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Hawthorn: The three-in-one natural remedy for high blood pressure


- by Dr. James Meschino, DC, MS, ROHP

Introduction

High blood pressure affects approximately twenty-five percent of the adult population in developed countries like the United States and Canada. In up to 75% of these cases, hypertension manifests in a mild form which is highly sensitive to nutrition, supplementation and lifestyle practices.

Hawthorn has been prescribed by European doctors for years to treat various heart conditions including hypertension, ischemic heart disease (angina), and congestive heart failure. Hawthorn's cardiovascular benefits are primarily due to the unique complement of flavonoid compounds found in its leaves, berries and blossoms, particularly anthocyanidins and proanthocyanidins. These active constituents have been shown to act in three ways to help reduce high blood pressure, and clinical studies have proven that supplementation with hawthorn extract can be a safe, natural method to treat mild to moderate hypertension.

As mentioned, hawthorn has been shown to provide three distinctive physiological effects, each of which contribute to its anti-hypertensive properties. These include:

  1. ACE – inhibitor 
  2. Calcium channel blocker 
  3. Nitric oxide release (vasodilator)

ACE-Inhibitors

ACE-inhibitors are agents that block the conversion of angiotensin I to angiotensin II, thereby reducing high blood pressure.

Under normal conditions, the angiotensin system is activated in response to hypotension, decreased sodium concentration in the distal tubule, decreased blood volume and/or renal sympathetic nerve stimulation. In response, the kidneys release renin which cleaves the liver-derived angiotensinogen into angiotensin I. Angiotensin I is then converted to angiotensin II via the angiotensin converting enzymes (ACE) in the pulmonary circulation, as well as in the endothelium of blood vessels in many parts of the body. The system, in general, aims to increase blood pressure

How Does Angiotensin II Increase Blood Pressure

Angiotensin II is a potent vasoconstrictor, which constricts arteries and veins and increases blood pressure. Angiotensin II also has prothrombotic potential through adhesion and aggregation of platelets and production of PAI-1 and PAI-2 (plasminogen activator inhibitor) – which decreases fibrinolysis. Angiotensin II also potentiates the release of norepinephrine by direct action on postganglionic sympathetic fibers. Angiotensin II also increases sodium resorption in the proximal tubules of the kidney.

All of these effects increase blood pressure and can increase risk of thrombosis and hypertension in a state of dysregulation. With ACE inhibitor use, the effects of angiotensin II are prevented, leading to decreased blood pressure (ACE-Inhibitors inhibit the enzyme that converts Angiotensin I into Angiotensin II) and decreased platelet adhesion.

ACE-inhibitors are also the drug of choice in the management of diabetes to retard progress of diabetic nephropathy. Although many prescription drugs are prescribed for their ACE-inhibitor properties, hawthorn extract has been shown to lower blood pressure by acting as a natural ACE-inhibitor, in cases of mild to moderate hypertension.

Calcium-Channel Blockers

Calcium channel blockers work by blocking voltage-gated calcium channels (VGCCs) in muscle cells of the heart and blood vessels. This prevents calcium levels from increasing as much in the cells when stimulated, leading to less muscle contraction. In the heart, this decreases cardiac contractility (systolic pressure). In blood vessels, a decrease in calcium results in less contraction of the vascular smooth muscle and therefore an increase vasodilation (diastolic pressure). Vasodilation decreases total peripheral resistance, while a decrease in cardiac contractility decreases cardiac output. Thus, these effects lower diastolic and systolic blood pressure. Although many anti-hypertensive prescription drugs act as calcium channel blockers, studies have shown that the active constituents in hawthorn can help to lower mild to moderate hypertension via their natural calcium channel blocker properties.

Nitric Oxide Release (Vasodilation)

Under normal conditions, the endothelial cells that line our blood vessels secrete nitric oxide, which dilates the vessel in accordance with the oxygen required by the tissues supplied by the vessel. In atherosclerosis, and under certain other conditions (cigarette smoking, high cholesterol, lack of antioxidant or folic acid status), individuals experience endothelial dysfunction, whereby the arterioles remain in a relative state of vasoconstriction. In turn, this reduces blood flow to the tissues supplied by these vessels, which can exacerbate angina, ischemic heart disease and hypertension.

In addition to dietary modification, exercise and medication use (e.g. nitroglycerine) to modify endothelial dysfunction, hawthorn extract has shown an ability to increase release of nitric oxide and promote vasodilation. This is another way in which hawthorn extract may reduce high blood pressure and promote improved circulation to the heart muscle.

