Evening primrose oil
Identification
- Generic Name
- Evening primrose oil
- DrugBank Accession Number
- DB11358
- Background
Evening primrose oil comes from the extraction from Oenothera biennis seeds and it is commonly used as an alternative source for omega-6 essential fatty acids. In its composition it presents some fatty acids such as Linolenic acid and Gamolenic acid.1 Evening primrose oil has been filled for the FDA by Humanetics Corporation on April 2000 to be a new dietary ingredient but its current status is "Inadequate basis for expectation of safety".5 By Health Canada, evening primrose oil is approved in over-the-counter combination dietary supplements.6 By the EMA, evening primrose oil is approved in herbal preparations.7
- Type
- Biotech
- Groups
- Investigational, Nutraceutical
- Synonyms
- Oenothera biennis (evening primrose) oil
- Oenothera biennis (evening primrose) seed extract
- Oenothera biennis l. oil
- Oenothera biennis seed extract
- Oenothera biennis seed oil
- Oenothera lamarckiana l. oil
- Oenothera muricata seed oil
- Oenothera oil
- Oenothera pycnocarpa seed oil
- Oenotherae biennis oleum
- Oils, glyceridic, evening primrose
- Oleum oenotherae erythrospinae
- Primrose oil
Pharmacology
- Indication
Evening primrose oil is used as part of over-the-counter dietary supplements.6
It is also used for the treatment of systemic inflammatory diseases and for women's health conditions such as cyclical mastalgia. These indications do not have sufficient evidence of their effectiveness. It was used for the treatment of atopic dermatitis in the United Kingdom but it is currently withdrawn due to lack of evidence of effectiveness.1
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- Contraindications & Blackbox Warnings
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- Pharmacodynamics
The effectivity of evening primrose oil is debatable as the evidence is very limited.9 Evening primrose oil improves the essential fatty acid content in plasma, erythrocyte, and platelet lipids. It has also been registered to increase alpha-tocopherol levels in non-diabetic and type I diabetic patients. Evening primrose oil affects the fatty acid composition of serum lipids and adipose tissue as well as it helps maintain normal cellular structures and it serves as a prostaglandin precursor. Administration of evening primrose oil is part of long-term therapy and thus, immediate results are never expected.4
- Mechanism of action
Evening primrose oil presents a content of 74% Linolenic acid and 9% Gamolenic acid from which the later seems to be the key active ingredient of this oil. These major essential fatty acids are required for the normal structure of cell membranes and they are not synthesized endogenously.4 The therapeutic activity of evening primrose oil is attributed to the direct action of its essential fatty acids on immune cells as well as to an indirect effect on the synthesis of eicosanoids. The actions of highly unsaturated fatty acids in tissues and eicosanoids are thought to be implicated in inflammatory and immunologic pathogeneses.1
The essential fatty acids found in evening primrose oil are involved in the biosynthesis of prostaglandin. For this activity, the main involved component is the Gamolenic acid. The presence of this essential fatty acid allows the synthesis of anti-inflammatory substances such as 15-hydroxy-eicosatrienoic acid and prostaglandin E1.4
- Absorption
The pharmacokinetics of evening primrose oil is mainly studied by analyzing its active ingredient Gamolenic acid. After administration, Gamolenic acid is rapidly absorbed and converted directly to Dihomo-gamma-linolenic acid and other precursors.4 When orally administered, the tmax was directly dependent to the time of administration, being of 2.7 hours in the evening and 4.4 hours in the morning. The Cmax and AUC were registered to be approximately 21 mcg/ml and 274 mcg.h/ml.2 The bioavailability of Gamolenic acid acid is influenced by triglyceride composition, cellular kinetics of phospholipases and acyltransferases.3
- Volume of distribution
No pharmacokinetic data available.
- Protein binding
No pharmacokinetic data available.
- Metabolism
The main component of evening primrose oil, Linolenic acid is usually desaturated by delta-6-desaturase which transforms this fatty acid to Gamolenic acid. This metabolic activity usually is limited by external factors such as stress, aging, alcohol, smoking, inflammation, diabetes, etc. In presence of these circumstances, the linoleic acid gets accumulated in the body and it inhibits the activity of the enzyme delta-6-desaturase. In proper conditions, Gamolenic acid forms Dihomo-gamma-linolenic acid by the action of elongases and it can further act as a substrate for production of prostaglandins or to be denaturated to arachidonic acid.4
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- Route of elimination
The major components of the primrose oil are highly metabolized and the majority of the generated metabolites are excreted in the urine.8
- Half-life
No pharmacokinetic data available.
- Clearance
No pharmacokinetic data available.
