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IN THIS ISSUE:

Enhancing Peak Male Performance with Scientifically Validated Botanicals

By Chris D. Meletis, ND

We live in challenging times where chronic stress, environmental pollutants and a myriad of other burdens are eroding away health, wellness and sexuality. As the result of the accumulation of burdens that come with modern existence, an alarming 1 in 4 men at the age of 30 now have measurable low testosterone levels. This makes it difficult to survive, let alone thrive, when the very hormone that helps support inner health is fleeting.

Overt symptoms of low testosterone are believed to affect 50 percent of men with measurable low levels. Yet the slow erosion of wellness and zeal for life that occurs with low testosterone may be so gradual, that human perception is insufficient to note the change during the short term.

It is well known that testosterone levels decline with the passage of time, and the average man passively accepting the aging process may expect deterioration of performance. Without taking a proactive stance, men undergo such changes as a slow decrease in sex drive, diminished erectile strength, sleep disturbance, depressed mood, or lethargy.

In this article, I will discuss two mile markers of male wellness: libido and erectile performance.

Enhancing Male Performance

Erectile dysfunction affects 50 percent of men ages 40-70 in the United States and is considered an important public health problem by the National Institutes of Health. Clinically, I work with many men in their late twenties and early 30s that present to my office with decreased erectile performance or overt inability at times to perform. An even greater number of men report a "take it or leave it" approach when it comes to libido. These changes are symptoms of deeper health needs and serve as a barometer of ones wellness status.

Libido and pelvic responsiveness in both the male and female share many of the same biochemical pathways. Thus, much of what follows possesses relevance for both sexes.

Before I discuss the ways that both men and women can improve their libido and enhance intimacy performance, it's important to acknowledge that maintaining healthy cardiovascular, neurological and mental wellness is also important for peak performance.

Natural Libido-Enhancing Strategies

A number of natural ingredients have been shown to affect the pathways involved in enhancing libido and improving sexual performance. Epimedium brevicornum, Tribulus terrestris, Panax ginseng, Ashwaghanda, grape seed extract, Eurycoma longifolia, pomegranate and green tea extracts (all found in the new e formula) have a synergistic role to play in helping men operate at peak performance.

Epimedium brevicornum

Epimedium brevicornum has been widely used for impotence, infertility, osteoporosis, cardiovascular diseases, amnesia, and senile functional diseases.1 One of the mechanisms of action is that it supports nitric oxide levels, which are essential for arousal and erectile tissue engorgement. Nitric oxide (NO) is formed from the conversion of L-arginine by nitric oxide synthase (NOS), which exists in three isoforms: neuronal (nNOS), endothelial (eNOS), and inducible (iNOS). nNOS is expressed in penile neurons innervating the corpus cavernosum (CC), and eNOS has been identified primarily in both cavernosal smooth muscle of penileand clitoral tissue. Researchers have concluded that and extract of Epimedium relaxes the CC smooth muscle through multitargets in NO/cGMP/PDE 5 pathway and helps address erectile dysfunction.2 Epimedium can prove very helpful as part of a male wellness protocol, relative to enhanced sexual performance.

Tribulus terrestris

Tribulus terrestris is another botanical commonly used to enhance libido. After conducting a study of Tribulus terrestris in rodents, researchers concluded, "Tribulus terrestris extract appears to possess aphrodisiac activity probably due to androgen increasing property of Tribulus terrestris."3 Similar findings were found in another study on primates, where researchers noted that Tribulus increased testosterone in the animals, and another later study on rodents, leading researchers to conclude, "The increase in intracavernous pressure which confirms the proerectile aphrodisiac property of Tribulus terrestris could possibly be the result of an increase in androgen and subsequent release of nitric oxide from the nerve endings innervating the corpus cavernosum."4-5 Tribulus also is known to decrease levels of prolactin in women, which is important since increased prolactin is associated with reduced libido.6

Panax

Panax ginseng has long been known to help support the adrenal glands and thus help cope with stress, important because stress is known to affect sexual performance. In addition Panax ginseng also helps increase circulation as well as nitric oxide production.7 The ginsenosides contained in ginseng have been shown to cause a dose-dependent relaxation of the corpus cavernosal smooth muscle in rabbits by increasing nitric oxide release.8-9 In a human study, 90 patients were divided into three groups and given Panax ginseng, a placebo, or the antidepressant drug trazodone orally. In the Panax ginseng group a significant improvement in erectile parameters such as penile rigidity, girth, duration of erection, improved libido, and patient satisfaction were reported. The overall therapeutic efficacy for erectile dysfunction was 60 percent for the Panax ginseng group but only 30 percent for the trazodone and placebo groups.10

