Estrogen Metabolism and the Gut Microbiome: Clinical Strategies for Hormone Detoxification

2026 | May

Dr. Holly Lucille, RN, ND

 

Subheadline 

A comprehensive review of liver detoxification phases, the estrobolome, and lifestyle, nutritional, and botanical strategies to support healthy estrogen balance.

 

Short Description 

This article explores estrogen metabolism through a whole-person lens, emphasizing the interconnected roles of liver detoxification, gut microbiota, and stress physiology. It outlines evidence-based integrative strategies—including nutrition, supplementation, lifestyle, and botanical medicine—to optimize hormone balance and support long-term health.

 

Abstract:

One of the most common concerns I hear from patients is about the potential negative effects of hormones, especially estrogen metabolism. But as practitioners, we know that we never treat hormones, or any health issues, in isolation—we support the overall terrain they live in. And estrogen metabolism, like so many things, depends on multiple systems: the liver, gut, adrenal glands, and even emotional resilience. So that’s why a whole-person approach, one that combines nutrients, lifestyle recommendations, and mindset is so essential for long-term balance and vitality. In my practice, and I’m sure in yours, the best results come from treating estrogen balance as a system, not a symptom.

Introduction:

One of the most common concerns I hear from patients is about the potential negative effects of hormones, especially how the body is dealing with estrogen’s which interestingly enough, it treats the molecules like a toxin. But as practitioners, we know that we never treat hormones, or any health issues, in isolation—we support the overall terrain they live in. And estrogen metabolism, like so many things, depends on multiple systems: the liver, gut, adrenal glands, and even emotional resilience.

A whole-person approach, one that combines nutrients, lifestyle recommendations, and mindset, is so essential for long-term balance and vitality. In my practice, and I’m sure in yours, the best results come from treating estrogen balance as a system, not a symptom.

That said, one of the crucial aspects of modulating estrogen is by supporting each phase of liver detoxification.

 

Phase I Liver Detoxification — Modulating Estrogen Safely

The process of ridding the body of various substances is primarily focused on the liver and, for the most part, involves a series of cytochrome P450-related enzyme reactions. But those reactions aren’t always in a person’s favor. While they ideally make estrogen metabolites inactive and ready for phase II, any dysfunction in this phase may also leave them active with potentially harmful results.1

Phase I detoxification readies estrogen metabolites and other fat-soluble molecules through hydroxylation to begin their path of elimination. While this is a very simplified description, at this stage, there are two main pathways that apply: the 16α-hydroxylation pathway that forms active estrogen metabolites and the 2-hydroxy pathway, which renders them inactive.

So, it is critical to safely modulate estrogen through supporting 2-hydroxy metabolism. Some researchers believe that the dominance of this pathway alone may be even more important than the sheer numbers of estrogen metabolites produced in the body. That is, the pathway is the primary issue.2

And this bears out in other facets of estrogen metabolism, too. Clinical research has found that women with increased 2-hydroxylation of estrogen towards inactive metabolites have more lean body mass and less body fat than those women with estrogen not guided down that healthy path.2

Clinical work also shows that encouraging increased 2-hydroxylation may lower systolic blood pressure in women post menopause, so bolstering proper estrogen metabolism has far-reaching effects.3

Additionally, insufficient 2-hydroxy metabolism is associated with reduced bone mass, issues with blood sugar, and increased potential for hormone-related cancers.2,4

So, how do you support it?

One way to help channel estrogen down proper pathways is through effective supplementation that is easily incorporated into a patient’s regimen. A well-studied option here is 3,3′-diindolelmethane, better known as DIM.

My guess is that most of your patients have probably heard about the powerful health benefits of broccoli, kale, brussels sprouts, and other cruciferous vegetables.

One of the reasons these vegetables are so highly regarded is because they contain indole-3-carbinol (I3C) a compound that converts to DIM following exposure to stomach acid.5

Getting therapeutic levels of DIM through diet alone can be difficult—it’s been estimated that it would take about two pounds of broccoli in one sitting to do so. Fortunately, clinical research shows that supplemental DIM assists liver enzymes during phase I and phase II to detoxify estrogen, direct it towards the 2-hydroxy pathway, and help shuttle estrogen metabolites and xenoestrogens (like estrogen mimics found in plastics and other environmental chemicals) more efficiently.5-7

The downstream effects of this can’t be overestimated. A Canadian clinical study found that women taking 300 mg per day of an absorption-enhanced DIM showed an increase in BRCA1 expression, which can help inhibit breast cancer, by 34 percent.8

A study at the University of California at Berkeley found that DIM had an anti-tumor effect on endometrial cancer cells, and other research shows that adding DIM to a regimen of Dienogest (a prescription progestin found in combination formulas with estradiol valerate in the United States) can make the medication more effective and help reduce pelvic pain and bleeding in patients with endometriosis.9,10

Other cell research shows that DIM inhibits the formation and growth of gastrointestinal, liver, and pancreatic cancer, so there are far-ranging reasons to recommend it.11

The form of DIM recommended here matters. Supplemental I3C and food sources still require processing by the stomach’s acid environment in order to convert to usable DIM. Clinical work has shown that absorption-enhanced DIM has a peak plasma concentration that is 200 to 300 percent higher compared to I3C doses.12,13

Along with DIM, I recommend curcumin from turmeric (Curcuma longa). Curcumin can affect the synthesis of steroid hormones and inhibit CYP17A1 activities, so it has the potential to balance endocrine activity and assist in phase I detoxification.14

A recent clinical study found that 1500 mg of curcumin per day reduced tumor necrosis factors (TNF) throughout the course of the 12-month regimen, significantly increased superoxide dismutase and glutathione peroxidase levels, and significantly reduced non-esterified fatty acids, hepatic steatosis, and liver stiffness compared to placebo in patients with type 2 diabetes and metabolic dysfunction-associated steatotic liver disease (MASLD). In this study, participants in the curcumin group also saw lower body mass index (BMI) numbers and a reduction in total body fat.15

One thing to note is that curcumin can be difficult for the body to absorb and limit its efficacy. Because of this, I recommend a curcumin blended with turmeric essential oil for enhanced absorption, plus the anti-inflammatory properties of ar-turmerone, a compound present in the oil.16,17

One other botanical extract I’d recommend in combination with DIM and curcumin is grape seed extract. Grape seed extract has been shown to partially inhibit aromatase, an enzyme that converts androgen into estrogen, which can make a critical difference for women concerned about breast cancer, because breast tissue typically has higher levels of aromatase. A study published in the journal Cancer Research, showed that in addition to limiting aromatase activity, grape seed extract reduced growth in MCF-7 breast cancer cells.18

Other clinical work has found that supplementation with grape seed extract containing 250 mg of proanthocyanidins improved quality of life and reduced markers of oxidative stress in participants with non-alcoholic fatty liver disease.19

 

Lifestyle + Diet: Absolute Musts for Estrogen Metabolism and Whole Person Health

I realize that for some, hearing the words “diet and lifestyle” may seem so familiar as to lose any meaning or urgency. But the truth is, it is a foundational pillar of our health that is all too easy  to overlook in the swirl of daily life. Often, when patients arrive in our care, they are seeking to make a major change from whatever in their past may have led to less-than-optimal conditions in their present. So, I typically find that their ears and hearts are open to change when it comes to what to eat and how much to exercise. Here are four key tips that I think are valuable takeaways to educate and encourage patients regarding lifestyle and diet.

