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Repair Your Cardiovascular System Improvements demonstrated within 2 hours* |
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Take The BioAnue Challenge:
We are confident that once you start following the science you will obtain your desired results.
If for any reason you are dissatisfied with this product,
we will refund you your money... no questions asked. |
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$12.65
Sample
10 Count Bottle
500mg Capsules |
$47.44
1 Month Supply
60 Count Bottle
500mg Capsules |
$130.94
Therapeutic Dosages

180 Count Bottle
500mg Capsules |
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- Overview
- Ingredients
- Directions
- Side Effects
Cardiovascular Disease & Stroke Contribute To 40% Of All US Deaths!
Cardiovascular Mender is a nutrient enzyme blend that promotes a healthy cardiovascular system. When one has symptoms of Cardiovascular Disease (CVD), an aggressive supplementation with this product will be required to obtain optimal results. Remember that approximately 40% of all deaths in the United States are directly linked to CVD.
How Can You Avoid Becoming a Part of this Statistic?
Cardiovascular disease is the broad term used to describe the different types of heart and blood vessel problems. Educate and monitor yourself for the classic symptoms of CVD. You alone know yourself better than does any one else. However, you must know the symptoms in order to take a proactive approach to your health.
To strengthen and protect your heart against disease and failure and slash up to 46 points off your high blood pressure- while strengthening your heart, organs and glands... use Cardiovascular Mender!
This Full-Strength Hybrid Systemic Enzyme Formula - Specifically Designed For Cardiovascular Health can truly be “Your Edge -Your New Beginning.”
Cardiovascular Mender Hybrid is a combination of pancreatic enzymes blended with fermented enzymes like Nattokinase, Serrapeptase, and the plant-based enzyme Bromelain. This one of a kind formulation is designed specifically for cardiovascular health. Additionally, BioAnue Laboratories has added other vital heart nutrients to the formula- natural benzoquinone (vitamin CoQ10) and adenosine triphosphate, otherwise known as ATP the body’s “cellular energy source.”
Proprietary Blend
Amylase
Pancreatin Protease*
Serrpeptase enteric coated granules
Lipase
Nattokinase enteric coated granules
Bromelain
ATP (adenosine triphosphate)
CoQ10 (natural benzoquinone)
* Protease Mixture Contains Trypsin, Chymotrypsin, Elastase, Carboxypeptidase (Alkalizing Enzyme) A1, CarboxypeptidaseA2 and Carboxypeptidase B…the full Protease Family.
This product is pure nutrition; no fillers, additives or synthetic chemicals.
The gelatin capsule complies with the requirements published in:
The United States Pharmacopoeia (USP); XXIV / National Formulary (NF) 19
The European Pharmacopoeia (EP); 3rd Edition
Kosher and Halal certified
Only one capsule per day is needed for healthy individuals to achieve the levels of activity as shown in peer-reviewed studies.
Lowering blood pressure:
Before starting the regiment, test your blood pressure. This will allow you to have an accurate baseline.
Take 2 capsules daily for the first two weeks; check your blood pressure at the end of these two weeks. Most people will find that 2 capsules per 24 hours are enough to lower blood pressure to ideal range.
If your blood pressure is not adequately lowered after two weeks, then increase dosage to 4 capsules per 24 hours. Check your blood pressure after one week and again after two weeks.
In the unlikely event that you still have not lowered your blood pressure, you can keep increasing by 2 capsules every 2 weeks until you are taking 6 capsules per 24 hours.
If 6 capsules per 24 hours does not lower your blood pressure, please call customer support.
Live blood cell analysis has confirmed that dehydration and blood aggregation can negatively affect blood pressure.
This product is an all natural, non-toxic substance. Over time, it can and will reverse the effects of Cardiovascular disease.
This product has no counter-indications with other medications or herbs.
Eaten on an empty stomach or if needed consume with food. The enzymes are in elevated dosages and will work systemically even when taken with food.
No Side effects in most cases.
Diarrhea, constipation, abdominal pain/cramps, nausea, or vomiting may occur.
Mega dosing could potentially remove too much fibrin (the glue that allows blood clotting to take place.). This condition could inhibit proper blood clotting. [The writer does not know of any proven instance where enzymes used in this formula have promoted this action, however fundamentally, this action is possible.]
If one is using dangerous drugs such as Warfarin (also known under the brand names: Coumadin, Jantoven, Marevan, Lawarin, and Waran) beware that these are anticoagulants.Warfin was initially marketed as a pesticide against rats and mice and is still popular for this purpose.
Vitamin K1 is reduced to vitamin KH2 by two warfarin-sensitive enzymes (KO-reductase to K-reductase), and the nicotinamide adenine dinucleotide-dependent reductase system that is insensitive to warfarin.
Consult your Allopathic Doctor when using Cardiovascular Mender and Warfarin.
This potent combination of unadulterated enzymes and nutrients is what gives Cardiovascular Mender the ability to Reverse heart condition, lower blood pressure, and melt away blood clots in a way unrealized in mainstream medicine!
A Few Research Examples by Dr. Raber, Sc. D.
Heart Wave-Form 63 year old Female
Demonstrating
Stage1 Hypertension.
