Oenothera biennis
is the plant commonly referred to as
evening primrose, tree
primrose, and sun drop. It is a
member of the Onagraceae, or willow, family.
[1]
Botanically, evening primrose
is a biennial plant; Characterized
by an erect,
rough branching stem growing 2 to 5
feet in height. [2] The leaves are ovate-lanceolate. The
large flowers are numerous and appear
in a pale-yellow in color. They
are considered nocturnal plants, blooming
only once and lasting for only one day. The
leaves and oil of evening primrose are the
parts of the plant used
medicinally. However, most
preparations only consist of the oil and
are referred to as EPO (evening
primrose oil).
In understanding how
evening primrose oil
works, one must first comprehend the
metabolism of essential fatty acids. Essential fatty acids are termed as
such because they cannot be
synthesized, or are not naturally
occuring, within the body and
therefore must be provided for in
the diet. The metabolic pathways of
essential fatty acids fall into two
categories, based on their chemical
structures: omega-3 fatty acids and
omega-6 fatty acids. Omega-3 fatty
acids are commonly found in cold
water fish, as eicosapentaenoic acid
(EPA) and docosahexaenoic acid (DHA).
Evening primrose
oil contains a fatty acid that is
categorized in the omega-6 fatty
acid pathway; beginning with linoleic acid. Linoleic acid is
found in plants and cannot be made
in the body. It is converted to
gamma-linolenic acid (GLA) by the
enzyme, delta-6 desaturase, which
removes two hydrogen molecules
effectively adding another double
bond (these essential fatty acids
are all polyunsaturated meaning they
have more than one double bond). GLA
is the fatty acid found in evening
primrose oil.
Although GLA can be
made in the body, in some
individuals the
conversion is problematic due to
polymorphisms in the enzyme.
Persons may also by lacking in enzyme cofactors
like vitamin B6, magnesium, and zinc. Furthermore, the delta-6 desaturase
enzyme can be inhibited by other
compounds, such as trans fatty acids,
alcohol, and saturated fats. [3] Therefore, it can be quite important
to have a preformed source of GLA as
is found in evening primrose oil.
Following either
conversion or consumption of GLA,
it is then metabolized to dihomo-GLA
(D-GLA) by an elongase enzyme which
adds two carbon units to the chain. This is an important point in the
omega-6 pathway because it is then
shuttled into one of two pathways:
-
Prostaglandin
1 series - the most
favorable. Aids GLAs conversion to arachadonic acid; which is
further metabolized via the,
-
Prostaglandin
2 series - or inflammatory leukotriene pathway
(associated with
inflammation and are unfavorable).
Interestingly, and
fortunately, the enzyme that converts
D-GLA to arachidonic acid is also
used in the omega-3 series pathway.
When there are more of these
favorable omega-3 fatty and omega-6 fatty acids, like GLA
in evening primrose oil, the
enzyme prefers to act on the omega-3
series, which often results in D-GLA being
converted to the prostaglandin 1
series (the series not associated
with inflammation). The balance of
dietary essential fatty acids in the
body is vital to proper functioning. Imbalances can lead to
a variety of disorders linked mainly
to inflammation, platelet
aggregation, and smooth muscle spasm. These problems can be addressed
through diet and supplementation
with certain omega-3 and omega-6
fatty acids, like evening primrose
oil.
Constituents in
evening primrose include;
fixed oil (15 - 20%), 65% essential fatty acids
(i.e. linoleic acid), gamma-linolenic acid
(8 - 10%), and triacylglycerols (trilinolein
and dilinoleoyl-mono-gamma-linolenin).[4
-6] GLA is also found in borage
oil, blackcurrant oil, and even certain
fungal lipids. However, most of the
evidence on the medicinal uses of GLA
is derived from studies
using evening primrose oil.
Medicinal actions
ascribed to the evening primrose oil
include:
The
leaves also possess digestive restorative
and anti-inflammatory properties. [1,
2]
Many herbs have a
long history of use.
Evening primrose, however, can be
considered part of the new
generation of supplementation. The
oil extracted from the seed,
commonly referred to as EPO, has
been extensively studied in the
treatment of various disorders,
ranging from specific dermatologic
to gynecologic conditions.
