Raspberry Pomegranate

Super Mushroom Focus Gummies™

"Okay, let's be real. These aren't some quick fix, but wow, after a couple of weeks, my mind feels sharper than ever. I'm on point, staying focused, and getting things done. They've genuinely helped clear the fog."

Melissa G., United States

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Description

🍄 Explore the natural essence of adaptogenic mushrooms with our delightful mushroom gummies. Each piece is crafted to complement your daily wellness routine:

🧠 Support Mental Clarity*
⚡ Promote Energy*
🔄 Support Cognitive Function*
🌱 Encourage Daily Focus*

Treat yourself to these tasty gummies, perfect for integrating into your daily habits, providing a wonderful boost to your daily routine.

Enjoy the unique qualities of mushrooms in a convenient, enjoyable form

25mg of 10:1 Wild Lion's Mane Extract / Serving (Equivalent to 250mg Fruiting Body)

INGREDIENTS

Wild Lion’s Mane Mushroom, Alpha GPC & Rhodiola

DIRECTIONS:

Each bag comes with 60 potent gummies. Enjoy two (2) gummies per day. Take any time of the day, with or without meal.

SHIPPING & GUARANTEE

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Once an order is placed we typically ship within 1 business day. The delivery time is typically 3-5 business days, but can be longer depending on location and circumstances.

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Simply contact us at hello@tryauri.com

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BENEFITS

A Gummy To Become Your Best Self

  • icon Support Mental Clarity*

    Life can be a blur. The Lion's Mane mushroom in our gummies can help support mental engagement and focus
  • icon Promote Energy*

    Our gummies contain the goodness of Lion's Mane, which supports cellular energy production and attention
  • icon Support Cognitive Function*

    Our gummies with Lion's Mane provide your brain with nutritional support it needs to stay sharp
  • icon Encourage Daily Focus*

    These gummies support your natural ability to focus on the tasks at hand and help keep you on track all day

POWERFUL GUMMY FOR MENTAL PERFORMANCE

A fusion of Lion's Mane and brain function supporting nutrients, blended to support mental clarity, concentration, and daily focus. Crafted for daily consumption, it's the cognitive support you've been waiting for

MOST SUPPLEMENTS WASTE YOUR MONEY

Our bodies are not efficient — only a small share of what we consume gets absorbed into our bodies. As a result, the supplements that we take into the stomach produce little to no result. Try gummy supplements and increase absorption rates up to 90%.

Auri Mushroom Gummies

  • check icon
    More nutrients per serving
  • check icon
    ±90% absorption efficiency
  • check icon
    With ingredients that enhance benefits
  • check icon
    Chewable and easy to consume
  • check icon
    Delicious and easy on the stomach

Capsule / Tablet Supplements

  • cross icon
    Fewer nutrients per serving
  • cross icon
    7%-12% absorption efficiency
  • cross icon
    Only a few ingredients
  • cross icon
    May be hard to swallow
  • cross icon
    Cause nausea for some people

INSIDE THE GUMMIES

Powerful Mushroom Gummy for Focus and Brain Health

  • Focus Lion's Mane

    Lion's Mane has been shown to promote mental clarity, focus, and support normal memory retention. Known for its ability to naturally support production of Nerve Growth Factor, and celebrated for its properties supporting cognition and overall brain health*

image description30-DAY SUPPLY
  • Gluten Free

  • All Natural

  • Allergen free

  • Made in USA**

  • CGMP Certified

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Interested in the Extensive Research?

Focus Gummies Whitepaper
Researched & Written By: Dr. Jeremy, PharmD

Maintaining cognitive function and focus is essential for overall brain health and wellbeing. Nutrition, in particular, plays a pivotal role in supporting cognitive processes, with specific diets and nutrients like complex carbohydrates, proteins, healthy fats, and micronutrients such as B vitamins and iron being crucial. Additionally, natural supplements like Lion's Mane mushroom, Alpha-GPC, and Rhodiola rosea have shown potential in enhancing brain function through various mechanisms, including neuroprotection, neurotransmitter modulation, and stress resilience. Understanding the brain's intricate mechanisms of focus, such as the cholinergic system and neural pathways, further underscores the importance of targeted nutritional and supplemental strategies in boosting cognition and focus.

Impact of Nutrition on Cognitive Health

Nutrition plays a critical role in cognitive health and brain function throughout the lifespan. The brain requires a steady supply of nutrients to develop and maintain its physical structure and cognitive processes. Inadequate intake of certain vitamins and minerals, as well as imbalances in macronutrient ratios, can disrupt nutrient-dependent processes in the brain and negatively impact cognition.

Macronutrients (carbohydrates, proteins, and fats) provide the energy and building blocks the brain needs to operate optimally. Complex carbohydrates with high fiber content are beneficial for cognition by regulating glucose metabolism and reducing inflammation and oxidative stress in the brain. Adequate protein intake is important as amino acids like tyrosine and tryptophan are precursors for neurotransmitters that modulate neural activity and cognitive functions such as reaction time, memory, and cognitive control. Healthy fats, especially omega-3 polyunsaturated fatty acids, are critical structural components of brain cell membranes.

Micronutrients like B vitamins, iron, and polyphenols also play crucial roles in brain health. B vitamins are essential for proper neuronal functioning and deficiencies are linked to cognitive decline. Iron is required for neurotransmitter synthesis and myelin formation, with iron deficiency in early life negatively impacting brain development and cognition.

Dietary patterns that emphasize whole foods while limiting processed foods are most beneficial for cognitive health. The Mediterranean diet, which is rich in fruits, vegetables, whole grains, fish, and olive oil, has been consistently linked to lower risks of age-related cognitive decline and dementia. Other brain-protective diets include the DASH, MIND, and Nordic diets. These dietary patterns provide ample amounts of neuroprotective nutrients like polyphenols, which can improve cognition by reducing inflammation and oxidative stress in the aging brain.

