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Creature Companion 2017; December: 32, 34.
Anton C. Beynen
Flax in dog food
Flax is a plant grown mainly for its oil and occasionally as linen-fiber crop. Flaxseeds, also known
as linseeds, are small, flat and oval-shaped. Flaxseed or its oil component is found in the ingredient
lists of many commercial dog foods. Dry foods may contain up to 10% flaxseed or 4% flaxseed oil.
Flaxseed meal (defatted seeds) is scarcely used.
Alpha-linolenic acid (ALA), an omega-3 fatty acid, is an essential nutrient that must be present in
the diet. Various ingredients provide ALA, but flaxseed (oil) has a uniquely rich content. The dog
can convert ALA into EPA (eicosapentaenoic acid), which elicits biological activity. The conversion
forms the basis for claims that flaxseed (oil) supports healthy skin, hair coat, joints and heart, but
these enhancements are unproven for flaxseed incorporated into an ALA-sufficient diet.
Supplemental flaxseed oil may ameliorate inflammatory skin disease.
Some internet discussions convey the impression that flaxseed causes food allergy. A manufacturer
offers a dog food line with an explicit flax-free claim. In fact, canine food allergy is rare (1),
rendering flaxseed allergy exceptionally rare. Another concern is that dietary flax releases
potentially toxic cyanide. No adverse cyanide-related effects have been reported for practical
flaxseed-containing dog diets, but this status quo awaits controlled study for confirmation (Note
1).
Flaxseed is high in lignans, compounds that can imitate or oppose female sex hormone activity.
Some dog breeders use flaxseed supplements for reproductive health (2). In female rats, dietary
flaxseed altered reproductive development and reduced the risk of chemical-induced breast
cancer. These topics are still unaddressed in dogs. Flaxseed-containing dog foods might affect
long-term health positively or negatively. For now, flaxseed (oil) is a suitable, but dispensable
ingredient.
Composition
The approximate composition of whole flaxseed is 36% crude fat, 22% crude protein, 8% crude fiber,
4% ash and 8% moisture. The specialities, ALA and secoisolariciresinol diglucoside (SDG), constitute
about 20 and 1%. Total SDG (3) consists of various oligomers (4). Measurable amounts of undesired
cyanogenic glucosides, tannins and seed-coat mucilage fall markedly upon heat treatment (5, 6) such
as applied in the production of kibbled or canned food.
Flaxseeds have a tough hull. Human subjects consuming muffins with identical amounts of ALA as
whole flaxseed, milled seed or flax oil, had increasing plasma ALA concentrations, in this order (7).
Grinding seeds or isolating oil enhances ALA availability, but also its oxidation susceptibility. In stored
oil, oxidation (8) and bitter products (9) appear.
Total-tract digestibility
Incorporating flaxseed, presumably ground and at 5.6%, into an extruded food, without changing
macronutrient composition, lowered apparent protein and fat digestibility in dogs by about one
percent unit, while fecal moisture was unaffected (10). Flaxseed fermentation by canine fecal flora
gave uninterpretable results (11).
Solvent-extracted flaxseed meal, as component of extruded kibbles, had an apparent protein
digestibility of 79% (12). It was 77% for pressed flaxseed cake, soaked in hot water and then mixed
with wetted kibbles (13). Intake of dietary dry matter with 1% flaxseed mucilage, which matches
about 9% whole flaxseed (6, 14, 15), resulted in lower fat digestibility and more moist stools (16).
Alpha-linolenic acid
Feeding ground flaxseed or flax oil to dogs raises ALA, EPA and docosapentaenoic acid (DPA), but not
docosahexaenoic acid (DHA), in blood total lipids, phospholipids, triglycerides, erythrocytes,
neutrophils, and heart tissue (17-22). ALA intakes were increased up to 6.5 g per MJ metabolizable
energy for at least 4 weeks.
The fatty acid changes endorse that the dog is capable of converting ALA. The liver desaturates both
linoleic acid (LA) and ALA (23), releases arachidonic acid (24) and likely EPA and DPA also. Canine
retina and brain functionality requires DHA, plasma DPA serving as (co-)precursor (25). Milk fat from
dogs fed flax oil during gestation and lactation was enriched in ALA, but not in EPA, DPA and DHA
(26).
