Guest User Guest User

Health Article: Grape seed Extract (GBE) Emerges as Anti-Cancer Powerhouse Thanks to Pro-Active Supplement Users

Article By Ethan Evers

(NaturalNews) The therapeutic potential of grape seed extract as anti-oxidant, anti-hypertensive and anti-inflammatory is so well established that this natural supplement is now being used in seven on-going clinical trials, only one of which is on cancer (of the breast). But the spotlight may soon shift to grape seed extract’s anti-cancer potential as recent landmark studies on human patients have just uncovered its remarkable protective effects against three major cancers: squamous cell carcinoma, prostate and hematologic malignancies.

Article By Ethan Evers

(NaturalNews) The therapeutic potential of grape seed extract as anti-oxidant, anti-hypertensive and anti-inflammatory is so well established that this natural supplement is now being used in seven on-going clinical trials, only one of which is on cancer (of the breast). But the spotlight may soon shift to grape seed extract’s anti-cancer potential as recent landmark studies on human patients have just uncovered its remarkable protective effects against three major cancers: squamous cell carcinoma, prostate and hematologic malignancies. Even more remarkable is that this breakthrough in the science of natural medicine was not due to the foresight of medical practitioners who designed the trials, but to the patients who took grape seed extract, on their volition, as a nutritional supplement to support general health.

74% Risk Reduction of Skin Cancer (SCC)
A recent study, just published in June 2011, was carried out in northern California on 830 participants to test the effects of general supplement use on the occurrence of squamous cell carcinoma (the second most common skin cancer). The supplements in use included vitamins A, C, D, E, multivitamins and grape seed extract. Only the users of grape seed extract experienced a significant reduction in risk (P = 0.031) of squamous cell carcinoma–by an astounding 74%. Multivitamin users experienced 29% reduced risk, but this was only borderline statistically significant.

62% Risk Reduction of Prostate Cancer
A much larger study conducted in Washington State tracked 35,239 male participants starting in the year 2000 in the Vitamins and Lifestyle (VITAL) cohort. Participants, aged 50-76 years, answered detailed questionnaires about specialty supplement use for the 10 years prior to the start of the study. Prostate cancer risk was assessed after a median follow-up time of 6.1 years. The results showed grape seed extract to be the stand-alone winner. Men, who used an individual grape seed extract supplement with “high average use” over 10 years, experienced a significant 62% risk reduction of prostate cancer compared to non-users, while average users of grape seed extract supplements experienced a 41% risk reduction. None of the other supplements observed in this study (CoQ10, fish oil, garlic pills, ginkgo biloba, ginseng, glucosamine, chondroitin or saw palmetto) were seen to offer protection against prostate cancer. Note, however, that green tea was not one of the supplements considered. This study was published in May 2011.

43% Risk Reduction of Hematologic Cancers
The same VITAL cohort as used for the prostate cancer study was also used to assess risk of hematologic cancers (involving blood, bone marrow or lymph nodes). The population was expanded to include women, for a total of 66,227 participants. Those who had ever used grape seed supplements saw a 43% risk reduction for hematologic cancers. This was only matched by those with a “high use” of garlic, who saw a 47% reduction of risk. No other supplements offered significant protection. This study was published in August 2011.

In addition to the above cancers, grape seed extract has already demonstrated cytotoxicity against breast cancer, colon cancer, glioblastoma, and NSC lung cancer cells in laboratory studies. But the three study results on human populations given above provide a dramatic leap forward for the science backing grape seed extract as an anti-cancer supplement. It is astounding, then, that none of the above studies received much media attention. That will likely require full-blown clinical trials, which will almost certainly be kicked-off as a result of these studies, but will take years to complete. Until then, the latest findings on grape seed extract make a compelling case for its consideration in any program or supplement regimen meant to reduce cancer risk.

Sources:

http://www.clinicaltrials.gov/ct2/results?te…

http://www.sciencedirect.com/science/article…

http://www.ncbi.nlm.nih.gov/pubmed/21598177

http://www.ncbi.nlm.nih.gov/pubmed/21803844

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC…

About the author
Ethan Evers is author of the award-winning medical thriller “The Eden Prescription,” in which natural medicine outperforms a billion-dollar chemo drug and threatens the entire $50 billion cancer drug industry. Ethan based The Eden Prescription on the latest science on natural medicine for cancer, and wrote it to show the future reality that natural medicine can bring us—and to warn of the strategies now being used by those who are trying to stop it. Ethan has a PhD in Applied Science.

