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Ela

Elettaria cardamomum

Ela (Elettaria cardamomum) is a plant used in Ayurveda, from the Zingiberaceae family. Listed in the Ayurvedic Pharmacopoeia of India (API) and referenced in traditional Ayurveda, Unani, and Siddha medicine systems.

Key facts
Botanical nameElettaria cardamomum
FamilyZingiberaceae · other entries in this family
OrderZingiberales
Also known asEla, Elettaria cardamomum, Cardamom, Green Cardamom, Elaichi, Sukshma Ela
Pharmacopoeia statusListed in the Ayurvedic Pharmacopoeia of India (API) and referenced in traditional Ayurveda, Unani, and Siddha medicine systems. Historical use documented since 4th century BCE. Not currently listed as a standalone WHO monograph; recognized by Indian pharmacopoeia standards for digestive, anti-inflammatory, and antimicrobial properties.
Taxon identifiersGBIF 2759871 · Wikidata Q33466 · NCBI Taxonomy 105181

Names and identification

LanguageName
EnglishEla
Latin/BotanicalElettaria cardamomum

Key Phytochemical Constituents

How does it work?

  • 1,8-Cineole (eucalyptol) exerts anti-inflammatory activity by inhibiting TNF-alpha, IL-1beta, and IL-6 production via NF-kB pathway suppression
  • Antihypertensive mechanism through diuretic action, calcium channel blocking, and ACE (angiotensin-converting enzyme) inhibition
  • Antioxidant activity via polyphenol-mediated free radical scavenging and enhancement of endogenous antioxidant defense systems (SOD, catalase)
  • Anticancer mechanisms include induction of apoptosis, cell cycle arrest, and inhibition of cell migration through modulation of PI3K/Akt and MAPK pathways
  • Antimicrobial action of 1,8-cineole and terpinen-4-ol through disruption of microbial cell membrane and interference with cellular respiration

Which traditional uses are supported by research?

  • Digestive aid for nausea, flatulence, and indigestion - confirmed by pharmacological studies showing carminative and antispasmodic effects
  • Respiratory relief for asthma and bronchitis - validated by studies demonstrating bronchodilatory effects of 1,8-cineole (eucalyptol)
  • Oral health for teeth and gum infections - confirmed by RCTs showing antibacterial and anti-inflammatory activity against periodontal pathogens
  • Blood pressure lowering - validated by meta-analysis of RCTs showing significant reduction in both systolic and diastolic blood pressure
  • Anti-inflammatory for metabolic disorders - confirmed by RCTs demonstrating significant reduction in TNF-alpha, hs-CRP, and IL-6

What do recent clinical trials show?

1 further claim previously listed here could not be traced to a published paper and has been removed. An absence here means we could not identify the source, not that no work exists.

Recent safety updates

  • Generally considered non-toxic and safe for culinary use; no mortalities observed in animal studies up to doses of 2 g/kg extract and 0.75 mL/kg essential oil
  • Neurotoxicity observed at high doses (1.5 g/kg extract, 0.75 mL/kg essential oil) in rotarod tests in animal studies; excessive consumption may cause gastrointestinal disturbances
  • Limited number of human clinical trials with small sample sizes; further large-scale prospective studies with longer treatment durations needed to establish complete safety profile for therapeutic use

What is it made of?

Key Active Markers

  • Cineole
  • Sabinene
  • Myrcene
  • Limonene
  • Quercetin
  • Kaempferol
  • Flavonoids
  • Rutin

Analytical Methods: HPLC fingerprinting, TLC (identity), LC-MS/MS (marker quantification)

Dosage forms and preparation

Dosage Forms: Churna (seed powder), Essential oil, Tablet, Capsule, Arka (distillate), Tincture, Confectionery/culinary preparations

Standard Dosage: 1-3g seed powder twice daily; 500mg extract capsule twice daily; essential oil: 1-2 drops in warm water or carrier; 2-5ml tincture

Bioavailability: Elettaria cardamomum (green cardamom) essential oil (2-8% in seeds) contains 1,8-cineole (20-50%) and alpha-terpinyl acetate (30-40%) as major components. These small monoterpenoids have excellent oral bioavailability (>60%) due to high lipophilicity and small molecular size. Rapid absorption from GI tract with peak plasma levels at 30-60 minutes. First-pass metabolism is moderate. The volatile nature means hot preparations lose significant active content - cold or warm (not boiling) preparations preferred. Enhancement not typically required due to inherent good bioavailability; however, enteric coating of essential oil capsules prevents gastric volatilization.

Optimal Timing: After meals as digestive aid; chewed directly after meals (traditional); with warm milk at bedtime for sleep quality

Standardized Extract: Essential oil: standardized to NLT 35% alpha-terpinyl acetate and NLT 20% 1,8-cineole by GC-MS. Oleoresin: 50-55% volatile oil. Seed extract: NLT 4% essential oil by distillation assay.

Shelf Life: Whole pods: 2-3 years; Powder: 6-12 months (volatile loss); Essential oil: 3-5 years (sealed amber bottle); Capsule/tablet: 2 years

Storage: Whole pods in airtight containers at room temperature - most stable form. Powder: airtight, nitrogen-flushed, opaque containers, use quickly. Essential oil: amber glass, cool dark place, tightly sealed. Avoid heat and light exposure.

Marker Compounds: 1,8-Cineole (eucalyptol), Alpha-terpinyl acetate, Linalool, Linalyl acetate, Limonene, Alpha-terpineol, Myrcene

Extraction Methods

  • Steam distillation of crushed seeds for essential oil
  • Supercritical CO2 extraction (superior quality, higher alpha-terpinyl acetate retention)
  • Hydrodistillation (traditional Arka)
  • Hydroalcoholic extraction (60:40) for non-volatile constituents
  • Cold-pressing of seeds (low yield)

Synergistic Combinations

  • With Sunthi (ginger) and Twak (cinnamon) in Trikatu-related digestive formulations
  • With Yashtimadhu for gastric soothing and carminative combination
  • With Lavanga (clove) for oral care formulations
  • With Jatiphala (nutmeg) for digestive and anti-emetic synergy
  • As Prakshepa Dravya (flavoring agent) in many Ayurvedic formulations

Published research

Literature indexed in PubMed that concerns this subject, grouped by study type. A paper appearing here is a record of what has been published, not evidence that the subject works, and laboratory or animal results do not transfer to people. Study titles link to PubMed so you can read the source rather than take our word.

Systematic reviews and meta-analyses3

  1. Nasimi Doost Azgomi R, Karimi A, Moini Jazani A. 2024. The favorable impacts of cardamom on related complications of diabetes: A comprehensive literature systematic reviewDiabetes & metabolic syndrome. PMID 38325073 · doi:10.1016/j.dsx.2024.102947
  2. Izadi B, Joulaei H, Lankarani KB and others. 2023. The effect of green cardamom on blood pressure and inflammatory markers among patients with metabolic syndrome and related disorders: A systematic review and meta-analysis of randomized clinical trialsPhytotherapy research : PTR. PMID 36181264 · doi:10.1002/ptr.7648
  3. Khorasani F, Aryan H, Sobhi A and others. 2020. A systematic review of the efficacy of alternative medicine in the treatment of nausea and vomiting of pregnancyJournal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology. PMID 31215276 · doi:10.1080/01443615.2019.1587392

Available from Age Ayurveda

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  • Acid ReliefTraditionally used to support comfortable digestion after meals.

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