- Adverse Effects
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- Toxicity
Evening primrose oil seems to have little toxicological effect in humans. The reported LD50 values in the mouse are 3.12 x 10^4 mcg/kg. The toxicological effects are very minimal and it has proven to not have an effect on tumor incidence nor to present effects on fertility studies.9
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs Browse all" title="About SNP Mediated Effects/ADRs" id="snp-actions-info" class="drug-info-popup" href="javascript:void(0);">
- Not Available
Interactions
- Drug Interactions Learn More" title="About Drug Interactions" id="structured-interactions-info" class="drug-info-popup" href="javascript:void(0);">
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Drug Interaction Integrate drug-drug
interactions in your softwareAbacavir Abacavir may decrease the excretion rate of Evening primrose oil which could result in a higher serum level. Aceclofenac Aceclofenac may decrease the excretion rate of Evening primrose oil which could result in a higher serum level. Acemetacin Acemetacin may decrease the excretion rate of Evening primrose oil which could result in a higher serum level. Acetaminophen Acetaminophen may decrease the excretion rate of Evening primrose oil which could result in a higher serum level. Acetazolamide Acetazolamide may increase the excretion rate of Evening primrose oil which could result in a lower serum level and potentially a reduction in efficacy. - Food Interactions
- Not Available
Products
- Drug product information from 10+ global regionsOur datasets provide approved product information including:dosage, form, labeller, route of administration, and marketing period.Access drug product information from over 10 global regions.
- Mixture Products
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image Efamol Cap Evening primrose oil (.6 mL) + Vitamin E (13.6 unit) Capsule Oral Efamol Research Inc. 1982-12-31 1999-10-25 Canada Evening Primrose Oil Cap Evening primrose oil (500 mg / cap) + Vitamin E (13.6 unit / cap) Capsule Oral Nature's Way Of Canada Ltd. 1984-12-31 2004-07-26 Canada Evening Primrose Oil With Vitamin E Evening primrose oil (500 mg/1) + Vitamin E (15 unit/1) Capsule Oral Ashbury Research Corporation Not applicable Not applicable Canada Gamma Oil Evening primrose oil (500 mg / cap) + Vitamin E (14.9 unit / cap) Capsule Oral Quest Vitamins A Div Of Purity Life Health Products 1985-12-31 2000-07-20 Canada Hovid Omega-3 + 6 Evening primrose oil (500 mg) + Fish oil (500 mg) Capsule, gelatin coated Oral Hovid Berhad 2020-09-08 Not applicable Malaysia - Unapproved/Other Products
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image Rhodd Ato Repair Body So Ap Evening primrose oil (6.0 g/100g) + Chamaecyparis obtusa leaf (2.0 g/100g) + Olive oil (13.0 g/100g) Soap Topical SJ NATURAL 2018-08-01 Not applicable US VP-Precip Evening primrose oil (500 mg/1) + Bilberry (40 mg/1) + Linseed oil (1000 mg/1) Capsule, gelatin coated Oral Virtus Pharmaceuticals 2012-05-18 2016-03-03 US
Categories
- Drug Categories
- Agents that reduce seizure threshold
- Angiosperms
- Anti-Inflammatory Agents
- Antirheumatic Agents
- Biological Products
- Complex Mixtures
- Dermatologicals
- Dietary Fats, Unsaturated
- Drugs that are Mainly Renally Excreted
- Embryophyta
- Eukaryota
- Fatty Acids
- Fatty Acids, Essential
- Fatty Acids, Omega-6
- Fatty Acids, Unsaturated
- Hypolipidemic Agents
- Linolenic Acids
- Lipid Regulating Agents
- Lipids
- Oenothera
- Oils
- Onagraceae
- Peripheral Nervous System Agents
- Plant Oils
- Plant Preparations
- Sensory System Agents
- Streptophyta
- Tracheophyta
- Viridiplantae
- Classification
- Not classified
- Affected organisms
- Humans and other mammals
Chemical Identifiers
- UNII
- 3Q9L08K71N
- CAS number
- 308064-97-3
References
- General References
- Bayles B, Usatine R: Evening primrose oil. Am Fam Physician. 2009 Dec 15;80(12):1405-8. [Article]
- Martens-Lobenhoffer J, Meyer FP: Pharmacokinetic data of gamma-linolenic acid in healthy volunteers after the administration of evening primrose oil (Epogam). Int J Clin Pharmacol Ther. 1998 Jul;36(7):363-6. [Article]
- Fan YY, Chapkin RS, Ramos KS: Dietary lipid source alters murine macrophage/vascular smooth muscle cell interactions in vitro. J Nutr. 1996 Sep;126(9):2083-8. doi: 10.1093/jn/126.9.2083. [Article]
- Wollschlaeger B. (2003). The ABC Clinical Guide to Herbs. American botanical council.
