Bioactive Compounds and Their Effect on Blood Pressure—A Review
Abstract
:1. Introduction
2. Materials and Methods
2.1. Data Sources and Searches
2.2. Eligibility Criteria
- Population: individuals with hypertension, normotension;
- Intervention: individuals with supplementation of described nutrients;
- Comparison: individuals without supplementation of any nutrients;
- Outcome: presence/absence of changes in blood pressure;
2.3. Study Selection
2.4. Data Collection Process and Data Items
3. Results
3.1. Anthocyanin
3.2. Lycopene
3.3. Docosahexaenoic Acid (DHA)
3.4. Caffeine
3.5. Dietary Fiber
3.6. Licorice
3.7. Epigallocatechin-3-gallate (EGCG)
3.8. Bioactive Peptides
4. Discussion
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
References
- World Health Organisation. Available online: https://www.who.int/news-room/fact-sheets/detail/hypertension (accessed on 16 February 2020).
- World Health Organisation. Available online: https://www.who.int/features/qa/82/en/ (accessed on 16 February 2020).
- Centers for Disease Control and Prevention. Available online: https://nccd.cdc.gov/ckd/detail.aspx?Qnum=Q646&Strat=Age%2c+Gender#refreshPosition (accessed on 16 February 2020).
- Stanaway, J.D.; Afshin, A.; Gakidou, E.; Lim, S.S.; Abate, D.; Abate, K.H.; Abbafati, C.; Abbasi, N.; Abbastabar, H.; Abd-Allah, F.; et al. Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990–2017: A systematic analysis for the global burden of disease study 2017. Lancet 2018, 392, 1923–1994. [Google Scholar]
- Yusuf, S.; Joseph, P.; Rangarajan, S.; Islam, S.; Mente, A.; Hystad, P.; Brauer, M.; Kutty, V.R.; Gupta, R.; Wielgosz, A.; et al. Modifiable risk factors, cardiovascular disease, and mortality in 155 722 individuals from 21 high-income, middle-income, and low-income countries (PURE): A prospective cohort study. Lancet 2020, 395, 795–808. [Google Scholar] [CrossRef] [Green Version]
- Williams, B.; Mancia, G.; Spiering, W.; Agabiti Rosei, E.; Azizi, M.; Burnier, M.; Clement, D.L.; Coca, A.; de Simone, G.; Dominiczak, A.; et al. 2018 ESC/ESH guidelines for the management of arterial hypertension. Eur. Heart J. 2018, 39, 3021–3104. [Google Scholar] [CrossRef] [PubMed]
- Ehret, G.B.; Caulfield, M.J. Genes for blood pressure: An opportunity to understand hypertension. Eur. Heart J. 2013, 34, 951–961. [Google Scholar] [CrossRef] [Green Version]
- Hamano, T.; Kimura, Y.; Takeda, M.; Yamasaki, M.; Isomura, M.; Nabika, T.; Shiwaku, K. Effect of environmental and lifestyle factors on hypertension: Shimane COHRE study. PLoS ONE 2012, 7, e49122. [Google Scholar] [CrossRef]
- Rimoldi, S.F.; Scherrer, U.; Messerli, F.H. Secondary arterial hypertension: When, who, and how to screen? Eur. Heart J. 2013, 35, 1245–1254. [Google Scholar] [CrossRef] [Green Version]
- Chow, C.K. Prevalence, awareness, treatment, and control of hypertension in rural and urban communities in high-, middle-, and low-income countries. JAMA 2013, 310, 959. [Google Scholar] [CrossRef] [Green Version]
- Martinez-Lacoba, R.; Pardo-Garcia, I.; Amo-Saus, E.; Escribano-Sotos, F. Mediterranean diet and health outcomes: A systematic meta-review. Eur. J. Public Health 2018, 28, 955–961. [Google Scholar] [CrossRef] [Green Version]
- Malinowski, B.; Zalewska, K.; Węsierska, A.; Sokołowska, M.M.; Socha, M.; Liczner, G.; Pawlak-Osińska, K.; Wiciński, M. Intermittent fasting in cardiovascular disorders—An overview. Nutrients 2019, 11, 673. [Google Scholar] [CrossRef] [Green Version]
- Chiavaroli, L.; Viguiliouk, E.; Nishi, S.K.; Mejia, S.B.; Rahelić, D.; Kahleová, H.; Salas-Salvadó, J.; Kendall, C.W.; Sievenpiper, J.L. DASH dietary pattern and cardiometabolic outcomes: An umbrella review of systematic reviews and meta-analyses. Nutrients 2019, 11, 338. [Google Scholar] [CrossRef] [Green Version]