  • Recommend a diet rich in cruciferous vegetables, including broccoli, kale, Brussels sprouts: Cruciferous vegetables are packed with protective nutrients that have demonstrably beneficial actions.

For example, they protect against the effects of benzo(a)pyrene [B(a)P], an all-too-common hydrocarbon from car exhaust, smoke, and charred, grilled, or deep-fried foods (which I encourage patients to avoid). Cruciferous vegetable consumption also boosts glutathione-S-transferase (GST) levels, which leads to increased glutathione production, and positively affects microbiome balance for better control and elimination of toxins.20-22

In one four-week clinical trial featuring organic vegetables, whole grains, nuts, and fruits, participants not only showed reduced levels of toxic trace elements including nickel (Ni), rhodium (Rh), tin (Sn), and gallium (Ga), but they also showed greater weight loss, BMI, waist circumference, and body fat mass.23 Considering how extra body fat can also act as an endocrine disruptor by storing environmental pollutants and spent hormones, this kind of dietary change is valuable for many reasons.24,25

  • Watch out for plastics, fragrances, and other synthetic estrogens: Plastics, fragrances, and other synthetic estrogens are not benign players in our lives, but play an active, and damaging role in overall health. We’re at a point now that we know endocrine-disrupting chemicals can have a very real, and very detrimental, effect on our health. They affect DNA methylation, improperly express microRNA signals, and can cause deep epigenetic changes that aren’t readily apparent until issues notably come to the fore.26

    Common chemicals and materials, including cadmium, arsenic, lead, bisphenol A, and phthalates are tied to breast cancer and endometriosis because they act as xenoestrogens, disrupting progesterone signaling creating oxidative damage, and weakening immune responses.26-28 
  • Avoid grilled and charred meats: High-temperature cooking methods generate a reaction between creatine, amino acids, and sugar that creates heterocyclic amines (HCAs) and polycyclic aromatic hydrocarbons (PAHs), carcinogens that are linked to an increased risk of cancer.29-33
  • Add herbs like rosemary and artichoke for gentle liver support: Both of these herbs add a natural and time-tested recommendation to any patient protocol for liver health. Rosemary essential oil alleviates oxidative stress but has been specifically found to reduce aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activity, protect healthy liver cells and prevent lipid peroxidation.34

Rosemary extracts also protect liver cells, inhibit tumor formation, and can relax the smooth muscle of the intestine, making it especially helpful for all phases of liver detoxification.35

Scientific research shows that rosemary water-soluble extracts and essential oil can promote CYP enzyme and other detoxification enzyme activity, and promote glutathione S-transferase expression, making it especially useful for modulating phase I detoxification.36

Artichoke, likewise, has positive effects here, too. Leaf extracts have been found to improve liver enzyme activity in participants with nonalcoholic steatohepatitis, as well as lowering levels of triglycerides in just two months.37

  • Encourage daily sweating, like exercise or taking a sauna, to enhance circulation and detox: Not only does regular exercise help keep weight down, boost mental wellness, and build bone strength, but it also assists the liver in its detoxifying actions. The liver responds to exercise by increasing fat oxidation due to pancreatic glucagon and insulin actions that occur during and right after exercise. In fact, regular activity alone may protect against fatty liver disease—or even reverse it—so it’s definitely a must for all phases of liver detoxification.38

 

Phase I Detoxification Key Points

While phase I readies estrogen for elimination, that estrogen may still be active. The major actions in phase I, carried out primarily by cytochrome P450 enzymes Include:

  • Oxidation
  • Hydration
  • Reduction
  • Hydrolysis1

The Next Step: Phase II Conjugation

Phase II completes the process of taking fat-soluble toxins, estrogens, and other materials and turning them into inactive, water-soluble wastes for elimination. While methylation, sulfation, and amino acid conjugation are all part of this picture, glucuronidation is the name of the game here. Toxins from the liver or intestinal bile attach to glucuronic acid and form the packages so critical to detoxification. It is the most common conjugation pathway, to help package estrogen metabolites for excretion. But that process isn’t guaranteed.39,40

In my own practice, I’ve found that nutraceutical support for phase II detoxification may be necessary for some patients. One sure place to start is with calcium-d-glucarate.

 

Calcium-D-Glucarate

Supplemental calcium-D-glucarate can assist patients with compromised ability to naturally synthesize D-glucaric acid from dietary sources, including apples, grapefruits, alfalfa sprouts, or cruciferous foods that contain glucarate salts. If their diets are currently low in fruits and vegetables, it is one more reason to recommend amendments there as well.39,40

Calcium-D-glucarate helps overcome one of the primary threats to phase II liver detoxification of estrogen metabolites: beta-glucuronidase.

Beta-glucuronidase is an enzyme produced in the colon by microflora, and essentially ‘unwraps’ the tidy package of toxins being readied for elimination. The result is estrogen metabolites being reactivated and reabsorbed, creating imbalances that account for a variety of health issues. As you’d expect, higher levels of beta-glucuronidase activity have been associated in scientific studies with an increased risk of hormone-related cancers, including breast and prostate cancers.40

Fortunately, calcium-D-glucarate supplementation can inhibit the actions of this enzyme and allow estrogen to continue along its appropriate detoxification pathway. Scientific research indicates that it can also reduce reactive oxygen species (ROS) production, help prevent liver cell damage and death, and neutralize other threats to deconjugation that would otherwise unravel the work of phase II metabolism.39

 

Curcumin for continued detoxification

Like many nutrients for liver detoxification and proper estrogen metabolism, curcumin affects more than one particular phase or pathway. As is necessary throughout the liver’s metabolizing and conjugating processes, curcumin reduces inflammatory markers and prevents damage or repairs injured liver cells to ensure more optimal packaging of estrogen and other materials for elimination.41,42

A clinical study found curcumin supplementation (1000 mg per day in divided doses) improved ultrasonographic findings in 75 percent of participants in the curcumin group compared to only 4.7 percent in the control group. Curcumin also reduced serum levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT), while the control group saw levels increase by the conclusion of the 8-week study period.43

Again, I recommend a curcumin that is combined with turmeric essential oil for enhanced absorption, because I see more consistent results in patients with a workable and convenient dosage.

B vitamins are crucial as co-factors for enzyme reactions and are often in depleted states in individuals with compromised liver health. As just one example, vitamin B6 levels can compromise the liver’s antioxidant abilities and reduce glutathione synthesis, leaving the liver at risk and potentially reducing its estrogen-metabolizing actions.44,45 In cases where patients need a boost in their Bs, I recommend bioactive forms that include B12 as L-methylcobalamin and L-methylfolate as a folate source. Bioactive forms don’t require conversion by the liver and can help overcome low levels of intrinsic factor, which may be an issue for some older patients.

