Анализ тенденций рынка пищевых добавок в 2026 году
1. www.grandviewresearch.com/industry-analysis/dietary-supplements-market-report.
3. www.marketsandmarkets.com/Market-Reports/plant-based-protein-market-14715651.html.
4. Gausserès N., Mahè S. et al. The gastro-ileal digestion of 15N-labelled pea nitrogen in adult humans // Br J Nutr. — 1996. — Jul. — 76 (1): 75–85. DOI: 10.1079/bjn19960010.
5. Smith C. E., Mollard R. C. et al. The effect of yellow pea protein and fibre on short-term food intake, subjective appetite and glycaemic response in healthy young men // Br J Nutr. — 2012. — Aug. — 108. — Suppl. 1: 74–80. DOI: 10.1017/S0007114512000700.
6. Abou-Samra R., Keersmaekers L. et al. Effect of different protein sources on satiation and short-term satiety when consumed as a starter // Nutr J. — 2011. — Dec. — 23; 10: 139. DOI: 10.1186/1475-2891-10-139.
7. Diepvens K., Häberer D., Westerterp-Plantenga M. Different proteins and biopeptides differently affect satiety and anorexigenic/orexigenic hormones in healthy humans // Int J Obes (Lond). — 2008. — Mar. — 32 (3): 510–518. DOI: 10.1038/sj.ijo.0803758.
8. Claessens M., Calame W. et al. The thermogenic and metabolic effects of protein hydrolysate with or without a carbohydrate load in healthy male subjects // Metabolism. — 2007. — Aug. — 56 (8): 1051–1059. DOI: 10.1016/j.metabol.2007.04.001.
9. Li H., Prairie N. et al. Blood pressure lowering effect of a pea protein hydrolysate in hypertensive rats and humans // J Agric Food Chem. — 2011. — Sep. — 28; 59 (18): 9854–9860. DOI: 10.1021/jf201911p.
10. Feng T., Huang Y. et al. Anti-fatigue effects of pea (Pisum sativum L.) peptides prepared by compound protease // J Food Sci Technol. — 2021. — Jun. — 58 (6): 2265-2272. DOI: 10.1007/s13197-020-04737-3.
11. Michelet M., Schluckebier D. et al. Food protein-induced enterocolitis syndrome — a review of the literature with focus on clinical management // J Asthma Allergy. — 2017. — Jun. — 27; 10: 197–207. DOI: 10.2147/JAA.S100379.
12. Purpura M., Lowery R. P. et al. A Comparison of Blood Amino Acid Concentrations Following Ingestion of Rice and Whey Protein Isolate: A Double-Blind Crossover Study // J Nutr Health Sci. — 2014. — Oct. — 1 (3): 306. DOI: 10.15744/2393-9060.1.306.
13. Joy J. M., Lowery R. P. et al. The effects of 8 weeks of whey or rice protein supplementation on body composition and exercise performance // Nutr J. — 2013. — Jun. — 20: 12–86. DOI: 10.1186/1475-2891-12-86.
14. Kalman D., Escalante A. et al. The body composition effects of extra protein in elite mixed martial artists undergoing frequent training over a six-week period // JISSN. — 2018. — May.
15. www.gminsights.com/industry-analysis/nootropic-supplements-market.
16. Brown R. P., Gerbarg P. L., Ramazanov Z. Rhodiola rosea: A Phytomedicinal Overview // HerbalGram. — 2002. — Jan. — 56: 40–52.
17. Darbinyan V., Kteyan A. et al. Rhodiola rosea in stress induced fatigue — a double blind cross-over study of a standardized extract SHR-5 with a repeated low-dose regimen on the mental performance of healthy physicians during night duty // Phytomedicine. — 2000. — Oct. — 7 (5): 365–371. DOI: 10.1016/S0944-7113(00)80055-0.
18. Spasov A. A., Wikman G. K. et al. A double-blind, placebo-controlled pilot study of the stimulating and adaptogenic effect of Rhodiola rosea SHR-5 extract on the fatigue of students caused by stress during an examination period with a repeated low-dose regimen // Phytomedicine. — 2000. — Apr. — 7 (2): 85–89. DOI: 10.1016/S0944-7113(00)80078-1.
19. Shevtsov V. A., Zholus B. I. et al. A randomized trial of two different doses of a SHR-5 Rhodiola rosea extract versus placebo and control of capacity for mental work // Phytomedicine. — 2003. — Mar. — 10 (2–3): 95–105. DOI: 10.1078/094471103321659780.