For breaking news and research updates on natural medicine for cancer, see Ethan’s Facebook Page: https://www.facebook.com/TheEdenPrescription

Learn more: http://www.naturalnews.com/033754_grape_seed_extract_cancer_prevention.html#ixzz2rpOZrWYD

Read More
Guest User Guest User

Health Article: Tart Cherries Relieve Osteoarthritis Pain

HIGHEST ANTI-INFLAMATORY CONTENT OF ANY FOOD

By Margie King, Health Coach

Tart Cherries Relieve Osteoarthritis Pain

If you are among the millions of Americans suffering from joint pain and arthritis, there’s good news about a favorite summer treat. According to research from Oregon Health & Science University, tart cherries help reduce the chronic inflammation that leads to pain.[1]

In fact, the Oregon researchers declared that tart cherries have the “highest anti-inflammatory content of any food” and can help osteoarthritis patients manage their condition.

HIGHEST ANTI-INFLAMATORY CONTENT OF ANY FOOD

By Margie King, Health Coach

Tart Cherries Relieve Osteoarthritis Pain

If you are among the millions of Americans suffering from joint pain and arthritis, there’s good news about a favorite summer treat. According to research from Oregon Health & Science University, tart cherries help reduce the chronic inflammation that leads to pain.[1]

In fact, the Oregon researchers declared that tart cherries have the “highest anti-inflammatory content of any food” and can help osteoarthritis patients manage their condition.

The study specifically dealt with tart cherries (e.g., Montmorency and Balaton) and not sweet cherries (e.g., Bing, Lambert, Rainier), although both varieties have healing benefits. Tart cherries are grown mostly in Michigan while the sweet varieties are found mostly in Washington, Oregon and Idaho.

Both types have traditionally been used to combat gout by reducing the body’s levels of uric acid. Tart cherries, however, have higher concentrations of phenolics and anthocyanins. These compounds have been specifically linked to high antioxidant capacity and reduced inflammation.

Read more here.

Read More
Guest User Guest User

Health Article: The Rest and Digest State!

HOW YOU EAT IS AS POWERFUL AS WHAT YOU EAT!
By Brittany Wood Nickerson, Practicing Herbalist

Our digestive system takes in and breaks down food and experiences. It is through the process of digestion that bits of food are transformed into vital nutrients – complex chemical processes work to extract vitamins and minerals, break down fats into lipids, and proteins into amino acids. A well functioning digestive system has the wisdom to break down, absorb and utilize the nutrition it needs from the food we eat and let go of the parts and pieces that it does not.

HOW YOU EAT IS AS POWERFUL AS WHAT YOU EAT!
By Brittany Wood Nickerson, Practicing Herbalist

Our digestive system takes in and breaks down food and experiences. It is through the process of digestion that bits of food are transformed into vital nutrients – complex chemical processes work to extract vitamins and minerals, break down fats into lipids, and proteins into amino acids. A well functioning digestive system has the wisdom to break down, absorb and utilize the nutrition it needs from the food we eat and let go of the parts and pieces that it does not. When digestion is not working well, one can eat the healthiest, most pure, organic food in the world, but not absorb any of the nutrients. In fact, improperly digested food (whether of poor or high quality) over time can lead to larger health concerns. We spend so much time focusing on WHAT we eat in our culture, I think we often forget to look at HOW we eat and whether or not our body is able to process and assimilate nutrition from that food.

Our digestive processes are integrally connected to our nervous system. The enteric nervous system, which has almost as many neurons as the spinal cord, runs the length of our digestive system from our mouth to our anus. The enteric nervous system is responsible for the secretion of digestive enzymes, bile and other fluids, the movement of peristalsis and the opening and closing of sphincters that allow food to pass from one digestive organ to another. The enteric nervous system is often called a second brain because it contains neurons, neurotransmitters and proteins that are responsible for communicating and thinking. Tissues that contain these “communicating and thinking” neurons and neurotransmitters (the same as those found in the brain) surround the primary organs of the digestive system – esophagus, stomach, small intestine, and large intestine – and are responsible for much of its functioning. When our senses are stimulated (the smell, sight or taste of food are a few examples), the enteric nervous system is triggered to begin the digestive process.

