Raw Oats for Gastrointestinal Health

Jeff Clark, ND

Oats are the seeds of the plant Avena sativa, a cereal grain that has been used as a foodstuff for both humans and livestock for millennia.1 As a dermatological agent colloidal extracts of oats have been used for their antioxidant, anti-inflammatory, moisturizing, cleansing and even ultraviolet protective properties.2 Oats are an excellent source of soluble fiber in the form of beta-glucans, alpha-tocopherols, B vitamins, minerals, proteins, and plant fats. As a grain without gluten, oat flour and bran are used as an alternative food for persons suffering from celiac disease.3,4

As a health food, oats have received extensive attention in recent times for their ability to lower serum cholesterol levels.5 Oat beta glucan isolates have been shown to shift serum cholesterol profiles to contain less low-density lipoproteins (LDL) and more of the desired high-density lipoproteins (HDL).6,7 Oat bran products have been shown to reduce postprandial glucose spike after a glucose load in patients with type 2 diabetes.8

In overweight patients, beta glucan from oats has been shown to decrease hypertension.9 Avenanthramide is an oat polyphenol that has been shown to enhance production of nitric oxide, a potent vasodilator, and to inhibit thickening of vascular smooth muscle. Both are actions preventative to developing atherosclerosis.10 Beta glucans extracted from oats have been shown to enhance the protective activity of immune system neutrophil cells.11

Oat bran has been shown to both increase endogenous butyrate production and to provide symptomatic relief in the reduction of abdominal pain and refluxIn the gastrointestinal (GI) tract, oat beta glucans are a prebiotic that is selectively fermented by butyrate-producing microorganisms.12 Oat bran has been proposed as a dietary treatment for ulcerative colitis and has been shown to both increase endogenous butyrate production and to provide symptomatic relief in the reduction of abdominal pain and reflux.13

Room temperature water extracts of uncooked oats have been shown to have a significant ability to inhibit fungal growth when applied to rye bread as a food preservative. The method of action is the presence of a chitinase enzyme with activity that is at least 10 times more abundant in oat extracts (Avena sativa) than from other grains. Oat chitinase enzyme activity is deactivated by heating. Optimal chitinase enzyme pH is 7.0 with a loss of 80% of activity at a pH of 8.0, yet only a loss of 40% of activity at a pH of 4.0. While Penicillium roqueforti is the rye bread mold species examined in most detail, activity against other species of yeast and fungi has been observed including species from the genuses Penicillium, Aspergillus, Eurotium, Phoma, Trichoderma, Alternaria, Geotrichum, Cladosporium, Botrytis, Paecilomyces, Rhizopus, and Candida.14

In conventional medical literature, Candida species are viewed as either completely benign commensal microflora in persons with competent immune systems, or a deeply invasive and potentially deadly infection in persons with a compromised immune system.15 Whether a semi-invasive Candida colonization in Gi tissues or intolerance of Candida can be a cause for ill health is a controversial and complex topic in the peer-reviewed science literature.16,17

Patients having a Candida problem often complain of fatigue, malaise, cloudy thinking, spastic colitis, alternating or chronic diarrhea and/or constipation, and a craving for sweet and high glycemic foods. Consumption of simple sugars and high glycemic foods aggravate the experience of symptoms. A diet that limits high glycemic foods moderates symptoms. Antifungal therapy using nystatin, azole drugs and various herbal preparations containing berberine, essential oil of oregano and other antifungal principals, at first spike symptoms, commonly referred to as a “die-off” or Herxheimer reaction, followed by a relief of symptoms. Candida species can be isolated from fecal samples and elevated Candida IgG is found in serum.17

The development of semi-invasive or Candida intolerance symptoms often follows a history of extensive antibiotic and/or corticosteroid use. It also may follow a history of heavy metal problems due to fish eating, dental amalgams, and/or inoculation with thimerosal vaccine preservatives. Low-dose heavy metal intolerance is a functional health problem typically without gross pathology. The MELISA test provides an unambiguous diagnostic demonstrating heavy metal pathology when type IV hypersensitivity to the metal is present.20

Human hosted colonies of Candida species develop resistance to chronic antifungal treatments and there is a research effort underway to learn how to best subvert that resistance.18,19 What if an effective therapy for GI Candida colonization, invasion and intolerance is as simple as eating raw oats? That is the proposal of this paper. The answer will likely be built on anecdotal data as there is no apparent way to constrain the use of raw oats and their extracts to a patent and pharmaceutical franchise model. Attracting adequate funding for a systematic clinical evaluation of raw oats also seems unlikely.

For those who suspect that intolerance to Candida species colonizing their GI tract is diminishing their health, what is the risk of trying raw oats? Outside of type I immune hypersensitivity (anaphylactic allergy) that is always possible for any substance, it would seem little. Raw oat meal is an easy to prepare food that has many health benefits to offer. Raw oat milk is a food product that contains prebiotic soluble fiber and antifungal chitinase enzymes that can be taken therapeutically between meals to diminish GI fungal load and encourage a healthier bowel flora by selectively feeding butyrate-producing microflora.

Raw (unkilned) organic oat groats are sometimes called sprouting oats or Scottish oats. Oat groats are the unbroken inner oat seed kernels with the outer husks removed. Raw oat groats have not been cooked nor heat treated in any way; they are living seeds that will sprout.