The ejection and reflected back pulse produced by the blood exiting and returning to the heart which formed a bell shape wave-form, possibly caused by cardiomyopathy "heart muscle disease".
*Improvements demonstrated two hours after consuming Cardiovascular Mender
Verified with A-CASPRO device
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| "A" The lower left hand corner of Image graph shows indications of delay in the injecting of the blood into the aorta. |
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"B" Demonstrates classic release into the aorta in contrast to the previous image "A." |
Conclusions are as follows:
Heart valves not opening nor closing quickly Heart valves out of sequence Heart beating twice as fast as needed Insignificant resting period (does not allow the heart to properly oxygenate the muscle / cells) The graph shows the heart is beating every .45 seconds; ideally the heart should beat every second.
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Before |
After |
Improvements after 2 Hours |
| CASP |
139 |
116 |
-23 points |
| Systolic |
147 |
122 |
-25 points |
| Diastolic |
82 |
72 |
-10 points |
| Heart beat |
.45 |
.98 |
+.53 Relative time in seconds |
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| Subject's Central Aortic Systolic Pressure (CASP) was lowered into the ideal range within the first two hours of using 2 capsules of Cardiovascular Mender, thus decreasing the likelihood of an upcoming event. |
- Science Behind CAP
- End-Stage Renal Disease (ESRD)
It is well known that blood pressure management is important for the prevention of cardiovascular events. Elevation of the central aortic blood pressure induces coronary arteriosclerosis, which easily causes various adverse events such as stenosis and myocardial infarction. Brachial blood pressure, which is usually measured in clinical settings, is an essential parameter for the evaluation and management of central aortic pressure. Since the observation and reduction of central aortic pressure contribute to the prevention of cardiovascular events, simple measurement of not only brachial blood pressure but also central aortic pressure may be useful in the prevention and treatment of cardiovascular diseases.
The large-scale ASCOT-CAFE study reported that central aortic pulse pressure may be a determinant of clinical outcomes and that brachial blood pressure is not always a good indicator of the effect of blood pressure–lowering drugs on arterial hemodynamics. Wilkinson et al. also insisted that the CAFE study would seem to support the view that blood pressure lowering per se matters, but that it is central and not brachial pressure they should be interested in, and predicted that the importance of central aortic pressure management will increase.
(Hypertens Res Vol. 30, No. 3 (2007))
Click Here to Read Study
Damage of large arteries is a major factor in the high cardiovascular morbidity and mortality of patients with end-stage renal disease (ESRD). Increased aortic pulse wave velocity (PWV) and brachial pulse pressure (PP) are the
principal arterial markers of cardiovascular mortality described in these patients. Whether central (carotid) PP and
brachial-carotid PP amplification may predict all-cause (including cardiovascular) mortality has never been investigated.
A cohort of 180 patients with ESRD who were undergoing hemodialysis was studied between January 1990 and March 2000. The mean duration of follow-up was 5236 months (meanSD). Mean age at entry was 51.516.3 years. Seventy deaths occurred, including both cardiovascular and noncardiovascular fatal events. At entry, patients underwent carotid PP measurements (pulse wave analysis), echocardiography, and aortic PWV (Doppler ultrasonography), together with standard clinical and biochemical analyses. On the basis of Cox analyses, after adjustment of age, time on dialysis before inclusion, and previous cardiovascular events, 3 factors emerged as predictors of all-cause mortality: carotid PP, brachial/carotid PP, and aortic PWV. Adjusted hazard ratios for 1-SD increments were 1.4 (1.1 to 1.8) for carotid PP, 0.5 (0.3 to 0.8) for brachial/carotid PP, and 1.3 (1.0 to 1.7) for PWV. Brachial blood pressure, including PP, had no predictive value for mortality after adjustment. These results provide the first direct evidence that in patients with ESRD, the carotid PP level and, mostly, the disappearance of PP amplification are strong independent predictors of all-cause
(including cardiovascular) mortality. (Hypertension. 2002;39:735-738.)
Click Here to Read Study
Heart Wave-Form of 56 Year-old Female Demonstrating Stage 3 Hypertension
Improvements demonstrated two hours after consuming Cardiovascular Mender
Verified with
a CASPRO device.
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"A" Indicates thick blood possibly due to rouleaux and/or aggregation, making the heart work harder to pump blood throughout the body.
The stiffening of the aortic tree can lead to everything from blood clots, heart attacks and stroke-- just to name a few potential issues. |
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"B" Demonstrates classic release into the aorta in contrast to the previous image.
"B" The dichotic notch that was not previously seen is now present. As the blood flows into atrium some relaxation is seen within the first two hours. |
The wave form indicates the subject is suffering from hardening of the arteries(arteriosclerosis), the dichotic notch is not present in image A, this is believed to be caused from the lack of flux in the aortic tree.