That being said, our digestive processes are influenced by all the same factors that influence our nervous system and to all those things that relax and worry us. When the body is stressed out, anxious, sad or angry, these emotions trigger our sympathetic nervous system, initiating the fight or flight response – when the body is in this state it goes into survival mode and digestion slows way down. On the contrary, when we are relaxed, happy and at ease, the parasympathetic nervous system is active; this is the rest and digest state. When we are in the rest and digest state, the enteric nervous system functions optimally and there is better digestion, absorption and elimination.

If you want to get the most out of your food, to digest properly, the body has to be in a relaxed, parasympathetic dominant state. Otherwise, the enteric nervous system, which makes all these amazing digestive processes work, will be impaired and sluggish. The most important first step is to make space to eat and digest. Making space to eat might include taking a few deep breaths before meals or taking a quiet moment to shut your eyes and soften into your body. A quiet moment of reflection such as this can help to lower the stress response. One of the other important ways that we can make space to enjoy and appreciate the food we eat is to practice gratitude – even if we are just eating a quick snack or a meal on the go. You can express your gratitude toward the food you are eating, those who prepared it or grew it, or to something else entirely. Giving thanks is an act that stimulates a parasympathetic (rest and digest) state, enhancing the digestive process.

There is ancient wisdom in saying grace before meals, as practiced by many cultures around the world.

Digestion is about breaking down, absorbing, processing and letting go of far more than just the food we eat. Supporting healthy digestion is also about acknowledging how we process experiences, emotions and energy. The state and health of our digestion can have a direct impact on our emotional state and vice versa. If you have an irritated, inflamed gut, you will feel irritated in your life. If you have sluggish, slow digestion, you will feel slow, unmotivated and perhaps depressed in your life. Supporting your digestion (including the ways we prepare and consume food) will positively influence how you feel, perceive, respond, react and initiate in your life. Supporting digestion is a broad topic, but here are a few straightforward suggestions to get you started!

Lifestyle and Dietary Suggestions to Support Better Digestion and Absorption:

1. Don’t eat late at night.

2. Eat regular, balanced meals and don’t snack when you are not hungry.

3. Don’t go for long periods without eating, do not suppress or ignore your hunger.

4. Have a bowel movement every day.

5. Do not drink cold liquids with meals.

6. Do not drink more than 6 – 8 oz. of liquid with meals.

7. Give thanks for the food you are eating, for those who grew it and prepared it and for anything else you want to honor.

8. Take a quiet moment before eating to relax and take a few deep breaths.

9. Chew slowly and mindfully.

10. Prepare and eat your food with love (no matter how simple or elaborate the meal).

11. Got bitter? Bitter is the most metabolically active of all flavors, it stimulates the entire digestive process, supports absorption and elimination and is excellent for liver health. Bitter foods include bitter lettuce, radicchio, dark leafy greens like dandelion greens and kale, and herbs like gentian, elecampane, angelica, artichoke leaf and dandelion root.

12. Support your digestive fire with carminative spices. Carminatives increase metabolism and the absorption of nutrients. They also help to relieve gas and bloating. All culinary herbs are carminative, so start cooking with herbs and spices!

13. Eat fermented foods. Fermented foods are full of probiotic bacteria that help support the health of our colon. They support absorption of B vitamins, fat-soluble vitamins and folic acid and play a large role in immunity. Healthy probiotic flora have also been linked to mental and emotional health. Fermented foods include: sauerkraut, kim chi, kombucha, plain yogurt, kefir, sour cream, crème fraiche, buttermilk, lacto fermented pickles, miso, raw apple cider vinegar.

Brittany Wood Nickerson is a practicing herbalist. She grows herbs, keeps a homestead, sees clients, runs an herbal school and writes zines at Thyme Herbal in Amherst Massachusetts. She will be teaching Daily Nourishment at HERBSTALK on June 8th.

Brittany can be found at Thyme Herbal: www.thymeherbal.com

This article was originally posted at: http://herbstalk.org/2013/06/the-rest-and-digest-state-how-you-eat-is-as-powerful-as-what-you-eat/

READ MORE HERE: Rest & Digest By Brittany Nickerson

Read More
Guest User Guest User

Health Article: The Power of Peppermint

A favorite herbal medicine of the ancients, peppermint leaves have been found in Egyptian pyramids dating back to 1,000 BC. Modern scientific investigations have now confirmed that this remarkable plant has over a dozen healing properties.