- Wu, X.; Beecher, G.R.; Holden, J.M.; Haytowitz, D.B.; Gebhardt, S.E.; Prior, R.L. Concentrations of anthocyanins in common foods in the united states and estimation of normal consumption. J. Agric. Food Chem. 2006, 54, 4069–4075. [Google Scholar] [CrossRef] [PubMed]
- Dreiseitel, A.; Schreier, P.; Oehme, A.; Locher, S.; Rogler, G.; Piberger, H.; Hajak, G.; Sand, P.G. Inhibition of proteasome activity by anthocyanins and anthocyanidins. Biochem. Biophys. Res. Commun. 2008, 372, 57–61. [Google Scholar] [CrossRef] [PubMed]
- Yi, L.; Chen, C.; Jin, X.; Zhang, T.; Zhou, Y.; Zhang, Q.; Zhu, J.; Mi, M. Differential suppression of intracellular reactive oxygen species-mediated signaling pathway in vascular endothelial cells by several subclasses of flavonoids. Biochimie 2012, 94, 2035–2044. [Google Scholar] [CrossRef]
- Jung, H.; Kwak, H.-K.; Hwang, K.T. Antioxidant and antiinflammatory activities of cyanidin-3-glucoside and cyanidin-3-rutinoside in hydrogen peroxide and lipopolysaccharide-treated RAW264.7 cells. Food Sci. Biotechnol. 2014, 23, 2053–2062. [Google Scholar] [CrossRef]
- Thilavech, T.; Abeywardena, M.Y.; Adams, M.; Dallimore, J.; Adisakwattana, S. Naturally occurring anthocyanin cyanidin-3-rutinoside possesses inherent vasorelaxant actions and prevents methylglyoxal-induced vascular dysfunction in rat aorta and mesenteric arterial bed. Biomed. Pharmacother. 2017, 95, 1251–1259. [Google Scholar] [CrossRef]
- Cassidy, A.; Mukamal, K.J.; Liu, L.; Franz, M.; Eliassen, A.H.; Rimm, E.B. High anthocyanin intake is associated with a reduced risk of myocardial infarction in young and middle-aged women. Circulation 2013, 127, 188–196. [Google Scholar] [CrossRef] [Green Version]
- Cassidy, A.; Bertoia, M.; Chiuve, S.; Flint, A.; Forman, J.; Rimm, E.B. Habitual intake of anthocyanins and flavanones and risk of cardiovascular disease in men. Am. J. Clin. Nutr. 2016, 104, 587–594. [Google Scholar] [CrossRef] [Green Version]
- Xu, J.-W.; Ikeda, K.; Yamori, Y. Upregulation of endothelial nitric oxide synthase by cyanidin-3-glucoside, a typical anthocyanin pigment. Hypertension 2004, 44, 217–222. [Google Scholar] [CrossRef] [Green Version]
- Horie, K.; Nanashima, N.; Maeda, H. Phytoestrogenic effects of blackcurrant anthocyanins increased endothelial nitric oxide synthase (eNOS) expression in human endothelial cells and ovariectomized rats. Molecules 2019, 24, 1259. [Google Scholar] [CrossRef] [Green Version]
- Landmesser, U.; Dikalov, S.; Price, S.R.; McCann, L.; Fukai, T.; Holland, S.M.; Mitch, W.E.; Harrison, D.G. Oxidation of tetrahydrobiopterin leads to uncoupling of endothelial cell nitric oxide synthase in hypertension. J. Clin. Investig. 2003, 111, 1201–1209. [Google Scholar] [CrossRef]
- Furuuchi, R.; Shimizu, I.; Yoshida, Y.; Hayashi, Y.; Ikegami, R.; Suda, M.; Katsuumi, G.; Wakasugi, T.; Nakao, M.; Minamino, T. Boysenberry polyphenol inhibits endothelial dysfunction and improves vascular health. PLoS ONE 2018, 13, e0202051. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Won, K.J.; Jung, S.H.; Jung, S.H.; Lee, K.P.; Lee, H.M.; Lee, D.-Y.; Park, E.-S.; Kim, J.; Kim, B. DJ-1/park7 modulates vasorelaxation and blood pressure via epigenetic modification of endothelial nitric oxide synthase. Cardiovasc. Res. 2013, 101, 473–481. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Cassidy, A.; O’Reilly, É.J.; Kay, C.; Sampson, L.; Franz, M.; Forman, J.; Curhan, G.; Rimm, E.B. Habitual intake of flavonoid subclasses and incident hypertension in adults. Am. J. Clin. Nutr. 2010, 93, 338–347. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jennings, A.; Welch, A.A.; Fairweather-Tait, S.J.; Kay, C.; Minihane, A.-M.; Chowienczyk, P.; Jiang, B.; Cecelja, M.; Spector, T.; Macgregor, A.; et al. Higher anthocyanin intake is associated with lower arterial stiffness and central blood pressure in women. Am. J. Clin. Nutr. 2012, 96, 781–788. [Google Scholar] [CrossRef] [Green Version]