In addition, hawthorn extract has a proven positive inotropic effect on the heart muscle (similar to coenzyme Q10), enabling the heart muscle to generate more ATP energy for myocardial contraction. This is why it remains a key intervention of choice in the management of congestive heart failure among European physicians, who have used hawthorn extensively over the years for various cardiovascular conditions, including congestive heart failure and the management of hypertension.

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Hawthorn: The three-in-one natural remedy for high blood pressure

Dr. James Meschino, 

DC, MS, ROHP

Hawthorn Dosage in Hypertension

In cases of mild to moderate high blood pressure you may consider recommending a daily dosage of 150-300 mg per day of hawthorn extract (standardized to contain 3-5% flavonoid content). I usually recommend a combination supplement product containing coenzyme Q10 and hawthorn, as both CoQ10 and hawthorn have blood pressure-lowering effects, improve endothelial function and have a positive inotropic effect on the heart muscle. Each capsule of the combination supplement I recommend contains:

  1. Co Q10 – 30 mg 
  2. Hawthorn Extract - 37.5 mg (std to 5% flavonoids) 
  3. Quercetin – 50 mg (quercetin is associated with lower cardiovascular risk in some studies)

I recommend that the patient take 2 capsules, 2 to 4 times per day, depending on the degree of hypertension, co-morbidity issues (overweight, high cholesterol, etc.) and other factors (fitness level, smoking, etc.), as well as monitoring their response. I often start with lower dosage (2 capsules, twice per day) and increase the dosage weekly if necessary, depending on the patient’s blood pressure response to treatment.

Note that the patient can take a supplement combination of this type in association with any other anti-hypertensive drug prescribed by their physician. However, hawthorn is not safe to take in conjunction with digitalis or digoxin, which are prescribed in some cases of congestive heart failure and arrhythmias.

You should also make the patient aware of other lifestyle practices that help to reduce high blood pressure:

  • Weight loss (if over weight)
  • Eliminate or reduce alcohol consumption
  • Reduce sodium intake
  • Calcium/magnesium supplementation (1200-1500/250-600 mg respectively)
  • Endurance Exercise (4-6 times per week for at least 20-30 minutes)
  • Stress reduction (biofeedback, yoga, progressive relaxation etc)

Summary

Scientific and clinical investigations have shown that active constituents in hawthorn extract can reduce high blood pressure via their influence on the angiotensin system, by acting as calcium channel blockers and by improving endothelial function. When taken with coenzyme Q10, and in conjunction with other anti-hypertensive lifestyle measures, hawthorn supplementation is a key element in the natural management of mild to moderate high blood pressure. In North America, hawthorn is often overlooked in this regard. As such, natural health practitioners should bring this information to the attention of their hypertensive patients for the purpose of enhancing the management of their condition, and reducing their dependency on other medications which may carry a greater risk of untoward side effects.