Additionally, supplemental magnesium may be helpful, especially for older patients, or those whose diets don’t currently incorporate magnesium-rich foods. Supplemental magnesium may be required to help regenerate liver tissue in individuals with previous liver health concerns to restore strength to its detoxification abilities.46

One review reported that up to 50 percent of patients with type 2 diabetes may be suffering from hypomagnesemia, due to low food intake and urinary excretion, so this issue is a sadly common one.47

 

Lifestyle and Diet Recommendations for Phase II Detoxification

As far as supporting phase II detoxification, lifestyle and diet recommendations generally mirror those for phase I:

  • Encourage daily physical activity: Attainable exercise levels help keep weight and any co-existing hormone issues better controlled and encourage healthy brain and body chemistry that aids in digestion and detoxification.48
  • Recommend a diet rich in whole, unprocessed foods: Leafy greens, beets, eggs and seeds help support methylation. Clinical research also shows that robust fruit and vegetable intake can reduce beta-glucuronidase activity.49 Diet—as always—is a key to keeping phase II and phase III detoxification running smoothly to eliminate harmful estrogen metabolites.50
  • Emphasize the importance of hydration: This keeps the detoxification process moving along smoothly and provides ample water to create water-soluble estrogen packages.
  • Promote healthy protein intake for amino acid conjugation: Along with a plant-rich diet, and make sure your patients are getting the requisite protein they need as sources of taurine, glycine, and arginine for amino acid conjugation. Plant or animal sources of proteins are appropriate here, including beans, lentils, pumpkin seeds, almonds, walnuts, chicken, turkey, and fish—just to name a few—so there are options for every taste and diet type that can help.

 

Phase II: Readying the Package of Estrogen

Phase II gets estrogen metabolites ready for elimination by wrapping them up in a water-soluble form that renders them inactive. These processes include:

  • Glucuronidation, the most common
  • Conjugation with amino acids
  • Methylation
  • Acetylation
  • Conjugation with glutathione
  • Sulfation1

 

Phase III — The Gut-Microbiome Axis (The “Estrobolome”)

Phase III is heavily influenced by the microbes in the gut, of which there are over 1,000 bacterial species in the colon, all influenced by food and medicine intake, immune system function, pathogens, and endocrine activity.

Our understanding of the connection between the gut microbiome and hormone-related conditions is continually being updated and expanded. Developing research on the estrobolome, the axis of gut prebiotics, probiotics, and hormone regulation, shows the importance of keeping estrogen metabolites moving through the body, and not being slowed while in transit. Because that’s when the neat packages of glucuronidation are likely to become unwrapped by beta-glucuronidase.51

The influence of beta-glucuronidase is so strong on estrogen levels that some researchers propose specific beta-glucuronidase inhibitors as a way of reducing ovarian and other estrogen-related cancers. Or, failing that, to at least make chemotherapy treatments for those cancers more effective and reduce the dosages and toxic effects of chemotherapy drugs.51

 

Supplemental recommendations for phase III detoxification

Keeping waste moving through the system gives beta-glucuronidase less time to interfere with proper estrogen metabolism, so constipation or other gut disorders that slow digestive transit time must be addressed.

In addition to calcium-D-glucarate for maintaining a well-sealed estrogen package and curcumin for helping maintain gut lining integrity and microbial balance, probiotics are a sensible choice.52-56

Gut microbiota and sex hormones have a reciprocal relationship, with hormones influencing the type and number of bacteria in the gut, and those bacteria modulating the level of circulating hormones.57,58

One thing to note is that while probiotic supplementation can promote regularity, reduce gut transit time, and help overcome pathogenic bacteria, some probiotics have also shown pro beta-glucuronidase activity.59-61 This can vary among species and strains, and of course, the individual biome of the patient.

In my practice, I’ve seen positive results with a probiotic blend of Lactobacillus plantarum, Lactobacillus rhamnosus, and Bifidobacterium bifidum. I find that a non-dairy based option overcomes any dietary sensitivities or requirements that would otherwise interfere with compliance. Each species has plenty to recommend it. Clinical studies report that they are helpful for cases of irritable bowel syndrome, Crohn’s disease, and, in the case of Lactobacillus plantarum, even Clostridium difficile infection in critically ill patients.62-66

Interestingly, Lactobacillus plantarum was recently found to degrade bisphenol A (BPA) and has been proposed as one way to remediate the contamination of foods due to plastics.67

Lactobacillus species also reduce oxidative stress in the gut through transcription factors nuclear factor erythroid 2-related factor 2 (Nrf-2) and nuclear factor kappa B (NF-κB) and may protect intestinal epithelial cells.68

And in addition to digestion-related concerns, a clinical study reported 75 percent of participants saw alleviation of menopause symptoms according to the Simplified Menopause Index (SMI) scale after supplementing with Lactobacillus gasseri.69-71

But the fact remains that circulating estrogen levels are affected by the gut microbiota and the actions of beta-glucuronidase. And those actions can release estrogen metabolites or keep them bound for excretion. So, estrogen levels—and any attendant issues relating to them—should be monitored when probiotics are part of a patient’s protocol.

 

Lifestyle and Diet Recommendations for Phase III Detoxification:

  • Recommend 25–35 g of fiber daily: Encourage your patients to keep things moving by consuming a variety of fiber-rich foods that include soluble and insoluble fiber, to build healthy form to the stool and keep estrogen metabolites moving out of the body.
  • Emphasize regular bowel movements as an “estrogen exit strategy:” Constipation is an enemy to good health and comfort in any circumstance, but it also creates greater opportunities for beta-glucuronidase to free bound estrogens, which are then reabsorbed. This is why having a high fiber intake, healthy hydration, and probiotics is imperative.
  • Recommend limited alcohol and processed sugar intake: Alcohol and sugar cause inflammatory conditions in the gut, interfere with healthy sleep, slow metabolism, and can add unwanted weight, which then becomes storage for hormones as well.
  • Encourage patients to manage dysbiosis with diet, water, and stress reduction: The Western diet makes individuals especially prone to suffering dysbiosis, and these imbalances in the microbiome benefit from a multi-faceted approach. Recommend patients tune up their gut with fermented foods, including yogurt, miso soup, kimchi, sauerkraut, and other choices rich in prebiotic and probiotics. Hydration is also key here because it, combined with increased fiber intake (which probably contains a good share of prebiotics) can help keep the digestive system running more regularly and smoothly. Stress reduction through gentle yoga practice, light exercise, meditation, and fasting from too much media can reduce emotional reactivity and settle the brain and gut.72-75

Stress and Cortisol: Addressing the Adrenal-Estrogen Connection

Stress, coupled with cyclic hormonal changes, can spike cortisol levels, deplete progesterone, and interfere with detoxification and digestion.76 Some research has reported rapid declines in estrogen and progesterone levels during the late luteal phase create conditions that that contribute to premenstrual dysphoric disorder (PMDD), making coping with ordinary stresses feel even more challenging.77,78

Other clinical work shows that low estrogen and progesterone levels may also be tied to postpartum depression symptoms.78,79 But one thing that remains common is that out of balance cortisol release has negative consequences.