- Hassellund, S.S.; Flaa, A.; Sandvik, L.; Kjeldsen, S.E.; Rostrup, M. Effects of anthocyanins on blood pressure and stress reactivity: A double-blind randomized placebo-controlled crossover study. J. Hum. Hypertens. 2011, 26, 396–404. [Google Scholar] [CrossRef]
- Rao, A.; Rao, L. Carotenoids and Human Health. Pharmacol. Res. 2007, 55, 207–216. [Google Scholar] [CrossRef]
- Di Mascio, P.; Kaiser, S.; Sies, H. Lycopene as the most efficient biological carotenoid singlet oxygen quencher. Arch. Biochem. Biophys. 1989, 274, 532–538. [Google Scholar] [CrossRef]
- Cantrell, A.; McGarvey, D.; George Truscott, T.; Rancan, F.; Böhm, F. Singlet oxygen quenching by dietary carotenoids in a model membrane environment. Arch. Biochem. Biophys. 2003, 412, 47–54. [Google Scholar] [CrossRef]
- Hung, C.-F.; Huang, T.-F.; Chen, B.-H.; Shieh, J.-M.; Wu, P.-H.; Wu, W.-B. Lycopene inhibits TNF-α-induced endothelial ICAM-1 expression and monocyte-endothelial adhesion. Eur. J. Pharmacol. 2008, 586, 275–282. [Google Scholar] [CrossRef]
- Armoza, A.; Haim, Y.; Basiri, A.; Wolak, T.; Paran, E. Tomato extract and the carotenoids lycopene and lutein improve endothelial function and attenuate inflammatory NF-κB signaling in endothelial cells. J. Hypertens. 2013, 31, 521–529. [Google Scholar] [CrossRef]
- Wolak, T.; Sharoni, Y.; Levy, J.; Linnewiel-Hermoni, K.; Stepensky, D.; Paran, E. Effect of tomato nutrient complex on blood pressure: A double blind, randomized dose–response study. Nutrients 2019, 11, 950. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Engelhard, Y.N.; Gazer, B.; Paran, E. Natural antioxidants from tomato extract reduce blood pressure in patients with grade-1 hypertension: A double-blind, placebo-controlled pilot study. Am. Heart J. 2006, 151, 100. [Google Scholar] [CrossRef] [PubMed]
- Paran, E.; Novack, V.; Engelhard, Y.N.; Hazan-Halevy, I. The effects of natural antioxidants from tomato extract in treated but uncontrolled hypertensive patients. Cardiovasc. Drugs Ther. 2008, 23, 145–151. [Google Scholar] [CrossRef] [PubMed]
- Thies, F.; Masson, L.F.; Rudd, A.; Vaughan, N.; Tsang, C.; Brittenden, J.; Simpson, W.G.; Duthie, S.; Horgan, G.W.; Duthie, G. Effect of a tomato-rich diet on markers of cardiovascular disease risk in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. Am. J. Clin. Nutr. 2012, 95, 1013–1022. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hu, Y.; Hu, F.B.; Manson, J.E. Marine omega-3 supplementation and cardiovascular disease: An updated meta-analysis of 13 randomized controlled trials involving 127 477 participants. J. Am. Heart Assoc. 2019, 8, e013543. [Google Scholar] [CrossRef]
- Theobald, H.E.; Goodall, A.H.; Sattar, N.; Talbot, D.C.S.; Chowienczyk, P.J.; Sanders, T.A.B. Low-dose docosahexaenoic acid lowers diastolic blood pressure in middle-aged men and women. J. Nutr. 2007, 137, 973–978. [Google Scholar] [CrossRef] [Green Version]
- Liu, J.C.; Conklin, S.M.; Manuck, S.B.; Yao, J.K.; Muldoon, M.F. Long-chain omega-3 fatty acids and blood pressure. Am. J. Hypertens. 2011, 24, 1121–1126. [Google Scholar] [CrossRef] [Green Version]
- Sagara, M.; Njelekela, M.; Teramoto, T.; Taguchi, T.; Mori, M.; Armitage, L.; Birt, N.; Birt, C.; Yamori, Y. Effects of docosahexaenoic acid supplementation on blood pressure, heart rate, and serum lipids in scottish men with hypertension and hypercholesterolemia. Int. J. Hypertens. 2011, 2011, 1–7. [Google Scholar] [CrossRef] [Green Version]
- Chen, J.; Sun, B.; Zhang, D. Association of dietary n3 and n6 fatty acids intake with hypertension: NHANES 2007–2014. Nutrients 2019, 11, 1232. [Google Scholar] [CrossRef] [Green Version]