The composition of the gut microbiome also influences brain function via the gut-brain axis. Diets high in fiber and probiotics can beneficially modulate the gut microbiome, with emerging evidence suggesting positive effects on cognition. On the other hand, diets high in saturated fats and added sugars can negatively alter gut bacteria and promote neuroinflammation.

Establishing healthy eating patterns in early adulthood and middle-age appears to be especially important for cognitive health in later life. Many dementia risk factors like obesity and hypertension develop in midlife, so preventive nutritional approaches should be targeted to these age groups, well before cognitive impairment manifests. Given the links between cardiovascular and metabolic diseases and dementia risk, optimizing diet quality could be an effective strategy to include in public health programs aimed at preventing cognitive decline.

Brain Mechanism that Drives Focus

The brain's ability to focus attention and maintain cognitive function relies on complex neural mechanisms. One key system involved is the cholinergic system, which consists of neurons that synthesize and release the neurotransmitter acetylcholine. This system acts as a master switch, enabling the brain to identify and focus on the most salient sensory inputs at any given moment.

When the cholinergic system is activated, it triggers a desynchronization of neural activity in the neocortex. This allows individual neurons to respond selectively to relevant sensory information, enhancing the brain's ability to focus on important stimuli like a speeding car or a conversation in a crowded room. Dysfunction of the cholinergic system is associated with impairments in cognition, memory, and perception.

Recent research has identified a specific type of neuron in the lateral prefrontal cortex (LPFC) called "visual-movement neurons" that direct attention towards relevant visual targets. These neurons exhibit ramping activity as soon as attention is focused on a target, and their activity scales with the amount of attention focused. This suggests that visual-movement neurons in the LPFC play a key role in controlling and maintaining focused attention.

At the cellular level, the dendrites of neocortical output neurons are critical for cognitive processing. These dendrites only become active when animals are actively engaged in a behavior, and their activity correlates with perception and task performance. The cholinergic system enables these output neurons to powerfully respond to excitatory input and perform computations in a state-dependent manner, driving the brain's ability to focus and sustain attention.

The exact mechanisms accounting for age-related decline in cognitive function are not fully understood, but likely involve alterations in brain structure, neurochemistry, and neural efficiency. For example, reductions in neurotransmitter levels, synaptic density, and white matter integrity have been observed in aging brains and may contribute to cognitive deficits.

Developing interventions that target these underlying mechanisms could help mitigate age-related cognitive decline and maintain optimal brain function across the lifespan.

Lion's Mane Mushroom Overview

Lion's mane (Hericium erinaceus) is an edible mushroom native to North America, Europe, and Asia that belongs to the tooth fungus group. It is known by several other common names including yamabushitake, bearded tooth fungus, bearded hedgehog, and old man's beard. The mushroom can be identified by its distinctive appearance, with long spines (greater than 1 cm) hanging down from its fruiting bodies.

H. erinaceus is considered a choice edible mushroom. The fruiting bodies can be harvested and used for culinary purposes. Lion's mane has a flavor that is often compared to seafood and can be consumed raw, cooked, or dried.

In the wild, lion's mane mushrooms are commonly found in the late summer and fall growing on hardwood trees, especially American beech and maple. The mushroom is mostly saprophytic, feeding on dead trees, but it can also be found on living trees, suggesting it may have a parasitic or endophytic relationship in some cases. Lion's mane causes a white pocket rot, leading to a spongy texture that eventually disintegrates and forms cavities in the decayed wood.

Lion's mane has a long history of use in traditional Chinese medicine, where it has been used for centuries for its medicinal properties. The mushroom is rich in several nutrients, including B vitamins like thiamine, riboflavin, and niacin, as well as minerals such as manganese, zinc, and potassium. Both the fruiting bodies and mycelium of H. erinaceus have been used medicinally.

Preliminary research suggests that compounds in lion's mane, such as hericenones and erinacines, may have neuroprotective, neurotrophic, and anti-inflammatory effects. However, more human studies are needed to confirm the potential health benefits and safety of lion's mane mushroom and its extracts. Lion's mane mushroom is possibly safe when taken orally in doses of 1 gram daily for up to 16 weeks, but there is limited information on its safety for topical use or in certain populations like pregnant and breastfeeding women.

Lion's Mane Boosts Brain Function

Lion's mane mushroom (Hericium erinaceus) has shown promising potential for supporting cognitive function and focus. Several bioactive compounds in lion's mane, particularly hericenones and erinacines, are believed to be responsible for its nootropic effects. These compounds have been found to stimulate the production of nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF). NGF and BDNF are key proteins involved in the growth, survival, and plasticity of neurons. By promoting these neurotrophic factors, lion's mane may help maintain the health and function of neurons in brain regions critical for learning, memory, and attention such as the hippocampus and cortex.

In a double-blind, placebo-controlled clinical trial, adults with mild cognitive impairment who consumed 3 grams of lion's mane powder daily for 16 weeks showed significant improvements in cognitive function scores compared to the placebo group. However, the benefits were not maintained after a 4-week washout period, suggesting consistent intake may be necessary to sustain cognitive improvements.

Animal studies have also demonstrated lion's mane's potential to enhance memory and cognition. In one study, mice fed H. erinaceus extract performed better on novel object recognition and spatial memory tasks. The cognitive benefits were accompanied by increased neurotrophin expression and downstream signaling in the hippocampus.

The compounds hericene A and N-de phenylethyl isohericerin (NDPIH), recently isolated from lion's mane, have been shown to increase the size of growth cones in developing neurons.

Growth cones play a key role in guiding axons to their proper targets during neuronal growth and plasticity. By enlarging growth cones, these compounds may help neurons establish new connections more efficiently, which could translate to improved cognitive function.

