Amla

Amla (Indian Gooseberry) is a potent antioxidant-rich fruit containing vitamin C, polyphenols, and tannins that neutralize free radicals while enhancing endogenous antioxidant enzymes, with clinical evidence supporting its ability to reduce inflammation through NF-κB inhibition, improve lipid profiles, enhance insulin sensitivity, and protect endothelial function, typically supplemented at 500-1,000mg daily of dried fruit powder or standardized extract.

Alternative Names: Indian Gooseberry, Phyllanthus emblica, Emblica officinalis, Amalaki, Dhatriphala, Emblic Myrobalan

Categories: Fruit Extract, Ayurvedic Herb, Antioxidant

Primary Longevity Benefits


  • Potent antioxidant activity
  • Anti-inflammatory effects
  • Immune system support
  • Cellular protection

Secondary Benefits


  • Cardiovascular health
  • Blood glucose regulation
  • Digestive health
  • Liver protection
  • Hair and skin health
  • Cognitive function
  • Eye health
  • Respiratory support

Mechanism of Action


Amla (Indian Gooseberry) exerts its diverse biological effects through multiple mechanisms, primarily centered around its exceptional antioxidant and anti-inflammatory properties. The fruit contains a rich array of bioactive compounds, including vitamin C, polyphenols, tannins, flavonoids, and various phytochemicals that work synergistically. Amla’s most notable mechanism is its potent antioxidant activity, which neutralizes free radicals and reactive oxygen species (ROS) that contribute to cellular damage and aging. Unlike isolated antioxidants, amla’s complex phytochemical profile provides a cascade of antioxidant protection through both direct scavenging of free radicals and enhancement of endogenous antioxidant systems.

It upregulates antioxidant enzymes such as superoxide dismutase (SOD), catalase, and glutathione peroxidase, creating a multi-layered defense against oxidative stress. Amla’s anti-inflammatory effects stem from its ability to inhibit pro-inflammatory cytokines and mediators. It suppresses nuclear factor-kappa B (NF-κB) activation, a master regulator of inflammation, and reduces the production of inflammatory molecules like tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and cyclooxygenase-2 (COX-2). This anti-inflammatory action contributes to its benefits for various chronic conditions.

In cardiovascular health, amla improves lipid profiles by enhancing cholesterol metabolism and inhibiting HMG-CoA reductase, the rate-limiting enzyme in cholesterol synthesis. It also protects endothelial function, reduces platelet aggregation, and maintains vascular integrity through its antioxidant effects. For blood glucose regulation, amla enhances insulin sensitivity and secretion while inhibiting alpha-glucosidase and alpha-amylase enzymes, which slows carbohydrate digestion and reduces postprandial glucose spikes. It also protects pancreatic beta cells from oxidative damage.

Amla supports digestive health through multiple mechanisms, including stimulating digestive enzyme secretion, protecting the gastric mucosa, promoting beneficial gut microbiota, and exhibiting mild laxative effects through its fiber content. Its hepatoprotective effects involve scavenging free radicals in liver tissue, enhancing detoxification enzymes, and reducing lipid peroxidation. For immune function, amla enhances both innate and adaptive immunity by increasing natural killer cell activity, macrophage function, and lymphocyte proliferation. Its high vitamin C content supports immune cell function and antibody production.

In skin and hair health, amla promotes collagen synthesis, inhibits collagenase and elastase enzymes that break down skin proteins, and provides photoprotection against UV damage. It also strengthens hair follicles and may inhibit 5-alpha-reductase, an enzyme involved in hair loss. Amla’s neuroprotective effects stem from its ability to reduce oxidative stress in neural tissues, modulate neurotransmitter systems, and potentially inhibit acetylcholinesterase, supporting cognitive function. Additionally, amla exhibits antimicrobial properties against various pathogens, supports respiratory health through anti-inflammatory and bronchodilatory effects, and provides adaptogenic benefits by modulating the stress response and supporting adrenal function.

Optimal Dosage


Disclaimer: The following dosage information is for educational purposes only. Always consult with a healthcare provider before starting any supplement regimen, especially if you have pre-existing health conditions, are pregnant or nursing, or are taking medications.