A clinical trial of
patients with atopic dermatitis (or
eczema) presenting with itchy dry
scaly skin examined EPO's effect. The results showed that
supplementation with EPO reduced the
extent of the skin lesions and
pruritis (itching) in all patients studied. Serum interferon (IFN)-gamma levels
were increased after the treatment
to those of the normal control
group, while serum IgE levels showed
a significant decrease. The authors
concluded that EPO could be a highly
effective treatment for 'grossly,'
non-inflammatory type atopic
dermatitis. The effect of EPO may be
through the modulation of the
immunological mechanism involving
IFN-gamma. [7]
Another double-blind,
placebo-controlled clinical trial in
children with atopic dermatitis
supports the use of EPO. A
significant improvement in the
overall severity of the clinical
condition, independent of whether
the children had manifestations of IgE-mediated allergy was recorded. The
content percentage of omega-6
fatty acids in the erythrocyte cell
membrane increased, especially in
the children treated with high doses
of EPO. In this high dose group, dihomo-gamma-linolenic acid (D-GLA)
also increased. [8]
It appears that EPO
may also be equally beneficial for treating
patients with diabetic neuropathy. In one double-blind, placebo-controlled study, 111 people
with mild diabetic neuropathy
received either 480 milligrams (mg) of GLA
or placebo daily. After a year,
the group taking GLA improved
significantly in 13 of the 16
parameters measured. [9]
Smaller study, and comparative animal research, has also found that evening
primrose oil can protect nerves from
diabetes-induced injury. [10-12]
Evening primrose
oil has been recommended to women
for treatment of symptoms associated
with premenstrual syndrome. Evidence
supporting this use has been
conflicting, however a number of
negative studies were so small that
the effectiveness of EOP was
difficult to rule out. A positive
study demonstrated that EPO was
better than placebo for treating
depression and other PMS symptoms. [13] It appears that EPO most
effectively addresses mastalgia
(breast pain) associated with the
menstrual cycle. In fact, in a large
study of women with this symptom, EPO demonstrated an equal level of
effectiveness as bromocriptine (a
pharmaceutical commonly prescribed
for cyclical mastalgia). [14] Most importantly, EPO has a very low
incidence of adverse effects, unlike
its prescription drug counterparts.
Additionally, EPO may
be beneficial for the treatment of
obesity, Raynaud's phenomenon,
schizophrenia, withdrawal from
alcohol, rheumatoid arthritis,
chronic fatigue syndrome, systemic
lupus erythematosus, hepatic
carcinoma, preeclampsia,
endometriosis, and ulcerative
colitis. [15-20]
Dosages are dependent
on the type of preparation and the
intended condition to be treated. If
using the oil, a range of 250 - 500 mg
of GLA (or 2.6 - 5.2 grams of EPO)
daily can be an effective dose for
conditions like atopic dermatitis
and mastalgia. For many of the other
conditions listed above (i.e. diabetic
neuropathy and inflammatory
diseases) a higher range of
500 - 600 mg GLA would be necessary. [1]
|
Evening Primrose Toxicities and
Contraindications |
Caution must be taken
in patients with a history of
epilepsy. One case report described
seizures in a patient using
evening primrose oil capsules
along with Cimicifuga racemosa and
Vitex-agnus castus for four months.
Evening primrose oils may also have the potential
to instigate undiagnosed temporal
lobe epilepsy. [21,
22]
Based
on this information and the potentiation of phenothiazines, EPO
should be avoided in patients with
seizure disorders. There is also
speculation that EPO will adversely
affect those with mania, as it will increase PGE1,
which is already in excess in this
condition.
Evening primrose
may interact with a number of
prescription medications. [23]
It may potentiate the epileptogenic
potential of phenothiazines. There
is also speculation that
anticoagulants may be potentiated
due to decreases in plasma
heparin-neutralizing activity and
platelet aggregation inhibition
associated with PGE-1, formed
from metabolism of DGLA. On the
other hand, EPO may favorably affect
other medications, such as
administration of GLA with tamoxifen.
Study has shown a faster clinical
response to tamoxifen in 38 patients
with estrogen-dependent breast
cancer. Also, kidney damage induced
by cyclosporine was reduced by the co-administration of 10 mg/kd of EPO
in rats.
Adverse effects of
EPO can include headache and mild
nausea. [24] No overdose symptoms have been
reported with the use of EPO. [1]
|
Evening Primrose Products |
The following table lists various
products that contain a safe and
reliable source of Evening Primrose:
|
Manufacturer |
Ingredient |
Amount |
US RDA |
Learn More |
|
GNC |
Evening Primrose Oil
|
500mg |
-- |
Click Here
 |
|
Natrol |
Evening Primrose Oil |
500 mg |
-- |
Click Here
 |
|
Nature's Way |
Evening Primrose Oil (seed) |
500 mg |
-- |
Click Here
 |