A more recent, double-blind, placebo-controlled, crossover study confirmed these results. Forty-five men diagnosed with ED received either 900 mg Panax ginseng or placebo three times per day for eight weeks. The first eight weeks of treatment were followed by a two-week washout period, after which the patients switched groups-those who had initially received the placebo received ginseng and those who initially received ginseng received the placebo for an additional eight weeks. Researchers measured the efficacy of treatment through changes observed in indexes of erectile function, including the International Index of Erectile Function (IIEF). Mean scores on the IIEF for Panax ginseng were significantly higher than for placebo after eight weeks of each treatment. In addition, penile tip rigidity was significantly better after eight weeks of Panax ginseng compared to placebo.11

Ashwagandha (Withania somnifera)

In clinical practice, Ashwagandha is an effective tool to support adrenal health. Stressed patients routinely report noticing an increased sense of well being with its use. An intriguing rat study evaluated the combined effects of Withania somnifera and Panax ginseng extracts. The two extracts were compared for their ability to attenuate some deleterious impact of chronic stress (CS). Both botanicals were able to decrease the number and severity of CS-induced ulcers, reverse CS-induced inhibition of male sexual behavior, and inhibit the adverse effects of CS on retention of learned tasks. Both botanicals also reversed CS-induced immunosuppression, but only the Withania extract increased peritoneal macrophage activity in the rats.12 This latter observation emphasizes the importance that can be gained by blending synergistic botanicals.

Grape Seed Extract

Maintaining the 60,000 miles of blood vessels and overall integrity of the circulatory system is essential. It is this long-term, broader thinking that helps preventively protect the body from needing to depend on what can be termed "reactionary" medicine. Several epidemiological studies suggest that the regular consumption of foods and beverages rich in flavonoids is associated with a reduction in the risk of several pathological conditions ranging from hypertension to coronary heart disease, stroke and dementia. Grape seed is one of the major polyphenols shown to have some of these effects in humans.13

Grape seed extract is emerging as a nutrient that has profound effects on nitric oxide production. Studies investigating grape seed's ability to support healthy blood pressure levels have determined its mechanism of action is partly due to its ability to raise nitric oxide levels. As noted earlier, nitric oxide is essential for arousal and erectile tissue engorgement.14-15

Eurycoma longifolia

Eurycoma longifolia, often called Long Jack, has a long history of use as a performance enhancing substance. In one study, extracts from E. longifolia Jack were orally administered to rats twice daily for 10 days. Testosterone was used as a positive control. Results showed that E. longifolia Jack produced a dose-dependent increase in sexual performance of the treated animals. The authors reported, "The present study therefore gives further evidence of the folk use of E. longifolia as an aphrodisiac."16

Pomegranate Extract

A study using a rabbit model of arteriogenic erectile dysfunction (ED) measured the effect of pomegranate juice (PJ) concentrate on intracavernous blood flow and penile erection. The researchers found eight weeks administration of PJ concentrate daily significantly increased intracavernous blood flow and smooth muscle relaxation.17 These findings are preliminary, yet the results are promising.

As with many botanicals, there is not merely one potential clinical application. For instance, studies have shown that pomegranate can block the conversion of testosterone to estrogen, a process controlled by the aromatase enzyme. Pomegranate inhibited aromatase activity by 60â "80 percent thus helping protect estrogen sensitive tissues including prostate and breast tissue.18

Green Tea Extract

Green tea extract is another nutrient important for male health. In vitro and animal studies have shown that green tea is a natural aromatase inhibitor that modulates estrogen synthesis.19-20 This effect can play a role in libido enhancement and overall male health.

Antioxidant Protection

One of the additional ways that ED begins to manifest is from the accumulation of unquenched oxidative products in erectile tissue.21 Antioxidant therapy is important for overall wellness and can prove useful prophylactic tool for preventing smooth muscle dysfunction and fibrosis in ED. Many of the ingredients mentioned above, including grape seed and pomegranate, also act as potent antioxidants.

New e

In addition to incorporating all the ingredients mentioned above, the new Androprime Formula also contains Bioperine a proprietary black pepper extract. Bioperine was incorporated into e to augment the effectiveness of the individual constituent herbs and the overall synergy of the formula.

