In this topic we want to present toxins that naturally occur in plant foods. See also: Plant Food Contamination, Pesticides.
Toxins in Raw Food
Introduction
Plant defense against herbivores
Plants use several strategies to defend against damage caused by herbivores. Many plants produce allelochemicals, that influence the behavior, growth, or survival of herbivores. These chemical defenses can act as repellents or toxins to herbivores, or reduce plant digestibility. While most plant defenses are directed against insects, the most significant herbivores, other defenses have evolved that are aimed at vertebrate herbivores, such as birds and mammals.
http://en.wikipedia.org/wiki/Plant_defense_against_herbivoryAntiherbivory compounds and can be classified into three sub-groups: nitrogen compounds (including alkaloids, cyanogenic glycosides and glucosinolates), terpenoids, and phenolics.
Alkaloids are derived from various amino acids. Over 3000 known alkaloids exist, examples include nicotine, caffeine, morphine, colchicine, ergolines, strychnine, and quinine. Alkaloids have pharmacological effects on humans and other animals.
Cyanogenic glycosides are stored in inactive forms in plant vacuoles. They become toxic when herbivores eat the plant and break cell membranes allowing the glycosides to come into contact with enzymes in the cytoplasm releasing hydrogen cyanide which blocks cellular respiration. The products can cause gastroenteritis, salivation, diarrhea, and irritation of the mouth.
The terpenoids, sometimes referred to as isoprenoids, are organic chemicals similar to terpenes. There are over 10,000 known types of terpenoids. Monoterpenoids are volatile essential oils such as citronella, limonene, menthol, camphor, and pinene. Diterpenoids are widely distributed in latex and resins, and can be quite toxic. Plant steroids and sterols are also produced from terpenoid precursors, including vitamin D, glycosides (such as digitalis) and saponins (which lyse red blood cells of herbivores).
Phenolics, sometimes called phenols. Some phenols have antiseptic properties, while others disrupt endocrine activity. Phenolics range from simple tannins to the more complex flavonoids that give plants much of their red, blue, yellow, and white pigments. Complex phenolics called polyphenols are capable of producing many different types of effects on humans, including antioxidant properties. Condensed tannins inhibit herbivore digestion by binding to consumed plant proteins and making them more difficult for animals to digest, and by interfering with protein absorption and digestive enzymes. Silica and lignins, which are completely indigestible to animals, grind down insect mandibles.
In addition to the three larger groups, fatty acid derivates, amino acids and even peptides are used as defence.
http://www2.mcdaniel.edu/Biology/botf99/herbnew/alkaloids.htmPlant regulation of fruit consumption
Plants invest energy into the production of fruits. Plants have evolved to encourage mutualist frugivores to consume their fruit for seed dispersal but also evolved mechanisms to decrease consumption of fruits when unripe and from non-seed dispersing predators. Plants have chemical and physical adaptations.
Chemical deterrents in plants are called secondary metabolites. Secondary metabolites are compounds produced by the plant that are not essential for the primary processes such as growth and reproduction. Toxins might have evolved to prevent consumption by animals that disperse seeds into unsuitable habitats, to prevent too many fruits from being eaten per feeding bout by preventing too many seeds being deposited in one site, or to prevent digestion of the seeds in the gut of the animal.
Physical deterrents:
- Cryptic coloration (e.g. green fruits blend in with the plant leaves)
- Unpalatable textures (e.g. thick skins made of anti-nutritive substances)
- Resins and saps (e.g. prevent animals from swallowing)
- Repellent substances, hard outer coats, spines, thorns.
Levey DJ, Tewksbury JJ, Izhaki I, Tsahar E, Haak DC. 2007. Evolutionary ecology of secondary compounds in ripe fruit Smith, R. L. Ecology and Field Biology. 5th ed. New York: Harper Collins, 1996.
Common toxins
Goitrogens
Goitrogens are substances that suppress the function of the thyroid gland by interfering with iodine uptake, which can, as a result, cause an enlargement of the thyroid. Certain raw foods have been identified as lightly goitrogenic (cooking inactivates the goitrogens).
These foods include:
- soybeans, pine nuts, peanuts,
- strawberries, pears, peaches,
- spinach, bamboo shoots, , bok choy, broccoli, brussels sprouts, cabbage, canola, cauliflower, collard greens, horseradish, kale, kohlrabi, mustard greens,
- sweet potatoes, radishes, turnips,
- millet.