20. Engels G., Brinckmann J. Bacopa // HerbalGram. — 2011; 91: 1–4.
21. Morgan A., Stevens J. Does Bacopa monnieri Improve Memory Performance in Older Persons? Results of a Randomized, Placebo-Controlled, Double-Blind Trial // J Altern Complem Med. — 2010. — Jul. — 16 (7): 753–759. DOI: 10.1089/acm.2009.0342.
22. Calabrese C., Gregory W. L. et al. Effects of a Standardized Bacopa monnieri Extract on Cognitive Performance, Anxiety, and Depression in the Elderly: A Randomized, Double-Blind, Placebo-Controlled Trial // J Altern Complem Med. — 2008. — Jul. — 14 (6): 707–713. DOI: 10.1089/acm.2008.0018.
23. Roodenrys S., Booth D. et al. Chronic effects of Brahmi (Bacopa monnieri) on human memory // Neuropsychopharmacology. — 2002. — Aug. — 27 (2): 279–281. DOI: 10.1016/S0893-133X(01)00419-5.
24. Stough C., Lloyd J. et al. The chronic effects of an extract of Bacopa monniera (Brahmi) on cognitive function in healthy human subjects // Psychopharmacology (Berl). — 2001. — Aug. — 156 (4): 481–484. DOI: 10.1007/s002130100815.
25. Stough C., Downey L. A. et al. Examining the nootropic effects of a special extract of Bacopa monniera on human cognitive functioning: 90 day double-blind placebo-controlled randomized trial // Phytother Res. — 2008. — Dec. — 22 (12): 1629–1634. DOI: 10.1002/ptr.2537.
26. Raghav S., Singh H. et al. Randomized controlled trial of standardized Bacopa monniera extract in age-associated memory impairment // Indian J Psychiatry. —2006. — Oct-Dec. — 48 (4): 238–242. DOI: 10.4103/0019-5545.31555.
27. Pase M. P., Kean J. et al. The cognitive-enhancing effects of Bacopa monnieri: a systematic review of randomized, controlled human clinical trials // J Altern Complement Med. — 2012. — Jul. — 18 (7): 647–652. DOI: 10.1089/acm.2011.0367.
28. Saitsu Y., Nishide A. et al. Improvement of cognitive functions by oral intake of Hericium erinaceus // Biomed Res. — 2019. — 40 (4): 125–131. DOI: 10.2220/biomedres.40.125.
29. Mori K., Inatomi S. et al. Improving effects of the mushroom Yamabushitake (Hericium erinaceus) on mild cognitive impairment: a double-blind placebo-controlled clinical trial // Phytother Res. — 2009. — Mar. — 23 (3): 367–372. DOI: 10.1002/ptr.2634.
30. Nagano M., Shimizu K. et al. Reduction of depression and anxiety by 4 weeks Hericium erinaceus intake // Biomed Res. — 2010. — Aug. — 31 (4): 231–237. DOI: 10.2220/biomedres.31.231.
31. www.futuremarketinsights.com/reports/postbiotic-supplements-market.
32. Hirose Y., Murosaki S. et al. Daily Intake of Heat-Killed Lactobacillus plantarum L-137 Augments Acquired Immunity in Healthy Adults // J Nutr. — 2006. — Dec. — 136 (12): 3069–3073. DOI: 10.1093/jn/136.12.3069.
33. Arimori Y., Nakamura R. et al. Daily intake of heat-killed Lactobacillus plantarum L-137 enhances type I interferon production in healthy humans and pigs // Immunopharmacol Immunotoxicol. — 2012. — Dec. — 34 (6): 937–943. DOI: 10.3109/08923973.2012.672425.
34. Hirose Y., Yamamoto Y. et al. Oral intake of heat-killed Lactobacillus plantarum L-137 decreases the incidence of upper respiratory tract infection in healthy subjects with high levels of psychological stress // J Nutr Sci. — 2013. Dec. — 6: 2–39. DOI: 10.1017/jns.2013.35.
35. Tanaka Y, Hirose Y, Yamamoto Y, et al. Daily intake of heat-killed Lactobacillus plantarum L-137 improves inflammation and lipid metabolism in overweight healthy adults: a randomized-controlled trial. Eur J Nutr. — 2020. — Sep. — 59 (6): 2641–2649. DOI: 0.1007/s00394-019-02112-3.