In our continuing effort to educate folks to the vast array of healing agents found in the natural world around us, we are excited to feature peppermint, a member of the aromatic mint family that you may already have squirreled away somewhere in your kitchen cupboard. While most have experienced peppermint as a flavoring agent, or perhaps as a comforting cup of herbal tea, few are aware of its wide range of experimentally confirmed therapeutic properties.

The Power of Peppermint: 15 Health Benefits Revealed

By Sayer Ji, Founder GreenMedInfo, posted on greenmedinfo.com 03/15/2013

A favorite herbal medicine of the ancients, peppermint leaves have been found in Egyptian pyramids dating back to 1,000 BC. Modern scientific investigations have now confirmed that this remarkable plant has over a dozen healing properties.

In our continuing effort to educate folks to the vast array of healing agents found in the natural world around us, we are excited to feature peppermint, a member of the aromatic mint family that you may already have squirreled away somewhere in your kitchen cupboard. While most have experienced peppermint as a flavoring agent, or perhaps as a comforting cup of herbal tea, few are aware of its wide range of experimentally confirmed therapeutic properties.

The ancients certainly were aware of the mint family’s medicinal value, having been used as herbal medicines in ancient Egypt, Greek and Rome thousands of years ago.[i] Dried peppermint leaves have even been found in several Egyptian pyramids carbon dating back to 1,000 BC.

Today, modern scientific investigations are revealing an abundance of potential health benefits associated with the use of different components of the peppermint plant, including aromatherapeutic, topical and internal applications.

Most of the human research on peppermint performed thus far indicates this plant has great value in treating gastrointestinal disorders, including:

Irritable Bowel Syndrome – Since the late 90′s it was discovered that enteric-coated peppermint oil capsules are safe and effective in the treatment of this increasingly prevalent disorder.[ii] This beneficial effect extends to the pediatric community. In one children’s trial 75% of those receiving peppermint oil had reduced severity of pain associated with IBS within 2 weeks.[iii] Another 2005 trial in adults concluded that “Taking into account the currently available drug treatments for IBS Peppermint oil (1-2 capsules t.i.d. over 24 weeks) may be the drug of first choice in IBS patients with non-serious constipation or diarrhea to alleviate general symptoms and to improve quality of life.”[iv] In another 2007 trial 75% of patients receiving peppermint oil saw an impressive 50% reduction of “total irritable bowel syndrome score.”[v] Most recently, a study published January of this year found that peppermint oil was effective in relieving abdominal pain in diarrhea predominant irritable bowel syndrome.[vi]
Colonic spasm – Peppermint oil has been studied as a safe and effective alternative to the drug Buscopan for its ability to reduce spasms during barium enemas.[vii] [viii]
Gastric Emptying Disorders – Peppermint has been found to enhance gastric emptying, suggesting its potential use in a clinical setting for patients with functional gastrointestinal disorders.[ix]

Functional dyspepsia – A 2000 study published in the journal Ailment Pharmacology and Therapy found that 90 mg of peppermint oil and 50 mg of caraway oil resulted in 67% of patients reporting “much or very much improved” in their symptoms of functional dyspepsia. [x]
Infantile Colic: A 2013 study found that peppermint is at least as effective as the chemical simethicone in the treatment of infantile colic.[xi]

Other studied applications include:

Breastfeeding Associated Nipple Pain and Damage: A 2007 study found that peppermint water prevented nipple cracks and nipple pain in breastfeeding mothers.[xii]
Tuberculosis: A 2009 study found that inhaled essential oil of peppermint was able to rapidly regress tuberculous inflammation, leading the authors to conclude: “This procedure may be used to prevent recurrences and exacerbation of pulmonary tuberculosis.”[xiii]

Allergic rhinitis (hay fever): A 2001 preclinical study found that extracts of the leaves of peppermint inhibit histamine release indicating it may be clinically effective in alleviating the nasal symptoms of allergic rhinitis.[xiv]

Shingles Associated Pain (Post-Herpetic Neuralgia): A 2002 case study found that topical peppermint oil treatment resulted in a near immediate improvement of shingles associated neuropathic pain symptoms; the therapeutic effects persisted throughout the entire 2 months of follow-up treatment. [xv]