Conclusion

It is clear that ultimate sexual functioning depends on a strong and well-nourished body that provides the ability to attain or maintain an erection. Epimedium brevicornum, Tribulus terrestris, Panax ginseng, Ashwaghanda, grape seed extract, Eurycoma longifolia, and pomegranate extract along with Bioperine (all found in the new e) can provide synergistic support for optimal male performance.

Editor's Note: Dr. Meletis is author of the book Better Sex Naturally, published by HarperCollins and co-author of His Change of Life, published by Greenwood Publishing.

References

1. Li HB, Chen F. Separation and purification of epimedin A, B, C, and icariin from the medicinal herb Epimedium brevicornum maxim by dual-mode HSCCC. J Chromatogr Sci. 2009; 47(5):337-40.

2. Chiu JH, Chen KK, Chien TM, Chiou WF, Chen CC, Wang JY, Lui WY, Wu CW Epimedium brevicornum Maxim extract relaxes rabbit corpus cavernosum through multitargets on nitric oxide/cyclic guanosine monophosphate signaling pathway. Int J Impot Res. 2006 Jul-Aug;18(4):335-42.

3. Gauthaman K, Adaikan PG, Prasad RN. Aphrodisiac properties of Tribulus Terrestris extract (Protodioscin) in normal and castrated rats. Life Sci. 2002 Aug 9;71(12):1385-96.

4. Gauthaman K, Ganesan AP, Prasad RN. Sexual effects of puncturevine (Tribulus terrestris) extract (protodioscin): an evaluation using a rat model. J Altern Complement Med.. 2003 Apr;9(2):257-65.

5. Gauthaman K, Ganesan AP. The hormonal effects of Tribulus terrestris and its role in the management of male erectile dysfunction-an evaluation using primates, rabbit and rat. Phytomedicine. 2008 Jan;15(1-2):44-54.

6. Dean W. The Neuroendocrine Theory of Aging Chapter 5. The Female Reproductive Homeostat. Vitamin Research News. December 1, 2005; 19(11).

7. Chen X, et al. Extracts of Ginkgo bilobaand ginsenoside exert cerebral vasodilation via a nitric oxide pathway. Clin Exp Pharmacol Physiol. 1997;24:958â "959.

8. Choi YD, Xin ZC, Choi HK. Effect of Korean red ginseng on the rabbit corpus cavernosal smooth muscle. Int J Impot Res. 1998;10:37-43.

9. Kim HJ, Woo DS, Lee G, Kim JJ. The relaxation effects of ginseng saponin in rabbit corporal smooth muscle: is it a nitric oxide donor? Br J Urol. 1998;82:744-748.

10. Choi HK, Seong DH, Rha KH. Clinical efficacy of Korean red ginseng for erectile dysfunction. Int J Impot Res. 1995;7:181-186.

11. Hong B, Ji YH, Hong JH, et al. A double-blind crossover study evaluating the efficacy of Korean red ginseng in patients with erectile dysfunction: a preliminary report. J Urol. 2002;168:2070-2073.

12. Bhattarcharya SK, Muruganandam AV. Adaptogenic activity of Withania somnifera: an experimental study using a rat model of chronic stress. Pharmacol Biochem Behav 2003;75:547-53.

13. Ghosh D, Scheepens A. Vascular action of polyphenols. Mol Nutr Food Res. 2009 Mar;53(3):322-31.

14. Edirisinghe I, Burton-Freeman B, Tissa Kappagoda C. Mechanism of the endothelium-dependent relaxation evoked by a grape seed extract. Clin Sci (Lond). 2008 Feb;114(4):331-7.

15. Zhang TX, Niu CQ, Hu JM, Liu H, Jing HE. Vasorelaxational effects of procyanidins on rabbit aorta in vitro and decreasing arterial blood pressure in vivo. Zhongguo Zhong Yao Za Zhi. 2008 Jul;33(14):1720-3.

16. Ang HH, Cheang HS, Yusof AP. Effects of Eurycoma longifolia Jack (Tongkat Ali) on the initiation of sexual performance of inexperienced castrated male rats. Exp Anim. 2000 Jan;49(1):35-8.

17. Azadzoi K, Schulman R, Aviram M, Siroky M. Oxidative Stress in Arteriogenic Erectile Dysfunction: Prophylatic Role of Antioxidants The Journal of Urology, 2005(174) 1:386-393.

18. Kim ND, Mehta R, Yu W, et al. Chemopreventive and adjuvant therapeutic potential of pomegranate (Punica granatum) for human breast cancer. Breast Cancer Res Treat. Feb 2002;71(3):203-217.