Eicosapentaenoic acid
EPA gives rise to eicosanoids with wide-ranging biological properties. Dogs gather bodily EPA more
efficiently from dietary EPA than from ALA (22) or ALA’s delta-6-desaturase product, stearidonic acid
(27). Using the observed (22) build-up of plasma phospholipid EPA as criterion, it follows (Note 2)
that 1.5 g of flaxseed oil (55% ALA) is as effective as 1 g of fish oil (10% EPA).
Skin health
Increasing the dietary ALA level from 0.08 g/MJ, which met the dog’s requirement (28, Note 3), to
0.56 g/MJ by inclusion of ground flaxseed, did not affect skin and hair coat condition in healthy dogs
(29, 30). Among four canine diets, the diet containing flax was not associated with healthier skin and
hair (31). Supplemental flaxseed oil (0.44 g ALA/MJ diet) improved canine atopic dermatitis
somewhat less than pure EPA (0.20 g/MJ diet) (32), while EPA amounted to twice the maximum
effective dose (33).
Heart and joint health
Fish oil (0.13 g EPA/MJ diet), but not flax oil (0.17 g ALA/MJ diet) supplementation, distinctly
elevated group-mean plasma EPA and reduced ventricular arrhythmia in Boxers (34). Fish oil (0.2-0.4
g EPA/MJ diet) has a small beneficial impact on canine osteoarthritis (35), but flax oil’s position
remains unknown.
Cancer
In specific rat studies (36, 37), flaxseed mitigated cancer risk. Exposure to a diet with 10% ground
flaxseed or 0.02% SDG during suckling, reduced the incidence of dimetylbenzanthracene-induced
palpable mammary tumors later in life (37).
Reproductive development
Dietary flaxseed activated oestrogen-receptor signaling in murine mammary gland (38). Diets
containing 5 or 10% flaxseed delayed or accelerated puberty onset in female rats (39, 40).
Note 1
Cyanogenic glycosides (CG) are plant chemicals consisting of a nitrile aglycone and a carbohydrate
moiety (glucose or gentobiose). Upon destruction of the plant cell structure, CG’s are hydrolysed by
endogenous enzymes, yielding hydroxypropanenitrile, which decomposes in aqueous solution to
hydrogen cyanide. In flaxseed, the main CG’s are linamarin, linustatin and neolinustatin. The
contents differ among flaxseed varieties (41).
The releasable amount of cyanide in flaxseed, as determined by alkaline titration, is about 200
mg/kg (5, 6). This amount translates to 10 mg/kg dry petfood at 10% flaxseed inclusion level and
50% loss (5, 6) during processing. In young dogs fed a diet based on cooked rice and pork, the
addition of sodium cyanide to a level of 9 mg cyanide/kg dry matter markedly reduced body-weight
gain (42). In contrast, a diet containing cooked cassava instead of rice and providing 11 mg
cyanide/kg dry matter, had no effect on growth.
Note 2
Dogs were fed diets (1.9 MJ/100 g) containing either beef tallow (0.09 g ALA and 0 g EPA/MJ)
flaxseed oil (5.42 g ALA and 0 g EPA/MJ) or menhaden oil (0.12 g ALA and 1.62 g EPA/MJ) (22). After
feeding the diets for 28 days, the EPA contents of plasma phospholipids were 0.53, 4.42 and 10.17
mol% of total fatty acids. The diets with flaxseed and menhaden oil had increased phospholipid EPA
by 3.89 and 9.64 mol%, which was caused by the additional intakes of 5.33 g ALA and 1.62 g EPA/MJ,
respectively. Thus, 1 g ALA and 1 g EPA would raise phospholipid EPA by 0.73 and 5.95 mol%, while 1
g flaxseed oil (0.55 g ALA) and 1 g fish oil (0.10 g EPA) would induce increments of 0.40 and 0.60
mol%. In other words, 1.5 g flaxseed oil is equivalent to 1.0 g fish oil. Some of the flaxseed
inefficiency is likely due to its LA which competes with ALA for the delta-6-desaturase. The flaxseed
and menhaden-oil diets contained 2.11 and 0.69 g LA/MJ (22).