Conclusions before treatment:
The blood appears viscous (not evacuating from the heart chamber quickly)
The aortic tree is hard and virtually inflexible
Conclusions After treatment:
The blood appears less viscous (evacuating from the heart chamber quickly)
The aortic tree has begun softening & showing signs of flexibility
The dichotic notch is present in the wave form (demonstrating softening of the aortic tree)
| |
Before |
After |
Improvements after 2 hours |
| CASP |
193 |
139 |
-54 points |
| Systolic |
196 |
149 |
-46 points |
| Diastolic |
95 |
87 |
-8 points |
| Heart beat |
.97 |
.77 |
-20 Relative time in seconds |
Subject's Central Aortic Systolic Pressure (CASP) was lowered close to ideal range within the first two hours of using 2 capsules of Cardiovascular Mender, thus decreasing the likelihood of an upcoming event.
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Subject's Central Aortic Systolic Pressure (CASP) was lowered close to ideal range within the first two hours of using 2 capsules of Cardiovascular Mender, thus decreasing the likelihood of an upcoming event. |
Cardiovascular Test
I performed about 600 atherosclerosis tests using the A-PULSE CASPro testing devise. This devise is a noninvasive blood pressure monitoring system that is designed to measure Central Aortic Systolic Pressure (CASP). Data is gathered by using arterial pulse waveforms gathered from arterial tonometry at the radial artery of the wrist.
The subjects' tested ages ranged from late 20's to over 80-years-old. Male and female participants were used; some of the participants were on prescription drugs, some we not on any medications. The majority of people who did not respond to the test showed symptoms of dehydration or caffeine stimulation- these two factors impaired the actions of the Cardiovascular Mender. Most of the patients who rehydrated or who were tested 24 hours later without caffeine stimulation, showed improvement within the test time of 2 hours. Other subject showed little improvement but were encouraged to try the product for 30 days. The latter subjects did see dramatic improvements within the next 30 days.
To read testimonials just click on the person's name to read about their experience in their own words.
To watch a video explaning about the A-PULSE CASPro testing devise, by Dr. Ting....Click Here
Testimonials
- Click Name to Open Testimonial
- Dave
- Jim
- Rose
The following testimonials are from people who have successfully used Cardiovascular Mender. When I was doing my experiments I found that about 90% of the people who used Cardiovascular Mender saw positive results within the first two hours of use.
Dave from Minnesota:
Dear Customer Survive,
February 17, 2011, at the age of 67, test results showed hardening of the arteries and the negative effect it was having on heart function. Was told this was normal for a person my age. "NORMAL" - I knew what that meant! My dad had dementia and was heading towards Alzheimer's disease and I wanted none of that. Called and spoke with a trained TumorX Protocol representative. I started on Cardiovascular Mender. Two months and two tests later showed a softening of arteries and improvement of heart function as I continue using this great product.
Jim from TX
Hello BioAnue,
I have severe heart issues and it was to the point I could not walk across the floor without complete exhaustion. I found your cardiovascular mender and decided to give it a try. I have been amazed at the results. In less than one month of taking the product I am now able to walk wherever I desire with no problems.
Thank you for this wonderful product.
It has changed my life for the better.
Rose from Vermont,
I started using Cardiovascular Mender on March 10, 2010, after 14 days of use the product symptoms of atrial fibrillation had completely ceased.
It has now been three more weeks and I've had zero episodes. I am now able to walk upstairs, garden and do the day-to-day joys of which I had been deprived. Due to my irregular heartbeats, as soon as I would start some strenuous exertions my heart would begin to have irregular palpitations; they would last anywhere from 2 to 8 hours at a time. I would typically have these episodes every other day and sometimes everyday weeks on end even though I was not putting exertion on my system.
I was desperate to find something that would help. My medical doctor offered no real hope. I found it difficult to keep down a full-time job as I needed two naps a day and I suffered from lack of energy.
Your product has completely turned things around for I feel like a new person.
I'm very grateful for Cardiovascular Mender.
Thank you BioAnue Laboratories
Testimonials
- Russ
- Ronald
- Mariene
- Randy
Russ From VA
I tried Cardiovascular Mender. I was extremely surprised to find that in the very first week (1 capsule per day) that the pounding of my heart started to dissipate. I could sit at a desk and feel my heart beating in my neck and head. I also had neuropathy in my feet. My feet felt as if they were on fire and liked to put them on a cold floor. The naturopathy has gone away in three weeks.
I used to wake up in my sleep due to the pounding of my heart. The pounding has gone.
We still do not know the cause of high blood pressure but the product is working, at least for me.
Case History
I am a 67 year old white male, O neg blood type. In 2005, I was diagnosed with Arial Fibrillation and a blood pressure of 205 over 170 with a heart rate of 250 beats per minute. At the local emergency room they gave me a calcium channel blocker and a blood thinner. I was put on a program at my local hospital of calcium channel blockers and Coumadin blood thinner. I later underwent a series of heart examinations.
Six months later I went for another physical. I still had the atrial fibrillation. I then realized that conventional medicine had absolutely no idea what the cause of high blood pressure or atrial fibrillation was. I discovered that the channel blocker only affects the symptoms and does nothing to rectify the cause. Coumadin is a recognized rat killer by causing rats internally to bleed to death.
I then visited three naturopaths in an attempt to solve my problem. In spite of vitamins, magnesium citrate and blood thinning products my blood pressure still stayed in the 170/125 range.