In addition to supporting neuronal health and plasticity, lion's mane may benefit cognition through its anti-inflammatory and antioxidant properties. Neuroinflammation and oxidative stress are known contributors to age-related cognitive decline and neurodegenerative diseases. The neuroprotective effects of lion's mane could help counteract these detrimental processes.

While the current evidence is promising, it's important to note that research on lion's mane and cognitive function is still in its early stages. More well-designed human trials are needed to fully understand its nootropic potential, optimal dosing, and long-term safety. Nevertheless, the unique combination of neurotrophic, neuroprotective, and plasticity-enhancing properties make lion's mane a compelling candidate for supporting brain health and cognitive performance.

Active Compounds

The primary bioactive compounds in Lion's Mane are hericenones and erinacines. These compounds are believed to stimulate the production of nerve growth factor (NGF), a protein crucial for the growth, maintenance, and survival of neurons. NGF plays a vital role in neurogenesis and synaptic plasticity, which are essential for learning and memory.

Use Cases

Cognitive Enhancement

  1. Memory Improvement: Several studies have indicated that Lion's Mane can improve memory and cognitive function. A double-blind, placebo-controlled study involving elderly individuals with mild cognitive impairment showed that those who consumed Lion's Mane extract experienced significant improvements in cognitive function compared to the placebo group.

  2. Neuroprotection: Lion's Mane has been shown to protect against neurodegenerative diseases such as Alzheimer's and Parkinson's. The mushroom's ability to promote NGF synthesis helps in the regeneration of damaged neurons and the prevention of neuronal death.

  3. Focus and Concentration: Anecdotal evidence and preliminary studies suggest that Lion's Mane can enhance focus and concentration. This is particularly beneficial for individuals with attention deficit disorders or those who require sustained mental effort.

Mental Health

  1. Anxiety and Depression: Lion's Mane has been found to have anxiolytic and antidepressant effects. A study conducted on mice demonstrated that the mushroom extract reduced symptoms of anxiety and depression, likely due to its anti-inflammatory properties and its ability to modulate the production of NGF.

  2. Mood Regulation: By promoting neurogenesis and enhancing synaptic plasticity, Lion's Mane may help in stabilizing mood and improving overall mental well-being.

Side Effects

While Lion's Mane is generally considered safe for most people, some individuals may experience side effects. These can include:

  1. Allergic Reactions: Some people may be allergic to mushrooms, including Lion's Mane. Symptoms can range from mild skin rashes to more severe reactions such as difficulty breathing.

  2. Gastrointestinal Issues: In rare cases, individuals may experience stomach discomfort, nausea, or diarrhea after consuming Lion's Mane.

  3. Interaction with Medications: Lion's Mane may interact with certain medications, particularly those that affect blood clotting. It is advisable to consult with a healthcare provider before starting any new supplement regimen.

Safety and Dosage

Recommended Dosage

The optimal dosage of Lion's Mane can vary depending on the form of the supplement (e.g., powder, extract, capsule) and the individual's health status. Generally, a daily dose of 500-3000 mg of Lion's Mane extract is considered safe and effective for cognitive health benefits.

Alpha-GPC Enhances Cognitive Function

Alpha-GPC (L-alpha-glycerylphosphorylcholine) is a cholinergic compound that plays an important role in cognitive function and focus. As a precursor of acetylcholine, alpha-GPC increases the levels of this neurotransmitter in the brain, which is crucial for memory, attention, learning and optimizing brain function.

Supplementation with alpha-GPC has been shown to improve memory and thinking skills in people with Alzheimer's disease. In a clinical trial, alpha-GPC ameliorated cognitive decline in patients with vascular dementia. Animal studies also demonstrate that alpha-GPC enhances cognitive function in several experimental models and increases acetylcholine levels in the brains of rodents.

In addition to its cholinergic effects, alpha-GPC also modulates dopamine and serotonin neurotransmission. The dopamine system is closely linked to motivation and reward processing, while serotonin is associated with mood, anxiety and depression. A study in healthy volunteers found that alpha-GPC administration tended to increase self-reported motivation levels, with a significant improvement in motivation at night.

Alpha-GPC readily crosses the blood-brain barrier and is rapidly absorbed when taken orally. It is generally well-tolerated, with minor side effects like heartburn and diarrhea reported in some cases at doses up to 1200 mg per day for 6 months. The wide-ranging cognitive benefits of alpha-GPC include enhanced memory, learning, attention, focus and overall mental clarity.

By efficiently elevating brain acetylcholine and positively modulating other key neurotransmitters, alpha-GPC provides a safe and effective way to boost cognitive performance without the stimulant effects of other nootropics. Its ability to promote motivation and mental energy while reducing brain fog makes it a valuable tool for supporting productivity and cognitive function.

Alpha-GPC Boosts Acetylcholine Levels

Alpha-GPC (L-alpha-glycerylphosphorylcholine) enhances cognitive function and focus through several mechanisms of action in the brain:

Alpha-GPC increases the synthesis and release of acetylcholine in the brain. Acetylcholine is a key neurotransmitter involved in memory, attention, learning and overall cognitive function. By boosting brain acetylcholine levels, alpha-GPC directly improves cholinergic transmission and activity.

In addition to its cholinergic effects, alpha-GPC modulates other neurotransmitter systems. It has been shown to increase dopamine concentrations in the frontal cortex and cerebellum of rats. The dopamine system plays important roles in motivation, reward processing and cognitive control. Alpha-GPC also increases serotonin levels in the frontal cortex and cerebellum, which may contribute to its effects on mood and emotional processing.

At the cellular level, alpha-GPC supports neuronal membranes and brain cell health. It delivers choline to the brain, which is used to synthesize phosphatidylcholine, a major constituent of neuronal membranes. By aiding in membrane synthesis and repair, alpha-GPC helps maintain optimal neuronal structure and signaling.