Memory problems: A 2006 study found that the simple aroma of peppermint enhances memory and increases alertness in human subjects.[xvi]

Chemotherapy-Induced Nausea: A 2013 study found that peppermint oil was found to be effective in reducing chemotherapy-induced nausea, and at reduced cost versus standard drug-based treatment.[xvii]

Prostate Cancer: Preclinical research indicates that peppermint contains a compound known as menthol which inhibits prostate cancer growth.[xviii] [xix]

Radiation Damage: Preclinical research indicates peppermint protects against radiation-induced DNA damage and cell death.[xx] [xxi]

Herpes Simplex Virus Type 1: Peppermint has been found to have inhibitory activity against acyclovir-resistant Herpes Simplex virus type 1.[xxii] [xxiii]

Dental Caries/Bad Breath: Peppermint oil extract has been found to be superior to the mouthwash chemical chlorhexidine inhibiting Streptococus mutans driven biofilm formation associated with dental caries.[xxiv] [xxv]

This may explain why powdered peppermint leaves were used in the Middle Ages to combat halitosis and whiten teeth.

Peppermint is actually a hybridized cross between Water Mint (Mentha aquatica) and Spearmint (Mentha spicata),[xxvi] the latter of which has also been researched to possess remarkable therapeutic properties, such as the ability to exert significant anti-androgenic effects in polycystic ovarian syndrome[xxvii] and ameliorating the related condition of mild hirsutism, marked by excessive hair growth in females.[xxviii]

Like all plant medicines, extreme caution must be exercised when using extracts and especially essential oils. Also, remember that more is not always better. A recent study on the use of rosemary in improving cognitive performance in the elderly found that a lower ‘culinary’ dose (750 mg) was not only more effective in improving cognition (as measured by memory speed) than a higher dose, but the highest dose (6,000 mg) had a significant memory impairing effect.[xxix] This illustrates quite nicely how less can be more, and why an occasional nightly cup of peppermint tea may be far superior as preventive strategy than taking large ‘heroic’ doses of an herb only after a serious health problem sets in.