19. Monteiro R, Azevedo I, Calhau C. Modulation of aromatase activity by diet polyphenolic compounds. J Agric Food Chem. 2006 May 17;54(10):3535-40.

20. Satoh K, Sakamoto Y, Ogata A, Nagai F, Mikuriya H, Numazawa M, Yamada K, Aoki N. Inhibition of aromatase activity by green tea extract catechins and their endocrinological effects of oral administration in rats. Food Chem Toxicol. 2002 Jul;40(7):925-33.

21. Azadzoi KM, Schulman RN, Aviram M, Siroky MB. Oxidative stress in arteriogenic erectile dysfunction: prophylactic role of antioxidants. J Urol 2005;174:386-393.

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Candida – The Hidden Cause Behind A Host of Health Concerns

By Chris D. Meletis, ND

Over the years, in clinical practice I have encountered thousands of patients who do not feel their best, are fatigued and are suffering from a complex of symptoms. For example, a patient may be suffering from one or more of the following: chronic diarrhea, constipation, bloating and flatulence, lethargy and fatigue, reduced or hyperactive immune function, skin eruptions, rectal itching, vaginal yeast infections, fungal infections (including nail fungus), urinary or bacterial infections, or oral thrush. When these are the symptoms manifested, along with performing basic testing for food allergies, I often consider that a patient may be suffering from candidiasis, a condition caused by candida albicans or a number of other candida species.

Candida infections can be insidious in that they manifest in the form of a number of symptoms that either seem unrelated to one another or mimic another disease. Yet, once candida is detected, eliminating this infection can result in improved overall health and increased energy.

In this article, I will discuss a new test that is particularly helpful in identifying the presence of candida along with natural strategies to combat this fungal infection. First, however, I will review what candida is and why it can be a problem.

Often Overlooked Cause Behind Poor Health

The genus candida comprises about 154 species. Six of these species most commonly inhabit the skin and mucous membranes as normal flora. Candida albicans represents the most abundant opportunistic strain while candida tropicalis, candida glabrata, candida krusei, candida parapsilosis and candida lusitaniae may also mount infection under opportunistic conditions.

Candida albicans is often considered a harmless yeast when present in very small quantities in the gastrointestinal tract and vaginas of warm-blooded animals. A healthy immune system and beneficial bacteria keep candida under control, but disruption to this internal balance can lead to yeast overgrowth. Hormonal imbalances, diabetes, metabolic syndrome, antibiotics and oral contraceptives, excessive consumption of sugar and simple carbohydrates, food allergies and sensitivities, stress, or exposure to environmental toxins can all lower immune defenses and contribute to candida's transformation from a benign, round yeast into a filament-shaped fungus with long hyphae or "roots" that penetrate intestinal cells in search of food. Candida albicans also can be spread by direct contact during intercourse, other intimate contact and through intravenous feedings, dialysis, surgery, underlying disease (diabetes mellitus, Addison's disease), immunodeficiency, pregnancy, age (elderly, infancy), and malnutrition.

Furthermore, parasitic infections can in and of themselves weaken the gastrointestinal tract enough to tip the balance in favor of candida turning into the more harmful fungal form of the organism.

Symptoms of Candida Related Complex:
  • Gastrointestinal: Bloating, intestinal gas, belching, constipation, diarrhea, heartburn, bad breath, abdominal pain, and indigestion
  • Urinary: Frequent urination, burning and desire to urinate, fluid retention, and edema (tissue swelling)
  • Male Sexual System: Loss of sex drive, impotency, prostate problems, genital itch, and bumps with fluid or pus at the tip of the penis forming patches that may spread to the scrotum
  • Female Sexual System: Vaginal inflammation, vaginal discharge, vaginal burning itching, vaginal pain, urinary tract infections, painful urination, premenstrual problems, menstrual problems, painful intercourse, decreased sex drive, and infertility
  • Mental and Emotional Distrubances: Chronic fatigue, drowsiness, and loss of energy, mental fog, decreased concentration, loss of alertness, poor work perfomance, memory loss or learning difficulty, severe mood swings, depression, irritability or periods of anger, hyperactivity and agitation, anxiety, insomnia, cravings for sweets, bread, sugar, alcohol, or yeast-containing foods (cheese)
  • Allergic and Somatic Reactivity: Numbness, burning or tingling, painful joints; swollen or stiff joints; muscle aches; muscle tension; nasal congestion; tension in the head; headaches; blurred vision; dizziness; ear ringing; shortness of breath; chest pains; acne, hives or other skin eruptions; increased sensitivity to foods, environmental substances, pollution, household chemicals, toiletries; symptoms worsen in moldy locations or on damp, muggy days


In an advanced stage, candida expels waste products into the circulatory system, depressing immunity and leading to numerous ailments that may fall within the syndrome called the Candida Related Complex or candidiasis.1-2 This results in the symptoms I mentioned in Table 1.