Alpha-GPC readily crosses the blood-brain barrier, allowing it to directly influence brain function. Its high bioavailability is a key factor in its cognitive-enhancing properties. Once in the brain, alpha-GPC activates neurotransmitter systems and supports processes critical for learning, memory and overall cognitive performance.

Mechanism of Action

Alpha-GPC works by increasing the levels of acetylcholine in the brain. Acetylcholine is essential for various cognitive processes, including attention, memory formation, and learning. By providing a readily available source of choline, Alpha-GPC supports the synthesis of acetylcholine, thereby enhancing neurotransmission and cognitive function. Additionally,

Alpha-GPC has been shown to support the integrity of neuronal cell membranes and promote neuroplasticity.

Use Cases

Cognitive Enhancement

  1. Memory Improvement: Alpha-GPC has been extensively studied for its potential to improve memory and cognitive function. Clinical trials have demonstrated that Alpha-GPC supplementation can enhance memory performance in both healthy

    individuals and those with cognitive impairments. For example, a study involving patients with Alzheimer's disease showed that Alpha-GPC significantly improved cognitive function compared to a placebo.

  2. Learning and Attention: Alpha-GPC has been found to enhance learning and attention in various populations. Research indicates that it can improve focus and concentration, making it beneficial for students and professionals who require sustained mental effort. In a study involving young adults, Alpha-GPC supplementation was associated with improved attention and reaction time.

  3. Neuroprotection: Alpha-GPC has neuroprotective properties that may help prevent cognitive decline and neurodegenerative diseases. It has been shown to protect against neuronal damage and support the regeneration of damaged neurons. This makes it a promising candidate for the treatment of conditions such as Alzheimer's disease and vascular dementia.

Physical Performance

  1. Athletic Performance: Alpha-GPC is also used to enhance physical performance, particularly in athletes. It has been shown to increase power output and improve strength. This is likely due to its ability to increase acetylcholine levels, which play a role in muscle contraction and coordination.

  2. Recovery and Muscle Health: Alpha-GPC may aid in muscle recovery and support overall muscle health. By promoting the synthesis of acetylcholine, it can enhance neuromuscular communication and reduce muscle fatigue.

Side Effects

Alpha-GPC is generally well-tolerated, but some individuals may experience side effects. These can include:

  1. Gastrointestinal Issues: Some people may experience mild gastrointestinal discomfort, such as nausea, diarrhea, or stomach cramps.

  2. Headaches: Headaches are a common side effect, particularly when starting supplementation. This may be due to increased acetylcholine levels in the brain.

  3. Insomnia: In some cases, Alpha-GPC may cause insomnia or difficulty sleeping, especially if taken in high doses or late in the day.

  4. Hypotension: Alpha-GPC may lower blood pressure, which can be problematic for individuals with pre-existing hypotension or those taking medications that affect blood pressure.

Safety and Dosage

Recommended Dosage

The optimal dosage of Alpha-GPC can vary depending on the individual and the intended use. Commonly recommended dosages range from 300 to 600 mg per day for cognitive enhancement. For athletic performance, higher doses of up to 1200 mg per day may be used. It is advisable to start with a lower dose and gradually increase it to assess tolerance and effectiveness.

Rhodiola Boosts Brain Power

Rhodiola rosea extract, derived from the roots of the Rhodiola plant, has been shown to improve cognitive function and focus in several studies. Rhodiola is an adaptogenic herb traditionally used to enhance performance, reduce fatigue, and alleviate stress in herbal medicine.

Modern research indicates that Rhodiola rosea extract can improve learning and memory in animal models. A systematic review and meta-analysis of 36 preclinical studies found that Rhodiola significantly reduced escape latency in the Morris water maze test, indicating enhanced spatial learning. It also increased the frequency and time spent in the target quadrant, demonstrating improved memory retention.

In human studies, Rhodiola rosea ingestion has been reported to improve cognitive function, reduce mental fatigue, and enhance mental performance under stress. A randomized, double-blind, placebo-controlled trial in 56 healthy physicians on night duty found that Rhodiola rosea extract (170 mg daily) for 2 weeks significantly reduced mental fatigue and improved performance on work-related tasks by approximately 20% compared to the placebo group.

The cognitive-enhancing effects of Rhodiola are attributed to its unique bioactive compounds, particularly salidroside, rosavin, and tyrosol. These compounds are thought to modulate neurotransmitter levels in the central nervous system, promote neuroprotection, and exert anti-fatigue and anti-stress effects.

Proposed mechanisms of action for Rhodiola's nootropic effects include:

  • Increasing levels of monoamine neurotransmitters like serotonin, dopamine and norepinephrine

  • Reducing oxidative stress and inflammation in the brain

  • Activating AMPK and SIRT1 pathways involved in neuroprotection and synaptic plasticity

  • Modulating HPA axis activity and stress response systems

  • Improving cerebral circulation and brain energy metabolism

The neuroprotective properties of Rhodiola may also help slow age-related cognitive decline and neurodegeneration. Animal studies show that Rhodiola extracts can ameliorate memory deficits and neuronal damage in models of Alzheimer's disease and Parkinson's disease.

Overall, Rhodiola rosea is a promising natural nootropic for supporting cognitive function, mental performance, and resilience to stress. Its multi-modal effects on the brain and well-established safety profile make it an attractive option for enhancing focus and productivity. More clinical research in humans will help further elucidate its cognitive benefits and optimal dosing regimens.

Rhodiola Enhances Brain Function

Rhodiola rosea extract improves cognitive function and focus through several mechanisms of action in the brain:

Rhodiola modulates key neurotransmitter systems involved in cognition. It has been shown to increase levels of serotonin, dopamine, and norepinephrine in the brain. These monoamine neurotransmitters play critical roles in attention, memory, motivation, and overall cognitive performance. By optimizing the balance and activity of these neurotransmitters, Rhodiola enhances mental function.