Excessively activating the hypothalamus-pituitary-adrenal axis (HPA) and the sympathetic-adrenal-medullary (SAM) can increase the risk of cancer as well through actions of adrenaline and noradrenaline receptor that signal breast cancer cell invasion.80

Regardless of the severity of health concerns associated with stress and hormones, disadvantageous responses can disrupt the best intentions to detoxify through amendments in diet and lifestyle.

And, since higher levels of progesterone are associated with improved mental recall following stressful events, and better overall memory and mood resilience, the question becomes, how do you manage cortisol?81

For patients whose battle against stressors appears especially difficult, I have found that there are botanical options that can help: magnolia and ashwagandha.

Magnolia (Magnolia officinalis ) has a long history of use as a stress-relieving herb, being used in Traditional Chinese Medicine as a tea, and more recently as a supplement. Magnolia bark is a source of honokiol, a phenolic compound that shows stress-relieving and cortisol moderating actions.82

In one clinical study, magnolia tea was consumed by women diagnosed with postpartum depression for three weeks, while a placebo group received standard postpartum care. Those in the tea group saw better sleep scores according to the Postpartum Sleep Quality Scale (PSQS), improved energy according to the Postpartum Fatigue Scale (PFS) scores, and relief for symptoms of depression according to the Edinburgh Postnatal Depression Scale (EPDS) at both three and six weeks following the study.82

In another clinical study, a combination of magnolia bark (Magnolia officinalis) and phellodendron bark (Phellodendron amurense) extracts reduced cortisol levels by 18 percent compared to placebo at the conclusion of a four-week study. Those taking the botanical combination also reported less tension, fatigue, anger, and confusion and more vigor.83

Ashwagandha (Withania somnifera) is an adaptogenic herb that has been well-recognized in traditional practice and current research for its ability to help people remain energetic, focused, and better able to cope with stress.

Numerous clinical studies have validated the use of ashwagandha as an aid to navigating and better responding to stressors. One clinical study found that ashwagandha significantly reduced stress in men and women, according to the Hamilton Anxiety Rating Scale (HAM-A) measurement scale. The researchers noted that ashwagandha accomplished this in four different ways:

  • Through the HPA axis: Ashwagandha may regulate how much cortisol and DHEA we generate in response to stressors. People taking ashwagandha have lower levels of these compounds in the morning, which suggests that it may be working to lower stress levels, and by extension, how much of these natural chemicals the body produces.
  • By stopping oxidative damage: Ashwagandha is a powerful antioxidant. The demands that free-radical damage does to the body and mind, and subsequent effects on mood, can’t be overstated. This herb puts a stop to that cycle.
  • By reducing inflammation: Ashwagandha is also a powerful anti-inflammatory. Inflammation, along with oxidation, is a major factor in weakening responses to stress and deepening symptoms of depression.
  • By working directly with brain chemistry: Ashwagandha influences gamma-aminobutyric acid (GABA) and serotonin activity. Each of these actions working in synchronicity appears to be the reason this herb is so effective at helping people become resilient to stress.

Additionally, for women concerned about hormonal effects of the herb, the ashwagandha used in this study was found to boost testosterone levels only in men but not in women.84

 

Lifestyle and Care Practices for Stress and Cortisol Management

Stress and cortisol management are also highly dependent on what our own physical and mental input and efforts, so I have a few recommendations I make to any patient struggling to remain resilient:

  • Consider mindfulness, breathwork, and nature exposure to lower cortisol: Mindfulness-based stress reduction (MBSR) has been shown to lower symptoms of anxiety, depression, and stress in what you could call a dose-dependent manner. That is, the more participants practiced, the better they felt.85

    Connecting mindfulness and time in nature combines two wholesome approaches to stress reduction in a way that makes it seem effortless. It’s a good method for bolstering levels of exercise and sharpening attentiveness without making it another thing to add to a “to-do” list. Nature therapy, or “forest bathing” has become a popular topic in recent years as people seek an alternative to artificial environments and overstimulating media.86,87 
  • Prioritize restorative sleep, strive for 7–9 hours each night: Lack of sleep throws off circadian rhythms, spikes cortisol levels, and sets people up to indulge in poor dietary habits and skip exercise. The best recommendation for patients is that they establish a sleep routine, and stick with it as much as possible. That means keeping the bedroom a place of rest, and not of screen time, watching caffeine intake, and setting a regular bedtime.88 
  • Create boundaries around screen time and overstimulation: Our screens may be useful, but they are not our friends. Reducing screen time, doomscrolling, and the habits that can keep people hooked on our devices can almost instantly create a more relaxing mode for blood pressure, cortisol levels, and cognitive strength. I especially recommend cutting screen time at least two hours before bedtime to reduce the effects of blue light on melatonin levels. 
  •  Reconnect with joy, and participate and relax with music, laughter, and community: We are social creatures, and stress makes us want to hide out in our own hermitages. That’s why I emphasize to my patients that healthy connections to hobbies, lightheartedness, and true friends are so important. They are already inherently valuable, but they are absolute must-haves for overall well-being.

 

Hormone Harmony Checklist

Pillar Key Practices Clinical Rationale
Nutrition Colorful phytonutrient-dense diet, crucifers, omega-3s, hydration Supports detox enzymes, reduces inflammation
Movement 30 min/day, mix resistance + aerobic Improves insulin sensitivity, lymphatic flow
Sleep 7–9 hrs nightly, consistent schedule Regulates cortisol and reproductive hormone rhythm
Emotional Health Mindfulness, gratitude, connection Calms HPA axis, supports gut-brain balance
Environment Minimize plastics, fragrances, pesticides Reduces xenoestrogen load and liver burden

The Synergy of Botanicals and Behavior

I always remind my patients that botanical recommendations are meant to support lifestyle alignments, not replace them. They truly are tools that amplify what their body already knows how to do when given the right inputs. DIM and curcumin, calcium-D-glucarate, magnolia bark extract ,and ashwagandha can help keep detoxification, estrogen balance, cellular strength, and stress reduction performing at their peak. But the real effort must come from the patient who wants to be well and the practitioner who is willing to guide them. They can go from detox to dynamic balance.

Ultimately, when a patient’s liver, gut, and adrenal systems are in harmony, and their lifestyle supports that flow, estrogen metabolism becomes effortless, not elusive.

 

Estrogen Balance and Detoxification Supplement Recommendations

These are supplemental ingredients that have produced positive results in my own practice.

Calcium-D-Glucarate: Calcium (as calcium-D-glucarate) 180 mg 14% calcium-D-glucarate 1.5g. Recommendations: 1 to 3 capsules twice daily with meals.

Curcumin Complex (Curcumin combined with turmeric essential oil for enhanced absorption) 750 mg

Curcumin (Curcuma longa) rhizome extract enhanced with turmeric essential oil and standardized for curcuminoid complex (curcumin, demethoxycurcumin and bisdemethoxycurcumin), phospholipids (from sunflower lecithin), supplying 500 mg of curcuminoids. Recommendations: 1 to 2 softgels daily.

