Revive MD Complete Vital: Support Heart Health and Detoxification

Revive MD Logo Revive MD is one of the few supplement brands to be started by a licensed medical doctor. And just as you’d expect from an M.D. who got into the supplement game, the brand has continually impressed us with its out-of-the-box approach to long-standing problems in the health and wellness product category.

We’re talking about Dr. Domenic Iacovone, and today we’ve got a new product to support your quest for better health:

Revive MD Complete Vital – Address the Underlying Issues

Revive MD Complete Vital

Revive MD Complete Vital is a potent cardiovascular support supplement with added liver detoxification and anti-inflammatory support

When it comes to optimizing and preserving health, shoring up nutritional deficiencies is obviously very important. Naturally, vitamins and minerals are the traditional province of the supplement industry.

Once you’re ready to move beyond the basics, though, there are two physiological mechanisms that should be addressed before anything else: Inflammation and oxidative stress.

Revive MD’s Complete Vital is based on that understanding – and it’s been too long since we saw a more focused or sophisticated selection of ingredients for that purpose.

The big headliners here, in our opinion, are NAC (N-acetyl-cysteine) and curcuminoids, which should be considered for inclusion in anyone’s longevity stack. These ingredients have been around for a while, but both, in our opinion, are still underrated – especially NAC.

The real sleeper here is red yeast rice, whose main bioactive constituent was actually captured by the pharmaceutical industry because it works so well.

So, what does it do? Read on to find out. But first, check PricePlow for product availability, coupon-based deals, and sign up for our Revive MD news alerts:

Revive MD Complete Vital – Deals and Price Drop Alerts

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  • Red Yeast Rice (Monascus purpureus) [Seed] Powder – 600 mg

    Revive MD Complete Vital

    Red yeast rice is a natural cholesterol-lowering ingredient.[1] Its anti-hyperlipidemic properties are so profound that one 2019 research review on the supplement refers to it as “the most effective cholesterol-lowering nutraceutical on the market.”[1]

    As a matter of fact, its main bioactive constituent, monacolin K, has the same chemical structure as Lovastatin, a pharmaceutical anti-hyperlipidemic drug.[1]

    A 600 milligram serving of red yeast rice extract should contain approximately 9 milligrams of monacolin K – research shows that monacolin K doses in this range, when taken every day for 6 to 8 weeks, can be expected to decrease low-density lipoprotein (LDL) cholesterol by 15%-25%.[1]

    Of course, to be absolutely sure of how much monacolin K we’re getting per serving of Revive MD Complete Vital, we would want to see a standardized extract used, with the precise standardization disclosed on the supplement facts label, which we don’t have here.

    Red Yeast Rice: Cholesterol-Lowering Mechanism

    The main bioactive molecule in ready yeast rice, monacolin K, is identical to Lovastatin, a prescription cholesterol-lowering drug in the statin class. Or, better said, Lovastatin is is identical to monacolin K! This image shows the cholesterol-lowering mechanism.[1]

    The good news, though, is that according to the research review cited above,[1] there’s an established range of variation when it comes to monacolin K content in red yeast rice, and 9 mg per 600 mg is actually on the lower end of that range. In other words, this supplement very likely contains more than that!

    The trifecta: improved HDL, Triglycerides, and LDL

    Red yeast extract can also improve serum apolipoprotein B, triglyceride, and HDL-C levels, as well as flow-mediated dilation and pulse wave velocity.[1]

    This is important because we’ve long commented on the knowledge that the ratio of triglycerides to HDL are far more powerful biomarkers than LDL alone.[2-6] The fact that this can support all of them is even more impressive.

  • N-Acetyl-L-Cysteine – 600 mg

    N-acetyl-L-cysteine, also known as N-acetyl cysteine or NAC, is a crucial building block for the synthesis of glutathione (GSH), your body’s most powerful endogenous antioxidant.[7] As such, optimizing GSH synthesis is absolutely critical for maintaining the body’s redox-oxidation balance, and ultimately, overall health.