The First Step: Diagnosing Candidiasis

When a candida imbalance is suspected, one of the most useful tools for confirming the diagnosis is to utilize a new test for detecting candida. This new ELISA Candida Antibodies and Antigen Panel is impressive in its comprehensiveness. The test can detect immediate, past and localized infections by testing for serum candida antigen, in addition to IgM, IgG, and IgA antibodies specific for Candida spp. An antigen is a protein marker on the surface of cells that identifies the cell as self or non-self. Antigens stimulate the production of antibodies by immune cells that will neutralize or destroy the cell if necessary.

IgM is the first antibody formed after primary exposure to an antigen, and reflects a present infection. IgM readily activates complement, a group of proteins in the blood that play a vital role in the body's immune defenses. IgM also assists the phagocytic system to eliminate foreign pathogens from the intravascular space.

IgG is the predominant antibody formed from secondary exposure to an antigen, and reflects a past or ongoing infection. It is produced as IgM antibody levels decrease after primary exposure. IgG also activates complement, and assists the phagocytic system to eliminate foreign pathogens from the extravascular space.

IgA is found in mucous secretions and is important in local (mucosal) immunity. Elevated IgA antibodies may reflect a more superficial candida infection.

The Candida Antibodies and Antigen Panel is now being offered here. You can now perform a simple fingerstick at home, send the results to the lab and receive your results within a couple weeks. Then you can discuss the findings with your healthcare providers.

The Second Step: Lifestyle Alterations

Once a diagnosis of candidiasis is confirmed, the first step is for affected individuals to eliminate from their diets any of the foods that feed candida. Consequently, all foods containing sugar and yeast should be eliminated from the diet in order to starve the candida organism. Baked goods, pastas, breads, cereals, rice, most grains, fruit, honey, and any sweetened foods should not be consumed. Many practitioners also recommend avoiding dairy products due to the fact they contain lactose, which is a sugar, and cheese because it contains mold. Fermented beverages such as alcohol should also be avoided. Diet should consist of meat protein such as chicken (preferable free range or organic) or wild fish and vegetables, with the exception of potatoes, sweet potatoes, and carrots, which may also feed the candida organism.

It is also important for those with elevated blood sugars, such as in the case of diabetes mellitus and metabolic syndrome, to actively work to maintain healthy blood sugar levels, so as to not inadvertently fuel the growth of candida.

Additionally, avoiding foods to which you are sensitive (as measured by a Food Allergy Test) can be especially helpful.

It is important to read labels carefully on any packaged foods.

The Third Step: Killing Candida

A number of natural substances (all found in the formula KandidaPlex) have been found to be very effective in killing candida, especially when they are combined with an anti-candida diet.

Undecylenic acid, commonly used in the form of calcium undecylenate, is an extremely effective, well-tolerated, broad-spectrum antifungal compound derived from the vacuum distillation of castor bean oil. It works, in part, by inhibiting the ability of candida to convert to its virulent mycelial phase. Several studies have demonstrated that undecylenic acid is 4-5 times as powerful an antifungal agent as caprylic acid in the same dosage.3-5 Undecylenic acid has been found to inhibit the switch from the harmless yeast form of candida to the invasive fungal form.5

Another anti-candida substance is Pau d'Arco (Tabebuia heptaphylla) The inner bark of the South American tree Pau d'Arco, also known as lapacho or taheebo, has long been used as a folk remedy in numerous afflictions. Pau d' Arco contains phytochemical compounds with antibacterial and antifungal activity. Among these compounds are lapachol and a series of napthoquinones, natural fungicidals effective against candida albicans. Lapachol is also antiviral and antiparasitic. Pau d'Arco selectively inhibits unfriendly bacteria such as the anaerobic Clostridium difficile and E. coli without affecting beneficial probiotic bacteria.6-7