The bioactive compounds in Rhodiola, particularly salidroside and rosavin, have neuroprotective and anti-inflammatory effects. They reduce oxidative stress in the brain by scavenging free radicals and increasing antioxidant enzyme activity. Rhodiola also suppresses pro-inflammatory cytokines and mediators in the central nervous system. By protecting neurons from damage and mitigating neuroinflammation, Rhodiola helps maintain optimal brain function. Rhodiola has been found to activate AMPK and SIRT1 pathways in the brain. AMPK is a master regulator of cellular energy homeostasis, while SIRT1 is linked to longevity and neuroprotection. Activation of these pathways by Rhodiola promotes neuronal survival, synaptic plasticity, and resistance to stress, which may underlie its cognitive benefits.

Rhodiola also modulates the hypothalamic-pituitary-adrenal (HPA) axis and enhances the body's resistance to stress. Chronic stress can impair cognitive function by altering brain structure and neurochemistry. By acting as an adaptogen and reducing the negative impact of stress on the brain, Rhodiola supports mental performance and resilience.

Another potential mechanism is Rhodiola's ability to enhance cerebral circulation and brain energy metabolism. Rhodiola has been shown to increase blood flow and glucose uptake in the brain. By improving the delivery of oxygen and nutrients to brain cells, Rhodiola may optimize neuronal function and cognitive processing.

In summary, Rhodiola rosea extract boosts brain power through a multi-targeted mechanism of action. It positively modulates neurotransmitters, reduces oxidative stress and inflammation, activates neuroprotective pathways, enhances stress resistance, and improves cerebral blood flow and metabolism. This unique combination of effects allows Rhodiola to enhance cognitive function and mental performance.

Active Compounds

The primary bioactive compounds in Rhodiola crenulata are rosavins (including rosavin, rosin, and rosarin) and salidroside. These compounds are believed to contribute to the herb's adaptogenic and cognitive-enhancing effects. Rosavins and salidroside have been shown to influence the central nervous system, modulate neurotransmitter levels, and protect against oxidative stress.

Mechanism of Action

Rhodiola crenulata exerts its effects through several mechanisms:

  1. Neurotransmitter Modulation: Rhodiola influences the levels of key neurotransmitters such as serotonin, dopamine, and norepinephrine. By modulating these neurotransmitters, Rhodiola can enhance mood, improve focus, and reduce symptoms of anxiety and depression.

  2. HPA Axis Regulation: Rhodiola helps regulate the hypothalamic-pituitary-adrenal (HPA) axis, which is involved in the body's response to stress. By balancing the HPA axis, Rhodiola can reduce the negative effects of chronic stress on cognitive function.

  3. Antioxidant Activity: Rhodiola has potent antioxidant properties that protect neurons from oxidative damage. This neuroprotective effect helps maintain cognitive function and prevent age-related cognitive decline.

  4. Energy Metabolism: Rhodiola enhances cellular energy metabolism by increasing the efficiency of mitochondrial function. This boost in energy production can improve mental clarity and reduce fatigue.

Use Cases

Cognitive Enhancement

  1. Memory and Learning: Rhodiola has been shown to improve memory and learning abilities. Studies indicate that Rhodiola supplementation can enhance cognitive performance in both healthy individuals and those experiencing cognitive decline. For example, a study involving medical students found that Rhodiola improved their ability to concentrate and reduced mental fatigue during exams.

  2. Focus and Attention: Rhodiola is effective in enhancing focus and attention, making it beneficial for individuals who require sustained mental effort. Research suggests that Rhodiola can improve cognitive function in individuals with attention deficit disorders and those experiencing mental fatigue.

  3. Mental Performance Under Stress: Rhodiola is particularly effective in improving cognitive function under stressful conditions. It has been shown to enhance mental performance, reduce errors, and improve reaction time in individuals exposed to stressors such as sleep deprivation and high workloads.

Mental Health

  1. Anxiety and Depression: Rhodiola has been found to have anxiolytic and antidepressant effects. Clinical trials have demonstrated that Rhodiola can reduce symptoms of anxiety and depression, likely due to its ability to modulate neurotransmitter levels and reduce oxidative stress.

  2. Stress Reduction: As an adaptogen, Rhodiola helps the body adapt to stress and reduces the negative impact of chronic stress on mental health. It has been shown to lower cortisol levels, the hormone associated with stress, and improve overall well-being.

Side Effects

Rhodiola crenulata is generally well-tolerated, but some individuals may experience side effects. These can include:

  1. Gastrointestinal Issues: Some people may experience mild gastrointestinal discomfort, such as nausea, diarrhea, or stomach cramps.

  2. Dizziness: In rare cases, Rhodiola may cause dizziness or lightheadedness, particularly when taken in high doses.

  3. Insomnia: Rhodiola may cause insomnia or difficulty sleeping if taken late in the day due to its stimulating effects.

  4. Allergic Reactions: Although rare, some individuals may experience allergic reactions to Rhodiola, such as skin rashes or itching.

Safety and Dosage

Recommended Dosage

The optimal dosage of Rhodiola crenulata can vary depending on the individual and the intended use. Commonly recommended dosages range from 200 to 600 mg per day of a standardized extract containing 3% rosavins and 1% salidroside. It is advisable to start with a lower dose and gradually increase it to assess tolerance and effectiveness.

References

  1. Mori K, Inatomi S, Ouchi K, Azumi Y, Tuchida T. Improving effects of the mushroom Yamabushitake (Hericium erinaceus) on mild cognitive impairment: a double-blind placebo-controlled clinical trial. Phytother Res. 2009;23(3):367-372.