- Fischer, R.; Dechend, R.; Qadri, F.; Markovic, M.; Feldt, S.; Herse, F.; Park, J.-K.; Gapelyuk, A.; Schwarz, I.; Zacharzowsky, U.B.; et al. Dietary N-3 polyunsaturated fatty acids and direct renin inhibition improve electrical remodeling in a model of high human renin hypertension. Hypertension 2008, 51, 540–546. [Google Scholar] [CrossRef]
- Nestel, P.; Shige, H.; Pomeroy, S.; Cehun, M.; Abbey, M.; Raederstorff, D. The n−3 fatty acids eicosapentaenoic acid and docosahexaenoic acid increase systemic arterial compliance in humans. Am. J. Clin. Nutr. 2002, 76, 326–330. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- van den Elsen, L.W.J.; Spijkers, L.J.A.; van den Akker, R.F.P.; van Winssen, A.M.H.; Balvers, M.; Wijesinghe, D.S.; Chalfant, C.E.; Garssen, J.; Willemsen, L.E.M.; Alewijnse, A.E.; et al. Dietary fish oil improves endothelial function and lowers blood pressure via suppression of sphingolipid-mediated contractions in spontaneously hypertensive rats. J. Hypertens. 2014, 32, 1050–1058. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- International Coffe Organization. Available online: http://www.ico.org/monthly_coffee_trade_stats.asp (accessed on 9 March 2020).
- Greenberg, J.A.; Boozer, C.N.; Geliebter, A. Coffee, diabetes, and weight control. Am. J. Clin. Nutr. 2006, 84, 682–693. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Teng, C.L.; Lim, W.Y.; Chua, C.Z.; Teo, R.S.K.; Lin, K.T.H.; Yeoh, J.C. Does a single cup of caffeinated drink significantly increase blood pressure in young adults? A randomised controlled trial. AFP 2016, 45, 65–68. [Google Scholar]
- Grosso, G.; Stepaniak, U.; Polak, M.; Micek, A.; Topor-Madry, R.; Stefler, D.; Szafraniec, K.; Pajak, A. Coffee consumption and risk of hypertension in the polish arm of the HAPIEE cohort study. Eur. J. Clin. Nutr. 2015, 70, 109–115. [Google Scholar] [CrossRef] [Green Version]
- Acar-Tek, N.; Aǧagündüz, D.; Ayhan, B. Effect of green coffee consumption on resting energy expenditure, blood pressure, and body temperature in healthy women: A pilot study. J. Am. Coll. Nutr. 2018, 37, 691–700. [Google Scholar] [CrossRef]
- Farag, N.H.; Whitsett, T.L.; McKey, B.S.; Wilson, M.F.; Vincent, A.S.; Everson-Rose, S.A.; Lovallo, W.R. Caffeine and blood pressure response: Sex, age, and hormonal status. J. Women Health 2010, 19, 1171–1176. [Google Scholar] [CrossRef] [Green Version]
- Washio, T.; Sasaki, H.; Ogoh, S. Acute impact of drinking coffee on the cerebral and systemic vasculature. Physiol. Rep. 2017, 5, e13288. [Google Scholar] [CrossRef]
- Tungland, B.C.; Meyer, D. Nondigestable-oligo and polysaccharides (Dietary Fiber): Their physiology and role in human health and food. Compr. Rev. Food Sci. Food Saf. 2002, 1, 90–109. [Google Scholar] [CrossRef]
- Hull, M.A. Nutritional prevention of colorectal cancer. Proc. Nutr. Soc. 2020, 1–6. [Google Scholar] [CrossRef]
- Masrul, M.; Nindrea, R.D. Dietary fibre protective against colorectal cancer patients in Asia: A meta-analysis. Open Access Maced. J. Med. Sci. 2019, 7, 1723–1727. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Brennan, C.S. Dietary fibre, glycaemic response, and diabetes. Mol. Nutr. Food Res. 2005, 49, 560–570. [Google Scholar] [CrossRef] [PubMed]
- Threapleton, D.E.; Greenwood, D.C.; Evans, C.E.L.; Cleghorn, C.L.; Nykjaer, C.; Woodhead, C.; Cade, J.E.; Gale, C.P.; Burley, V.J. Dietary fibre intake and risk of cardiovascular disease: Systematic review and meta-analysis. BMJ 2013, 347, f6879. [Google Scholar] [CrossRef] [Green Version]
- Eshak, E.S.; Iso, H.; Date, C.; Kikuchi, S.; Watanabe, Y.; Wada, Y.; Wakai, K.; Tamakoshi, A. Dietary fiber intake is associated with reduced risk of mortality from cardiovascular disease among japanese men and women. J. Nutr. 2010, 140, 1445–1453. [Google Scholar] [PubMed] [Green Version]