    There’s just one problem with taking supplemental GSH, though: its oral bioavailability is too low to be effective.[8] The bioavailability of the precursor, NAC, is much higher, making NAC supplementation a better strategy for upregulating GSH.

    Revive MD Complete Vital Benefits

    More specifically, it’s the cysteine in NAC that’s the precursor to GSH. We could take regular old L-cysteine instead of NAC, except that, once again, there’s a bioavailability issue. Free cysteine gets prematurely degraded by first pass metabolism, but NAC, the acetylated form, doesn’t.[9,10]

    A 2017 research review on the benefits of NAC concluded that this acetylated amino acid is capable of:[11]

    • Supporting female endocrine and ovarian health
    • Improving successful birth outcomes
    • Limiting liver damage caused by acetaminophen
    • Supporting fertility
    • Mitigating bronchitis symptoms
    • Optimizing muscular performance
    • Supporting hemodialysis
    • Managing asthma symptoms
    • Decreasing risk of neurodegenerative conditions

    Everything on this list is great, but what makes NAC particularly compelling for the average person is its liver-protective effect.[12] As the liver is the “seat of all health”, if you support its ability to do its job, you support your overall health in general.

    Revive MD Complete Vital Detoxification

    However, the use of certain substances in everyday living, ranging from pain relievers to alcohol to excessive fat soluble vitamins, or engaging in aggressive forms of athletic training, can put one’s liver in serious jeopardy.

    Incredibly, NAC appears to selectively protect good cells, without impairing your body’s natural response to bad cells. For example, some research has found that NAC can help keep healthy cells alive and flourishing during chemotherapy,[13,14] without protecting cancerous cells from the drug effect.

    Importantly, NAC can also play a role in protecting DNA from being damaged by oxidative stress and inflammation.[14]

    Immunological benefits

    Since GSH is absolutely crucial for proper immune function,[15] it’s not surprising that supplementing with NAC can improve immunity.[16,17] One study even found that NAC supplementation completely restored natural killer cell activity in people with immunological deficiencies and toxicities.[15]

    NAC supplementation can also directly inhibit viral replication,[18] and has some documented activity supporting outcomes against “modern” health infections.[19,20]

    NAC and alcohol

    Revive MD NAC

    We went even deeper on our article on the standalone Revive MD NAC. The much-discussed glutathione precursor has a wide-ranging array of benefits, from supporting liver function to psychological support.

    You’ve probably heard that NAC supplementation can be a good preventative measure against hangovers. While this may sound like an old wives’ tale, it turns out that peer-reviewed studies back this up – NAC can help mitigate alcohol-induced liver damage as well.[21-23]

    We don’t endorse heavy drinking in any case, but if you do imbibe, then you should consider adding NAC to your before and after toolkit. Be smart.

    Cardioprotective

    Cysteine supplementation in general,[24] and NAC specifically,[25] have been shown to exert cardioprotective effects.

    The history and legality of NAC

    Given the many incredible benefits of NAC, it’s wild to consider the fact that the FDA made a very suspicious attempt to ban NAC from dietary supplements back in 2021. Fortunately, the Natural Products Association (NPA) fought back, pointing out that NAC’s commercial sale as a dietary supplement predates 1994, meaning it was legally eligible to be grandfathered into the “old dietary ingredient” status.

  • Terminalia arjuna [Bark] Extract – 500 mg

    The arjuna tree is native to India, and has a long history of use in Ayurvedic medicine for the management of cardiovascular issues like high blood pressure, heart congestion, chest pain, and high cholesterol.[26]

    Grapeseed Extract Arjuna

    Arjuna naturally contains high concentrations of potent phytochemicals like triterpenoids, flavonoids, glycosides, and β-sitosterol.[26] Most of its beneficial effects can be attributed to the triterpenoids and flavonoids.[26]

    One double-blind, randomized, placebo-controlled study found that two months of supplementing with 500 mg/day of arjuna extract, when administered alongside allopathic treatments, can increase cardiovascular function to a greater extent than prescription medication alone.[27] Note that we have the same dose here in Revive MD Complete Vital.