36. Depommier C., Everard A. et al. Supplementation with Akkermansia muciniphila in overweight and obese human volunteers: a proof-of-concept exploratory study // Nat Med. — 2019. — Jul. — 25 (7): 1096–1103. DOI: 10.1038/s41591-019-0495-2.
37. Proksch E., Schunck M. et al. Oral intake of specific bioactive collagen peptides reduces skin wrinkles and increases dermal matrix synthesis // Skin Pharmacol Physiol. — 2014. — 27 (3): 113–119. DOI: 10.1159/000355523.
38. Fry D., Morales M. A reexamination of the effects of creatine on muscle protein synthesis in tissue culture // J Cell Biol. — 1980. — Feb. — 84 (2): 294–297. DOI: 10.1083/jcb.84.2.294.
39. Ingwall J. S., Weiner C. D. et al. Specificity of creatine in the control of muscle protein synthesis // J Cell Biol. — 1974. — Jul. — 62 (1): 145–151. DOI: 10.1083/jcb.62.1.145.
40. www.grandviewresearch.com/horizon/outlook/womens-health-and-beauty-supplements-market-size/global.
41. www.grandviewresearch.com/industry-analysis/urology-supplements-market-report.
42. Howell A. B., Botto H. et al. Dosage effect on uropathogenic Escherichia coli anti-adhesion activity in urine following consumption of cranberry powder standardized for proanthocyanidin content: a multicentric randomized double blind study // BMC Infect Dis. — 2010. — Apr. — 14; 10: 94. DOI: 10.1186/1471-2334-10-94.
43. Nicolosi D., Tempera G. et al. Anti-Adhesion Activity of A2-type Proanthocyanidins (a Cranberry Major Component) on Uropathogenic E. coli and P. mirabilis Strains // Antibiotics (Basel). — 2014. — Apr. — 3 (2): 143–154. DOI: 10.3390/antibiotics3020143
44. Wagenlehner F. M., Abramov-Sommariva D. et al. Non-Antibiotic Herbal Therapy (BNO 1045) versus Antibiotic Therapy (Fosfomycin Trometamol) for the Treatment of Acute Lower Uncomplicated Urinary Tract Infections in Women: A Double-Blind, Parallel-Group, Randomized, Multicentre, Non-Inferiority Phase III Trial // Urol Int. — 2018. — 101 (3): 327–336. DOI: 10.1159/000493368.
45. Höller M., Steindl H. et al. Treatment of Urinary Tract Infections with Canephron® in Germany: A Retrospective Database Analysis // Antibiotics (Basel). — 2021. — Jun. — 8; 10 (6): 685. DOI: 10.3390/antibiotics10060685.
46. Butler D. S. C., Wagenlehner F. et al. Phytotherapy (BNO 1045) of Acute Lower Uncomplicated Urinary Tract Infection in Women Normalizes Local Host Responses // Urol Int. — 2023. — 107 (8): 778–784. DOI: 10.1159/000531206.
47. Beerepoot M. A., ter Riet G. et al. Lactobacilli vs antibiotics to prevent urinary tract infections: a randomized, double-blind, noninferiority trial in postmenopausal women // Arch Intern Med. — 2012. — May. — 14; 172 (9): 704–712. DOI: 10.1001/archinternmed.2012.777
48. Anukam K., Osazuwa E. et al. Augmentation of antimicrobial metronidazole therapy of bacterial vaginosis with oral probiotic Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14: randomized, double-blind, placebo controlled trial // Microbes Infect. — 2006. — May. — 8 (6): 1450–1454. DOI: 10.1016/j.micinf.2006.01.003
51. Heger M., Ventskovskiy B. M. et al. Efficacy and safety of a special extract of Rheum rhaponticum (ERr 731) in perimenopausal women with climacteric complaints: a 12-week randomized, double-blind, placebo-controlled trial // Menopause. — 2006. — Sep-Oct. — 13 (5): 744–759. DOI: 10.1097/01.gme.0000240632.08182.e4.
52. Kaszkin-Bettag M., Beck S. et al. Efficacy of the special extract ERr 731 from rhapontic rhubarb for menopausal complaints: a 6-month open observational study // Altern Ther Health Med. — 2008. — Nov-Dec. — 14 (6): 32–38.