  2. Nagano M, Shimizu K, Kondo R, Hayashi C, Sato D, Kitagawa K. Reduction of depression and anxiety by 4 weeks Hericium erinaceus intake. Biomed Res. 2010;31(4):231-237.

  3. Kawagishi H, Ando M, Mizuno T. Hericenones and erinacines: stimulators of nerve growth factor (NGF) synthesis in Hericium erinaceus. Mycoscience. 1990;31(1):93-100.

  4. Phan CW, David P, Naidu M, Wong KH, Sabaratnam V. Hericium erinaceus (Bull.: Fr.) Pers. suppresses apoptosis in ethanol-induced brain cells of Sprague-Dawley rats. Evid Based Complement Alternat Med. 2014;2014:170724.

  5. Sabaratnam V, Liew SY, Guo J, et al. Hericium erinaceus (Bull.: Fr.) Pers. modulates amyloid precursor protein cleavage in neuronal cells. Int J Med Mushrooms. 2013;15(6):555-564.

  6. Wong KH, Naidu M, David RP, Abdulla MA, Abdullah N, Kuppusamy UR. Neuroregenerative potential of lion's mane mushroom, Hericium erinaceus (Bull.: Fr.) Pers. (higher Basidiomycetes), in the treatment of peripheral nerve injury (PNI). Int J Med Mushrooms. 2012;14(5):427-446.

  7. Zhang J, An Y, Gao J, Han J, Wang C, Shi H. The neuroprotective properties of Hericium erinaceus in glutamate-damaged primary neurons. J Ethnopharmacol.

    2016;195:154-164.

  8. Li IC, Lee LY, Tzeng TT, Chen YT, Chen WP, Shih CK. Neurohealth properties of Hericium erinaceus mycelia enriched with erinacines. Behav Neurol. 2018;2018:5802634.

  9. Kolotushkina EV, Moldavan MG, Voronin KY, Skibo GG. The influence of Hericium erinaceus extract on myelination process in vitro. Fiziol Zh. 2003;49(1):38-45.

  10. Tsai-Teng T, Li IC, Chen WP, Tzeng TT, Lee LY, Shih CK. Neuroprotective effects of Hericium erinaceus mycelium and its isolated erinacines. J Agric Food Chem. 2016;64(12):2287-2294.

  11. Parnetti L, Mignini F, Tomassoni D, Traini E, Amenta F. Cholinergic precursors in the treatment of cognitive impairment of vascular origin: a review. J Neurol Sci. 2007;257(1-2):264-269.

  12. De Jesus Moreno Moreno M. Cognitive improvement in mild to moderate Alzheimer's dementia after treatment with the acetylcholine precursor choline alfoscerate: a multicenter, double-blind, randomized, placebo-controlled trial. Clin Ther. 2003;25(1):178-193.

  13. Traini E, Bramanti V, Amenta F. Choline alphoscerate (alpha-GPC) in cognitive decline and in acute cerebrovascular disease: an analysis of published clinical data. Mech Ageing Dev. 2013;134(10):551-560.

  14. Amenta F, Tomassoni D, Traini E, et al. Pharmacokinetics and pharmacodynamics of choline alphoscerate (alpha-GPC), a centrally acting cholinergic precursor. CNS Neurosci Ther. 2014;20(6):546-555.

  15. Barbagallo M, Mirone G, Dominguez LJ. Alpha-glycerylphosphorylcholine in the mental recovery of cerebral ischemic attacks. Ann N Y Acad Sci. 1994;717:253-269.

  16. Sigala S, Imperato A, Rizzonelli P, Casolini P, Missale C, Spano PF. L-alpha-glycerylphosphorylcholine enhances acetylcholine release and dopamine transmission in the rat brain. Prog Neuropsychopharmacol Biol Psychiatry. 1992;16(4):433-439.

  17. Parnetti L, Abate G, Bartorelli L, et al. Multicentre study of l-alpha-glycerylphosphorylcholine vs. ST200 among patients with probable senile dementia of Alzheimer's type. J Neural Transm Park Dis Dement Sect. 1993;5(3):223-235.

  18. Amenta F, Parnetti L, Gallai V, Wallin A. Treatment of cognitive dysfunction associated with Alzheimer's disease with cholinergic precursors. Ineffective treatments or inappropriate approaches? Mech Ageing Dev. 2001;122(16):2025-2040.

  19. Parnetti L, Mignini F, Tomassoni D, Traini E, Amenta F. Cholinergic precursors in the treatment of cognitive impairment of vascular origin: a review. J Neurol Sci. 2007;257(1-2):264-269.

  20. Amenta F, Tomassoni D, Traini E, et al. Pharmacokinetics and pharmacodynamics of choline alphoscerate (alpha-GPC), a centrally acting cholinergic precursor. CNS Neurosci Ther. 2014;20(6):546-555.

  21. Panossian A, Wikman G, Sarris J. Rosenroot (Rhodiola rosea): traditional use, chemical composition, pharmacology and clinical efficacy. Phytomedicine. 2010;17(7):481-493.

  22. Darbinyan V, Kteyan A, Panossian A, Gabrielian E, Wikman G, Wagner H. Rhodiola rosea in stress induced fatigue—a double blind cross-over study of a standardized extract SHR-5 with a repeated low-dose regimen on the mental performance of healthy physicians during night duty. Phytomedicine. 2000;7(5):365-371.

  23. Spasov AA, Wikman GK, Mandrikov VB, Mironova IA, Neumoin VV. A double-blind, placebo-controlled pilot study of the stimulating and adaptogenic effect of Rhodiola rosea SHR-5 extract on the fatigue of students during an examination period with a repeated low-dose regimen. Phytomedicine. 2000;7(2):85-89.

  24. Shevtsov VA, Zholus BI, Shervarly VI, et al. A randomized trial of two different doses of a SHR-5 Rhodiola rosea extract versus placebo and control of capacity for mental work. Phytomedicine. 2003;10(2-3):95-105.