Enlyse is another important part of an anti-candida program. It is a blend of powerful all-vegetarian enzymes designed to help prevent overgrowth of candida. This blend improves the intestinal environment by hydrolyzing putrefying food trapped in between the intestinal villi and digesting non-starch polysaccharides that are known to create gas and bloating. Hemicellulases in Enlyse help remove the biofilm layer, which surrounds candida albicans. Removal of the yeast's protective biofilm facilitates the penetration of the antifungal ingredients calcium undecylenate, berberine and resveratrol directly to the yeast cell.8 Chitosanase in Enlyse is a special enzyme that helps break down chitin, which is an important part of the structure of the candida cell wall. This can be a significant factor in the prevention of overgrowth of this potentially pathogenic yeast.9

Berberine is an antifungal agent found in goldenseal, barberry and Oregon grape. Extracellular enzymes secreted by candida albicans are claimed to be virulent factors responsible for penetration of the yeast into host cells. Berberine was able to suppress candida's enzyme activity and prevented its adherence to epithelial cells. Berberine also interrupts the process of chitin synthesis by which candida constructs its cell walls.10 Berberine also has been shown to work synergistically with other antifungal agents.11

Trans-resveratrol demonstrates potent antifungal activity at very low concentrations; it acts to disrupt the formation of the hyphae, or mycelia, which are required for candida to penetrate the epithelial cells lining the gastrointestinal tract.12-13

According to one group of researchers, "Therefore, the fungicidal effects of resveratrol demonstrate that this compound is a potential candidate as an antifungal agent in treating... candidal infections."12

Finally, biotin is a powerful addition to an anti-candida regimen and works with the other compounds mentioned above. In vitro, biotin has been shown to prevent the budding yeast form of candida albicans from "morphing" into its invasive mycelial form.14

The Final Step: Counteracting the Die-Off Reaction

When yeast cells are rapidly killed by the immune system, drug treatment, or dietary intervention, a die-off or Herxheimer reaction occurs. This reaction is caused by the massive release of toxins from dying candida cells. Toxic proteins from the dead yeasts cross cell membranes, enter the bloodstream, and trigger an intense immune reaction.

Other chemicals released during candida die off cause direct cellular toxicity throughout the body. Immune/yeast complexes trigger the release of histamine, an irritating tissue hormone that initiates tissue inflammation and causes discomfort. Severe allergic and toxic reactions exacerbate the symptoms of candida. Die-off reactions may last from a few days to a few weeks but usually clear up in less than a week. Even though a strong die-off reaction causes a significant amount of discomfort, it is a sign of a successful treatment.

Perhaps one of the most unfortunate aspects of a severe Herxheimer reaction is that it may cause individuals to abandon a successful treatment prematurely. The Herxheimer reaction keeps many individuals indulging in their pro-yeast lifestyle like the withdrawal reaction keeps drug abusers addicted.

In order to ease the discomfort associated with the die-off reaction, I recommend that my patients consume EnteraKlenz and a good fiber supplement such as EZ Fiber. The fiber will help escort the toxic debris out of the body. A good probiotic such as BioPRO also can help support the health of the GI tract.

Conclusion

A modern day lifestyle that includes stress, an excessive amount of sugary foods, oral contraceptives and antibiotics can disrupt the body's balance. When this happens, the normally harmless yeast form of candida albicans can transform into the pathogenic fungal form. A new comprehensive Candida Antibodies and Antigen Panel is now being offered here to detect this insidious but prevalent infection. Altering the diet and taking the synergistic combination of anti-candida substances found in KandidaPlex can help rid the body of this organism and create a greater degree of energy and overall health.



References

1. Crook WG. The Yeast Connection, A Medical Breakthrough. 2nd Addition. Professional Books. Jackson, TN, 1984.

2. Crook WG. The Yeast Connection and the Woman. Professional Books. Jackson, TN. 1987.

3. Birdsall C. Gastrointestinal Candidiasis: Fact or Fiction. Alt Med Rev. 1997; 2(5):346-54.

4. Li XC, Jacob MR, Khan SI, Ashfaq MK, Babu KS, Agarwal AK, Elsohly HN, Manly SP, Clark AM. Potent in vitro antifungal activities of naturally occurring acetylenic acids. Antimicrob Agents Chemother. 2008. Jul;52(7):2442-8. Epub 2008 May 5.

5. McLain N, Ascanio R, Baker C, Strohaver RA, Dolan JW. Undecylenic acid inhibits morphogenesis of Candida albicans. Antimicrob Agents Chemother. 2000 Oct;44(10):2873-5.

6. Park, B. S., et al. Selective growth-inhibiting effects of compounds identified in Tabebuia impetiginosa inner bark on human intestinal bacteria. J. Agric. Food Chem. 2005 Feb; 23;53(4): 1152-7.