The typical dosage range for amla (Indian gooseberry) supplements is 500-1,000 mg of dried fruit powder or standardized extract daily. For fresh amla fruit, 1-2 fruits daily are traditionally recommended. There is no established Recommended Dietary Allowance (RDA) for amla as it is not classified as an essential nutrient. Dosages may vary based on the specific form, concentration, and intended health benefit.

By Condition

Condition Dosage Notes
General antioxidant support 500 mg of dried fruit powder or standardized extract daily Can be taken in divided doses with meals for better tolerance.
Cardiovascular health/Cholesterol management 500-1,000 mg of standardized extract daily Clinical studies showing lipid-lowering effects typically used 500 mg twice daily of standardized extract for 12 weeks.
Blood glucose regulation 1,000-3,000 mg of dried fruit powder daily Studies showing benefits for glycemic control used 1-3 g daily, often divided into 2-3 doses with meals.
Digestive health 500-1,000 mg of dried fruit powder daily Traditional Ayurvedic practice recommends taking before or after meals for digestive support.
Immune support 500-1,000 mg daily May be increased to 1,500 mg during periods of increased immune challenge.
Skin and hair health 500-1,000 mg daily Consistent use for at least 8-12 weeks is typically recommended to observe benefits.
Liver support 750-1,500 mg daily Often used in divided doses for hepatoprotective effects.
Cognitive function 500-1,000 mg daily Limited clinical data; dosage based on traditional use and preliminary studies.

By Age Group

Age Group Dosage Notes
Children (under 12 years) Not recommended unless prescribed by a healthcare provider Safety and appropriate dosing not well established in children.
Adolescents (12-17 years) 250-500 mg daily, if recommended by healthcare provider Limited research in this age group; use with caution and medical supervision.
Adults (18-65 years) 500-1,000 mg daily Most research has been conducted in this age group.
Older adults (over 65 years) 500-1,000 mg daily, starting with lower doses May be more sensitive to effects; start with lower doses and increase gradually if needed.
Pregnant or breastfeeding women Not recommended unless prescribed by healthcare provider Insufficient safety data; traditional use in some cultures but medical supervision is advised.

Bioavailability


Absorption Rate

The bioavailability of amla’s active compounds varies significantly depending on the form and preparation method. The vitamin C content in amla has unique stability compared to synthetic vitamin C, with studies suggesting

it remains bioavailable even in conditions that would degrade isolated ascorbic acid. The polyphenols, tannins, and other phytochemicals in amla have moderate bioavailability, estimated between 10-40% depending on the specific compound and individual factors. Standardized extracts typically offer enhanced bioavailability compared to raw fruit powder due to concentration of active compounds and sometimes improved delivery systems.

Enhancement Methods

Consuming amla with a small amount of healthy fat (such as ghee in traditional preparations) may enhance absorption of fat-soluble compounds, Combining with black pepper extract (piperine) can increase bioavailability of certain phytochemicals through inhibition of metabolizing enzymes, Liposomal formulations encapsulate amla compounds in phospholipid bilayers, potentially improving absorption, Fermented amla preparations may enhance bioavailability through breakdown of complex compounds into more absorbable forms, Taking with vitamin C-rich foods may have synergistic effects and improve overall antioxidant absorption, Standardized extracts with higher concentrations of active compounds generally offer better bioavailability than raw powder, Consuming with meals containing protein may enhance absorption of certain compounds, Traditional Ayurvedic processing methods like triphala formulation (combining with other herbs) may enhance therapeutic effects

Timing Recommendations

For general health benefits, amla supplements can be taken at any time of day, though taking with food may reduce potential mild gastrointestinal effects in sensitive individuals. For blood glucose management, taking 15-30 minutes before meals may help reduce post-meal glucose spikes. When used for digestive support, traditional Ayurvedic practice recommends taking amla before meals to stimulate digestive enzymes or after meals to soothe the digestive tract. For cardiovascular benefits, consistent daily timing is more important than specific time of day.