    Another study, using the same treatment dose and duration, found a substantial increase in VO2max and systolic blood pressure.[28]

  • Curcumin C3 Complex (Curcuma longa) [Rhizome] Extract – 400 mg

    Turmeric is an orange spice that’s in the same taxonomic family as ginger. It’s been used for centuries, if not millennia, to treat or manage a seemingly endless list of ailments.[29,30]

    Revive MD Complete Vital

    The star players in turmeric are its curcuminoids, a category that includes curcumin. While curcumin is definitely the most famous and well-researched in the group, all of the curcuminoids have similar effects on the human body – they’re all powerful anti-inflammatory and antioxidant compounds.[16]

    That’s why it’s cool to see Revive MD using C3 Complex, an ingredient that’s standardized to contain 95% curcuminoids by weight, and not only curcumin.

    Peer-reviewed studies indicate that curcuminoids are as close to a silver bullet as you can get in the world of dietary supplements. The laundry list of symptoms that curcuminoids might improve or resolve touches in some way on almost every known affliction, including the diseases of civilization, like depression or diabetes.[31,32]

    The near-universal power of the curcuminoids is thanks to their powerful anti-inflammatory effects.[31-33] Since chronic inflammation drives so many different kinds of physical and mental illnesses, it’s not that surprising to see that down regulating inflammation could have such far-reaching benefits.

    Importantly, curcuminoids can help support immune function by supporting specific immune cells like T cells, B cells, macrophages, neutrophils, NK cells, and dendritic cells.[29,30]

    Summing it all up, one study simply calls curcumin a “nature-made Jack-of-all-trades.”[32]

  • Grape (Vitis vinifera) [Seed] Extract – 400 mg

    Grape seed extract (GSE) can significantly increase blood flow and cardiovascular function. It’s loaded with powerful antioxidants including phenolic acids, flavonoids, and proanthocyanidins.[34]

    Cardiovascular Support from Revive

    Proanthocyanidin polyphenols are the main bioactive constituents here. Peer-reviewed research shows that these compounds have potent antioxidant, antidiabetic, anticancer, antimicrobial, antitumor, immunomodulatory, anti-inflammatory, cardioprotective, and neuroprotective effects.[34]

    Proanthocyanidins can induce vasodilation by triggering endothelial cells to release nitric oxide (NO).[34]

    Studies on GSE specifically have found that it can:[35-41]

    • Increase circulation
    • Decrease blood pressure
    • Reduce oxidative stress
    • Increase bone density
    • Improve liver, kidney, and brain health

    This means that users of Complete Vital may also get some athletic performance enhancement, thanks to its blood flow improvements — we do find grape seed extract in numerous pre-workout supplements for a reason.

  • Co-Enzyme Q10 (Ubiquinone) – 200 mg

    Coenzyme Q10 (CoQ10) is a powerful antioxidant that’s especially effective when it comes to supporting mitochondrial respiration.[42]

    Revive MD Complete Vital Key Ingredients

    Recall that mitochondria are the cellular organelles responsible for synthesizing all of your body’s adenosine triphosphate (ATP), which is the form of consumable chemical energy that your cells require for performing all their metabolic functions – ATP is your body’s gasoline! Unsurprisingly, if your body’s ATP supply becomes inadequate due to mitochondrial dysfunction, that can be a major contributing factor to devastating illnesses like diabetes, cancer, neurodegenerative illness, and cardiovascular disease.[43]

    CoQ10 is especially good at improving cardiovascular health and function, thanks to its ability to stabilize the notoriously unstable nitric oxide (NO) molecule. Remember, NO plays an indispensable role in vasodilation, so we need it to function properly in order to maintain healthy blood pressure and heart rate.[44]

  • Nattokinase – 100 mg (2,000 FU)

    Nattokinase is a fibrinolytic enzyme that’s seen a surge in popularity since 2020, and especially 2021 ongoing.