_____________________________________________________
Resources
[i] A. Sustrikova, I. Salamon, Essential oil of peppermint (Mentha x piperita L.) from fields in Eastern Slovakia., 2004: Zahradnictvi Horticultural Science 31(1): 31-36
[ii] J H Liu, G H Chen, H Z Yeh, C K Huang, S K Poon. Enteric-coated peppermint-oil capsules in the treatment of irritable bowel syndrome: a prospective, randomized trial. J Gastroenterol. 1997 Dec;32(6):765-8. PMID: 9430014
[iii] R M Kline, J J Kline, Di Palma J, G J Barbero. Enteric-coated, pH-dependent peppermint oil capsules for the treatment of irritable bowel syndrome in children. J Pediatr. 2001 Jan;138(1):125-8. PMID: 11148527
[iv] H G Grigoleit, P Grigoleit. Peppermint oil in irritable bowel syndrome. Phytomedicine. 2005 Aug;12(8):601-6. PMID: 16121521
[v] G Cappello, M Spezzaferro, L Grossi, L Manzoli, L Marzio. Peppermint oil (Mintoil) in the treatment of irritable bowel syndrome: a prospective double blind placebo-controlled randomized trial. Dig Liver Dis. 2007 Jun;39(6):530-6. Epub 2007 Apr 8. PMID: 17420159
[vi] M S Alam, P K Roy, A R Miah, S H Mollick, M R Khan, M C Mahmud, S Khatun. Efficacy of Peppermint Oil in Diarrhea Predominant IBS – A Double Blind Randomized Placebo – Controlled Study. Mymensingh Med J. 2013 Jan ;22(1):27-30. PMID: 23416804
[vii] M J Sparks, P O’Sullivan, A A Herrington, S K Morcos. Does peppermint oil relieve spasm during barium enema? Br J Radiol. 1995 Aug;68(812):841-3. PMID: 7551780
[viii] T Asao, H Kuwano, M Ide, I Hirayama, J-I Nakamura, K-I Fujita, R Horiuti. Spasmolytic effect of peppermint oil in barium during double-contrast barium enema compared with Buscopan. Clin Radiol. 2003 Apr;58(4):301-5. PMID: 12662951
[ix] Masahiko Inamori, Tomoyuki Akiyama, Keiko Akimoto, Koji Fujita, Hirokazu Takahashi, Masato Yoneda, Yasunobu Abe, Kensuke Kubota, Satoru Saito, Norio Ueno, Atsushi Nakajima. Early effects of peppermint oil on gastric emptying: a crossover study using a continuous real-time 13C breath test (BreathID system). J Gastroenterol. 2007 Jul;42(7):539-42. Epub 2007 Jul 25. PMID: 17653649
[x] B May, S Köhler, B Schneider. Efficacy and tolerability of a fixed combination of peppermint oil and caraway oil in patients suffering from functional dyspepsia. Aliment Pharmacol Ther. 2000 Dec;14(12):1671-7. PMID: 11121917
[xi] João Guilherme Bezerra Alves, Rita de Cássia Coelho Moraes de Brito, Telma Samila Cavalcanti. Effectiveness of Mentha piperita in the Treatment of Infantile Colic: A Crossover Study. Evid Based Complement Alternat Med. 2012 ;2012:981352. Epub 2012 Jul 12. PMID: 22844342
[xii] Manizheh Sayyah Melli, Mohammad Reza Rashidi, Abbas Delazar, Elaheh Madarek, Mohammad Hassan Kargar Maher, Alieh Ghasemzadeh, Kamran Sadaghat, Zohreh Tahmasebi. Effect of peppermint water on prevention of nipple cracks in lactating primiparous women: a randomized controlled trial. Int Breastfeed J. 2007;2:7. Epub 2007 Apr 19. PMID: 17442122
[xiii] V A Shkurupiĭ, O A Odintsova, N V Kazarinova, K G Tkrachenko. [Use of essential oil of peppermint (Mentha piperita) in the complex treatment of patients with infiltrative pulmonary tuberculosis]. Virol J. 2009 Jan 20;6:8. PMID: 17128800
[xiv] T Inoue, Y Sugimoto, H Masuda, C Kamei. Effects of peppermint (Mentha piperita L.) extracts on experimental allergic rhinitis in rats. Biol Pharm Bull. 2001 Jan;24(1):92-5. PMID: 11201253
[xv] Simon J Davies, Louise M Harding, Andrew P Baranowski. A novel treatment of postherpetic neuralgia using peppermint oil. Clin J Pain. 2002 May-Jun;18(3):200-2 PMID: 12048423
[xvi] Mark Moss, Steven Hewitt, Lucy Moss, Keith Wesnes. Modulation of cognitive performance and mood by aromas of peppermint and ylang-ylang. Nutr Cancer. 2006;55(1):53-62. PMID: 18041606
[xvii] Z Tayarani-Najaran, E Talasaz-Firoozi, R Nasiri, N Jalali, Mk Hassanzadeh. Antiemetic activity of volatile oil from Mentha spicata and Mentha× piperita in chemotherapy-induced nausea and vomiting. Ecancermedicalscience. 2013 ;7:290. Epub 2013 Jan 31. PMID: 23390455
[xviii] Eun-Jung Park, Su-Hwa Kim, Byung-Joo Kim, Sung-Young Kim, Insuk So, Ju-Hong Jeon. Menthol Enhances an Antiproliferative Activity of 1alpha,25-Dihydroxyvitamin D(3) in LNCaP Cells. J Clin Biochem Nutr. 2009 Mar;44(2):125-30. Epub 2009 Feb 28. PMID: 19308266
[xix] Su-Hwa Kim, Joo-Hyun Nam, Eun-Jung Park, Byung-Joo Kim, Sung-Joon Kim, Insuk So, Ju-Hong Jeon. Menthol regulates TRPM8-independent processes in PC-3 prostate cancer cells. Biochim Biophys Acta. 2007 Apr;1770(4):659-65. Epub 2006 Nov 23. PMID: 18955132
[xx] Hanaa A Hassan, Hani S Hafez, Mona S Goda. Mentha piperita as a pivotal neuro-protective agent against gamma irradiation induced DNA fragmentation and apoptosis : Mentha extract as a neuroprotective against gamma irradiation. Cytotechnology. 2013 Jan ;65(1):145-56. Epub 2012 Sep 21. PMID: 23011739
[xxi] Ravindra M Samarth, Meenakshi Samarth. Protection against radiation-induced testicular damage in Swiss albino mice by Mentha piperita (Linn.). Basic Clin Pharmacol Toxicol. 2009 Apr;104(4):329-34. PMID: 19320637
[xxii] Silke Nolkemper, Jürgen Reichling, Florian C Stintzing, Reinhold Carle, Paul Schnitzler. Antiviral effect of aqueous extracts from species of the Lamiaceae family against Herpes simplex virus type 1 and type 2 in vitro. Planta Med. 2006 Dec;72(15):1378-82. Epub 2006 Nov 7. PMID: 17091431
[xxiii] A Schuhmacher, J Reichling, P Schnitzler. Virucidal effect of peppermint oil on the enveloped viruses herpes simplex virus type 1 and type 2 in vitro. Phytomedicine. 2003;10(6-7):504-10. PMID: 13678235
[xxiv] Iraj Rasooli, Shojaedin Shayegh, Massoud Taghizadeh, Shakiba Darvish Alipoor Astaneh. Phytotherapeutic prevention of dental biofilm formation. Phytother Res. 2008 Sep;22(9):1162-7. PMID: 18729251
[xxv] Shojaedin Shayegh, Iraj Rasooli, Massoud Taghizadeh, Shakiba Darvish Alipoor Astaneh. Phytotherapeutic inhibition of supragingival dental plaque. Nat Prod Res. 2008 Mar 20;22(5):428-39. PMID: 18404563
[xxvi] The Complete Illustrated Book of Herbs, Alex Frampton, The Reader’s Digest Association, 2009
[xxvii] Paul Grant. Spearmint herbal tea has significant anti-androgen effects in polycystic ovarian syndrome. A randomized controlled trial. Phytother Res. 2009 Jul 7. PMID: 19585478
[xxviii] Mehmet Akdoğan, Mehmet Numan Tamer, Erkan Cüre, Medine Cumhur Cüre, Banu Kale Köroğlu, Namik Delibaş. Effect of spearmint (Mentha spicata Labiatae) teas on androgen levels in women with hirsutism. Phytother Res. 2007 May;21(5):444-7. PMID: 17310494
[xxix] Andrew Pengelly, James Snow, Simon Y Mills, Andrew Scholey, Keith Wesnes, Leah Reeves Butler. Short-term study on the effects of rosemary on cognitive function in an elderly population. J Med Food. 2012 Jan ;15(1):10-7. Epub 2011 Aug 30. PMID: 21877951