53. Kaszkin-Bettag M., Ventskovskiy B. M. et al. The special extract ERr 731 of the roots of Rheum rhaponticum decreases anxiety and improves health state and general well-being in perimenopausal women // Menopause. — 2007. — Mar-Apr. — 14 (2): 270–283. DOI: 10.1097/01.gme.0000251932.48426.35.
54. Ross S. M. Menopause: a standardized isopropanolic black cohosh extract (remifemin) is found to be safe and effective for menopausal symptoms // Holist Nurs Pract. — 2012. — Jan-Feb. — 26 (1): 58-61. DOI: 10.1097/HNP.0b013e31823d1f67.
55. Osmers R., Friede M. et al. Efficacy and safety of isopropanolic black cohosh extract for climacteric symptoms // Obstet Gynecol. — 2005. — May. — 105 (5 Pt 1): 1074–1083. DOI: 10.1097/01.AOG.0000158865.98070.89.
56. Frei-Kleiner S., Schaffner W. et al. Cimicifuga racemosa dried ethanolic extract in menopausal disorders: a double-blind placebo-controlled clinical trial // Maturitas. — 2005. — Aug. — 16; 51 (4): 397–404. DOI: 10.1016/j.maturitas.2004.10.003.
57. Wuttke W., Seidlová-Wuttke D., Gorkow C. The Cimicifuga preparation BNO 1055 vs. conjugated estrogens in a double-blind placebo-controlled study: effects on menopause symptoms and bone markers // Maturitas. — 2003. — Mar. — 14: 44 Suppl 1: 67–77. DOI: 10.1016/s0378-5122(02)00350-x.
58. Udani J. K., Brown D. J. et al. Pharmacokinetics and Bioavailability of Plant Lignan 7-Hydroxymatairesinol and Effects on Serum Enterolactone and Clinical Symptoms in Postmenopausal Women: A Single-Blinded, Parallel, Dose-Comparison Study // J Am Coll Nutr. — Dec. — 2013. — 32 (6): 428–435. DOI: 10.1080/07315724.2013.849578.
59. www.grandviewresearch.com/industry-analysis/fertility-supplements-market.
60. Gerhard I. I., Patek A. et al. Mastodynon for female infertility // Forsch Komplementarmed. — 1998. — 5 (6): 272–278. DOI: 10.1159/000021154.
61. Gonzales G. F. Ethnobiology and Ethnopharmacology of Lepidium meyenii (Maca), a Plant from the Peruvian Highlands // Evid Based Complement Alternat Med. — 2012. — 193496. DOI: 10.1155/2012/193496.
62. Stojanovska L., Law C. et al. Maca reduces blood pressure and depression, in a pilot study in postmenopausal women // Climacteric. — 2015. — Feb. — 18 (1): 69–78. DOI: 10.3109/13697137.2014.929649.
63. Meissner H. O., Mscisz A. et al. Hormone-Balancing Effect of Pre-Gelatinized Organic Maca (Lepidium peruvianum Chacon): (II) Physiological and Symptomatic Responses of Early-Postmenopausal Women to Standardized doses of Maca in Double Blind, Randomized, Placebo-Controlled, Multi-Centre Clinical Study // Int J Biomed Sci. — 2006. — Dec. — 2 (4): 360–374.
64. Fung J. L., Hartman T. J. et al. Association of vitamin D intake and serum levels with fertility: results from the Lifestyle and Fertility Study // Fertil Steril. —2017. — Aug. — 108 (2): 302–311. DOI: 10.1016/j.fertnstert.2017.05.037.
65. Purswani J., Gala P. et al. The role of vitamin D in pre-eclampsia: a systematic review // BMC Pregnancy Childbirth. — 2017. — Jul. — 15; 17 (1): 231. DOI: 10.1186/s12884-017-1408-3.
66. www.grandviewresearch.com/industry-analysis/weight-loss-supplements-market-report.
67. De Jesus M., Berquist K., Bruno G. Effects of Somato® tomato fruit extract on key physiological and psychological domains associated with sleep quality, autonomic function, and health-related quality of life (HRQoL) — A Pilot Study // Altern Ther Health Med. — 2025. — Sep. — 24: AT11745.
68. Bannai M., Kawai N. New therapeutic strategy for amino acid medicine: glycine improves the quality of sleep // J Pharmacol Sci. — 2012. — 118 (2): 145–148. DOI: 10.1254/jphs.11r04fm.