Note 3
The recommended LA and ALA allowances for adult dogs at maintenance have been set at 0.66 and
0.026 g/MJ while the LA:ALA ratio should be between 2.6 and 26 (28). Thus, the 0.026 g ALA/MJ
value is the minimum requirement at 0.66 g LA/MJ as the LA:ALA ratio results in 25.4. The role of the
ratio relates to the competition between LA and ALA for the delta-6-desaturase.
With regard to skin and hair coat condition in healthy dogs, diets containing ground sunflowerseed
(2.51 g LA and 0.12 g ALA/MJ, ratio 20.9) or ground flaxseed (1.97 g LA and 0.68 g ALA/MJ, ratio 2.9)
have been compared (29). Diets with either beef tallow (0.66 g LA and 0.05 g ALA/MJ, ratio 13.2),
sunflower oil (2.37 g LA and 0.07 g ALA, ratio 33.9) or ground flaxseed (2.37 g LA and 0.61 g ALA/MJ,
ratio 3.9) have also been compared (30). Two control diets within the comparisons can be
considered ALA sufficient. The sunflowerseed and tallow diets contained more than 0.026 g ALA/MJ
and had a LA:ALA ratio lower than 26. The sunflower-oil diet had a LA:ALA ratio of 33.9 so that the
ALA content of 0.07 g/MJ may be considered deficient. On the other hand, the 0.07 g ALA/MJ is 2.7
times higher than the minimum requirement at the LA:ALA ratio of 26.
The situation is further complicated by the fact that the diets differed as to contents of EPA, which
could be ALA’s mediator in potentially affecting skin and hair condition. The diets with
sunflowerseed and flaxseed contained 7 and 19 mg EPA/MJ (18, 29). The diets with beef tallow,
sunflower oil and flaxseed contained 11, 7 and 34 mg EPA/MJ (30). Thus, the flaxseed diets
contained more EPA than their control diets. The proposed requirement for EPA is 14 mg/MJ (28).
Even though the flaxseed versus sunflower-oil-diet increased both ALA and EPA intake above their
requirements, there was no improvement of skin and hair coat condition (30).
A third study was published in abstract form (31). The data show that dietary flax was not associated
with changes in skin and hair coat condition in healthy dogs. A diet containing flax as ALA source was
compared with three traditional canine diets. The ingredient and analysed compositions of the four
diets, including the fatty acid profiles, are not reported.
Literature
1. Beynen A.C. Hypoallergenic dog foods: supply and demand overwhelm need. All About Feed 2015;
23/9: 34.
2. Lans C, Turner N, Brauer G, Khan T. Medicinal plants used in British Columbia, Canada for
reproductive health in pets. Prev Vet Med 2009; 90: 268-273.
3. Johnsson P, Kamal-Eldin A, Lundgren LN, Åman P. HPLC method for analysis of secoisolariciresinol
diglucoside in flaxseeds. J Agric Food Chem 2000; 48: 5216-5219.
4. Li X, Yuan J-P, Xu S-P, Wang J-H, Liu X. Separation and determination of secoisolariciresinol
diglucoside oligomers and their hydrolysates in the flaxseed extract by high-performance liquid
chromatography. J Chromatogr A 2008; 1185: 223-232.
5. Feng D, Shen Y, Chavez ER. Effectiveness of different processing methods in reducing hydrogen
cyanide content of flaxseed. J Sci Food Agric 2003; 83: 836-841.
6. Imran M, Anjum FM, Ahmad N, Khan MK, Mushtaq Z, Nadeem M, Hussain S. Impact of extrusion
processing conditions on lipid peroxidation and storage stability of full-fat flaxseed meal. Lipids
Health Dis 2015; 14: 92.
7. Austria JA, Richard MN, Chahine MN, Edel AL, Malcolmson LJ, Dupasquier CMC, Pierce GN.
Bioavailability of alpha-linolenic acid in subjects after ingestion of three different forms of flaxseed. J
Am Coll Nutr 2008; 27: 214-221.