If using multiple doses, spreading them throughout the day (morning and evening) may provide more consistent blood levels of active compounds. For sleep quality improvement, taking the last dose in the early evening rather than right before bed is recommended. When using amla for immune support during illness, more frequent smaller doses throughout the day may be beneficial. If experiencing any acid reflux or digestive discomfort, taking with or shortly after meals rather than on an empty stomach is advised.

Safety Profile


Safety Rating i

4High Safety

Side Effects

  • Mild gastrointestinal discomfort (uncommon)
  • Loose stools or diarrhea at high doses (rare)
  • Temporary increase in stomach acidity (uncommon)
  • Mild allergic reactions in sensitive individuals (rare)
  • Hypoglycemia when used with diabetes medications (rare)
  • Temporary increase in bleeding time (rare)
  • Mild headache (very rare)
  • Skin rash (very rare)

Contraindications

  • Known allergy or hypersensitivity to amla or plants in the Phyllanthaceae family
  • Severe liver or kidney disease (use with caution due to limited safety data)
  • Bleeding disorders (theoretical concern due to potential antiplatelet effects)
  • Scheduled surgery (discontinue 2 weeks before due to potential antiplatelet effects)
  • Pregnancy and breastfeeding (insufficient safety data, though traditionally used in some cultures)
  • Very low blood pressure (theoretical concern due to potential hypotensive effects)
  • Severe hypoglycemia or unstable diabetes (may enhance effects of diabetes medications)

Drug Interactions

  • Anticoagulant/antiplatelet medications (warfarin, aspirin, clopidogrel): May enhance blood-thinning effects
  • Diabetes medications (insulin, metformin, sulfonylureas): May enhance hypoglycemic effects
  • Antihypertensive medications: May enhance blood pressure-lowering effects
  • Hepatotoxic medications: Theoretical concern for additive effects, though amla is generally hepatoprotective
  • Immunosuppressants: Potential interaction due to amla’s immunomodulatory effects
  • Thyroid medications: May affect thyroid hormone levels with long-term use
  • Iron supplements: Tannins in amla may reduce iron absorption if taken simultaneously
  • Medications metabolized by cytochrome P450 enzymes: Potential for interactions, though clinical significance is unclear

Upper Limit

No official Upper Tolerable Intake Level (UL) has been established for amla. Traditional use and clinical studies suggest that doses up to 3 grams of dried fruit powder daily are generally well-tolerated in healthy adults. Higher doses of 3-5 grams daily have been used in some clinical studies without significant adverse effects, but may increase the risk of gastrointestinal discomfort in sensitive individuals. Long-term safety studies beyond 12 months are limited.

As with any supplement, it is advisable to use the lowest effective dose for the intended purpose. Standardized extracts should be used according to manufacturer recommendations, as potency varies between products. Individuals with pre-existing health conditions or those taking medications should consult healthcare providers before using high doses of amla.

Regulatory Status


Fda Status

In the United States, amla (Indian gooseberry) is regulated as a dietary supplement under the Dietary Supplement Health and Education Act (DSHEA) of 1994. It is not approved as a drug for the treatment, prevention, or cure of any disease. As a dietary supplement, amla products can be marketed without pre-approval from the FDA, provided they contain ingredients that were marketed in the U.S. before October 15, 1994, or have been determined to be Generally Recognized as Safe (GRAS).

Manufacturers are responsible for ensuring the safety of their products and for making truthful claims. The FDA does not allow disease treatment claims for amla supplements, though structure/function claims (e.g., ‘supports immune health’ or ‘promotes healthy digestion’) are permitted with appropriate disclaimers. Amla is also permitted as a food ingredient in certain contexts, particularly in ethnic food products.

International Status

Eu: In the European Union, amla is regulated under the Food Supplements Directive (2002/46/EC) and the Novel Food Regulation (EU) 2015/2283. Traditional amla preparations are generally permitted in food supplements, though novel extraction methods or highly concentrated extracts may require novel food authorization. The European Food Safety Authority (EFSA) has not approved any specific health claims for amla under Regulation (EC) No 1924/2006. Amla is also used in some traditional herbal medicinal products regulated under Directive 2004/24/EC, though such products must meet quality, safety, and traditional use requirements.