Fruit
Nightshades
The toxins found in Nightshades (scopolamine , atropine, solanine, nicotine and more) may be the leading cause of Arthritic inflammation, cancer, Alzheimer’s, Migraine headaches, birth defects, miscarriages, inflammatory bowel disorder, and Crohn’s Disease.
http://www.nightshadefree.com/Then, in the 1600s and 1700s food and drug crops based on nightshades were imported from the Americas and for the past 400 years have penetrated and become ubiquitous in the Western diet. These include tobacco, tomatoes, potatoes and chili peppers. It is not surprising that these novel foods, being nightshades, were regarded with suspicion at first and were slow to take hold in the European diet. They all contain solanine in some form, named as solanine (potatoes), tomatine (tomatoes), alpha-solanine (aubergine) or solanadine (chillies and capsicums). They also contain nicotine in small amounts. Nicotine has a synergistic action with solanine -it stimulates the production of acetylcholine.
It is now apparent that there are groups of people who cannot tolerate nightshades in their diets, wish to avoid them anyway or find that eliminating them helps alleviate a variety of mental, emotional and physical problems.
http://www.craigsams.com/pages/tobac.htmlTomato
The leaves, stems, and green unripe fruit of the tomato plant contain small amounts of the poisonous alkaloid tomatine.
http://www.sciencedirect.com/science?...&md5=915d12d736cf571ed7793e94eec98a4dGreens
Celery
Celery is known to contain psoralens, a group of substances that cause a toxic dermal reaction on exposure to ultraviolet A rays (UVA).
http://www.ncbi.nlm.nih.gov/pubmed/8157392?dopt=abstracthttp://www.ncbi.nlm.nih.gov/pubmed/2960270?dopt=abstractParsnip
Wild parsnip contains furanocoumarins, which deter herbivores from eating its foliage.
http://www.bioone.org/doi/abs/10.1614/WT-05-186.1
Roots
Sweet potato
Lin et al. (1985) have established that sweet potato shows trypsin inhibitor activity (TIA) ranging from 90 percent inhibition in some varieties to 20 percent in others. There is a significant correlation between the trypsin inhibitor content and the protein content of the sweet potato variety. Heating to 90°C for several minutes inactivates trypsin inhibitors.
In response to injury, or exposure to infectious agents, in reaction to physiological stimulation or on exposure of wounded tissue to fungal contamination, sweet potato will produce certain metabolites. Some of these compounds, especially the furano-terpenoids are known to be toxic (Uritani, 1967). Fungal contamination of sweet potato tubers by Ceratocystis fimbriata and several Fusarium species leads to the production of ipomeamarone, a hepatoxin, while other metabolites like 4-ipomeanol are pulmonary toxins. Baking destroys only 40 percent of these toxins.
Potato
Potato contains the glycoalkaloids alpha-solanine and alpha-chaconine (Maya, 1980), concentrated mainly in the flowers and sprouts (200 to 500 mg/100 g). In healthy potato tubers the concentration of the glycoalkaloids is usually less than 10 mg/100 g and this can normally be reduced by peeling (Wood and Young, 1974; Bushway et al., 1983). In bitter varieties the alkaloid concentration can go up to 80 mg/100 g in the tuber as a whole and up to 150220 mg/100 g in the peel. The presence of these glycoalkaloids is not perceptible to the taste buds until they reach a concentration of 20 ma/100 g when they taste bitter. At higher concentrations they cause a burning and persistent irritation similar to hot pepper. At these concentrations solanine and other potato glycoalkaloids are toxic. They are not destroyed during normal cooking because the decomposition temperature of solanine is about 243 C.
Levels of glycoalkaloids may build up in potatoes which are exposed to bright light for long periods. They may also result from wounding during harvest or during post-harvest handling and storage, especially at temperatures below 10°C (Jadhav and Salunkhe, 1975). Glycoalkaloids are inhibitors of choline esterase and cause haemorrhagic damage to the gastrointestinal tract as well as to the retina (Ahmed, 1982). Solanine poisoning has been known to cause severe illness but it is rarely fatal (Jadhav and Salunkhe, 1975).
Potato also contains proteinase inhibitors which act as an effective defense against insects and micro-organisms but are no problem to humans because they are destroyed by heat.