- Du, H.; van der A, D.L.; Boshuizen, H.C.; Forouhi, N.G.; Wareham, N.J.; Halkjær, J.; Tjønneland, A.; Overvad, K.; Jakobsen, M.U.; Boeing, H.; et al. Dietary fiber and subsequent changes in body weight and waist circumference in european men and women. Am. J. Clin. Nutr. 2009, 91, 329–336. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- McKeown, N.M.; Yoshida, M.; Shea, M.K.; Jacques, P.F.; Lichtenstein, A.H.; Rogers, G.; Booth, S.L.; Saltzman, E. Whole-grain intake and cereal fiber are associated with lower abdominal adiposity in older adults. J. Nutr. 2009, 139, 1950–1955. [Google Scholar] [CrossRef] [PubMed]
- Gunness, P.; Gidley, M.J. Mechanisms underlying the cholesterol-lowering properties of soluble dietary fibre polysaccharides. Food Funct. 2010, 1, 149. [Google Scholar] [CrossRef]
- Brown, L.; Rosner, B.; Willett, W.W.; Sacks, F.M. Cholesterol-lowering effects of dietary fiber: A meta-analysis. Am. J. Clin. Nutr. 1999, 69, 30–42. [Google Scholar] [CrossRef]
- Clark, C.C.T.; Salek, M.; Aghabagheri, E.; Jafarnejad, S. The effect of psyllium supplementation on blood pressure: A systematic review and meta-analysis of randomized controlled trials. Korean J. Intern. Med. 2020. [Google Scholar] [CrossRef] [Green Version]
- Sekgala, M.; Mchiza, Z.; Parker, W.; Monyeki, K. Dietary fiber intake and metabolic syndrome risk factors among young south african adults. Nutrients 2018, 10, 504. [Google Scholar] [CrossRef] [Green Version]
- Khan, K.; Jovanovski, E.; Ho, H.V.T.; Marques, A.C.R.; Zurbau, A.; Mejia, S.B.; Sievenpiper, J.L.; Vuksan, V. The effect of viscous soluble fiber on blood pressure: A systematic review and meta-analysis of randomized controlled trials. Nutr. Metab. Cardiovasc. Dis. 2018, 28, 3–13. [Google Scholar] [CrossRef] [PubMed]
- Streppel, M.T.; Arends, L.R.; van ’t Veer, P.; Grobbee, D.E.; Geleijnse, J.M. Dietary fiber and blood pressure: A meta-analysis of randomized placebo-controlled trials. Arch. Intern. Med. 2005, 165, 150–156. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Becerril-Alarcón, Y.; Campos-Gómez, S.; Valdez-Andrade, J.J.; Campos-Gómez, K.A.; Reyes-Barretero, D.Y.; Benítez-Arciniega, A.D.; Valdés-Ramos, R.; Soto-Piña, A.E. Inulin supplementation reduces systolic blood pressure in women with breast cancer undergoing neoadjuvant chemotherapy. Cardiovasc. Ther. 2019, 2019, 1–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Yang, R.; Wang, L.; Yuan, B.; Liu, Y. The pharmacological activities of licorice. Planta Med. 2015, 81, 1654–1669. [Google Scholar] [CrossRef] [Green Version]
- Asl, M.N.; Hosseinzadeh, H. Review of pharmacological effects of glycyrrhiza Sp. and its bioactive compounds. Phytother. Res. 2008, 22, 709–724. [Google Scholar] [CrossRef]
- Allcock, E.; Cowdery, J. Hypertension induced by liquorice tea. BMJ Case Rep. 2015, 2015, bcr2015209926. [Google Scholar] [CrossRef] [Green Version]
- Gomez-Sanchez, E.P.; Gomez-Sanchez, C.E. Central hypertensinogenic effects of glycyrrhizic acid and carbenoxolone. Am. J. Physiol. Endocrinol. Metab. 1992, 263, E1125–E1130. [Google Scholar] [CrossRef]
- Leskinen, M.H.; Hautaniemi, E.J.; Tahvanainen, A.M.; Koskela, J.K.; Päällysaho, M.; Tikkakoski, A.J.; Kähönen, M.; Kööbi, T.; Niemelä, O.; Mustonen, J.; et al. Daily liquorice consumption for two weeks increases augmentation index and central systolic and diastolic blood pressure. PLoS ONE 2014, 9, e105607. [Google Scholar] [CrossRef]
- Sigurjónsdóttir, H.Á.; Franzson, L.; Manhem, K.; Ragnarsson, J.; Sigurdsson, G.; Wallerstedt, S. Liquorice-induced rise in blood pressure: A linear dose-response relationship. J. Hum. Hypertens. 2001, 15, 549–552. [Google Scholar] [CrossRef] [Green Version]
- Penninkilampi, R.; Eslick, E.M.; Eslick, G.D. The association between consistent licorice ingestion, hypertension and hypokalaemia: A systematic review and meta-analysis. J. Hum. Hypertens. 2017, 31, 699–707. [Google Scholar] [CrossRef]