Canada: Health Canada regulates amla as a Natural Health Product (NHP) under the Natural Health Products Regulations. Amla products must have a Natural Product Number (NPN) to be legally sold in Canada. Health Canada’s Natural Health Products Ingredients Database lists amla with approved uses for antioxidant support, digestive health, and as a source of vitamin C. Traditional Ayurvedic claims may be permitted with appropriate evidence of traditional use. Amla is also permitted as a food ingredient in certain contexts.

Australia: The Therapeutic Goods Administration (TGA) in Australia regulates amla-containing products as listed complementary medicines. Such products must be included in the Australian Register of Therapeutic Goods (ARTG) before they can be marketed. Amla is recognized in the TGA’s list of permissible ingredients for use in listed medicines. Claims must be supported by evidence and comply with the Therapeutic Goods Advertising Code. Amla is also permitted as a food ingredient in certain contexts under Food Standards Australia New Zealand (FSANZ) regulations.

India: In India, amla has special regulatory status as it is a key component of traditional Ayurvedic medicine. It is regulated under the Drugs and Cosmetics Act, 1940, and Rules 1945, which include provisions for Ayurvedic, Siddha, and Unani drugs. The Ministry of AYUSH (Ayurveda, Yoga & Naturopathy, Unani, Siddha, and Homeopathy) oversees traditional medicine products containing amla. Amla is listed in the Ayurvedic Pharmacopoeia of India, which establishes quality standards. As a food, amla is regulated by the Food Safety and Standards Authority of India (FSSAI) and is recognized as a traditional food ingredient.

Synergistic Compounds


Compound Synergy Mechanism Evidence Rating
Turmeric (Curcumin) Both amla and turmeric have potent anti-inflammatory and antioxidant properties that work through complementary pathways. While amla is rich in vitamin C and tannins, turmeric contains curcuminoids that inhibit different inflammatory mediators, creating a more comprehensive anti-inflammatory effect. 3
Black Pepper Extract (Piperine) Piperine enhances the bioavailability of amla’s active compounds by inhibiting certain metabolizing enzymes and promoting absorption in the gastrointestinal tract. This combination can significantly increase the efficacy of amla supplementation. 3
Triphala Components (Haritaki and Bibhitaki) In the traditional Ayurvedic formulation Triphala, amla is combined with Terminalia chebula (Haritaki) and Terminalia bellirica (Bibhitaki). Each herb targets different aspects of digestive health and detoxification, creating a balanced and comprehensive effect on the gastrointestinal system. 3
Ashwagandha Amla’s antioxidant properties complement ashwagandha’s adaptogenic effects. While amla helps reduce oxidative stress, ashwagandha helps modulate stress hormone levels, potentially creating a more balanced response to both physical and psychological stressors. 2
Vitamin C (additional sources) While amla is already rich in vitamin C, combining it with additional vitamin C can create a more sustained antioxidant effect. Amla’s tannins help stabilize vitamin C, potentially extending its activity in the body. 3
Olive Extract Recent clinical research has shown that the combination of amla and olive extracts has synergistic effects on blood glucose regulation and lipid profiles in individuals with prediabetes and type 2 diabetes, beyond what either extract achieves alone. 3
Berberine Amla’s antioxidant effects complement berberine’s metabolic benefits. While berberine activates AMPK and improves insulin sensitivity, amla helps reduce oxidative stress that can impair insulin signaling, potentially creating a more comprehensive approach to metabolic health. 2
Omega-3 Fatty Acids Amla’s anti-inflammatory properties may complement the anti-inflammatory effects of omega-3 fatty acids, particularly for cardiovascular health. Amla helps improve lipid profiles while omega-3s reduce triglycerides and inflammation. 2
Probiotics Amla’s prebiotic fiber content and antimicrobial properties may support the growth of beneficial bacteria while inhibiting pathogenic ones. This creates a synergistic effect with probiotic supplementation for gut health. 2
Milk Thistle (Silymarin) Both amla and milk thistle support liver health through different mechanisms. Amla provides antioxidant protection while silymarin enhances glutathione production and promotes liver cell regeneration, creating a more comprehensive hepatoprotective effect. 2
Zinc Amla’s vitamin C content enhances zinc absorption, while zinc complements amla’s immune-supporting properties. Together they provide more comprehensive immune support than either alone. 2
Ginger Amla and ginger both support digestive health and have anti-inflammatory properties, but through different bioactive compounds and mechanisms, creating a more comprehensive approach to gastrointestinal health and inflammation. 2