7. Portillo, A., et al. Antifungal activity of Paraguayan plants used in traditional medicine. J. Ethnopharmacol. 2001; 76(1): 93â "8.

8. Al-Fattani MA, Douglas LJ. Biofilm matrix of Candida albicans and Candida tropicalis: chemical composition and role in drug resistance. J. Med. Microbiol. 2006 Aug; 55(Pt 8):999-1008.

9. Chattaway FW, Shenolikar S, O'Reillt J, Barlow AJ. Changes in the cell surface of the dimorphic forms of Candida albicans by treatment with hydrolytic enzymes. J. Gen Microbiol. 1976 Aug; 96(2):335-47.

10. Yordanov M, Dimitrova P, Patkar S, Saso L, Ivanovska N. Inhibition of Candida albicans extracellular enzyme activity by selected natural substances and their application in Candida infection. Can J Microbiol. 2008 Jun;54(6):435-40.

11. Quan H, Cao YY, Xu Z, Zhao JX, Gao PH, Qin XF, Jiang YY. Potent in vitro synergism of fluconazole and berberine chloride against clinical isolates of Candida albicans resistant to fluconazole. Antimicrob Agents Chemother. 2006 Mar;50(3):1096-9.

12. Jung HJ, Seu YB, Lee DG Candicidal action of resveratrol isolated from grapes on human pathogenic yeast C. albicans. J Microbiol Biotechnol. 2007 Aug; 17(8):1324-9.

13. Jung HJ, Hwang IA, Sung WS, Kang H, Kang BS, Seu YB, Lee DG. Fungicidal effect of resveratrol on human infectious fungi. Arch Pharm Res. 2005 May;28(5):557-60.

14. Yamaguchi H. Mycelial development and chemical alteration of Candida albicans from biotin insufficiency. Sabouraudia. 1974 Nov;12(3):320â "328.

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Hormone Replacement Users Still Face Risks

Posted Feb 16, 2009

Women who take combined estrogen-progestin hormone therapy for at least five years increase their risk of breast cancer, according to a Stanford University study.

The study confirms findings of a landmark 2002 report by the Women’s Health Initiative.

However, Ellen Matloff, director of Cancer Genetic Counseling at the Yale Cancer Center, said women should not end their hormone-replacement therapy without weighing the risks and benefits with their doctors.

“When you look at the average risk to the average woman who is using hormone-replacement therapy, their average risk is quite small,” Matloff said. “It might be that, before this, 10 of 1,000 women were at risk for breast cancer, and now it might be 18 (of 1,000).”

After the 2002 study was published, hormone therapy prescriptions dropped from 60 million in 2001 to 20 million in 2005, according to a Stanford University Medical Center. However, not all doctors agreed that ending hormone therapy was the reason.

The new study settles the question, according to Marcia Stefanick, professor of medicine at Stanford University School of Medicine and a coauthor of the study.

“This is very strong evidence that estrogen plus progestin causes breast cancer,” said Stefanick. “You start women on hormones and within five years, their risk for breast cancer is clearly elevated. You stop the hormones and within one year their risk is essentially back to normal. It’s reasonably convincing cause-and-effect data.”

Results of the multi-center study were published in Thursday’s issue of the New England Journal of Medicine. The results do not apply to women who take estrogen only, such as those who have had hysterectomies.

The study looked at two groups of women, 15,000 in the original Women’s Health Initiative Study and 41,449 women in a separate trial started in 1994. Breast cancer rates in the first group dropped 28 percent within a year of ending hormone-replacement therapy, Stanford researchers found. In the second, half of the women stopped using estrogen-progestin therapy; they experienced a 43 percent drop in breast cancer rates, the study found.

Matloff said stoppinghormone therapy carries risks and side effects as well, such as osteoporosis, night sweats, depression, mood swings and loss of sex drive and functioning.

If a woman stays on estrogen-progestin therapy, “I would encourage her to take a step back, speak to her physician and weigh whether the risks outweigh the benefits before you go off our medication,” Matloff said. “I would just advise some caution.

Date Feb 14, 2009

To see more of New Haven Register, or to subscribe to the newspaper, go to http://www.nhregister.com.

Copyright © 2009, New Haven Register, Conn.

Women who take combined estrogen-progestin hormone therapy for at least five years increase their risk of breast cancer, according to a Stanford University study.

The study confirms findings of a landmark 2002 report by the Women's Health Initiative.