- van Gelderen, C.E.M.; Bijlsma, J.A.; van Dokkum, W.; Savelkoull, T.J.F. Glycyrrhizic acid: The assessment of a no effect level. Hum. Exp. Toxicol. 2000, 19, 434–439. [Google Scholar] [CrossRef] [PubMed]
- Basso, A.; Paola, L.D.; Erle, G.; Boscaro, M.; Armanini, D. Licorice ameliorates postural hypotension caused by diabetic autonomic neuropathy. Diabetes Care 1994, 17, 1356. [Google Scholar] [CrossRef] [PubMed]
- Koch, W.; Kukula-Koch, W.; Komsta, Ł.; Marzec, Z.; Szwerc, W.; Głowniak, K. Green tea quality evaluation based on its catechins and metals composition in combination with chemometric analysis. Molecules 2018, 23, 1689. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Rice-Evans, C. Implications of the mechanisms of action of tea polyphenols as antioxidants in vitro for chemoprevention in humans. Exp. Biol. Med. 1999, 220, 262–266. [Google Scholar]
- Yan, J.; Zhao, Y.; Suo, S.; Liu, Y.; Zhao, B. Green tea catechins ameliorate adipose insulin resistance by improving oxidative stress. Free Radic. Biol. Med. 2012, 52, 1648–1657. [Google Scholar] [CrossRef]
- Matsuo, N.; Yamada, K.; Yamashita, K.; Shoji, K.; Mori, M.; Sugano, M. Inhibitory effect of tea polyphenols on histamine and leukotriene b4 release from rat peritoneal exudate cells. Vitro Cell. Dev. Biol. Animal 1996, 32, 340–344. [Google Scholar] [CrossRef]
- Du, G.-J.; Zhang, Z.; Wen, X.-D.; Yu, C.; Calway, T.; Yuan, C.-S.; Wang, C.-Z. Epigallocatechin gallate (EGCG) is the most effective cancer chemopreventive polyphenol in green tea. Nutrients 2012, 4, 1679–1691. [Google Scholar] [CrossRef]
- Wolfram, S. Effects of green tea and EGCG on cardiovascular and metabolic health. J. Am. Coll. Nutr. 2007, 26, 373S–388S. [Google Scholar] [CrossRef]
- Yang, Y.-C.; Lu, F.-H.; Wu, J.-S.; Wu, C.-H.; Chang, C.-J. The protective effect of habitual tea consumption on hypertension. Arch. Intern. Med. 2004, 164, 1534. [Google Scholar] [CrossRef] [Green Version]
- Brown, A.L.; Lane, J.; Coverly, J.; Stocks, J.; Jackson, S.; Stephen, A.; Bluck, L.; Coward, A.; Hendrickx, H. Effects of dietary supplementation with the green tea polyphenol epigallocatechin-3-gallate on insulin resistance and associated metabolic risk factors: Randomized controlled trial. Br. J. Nutr. 2008, 101, 886–894. [Google Scholar] [CrossRef]
- Nantz, M.P.; Rowe, C.A.; Bukowski, J.F.; Percival, S.S. Standardized capsule of camellia sinensis lowers cardiovascular risk factors in a randomized, double-blind, placebo-controlled study. Nutrition 2009, 25, 147–154. [Google Scholar] [CrossRef] [PubMed]
- Bogdanski, P.; Suliburska, J.; Szulinska, M.; Stepien, M.; Pupek-Musialik, D.; Jablecka, A. Green tea extract reduces blood pressure, inflammatory biomarkers, and oxidative stress and improves parameters associated with insulin resistance in obese, hypertensive patients. Nutr. Res. 2012, 32, 421–427. [Google Scholar] [CrossRef] [PubMed]
- Maeda-Yamamoto, M.; Nishimura, M.; Kitaichi, N.; Nesumi, A.; Monobe, M.; Nomura, S.; Horie, Y.; Tachibana, H.; Nishihira, J. A randomized, placebo-controlled study on the safety and efficacy of daily ingestion of green tea (Camellia Sinensis L.) Cv. “Yabukita” and “Sunrouge” on eyestrain and blood pressure in healthy adults. Nutrients 2018, 10, 569. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Li, F.; Ohnishi-Kameyama, M.; Takahashi, Y.; Yamaki, K. Tea polyphenols as novel and potent inhibitory substances against renin activity. J. Agric. Food Chem. 2013, 61, 9697–9704. [Google Scholar] [CrossRef] [PubMed]
- Persson, I.A.-L.; Josefsson, M.; Persson, K.; Andersson, R.G.G. Tea flavanols inhibit angiotensin-converting enzyme activity and increase nitric oxide production in human endothelial cells. J. Pharm. Pharmacol. 2006, 58, 1139–1144. [Google Scholar] [CrossRef] [PubMed]