    Why? As you can probably guess from the word fibrinolytic, it degrades fibrin, a stiff, insoluble protein that the body uses for blood clotting and scar tissue generation.[45]

    Nattokinase Blood Pressure

    Nattokinase led to significant reductions in blood pressure, especially in men.[46]

    When fibrin interacts with neutrophil extracellular traps (NETs), the result is a composite matrix in your bloodstream that has the potential to increase blood viscosity, cardiovascular resistance, and blood pressure.[47] Taking fibrinolytic enzymes breaks down the fibrin component of this matrix, thus dissolving it and reversing its effects – bringing blood viscosity and blood pressure back under control.[48,49]

    One 2008 randomized, double-blind, placebo-controlled study showed that supplementation with nattokinase substantially decreased the severity of hypertension.[49] It could potentially even decrease one’s likelihood of developing such problems in the first place, although that’s researcher speculation.

    Another randomized controlled trial published in 2016 found that nattokinase consumption caused a 3 mmHg decrease in systolic blood pressure, and a whopping 6 mmHg in diastolic. Both effects achieved statistical significance.[46]

    While nattokinase can improve cardiovascular function in both men and women, that study found that it has a greater beneficial effect in men.[46] Given that exogenous testosterone therapy is linked to a higher risk of clotting,[50] it’s reasonable to assume that nattokinase works better in men partly because it’s minimizing the downsides of high testosterone levels.

    Nattokinase can potentially help preserve the long-term health and function of your cardiovascular system – studies show it can decrease cholesterol and significantly reduce the progression of atherosclerosis in people with hyperlipidemia.[51]

Dosage and Instructions

Revive MD Complete Vital Directions

Take 4 capsules per day, preferably about 30 minutes before bed or as directed by your doctor.

Complete Vital is What We Expect from Revive MD

As the industry continues to double down on new initiatives around product efficacy and purity, consumer sentiment toward supplements is improving across the board. As the average person is taking supplements more seriously, health and wellness is a huge growth category in the overall supplement market.

Complete Vital is an amazing formula, and it’s a great reminder of how far the industry has come in understanding how to appeal to the health and wellness demographic. Formulas like this are what we’ve come to expect from Dr. Iacovone and his team at Revive MD.

Revive MD Complete Vital Purpose

Supplement research is now developing more quickly than ever, and the industry has seen its share of trial-and-error. It’s exceedingly difficult to keep up with the amount of toxicity that the agri-food and pharmaceutical industries have thrust upon us. But Revive MD’s actually doing quite a good job of it.

This formula is so sophisticated that it’s almost as if Revive MD watched all the industry trial and error of the past decade, kept an eye on society’s transgressions against the liver, and then set out to create a product using only the very best ingredients to best survive these times of toxicity.

Since Revive MD was one of the first brands to base its entire business model on premium, clinically-validated, multi-ingredient wellness formulas, it’s not surprising that they would know how to do this right.

Revive MD Complete Vital – Deals and Price Drop Alerts

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About the Author: Mike Roberto

Mike Roberto

Mike Roberto is a research scientist and water sports athlete who founded PricePlow. He is an n=1 diet experimenter with extensive experience in supplementation and dietary modification, whose personal expertise stems from several experiments done on himself while sharing lab tests.

Mike's goal is to bridge the gap between nutritional research scientists and non-academics who seek to better their health in a system that has catastrophically failed the public.

