ARTICLE
Auteur(s) : R.G. ACKMAN
Professor Emeritus, Department of Food Science and
Technology, Dalhousie University, Box 1000, Halifax, Nova Scotia,
B3J 2X4, Canada
Tel.: 902 494 6030
Fax: 902 420 0219
<robert.ackman@dal.ca>
Among the peculiar statements or assertions recently made promoting
omega 3 nutrition and nutraceutical products two are worth
discussing. One is that the menhaden oil used in a new margarine
type in the USA is “organic”. This can only be compared with the
term “organic farming” which has become to refer to foodstuffs
produced without fertilizers or chemical pesticides. A second claim
of note is that it is a supplemental source of DHA. It can also be
described as “vegetarian”. In fact the well-known infant formula
Martek Biosciences Corp. product [1] for DHA supplementation of
infant formulas is derived from a cultured single-celled
Crypthecodinium cohnii alga. It is interesting that Martek
are taking legal action against a competing product advertised as
“vegetarian” by Nutrinova Inc.
The application of such products during pregnancy and infant
nursing has recently been included in a review in this journal by
J.-M. Bourre [2]. The second is that although I have been
associated with marine and freshwater fish lipids for many years,
it was only a few years ago that I began to question the facile and
neatly drawn conversions of alpha-linolenic acid (ALA, 18:3n-3) to
EPA and DHA in fish as well as other marine organisms. This was
stimulated by the recent critical works published on humans
achieving the same conversion but only to a limited degree [3, 4].
It now may seem strange that there was a prolonged struggle to get
ALA the status of an “essential” fatty acid [5]. Originally this
was cautiously accepted but primarily because it apparently could
not be biosynthesized by animals. ALA as “essential” was only
tolerated in nutrition because it might have a role in keeping skin
in good health. In contrast the n-6 linoleic acid (LA, 18:2n-6) was
enthusiastically stuffed into our diets from the 1950s on in
attempts to reduce serum cholesterol [6, 7] and at that time not
because of any other obvious clinical need except for the clotting
aid thromboxane B2. Now we know that this was adding to the
pre-existing n-6/n-3 imbalance in our diets with dubious
consequences.
In respect to EPA (20:5n-3) and DHA (22:6n-3) they were simply
ignored as they were presumed to be easily made by the body from
ALA. In an attempt to promote our understanding of the
“essentiality” of three different chain lengths, S. Cunnane coined
the phrase “conditionally essential” for both LA and ALA [8]. It
has however not been widely accepted. We have in fact only lately
sorted out reports showing that only a small percentage of the ALA
consumed daily is utilized by the human body [9], and that the
reason for DHA being truly essential is probably the very low
activity of the delta-6 desaturase step in the Sprecher shunt
necessary to produce DHA [10, 11]. This introduces a new ethylenic
bond in 24:5n-3 to give 24:6n-3 which is then chain-shortened to
22:6n-3. This route can apply along with dietary sources as the
origin of the DHA normally found in human milk [11] and is included
in the most recent review of the essentiality of DHA in humans
[12].
Before closing the health/biomedical situation with apologies to
Dr. Bourre for duplicating some of his recent papers [2], it should
be noted that table 1 provides a partial
listing of the n-3 fatty acids commonly found in marine oils. In an
attempt to produce the highest possible numbers for labelling of
health-related products to overawe consumers [13], two less
well-known n-3 polyunsaturated fatty acids may be included. These
are obvious in the phytoplankton and zooplankton in Table 1 and are found in our edible marine
products, being respectively 18:4n-3 and 18:5n-3. Although only
traces of 18:5n-3 can be discerned in many fish oils, 1-3% of
18:4n-3 is usually there. The 18:5n-3 is readily converted to
18:4n-3 in fish cells [14], and the 18:4n-3 itself is useful in
humans [4]. The interconversion of the three
C20-C22 polyunsaturated n-3 fatty acids EPA, DPA and DHA has
been known for years and is of special interest in tissues such as
the endothelium of blood vessels [15]. It should be noted here that
the marine world considers that only the n-3 docosapentaenoic acid
(22:5n-3) is of interest and common at the 1-2% level in all fish
oils, while the alternative DPA isomer 22:5n-6 is present only in
traces compared to the 22:5n-3.
Table 1. Proportions* of
recovered unsaturated fatty acids in an experiment where mixed
phytoplankton were grazed on by copepods in a natural enviornment
and subsequently the copepods were the food of herring larvae**. A
partial single analysis of northern Atlantic herring oil is given
for comparison.
| Fatty acid total lipid |
Phytoplankton, total lipid |
Zooplankton, total lipid |
Herring larvae, triacylglycerols |
North Sea herring oil |
| 16:1n-7 |
13 |
4 |
5 |
7 |
| 18:1n-9 |
3 |
4 |
5 |
10 |
| 18:2n-6 |
2 |
2 |
2 |
1 |
| 18:3n-3 |
2 |
2 |
3 |
2 |
| 18:4n-3 |
10 |
6 |
17 |
3 |
| 18:5n-3 |
8 |
1 |
1 |
|
| 20:4n-6 |
Trace |
1 |
Trace |
Trace |
| 20:5n-3 |
13 |
18 |
15 |
7 |
| 22:5n-3 |
Trace |
1 |
1 |
1 |
| 22:6n-3 |
15 |
24 |
20 |
7 |
* w/w percent; ** From Fraser et al. [23].
The results of my own evaluation of the origins of EPA and DHA,
shown in figure
1, first appeared in an article promoting salmon as a
source of DHA [16]. In this brief review not all arguments can be
presented, but in a more extensive review D.R.Tocher has come to
similar conclusions [17.