- Antonello, M.; Montemurro, D.; Bolognesi, M.; Dipascoli, M.; Piva, A.; Grego, F.; Sticchi, D.; Giulani, L.; Garbisa, S.; Rossi, G. Prevention of hypertension, cardiovascular damage and endothelial dysfunction with green tea extracts. Am. J. Hypertens. 2007, 20, 1321–1328. [Google Scholar] [CrossRef] [Green Version]
- Lorenz, M.; Wessler, S.; Follmann, E.; Michaelis, W.; Düsterhöft, T.; Baumann, G.; Stangl, K.; Stangl, V. A constituent of green tea, epigallocatechin-3-gallate, activates endothelial nitric oxide synthase by a phosphatidylinositol-3-OH-Kinase-, cAMP-dependent protein kinase-, and akt-dependent pathway and leads to endothelial-dependent vasorelaxation. J. Biol. Chem. 2003, 279, 6190–6195. [Google Scholar] [CrossRef] [Green Version]
- Kim, J.; Formoso, G.; Li, Y.; Potenza, M.A.; Marasciulo, F.L.; Montagnani, M.; Quon, M.J. Epigallocatechin gallate, a green tea polyphenol, mediates NO-dependent vasodilation using signaling pathways in vascular endothelium requiring reactive oxygen species and fyn. J. Biol. Chem. 2007, 282, 13736–13745. [Google Scholar] [CrossRef] [Green Version]
- Roy, M.K.; Kuwabara, Y.; Hara, K.; Watanabe, Y.; Tamai, Y. Peptides from the n-terminal end of bovine lactoferrin induce apoptosis in human leukemic (HL-60) cells. J. Dairy Sci. 2002, 85, 2065–2074. [Google Scholar] [CrossRef] [Green Version]
- guilar-Toalá, J.E.; Santiago-López, L.; Peres, C.M.; Peres, C.; Garcia, H.S.; Vallejo-Cordoba, B.; González-Córdova, A.F.; Hernández-Mendoza, A. Assessment of multifunctional activity of bioactive peptides derived from fermented milk by specific lactobacillus plantarum strains. J. Dairy Sci. 2017, 100, 65–75. [Google Scholar] [CrossRef]
- Lee, S.Y.; Hur, S.J. Antihypertensive peptides from animal products, marine organisms, and plants. Food Chem. 2017, 228, 506–517. [Google Scholar] [CrossRef] [PubMed]
- Fekete, Á.; Givens, D.; Lovegrove, J. Casein-derived lactotripeptides reduce systolic and diastolic blood pressure in a meta-analysis of randomised clinical trials. Nutrients 2015, 7, 659–681. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Fekete, Á.A.; Giromini, C.; Chatzidiakou, Y.; Givens, D.I.; Lovegrove, J.A. Whey protein lowers blood pressure and improves endothelial function and lipid biomarkers in adults with prehypertension and mild hypertension: Results from the chronic whey2Go randomized controlled trial. Am. J. Clin. Nutr. 2016, 104, 1534–1544. [Google Scholar] [CrossRef] [PubMed]
- He, J.; Gu, D.; Wu, X.; Chen, J.; Duan, X.; Chen, J.; Whelton, P.K. Effect of soybean protein on blood pressure: A randomized, controlled trial. Ann. Intern. Med. 2005, 143, 1. [Google Scholar] [CrossRef]
- Fujita, H.; Yamagami, T.; Ohshima, K. Effects of an ace-inhibitory agent, katsuobushi oligopeptide, in the spontaneously hypertensive rat and in borderline and mildly hypertensive subjects. Nutr. Res. 2001, 21, 1149–1158. [Google Scholar] [CrossRef]
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Cassidy et al., 2011 [26] | 156,952 | Prospective | Healthy women and men | 14 years | Risk of hypertension |
Jennins et al., 2012 [27] | 1898 | Cross-sectional | Hypertensive women | – | cSBP Map Arterial stiffness |
Hasselund et al., 2011 [28] | 27 | Crossover | Mildly hypertensive men | 8 Weeks | Slight of resting BP No other significant changes |
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Wolak et al., 2019 [34] | 61 | Double-blind | Hypertensive women and men | 8 weeks | SBP |
Wolak et al., 2019 [34] | 31 | Single-blind | Hypertensive women and men | 4 months | SBP |
Engelhard et al., 2005 [35] | 31 | Double-blind | Grade-1 hypertension women and men | 16 weeks | SBP and DBP |
Paran et al., 2008 [36] | 50 | Crossover | Moderate hypertensive women and men | 12 weeks | SBP |