8. Tańska M, Roszkowska B, Skrajda M, Dąbrowski G. Commercial cold pressed flaxseed oils quality
and oxidative stability at the beginning and end of their shelf life. J Oleo Sci 2016; 65: 111-121.
9. Brühl L, Matthäus B, Fehling E, Wiege B, Lehmann B, Luftmann H, Bergander K, Quiroga K,
Scheipers A, Frank O, Hofmann T. Identification of bitter off-taste compounds in the stored cold
pressed linseed oil. J Agric Food Chem 2007; 55: 7864-7868.
10. Martinez Sotelo PG, Quinteros Granja AG. Evalución de la digestibilidad aparente de dietas con
semilla de linaza (Linum usitatissimun) vs. dietas con sebo en perros. DVM thesis, Universidad
Central del Ecuador, Facultad de Medicina Veterinaria y Zootechnia, Quito, Ecudaor, 2012.
11. Swanson KS, Grieshop CM, Clapper GM, Shields Jr RG, Belay T, Merchen NR, Fahey Jr GC. Fruit
and vegetable fiber fermentation by gut microflora from canines. J Anim Sci 2001; 79: 919-926.
12. Gröner T, Pfeffer E. Digestibility of organic matter and digestible energy in single ingredients of
extruded dog foods and their effects on faecal dry matter concentration and consistency. J Anim
Physiol Anim Nutr 1997; 77: 214-220.
13. Kempe R, Saastamoinen M. Effect of linseed cake supplementation on digestibility and faecal and
haematological parameters in dogs. J Anim Physiol Anim Nutr 2007; 91: 319-325.
14. Bhatty RS, Cherdkiatgumchai P. Compositional analysis of laboratory-prepared and commercial
samples of linseed meal and of hull isolated from flax. J Am Oil Chem Soc 1990; 67: 79-84.
15. Bhatty RS. Further compositional analyses of flax: mucilage, trypsin inhibitors and hydrocyanic
acid. J Am Oil Chem Soc 1993; 70: 899-904.
16. Nybroe S, Astrup A, Bjørnvad CR. Dietary supplementation with flaxseed mucilage alone or in
combination with calcium in dogs – effects on apparent digestibility of fat and energy and fecal
characteristics. Int J Obes 2016; 40: 1884-1890.
17. Anderson RE, Maude MB, Acland G, Aguirre GD. Plasma lipid changes in PRCD-affected and
normal miniature poodles given oral supplements of linseed oil. Indications for the involvement of n-
3 fatty acids in inherited retinal degenerations. Exp Eye Res 1994; 58: 129-137.
18. Bauer JE, Dunbar BL, Bigley KE. Dietary flaxseed in dogs results in differential transport and
metabolism of (n-3) polyunsaturated fatty acids. J Nutr 1998; 128: 2641S-2644S.
19. Bibus DM, Stitt PA. Metabolism of α-linolenic acid from flaxseed in dogs. World Rev Nutr Diet
1998; 83: 186-198.
20. Dunbar BL, Bigley KE, Bauer JE. Early and sustained enrichment of serum n-3 long chain
polyunsaturated fatty acids in dogs fed a flaxseed supplemented diet. Lipids 2010; 45: 1-10.
21. Purushothaman D, Brown WY, Wu S-H, Vanselow B. Evaluation of breed effects on n-3 PUFA
metabolism with dietary flaxseed oil supplementation in dogs. Br J Nutr 2011; 106: S139-S141.
22. Waldron MK, Hannah SS, Bauer JE. Plasma phospholipid fatty acid and ex vivo neutrophil
responses are differently altered in dogs fed fish- and linseed-oil containing diets at the same n-6:n-3
fatty acid ratio. Lipids 2012; 47: 425-434.
23. Dunbar BL, Bauer JE. Conversion of essential fatty acids by delta 6-desaturase in dog liver
microsomes. J Nutr 2002; 132: 1701S-1703S.
24. Caren R, Corbo L. The origin of plasma arachidonic acid in dogs. Metabolism 1968; 11: 1043-
1050.
