Life Extension Magazine 2004
Sesame Lignans Dramatically Increase Vitamin E Activity
|LE Magazine Special Edition, Winter 2004/2005|
|Sesame Lignans Dramatically Increase Vitamin E Activity|
Sesame seeds and its oil have long been considered a health food in Japan and China.1,2 Sesame’s biological effects, however, have only been identified in the past decade. Sesame lignans are the 1% solid portion of sesame oil and are responsible for all the beneficial effects of sesame.3
Sesame and its lignans have a broad range of applications in human health. This includes increasing the anti-inflammatory index of fish oils,4,5 decreasing LDL oxidation,6,7 inhibiting lipid peroxidation,6-8 lowering LDL levels in humans,9,10 and guarding against DNA mutating toxins.11-13
The most significant finding about sesame lignans, however, is their unique ability to increase tissue levels of vitamin E (including gamma tocopherol) via several different mechanisms.14-17 Elevation of gamma tocopherol is of particular importance because gamma tocopherol, but not alpha tocopherol, quenches a particularly dangerous type of free radical (peroxynitrite radical) that plays a major role in the development of age-related disorders.18,19
The primary purpose for taking vitamin E is to suppress free radicals. Over the past year, four prestigious scientific journals have recognized the unique benefits of gamma tocopherol and have published articles indicating that gamma tocopherol may be the critically important form of supplemental vitamin E.20-23
For the first time, gamma tocopherol has been combined with sesame lignans in a human study that measured tissue oxidative stress and inflammatory levels. The results show that sesame boosts the efficacy of gamma tocopherol by an average of 25% compared to the same amount of gamma tocopherol combined with tocotrienols.LEF study
Increased Gamma Tocopherol Results in Decreased Free Radicals
In animal studies, supplementing with gamma tocopherol alone resulted in only small concentrations of gamma tocopherol in the blood and liver of rats. In sharp contrast, feeding of sesame lignans resulted in high concentrations of gamma tocopherol in blood and liver.25 Lipid peroxidation is an important measurement of cell membrane free radical damage. In this study, lipid peroxidation levels were 50% lower in the blood of the sesame+gamma tocopherol group compared to the group fed only gamma tocopherol, while liver peroxidation rates were 30% lower.25
The bar graphs in figure 1 show the differences in gamma tocopherol and levels between the groups of animals fed only gamma tocopherol versus the gamma tocopherol plus sesame lignans-fed group.25
In another study, adding sesame seed to a rat diet increased alpha tocopherol serum levels 40%, and gamma tocopherol levels 800%.26 Sesame lignans have also demonstrated the ability to lower a measure of oxidative cell membrane/DNA damage by 82.8% (thiobarbituric reactive liver levels).7
Figure 2 shows the remarkable effects that sesame has on decreasing levels of destructive free radicals.
How Sesame Boosts Vitamin E
Human and animal studies show that supplementing with sesame or its lignans produces similar effects in raising all tocopherol levels. In one study, liver, brain, kidney and serum levels of gamma tocopherol in rats were measured after being given gamma tocopherol alone or being given gamma tocopherol and sesame.
The gamma-tocopherol-only fed group increased liver, kidney, brain and blood levels of gamma tocopherol only 3 nmol per gram in tissues and 3 micromoles per liter in blood. When fed sesame and gamma tocopherol together, the rats had gamma tocopherol levels of 25-30 nmol per gram in tissue and 30 nmol per liter in blood, an increase between 833 to 1000% compared to no sesame.26 This study also showed that the urinary excretion of the metabolite of gamma tocopherol (gamma-CEHC) dropped 50% in the sesame-supplemented rats, a factor that helps explain the dramatic increase in tissue and blood levels of in the group fed sesame + gamma tocopherol (see figure 3).
Sesame inhibits the specific enzyme that breaks down tocopherols (tocopherol gamma- hydroxylase, or CYP-3A),17,26 which further clarifies how sesame boosts gamma and alpha tocopherol levels in the body.
Life Extension Tests Sesame Lignans in Humans
Three markers of oxidative stress and inflammation were measured in the blood of a group of human test subjects to establish a baseline. The group was then divided, with one group given gamma tocopherol plus tocotrienols, while another received the same amount of gamma tocopherol plus sesame lignans.
The three blood markers of oxidative stress and inflammation measured were:
The dityrosine marker measures serum levels of deep tissue protein oxidation caused by the peroxynitrite radical reacting with tyrosine, an amino acid found in all human proteins.29 Tyrosine is the amino acid most readily attacked by peroxynitrite radical. Peroxynitrite is an extremely powerful free radical that has been implicated in a host of disorders. Gamma tocopherol is the only tocopherol that reacts with, or traps, the peroxynitrite radical to any appreciable degree.18 Compared to the gamma tocopherol-tocotrienol group, those taking gamma tocopherol-sesame showed a 45% reduction in serum dityrosine oxidation levels after two weeks of supplementation.