However, Ellen Matloff, director of Cancer Genetic Counseling at the Yale Cancer Center, said women should not end their hormone-replacement therapy without weighing the risks and benefits with their doctors.

"When you look at the average risk to the average woman who is using hormone-replacement therapy, their average risk is quite small," Matloff said. "It might be that, before this, 10 of 1,000 women were at risk for breast cancer, and now it might be 18 (of 1,000)."

After the 2002 study was published, hormone therapy prescriptions dropped from 60 million in 2001 to 20 million in 2005, according to a Stanford University Medical Center. However, not all doctors agreed that ending hormone therapy was the reason.

The new study settles the question, according to Marcia Stefanick, professor of medicine at Stanford University School of Medicine and a coauthor of the study.

"This is very strong evidence that estrogen plus progestin causes breast cancer," said Stefanick. "You start women on hormones and within five years, their risk for breast cancer is clearly elevated. You stop the hormones and within one year their risk is essentially back to normal. It's reasonably convincing cause-and-effect data."

Results of the multi-center study were published in Thursday's issue of the New England Journal of Medicine. The results do not apply to women who take estrogen only, such as those who have had hysterectomies.

The study looked at two groups of women, 15,000 in the original Women's Health Initiative Study and 41,449 women in a separate trial started in 1994. Breast cancer rates in the first group dropped 28 percent within a year of ending hormone-replacement therapy, Stanford researchers found. In the second, half of the women stopped using estrogen-progestin therapy; they experienced a 43 percent drop in breast cancer rates, the study found.

Matloff said stoppinghormone therapy carries risks and side effects as well, such as osteoporosis, night sweats, depression, mood swings and loss of sex drive and functioning.

If a woman stays on estrogen-progestin therapy, "I would encourage her to take a step back, speak to her physician and weigh whether the risks outweigh the benefits before you go off our medication," Matloff said. "I would just advise some caution.

Date Feb 14, 2009

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Herb helps postmenopausal anxiety, sex drive

Postmenopausal women experiencing anxiety, depression or low sex drive may find help from the herb maca. Australian researchers at Victoria University report on a recent study in which 14 postmenopausal women supplemented with powdered Maca. The dose was 3.5grams per day for a period of 6 weeks. They found that the herb significantly reduced psychological symptoms, including anxiety and depression, and also reduced sexual dysfunction in the women, independent of estrogenic and androgenic activity.

Maca improved both mood and sex drive without affecting hormones

Unlike some other herbs that affect hormone levels, maca appeared to exhibit no significant effects on serum concentrations of estradiol, FSH, LH, and sex hormone-binding globulin. The researchers conclude that "supplementation with the herb, maca, may reduce anxiety, depression and sexual dysfunction in postmenopausal women" and that additional research is warranted.

Research on men, backed by animal studies, indicates that maca is also effective for improving male sexual function. A 12-week study in2002 aimed to determine if reports of increased sexual desire were due to effect on mood or on serum testosterone levels. At the 8-week mark, researchers noted a marked improvement in sexual desire; however, serum testosterone andestradiol levels were not different in men treated with maca and in those treated with placebo. The researchers were not able to determine the exact mode of action for maca.

Sources: Menopause, 2008 September 6[Epub ahead of print]; Andrologia, 2002 34(6):367-372

Postmenopausal women experiencing anxiety, depression or low sex drive may find help from the herb maca. Australian researchers at Victoria University report on a recent study in which 14 postmenopausal women supplemented with powdered Maca. The dose was 3.5grams per day for a period of 6 weeks. They found that the herb significantly reduced psychological symptoms, including anxiety and depression, and also reduced sexual dysfunction in the women, independent of estrogenic and androgenic activity.

Maca improved both mood and sex drive without affecting hormones

Unlike some other herbs that affect hormone levels, maca appeared to exhibit no significant effects on serum concentrations of estradiol, FSH, LH, and sex hormone-binding globulin. The researchers conclude that "supplementation with the herb, maca, may reduce anxiety, depression and sexual dysfunction in postmenopausal women" and that additional research is warranted.

Research on men, backed by animal studies, indicates that maca is also effective for improving male sexual function. A 12-week study in2002 aimed to determine if reports of increased sexual desire were due to effect on mood or on serum testosterone levels. At the 8-week mark, researchers noted a marked improvement in sexual desire; however, serum testosterone andestradiol levels were not different in men treated with maca and in those treated with placebo. The researchers were not able to determine the exact mode of action for maca.

Sources: Menopause, 2008 September 6[Epub ahead of print]; Andrologia, 2002 34(6):367-372

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