Russell Walker
Ronald from Madrid, Spain
I am Ronald, the brother of Russ Walker and live in Madrid, Spain
After suffering for years with atririal fibrilition of the heart, all sorts of palpitations, feelings of weakness, nervousness I noticed immediate relief with the Heart Mender and Cardiovascular Mender products.
Previously, I had spent many visits in the hospital without ever knowing why I was so aflicted.
I was resigned to beta blockers, tranquilizers, and any sort of medicine which relates to heart problems. If one is not already suffering from something, medicine will eventually make you sick.
Thank God that I am so releived with these products that I am totally free of these disturbances and my psychological disposition has also changed in the absense of the former apprehension.
I certainly look forward to continuing with these products when my current supply runs out and my interest is now perked towards any new formulas you may have regarding general health.
Thank you and best regards,
Ron Walker
From Marlene-GA,
Hello BioAnue,
I have used some of your products before and have found them to be of excellent quality. For some time I had been having pains shoot out my left arm unexpectedly and they would take my breath away, they did not last too long so I just went on about my business. I mentioned it to someone and they suggested I try the Cardiovascular Mender you carry.
I have been on the product for a little over 1 month now and I have had no episodes for a couple of weeks now. Once again you have brought a product to market that is not only what is needed but is of the highest quality.
Thank you.
Randy From GA
Hello,
I had taken some of your products in the past and was very pleased with them. When I saw you had the Cardiovascular Mender I decided to try it for my heart and artery issues. I know it was helping after I ran out and my system could tell immediately. I have some more on the way and do not plan to be without it again.
Thank you for making such good, high quality products.
Cardiovascular Mender: It’s All In The Mix!
In order to fully understand how Cardiovascular Mender can reverse heart condition and melt away blood clots, you need to know the science behind the enzymes and nutrients used in this formulation. So, let’s start with the pancreatic enzymes and finish with CoQ10.
Unlike other systemic enzyme products, we use real pancreatic enzymes derived from animal sources. These three enzymes are known as the Protease (family)– Lipase and Amylase.
Two of the many reasons we use pancreatic enzymes in our enzyme preparation, is the “lasting effects” in the body of these enzymes, and the fact that only pancreatic enzymes mutate into other types of enzymes. We only have a few organs in the body that produce enzymes, however 1,000 of enzymes have been detected inside the human body.
Pancreatic enzymes have the ability to last up to 42 hours in the human body. In comparison, fungi based Pancreatic enzymes only last on average 4-6 hours hours, not even a day ! Another fascinating aspect of pancreatic enzymes is their ability to fortify the organs and glands in a way that plant based enzymes cannot. Pancreatic enzymes have always been known to work on a cellular level and therefore will help to strengthen the whole body in balance.
Cardiovascular Mender not only rebuilds the cardiovascular system…it also has enough pancreatic enzymes in the blend to fortify digestion and work systemically on the whole system.
Putting It All Together – The Key Ingredient in Cardiovascular Mender
In addition to the pancreatic enzymes and their ability to fortify the heart, organs and glands, BioAnue Cardiovascular Mender utilizes two of the strongest fibrinolytic enzymes known to science… Nattokinase and Serrapeptase.
Nattokinase is a super high fibrinolytic enzyme capable of providing you with three amazing cardiovascular health benefits you should not be without. But First, what is Nattokinase and how does it work?
- ATP
- Bromelain
- Nattokinase
- Lipase
- Pancreatic Protease
- Q10
- Serrapeptase
Adenosine Triphosphate deficiency
ATP (adenosine triphosphate) can be used to increase the blood flow without increasing blood pressure. In an experiment, 11 healthy males were given 1 gram of ATP each. Two hours after administration blood flow was demonstrated to increase up to 58% in arteries.
ATP facilitates greater oxygen intake to the brain and vital organs which promotes accelerated healing at the cellular level.
Adenosine triphosphate (ATP) is a biological substance that stores the energy that the body needs for a wide variety of metabolic functions. In fact all the physiological mechanisms that need energy get it from ATP or one of its derivatives stored in cells. The breakdown of ATP releases energy which is then used as fuel for all our bodily functions. ATP is needed for the heart to beat, it is needed for muscular effort, in fact everything we do requires ATP as energy.
The body cannot function without ATP. That is why ATP is known as the “energy currency”. Each cell in your body must be supplied with energy continuously if it is to function correctly. Therefore when the cells in the body do not make ATP, because of low oxygen levels, the cells act anaerobically and lactate is produced.
Lactate Can Create Muscular Pain
Muscle fiber degeneration and regeneration, inflammation in intramuscular connective tissue, and hypoxia (low oxygen to the cell) occur with sustained muscular action. Severe muscle pain develops in this low oxygen environment. A combination of muscle tension and muscle hypoxia is the likely cause the chronic heart disease muscle pain syndrome, called angina.
Ischaemic or ischemic heart disease (IHD), or myocardial ischaemia, is a disease characterized by reduced blood supply to the heart muscle, usually due to coronary artery disease (atherosclerosis of the coronary arteries). Its risk increases with age, smoking, hypercholesterolemia (high cholesterol levels), diabetes, hypertension (high blood pressure) and is more common in men and those who have close relatives with ischaemic heart disease.
