein enzymes. By inhibiting certain enzymes BioPerine® (extract) may alter the effectiveness of certain medications by increasing bioavailability. The active ingredients in this previous diatary supplement were the amino acids L-citruline and L-arginine, which served as a substrate for NO generation. The previous diatary supplement was sold and administered as a capsule containing 500 mg of L-citrulline, 250 mg of L-arginine, and 1.5 mg of bioperine. The recommended dosage was two capsules per day. In spite of the success realized with the previous diatary supplement, there remains a need for additional formulations that provide improved effects.

SUMMARY OF THE INVENTION

Applicant has determined that the beneficial effects of the previous diatary supplement can be significantly improved by increasing the amount of piperine in the formulation from 1.5 mg to about 5 mg. Based on the suggested administration of two capsules per day, this represents an increase in the amount of piperine from 3.0 mg to about 10.0 mg per day.

Accordingly, in one embodiment the invention provides a unit dosage form suitable for oral administration to a human comprising: L-citrulline (500 mg±20 mg); L-arginine (250 mg ±20 mg); and at least about 5 mg piperine.

In another embodiment the invention provides a unit dosage form suitable for oral administration to a human comprising: about 500 mg of L-citrulline; about 250 mg of L-arginine; and about 5 mg of bioperine.

In another embodiment the invention provides a method to increase NO levels in the blood of a mammal comprising administering a unit dosage form of the invention to the mammal.

In another embodiment the invention provides a method to increase cerebral blood flow in a mammal comprising administering a unit dosage form of the invention to the mammal.

In another embodiment the invention provides a method to increase oxygenation of the brain in a mammal comprising administering a unit dosage form of the invention to the mammal.

In another embodiment the invention provides a method to improve cognitive function in a mammal comprising administering a unit dosage form of the invention to the mammal.

BRIEF DESCRIPTION OF THE FIGURES

FIGS. 1 shows the conversion of L-citrulline and L-argenine to NO.

FIG. 2 shows how Nitric Oxide Synthase (NOS) in endothelial cells converts L-arginine to L-hydroxyarginine and subsequently to nitric oxide (NO) and L-citrulline.

FIG. 3 shows the structure for piperine.

DETAILED DESCRIPTION

As used herein, the term “about” has its generally accepted meaning. In one embodiment, the term about means±10% of the associated value. For example, about 100 mg means 100 mg±10 mg. In one embodiment, the term about means±5% of the associated value. For example, about 100 mg means 100 mg±5 mg. In one embodiment, the term about means±2% of the associated value. For example, about 100 mg means 100 mg±2 mg. In one embodiment, the term about means±1% of the associated value. For example, about 100 mg means 100 mg±1 mg.

In one embodiment a unit dosage form of the invention may contain one or more pharmaceutical diluents or excipients. For example, in one embodiment a unit dosage form of the invention may comprise microcrystalline cellulose, silicon dioxide, and magnesium stearate.

In one embodiment a unit dosage form of the invention may comprise at least about 480 mg of L-citrulline.

In one embodiment a unit dosage form of the invention may comprise at least about 490 mg of L-citrulline.

In one embodiment a unit dosage form of the invention may comprise at least about 500 mg of L-citrulline.

In one embodiment a unit dosage form of the invention may comprise at least about 230 mg of L-arginine.

In one embodiment a unit dosage form of the invention may comprise at least about 240 mg of L-arginine.

In one embodiment a unit dosage form of the invention may comprise at least about 250 mg of L-arginine.

In one embodiment the piperine is synthetically produced piperine.

In one embodiment the piperine is an extract from the fruit of Piper.

L-Argenine is an α-amino acid that is used in the biosynthesis of proteins. It is the precursor for the biosynthesis of nitric oxide. L-Argenine has the following structure:

In humans, arginine is classified as a semiessential or conditionally essential amino acid, depending on the developmental stage and health status of the individual. L-Argenine is commercially available from a variety of sources.

L-Citrulline is an a-amino acid that is a key intermediate in the urea cycle, the pathway by which mammals excrete ammonia by converting it into urea. Citrulline is also produced as a byproduct of the enzymatic production of nitric oxide from the amino acid arginine, catalyzed by nitric oxide synthase. L-Citrulline has the following structure:

L-Citrulline is commercially available from a variety of sources.