There is much variation in the fatty acids of
phytoplankton (microalgae), and a recent paper in this publication
tabulated the principal fatty acids of five microalgae popular in
aquaculture [18]. Many other authors have conducted similar studies
in connection with aquaculture. What is not clear from these
studies is that there are often high degrees of selectivity in how
small marine animals consume the most desirable microalgae from
those available, perhaps primarily on the basis of relative size
(figure 2). The
immobile molluscan filter-feeders have to make do with whatever
food is delivered by the ocean currents. Some of this can be
detritus, particles including dead phytoplankton, or remains of
dead zooplankton or their feces, all with or without coating of
bacteria that can also be utilized for food [19]. From
phytoplankton they can also accumulate toxins deadly to humans
[20], but these animals have to have membranes with whatever are to
them “essential” fatty acids [21], including the long-chain
polyunsaturates. There may be an insufficient supply but apparently
they can utilize a delta-5 desaturase operating during the
biosynthesis of monounsaturated C20 fatty acids to fill in the
orderly rows of phospholipids in membranes with 5,11-20:2.
Concurrently or subsequently they may be elongating these to
C22 if necessary, generally to 7,13-22:2 [22].
Fraser et al. [23] have reported on a laboratory-type food
chain conducted in a floating open-top plastic cylinder in a
Scottish Loch. Filled with filtered seawater, zooplankton suitable
as food for larval herring were introduced and later the predator
on the zooplankton, newly hatched herring larvae. There were
13 major species of phytoplankton initially present to provide
a good assortment of fatty acids when pooled from total lipids with
the results shown in table 1.
Excepting for the surprising accumulation of 18:4n-3, the herring
larva unsaturated fatty acids in the triacylglycerols already
resemble that of the composition of the oil from mature North sea
herring [24]. Another difference of note however is the absence of
more than 1% 20:1 and 22:1, fatty acids produced from the
alcohols of copepods [25], that could make up 35% of the fatty
acids in this particular type of oceanic herring oil [24]. The
larval herring present had been feeding for 28 days after
hatching and may have used up most of the initial egg lipids during
the initial 4-8 days of the study [23], but 20:1 and
22:1 were virtually absent. The role of selective feeding at
either the first or second stage of this experiment is discussed by
the authors.
Menhaden oil, from a fish species directly consuming North
Atlantic or Gulf of Mexico phytoplankton by filter feeding, also
shows [24] only 1.3% each of 18:2n-6 and 18:3n-3, but 11% of
20:5n-3 and 9% of 22:6n-3. These figures may represent those fatty
acid proportions in the phytoplankton of their diet.
It was on the basis of many such findings that figure 1 was prepared.
Although the simple disposal of the phytoplankton 18:2n-6 and
18:3n-3may be presumptuous, their absence as significant lipid
components in many marine invertebrates should be noted. Green
algae are the most likely phytoplankton species to show
accumulation of 18:2n-6 but only modest amounts of its successor
acid arachidonic (20:4n-6). Correspondingly the very long-chain EPA
and DHA may be modest in green algae except in Cryptomonads
[26].
These generalities are expressly applicable to the North Atlantic
and North Pacific ecosytems. In the tropics the sunlit coral reefs
have many organisms with more substantial accumulations of
arachidonic acid than in the colder northern latitudes. Possibly
this provides for a greater range of chemical signals in the water
in such crowded communities. We do not often think of fatty acids
as essential for this among humans! There are suspicions among
oceanographers that major changes in ocean water distribution are
pending, perhaps in hundreds of years instead of millennia. The
distribution of fish populations may be seriously affected, but the
importance of sources of omega 3 fatty acids is of concern.
Australian and New Zealand scientists are participating in many
similar studies [26, 27].
The invertebrates of figure 2 are often
concentrated and localized by mixing of water masses, but certainly
are one of the major biomasses in the world’s oceans. The work of
M.V. Bell and colleagues has shown that rainbow trout held in
freshwater were capable of catabolizing much of the dietary
labelled 18:3n-3 with very little conversion to DHA [28], and they
have followed biosynthesis in various organs and tissues [29]. This
latent route to EPA and DHA in the trout, which in the ocean would
normally be plentifully supplied with EPA and DHA in the wild, is
probably paralleled by the modern position of humans in their
handling of the conversion of ALA to DHA.
Whether the EPA and DHA situation of falling supplies of fish oil
in fish aquaculture can be offset by partial introduction of
vegetable oils remains to be seen. The regrettable aspect of the
natural supply of these two truly essential fatty acids, EPA and
DHA, is that over-harvesting of fish is rapidly becoming a scandal,
and the generous supply of natural vegetable EPA and DHA in the
oceans will be mostly wasted.
Some activists advocate fish oil capsules as safer than fish, and
some suspect that hidden benefits such as selenium may give fish a
nutritional edge over capsules. Both are equally satisfactory [30],
Recommendations for fish consumption by the American Heart
Association [31] are summarized in a very readable review from the
U.K. [32]. Part of its title is “Fishing for a natural
treatment”!
The safety of cultured algal supplies of the necessary long-chain,
highly unsaturated omega 3 fatty acids in our diets is assured
[1, 33, 34]. Unfortunately activist groups are prone to push
potential problems to the fore, and the media flourish on
exaggerating their interpretations of scientific data. Some such
newsletters are more trustworthy than others [35], and it is not
for nothing that BMJ (British Medical Journal) recently
devoted its entire cover to a simple but ironic message: “Trust me.
I’m a website.” This is a sad commentary on our efforts to promote
a natural source of our two truly essential fatty acids. n
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