- FDA new dietary ingredients [Link]
- Health Canada [Link]
- EMA [Link]
- Gamma-linolenic acid monograph [File]
- Chemical Information Document of the National Toxicology Program [File]
- External Links
- PubChem Substance
- 347911198
- 1437503
- Wikipedia
- Oenothera_biennis
- MSDS
- Download (46.8 KB)
Clinical Trials
- Clinical Trials Learn More" title="About Clinical Trials" id="clinical-trials-info" class="drug-info-popup" href="javascript:void(0);">
Phase Status Purpose Conditions Count 4 Completed Treatment Atopic Dermatitis / Neurodermatitis 1 4 Completed Treatment Benign Breast Disease / Breast Pain / Fibroadenoma / Fibrocystic Disease of Breast 1 4 Completed Treatment Missed Abortion 1 3 Unknown Status Treatment Missed Abortion 1
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
Form Route Strength Capsule Oral 450 mg Capsule Oral 1000 MG Capsule, liquid filled Oral Capsule, gelatin coated Oral 500 mg Capsule, gelatin coated Oral Capsule Oral Capsule Oral Capsule Oral 1300 mg Soap Topical Capsule, liquid filled Oral Capsule, gelatin coated Oral 1000 MG Oil 1000 mg Capsule, gelatin coated Oral Tablet Oral - Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Liquid
- Experimental Properties
Property Value Source boiling point (°C) 240 ºC 'MSDS' water solubility Insoluble 'MSDS'
Enzymes
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
- No
- Actions
- Ligand
- General Function
- Catalyzes the first and rate-limiting reaction of the four that constitute the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process, allows the addition of 2 carbons to the chain of long- and very long-chain fatty acids/VLCFAs per cycle. Condensing enzyme that acts specifically toward polyunsaturated acyl-CoA with the higher activity toward C18:3(n-6) acyl-CoA. May participate in the production of monounsaturated and of polyunsaturated VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators.
- Specific Function
- 3-oxo-arachidoyl-coa synthase activity
- Gene Name
- ELOVL5
- Uniprot ID
- Q9NYP7
- Uniprot Name
- Elongation of very long chain fatty acids protein 5
- Molecular Weight
- 35293.15 Da
References
- Timoszuk M, Bielawska K, Skrzydlewska E: Evening Primrose (Oenothera biennis) Biological Activity Dependent on Chemical Composition. Antioxidants (Basel). 2018 Aug 14;7(8). pii: antiox7080108. doi: 10.3390/antiox7080108. [Article]
- Wollschlaeger B. (2003). The ABC Clinical Guide to Herbs. American botanical council.
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
- No
- Actions
- Ligand
- General Function
- Oxidoreductase activity
- Specific Function
- Isoform 2 does not exhibit any catalytic activity toward 20:3n-6, but it may enhance FADS2 activity (By similarity). Isoform 1 is a component of a lipid metabolic pathway that catalyzes biosynthesi...
- Gene Name
- FADS1
- Uniprot ID
- O60427
- Uniprot Name
- Fatty acid desaturase 1
- Molecular Weight
- 51963.945 Da
References
- Timoszuk M, Bielawska K, Skrzydlewska E: Evening Primrose (Oenothera biennis) Biological Activity Dependent on Chemical Composition. Antioxidants (Basel). 2018 Aug 14;7(8). pii: antiox7080108. doi: 10.3390/antiox7080108. [Article]
- Wollschlaeger B. (2003). The ABC Clinical Guide to Herbs. American botanical council.
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
- Unknown
- Actions
- Ligand
- General Function
- Stearoyl-coa 9-desaturase activity
- Specific Function
- Component of a lipid metabolic pathway that catalyzes biosynthesis of highly unsaturated fatty acids (HUFA) from precursor essential polyunsaturated fatty acids (PUFA) linoleic acid (LA) (18:2n-6) ...
- Gene Name
- FADS2
- Uniprot ID
- O95864
- Uniprot Name
- Fatty acid desaturase 2
- Molecular Weight
- 52259.075 Da
References
- Timoszuk M, Bielawska K, Skrzydlewska E: Evening Primrose (Oenothera biennis) Biological Activity Dependent on Chemical Composition. Antioxidants (Basel). 2018 Aug 14;7(8). pii: antiox7080108. doi: 10.3390/antiox7080108. [Article]
- Wollschlaeger B. (2003). The ABC Clinical Guide to Herbs. American botanical council.
Drug created at December 03, 2015 16:52 / Updated at September 28, 2021 21:54