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References

  1. Cicero, Arrigo F G et al. “Red Yeast Rice for Hypercholesterolemia.” Methodist DeBakey cardiovascular journal vol. 15,3 (2019): 192-199. doi:10.14797/mdcj-15-3-192. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822657/
  2. Bertsch, Ruth Ann, and Maqdooda A Merchant. “Study of the Use of Lipid Panels as a Marker of Insulin Resistance to Determine Cardiovascular Risk.” The Permanente journal vol. 19,4 (2015): 4-10. doi:10.7812/TPP/14-237. https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4625988/
  3. Bartlett, Jacquelaine, et al. “Is Isolated Low High-Density Lipoprotein Cholesterol a Cardiovascular Disease Risk Factor?” Circulation: Cardiovascular Quality and Outcomes, vol. 9, no. 3, May 2016, pp. 206–212, 10.1161/circoutcomes.115.002436. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871717/
  4. Wang, T. D., et al. “Efficacy of Cholesterol Levels and Ratios in Predicting Future Coronary Heart Disease in a Chinese Population.” The American Journal of Cardiology, vol. 88, no. 7, 1 Oct. 2001, pp. 737–743, 10.1016/s0002-9149(01)01843-4. https://pubmed.ncbi.nlm.nih.gov/11589839
  5. Jeppesen, Jørgen, et al. “Low Triglycerides–High High-Density Lipoprotein Cholesterol and Risk of Ischemic Heart Disease.” Archives of Internal Medicine, vol. 161, no. 3, 12 Feb. 2001, p. 361, 10.1001/archinte.161.3.361. https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/647239
  6. Castelli, William P. “Epidemiology of Triglycerides: A View from Framingham.” American Journal of Cardiology, vol. 70, no. 19, 14 Dec. 1992, pp. H3–H9, 10.1016/0002-9149(92)91083-G. https://www.ajconline.org/article/0002-9149(92)91083-G/abstract
  7. Kasperczyk, Sławomir, et al. “The Administration of N-Acetylcysteine Reduces Oxidative Stress and Regulates Glutathione Metabolism in the Blood Cells of Workers Exposed to Lead.” Clinical Toxicology, vol. 51, no. 6, 4 June 2013, pp. 480–486, 10.3109/15563650.2013.802797; https://pubmed.ncbi.nlm.nih.gov/23731375/
  8. Witschi, A., et al. “The Systemic Availability of Oral Glutathione.” European Journal of Clinical Pharmacology, vol. 43, no. 6, 1992, pp. 667–669, 10.1007/BF02284971; https://pubmed.ncbi.nlm.nih.gov/1362956/
  9. Dean, Olivia, et al. “N-Acetylcysteine in Psychiatry: Current Therapeutic Evidence and Potential Mechanisms of Action.” Journal of Psychiatry & Neuroscience, vol. 36, no. 2, 1 Mar. 2011, pp. 78–86, 10.1503/jpn.100057; https://www.ncbi.nlm.nih.gov/pubmed/21118657
  10. Sjödin, Karin, et al. “Metabolism of N-Acetyl-l-Cysteine Some Structural Requirements for the Deacetylation and Consequences for the Oral Bioavailability.” Biochemical Pharmacology, vol. 38, no. 22, Nov. 1989, pp. 3981–3985, 10.1016/0006-2952(89)90677-1; https://www.ncbi.nlm.nih.gov/pubmed/2597179
  11. Mokhtari, Vida et al; “A Review on Various Uses of N-Acetyl Cysteine.”; Cell journal; vol. 19,1; 2017; 11-17; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241507/
  12. Green, Jody, et al. “Oral and Intravenous Acetylcysteine for Treatment of Acetaminophen Toxicity: A Systematic Review and Meta-Analysis.” Western Journal of Emergency Medicine, vol. 14, no. 3, 1 May 2013, pp. 218–226, 10.5811/westjem.2012.4.6885; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3656701/