The isoprostane marker measures the amount of cell membrane damage caused by free radicals.30,31 Cell membrane damage, also called lipid peroxidation, is a free radical chain reaction of cell membrane fatty acids. Normally, lipid peroxidation results in free radicals destroying normal molecules before being quenched. Supplementing with vitamin E has been shown to significantly reduce isoprostane generation and reduce aortic lesion areas.32 Compared to the gamma tocopherol-tocotrienol group, those taking gamma tocopherol and sesame showed a 22% reduction in serum isoprostane levels after two weeks of supplementation.
The PLGF-1 marker is an extremely sensitive new test for atherosclerotic risk in humans.33 PLGF-1 stands for “placental growth factor” because it was originally identified in the placenta.34 For adults, however, high levels of PLGF-1 are indicative of atherosclerotic lesions. PLGF-1 stimulates vascular smooth muscle cell growth, recruits macrophages into atherosclerotic lesions, up-regulates production of tumor-necrosis factor-a and stimulates undesirable angiogenesis.35 In the animal model, inhibition of PLGF-1 suppressed both atherosclerotic plaque growth and arterial wall inflammatory reactions. PLGF-1 may be considered a marker for the presence of unstable arterial wall plaque.36 Compared to the gamma tocopherol-tocotrienol group, those taking gamma tocopherol-sesame showed an 11.5% reduction in serum PLGF-1 levels after two weeks of supplementation.
Since this was a healthy group of people to begin with, whose baseline PLGF-1 was already in the lowest 1% of risk, the 11.5 reduction in the gamma tocopherol-sesame group was impressive. Presumably, those with arterial wall dysfunction, who normally have high PLGF-1 levels, would derive even greater benefit from supplements that lowered this very sensitive inflammatory marker. The same holds true for aging people whose baseline oxidative stress levels are very high compared to this healthy group of test subjects.
Based on these three advanced measurements of free radical and inflammatory damage, gamma tocopherol plus sesame lignans is 25% more effective than the more expensive gamma tocopherol plus tocotrienols.
What is so impressive about these recent findings is that unlike previous studies, it did not compare sesame to a placebo or control group. Instead, this human study compared low cost sesame to the effects of very expensive tocotrienols. The tocotrienols are considered nature’s most potent natural antioxidants. Yet sesame was found to work 25% better than the tocotrienols.
This is great news for vitamin consumers, since tocotrienols are costly, whereas the price of standardized sesame lignans is relatively modest.
1. Budowski P, Markley KS. The Chemical and Physiological Properties of Sesame Oil. Chem Rev. 1951;48:125-51.
2. Namiki, M, Kobayashi, T. Science of Sesame. Asakura Shoten, Tokyo, Japan. 1989.
3. Fukuda Y, Osawa T, Namiki M, et al. Studies on the antioxidative substances in sesame seed. Agric Biol Chem. 1985;49:301-306.
4. Chavali SR, Zhong WW, Forse AA. Dietary alpha-linolenic acid increases TNF-alpha, and decreases IL-6, IL-10 in response to LPS: effects of sesamin on the delta-5 desaturation of omega6 and omega3 fatty acids in mice. Prostaglandins Leukot Essent Fatty Acids 1998 Mar;58(3):185-91.
5. Tahir, KEH, Hamad,AM, Ageel, MA, et al. Effects of sesame and cod liver oils on prostacyclin synthesis by the rat thoracic aorta. Arch Int Pharmacodyn Ther 1988 Mar-Apr;292:182-8.
6. Miura S, Watanabe J, Sano M, et al. Effects of various natural antioxidants on the Cu(2+)-mediated oxidative modification of low density lipoprotein. Biol Pharm Bull. 1995 Jan;18(1):1-4.
7. Kang MH, Naito M. Mode of action of sesame lignans in protecting LDL against oxidative damage in vitro. Life Sci. 2000;66(2):161-7.
8. Ikeda S, Kagaya M, Kobayashi K, et al. Dietary sesame lignans decrease lipid peroxidation in rats fed docosahexenoic acid. J Nutr Sci Vitaminol. (Tokyo) 2003 Aug;49(4):270-6.
9. Hirata F, Fujita K, Ishikura Y, et al. Hypocholesteremic effect of sesame lignans in humans. Atherosclerosis. 1996. Apr 26;122(1):135-36.
10. Nakabayashi A, Kitagawa Y, Suwa Y, et al. Alpha-tocopherol enhances the hypocholesteremic action of sesamin in rats. Int J Vitam Nutr Res. 1995;65(3):162-8.
11. Kang MH. Katsuzaki H, Osawa T. Inhibition of 2,2’-azobis[2,4-dimethylaminovaleronitrile]-induced lipid peroxidation by sesaminols. Lipids. 1998 Oct;33(10):1031-6.
12. Kapadia GJ, Azuine MA, Tokuda H, et al. Chemopreventive effect of resveratrol, sesamol, sesame oil and sunflower oil in the Epstein-Barr virus early antigen activation assay and mouse skin two-stage carcinogenesis. Pharmacol Res. 2002 June;45(6):499-505.
13. Uchida M, Nakajin S, Toyoshima S, et al. Inhibitory effect of sesamol and related compounds on lipid peroxidation. Biol Pharm Bull 1996;19:623-6.