Symptoms of stable ischaemic heart disease include angina (characteristic chest pain on exertion) and decreased exercise tolerance. Unstable IHD presents itself as chest pain or other symptoms at rest, or rapidly worsening angina. It is the most common cause of death in most Western countries, and a major cause of hospital admissions. There is limited evidence for benefits of population screening. Prevention, by implementing a healthy diet and supplements to correct diabetes, cholesterol, and high blood pressure is used both to prevent IHD and to decrease the risk of complications.
With ample oxygen, the body is able to produce all the ATP it needs to maintain a healthy existence. However, when oxygen is low, for example during strenuous exercise, Thrombus occurs. The body may not be able to replace ATP fast enough during strenuous exercise. In order to achieve maximum athletic performance, as well as for overall health, it is important to keep ATP at the optimum level. ATP is critical for heart health as well as the health of all the other musculature in the body that allows us to function.
ATP not only keeps your heart beating, it also keeps oxygen circulating around your body which is vital for muscles to operate and for them to recover and develop. If ATP levels continue to be depleted, you may face a deficiency.
Thrombus
Taussig and Nieper, 1979, Kelly, 1996 showed:
Bromelain inhibits thrombus formation; studies have shown that bromelain prevents aggregation of human blood platelets in vivo in vitro e.g., Petri dish and human experiments. Both of the researches also demonstrated that bromelain prevents or minimizes the severity of angina and Transient Ischemic Attacks (TIA), which is a "warning stroke" or "mini-stroke" that produces stroke-like symptoms but no lasting damage. Recognizing and treating TIA's can reduce your risk of a major stroke.
Taussig and Nieper, 1979 and later, Hale et al, 2002, showed that in vitro bromelain treatment of leukocytes (white blood cells), markers studied, induced loss of CD41 and CD42A via enzymatic digestion, and also decreased platelet function, thus inhibiting thrombosis formation.
Oxygen and Nutrients Absorption
Taussig, Nieper and Kelly et. al, suggested that bromelain increases vessels' wall permeability to oxygen and nutrients while at the same time thinning the blood.
Heart Attach or Stroke
(Kelly, 1996). Heinicke et al. (1972) were the first to report that bromelain prevents abnormal clump together of blood platelets, using fibrinogen in the process. Their study was carried out among human volunteers with a history of heart attach or stroke, some with high fibrinogen values, as well as healthy subjects. Their study found that oral administration of bromelain (160-1000mg per day) decreased aggregation of blood platelets in all the subjects.
Stable Angina
Nieper in (1978), administered 400-1000mg per day of bromelain to 14 patients with stable angina. The study resulted in the disappearance of symptoms in all patients within 4 to 90 days, but reappeared after bromelain administration was discontinued. The ability of bromelain to influence these conditions could be due to its ability to breakdown fibrinous plaques, and to dissolve atherosclerosis plaque.
Nattokinase is an enzyme found in Nattō, a popular Japanese cheese made from fermented soybeans. Nattō is produced by a fermentation process by adding Bacillus Nattō, a beneficial bacterium, to boiled soybeans. The enzyme is then purified and isolated into a powdered form so that it can be used in a capsule or tablet.
Unlike aspirin and most other anticoagulant drugs which interfere with fibrin production, Nattokinase acts “directly on the fibrin that binds platelets and red blood cells that form blood clots. Nattokinase has the ability to help your cardiovascular system in three specific ways:
1.Thrombolytic Effect: Nattokinase dissolves existing thrombus (clotting) by dissolving the fibrin that binds platelets together. Nattō acts much like plasmin, the only enzyme produced by the human body that breaks down fibrin. As we age, our plasmin production decreases, making Nattō supplementation the ideal replacement. Nattokinase also enhances the body’s own production of plasmin and other blood clotting agents, including urokinase (endogenous) (Sumi, H. et al. “A novel fibrinolytic enzyme (Nattokinase) in the vegetable cheese Nattō….” Experientia 1987, 43:1110-11).
2. Blood Pressure: Nattokinase has been shown to lower blood pressure levels. People in Japan have been eating Nattō for this purpose for hundreds of years. Studies have shown it lowers blood pressure by inhibiting angiogenesis converting enzyme (ACE). Ace causes blood vessels to narrow and blood pressure to rise. Nattokinase’s ability to inhibit ACE, therefore, has a lowering effect on blood pressure (Maruyama M, Sumi H. Effect of Nattō Diet on Blood Pressure. JTTAS,1995.).
3. Circulation Enhancement: Nattokinase has been shown to aid in blood flow by assisting in the clearing of circulation. It has also been shown to help prevent the hardening and narrowing of arteries (Sumi H. Healthy Microbe "Bacillus Nattō". Japan Bio Science Laboratory Co. Ltd.).
As good as all of these benefits sound, obtaining the correct amounts of Nattokinase is essential if you are expecting to get real results. So, in order to make sure we had the right amounts, we went back and reviewed Dr. Sumi’s original research. The research showed that Nattō has an average of 40 fibrinolytic units per gram (fibrinolytic units are a determination of how much fibrin a specific amount of the enzyme breaks up in a test tube). In human clinical trials, dosages of between 50 and 200 grams of Nattō per day were shown to be effective in humans. This would equate to between 2,000 and 8,000 fibrinolytic units (Sumi H. Interview with Doctor of Medicine Hiroyuki Sumi. Japan Bio Science Laboratory Co. Ltd.).