  13. Wanamarta, A. H., et al. “Effect of N-Acetylcysteine on the Antiproliferative Action of X-Rays or Bleomycin in Cultured Human Lung Tumor Cells.” Journal of Cancer Research and Clinical Oncology, vol. 115, no. 4, 1989, pp. 340–344, 10.1007/BF00400960; https://pubmed.ncbi.nlm.nih.gov/2474548/
  14. Millea, Paul J. “N-Acetylcysteine: Multiple Clinical Applications.” American Family Physician, vol. 80, no. 3, 1 Aug. 2009, pp. 265–269; https://pubmed.ncbi.nlm.nih.gov/19621836/
  15. Dröge, W, and R Breitkreutz; “Glutathione and Immune Function.”; The Proceedings of the Nutrition Society; U.S. National Library of Medicine; Nov. 2000; https://pubmed.ncbi.nlm.nih.gov/11115795
  16. Dröge, W, et al; “HIV-Induced Cysteine Deficiency and T-Cell Dysfunction–a Rationale for Treatment with N-Acetylcysteine.”; Immunology Today; U.S. National Library of Medicine; June 1992; https://pubmed.ncbi.nlm.nih.gov/1378279
  17. de Quay, B, et al; “Glutathione Depletion in HIV-Infected Patients: Role of Cysteine Deficiency and Effect of Oral N-Acetylcysteine.”; AIDS (London, England); U.S. National Library of Medicine; Aug. 1992; https://pubmed.ncbi.nlm.nih.gov/1418777
  18. Geiler, Janina, et al; “N-Acetyl-L-Cysteine (NAC) Inhibits Virus Replication and Expression of pro-Inflammatory Molecules in A549 Cells Infected with Highly Pathogenic H5N1 Influenza A Virus.”; Biochemical Pharmacology; U.S. National Library of Medicine; 1 Feb. 2010; https://www.ncbi.nlm.nih.gov/pubmed/19732754
  19. Shi, Zhongcheng, and Carlos A Puyo. “N-Acetylcysteine to Combat COVID-19: An Evidence Review.” Therapeutics and Clinical Risk Management, vol. Volume 16, Nov. 2020, pp. 1047–1055, 10.2147/tcrm.s273700; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649937/
  20. Izquierdo-Alonso, José Luis, et al. “N-Acetylcysteine for Prevention and Treatment of COVID-19: Current State of Evidence and Future Directions.” Journal of Infection and Public Health, vol. 15, no. 12, Dec. 2022, pp. 1477–1483, 10.1016/j.jiph.2022.11.009; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651994/
  21. Aydin, Seval, et al. “N-Acetylcysteine Reduced the Effect of Ethanol on Antioxidant System in Rat Plasma and Brain Tissue.” The Tohoku Journal of Experimental Medicine, vol. 198, no. 2, 2002, pp. 71–77, 10.1620/tjem.198.71; https://pubmed.ncbi.nlm.nih.gov/12512991/
  22. Caro, Andres A., et al. “N-Acetylcysteine Inhibits the Upregulation of Mitochondrial Biogenesis Genes in Livers from Rats Fed Ethanol Chronically.” Alcoholism, Clinical and Experimental Research, vol. 38, no. 12, 1 Dec. 2014, p. 2896, 10.1111/acer.12576; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4293075/
  23. Ozaras, Resat, et al. “N-Acetylcysteine Attenuates Alcohol-Induced Oxidative Stress in the Rat.” World Journal of Gastroenterology, vol. 9, no. 1, 2003, p. 125, 10.3748/wjg.v9.i1.125; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4728225/
  24. Shackebaei, D, et al; “Mechanisms Underlying the Cardioprotective Effect of L-Cysteine.”; Molecular and Cellular Biochemistry; U.S. National Library of Medicine; Sept. 2005; https://pubmed.ncbi.nlm.nih.gov/16132711
  25. Cui, Yuqi, et al. “N-Acetylcysteine and Atherosclerosis: Promises and Challenges.” Antioxidants, vol. 12, no. 12, 4 Dec. 2023, pp. 2073–2073, doi:10.3390/antiox12122073. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10741030/