Antagonistic Compounds


Compound Interaction Type Evidence Rating
Iron Supplements The tannins in amla may bind to iron and reduce its absorption when taken simultaneously. This interaction is primarily a concern with non-heme iron (from plant sources and supplements) rather than heme iron (from animal sources). 3
Anticoagulant Medications (Warfarin, Heparin) Amla may enhance the blood-thinning effects of anticoagulant medications due to its own mild antiplatelet properties, potentially increasing the risk of bleeding. This interaction is primarily theoretical and based on amla’s known effects on platelet aggregation. 2
Diabetes Medications (Insulin, Sulfonylureas) Amla may enhance the blood glucose-lowering effects of diabetes medications, potentially leading to hypoglycemia. While this can be beneficial when properly managed, it requires careful monitoring and potential dosage adjustments of diabetes medications. 3
Antihypertensive Medications Amla may enhance the blood pressure-lowering effects of antihypertensive medications, potentially leading to hypotension in sensitive individuals. This interaction is based on amla’s observed effects on vascular function and blood pressure. 2
Certain Antibiotics (Tetracyclines, Quinolones) The tannins in amla may bind to certain antibiotics, reducing their absorption and efficacy. This interaction is similar to that observed with other tannin-containing foods and supplements. 2
Immunosuppressant Medications Amla’s immunomodulatory effects may potentially counteract the intended effects of immunosuppressant medications used in autoimmune conditions or post-transplant therapy. This interaction is primarily theoretical and based on amla’s known effects on immune function. 1
Thyroid Medications Some evidence suggests that long-term use of high-dose amla may affect thyroid function, potentially interfering with thyroid medication efficacy. This interaction requires further research but warrants caution in those with thyroid conditions. 1
Alcohol While not strictly antagonistic, the combination of amla’s hepatoprotective effects with alcohol’s hepatotoxic effects creates a mixed interaction. Amla may provide some protection against alcohol-induced liver damage, but should not be used to justify excessive alcohol consumption. 2

Cost Efficiency


Relative Cost

Low to Medium

Cost Per Effective Dose

The cost of amla supplements varies based on form, quality, and standardization level. Basic amla powder typically ranges from $0.10-0.30 per day for a 500-1,000 mg dose, making it one of the more affordable supplements. Standardized extracts are moderately priced at approximately $0.30-0.80 per day for an effective dose. Organic certified products generally cost 20-50% more than conventional options.

Specialized formulations like liposomal amla or proprietary blends can range from $0.75-1.50 per day. Traditional Ayurvedic preparations like Chyawanprash or Triphala containing amla range from $0.25-0.75 per daily serving. Fresh or frozen amla fruit, where available, costs approximately $0.50-1.00 per day for an effective amount (1-2 fruits).

Value Analysis

Amla offers excellent value for its cost when compared to many other supplements with similar antioxidant and health-promoting properties. Its multi-faceted benefits for cardiovascular health, blood glucose regulation, digestive function, and immune support make it cost-effective as a single supplement that may replace multiple targeted products. For antioxidant support, amla is particularly cost-efficient compared to isolated antioxidant supplements, as its complex phytochemical profile provides a spectrum of antioxidant compounds that work synergistically. When used for specific conditions like blood glucose management or cholesterol support, amla may be more cost-effective than some pharmaceutical options, especially when considering the absence of significant side effects.

However, it may take longer to see results compared to pharmaceutical interventions. The traditional forms of amla (powder, dried fruit) generally provide better value than highly processed proprietary formulations, though standardized extracts ensure consistent potency that may justify their higher cost for specific therapeutic purposes. For general health maintenance, basic amla powder offers excellent value, while those seeking specific clinical outcomes may find better value in standardized extracts with guaranteed levels of active compounds. When comparing organic versus conventional amla products, the additional cost of organic certification may be justified by the reduced exposure to pesticides, particularly important for a fruit-derived supplement.