Read More
Guest User Guest User

Health Article: Green Tea Changes Estrogen Metabolism and Breast Cancer Risk

By Case Adams, Naturopath, posted on greenmedinfo.com 03/09/2013

New research from the U.S. National Institutes of Health shows that the biochemicals in green tea change a women’s estrogen metabolism, revealing at least one of its mechanisms for reducing the risk of breast cancer.

The study comes from the NIH’s National Cancer Institute, and was led by Dr. Barbara Fuhrman. The researchers tested the levels of urinary estrogens and metabolites among 181 healthy Japanese American women from California and Hawaii. Of the group, 72 of the women were postmenopausal. The remainder of the group was premenopausal.

By Case Adams, Naturopath, posted on greenmedinfo.com 03/09/2013

green_tea_breast_cancer-e1362923104670-150x150.jpg

New research from the U.S. National Institutes of Health shows that the biochemicals in green tea change a women’s estrogen metabolism, revealing at least one of its mechanisms for reducing the risk of breast cancer.

The study comes from the NIH’s National Cancer Institute, and was led by Dr. Barbara Fuhrman. The researchers tested the levels of urinary estrogens and metabolites among 181 healthy Japanese American women from California and Hawaii. Of the group, 72 of the women were postmenopausal. The remainder of the group was premenopausal.

The data was compiled using a combination of urinary testing along with personal interviews with each women. The woman’s intake of not only green tea, but black tea, coffee (decaffeinated or not) and soda (decaffeinated or not) was also queried and recorded and measured, and the results were adjusted with respect to caffeine consumption. Considerations such as soy consumption, body mass index, age and others were also made and adjusted.

The research found that those postmenopausal women who drank green tea daily had 20% less urinary estrone and 40% less urinary estradiol levels, when compared to those levels of women who drank green tea less than one time per week.

These estrogen levels followed their categorization with regard to the estrogen metabolism pathway involved. This allowed the researchers to determine that these urinary estrogen differences were related to their estrogen metabolism and their future risk of breast cancer.