  26. Dwivedi, S. et al. Oct. 2014. “Revisiting Terminalia arjuna – An Ancient Cardiovascular Drug.” Journal of Traditional and Complementary Medicine vol. 4,4; 224–31. doi:10.4103/2225-4110.139103. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220499/
  27. Dwivedi S, et al. Oct. 1997. “Beneficial Effects of Terminalia arjuna in Coronary Artery Disease. Indian Heart Journal vol.49,5; 507-10. https://pubmed.ncbi.nlm.nih.gov/9505018/
  28. Sandhu, J. et al. Sept. 2010. “Effects of Withania somnifera (Ashwagandha) and Terminalia arjuna (Arjuna) on Physical Performance and Cardiorespiratory Endurance in Healthy Young Adults.” International Journal of Ayurveda Research vol. 1,3; 144–9. doi: 10.4103/0974-7788.72485. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996571/
  29. Gautam, S. et al. 2007. “Immunomodulation by Curcumin.” Advances in Experimental Medicine and Biology vol. 595, 321–41. doi:10.1007/978-0-387-46401-5_14. https://pubmed.ncbi.nlm.nih.gov/17569218/
  30. Jagetia G. et al. Jan. 2007. “Spicing Up” of the Immune system by Curcumin. Journal of Clinical Immunology vol. 27,1; 19-35. doi:10.1007/s10875-006-9066-7. https://pubmed.ncbi.nlm.nih.gov/17211725/
  31. ‌Peng, Ying et al. “Anti-Inflammatory Effects of Curcumin in the Inflammatory Diseases: Status, Limitations and Countermeasures.” Drug design, development and therapy vol. 15 4503-4525. 2 Nov. 2021, doi:10.2147/DDDT.S327378; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572027/
  32. Abdollahi, Elham, et al. “Therapeutic Effects of Curcumin in Inflammatory and Immune-Mediated Diseases: A Nature-Made Jack-of-All-Trades?” Journal of Cellular Physiology, vol. 233, no. 2, 31 Mar. 2017, pp. 830–848, doi:10.1002/jcp.25778. https://onlinelibrary.wiley.com/doi/10.1002/jcp.25778
  33. Jagetia GC, Aggarwal BB. “Spicing up” of the immune system by curcumin. J Clin Immunol. 2007 Jan;27(1):19-35. doi: 10.1007/s10875-006-9066-7; https://link.springer.com/article/10.1007/s10875-006-9066-7
  34. Rauf, A., et al. 2019. “Proanthocyanidins: A Comprehensive Review.” Biomedicine & Pharmacotherapy, 116. doi:10.1016/j.biopha.2019.108999. https://www.sciencedirect.com/science/article/pii/S0753332219305359
  35. Zhang, Haili, et al. 2016. “The Impact of Grape Seed Extract Treatment on Blood Pressure Changes: A Meta-Analysis of 16 Randomized Controlled Trials.” Medicine vol. 95,33: e4247. doi:10.1097/MD.0000000000004247. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370781/
  36. Shenoy SF., et al. 2007. “Effects of Grape Seed Extract Consumption on Platelet Function in Postmenopausal Women.” Thrombosis Research 121(3):431‐432. doi:10.1016/j.thromres.2007.09.004. https://pubmed.ncbi.nlm.nih.gov/17950783/
  37. Aloui F., et al. 2016. “Grape Seed and Skin Extract Reduces Pancreas Lipotoxicity, Oxidative Stress and Inflammation in High Fat Diet Fed Rats.” Biomed Pharmacother 84:2020‐2028 doi:10.1016/j.biopha.2016.11.017. https://pubmed.ncbi.nlm.nih.gov/27847215/
  38. Calapai G., et al.Oct. 31, 2017. “A Randomized, Double-Blinded, Clinical Trial on Effects of a Vitis vinifera Extract on Cognitive Function in Healthy Older Adults.” Frontiers in Pharmacology. 8:776. doi:10.3389/fphar.2017.00776. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671585/
  39. Khoshbaten M., et al. 2010. “Grape Seed Extract to Improve Liver Function in Patients with Nonalcoholic Fatty Liver Change.” Saudi Journal of Gastroenterology 16(3):194‐197. doi:10.4103/1319-3767.65197. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003214/