25. Alvarez RA, Aguirre GD, Acland GM, Anderson RE. Docosapentaenoic acid is converted to
docosahexaenoic acid in the retinas of normal and prcd-affected miniature poodle dogs. Invest
Ophthalmol Vis Sci 1994; 35: 402-408.
26. Heinemann KM, Waldron MK, Bigley KE, Lees GE, Bauer JE. Long-chain (n-3) polyunsaturated
fatty acids are more efficient than α-linolenic acid in improving electroretinogram responses of
puppies exposed during gestation, lactation and weaning. J Nutr 2005; 135: 1960-1966.
27. Harris WS, DiRienzo MA, Sands SA, George C, Jones PG, Eapen AK. Stearidonic acid increases the
red blood cell and heart eicosapentaenoic acid content in dogs. Lipids 2007; 42: 325-333.
28. National Research Council. Nutrient requirements of dogs and cats. National Academy of
Sciences, Washington DC, 2006.
29. Rees CA, Bauer JE, Burkholder WJ, Kennis RA, Dunbar BL, Bigley KE. Effects of dietary flax seed
and sunflower seed supplementation on normal canine serum polyunsaturated fatty acids and skin
and hair coat condition. Vet Dermatol 2001; 12: 111-117.
30. Hester SL. Effect of dietary polyunsaturated fatty acid and related nutrients on plasma lipids, and
skin and hair coat condition in canines. MSc thesis, Texas A&M University, College Station, TX, USA,
2004.
31. Campbell KL, Roudebush P. Effects of four diets on serum and cutaneous fatty acids,
transepidermal water losses, skin surface lipids, hydration and condition of the skin and hair coat of
dogs. Proceedings AAVD/ACVD Meeting 1995, pp 80-81.
32. Mueller RS, Fieseler KV, Fettman MJ, Zabel S, Rosychuk RAW, Ogilvie GK, Greenwalt TL. Effect of
omega-3 fatty acids on canine atopic dermatitis. J Small Anim Pract 2004; 45: 293-297.
33. Beynen A.C. Vetzuurtherapie bij honden met atopische dermatitis. Dier-en-Arts 2017; Nr. 8/9:
222-225.
34. Smith CE, Freeman LM, Rush JE, Cunningham SM, Biourge V. Omega-3 fatty acids in Boxer dogs
with arrhythmogenic right ventricular cardiomyopathy. J Vet Intern Med 2007; 21: 265-273.
35. Beynen A.C. Visolie en behandeling van osteoartritis bij honden en katten. Dier-en-Arts 2016; Nr.
10: 264-267.
36. Thompson LU, Seidl MM, Rickard SE, Orcheson LJ, Fong HHS. Antitumorigenic effect of a
mammalian lignan precursor from flaxseed. Nutr Cancer 1996; 26: 159-165.
37. Chen J, Tan KP, Ward WE, Thompson LU. Exposure to flaxseed or its purified lignan during
suckling inhibits chemically induced rat mammary tumorigenesis. Exp Biol Med 2003; 228: 951-958.
38. Penttinen-Damdimopoulou P, Power KA, Hurmerinta TT, Nurmi T, Van der Saag PT, Mäkelä SI.
Dietary sources of lignans and isoflavones modulate responses to estradiol in estrogen reporter
mice. Mol Nutr Food Res 2009; 53: 996-1006.
39. Tou JCL, Chen J, Thompson LU. Flaxseed and its lignan precursor, secoisolariciresinol diglycoside,
affect pregnancy outcome and reproductive development in rats. J Nutr 1998; 128: 1861-1868.
40. Tou JCL, Thompson LU. Exposure to flaxseed or its lignan component during different
developmental stages influences rat mammary gland structures. Carcinogenesis 1999: 20: 1831-
1835.
41. Russo R, Reggiani R. Variation in the content of cyanogenic glycosides in flaxseed meal from
twenty-one varieties. Food Nutr Sci 2014; 5: 1456-1462.
42. Kamalu BP. Digestibility of a nutritionally-balanced cassava (Manihot eculanta Crantz) diet and its
effect on growth in young male dogs. Br J Nutr 1991; 66: 199-208.