Considering that effective doses of amla are relatively low (500-1,000 mg daily for most purposes) compared to some other herbal supplements that require multiple grams daily, the overall monthly cost remains reasonable even for higher-quality products.

Stability Information


Shelf Life

The shelf life of amla products varies significantly based on form and processing methods. Fresh amla fruit has a relatively short shelf life of 1-2 weeks when refrigerated. Dried amla fruit can maintain quality for 1-2 years when properly stored in airtight containers away from heat and moisture. Amla powder typically has a shelf life of 1-3 years, depending on processing methods and storage conditions.

Standardized extracts in capsule or tablet form generally maintain potency for 2-3 years when stored properly. Liquid extracts and juices have shorter shelf lives of 1-2 years unopened, and 3-6 months after opening if refrigerated. Traditional preparations like Chyawanprash can last 2-3 years when commercially prepared with preservatives, or 6-12 months for homemade versions.

Storage Recommendations

Amla supplements should be stored in cool, dry places away from direct sunlight, heat, and moisture to preserve their active compounds. Capsules, tablets, and powders should be kept in airtight containers, preferably the original packaging designed to protect from light and moisture. Refrigeration is recommended for liquid extracts, juices, and fresh or frozen amla products after opening. Avoid storing amla products in bathrooms or kitchens where humidity levels fluctuate.

For long-term storage of amla powder, consider using moisture-absorbing packets in the container. Traditional preparations like Chyawanprash should be stored in glass containers rather than plastic when possible, and a clean, dry spoon should always be used to prevent contamination. If bulk amla powder is purchased, consider dividing it into smaller airtight containers to minimize exposure to air and moisture during regular use. For travel, transfer only the needed amount to a travel container rather than exposing the entire supply to varying environmental conditions.

Degradation Factors

Heat exposure, which accelerates the breakdown of vitamin C and other heat-sensitive compounds, Light exposure, particularly UV light, which degrades polyphenols and other photosensitive compounds, Oxygen exposure, which promotes oxidation of antioxidant compounds, Moisture, which can lead to microbial growth and enzymatic degradation, pH changes in liquid formulations, which can affect stability of various phytochemicals, Enzymatic activity in minimally processed products, which can break down active compounds, Microbial contamination, especially in liquid or high-moisture products, Metal ions (particularly iron and copper), which can catalyze oxidation reactions, Improper freeze-thaw cycles for frozen products, which can damage cellular structures, Chemical interactions with other ingredients in multi-component formulations, Processing methods that use high heat or harsh chemicals, which can destroy sensitive compounds, Extended storage time, which gradually reduces potency even under optimal conditions

Sourcing


Synthesis Methods

  • Standardized extracts produced through water extraction methods
  • Alcohol-based extraction to concentrate certain bioactive compounds
  • Supercritical CO2 extraction for certain applications
  • Freeze-drying of amla fruit or juice to preserve nutrient content
  • Spray-drying techniques for powder production
  • Traditional Ayurvedic processing methods involving drying, roasting, or cooking with other herbs
  • Fermentation processes to enhance bioavailability of certain compounds
  • Liposomal encapsulation for improved absorption

Natural Sources

  • Fresh amla fruit (Phyllanthus emblica/Emblica officinalis)
  • Dried amla fruit
  • Wild-harvested amla from forests in India, Nepal, Sri Lanka, and other parts of Southeast Asia
  • Cultivated amla from orchards in India (particularly in Uttar Pradesh, Madhya Pradesh, Tamil Nadu, and Rajasthan)
  • Amla trees grown in home gardens throughout South Asia
  • Amla incorporated in traditional Ayurvedic formulations like Chyawanprash and Triphala
  • Amla juice and preserves available in South Asian markets
  • Amla powder made from dried and ground fruit