References

1.Aesoph, Lauri M. A Holistic Approach to Skin Protection. Nutrition Science News 1998; V3, N4: 204-208
2.Boelsma, E et al. Nutritional skin care; Health effects of micronutrients and fatty acids. American Journal of Clinical Nutrition 2001; 73 (5): 853-64
3.Hoffman, Ronald L. The Holistic M.D.: Skin (Part One). Conscious Choice: The Journal of Ecology & Natural Living 1991; N.15; p.24
4.Colgan, M. Hormonal Health. Apple Publishing, 1996
5.Estrogen: Therapeutic Use. Women’s Health Weekly, March 16,1998, p.6, 2p
6.Estrogen: Skin, Aging & Prevention. Modern Medicine, may 97, Vol. 65 Issue 5, p.26, 2p
7.Dunn, LB et al. Does estrogen prevent skin aging? Results from the First National Health and Nutrition Examination Survey (NHANES I). Arch Dermatol, 1997; Vol. 133 (3), pp.339-42
8.Henderson, Alan. Skin, Aging & Treatment. Women’s Health Weekly, October 7, 1996-October 14 1996, issue N., p.19, 2p
9.Guttman, Cheryl. Estrogen Receptors; Scalp Physiology Dermatology Times, Sept. 2000, Vol.21, issue 9, p.42, 2/5p
10.Callens, A et al. Does hormonal skin aging exist? A study of the influence of different hormone therapy regimens on the skin of postmenopausal women using non-invasive measurement techniques. Dermatology, 1996; Vol. 193 (4), pp.289-94
11.Bolognia, JL. Dermatologic and cosmetic concerns of the older woman. Clinics in Geriatric Medicine 1993 Feb; 9(1): 209-29
12.Vänttinen, K, Moravcova, J. Transdermal absorption of phytoestrogens. Pharmazie, 2001 Sep; Vol. 56 (9), pp.711-7
13. Fuller, Kathleen E, PhD., Casparian, J. Michael, MD. Vitamin D: Balancing Cutaneous and Systemic Considerations. South Med J 94 (1): 58-64, 2001
14.de Gruijl, FR. Adverse effects of sunlight on the skin. Ned Tijdschr Geneeskd 1998; 142 (12): 620-5
15.Eberlein-Konig, B et al. Protective effect against sunburn of combined systemic ascorbic acid (vitamin C) and d-alpha-tocopherol (vitamin E). J Am Acad Dermatol 1998; 38(1): 45-8
16.Podda, M et al. UV irradiation depletes antioxidants and causes oxidative damage in a model of human skin. Free Radic Biol Med, 1998; 24 (1): 55-65
17.Emonet-Piccardi, N et al. Protective effects of antioxidants against UVA-induced DNA damage in human skin fibroblasts in culture. Free Radic Res 1998; 29 (4): 307-13
18.Firkle, T et al. Antioxidants and protection of the skin against the effect of ultraviolet rays. Cas Lek Cesk 2000; 139 (12): 358-60
19.Pugliese, PT. The skin’s antioxidant systems. Dermatol Nurs 1998; 10 (6): 401-16; quiz 417-8
20.Keller, KL, Fenske, NA. Uses of vitamins A, C, and E and related compounds in dermatology: a review. J Am Acad Dermatol 1998; 39 (4 Pt 1): 611-25
21.Stahl W et al. Carotenoids and carotenoids plus vitamin E protect against ultraviolet light-induced erythema in humans. Am J Clin Nutr 2000 Mar; 71 (3): 795-8
22.Shukla, A. Depletion of reduced glutathione, ascorbic acid, vitamin E and antioxidant defense enzymes in a healing cutaneous wound. Free Radic Res 1997; 26 (2): 93-101
23.Food, Nutrition and Diet Therapy (7th edition.) Krause M and Mahan K edit. W.B. Saunders Company 1984: 119-132
24.Clinical Nutrition (2nd edition) S. Halpern (edit) J.B. Lippincott Company. 1987: Chpt 24 — Cutaneous Aspects of Nutritional Disorders: 399-406
25.Pressman, A and Adams, A. Clinical Assessment of Nutritional Status: a working manual. (published by Management Enterprises, New York, 1982): 29-36
26.Werbach, M. Nutritional Influences on Illness. (published by Third Line press, Inc., California, 1987)
27.Pizzorno, J. Total Wellness. (published by Prima Publishing, U.S., 1996); Normalizing Inflammatory Function: 163-191
28.Gensler, HL et al. Oral niacin prevents photocarcinogenesis and photoimmunosuppression in mice. Nutr Cancer 1999; 34 (1): 36-41
29.United States Department of Agriculture, Food Technology, 1981; 35: 9. The National Health and Nutrition Examination Survey II (NHANES II)
30.Nutrition For Living – second Edition, The Benjamin/Cummings Publishing Companies, Inc., 1988: 12-14
31.Nutrition In Perspective – second Edition. Prentice-Hall, Inc. New Jersey, U.S., 1987

32.Seifter, E, Crowley, LV et al. Influence of vitamin A on wound healing in rats with femoral fracture. Ann Surg 1975; 181: 836-41
33.Demetriou, AA, et al. Vitamin A and retinoic acid: induced fibroblast differentiation in vitro. Surgery 1985; 98: 931-4
34.Kragballe, K. The future of vitamin D in dermatology. J Am Acad Dermatol 1997; 37 (3 pt 2): S72-6
35.Morimoto, S et al. An open study of vitamin D3 treatment in psoriasis vulgaris. Br J Dermatol 1986; 115:421-9
36.The New Encyclopedia of Vitamins, Minerals, Supplements and Herbs. (N. Reavley, edit.) M. Evans and Company, Inc. (pub.) 1998: 310-328. (Zinc): 668-676 (Skin Conditions
37.The Doctors’ Vitamin and Mineral Encyclopedia (S. Hendler). Simon and Schuster, 1990: 195-207 (Zinc)
38.Nutrition for Living – second Edition, The Benjamin/Cummins Publishing Companies, Inc., 1988:338


Don’t have time to read the whole book right now?

No worries. Let me send you a copy so you can read it when it’s convenient for you. Just let me know where to send it.

Hawthorn: The three-in-one natural remedy for high blood pressure

Dr. James Meschino, 

DC, MS, ROHP

Global Integrative Medicine Academy

The Global Integrative Medicine Academy was created to satisfy a need, expressed by many health professionals, to establish credentials as experts in Nutritional Medicine. But, health professionals also needed to be able to complete the programme with a minimum impact on their career, family, and lifestyle. That is why the Advanced Nutritional Medicine and Sports Nutrition Certification Program was created.

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