69. Abdou A. M., Higashiguchi S. et al. Relaxation and immunity enhancement effects of gamma-aminobutyric acid (GABA) administration in humans // Biofactors. — 2006. — 26 (3): 201–208. DOI: 10.1002/biof.5520260305.
70. Yamatsu A., Yamashita Y. et al. The Improvement of Sleep by Oral Intake of GABA and Apocynum venetum Leaf Extract // J Nutr Sci Vitaminol (Tokyo). — 2015. — 61 (2): 182–187. DOI: 10.3177/jnsv.61.182.
71. www.skyquestt.com/report/digestive-health-products-market.
73. Plaza-Diaz J., Ruiz-Ojeda F. J. et al. Mechanisms of Action of Probiotics // Adv Nutr. — 2019. — Jan. — 1; 10 (suppl_1): 49–66. DOI: 10.1093/advances/nmy063.
74. Lievin V., Peiffer I. et al. Bifidobacterium strains from resident infant human gastrointestinal microflora exert antimicrobial activity // Gut. — 2000. — Nov. — 47: 646–652. DOI: 10.1136/gut.47.5.646.
75. Rastall R. A. Bacteria in the gut: friends and foes and how to alter the balance // J Nutr. — 2004. — Aug. — 134: 2022-2026. DOI: 10.1093/jn/134.8.2022S.
76. Erickson K. L., Hubbard N. E. Probiotic Immunomodulation in Health and Disease // J Nutr. — 2000. — Feb. — 130: 403–409. DOI: 10.1093/jn/130.2.403S.
77. Di Pierro F., Adami T. et al. Clinical evaluation of the oral probiotic Streptococcus salivarius K12 in the prevention of recurrent pharyngitis and/or tonsillitis caused by Streptococcus pyogenes in adults // Expert Opin Biol Ther. — 2013. — Mar. — 13 (3): 339–343. DOI: 10.1517/14712598.2013.758711.
78. Masdea L., Kulik E. M. et al T. Antimicrobial activity of Streptococcus salivarius K12 on bacteria involved in oral malodour // Arch Oral Biol. — 2012. — Aug. — 57 (8): 1041–1047. DOI: 10.1016/j.archoralbio.2012.02.011.
79. Burton J. P., Chilcott C. N., Tagg J. R. The rationale and potential for the reduction of oral malodour using Streptococcus salivarius probiotics // Oral Dis. — 2005: 11 Suppl 1: 29–31. DOI: 10.1111/j.1601-0825.2005.01084.x.
80. https://ods.od.nih.gov/HealthInformation/dailyvalues.aspx.
82. Verhoef S. P., Meyer D., Westerterp K. R. Effects of oligofructose on appetite profile, glucagon-like peptide 1 and peptide YY3-36 concentrations and energy intake // Br J Nutr. — 2011. — Dec. — 106 (11): 1757–1762. DOI: 10.1017/S0007114511002194.
83. Finegold S. M., Li Z. et al. Xylooligosaccharide increases bifidobacteria but not lactobacilli in human gut microbiota // Food Funct. — 2014. — Mar. — 5 (3): 436–445. DOI: 10.1039/c3fo60348b.
84. Salyers A. A., Palmer J. K., Wilkins T. D. Degradation of polysaccharides by intestinal bacterial enzymes // Am J Clin Nutr. — 1978. — Oct. — 31: 128–130. DOI: 10.1093/ajcn/31.10.S128.
85. Johnstone N., Milesi C. et al. Anxiolytic effects of a galacto-oligosaccharides prebiotic in healthy females (18-25 years) with corresponding changes in gut bacterial composition // Sci Rep. — 2021. — Apr. — 15; 11 (1): 8302. DOI: 10.1038/s41598-021-87865-w.
86. Zhou K. Strategies to promote abundance of Akkermansia muciniphila, an emerging probiotics in the gut, evidence from dietary intervention studies // J Funct Foods. — 2017. — Jun. — 33: 194–201. DOI: 10.1016/j.jff.2017.03.045.
88. www.grandviewresearch.com/industry-analysis/creatine-supplements-market-report.
89. Kreider R. B., Kalman D. S. et al. International Society of Sports Nutrition position stand: safety and efficacy of creatine supplementation in exercise, sport, and medicine // J Int Soc Sports Nutr. — 2017. — Jun. — 13: 14–18. DOI: 10.1186/s12970-017-0173-z.