  40. Turki K, et al. Jun. 27, 2016. “Grape Seed Powder Improves Renal Failure of Chronic Kidney Disease Patients.” EXCLI Journal. 2016;15:424‐433. doi:10.17179/excli2016-363. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5083963/
  41. Ishikawa M., et al. 2005. “Grape Seed Proanthocyanidins Extract Promotes Bone Formation in Rat’s Mandibular Condyle.” European Journal of Oral Sciences 2005;113(1):47‐52. doi:10.1111/j.1600-0722.2004.00176.x. https://pubmed.ncbi.nlm.nih.gov/15693829/
  42. Hidalgo-Gutiérrez, Agustín et al. “Metabolic Targets of Coenzyme Q10 in Mitochondria.” Antioxidants (Basel, Switzerland) vol. 10,4 520. 26 Mar. 2021, doi:10.3390/antiox10040520. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066821/
  43. Garrido-Maraver J., et al; “Clinical applications of coenzyme Q10;” Frontiers in Bioscience; 2014. doi:10.2741/4231. https://www.ncbi.nlm.nih.gov/pubmed/24389208
  44. Rabanal-Ruiz, Yoana et al. “The Use of Coenzyme Q10 in Cardiovascular Diseases.” Antioxidants (Basel, Switzerland) vol. 10,5 755. 10 May. 2021, doi:10.3390/antiox10050755. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8151454/
  45. Weng, Yunqi et al. “Nattokinase: An Oral Antithrombotic Agent for the Prevention of Cardiovascular Disease.” International journal of molecular sciences vol. 18,3 523. 28 Feb. 2017, doi:10.3390/ijms18030523; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372539/
  46. Jensen, Gitte, et al. “Consumption of Nattokinase Is Associated with Reduced Blood Pressure and von Willebrand Factor, a Cardiovascular Risk Marker: Results from a Randomized, Double-Blind, Placebo-Controlled, Multicenter North American Clinical Trial.” Integrated Blood Pressure Control, vol. Volume 9, Oct. 2016, pp. 95–104, doi:10.2147/ibpc.s99553. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066864/
  47. Martinod, Kimberly, and Denisa D Wagner. “Thrombosis: tangled up in NETs.” Blood vol. 123,18 (2014): 2768-76. doi:10.1182/blood-2013-10-463646; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007606/
  48. Pais, Eszter et al. “Effects of nattokinase, a pro-fibrinolytic enzyme, on red blood cell aggregation and whole blood viscosity.” Clinical hemorheology and microcirculation vol. 35,1-2 (2006): 139-42; https://content.iospress.com/articles/clinical-hemorheology-and-microcirculation/ch914
  49. Kim, Ji Young et al. “Effects of nattokinase on blood pressure: a randomized, controlled trial.” Hypertension research : official journal of the Japanese Society of Hypertension vol. 31,8 (2008): 1583-8. doi:10.1291/hypres.31.1583; https://www.nature.com/articles/hr2008203
  50. Walker, Rob F et al. “Association of Testosterone Therapy With Risk of Venous Thromboembolism Among Men With and Without Hypogonadism.” JAMA internal medicine vol. 180,2 (2020): 190-197. doi:10.1001/jamainternmed.2019.5135 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865248/
  51. Chen, Hongjie et al. “Effective management of atherosclerosis progress and hyperlipidemia with nattokinase: A clinical study with 1,062 participants.” Frontiers in cardiovascular medicine vol. 9 964977. 22 Aug. 2022, doi:10.3389/fcvm.2022.964977 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441630/

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