Therefore, just 4- 500mg capsules per day equal the amounts used in the studies of 2,000-8,000 fibrinolytic units. If you are dealing with heart disease, 4 capsules per day should be adequate. However, if you are healthy and just looking to maintain your good health, we strongly recommend that you only consume one (1) or two (2) capsules per day.
Lipase Deficiency
Lipase is made in the pancreas, secreted in the duodenum, migrates into the gut, then into the cardiovascular system, where Lipase also functions in the blood to enzymatically act on the triacylglycerides converting it into very low density lipoprotein so that cells can take up the free fatty acids as energy.
For example, pancreatic lipase, which is the key enzyme to break down fats in the human digestive system, converts triglyceride substrates found in ingested oils to monoglycerides and free fatty acids. Regarding the amount and nature of lipids, diets rich in polyunsaturated fatty acid, mainly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), have been shown to reduce the risk of coronary heart disease. These substances can be made using lipase inside the human body
What Is Cholesterol? What Are Triglycerides?
Cholesterol and triglycerides are two forms of lipids, or fats. Both cholesterol and triglycerides are necessary for life itself. Cholesterol is necessary, among other things, for building cell membranes and for making several essential hormones. Triglycerides, which are chains of high-energy fatty acids, provide much of the energy needed for cells to function. But when one is deficient in lipase the body cannot use the cholesterol lipids, that is to say, the fat.
Lipase deficiency increases plasma triglycerides and reduces HDL levels and may thereby predispose carriers to ischemic heart disease. These findings were published in American Heart Association, Inc. Børge G. Nordestgaard, et al., Circulation. 2000;101:2393-2397. Nine thousand, two hundred, fifty-nine (9,259) individuals were studied for lipase deficiency. When lipase was corrected in serum, heart disease decreased. The lipoprotein lipase was found to degrade the triglycerides contained in chylomicrons (chylomicrons are large lipoprotein particles that consist of triglycerides (85-92%), phospholipids (6-12%), cholesterol (1-3%) and proteins (1-2%) , and very-low-density lipoproteins).
Pancreatic Protease
A.H. Elliot et al., published his finding in 1931; he demonstrated that taking pancreatic enzymes treated the cause of Angina, which is a disease of the cardiovascular system. He described the increase in the coronary flow as allowing adequate oxygen and essential nutrients through, thus feeding the heart. The body's antagonisms to the hypertension is created by a restricted cardiovascular system, caused by low blood oxygen levels, creating anaerobic cell respiration, creating lactate in the heart muscle, and leading to adrenalin production: "the fight or flight hormone". The action above describes the beneficial usage of Trypsin, Chymotrypsin, Elastase, Carboxypeptidase A1, A2, and Carboypeptidase B, also known as pancreatic protease. The actions explained by Dr. Elliot explained the beneficial influence of pancreatic enzymes in cleaning the debris and fibrin from the cardiovascular system, (fibrin is made from fibrinogen, a soluble plasma glycoprotein that is synthesized by the liver.). As we age, fibrin accumulates in the cardiovascular system . By cleaning the blood of fibrin, blood flow and oxygen is increased.
What are the Symptoms of Angina?
Chest pain or discomfort that typically occurs with activity or stress when more oxygen is required is a symptom of angina. The pain usually begins slowly and gets worse over the next few minutes before going away.
- A feeling of indigestion or heartburn
- Dizziness or light-headedness
- Nausea, vomiting, and cold sweats
- Palpitations
- Shortness of breath
- Unexplained tiredness after activity (more common in women)
Causes
Your heart muscle is working all the time, so it needs a continuous supply of oxygen. This oxygen is provided by the coronary arteries, which carry blood. When the heart muscle has to work harder, it needs more oxygen. Symptoms of angina occur when the coronary arteries are narrowed or blocked by hardening of the arteries (atherosclerosis), or by a blood clot. The most common cause of angina is coronary heart disease (CHD). Angina pectoris is the medical term for this type of chest pain. Stable angina is predictable chest pain. Although less serious than unstable angina, it can be very painful or uncomfortable. Anything that requires the heart muscle to need more oxygen can cause an angina attack, including:
- Cold weather
- Exercise
- Emotional tension
- Large meals
Other causes of angina include:
- Abnormal heart rhythms
- Anemia
- Coronary artery spasm (also called Prinzmetal's angina)
- Heart failure
- Heart valve disease
- Hyperthyroidism
Q10
This unique vitamin-like substance is present in every cell of the body, especially the heart. Q10 levels are reported to decrease with age and to be low in patients with cardiovascular disease. Q10 decreases the proliferation of free radicals, supporting a healthy immune system. Q10 also stimulates the metabolism to aid your body in the conversion of food to energy and aids in the reductions of cellular oxidation.
An excerpt from an article of the National Academy of Science states, “Therapy with CoQ10 can result in increasing and even normalizing the myocardial levels of CoQ10. Therapy with CoQ10 can result in a…profound increase both in cardiac function and in the quality of life of a failing cardiac patient. Cardiomyopathy (any disease that affects the structure and function of the heart) can be substantially, but not solely, a consequence of a deficiency of CoQ10.”