DIM + Curcumin Complex

Proprietary Complex Curcumin and French Grape Seed Extract 250 mg
Curcumin (Curcuma longa) rhizome extract enhanced with turmeric essential oil and standardized for curcuminoid complex (curcumin, demethoxycurcumin and bisdemethoxycurcumin), French grape (Vitis vinifera) seed extract standardized to contain ≥ 99% polyphenols and ≥ 80% OPCs.

Bioavailable DIM 120 mg
Enhanced bioavailability complex containing starch, a minimum 25% diindolylmethane [30 mg], vitamin E, phosphatidylcholine, silica.
Recommendations: 1 capsule daily with food. May increase to 1 capsule twice daily

Ashwagandha:
Withania somnifera) leaf and root extract (EP35™) standardized to ≥ 35% withanolides (≥52.5 mg). Recommendations: 1 capsule, once or twice daily.

Magnolia Bark Extract: Magnolia (Magnolia officinalis) (bark) extract standardized to 2% honokiol (6 mg) and 1% magnolol (3 mg), Recommendations: 400 mg, 1 tablet daily, may increase to 2 tablets daily if needed during stress.

Probiotic blend: Lactobacillus plantarum, Lactobacillus rhamnosus, and Bifidobacterium bifidum, 20 Billion CFU per capsule. Recommendations: Take 1 capsule daily, with food.

 

References:

  1.         Phang-Lyn S, Llerena VA. Biochemistry, Biotransformation. [Updated 2023 Aug 14]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK544353/. Accessed October 20, 2025
  2.         Napoli N, Vattikuti S, Yarramaneni J, et al. Increased 2-hydroxylation of estrogen is associated with lower body fat and increased lean body mass in postmenopausal women. Maturitas. 2012;72(1):66-71. doi:10.1016/j.maturitas.2012.02.002
  3.         Masi CM, Hawkley LC, Berry JD, Cacioppo JT. Estrogen metabolites and systolic blood pressure in a population-based sample of postmenopausal women. J Clin Endocrinol Metab. 2006 Mar;91(3):1015–1020. doi: 10.1210/jc.2005-2339. 
  4.         De Coster S, van Larebeke N. Endocrine-disrupting chemicals: associated disorders and mechanisms of action. J Environ Public Health. 2012;2012:713696. doi:10.1155/2012/713696 https://pmc.ncbi.nlm.nih.gov/articles/PMC3443608/
  5.         Banerjee S, Kong D, Wang Z, Bao B, Hillman GG, Sarkar FH. Attenuation of multi-targeted proliferation-linked signaling by 3,3′-diindolylmethane (DIM): from bench to clinic. Mutat Res. 2011;728(1-2):47-66. doi:10.1016/j.mrrev.2011.06.001
  6.         Dalessandri KM, Firestone GL, Fitch MD, Bradlow HL, Bjeldanes LF. Pilot study: effect of 3,3’diindolylmethane supplements on urinary hormone metabolites in postmenopausal women with a history of early-stage breast cancer. Nutr Cancer. 2004;50(2):161-7.
  7.         Rajoria S, Suriano R, Parmar PS, et al. 3,3′-diindolylmethane modulates estrogen metabolism in patients with thyroid proliferative disease: a pilot study. Thyroid. 2011;21(3):299–304.
  8.         Kotsopoulos J, Zhang S, Akbari M, et al. BRCA1 mRNA levels following a 4-6-week intervention with oral 3,3′-diindolylmethane. Br J Cancer. 2014 Sep 23;111(7):1269-74.
  9.         Leong H, Firestone GL, Bjeldanes LF. Cytostatic effects of 3,3′-diindolylmethane in human endometrial cancer cells result from an estrogen receptor-mediated increase in transforming growth factor-alpha expression. Carcinogenesis. 2001 Nov;22(11):1809-17.
  10.     Morales-Prieto DM, Herrmann J, Osterwald H, et al. Comparison of dienogest effects upon 3,3′-diindolylmethane supplementation in models of endometriosis and clinical cases. Reprod Biol. 2018 Sep;18(3):252-258.
  11.     Kim SM. Cellular and Molecular Mechanisms of 3,3′-Diindolylmethane in Gastrointestinal Cancer. Int J Mol Sci. 2016;17(7):1155. Published 2016 Jul 19. doi:10.3390/ijms17071155 https://pmc.ncbi.nlm.nih.gov/articles/PMC4964527/#abstract1
  12.     Pondugula SR, Flannery PC, Abbott KL, et al. Diindolylmethane, a naturally occurring compound, induces CYP3A4 and MDR1 gene expression by activating human PXR. Toxicol Lett. 2015;232(3):580-589. doi:10.1016/j.toxlet.2014.12.015 https://pmc.ncbi.nlm.nih.gov/articles/PMC4568078/#abstract1
  13.     Reed GA, Sunega JM, Sullivan DK, et al. Single-dose pharmacokinetics and tolerability of absorption-enhanced 3,3′-diindolylmethane in healthy subjects. Cancer Epidemiol Biomarkers Prev. 2008;17(10):2619-2624. doi:10.1158/1055-9965.EPI-08-0520. https://pmc.ncbi.nlm.nih.gov/articles/PMC2602858/#abstract1
  14.     Rodríguez Castaño P, Parween S, Pandey AV. Bioactivity of Curcumin on the Cytochrome P450 Enzymes of the Steroidogenic Pathway. Int J Mol Sci. 2019;20(18):4606. Published 2019 Sep 17. doi:10.3390/ijms20184606. https://pmc.ncbi.nlm.nih.gov/articles/PMC6770025/
  15.     Yaikwawong M, Jansarikit L, Jirawatnotai S, Chuengsamarn S. Curcumin for Inflammation Control in Individuals with Type 2 Diabetes Mellitus and Metabolic Dysfunction-Associated Steatotic Liver Disease: A Randomized Controlled Trial. Nutrients. 2025;17(12):1972. Published 2025 Jun 10. doi:10.3390/nu17121972
  16.     Antony B, Merina B, Iyer VS, Judy N, Lennertz K, Joyal S. A pilot cross-over study to evaluate human oral bioavailability of BCM-95 CG (Biocurcumax™) a novel bioenhanced preparation of curcumin. Ind J Pharm Sci. 2008:445-449.
  17.     Benny B, Antony B. Bioavailability of Biocurcumax (BCM-95). Spice India. September, 2006:11-15. 014 Jun 18;11:31. doi: 10.1186/1550-2783-11-31. eCollection 2014.
  18.     Kijima I, et al. Grape seed extract is an aromatase inhibitor and a suppressor of aromatase expression. Cancer Res. 2006;66(11):5960-7.
  19. Ghanbari P, Alboebadi R, Bazyar H, et al. Grape seed extract supplementation in non-alcoholic fatty liver disease. Int J Vitam Nutr Res. 2024;94(5-6):365-376. doi:10.1024/0300-9831/a000805
  20.     Steinkellner H, Rabot S, Freywald C, et al. Effects of cruciferous vegetables and their constituents on drug metabolizing enzymes involved in the bioactivation of DNA-reactive dietary carcinogens. Mutat Res. 2001;480-481:285-297. doi:10.1016/s0027-5107(01)00188-9
  21.     Ho E, Wong CP, Bouranis JA, Shannon J, Zhang Z. Cruciferous Vegetables, Bioactive Metabolites, and Microbiome for Breast Cancer Prevention. Annu Rev Nutr. 2025;45(1):171-195. doi:10.1146/annurev-nutr-062222-024321
  22.     Fujioka N, Fritz V, Upadhyaya P, Kassie F, Hecht SS. Research on cruciferous vegetables, indole-3-carbinol, and cancer prevention: A tribute to Lee W. Wattenberg. Mol Nutr Food Res. 2016;60(6):1228-1238. doi:10.1002/mnfr.201500889
  23.     Jung SJ, Kim WL, Park BH, Lee SO, Chae SW. Effect of toxic trace element detoxification, body fat reduction following four-week intake of the Wellnessup diet: a three-arm, randomized clinical trial. Nutr Metab (Lond). 2020;17:47. Published 2020 Jun 22. doi:10.1186/s12986-020-00465-9 https://pmc.ncbi.nlm.nih.gov/articles/PMC7310262/
  24.     Müllerová D, Kopecký J. White adipose tissue: storage and effector site for environmental pollutants. Physiol Res. 2007;56(4):375-382. doi:10.33549/physiolres.931022
  25.     Hodges RE, Minich DM. Modulation of Metabolic Detoxification Pathways Using Foods and Food-Derived Components: A Scientific Review with Clinical Application. J Nutr Metab. 2015;2015:760689. doi:10.1155/2015/760689
  26.     Singh DD. Epigenetic Mechanisms of Endocrine-Disrupting Chemicals in Breast Cancer and Their Impact on Dietary Intake. J Xenobiot. 2024;15(1):1. Published 2024 Dec 24. doi:10.3390/jox15010001
  27.     Moustakli E, Potiris A, Grigoriadis T, et al. Unraveling the Core of Endometriosis: The Impact of Endocrine Disruptors. Int J Mol Sci. 2025;26(15):7600. Published 2025 Aug 6. doi:10.3390/ijms26157600
  28.     Cano R, Pérez JL, Dávila LA, et al. Role of Endocrine-Disrupting Chemicals in the Pathogenesis of Non-Alcoholic Fatty Liver Disease: A Comprehensive Review. Int J Mol Sci. 2021;22(9):4807. Published 2021 May 1. doi:10.3390/ijms22094807
  29.     Nadeem HR, Akhtar S, Ismail T, et al. Heterocyclic Aromatic Amines in Meat: Formation, Isolation, Risk Assessment, and Inhibitory Effect of Plant Extracts. Foods. 2021;10(7):1466. Published 2021 Jun 24. doi:10.3390/foods10071466
  30.     Iko Afé OH, Douny C, Kpoclou YE, et al. Insight about methods used for polycyclic aromatic hydrocarbons reduction in smoked or grilled fishery and meat products for future re-engineering: A systematic review. Food Chem Toxicol. 2020;141:111372. doi:10.1016/j.fct.2020.111372
  31.     Yang L, Zhang H, Zhang X, et al. Exposure to Atmospheric Particulate Matter-Bound Polycyclic Aromatic Hydrocarbons and Their Health Effects: A Review. Int J Environ Res Public Health. 2021;18(4):2177. Published 2021 Feb 23. doi:10.3390/ijerph18042177
  32.     Duedahl-Olesen L, Ionas AC. Formation and mitigation of PAHs in barbecued meat – a review. Crit Rev Food Sci Nutr. 2022;62(13):3553-3568. doi:10.1080/10408398.2020.1867056