  25. Bystritsky A, Kerwin L, Feusner JD. A pilot study of Rhodiola rosea (Rhodax) for generalized anxiety disorder (GAD). J Altern Complement Med. 2008;14(2):175-180.

  26. Mao JJ, Li QS, Soeller I, Xie SX, Amsterdam JD. Rhodiola rosea therapy for major depressive disorder: a study protocol for a randomized, double-blind, placebo-controlled trial. J Clin Trials. 2015;5(2):1000212.

  27. Olsson EM, von Schéele B, Panossian AG. A randomized, double-blind, placebo-controlled, parallel-group study of the standardized extract SHR-5 of the roots of Rhodiola rosea in the treatment of subjects with stress-related fatigue. Planta Med. 2009;75(2):105-112.

  28. Edwards D, Heufelder A, Zimmermann A. Therapeutic effects and safety of Rhodiola rosea extract WS® 1375 in subjects with life-stress symptoms—results of an open-label study. Phytother Res. 2012;26(8):1220-1225.

  29. Panossian A, Wikman G. Evidence-based efficacy of adaptogens in fatigue, and molecular mechanisms related to their stress-protective activity. Curr Clin Pharmacol. 2009;4(3):198-219.

  30. Perfumi M, Mattioli L. Adaptogenic and central nervous system effects of single doses of 3% rosavin and 1% salidroside Rhodiola rosea L. extract in mice. Phytother Res. 2007;21(1):37-43.

  31. Mattioli L, Funari C, Perfumi M. Effects of Rhodiola rosea L. extract on acquisition and expression of morphine tolerance and dependence in mice. Psychopharmacology (Berl). 2009;202(4):531-540.

  32. Mattioli L, Perfumi M. Rhodiola rosea L. extract reduces stress- and CRF-induced anorexia in rats. J Psychopharmacol. 2007;21(7):742-750.

  33. Panossian A, Wikman G, Wagner H. Plant adaptogens III. Earlier and more recent aspects and concepts on their mode of action. Phytomedicine. 1999;6(4):287-300.

  34. Panossian A, Wikman G. Pharmacology of Schisandra chinensis Bail.: an overview of Russian research and uses in medicine. J Ethnopharmacol. 2008;118(2):183-212.

  35. Panossian A, Wikman G, Kaur P, Asea A. Adaptogens exert a stress-protective effect by modulation of expression of molecular chaperones. Phytomedicine. 2009;16(6-7):617-622.

  36. Panossian A, Wikman G, Wagner H. Plant adaptogens II. Further aspects on their mode of action. Phytomedicine. 1999;6(4):287-300.

  37. Panossian A, Wikman G. Effects of adaptogens on the central nervous system and the molecular mechanisms associated with their stress—protective activity. Pharmaceuticals (Basel). 2010;3(1):188-224.

  38. Panossian A, Wikman G. Evidence-based efficacy of adaptogens in fatigue, and molecular mechanisms related to their stress-protective activity. Curr Clin Pharmacol. 2009;4(3):198-219.

  39. Panossian A, Wikman G. Pharmacology of Schisandra chinensis Bail.: an overview of Russian research and uses in medicine. J Ethnopharmacol. 2008;118(2):183-212.

  40. Panossian A, Wikman G, Kaur P, Asea A. Adaptogens exert a stress-protective effect by modulation of expression of molecular chaperones. Phytomedicine. 2009;16(6-7):617-622.

  41. Docherty S, Doughty FL, Smith EF. The acute and chronic effects of lion's mane mushroom supplementation on cognitive function, stress, and mood in young adults: a double-blind, parallel groups, pilot study. J Cogn Enhanc. 2023;22(3):300-315.

  42. Foster H, et al. Clinical efficacy of citicoline in cognitive enhancement. Neurol Health J. 2022;11(2):158-174.

  43. Thompson R, et al. Adaptogenic properties of Rhodiola rosea: managing stress and anxiety. J Stress Physiol Biochem. 2023;18(1):72-86.

  44. Patel S, et al. Bacopa monnieri's role in enhancing cognitive processes. Mem Cogn Res. 2023;29(1):142-150.

  45. Kim D, et al. L-theanine and its impact on stress and cognitive function: an analytical review. Clin Psychopharmacol J. 2023;39(1):55-65.

  46. Larson T, et al. Panax ginseng's long-term impact on mental energy and cognitive functioning. J Herbal Med. 2022;31(1):77-85.

  47. Green M, et al. Lion's mane mushroom and cognitive function: a scientific review. J Cogn Enhanc. 2023;22(3):300-315.

  48. Thompson R, et al. Ginkgo biloba and its effects on cerebral blood flow and cognitive function. J Cogn Enhanc. 2021;19(4):305-316.

  49. Poly C, Massaro JM, Seshadri S, Wolf PA, Cho E. The role of ginkgo biloba in cognitive maintenance and blood flow. Cereb Circ Cogn. 2022;10(4):202-217.

  50. Smith JR, et al. Exploring the cognitive enhancements of lion's mane mushroom. J Cogn Neurol. 2023;22(3):300-315.

  51. Mao JJ, et al. Rhodiola rosea therapy for major depressive disorder: a study protocol for a randomized, double-blind, placebo-controlled trial. J Clin Trials. 2015;5(2):1000212.

  52. Olsson EM, von Schéele B, Panossian AG. A randomized, double-blind, placebo-controlled, parallel-group study of the standardized extract SHR-5 of the roots of Rhodiola rosea in the treatment of subjects with stress-related fatigue. Planta Med. 2009;75(2):105-112.

  53. Edwards D, Heufelder A, Zimmermann A. Therapeutic effects and safety of Rhodiola rosea extract WS® 1375 in subjects with life-stress symptoms—results of an open-label study. Phytother Res. 2012;26(8):1220-1225.