In a 90-day study, 2500 patients with congestive heart failure were given CoQ10. The percentages of patients with symptomatic improvement were as follows: sweating 82.4%, jugular reflux 81.5%, bluish skin discoloration 81%, lung noise 78.4%, fluid retention in organs 76.9%, awareness of heartbeat 75.7%, vertigo 73%, irregular heart beats 62%, insomnia 60.2%, shortness of breath 54.2%, night time urination 50.7%, enlargement of the liver area 49.3%.
Q10 Precursor to ATP
Q10 is essential for electron transport within the mitochondria and hence for ATP generation and cellular energy production.
Clinical Aspects of CoQ10 Primary CoQ10 Deficiency
Ogashara, et al, described the first patients (two sisters) with primary CoQ10 deficiency in 1989. The patients, aged 12 and 14, had progressive muscle weakness, abnormal fatigue, and central nervous system dysfunction from early childhood. The CoQ10 concentration in their muscles was markedly decreased, being about 5% of normal, but was normal in serum and cultured fibroblasts. It was concluded that the primary defect in these sisters probably involved a tissue-specific isozyme in the CoQ10 synthetic pathway of muscle and brain, and both patients improved remarkably with oral CoQ10
CoQ10 and Statin Myopathy
De Pinieux G, et al, Lipid-lowering drugs and mitochondrial function: Br J Clin Pharmacol 1996;42:333-7.
Studies have indicated up to 13.6% of statin treated patients experience some degree of myopathy (muscle weakness), and as targets for cholesterol reduction become progressively lower, necessitating higher statin doses. The risk of side effects, particularly myopathies, has increased. A number of studies have provided evidence of impaired mitochondrial function in statin-induced myopathy. Also observed was significant elevations in the lactate to pyruvate ratio, an indirect marker of mitochondrial dysfunction. Abnormalities resolved following discontinuation of statin therapy was confirmed in the patients who had repeat biopsies.
CoQ10 and Hypertension
A recent meta-analysis of Q10 in the treatment of hypertension (12 clinical trials, 362 patients) concluded that, in hypertensive patients, CoQ10 has the potential to lower systolic and diastolic blood pressure, without significant side effects. A blood pressure lowering effect of CoQ10 was found across three types of studies including randomised controlled, crossover, and open label. Decreases in systolic blood pressure ranged from 11 to 17 mmHg and in diastolic blood pressure from 8 to 10 mmHg. Rosenfeldt FL, et al. Coenzyme Q10 in the treatment of hypertension: meta-analysis of the clinical trials. J Hum Hypertens 2007;21:297-306.
The antihypertensive effect of CoQ10 occurs gradually over several months, and the CoQ10 dose required for effectiveness varies between patients. Mol Aspects Med 1994;15 (Suppl):S265-72. Langsjoen P, et al
Sarrapeptase
The Miracle Silk Worm Enzyme!
Serrapeptase digests non-living tissue, blood clots, cysts, and arterial plaque and helps to lower inflammation in all forms including C-Reactive Proteins. In fact, the late German physician, Dr. Hans Nieper, used Serrapeptase successfully to treat arterial blockage in his coronary patients. Serrapeptase protects against stroke and is reportedly more effective and quicker than EDTA Chelation treatments in removing arterial plaque. Dr. Nieper also reported that Serrapeptase dissolves blood clots and causes varicose veins to shrink or diminish. Dr. Nieper told of a woman scheduled for hand amputation and a man scheduled for bypass surgery who both recovered quickly without surgery after treatment with Serrapeptase.
Serrapeptase may well offer additional cardiovascular benefits not considered by Nieper. In particular, researchers have recently proposed that inflammation contributes to the development of arterial blockage. In one study, subjects with higher levels of CRP (C-Reactive Protein*, a marker for systemic inflammation) were found to have a greater risk of future heart attack and stroke, independently of other risk factors such as smoking, high blood pressure, or cholesterol levels.
Subjects with the highest levels of CRP who also used aspirin, however, showed dramatic decreases in their risk of heart attack, leading the researchers to speculate that the effectiveness of aspirin in preventing heart attack is due as much to its anti-inflammatory activity as to its anticlotting effects.
Serrapeptase, like aspirin, has both anti-inflammatory and anticlotting properties. In contrast to aspirin, however, serrapeptase can melt through existing fibrous deposits. Serrapeptase also lacks the serious gastrointestinal side effects associated with chronic use of NSAID's such as aspirin.
This combination of properties makes serrapeptase just about the perfect remedy for warding off cardiovascular disease, better even than the proverbial aspirin a day. It’s beginning to look more and more as though Dr. Nieper was right—serrapeptase is indeed a “miracle” enzyme.
Because serrapeptase is a blood-thinning agent, it’s wise to consult your physician if you’re already taking any form of anticoagulant therapy such as Warfarin. Despite these cautions, however, serrapeptase has an excellent tolerability profile in general.
*The C-reactive protein (CRP) test is a blood test that measures the level an inflammatory marker – a substance that the body releases in response to inflammation. High levels of CRP in the blood means there is inflammation somewhere in the body.