  33.     Reng Q, Zhu LL, Feng L, et al. Dietary meat mutagens intake and cancer risk: A systematic review and meta-analysis. Front Nutr. 2022;9:962688. Published 2022 Sep 23. doi:10.3389/fnut.2022.962688
  34.     Rašković A, Milanović I, Pavlović N, Ćebović T, Vukmirović S, Mikov M. Antioxidant activity of rosemary (Rosmarinus officinalis L.) essential oil and its hepatoprotective potential. BMC Complement Altern Med. 2014;14:225. Published 2014 Jul 7. doi:10.1186/1472-6882-14-225
  35.     al-Sereiti MR, Abu-Amer KM, Sen P. Pharmacology of rosemary (Rosmarinus officinalis Linn.) and its therapeutic potentials. Indian J Exp Biol. 1999;37(2):124-130.
  36.     Debersac P, Heydel JM, Amiot MJ, et al. Induction of cytochrome P450 and/or detoxication enzymes by various extracts of rosemary: description of specific patterns. Food Chem Toxicol. 2001;39(9):907-918. doi:10.1016/s0278-6915(01)00034-5
  37.     Rangboo V, Noroozi M, Zavoshy R, Rezadoost SA, Mohammadpoorasl A. The Effect of Artichoke Leaf Extract on Alanine Aminotransferase and Aspartate Aminotransferase in the Patients with Nonalcoholic Steatohepatitis. Int J Hepatol. 2016;2016:4030476. doi:10.1155/2016/4030476
  38.     Trefts E, Williams AS, Wasserman DH. Exercise and the Regulation of Hepatic Metabolism. Prog Mol Biol Transl Sci. 2015;135:203-225. doi:10.1016/bs.pmbts.2015.07.010
  39.     Ayyadurai VAS, Deonikar P, Fields C. Mechanistic Understanding of D-Glucaric Acid to Support Liver Detoxification Essential to Muscle Health Using a Computational Systems Biology Approach. Nutrients. 2023;15(3):733. Published 2023 Feb 1. doi:10.3390/nu15030733
  40.     Calcium-D-glucarate. Altern Med Rev. 2002;7(4):336-339.
  41.     Inzaugarat ME, De Matteo E, Baz P, et al. New evidence for the therapeutic potential of curcumin to treat nonalcoholic fatty liver disease in humans. PLoS One. 2017;12(3):e0172900. Published 2017 Mar 3. doi:10.1371/journal.pone.0172900
  42.     Zabihi NA, Pirro M, Johnston TP, Sahebkar A. Is There a Role for Curcumin Supplementation in the Treatment of Non-Alcoholic Fatty Liver Disease? The Data Suggest Yes. Curr Pharm Des. 2017;23(7):969-982. doi:10.2174/1381612822666161010115235
  43.     Panahi Y, Kianpour P, Mohtashami R, Jafari R, Simental-Mendía LE, Sahebkar A. Efficacy and Safety of Phytosomal Curcumin in Non-Alcoholic Fatty Liver Disease: A Randomized Controlled Trial. Drug Res (Stuttg). 2017;67(4):244-251. doi:10.1055/s-0043-100019
  44.     LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012-. Vitamin B. [Updated 2021 May 27]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK548710/
  45.     Licata A, Zerbo M, Como S, et al. The Role of Vitamin Deficiency in Liver Disease: To Supplement or Not Supplement?. Nutrients. 2021;13(11):4014. Published 2021 Nov 10. doi:10.3390/nu13114014
  46.     Bravo M, Simón J, González-Recio I, Martinez-Cruz LA, Goikoetxea-Usandizaga N, Martínez-Chantar ML. Magnesium and Liver Metabolism Through the Lifespan. Adv Nutr. 2023;14(4):739-751. doi:10.1016/j.advnut.2023.05.009 https://pmc.ncbi.nlm.nih.gov/articles/PMC10334155/
  47.     Piuri G, Zocchi M, Della Porta M, et al. Magnesium in Obesity, Metabolic Syndrome, and Type 2 Diabetes. Nutrients. 2021;13(2):320. Published 2021 Jan 22. doi:10.3390/nu13020320
  48.     Trefts E, Williams AS, Wasserman DH. Exercise and the Regulation of Hepatic Metabolism. Prog Mol Biol Transl Sci. 2015;135:203-225. doi:10.1016/bs.pmbts.2015.07.010
  49.     Lampe JW, Li SS, Potter JD, King IB. Serum beta-glucuronidase activity is inversely associated with plant-food intakes in humans. J Nutr. 2002;132(6):1341-1344. doi:10.1093/jn/132.6.1341
  50.     Hodges RE, Minich DM. Modulation of Metabolic Detoxification Pathways Using Foods and Food-Derived Components: A Scientific Review with Clinical Application. J Nutr Metab. 2015;2015:760689. doi:10.1155/2015/760689
  51.     He S, Li H, Yu Z, et al. The Gut Microbiome and Sex Hormone-Related Diseases. Front Microbiol. 2021;12:711137. Published 2021 Sep 28. doi:10.3389/fmicb.2021.711137 https://pmc.ncbi.nlm.nih.gov/articles/PMC8506209/
  52.     Lamichhane G, Godsey TJ, Liu J, et al. Twelve-Week Curcumin Supplementation Improves Glucose Homeostasis and Gut Health in Prediabetic Older Adults: A Pilot, Double-Blind, Placebo-Controlled Trial. Nutrients. 2025;17(13):2164. Published 2025 Jun 29. doi:10.3390/nu17132164 https://pmc.ncbi.nlm.nih.gov/articles/PMC12251931/
  53.     Pivari F, Mingione A, Piazzini G, et al. Curcumin Supplementation (Meriva®) Modulates Inflammation, Lipid Peroxidation and Gut Microbiota Composition in Chronic Kidney Disease. Nutrients. 2022;14(1):231. Published 2022 Jan 5. doi:10.3390/nu14010231 https://pmc.ncbi.nlm.nih.gov/articles/PMC8747135/
  54.     Peterson CT, Vaughn AR, Sharma V, et al. Effects of Turmeric and Curcumin Dietary Supplementation on Human Gut Microbiota: A Double-Blind, Randomized, Placebo-Controlled Pilot Study. J Evid Based Integr Med. 2018;23:2515690X18790725. doi:10.1177/2515690X18790725. https://pmc.ncbi.nlm.nih.gov/articles/PMC6083746/
  55.     Balaji S, Jeyaraman N, Jeyaraman M, et al. Impact of curcumin on gut microbiome. World J Exp Med. 2025;15(1):100275. Published 2025 Mar 20. doi:10.5493/wjem.v15.i1.100275. https://pmc.ncbi.nlm.nih.gov/articles/PMC11718586/
  56.     Ghosh SS, He H, Wang J, Gehr TW, Ghosh S. Curcumin-mediated regulation of intestinal barrier function: The mechanism underlying its beneficial effects. Tissue Barriers. 2018;6(1):e1425085. doi:10.1080/21688370.2018.1425085. https://pmc.ncbi.nlm.nih.gov/articles/PMC5823546/
  57.     Liaquat M, Minihane AM, Vauzour D, Pontifex MG. The gut microbiota in menopause: Is there a role for prebiotic and probiotic solutions?. Post Reprod Health. 2025;31(2):105-114. doi:10.1177/20533691251340491
  58.     Wang H, Shi F, Zheng L, et al. Gut microbiota has the potential to improve health of menopausal women by regulating estrogen. Front Endocrinol (Lausanne). 2025;16:1562332. Published 2025 Jun 9. doi:10.3389/fendo.2025.1562332 https://pmc.ncbi.nlm.nih.gov/articles/PMC12183514/
  59. Honda S, Tominaga Y, Espadaler-Mazo J, et al. Supplementation with a Probiotic Formula Having β-Glucuronidase Activity Modulates Serum Estrogen Levels in Healthy Peri- and Postmenopausal Women. J Med Food. 2024;27(8):720-727. doi:10.1089/jmf.2023.k.0320 https://www.liebertpub.com/doi/10.1089/jmf.2023.k.0320?url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org&rfr_dat=cr_pub++0pubmed
  60.     Liaquat M, Minihane AM, Vauzour D, Pontifex MG. The gut microbiota in menopause: Is there a role for prebiotic and probiotic solutions?. Post Reprod Health. 2025;31(2):105-114. doi:10.1177/20533691251340491
  61.     Flores R, Shi J, Fuhrman B, et al. Fecal microbial determinants of fecal and systemic estrogens and estrogen metabolites: a cross-sectional study. J Transl Med. 2012;10:253. Published 2012 Dec 21. doi:10.1186/1479-5876-10-253. https://pmc.ncbi.nlm.nih.gov/articles/PMC3552825/
  62.     Bixquert Jiménez M. Treatment of irritable bowel syndrome with probiotics. An etiopathogenic approach at last? Rev Esp Enferm Dig. 2009;101(8):553-64.
  63.     Wasilewski A, Zielińska M, Storr M, Fichna J. Beneficial Effects of Probiotics, Prebiotics, Synbiotics, and Psychobiotics in Inflammatory Bowel Disease. Inflamm Bowel Dis. 2015 Jul;21(7):1674-82.