Lectins or haemogglutenins are also present in potato. These toxins are capable of agglutinating the erythocytes of several mammalian species including humans (Goldstein and Hayes, 1978), but this is of minimal nutritional significance as haemogglutenins are also destroyed by heat, and potatoes are normally cooked before they are eaten.
http://www.fao.org/docrep/T0207E/T0207E08.htmThe modern practice of washing potatoes and packing them in plastic bags allows light to affect the potato and stimulate its production of solanine, the nightshade alkaloid that, in nature, sickens animals that might dig up potatoes for food. In 1976 the Department of Health, concerned about high levels of anencephaly and spina bifida, urged pregnant mothers to wear rubber gloves when preparing potatoes and to discard in their entirety any potatoes that showed signs of greening or of blight (black streaks in the potato) It is not enough to simply remove the discoloured part - the entire potato should not be eaten. The solanine in potatoes is 4 times greater in the skin than in the rest of the potato.
The fatal dose of solanine for an adult is 200-250 mg depending on body weight. Potatoes should not contain more than 20 mg of solanine per 100g, so it would take at least 1 Kg of potatoes (2.2 lbs) to be fatal. Potato peels have been found to contain up to 180 mg of solanine per 100g, so a person consuming 150-200g of deep fried potato peels with a high solanine content could be at considerable risk. Potatoes that have been properly stored and are from low solanine varieties will only contain 7 mg/100g. In 1996 the Committee on Toxicity stated that potatoes should not be eaten if they still taste bitter after the green parts and sprouts have been removed. However, few people taste-test a raw potato once it is peeled to assess its bitterness. Although spina bifida prevention now focuses on preconceptual consumption of folic acid, the world’s highest incidence of spina bifida is in Ireland, where the wet climate encourages late potato blight. A study in Belfast showed that mothers who had given birth to a child with spina bifida or anencephaly could reduce the risk of a similar defect in the second child by 50% if they maintained a potato-free diet.
http://www.craigsams.com/pages/tobac.htmlSolanine and chaconine in potatoes are not very dangerous unless big quantities are eaten. They don't accumulate in the body, but they are not destroyed by heat.
Cassava
Though not too widely used in the United States, cassava is a woody shrub that is generally found in the Caribbean and South America. When using cassava, it can either be made to be sweet or bitter. The taste, as well as the smell, all depends on the amount of cyanogenic glucosides, which are in fact, extremely poisonous. Most who prepare it like it to be bitter, as it keeps away insects and even animals. If cassava is prepared incorrectly, it can be deadly. Cassava poisoning, due to high levels of cyanide, is known as Konzo. Cassava poisoning leads to irreversible paralysis.
http://www.toptenz.net/top-10-toxic-foods-we-love-to-eat.phpMushrooms
Indeed, I recommend that no mushrooms be eaten raw. In addition to the heat labile hemolysin, some mushrooms contain potentially carcinogenic hydrazines that are deactivated on cooking. Others contain an enzyme that blocks protein uptake. Mushrooms can be very nutritious after cooking but are generally hard to digest or worse when eaten raw. Paradoxically, several strains of the common commercial button mushroom including the now popular Portobello, contain significant levels of Agaritine, a potentially carcinogenic hydrazine that is bioactivated by cooking.
http://academic.evergreen.edu/projects/mushrooms/phm/s49.htmMany hydrazines are known to be strong carcinogens and can be found in a lot of edible mushrooms. Cooking destroys some or all of the hydrazines, but the steam given off during cooking has been known to make some cooks ill. Besides this fact, the structural material or cell walls in mushrooms is made of chitin, and humans don’t have the ability to digest this derivative of cellulose. The body can do several things to this undigested chitin. It can expel it by vomiting or send it the other way with diarrhea. Small amounts may pass through the gut with other food and go unnoticed, or it may stay in the gut where bacteria will work on it causing bloating, gas, and other discomfort. Cooking does not destroy chitin but may ease its effect.
http://fungi-zette.com/mush12.htm#rawSamples of Shiitake, verified as being produced without any formaldehyde treatments, were found to produce similar levels of formaldehyde. In humans, it is known to have a number of damaging effects and there is limited evidence of a carcinogenic effect.
http://www.ncbi.nlm.nih.gov/pubmed/15764336?dopt=AbstractFormaldehyde, 2-Butoxyethanol and 1-tert-Butoxypropan-2-ol, IARC Monographs on the Evaluation of Carcinogenic Risks to Humans 88, Lyon, France: International Agency for Research on Cancer, 2006Flagellate skin lesions occur in some patients after eating the mushroom Lentinus edodes, and they are called shiitake dermatitis in Japan.
http://content.karger.com/produktedb/produkte.asp?typ=fulltext&file=drm97255