Quality Considerations

When selecting amla supplements, several quality factors should be considered. Look for products that specify the standardization of key compounds, particularly total polyphenols, tannins, or vitamin C content, as these indicate potency and consistency. Organic certification is important since amla, as a fruit, may contain pesticide residues if conventionally grown. The country of origin matters—amla from India, particularly from regions with traditional cultivation practices, often has higher phytochemical content due to optimal growing conditions. Processing methods significantly impact quality; low-temperature drying and extraction help preserve heat-sensitive compounds like vitamin C. For extracts, the extraction ratio (e.g., 10:1) indicates concentration level, with higher ratios generally offering more potent products. Third-party testing for contaminants, heavy metals, and microbial safety is essential, as is verification of identity through appropriate analytical methods. Fresh amla products should have minimal additives, while standardized extracts may contain necessary excipients for stability. Sustainable harvesting practices are becoming increasingly important as demand grows. Traditional knowledge in processing, such as methods used in Ayurvedic preparation, can enhance therapeutic properties. Finally, transparency in the supply chain, from harvesting to final product, indicates a manufacturer’s commitment to quality.

Historical Usage


Amla (Indian Gooseberry) has a rich and extensive history of traditional use spanning thousands of years, particularly in the Indian subcontinent. In Ayurveda, India’s ancient system of medicine dating back over 5,000 years, amla is revered as one of the most important medicinal fruits and is often referred to as ‘Dhatri’ (the nurse) or ‘Amrita’ (nectar) due to its extraordinary healing properties. The earliest documented references to amla appear in ancient Ayurvedic texts like the Charaka Samhita and Sushruta Samhita (circa 1000-500 BCE), where it is described as a rasayana (rejuvenative) that promotes longevity, enhances digestion, and balances all three doshas (vata, pitta, and kapha). Amla forms a crucial component of the renowned Ayurvedic formulation Triphala, a combination of three fruits (amla, haritaki, and bibhitaki) that has been used for digestive health, detoxification, and rejuvenation for millennia.

Another classical preparation, Chyawanprash, which contains amla as its primary ingredient, has been used since ancient times to boost immunity, vitality, and longevity. In traditional Chinese medicine, amla (known as Yu Gan Zi) has been used since at least the Tang Dynasty (618-907 CE) for liver health, improving eyesight, and treating various inflammatory conditions. Throughout South and Southeast Asia, amla has been incorporated into traditional medicine systems for treating respiratory conditions, enhancing digestion, purifying blood, strengthening hair, and improving skin health. In folk medicine practices across India, amla has been used to address diabetes, cough, asthma, menstrual disorders, and liver conditions.

The fruit was traditionally consumed fresh, dried, or preserved in various forms including pickles, jams, and candied preparations to make its sour taste more palatable while preserving its medicinal properties. Amla was also used in religious contexts, considered sacred in Hinduism and often offered in temples and religious ceremonies. The tree itself was venerated, with various parts including leaves, bark, and roots also used medicinally. In the medieval period, Unani medicine (Greco-Arabic medicine practiced in South Asia) incorporated amla for treating liver disorders, strengthening the heart, and improving eyesight.

Colonial-era European physicians in India documented the use of amla for scurvy (now known to be related to its high vitamin C content) and various digestive ailments. In modern times, scientific research has validated many of these traditional uses, confirming amla’s antioxidant, anti-inflammatory, immunomodulatory, and adaptogenic properties, bringing this ancient remedy into contemporary integrative medicine practices worldwide.

Scientific Evidence


Evidence Rating i

3Evidence Rating: Moderate Evidence – Multiple studies with generally consistent results

Key Studies

Study Title: Amla (Emblica officinalis Gaertn.) extract reduces oxidative stress in streptozotocin-induced diabetic rats
Authors: Rao TP, Sakaguchi N, Juneja LR, Wada E, Yokozawa T
Publication: Journal of Medicinal Food
Year: 2005
Doi: 10.1089/jmf.2005.8.362
Url: https://pubmed.ncbi.nlm.nih.gov/16176136/
Study Type: Animal study
Population: Streptozotocin-induced diabetic rats
Findings: Amla extract significantly reduced oxidative stress markers and improved antioxidant status in diabetic rats, suggesting potential benefits for diabetes-related oxidative damage.
Limitations: Animal study; results may not directly translate to humans.

