Pomegranate Seed Oil - NutraPedia
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Pomegranate Seed Oil Information
1) What conditions has it been studied for?
Pomegranate seed oil has been studied for a variety of conditions, including:
- Cardiovascular diseases
- Diabetes
- Obesity
- Inflammation
- Cancer
- Menopausal symptoms
- Skin conditions, such as psoriasis and eczema
2) Does it work in treating those conditions?
The effectiveness of pomegranate seed oil for these conditions is still under research, with some studies suggesting potential benefits due to its anti-inflammatory and antioxidant properties. However, more clinical trials are needed to establish definitive therapeutic effects for the conditions listed.
3) What health benefits does it have?
Pomegranate seed oil is known for its health benefits, which include:
- Antioxidant properties
- Anti-inflammatory effects
- Supporting heart health
- Improving skin elasticity and regeneration
- Potentially reducing the risk of certain cancers
- Modulating hormonal balance during menopause
4) Does it have any downsides?
Like any natural product, pomegranate seed oil may have downsides:
- Allergic reactions in individuals sensitive to pomegranates
- Possible interactions with medications, especially blood thinners
- High-caloric content, which could affect weight management if consumed in large amounts
5) Is it beneficial or harmful for any particular genetic variations?
Currently, there is limited research on the relationship between pomegranate seed oil and specific genetic variations. Some preliminary studies suggest that individuals with certain genetic profiles related to metabolism and inflammation might experience different levels of benefits or risks, but more research is needed to draw solid conclusions.
Pomegranate Seed Oil Research Summary
Effects on Obesity and Insulin Resistance
Pomegranate seed oil (PSO) supplementation in mice reduced body weight and fat mass, improved peripheral insulin sensitivity, and prevented obesity and insulin resistance induced by a high-fat diet, without altering food intake or energy balance.
Antioxidant Properties and Enzyme Inhibition
PSO demonstrated strong antioxidant activity, comparable to butylated hydroxyanisole (BHA) and green tea, and superior to that of red wine. PSO flavonoids inhibited key enzymes involved in inflammation, with punicic acid being the most abundant fatty acid.
Metabolism in Humans
In a study with healthy individuals, punicic acid from Trichosanthes kirilowii seed kernels was successfully incorporated into plasma and red blood cell membranes, indicating its potential as a dietary source of beneficial fatty acids.
Punicic Acid Production and Metabolism
Enzymes capable of producing punicic acid were identified from plants and effectively expressed in yeast and Arabidopsis seeds. In rats, punicic acid was metabolized into conjugated linoleic acid (CLA), which has known health benefits, suggesting its potential as a functional food ingredient.
Conversion of Fatty Acids in Rats
Alpha-eleostearic acid was converted into CLA in rats, a process independent of gut bacteria and facilitated by an enzyme-mediated reaction, underscoring the potential health benefits of dietary fatty acids.
Impact of CLA on Lipid Peroxidation
Dietary CLA affected the metabolism of lipid peroxidation markers in rats and human cells, indicating that CLA can impair the catabolism of isoprostanes, molecules associated with oxidative stress.
PSO and Blood Lipid Levels
A clinical trial showed that PSO intake significantly improved lipid profiles in hyperlipidemic subjects by lowering triglyceride levels and the TAG:HDL-C ratio, suggesting PSO's potential in managing high blood lipid levels.
PSO and Intestinal Health
PSO reduced the incidence of necrotizing enterocolitis in premature rats by improving intestinal epithelial homeostasis and exerting anti-inflammatory effects.
Punicic Acid and Breast Cancer
Punicic acid from PSO inhibited breast cancer cell proliferation, induced apoptosis, and disrupted mitochondrial membrane potential, with potential reliance on lipid oxidation and PKC signaling pathways.
Estrogen Receptors and Linolenic Acid Isomers
Punicic acid and alpha-eleostearic acid from PSO acted as selective estrogen receptor modulators, modulating estrogen receptor activity in breast cancer cells.
Weight Loss and Metabolic Improvement
Xanthigen, containing PSO and fucoxanthin, promoted weight loss, reduced body and liver fat, and improved liver function in obese non-diabetic women, potentially increasing resting energy expenditure.
Xanthigen and Fat Cell Development
Xanthigen disrupted the formation and storage of fat cells more effectively than its individual components by modulating key proteins and enzymes involved in fat cell development.
References:
- Pomegranate seed oil, a rich source of punicic acid, prevents diet-induced obesity and insulin resistance in mice
- Antioxidant and eicosanoid enzyme inhibition properties of pomegranate seed oil and fermented juice flavonoids
- Incorporation and metabolism of punicic acid in healthy young humans
- Delta 12-oleate desaturase-related enzymes associated with formation of conjugated trans-delta 11, cis-delta 13 double bonds
- Punicic acid from Trichosanthes kirilowii seed oil is rapidly metabolized to conjugated linoleic acid in rats
- Alpha-eleostearic acid (9Z11E13E-18:3) is quickly converted to conjugated linoleic acid (9Z11E-18:2) in rats
- Impairment of 8-iso-PGF(2ALPHA) isoprostane metabolism by dietary conjugated linoleic acid (CLA)
- Effect of pomegranate seed oil on hyperlipidaemic subjects: a double-blind placebo-controlled clinical trial
- Pomegranate seed oil reduces intestinal damage in a rat model of necrotizing enterocolitis
- Punicic acid is an omega-5 fatty acid capable of inhibiting breast cancer proliferation
- Pomegranate (Punica granatum) seed linolenic acid isomers: concentration-dependent modulation of estrogen receptor activity
- The effects of Xanthigen in the weight management of obese premenopausal women with non-alcoholic fatty liver disease and normal liver fat
- Xanthigen suppresses preadipocyte differentiation and adipogenesis through down-regulation of PPARγ and C/EBPs and modulation of SIRT-1, AMPK, and FoxO pathways
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