Thies et al., 2012 [37] | 225 | Single-blind | Moderate overweight women and men | 16 weeks | No significant changes |
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Theobald et al., 2007 [39] | 40 | crossover | Healthy women and men | 10 months | DBP |
Liu et al., 2011 [40] | 265 | Observational study | Healthy women and men | N/A | Resting DBP 24-h DBP |
Sagara et al., 2011 [41] | 38 | Double-blind | Hypertensive and/or hypercholesterolemic men | 5 weeks | SBP DBP HDL-c |
Cheng et al., 2019 [42] | 18 434 | Cross-sectional | General population | 7 years | Risk of hypertension |
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Teng CL et al., 2016 [48] | 104 | Double-blind | Normotensive young adults women and men | - | No significant changes |
Grosso G et al., 2016 [49] | 2725 | Prospective | Normotensive women and men | Average of 5 years | Risk of hypertension |
Acar-tek et al., 2018 [50] | 24 | Pilot | Healthy women | No significant changes | |
Farag et al., 2010 [51] | 165 | Crossover | Healthy women and men | 2 weeks | ↑BP |
Washio et al., 2017 [52] | 10 | Randomized and blinded | Healthy men | - | MAP |
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Clark CCT et al., 2020 [63] | 592 | Meta-analysis | Hypertensive women and men | - | SBP |
Sekgala et al., 2018 [64] | 627 | Cross-sectional | Random | 20 years | BP |
Khan et al., 2018 [65] | 2773 | Meta-analysis of RCT | - | ≥ 4 weeks | SBP DBP |
Streppel et. al., 2005 [66] | 1404 | Meta-analysis of RCT | - | - | DBP |
Barcerril-Alarcón et al., 2019 [67] | 38 | Double-blind | Normotensive and mildly hypertensive women with breast cancer | 21 days | SBP |
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Leskinen et al., 2014 [72] | 20 | Open-label | Normotensive women and men | 2 weeks | SBP DBP |
Sigurjónsdóttir et al., 2001 [73] | 64 | Intervention | Normotensive women and men | 2–4 weeks | SBP |
Penninkilampi R. et al., 2017 [74] | 337 | Meta-analysis | Healthy women and men | 1–8 weeks | SBP DBP |
van Gelderen et al., 2000 [75] | 39 | Comparative | Healthy women | 12 weeks | No changes |
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Brown et al., 2008 [84] | 100 | Parallel | Obese or overweight men | 8 weeks | DBP |
Nantz et al., 2008 [85] | 111 | Parallel | Healthy men and women | 3 months | SBP DBP |
Bogdanski et al., 20012 [86] | 56 | Parallel | Obese, hypertensive men and women | 3 months | SBP DBP LDL-C TG insulin resistance HDL-C |
Maeda-Yamamoto et al., 2018 [87] | 120 | Parallel | Healthy men and women | 12 weeks | DBP |
Author and Reference Number | Number of Participants | Study Design | Participants Description | Duration | Findings |
---|---|---|---|---|---|
Frekete et al., 2015 [4] | 2200 | Meta-analysis | Normotensive and hypertensive Men and women | 4–21 weeks | BP |
Frekete et al., 2016 [5] | 38 | Double-blind | Mild hypertensive Male and females | 8 weeks | BP |
He et al., 2005 [6] | 302 | Double-blind | Hypertensive Men and women | 12 weeks | BP |
Fujita et al., 2001 [7] | 65 | Double-blind | Males and Females Hypertensive | 10 weeks | BP |
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Share and Cite
Malinowski, B.; Fajardo Leighton, R.I.; Hill, C.G.; Szandorowski, P.; Wiciński, M. Bioactive Compounds and Their Effect on Blood Pressure—A Review. Nutrients 2020, 12, 1659. https://doi.org/10.3390/nu12061659
Malinowski B, Fajardo Leighton RI, Hill CG, Szandorowski P, Wiciński M. Bioactive Compounds and Their Effect on Blood Pressure—A Review. Nutrients. 2020; 12(6):1659. https://doi.org/10.3390/nu12061659
Chicago/Turabian StyleMalinowski, Bartosz, Raul Ignacio Fajardo Leighton, Christopher George Hill, Paweł Szandorowski, and Michał Wiciński. 2020. "Bioactive Compounds and Their Effect on Blood Pressure—A Review" Nutrients 12, no. 6: 1659. https://doi.org/10.3390/nu12061659