90. Zamani P., Rawat D. et al. Effect of inorganic nitrate on exercise capacity in heart failure with preserved ejection fraction // Circulation. — 2015. — Jan. — 27; 131 (4): 371–380. DOI: 10.1161/CIRCULATIONAHA.114.012957.
91. Hord N. G., Tang Y., Bryan N. S. Food sources of nitrates and nitrites: the physiologic context for potential health benefits // Am J Clin Nutr. — 2009. — Jul. — 90 (1): 1–10. DOI: 10.3945/ajcn.2008.27131.
92. Suzuki T., Morita M. et al. Oral L-citrulline supplementation enhances cycling time trial performance in healthy trained men: Double-blind randomized placebo-controlled 2-way crossover study // J Int Soc Sports Nutr. — 2016. — Feb. — 19: 13: 6. DOI: 10.1186/s12970-016-0117-z.
93. Cormio L., De Siati M. et al. Oral L-citrulline supplementation improves erection hardness in men with mild erectile dysfunction // Urology. — 2011. — Jan. — 77: 119–122. DOI: 10.1016/j.urology.2010.08.028.
94. Schwedhelm E., Maas R. et al. Pharmacokinetic and pharmacodynamic properties of oral L-citrulline and L-arginine: impact on nitric oxide metabolism // Br J Clin Pharmacol. — 2007. — Jul. — 27; 65 (1): 51–59. DOI: 10.1111/j.1365-2125.2007.02990.x.
95. Ghosal S. The aroma principles of Gomutra and Karpuragandha Shilajit // Indian J Indg Med. — 1994. — 11: 11–14.
96. David F., Vasant, L. The Yoga of Herbs. Twin Lakes, WI: Lotus Press. — 2001.
97. Biswas T. K., Pandit S. et al. Clinical evaluation of spermatogenic activity of processed Shilajit in oligospermia // Andrologia. — 2010. — Feb. — 42 (1): 48–56. DOI: 10.1111/j.1439-0272.2009.00956.x.
98. Pandit S., Biswas S. et al. Clinical evaluation of purified shilajit on testosterone levels in healthy volunteers // Andrologia. — 2016. — Jun. — 48 (5): 570–575. DOI: 10.1111/and.12482.
100. Tartar J. L., Kalman D., Hewlings S. A Prospective Study Evaluating the Effects of a Nutritional Supplement Intervention on Cognition, Mood States, and Mental Performance in Video Gamers // Nutrients. — 2019. — Oct. — 11 (10): 2326. DOI: 10.3390/nu11102326.
101. Stringham J. M., O’Brien K. J., Stringham N. T. Macular carotenoid supplementation improves disability glare performance and dynamics of photostress recovery // Eye Vis (Lond). — 2016. — Nov. — 11: 3–30. DOI: 10.1186/s40662-016-0060-8.
102. Stringham N. T., Holmes P. V., Stringham J. M. Supplementation with macular carotenoids reduces psychological stress, serum cortisol, and sub-optimal symptoms of physical and emotional health in young adults // Nutr Neurosci. — 2018. — May. — 21 (4): 286–296. DOI: 10.1080/1028415X.2017.1286445.
103. https://iovs.arvojournals.org/article.aspx?articleid=2563197.
104. www.marketresearchfuture.com/reports/herbal-supplements-market. 3231#:~:text=Herbal%20Supplements%20Market%20Size%20was,period%20(2024%20%2D%202032).
105. Blumenthal M. (eds) et al. The Complete German Commission E Monographs: Therapeutic Guide to Herbal Medicines. Austin: American Botanical Council and Boston: Integrative Medicine Communications. — 1998. — 425–426.
106. Platel K., Srinivasan K. Influence of dietary spices or their active principles on digestive enzymes of small intestinal mucosa in rats // Int J Food Sci Nutr. — 1996. — Jan. — 47 (1): 55–59. DOI: 10.3109/09637489609028561.
107. Ernst E., Pittler M. H. Efficacy of ginger for nausea and vomiting: a systematic review of randomized clinical trials // Br J Anesth. — 2000. — Mar. — 84 (3): 367–371. DOI: 10.1093/oxfordjournals.bja.a013442.
108. Schouenborg L. O., Honnens de Lichtenberg M. et al. Hyperemesis gravidarum // Ugeskrift for Laeger. — 1992. — 154 (15), 1015–1019.
109. Fischer-Rasmussen W., Kjaer S. K. et al. Ginger treatment of hyperemesis gravidarum // Eur J Obstet Gynecol Reprod Biol. — 1991. — Jan. — 4; 38 (1): 19–24. DOI: 10.1016/0028-2243(91)90202-v.