**Warfarin is prescribed to people with an increased tendency for thrombosis or as secondary prophylaxis (prevention of further episodes) in those individuals that have already formed a blood clot (thrombus). Warfarin treatment can help prevent formation of future blood clots and help reduce the risk of embolism (migration of a thrombus to a spot where it blocks blood supply to a vital organ). Common clinical indications for warfarin use are artial fibrillation, the presence of artificial heart valves, deep venous thrombosis, pulmonary embolism, antiphospholipid syndrome and, occasionally, after heart attacks (myocardial infarction).
Knowing The Symptoms of Heart Disease
Could Save your Live
- Angina
- Arrhythmias
- Atrial Fibrillation
- Heart Attack
The most common symptom of coronary artery disease is angina, or chest pain. Angina can be described as a discomfort, heaviness, pressure, aching, burning, fullness, squeezing, or painful feeling in your chest. It can be mistaken for indigestion or heartburn.
Angina is usually felt in the chest, but may also be felt in the shoulders, arms, neck, throat, jaw, or back.
Other symptoms of coronary artery disease include:
- Shortness of breath
- Palpitations (irregular heart beats, skipped beats, or a "flip-flop" feeling in your chest)
- A faster heartbeat
- Weakness or dizziness
- Nausea
- Sweating
Symptoms of Arrhythmias
When symptoms of arrhythmias, or an abnormal heart rhythm, are present, they may include:
- Palpitations (a feeling of skipped heart beats, fluttering or "flip-flops," or feeling that your heart is "running away").
- Pounding in your chest.
- Dizziness or feeling light-headed.
- Fainting.
- Shortness of breath.
- Chest discomfort.
- Weakness or fatigue (feeling very tired)
Symptoms of Atrial Fibrillation
Atrial fibrillation (AF) is a type of arrhythmia. Most people with AF experience one or more of the following symptoms:
- Heart palpitations (a sudden pounding, fluttering, or racing feeling in the heart).
- Lack of energy; tired.
- Dizziness (feeling faint or light-headed).
- Chest discomfort (pain, pressure, or discomfort in the chest).
- Shortness of breath (difficulty breathing during activities of daily living).
Some patients with artial fibrillation have no symptoms. Sometimes these episodes are briefer.
Allopathic doctors prescribe numerous drugs to mask CVD, this only make the problem worst over time.
An important thing to understand when wanting to correct your health, is that masking the problem to improve the numbers is not healthy and causes more harm to your health in the long term.
Symptoms of a heart attack can include:
- Discomfort, pressure, heaviness, or pain in the chest, arm, or below the breastbone
- Discomfort radiating to the back, jaw, throat, or arm
- Fullness, indigestion, or choking feeling (may feel like heartburn)
- Sweating, nausea, vomiting, or dizziness
- Extreme weakness, anxiety, or shortness of breath
- Rapid or irregular heartbeats
During a heart attack, symptoms typically last 30 minutes or longer and are not relieved by rest or oral medications (medications taken by mouth). Initial symptoms can start as a mild discomfort that progresses to significant pain.
Some people have a heart attack without having any symptoms (a "silent" MI). A silent MI can occur among all people, though it occurs more often among diabetics.
If you think you are having a heart attack, DO NOT DELAY. Call for emergency help (dial 911 in most areas). Immediate treatment of a heart attack is very important to lessen the amount of damage to your heart.
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Protecting and sustaining your heart is vital to a long healthy life.
Cardiovascular Mender is a systemic formula of natural glandular enzymes, blended with phyto-enzymes, then combined with fermented enzymes, Finally blended with coenzymes allowing synergy between the enzymes and the most important nucleotide our body needs to function on!
All of these nutrients well help you maintain a healthy lifestyle. You need to do your part in eating healthy food and having yourself tested to make sure you are on a path of complete health.
Resources
1. Heart Facts 2007: All Americans Cardiovascular Diseases Still No. 1 American Heart Association
2. Proc. Natl. Acad. Sci. USA Vol. 82, pp.901-904, February 1985 Medical Sciences
3. Proceedings of the National Academy of Sciences _ January 18, 2005 _ vol. 102 _ no. 3
4. British Journal of Nutrition (2005), 93, 131–135 DOI: 10.1079/BJN20041285
5. http://www.crestorfacts.com/sideeffects.aspx
6. http://en.wikipedia.org/wiki/Rhabdomyolysis
7. Goto K. Tsuda M. Sano M. Matsunaga T. The changes of blood flow in the vertebral artery and the common carotid artery by the oral administration of ATP. The Clinical Report 16(6):3617-20,1982
8. Journal of the American College of Nutrition, Vol. 20, No. 6, 591-598 (2001)
9. Archives of Neurology, October 2002, Vol. 59, No. 10, pp. 1541-1550.
10. Clin Investig (1993) 71:S 145-S 149
*Statin Drugs in the US include: Lipitor, Torvast, Lipobay, Baycol, Lescol, Mevacor, Altocor, Mevastatin (red yeast rice), Livalo, Pitava, Pravachol, Selektine, Lipostat, Crestor, Zocor, and Lipex. |
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