Raw Oatmeal

Place 1 cup groats into a 2 cup measuring container and cover with water. Let stand at least 2 hours. Overnight is a sufficient and convenient soaking time for morning oatmeal.

Macerate the soaked oats in a high speed blender. Dish out and serve as you would cooked oatmeal, consuming all the liquids and solids. The natural flavor of raw oatmeal is nutty and slightly sweet. Persons suspecting Candida problems should not sweeten the oatmeal further, but can season their meal with cinnamon or other spices.

Raw Oatmilk

1 cup raw (unkilned) organic oat groats

Place in 2 cup measuring container and fill water to the 2 cup level. Let stand 2 hours. Macerate in a high-speed blender. Add 2-3 more cups of water. Let stand 1-2 hours more. After the second soaking, thoroughly blend.

Pour mixture through a fine mesh strainer into a catching container, stirring the bran accumulating in the strainer, allowing the milk to pass into the catchment. The insoluble remainder can be saved as a thickening ingredient for other recipes and can be cooked. The antifungal chitinase enzymes are dissolved into the milk and the milk should not be heated.

Cover and refrigerate for use as a drinking milk. Oat milk can be flavored with the addition of vanilla or other non-sweetening seasoning allowed to permeate the stored milk. With storage the milk separates and the solids settle. Stir or shake before pouring and drinking. For therapeutic use, drink oat milk between meals, allowing the milk to coat oral and GI mucous membranes.


Jeff Clark JCbioJeff Clark, ND is a 2007 graduate of NCNM and former high tech design engineer and manager. Dr. Clark is a founder of True Health Medicine, PC in Tualatin, OR a group naturopathic and acupuncture clinic serving the whole family. Dr. Clark’s practice emphasis is treating adults with chronic health conditions using nutrition, detoxification, herbal medicine, and IV nutrient therapy.

 

References

  1. Gibson L, Benson G. Origin, history, and uses of oat (avena sativa) and wheat (triticum aestivum). Iowa State Agronomy Department Website. http://www.agron.iastate.edu/courses/agron212/Readings/Oat_wheat_history.htm. Accessed November 21, 2009.
  2. Kurtz ES,Wallo W. Colloidal oatmeal: history, chemistry and clinical properties. J Drugs Dermatol. 2007;6(2):167-170.
  3. Sadiq BM, et al. Oat: unique among the cereals. Eur J Nutr. 2008;47(2):68-79.
  4. Welch RW. Can dietary oats promote health? Br J Biomed Sci. 1994;51(3):260-270.
  5. Queenan KM, et al. Concentrated oat beta-glucan, a fermentable fiber, lowers serum cholesterol in hypercholesterolemic adults in a randomized controlled trial. Nutr J. 2007;6:6.
  6. Reyna-Villasmil N. Oat-derived beta-glucan significantly improves HDLC and diminishes LDLC and non-HDL cholesterol in overweight individuals with mild hypercholesterolemia. Am J Ther. 2007;14(2):203-212.
  7. Robitaille J, et al. Effect of an oat bran-rich supplement on the metabolic profile of overweight premenopausal women. Ann Nutr Metab. 2005;49(3):141-148.
  8. Tapola N, et al. Glycemic responses of oat bran products in type 2 diabetic patients. Nutr Metab Cardiovasc Dis. 2005;15(4):255-261.
  9. Maki KC, et al. Effects of consuming foods containing oat beta-glucan on blood pressure, carbohydrate metabolism and biomarkers of oxidative stress in men and women with elevated blood pressure. Eur J Clin Nutr. 2007;61(6):786-795.
  10. Nie L, et al. Avenanthramide, a polyphenol from oats, inhibits vascular smooth muscle cell proliferation and enhances nitric oxide production. Atherosclerosis. 2006;186(2):260-266.
  11. Murphy EA, et al. Oat beta-glucan effects on neutrophil respiratory burst activity following exercise. Med Sci Sports Exerc. 2007;39(4):639-644.
  12. Kedia G, et al. In vitro fermentation of oat bran obtained by debranning with a mixed culture of human fecal bacteria. Curr Microbiol. 2009;58(4):338-342.
  13. Hallert C, et al. Increasing fecal butyrate in ulcerative colitis patients by diet: controlled pilot study. Inflamm Bowel Dis. 2003;9(2):116-121.
  14. Sorensen HP. Oat (Avena sativa) seed extract as an antifungal food preservative through the catalytic activity of a highly abundant Class I Chitinase. Appl Biochem Biotechnol. 2009 Feb 18. [Epub ahead of print]
  15. Fidel PL. Immunity to Candida. Oral Dis. 2002;8(suppl 2):69-75.
  16. Lacour M, et al. The pathogenetic significance of intestinal Candida colonization–a systematic review from an interdisciplinary and environmental medical point of view. Int J Hyg Environ Health. 2002;205(4):257-268.
  17. Lewith GT, et al. Elevation of Candida IgG antibodies in patients with medically unexplained symptoms. J Altern Complement Med. 2007;13(10):1129-1133.
  18. Diwischek F, et al. Cerulenin analogues as inhibitors of efflux pumps in drug-resistant Candida albicans. Arch Pharm (Weinheim). 2009;342(3):150-164.
  19. Wilheim AB, et al. The resistance to fluconazole in patients with esophageal candidiasis. Arq Gastroenterol. 2009;46(1):32-37.
  20. The MELISA Test. Melisa Medica Foundation Web site. http://www.melisa.org/

 

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