14. Kamal-Eldin A, Frank J, Razdan A, et al. Effects of dietary phenolic compounds on tocopherol, cholesterol, and fatty acids in rats. Lipids 2000;35:427-435.
15. Kamal-Eldin A, Pettersson D, Appelqvist LA Sesamin (a compound from sesame oil) increases tocopherol levels in rats fed ad libitum. Lipids 1995;30:499-505.
16. Cooney RV, Custer LJ, Okinaka L, et al. Effects of dietary sesame seeds on plasma tocopherol levels. Nutr Cancer. 2001;39(1):66-71.
17. Parker RS, Sontag TJ, Swanson JE. Cytochrome P4503A-dependent metabolism of tocopherols and inhibition by sesamin. Biochem Biophys Res Commun. 2000 Nov 2;277(3):531-4.
18. Christen S, Woodall AA, Shigenaga MK, et al. Gamma-tocopherol traps mutagenic electrophiles such as NO(X) and complements alpha-tocopherol: physiological implications. Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3217-22.
19. Kontush A, Spranger T, Reich A, et al. Lipophilic antioxidants in blood plasma as markers of atherosclerosis: the role of alpha-carotene and gamma-tocopherol. Atherosclerosis 1999 May; 144(1):117-22.
20. Friedrich MJ. To “E” or not to “E,” vitamin E’s role in health and disease is the question. JAMA. 2004 Aug 11;292(6):671-3.
21. Galli F, Stabile AM, Betti M, et al. The effect of alpha- and gamma-tocopherol and their carboxyethyl hydroxychroman metabolites on prostate cancer cell proliferation. Arch Biochem Biophys. 2004 Mar 1;423(1):97-102.
22. Wagner KH, Kamal-Eldin A, Elmadfa I.Gamma-tocopherol—an underestimated vitamin? Ann Nutr Metab. 2004;48(3):169-88.
23. Hensley K, Benaksas EJ, Bolli R, et al.New perspectives on vitamin E: gamma-tocopherol and carboxyelthylhydroxychroman metabolites in biology and medicine. Free Radic Biol Med. 2004 Jan 1;36(1):1-15.
24. Lemcke-Norojarvi M. Corn and sesame oils increase serum gamma-tocopherol concentrations in healthy Swedish women. J Nutr. 2001; 131: 1195-1201.
25. Yamashita K, Nohara Y, Katayama K. Sesame seed lignans and gamma-tocopherol act synergistically to produce vitamin E activity in rats. J. Nutr. 1992 Dec;122:2440-6.
26. Ikeda S, Tohama T, Yamashita K. Dietary sesame seed and its lignans inhibit 2,7,8-trimethyl-2[2’-carboxyethyl]-6-hydroxychroman excretion into urine of rats fed gamma-tocopherol. J Nutr. 2002 May;132(5) :961-6.
27. Yamashita K, Lisuka Y. Sesame seed and its lignans produce marked enhancement of vitamin E activity in rats fed a low a-tocopherol diet. Lipids 1995 Nov;30: 1019-28.
28. Hosomi A, Arita M, Sato Y, et al. Affinity for alpha-tocopherol transfer protein as a determinant of the biological activities of vitamin E analogs. FEBS Lett. 1997 Jun 2;409(1):105-8.
29. Giulivi C, Traaseth NJ, Davies KJ. Tyrosine oxidation products: analysis and biological relevance. Amino Acids. 2003 Dec;25(3-4):227-32. Epub 2003 Jul 29.
30. Cracowski JL, Durand T, Bessard G. Isoprostanes as a biomarker of lipid peroxidation in humans: physiology, pharmacology and clinical implications. Trends Pharmacol Sci. 2002 Aug;23(8):360-6.
31. Roberts LJ, Morrow JD. Measurement of F(2)-isoprostanes as an index of oxidative stress in vivo. Free Radic Biol Med. 2000 Feb 15;28(4):505-13.
32. Pratico D, Tangirala RK, Rader DJ, et al. Vitamin E suppresses isoprostane generation in vivo and reduces atherosclerosis in ApoE-deficient mice. Nat Med. 1998 Oct;4(10):1189-92.
33. Heeschen C, Dimmeler S, Fichtlscherer S, et al. Prognostic value of placental growth factor in patients with acute chest pain. JAMA. 2004 Jan 28;291(4):435-41.
34. Maglione D, Guerriero V, Viglietto G, et al. Isolation of a human placenta cDNA coding for a protein related to the vascular permeability factor. Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):9267-71.
35. Luttun A, Tjwa M, Moons L, et al. Revascularization of ischemic tissues by PlGF treatment, and inhibition of tumor angiogenesis, arthritis and atherosclerosis by anti-Flt1. Nat Med. 2002 Aug;8(8):831-40.
36. Autiero M, Luttun A, Tjwa M, et al. Placental growth factor and its receptor, vascular endothelial growth factor receptor-1: novel targets for stimulation of ischemic tissue revascularization and inhibition of angiogenic and inflammatory disorders. J Thromb Haemost. 2003 Jul;1(7):1356-70.