  64.     Ducrotté P, Sawant P, Jayanthi V. Clinical trial: Lactobacillus plantarum 299v (DSM 9843) improves symptoms of irritable bowel syndrome. World J Gastroenterol. 2012;18(30):4012-8.
  65.     Nobaek S, Johansson ML, Molin G, Ahrné S, Jeppsson B. Alteration of intestinal microflora is associated with reduction in abdominal bloating and pain in patients with irritable bowel syndrome. Am J Gastroenterol. 2000;95(5):1231-1238. doi:10.1111/j.1572-0241.2000.02015.x
  66.     Klarin B, Wullt M, Palmquist I, Molin G, Larsson A, Jeppsson B. Lactobacillus plantarum 299v reduces colonisation of Clostridium difficile in critically ill patients treated with antibiotics. Acta Anaesthesiol Scand. 2008;52(8):1096-1102. doi:10.1111/j.1399-6576.2008.01748.x
  67.     Kyrila G, Katsoulas A, Schoretsaniti V, et al. Bisphenol A removal and degradation pathways in microorganisms with probiotic properties. J Hazard Mater. 2021;413:125363. doi:10.1016/j.jhazmat.2021.125363
  68.     Kong Y, Olejar KJ, On SLW, Chelikani V. The Potential of Lactobacillus spp. for Modulating Oxidative Stress in the Gastrointestinal Tract. Antioxidants (Basel). 2020;9(7):610. Published 2020 Jul 10. doi:10.3390/antiox9070610 https://pmc.ncbi.nlm.nih.gov/articles/PMC7402165/
  69.     Wang H, Shi F, Zheng L, et al. Gut microbiota has the potential to improve health of menopausal women by regulating estrogen. Front Endocrinol (Lausanne). 2025;16:1562332. Published 2025 Jun 9. doi:10.3389/fendo.2025.1562332
    https://pmc.ncbi.nlm.nih.gov/articles/PMC12183514/
  70.     Sawada D, Sugawara T, Hirota T, Nakamura Y. Effects of Lactobacillus gasseri CP2305 on Mild Menopausal Symptoms in Middle-Aged Women. Nutrients. 2022;14(9):1695. Published 2022 Apr 19. doi:10.3390/nu14091695
  71.     Forssten SD, Ouwehand AC, Griffin SM, Patterson E. One Giant Leap from Mouse to Man: The Microbiota-Gut-Brain Axis in Mood Disorders and Translational Challenges Moving towards Human Clinical Trials. Nutrients. 2022;14(3):568. Published 2022 Jan 27. doi:10.3390/nu14030568
  72.     Trefts E, Williams AS, Wasserman DH. Exercise and the Regulation of Hepatic Metabolism. Prog Mol Biol Transl Sci. 2015;135:203-225. doi:10.1016/bs.pmbts.2015.07.010
  73.     Hodges RE, Minich DM. Modulation of Metabolic Detoxification Pathways Using Foods and Food-Derived Components: A Scientific Review with Clinical Application. J Nutr Metab. 2015;2015:760689. doi:10.1155/2015/760689
  74.     “Dysbiosis.” Cleveland Clinic Health Library. Cleveland Clinic web site. Accessed: October 28, 2025. Available at: https://my.clevelandclinic.org/health/diseases/dysbiosis
  75.     Tomasello G, Mazzola M, Leone A, et al. Nutrition, oxidative stress and intestinal dysbiosis: Influence of diet on gut microbiota in inflammatory bowel diseases. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016;160(4):461-466. doi:10.5507/bp.2016.052
  76.     Lovick TA. Estrous cycle and stress: influence of progesterone on the female brain. Braz J Med Biol Res. 2012;45(4):314-320. doi:10.1590/s0100-879×2012007500044
  77.     Ko CH, Wong TH, Suen JL, Lin PC, Long CY, Yen JY. Estrogen, progesterone, cortisol, brain-derived neurotrophic factor, and vascular endothelial growth factor during the luteal phase of the menstrual cycle in women with premenstrual dysphoric disorder. J Psychiatr Res. 2024;169:307-317. doi:10.1016/j.jpsychires.2023.11.019
  78.     Mazza M, Marano G. Unmasking the cycle: Premenstrual and menstrual exacerbation of psychiatric disorders and impact on female mental health. World J Psychiatry. 2025;15(8):107132. Published 2025 Aug 19. doi:10.5498/wjp.v15.i8.107132
  79.     Harris B, Lovett L, Newcombe RG, Read GF, Walker R, Riad-Fahmy D. Maternity blues and major endocrine changes: Cardiff puerperal mood and hormone study II. BMJ. 1994;308(6934):949-953. doi:10.1136/bmj.308.6934.949
  80.     Yasuda MT, Sakakibara H, Shimoi K. Estrogen- and stress-induced DNA damage in breast cancer and chemoprevention with dietary flavonoid. Genes Environ. 2017;39:10. Published 2017 Feb 1. doi:10.1186/s41021-016-0071-7
  81.     Maki PM, Mordecai KL, Rubin LH, et al. Menstrual cycle effects on cortisol responsivity and emotional retrieval following a psychosocial stressor. Horm Behav. 2015;74:201-208. doi:10.1016/j.yhbeh.2015.06.023
  82.     Xue L, Zhang J, Shen H, Ai L, Wu R. A randomized controlled pilot study of the effectiveness of magnolia tea on alleviating depression in postnatal women. Food Sci Nutr. 2020;8(3):1554-1561. Published 2020 Feb 10. doi:10.1002/fsn3.1442
  83.     Talbott SM, Talbott JA, Pugh M. Effect of Magnolia officinalis and Phellodendron amurense (Relora®) on cortisol and psychological mood state in moderately stressed subjects. J Int Soc Sports Nutr. 2013;10(1):37. Published 2013 Aug 7. doi:10.1186/1550-2783-10-37 https://pmc.ncbi.nlm.nih.gov/articles/PMC3750820/#abstract1
  84.     Lopresti AL, Smith SJ, Malvi H, Kodgule R. An investigation into the stress-relieving and pharmacological actions of an ashwagandha (Withania somnifera) extract: A randomized, double-blind, placebo-controlled study. Medicine (Baltimore). 2019;98(37):e17186.
  85.     Alzahrani AM, Hakami A, AlHadi A, et al. The effectiveness of mindfulness training in improving medical students’ stress, depression, and anxiety. PLoS One. 2023;18(10):e0293539. Published 2023 Oct 31. doi:10.1371/journal.pone.0293539. https://pmc.ncbi.nlm.nih.gov/articles/PMC10617730/
  86.     Menardo E, Di Marco D, Ramos S, et al. Nature and Mindfulness to Cope with Work-Related Stress: A Narrative Review. Int J Environ Res Public Health. 2022;19(10):5948. Published 2022 May 13. doi:10.3390/ijerph19105948. https://pmc.ncbi.nlm.nih.gov/articles/PMC9140663/
  87.     Hansen MM, Jones R, Tocchini K. Shinrin-Yoku (Forest Bathing) and Nature Therapy: A State-of-the-Art Review. Int. J. Environ. Res. Public Health. 2017;14:851. doi: 10.3390/ijerph14080851. https://www.mdpi.com/1660-4601/14/8/851
  88.     Wright KP Jr, Drake AL, Frey DJ, et al. Influence of sleep deprivation and circadian misalignment on cortisol, inflammatory markers, and cytokine balance. Brain Behav Immun. 2015;47:24-34. doi:10.1016/j.bbi.2015.01.004. https://pmc.ncbi.nlm.nih.gov/articles/PMC5401766/

 

Author Bio: 

Dr. Holly Lucille, ND, RN, ONC is a nationally recognized naturopathic physician, registered nurse, educator, author, and media personality with over two decades of clinical experience. A graduate of the Southwest College of Naturopathic Medicine (now Sonoran University of Health Sciences), she maintains a clinical focus on whole-person, individualized care rooted in the principles of naturopathic medicine. 

Dr. Lucille is widely known for her work in integrative and natural medicine, having appeared on major media platforms including Dr. Oz, The Doctors, and national television networks, and being named to Time magazine’s “Alt List” of influential voices in health. She is the author of books on hormone health and wellness, host of the Mindful Medicine podcast, and a frequent lecturer to both clinicians and the public. 

In addition to her clinical and media work, Dr. Lucille serves in leadership roles within the profession, including positions with the Institute for Natural Medicine and as a past president of the California Naturopathic Doctors Association. Her Los Angeles–based practice emphasizes comprehensive, root-cause–oriented care that integrates science, nature, and patient empowerment.

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