110. Srivastava K. C., Mustafa T. Ginger (Zingiber officinale) in rheumatism and musculoskeletal disorders // Med Hypotheses. — 1992. — Dec. — 39 (4): 342–348. DOI: 10.1016/0306-9877(92)90059-l.
111. Hausenblas H. A., Saha D. et al. Saffron (Crocus sativus L.) and major depressive disorder: a meta-analysis of randomized clinical trials // J Integr Med. — 2013. — Nov. — 11 (6): 377–383. DOI: 10.3736/jintegrmed2013056.
112. Hosseinali E., Mojabi S. N. et al. Aqueous Extract of Saffron (Crocus sativus) Increases Brain Dopamine and Glutamate Concentrations in Rats // J Behav Brain Sci. — 2013. — Jul. — 3: 315–319. DOI: 10.4236/jbbs.2013.33031.
113. Akhondzadeh S., Tahmacebi-Pour N. et al. Crocus sativus L. in the treatment of mild to moderate depression: a double-blind, randomized and placebo-controlled trial // Phytother Res. — 2005. — Feb. — 19 (2): 148–151. DOI: 10.1002/ptr.1647.
114. Modabbernia A., Sohrabi H. et al. Effect of saffron on fluoxetine-induced sexual impairment in men: randomized double-blind placebo-controlled trial // Psychopharmacology (Berl). — 2012. — Oct. — 223 (4): 381–388. DOI: 10.1007/s00213-012-2729-6.
115. Smith T., Bauman H., Resetar H. US Sales of Herbal Supplements Decline Slightly in 2022 // HerbalGram. — 2024. — Dec. — 139: 52–69. DOI: 10.59520/hg.hmr/ylrj6395.
116. Chandra D., Gupta S. Anti-inflammatory and anti-arthritic activity of volatile oil of Curcuma longa (Haldi) // Ind J Med Res. — 1972. — Jan. — 60 (1): 138–142.
117. Toda S., Miyase T. et al. Natural antioxidants. Antioxidative compounds isolated from rhizome of Curcuma longa L // Chem Pharmacol Bull (Tokyo). — 1985. — Apr. — 33 (4): 1725–1728. DOI: 10.1248/cpb.33.1725.
118. Mortellini R., Foresti R. et al. Curcumin, an antioxidant and anti-inflammatory agent, induces heme oxygenase-1 and protects endothelial cells against oxidative stress // Free Radic Biol Med. — 2000. — Apr. — 15; 28: 1303–1312. DOI: 10.1016/s0891-5849(00)00294-x.
119. Pizorrno J. E., Murray M. T. Textbook of Natural Medicine, 2nd Ed. London: Churchill Livingstone. — 1999. — 689–693.
121. Iwamoto T., Hosoda K. et al. Inhibition of low-density lipoprotein oxidation by astaxanthin // J Atheroscler Thromb. — 2000. — 7 (4): 216–222. DOI: 10.5551/jat1994.7.216.
122. Yamashita E. The Effects of a Dietary Supplement Containing Astaxanthin on Skin Condition // Carotenoid Science. — 2006. — 10: 91–95.
123. Chalyk N. E., Klochkov V. A. et al. Continuous astaxanthin intake reduces oxidative stress and reverses age-related morphological changes of residual skin surface components in middle-aged volunteers // Nutr Res. — 2017. — Dec. — 48: 40–48. DOI: 10.1016/j.nutres.2017.10.006.
124. Bizot V., Cestone E. et al. Improving Skin Hydration and Age-related Symptoms by Oral Administration of Wheat Glucosylceramides and Digalactosyl Diglycerides: A Human Clinical Study // Cosmetics. — 2017. — 4 (4): 37. DOI: 10.3390/cosmetics4040037.
125. Proksch E., Schunck M. et al. Oral intake of specific bioactive collagen peptides reduces skin wrinkles and increases dermal matrix synthesis // Skin Pharmacol Physiol. — 2014. — 27 (3): 113–119. DOI: 10.1159/000355523.
126. Proksch E., Segger D. et al. Oral supplementation of specific collagen peptides has beneficial effects on human skin physiology: a double-blind, placebo-controlled study // Skin Pharmacol Physiol. — 2014. — 27 (1): 47–-55. DOI: 10.1159/000351376.