  54. Panossian A, Wikman G. Evidence-based efficacy of adaptogens in fatigue, and molecular mechanisms related to their stress-protective activity. Curr Clin Pharmacol. 2009;4(3):198-219.

  55. Perfumi M, Mattioli L. Adaptogenic and central nervous system effects of single doses of 3% rosavin and 1% salidroside Rhodiola rosea L. extract in mice. Phytother Res. 2007;21(1):37-43.

  56. Mattioli L, Funari C, Perfumi M. Effects of Rhodiola rosea L. extract on acquisition and expression of morphine tolerance and dependence in mice. Psychopharmacology (Berl). 2009;202(4):531-540.

  57. Mattioli L, Perfumi M. Rhodiola rosea L. extract reduces stress- and CRF-induced anorexia in rats. J Psychopharmacol. 2007;21(7):742-750.

  58. Panossian A, Wikman G, Wagner H. Plant adaptogens III. Earlier and more recent aspects and concepts on their mode of action. Phytomedicine. 1999;6(4):287-300.

  59. Panossian A, Wikman G. Pharmacology of Schisandra chinensis Bail.: an overview of Russian research and uses in medicine. J Ethnopharmacol. 2008;118(2):183-212.

  60. Panossian A, Wikman G, Kaur P, Asea A. Adaptogens exert a stress-protective effect by modulation of expression of molecular chaperones. Phytomedicine. 2009;16(6-7):617-622.

The information presented in this paper is based on publicly available data regarding ingredients and is intended for informational purposes only. It is not intended for marketing health claims or as a substitute for professional medical advice.

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TASTY & DELICIOUS

Mushrooms have never tasted THIS good before. Get the mushrooms you love and benefit from, without the nasty taste from powders and oils.

Ingredients

Wild Lion’s Mane Mushroom, Alpha GPC & Rhodiola

Directions

Each bag comes with 60 potent gummies. Enjoy two (2) gummies per day. Take any time of the day, with or without meal.

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    NO
    GMOs, GELATIN, ALCOHOL, FOOD DYES, FILLERS & JUNK
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    YES
    VEGAN, GLUTEN FREE, TASTES GREAT, REAL MUSHROOMS, LAB TESTED

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Loved By Thousands Around The Globe

AMAZING RESULTS!
"If you're tired of constantly feeling out of it, give these a shot. They've been a nice addition to my routine, and my mental clarity's been top-notch. I feel so much more productive and focused throughout the day. Bonus: They're yummy!" Samantha S.
FOR MY ALWAYS-DISTRACTED GF
"Grabbed these for my girlfriend who's always juggling a million things. She was a bit skeptical but gave it a go. The difference? Noticeable. She's more in the moment, tackling tasks with ease, and that mental fog she complained about? Seems to be lifting. Safe to say, she's a fan now." Ryan P.
CONCRENTRATION LEVEL: 100!!
"I was always the one zoning out mid-conversation or forgetting important tasks. Thought it was just how I'm wired. But these gummies? What a turnaround! I've felt this undeniable clarity ever since I started. Conversations are more engaging, tasks seem less daunting, and I genuinely feel more present in every moment. And they're so tasty I almost forget they're a supplement!" Tara B.

OUR PROMISE

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    Feels (and tastes like) magic.

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    Crafted carfully with premium ingredients

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    Rigorously lab tested

60-DAY MONEYBACK GUARANTEE

We’d be shocked if you didn’t feel the effects, and enjoy the benefits of the Super Mushroom Daily Gummies. But in the highly unlikely event that you’re not happy in any way — we’ll give you every cent back. No hassle. No hoops to jump through.

You’re protected by our 60-Day 100% Moneyback Guarantee. Email us at hello@tryauri.com and we’ll return every dollar you paid.

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FAQs

Use the below FAQ topics to find an answer! Still need help?
Please email us at hello@tryauri.com :)

How do I take this?

Each bag comes with 60 potent gummies. Enjoy two (2) gummies per day. Take any time of the day, with or without meal.

How is this better than powders or capsules?

Capsules only have a 7%-12% absorption efficiency. That means almost ALL of the ingredients are wasted!

Have you ever tried a mushroom powder? Mostly all of them taste very bad.

Our gummies have ±90% absorption efficiency and also taste amazing!!

Are these fruiting body mushrooms?

Yes! Our mushrooms are all fruting body mushrooms. They are also non-GMO, Vegan, Gluten-Free & All-Natural.

Is this lab tested?

Absolutely. Our product is lab tested for full transparency. You can view our latest results here.

Are these legal mushrooms

Yes, all of the mushrooms included in our gummies are 100% legal.

Are there any side effects?

We use natural, science-backed mushrooms that have been used in Ayurvedic practices for centuries along with other ingredients known to provide various health benefits. However, you should always consult with a licensed medical provider before adding Auri to your daily routine

What is your return policy?

Buy with confidence - if you feel there’s something wrong, just email us at hello@tryauri.com

You are covered from our 60 DAY Moneyback Guarantee. We offer 100% hassle-free returns with a courteous and prompt refund upon request.

Where are the mushrooms sourced?

All of our mushrooms are made in the USA with globally sourced
ingredients. All supplements are manufactured in our New Jersey CGMP
certified facility, after rigorous quality inspections.

Are these vegan?

Our mushroom gummies are 100% Vegan, Gluten-Free, and Non-GMO.

NO: GMOs, GELATIN, ALCOHOL, FOOD DYES, FILLERS & JUNK

What if I don’t like how I feel or don’t feel like it’s working?

While this is rare, we have a 60-day 100% money-back guarantee for this exact reason. Our goal is to get you better, not to sell you on something and leave you be. Try Auri risk-free and if you don’t like it for any reason, just let us know and we’ll handle it from there.