Bioperine® is a patented absorption enhancer, obtained from black pepper fruits (Piper nigrum). Bioperine® helps the body absorb the amino acids (see U.S. Pat. No. 5,536,506 and European Patent EP0810868B1). Bioperine® (extract) inhibits human CYP3A4 and P-glycoprotein enzymes. By inhibiting certain enzymes Bioperine® (extract) may alter the effectiveness of certain medications by increasing bioavailability. Bioperine is Generally Recognized As Safe (GRAS). Bioperine® (CAS Reg. No. 94-62-2) is named as 1-piperylpiperidine; 5-(1,3-benzodioxol-5-yl)-1-(piperidin-1-yl)penta-2,4-dien-1-one; and (2E,4E)-5-(1,3-benzodioxol-5-yl)-1-(piperidin-1-yl)penta-2,4-dien-1-one, and has the structure:

1-Piperylpiperidine is commercially available from a variety of sources.

The invention will now be illustrated by the following non-limiting Examples.

EXAMPLE 1.

The chart below describes the changes between the old formulation and the present invention based on the satisfaction rate for the customer's processing fees. The new formulation shows a 19.9 percent increase processing speed over four months as opposed to the old formulation with only as 2.9 percent increase in processing speed.

	Old Formulation	Present Invention
	Satisfaction Rate	Satisfaction Rate
	Baseline	688	59
	At 4 Month	62.3	78.9
	% Increase	2.9	19.9

All publications, patents, and patent documents are incorporated by reference herein, as though individually incorporated by reference. The invention has been described with reference to various specific and preferred embodiments and techniques. However, it should be understood that many variations and modifications may be made while remaining within the spirit and scope of the invention.

Claims

1-19. (canceled)

20. A method to increase NO levels in the blood of a mammal comprising administering two unit dosage forms a day to the mammal, wherein each unit dosage form comprises: L-citrulline 500 mg±20 mg;L-arginine 250 mg±20 mg; andat least about 5 mg piperine.

21. The method of claim 20 wherein each unit dosage form comprises at least about 5.5 mg piperine.

22. The method of claim 20 wherein each unit dosage form comprises at least about 480 mg of L-citrulline.

23. The method of claim 20 wherein each unit dosage form comprises at least about 230 mg of L-arginine.

24. The method of claim 20 wherein each unit dosage form further comprises microcrystalline cellulose, silicon dioxide, and magnesium sterate.

25. The method of claim 20 wherein each unit dosage form is formulated as a capsule, powder, or liquid.

26. A method to increase oxygenation of the brain in a mammal comprising administering two unit dosage forms a day to the mammal, wherein each unit dosage form comprises: L-citrulline 500 mg±20 mg;L-arginine 250 mg±20 mg; andat least about 5 mg piperine.

27. The method of claim 26 wherein each unit dosage form comprises at least about 5.5 mg piperine.

28. The method of claim 26 wherein each unit dosage form comprises at least about 480 mg of L-citrulline.

29. The method of claim 26 wherein each unit dosage form comprises at least about 230 mg of L-arginine.

30. The method of claim 26 wherein each unit dosage form further comprises microcrystalline cellulose, silicon dioxide, and magnesium sterate.

31. The method of claim 26 wherein each unit dosage form is formulated as a capsule, powder, or liquid.

32. A method to improve cognitive function in a mammal comprising administering two unit dosage forms a day to the mammal, wherein each unit dosage form comprises: L-citrulline 500 mg±20 mg;L-arginine 250 mg±20 mg; andat least about 5 mg piperine.

33. The method of claim 32 wherein each unit dosage form comprises at least about 5.5 mg piperine.

34. The method of claim 32 wherein each unit dosage form comprises at least about 480 mg of L-citrulline.

35. The method of claim 32 wherein each unit dosage form comprises at least about 230 mg of L-arginine.

36. The method of claim 32 wherein each unit dosage form further comprises microcrystalline cellulose, silicon dioxide, and magnesium sterate.

37. The method of claim 32 wherein each unit dosage form is formulated as a capsule, powder, or liquid.