The primary estrogen pathway connected with breast cancer is the 16-hydroxylated estrogens. As for the 16-hydroxylated estrogen pathway, both estradiol and estrone markers were 40% lower among those women who drank green tea at least one time daily compared to those women who drank less than one cup of green tea a week.

Levels of caffeine consumption did not change these dynamics among the women. And black tea consumption did not produce these decreases in estrogen metabolites.

Furthermore, estrogen levels of premenopausal women did not respond to green tea consumption. This did not surprise the researchers, as previous research has found that postmenopausal women respond differently to medications such as tamoxifen and aromatase inhibitors.

Interestingly, the research also found that the average urinary estrogen levels of the entire postmenopausal Japanese-American group was about half of the levels that were found in a recent study of postmenopausal women from New York who were primarily Caucasian. The researchers could not determine the reason for the difference – stating that it could be related to differences in diet, lifestyle factors or others.

While other studies have shown some differences in urinary estrogen levels and green tea drinking among women, this is the first study that analyzed a broad range of estrogen metabolites among peri- and postmenopausal women

Postmenopause follows one year after the stage of menopause, when a woman’s ovaries halt egg production. During this period, estrogen and progesterone production is reduced.

During this period a woman may experience symptoms related to lower levels of estrogen production. These include hot flashes, night sweating, insomnia, headaches, mood swings and other physical symptoms.

Many doctors recommend halting caffeine consumption during postmenopause, to help with menopause symptoms. This may run some conflict to green tea consumption, as a cup of green tea will typically contain about 20 milligrams of caffeine – as compared to about 30 milligrams in black tea and many sodas, and about 80 milligrams in a cup of coffee.

However, there are forms of green tea that contain less and even no caffeine. Gyokuro and Sencha Green teas will contain about half the caffeine content. The Joujicha green tea, the Genmaicha tea (mix of Bancha and Genmai – rice grain), and the Bancha green tea can contain up to ten times less caffeine than standard green teas.

In addition, there are now several decaffeinated green tea products available. The “Effervescence” decaffeination process, which uses water and carbon dioxide will retain over 90% of the green tea’s polyphenols. The other method, wherein ethyl acetate is used as a solvent, can lose as much as 70% of the green tea’s polyphenols during decaffeination.

And of course, black tea has the most caffeine, and does not provide the same medicinal benefits. Even though black tea is made from the same plant – Camellia sinensis – black teas are dried and oxidized under intense heat and/or sun, during which they lose much of their medicinal constituents.

These constituents include polyphenols such as epigallocatechin, epicatechin, epigallocatechin gallate and epicatechin gallate. These catechins can comprise up to 30% of the dry weight of fresh tea leaves.. These catechins have been shown to inhibit tumors in laboratory studies. The NIH researchers suggested that these polyphenols were the reason for the change in the estrogen metabolites:

“As a rich source of phytochemicals that can interact with and regulate xenobiotic metabolizing enzymes, green tea may modify metabolism or conjugation of estrogens and may thereby impact breast cancer risk.”

Another 2013 study from Italy’s University of Calabria found that epigallocatechin gallate specifically down-regulates a gene that stimulates cancer growth.

Other foods containing catechins, such as olives, blackberries, raspberries, cherries, grapes, apples, papayas, mangoes among many others, also have shown anti-cancer effects. Many herbal teas also contain catechins.

For additional research on Green Tea’s health benefits visit: Green Tea benefits.

For additional research on evidence-based, natural compounds with ant-breast cancer activity visit: natural Breast Cancer therapies

References
Fuhrman BJ, Pfeiffer RM, Wu AH, Xu X, Keefer LK, Veenstra TD, Ziegler RG. Green tea intake is associated with urinary estrogen profiles in
Japanese-American women. Nutr J. 2013 Feb 15;12(1):25.
Yang CS, Wang X, Lu G, Picinich SC: Cancer prevention by tea: animal studies, molecular mechanisms and human relevance. Nat Rev Cancer2009, 9(6):429–439.

Case Adams is a California Naturopath and holds a Ph.D. in Natural Health Sciences. His focus is upon science-based natural health solutions. He is the author of 20 books on natural health and numerous print and internet articles. His work can be found at http://www.caseadams.com.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff. This article is provided for informational use only.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of Cambridge Naturals or its staff. This article is provided for informational use only.

Read More