Study Title: Effect of Amla fruit (Emblica officinalis Gaertn.) on blood glucose and lipid profile of normal subjects and type 2 diabetic patients
Authors: Akhtar MS, Ramzan A, Ali A, Ahmad M
Publication: International Journal of Food Sciences and Nutrition
Year: 2011
Doi: 10.3109/09637486.2010.529072
Url: https://pubmed.ncbi.nlm.nih.gov/21495900/
Study Type: Randomized controlled trial
Population: Type 2 diabetic patients and healthy volunteers
Findings: Amla powder (1, 2, or 3 g daily for 21 days) significantly reduced fasting and post-prandial blood glucose levels in diabetic subjects and improved lipid profiles in both diabetic and normal subjects.
Limitations: Small sample size; relatively short duration.

Study Title: Efficacy of Phyllanthus emblica L. fruit extract in improving the antioxidant status of red blood cells during storage
Authors: Gupta A, Gautam MK, Singh RK, Kumar MV, Rao CV, Goel RK, Anupurba S
Publication: National Journal of Physiology, Pharmacy and Pharmacology
Year: 2016
Doi: 10.5455/njppp.2016.6.0718024072016
Url: https://www.njppp.com/fulltext/28-1470043128.pdf
Study Type: In vitro study
Population: Human red blood cells
Findings: Amla extract significantly improved the antioxidant status of stored red blood cells, reducing oxidative damage and potentially extending storage viability.
Limitations: In vitro study; clinical relevance needs further investigation.

Study Title: Clinical evaluation of Emblica officinalis Gaertn (Amla) in healthy human subjects: Health benefits and safety results from a randomized, double-blind, crossover placebo-controlled study
Authors: Kapoor MP, Suzuki K, Derek T, Ozeki M, Okubo T
Publication: Contemporary Clinical Trials Communications
Year: 2019
Doi: 10.1016/j.conctc.2019.100499
Url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926135/
Study Type: Randomized, double-blind, crossover placebo-controlled trial
Population: 15 healthy adult subjects
Findings: Amla supplementation (500 mg daily for 12 weeks) significantly improved blood fluidity, reduced oxidative stress markers, and improved lipid profiles without adverse effects.
Limitations: Small sample size; conducted in healthy subjects rather than those with specific health conditions.

Study Title: Amla (Emblica officinalis) improves endothelial function and reduces biomarkers of oxidation in patients with type 2 diabetes: A randomized, double-blind, controlled clinical trial
Authors: Usharani P, Fatima N, Muralidhar N
Publication: Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Year: 2013
Doi: 10.2147/DMSO.S46341
Url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658718/
Study Type: Randomized, double-blind, placebo-controlled trial
Population: 80 patients with type 2 diabetes
Findings: Amla extract (500 mg twice daily for 12 weeks) significantly improved endothelial function, reduced biomarkers of oxidative stress and systemic inflammation compared to placebo.
Limitations: Moderate sample size; relatively short duration for chronic condition assessment.

Meta Analyses

Variya BC, Bakrania AK, Patel SS. Emblica officinalis (Amla): A review for its phytochemistry, ethnomedicinal uses and medicinal potentials with respect to molecular mechanisms. Pharmacological Research. 2016;111:180-200. doi:10.1016/j.phrs.2016.06.013, D’souza JJ, D’souza PP, Fazal F, Kumar A, Bhat HP, Baliga MS. Anti-diabetic effects of the Indian indigenous fruit Emblica officinalis Gaertn: active constituents and modes of action. Food & Function. 2014;5(4):635-644. doi:10.1039/c3fo60366k

Ongoing Trials

Evaluation of Amla Extract on Glycemic Control in Type 2 Diabetes (NCT04571060), Effects of Amla Extract on Endothelial Function and Cardiovascular Risk Markers (NCT03656939), Amla Extract for Non-Alcoholic Fatty Liver Disease: A Randomized Controlled Trial, Efficacy of Standardized Amla Extract on Cognitive Function in Older Adults, Comparative Bioavailability of Different Amla Formulations

Disclaimer: The information provided is for educational purposes only and is not intended as medical advice. Always consult with a healthcare professional before starting any supplement regimen, especially if you have pre-existing health conditions or are taking medications.

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