Aspic

Also known as: Broad-Leaved Lavender, Spike Lavender

Botanical Overview

Aspic (Lavandula latifolia) belongs to the Lamiaceae family. Limited but reliable traditional records indicate this plant has recognized medicinal applications in one or more healing traditions. The mint family (Lamiaceae) includes aromatic herbs and shrubs with square stems, opposite leaves, and two-lipped flowers. Many species produce essential oils in glandular trichomes on their leaves and stems. This family is one of the most important sources of culinary and medicinal herbs worldwide.

General Description

Hybridization can occur in the wild with English lavender.

ⓘ Information
Description adapted from Wikipedia (CC BY-SA 4.0).

Family Context

The Lamiaceae family is large and widely distributed. Notable medicinal members include:

  • Basil — 86 documented uses
  • Rosemary — 60 documented uses
  • Agbo — 54 documented uses
  • Sage — 49 documented uses

Geographic Distribution

Aspic has been recorded in 10 countries and territories worldwide, including Andorra, Switzerland, Germany, Spain, France, and others.

Traditional Uses

Aspic has been traditionally used for digestive health, urinary tract health, and nervous system disorders, among other applications.

Digestive health.

  • Carminative
  • Vermifuge
  • Stomachic

For digestive complaints, the herb is typically prepared as a tea or decoction taken before meals. The bitter compounds stimulate digestive secretions and improve nutrient absorption. Some traditions use the powdered root or leaves in small doses as a stomachic tonic.

Urinary tract health.

  • Diuretic

Urinary tract applications typically involve drinking the herb as a mild tea, which increases urine production and helps flush the urinary system. It may be combined with other demulcent herbs to soothe irritated tissues.

Nervous system disorders.

  • Nervine
  • Spasm

Nervous system support involves taking the herb as a warm tea, often in the evening or before bed. The calming compounds interact with neurotransmitter systems to promote relaxation and restful sleep.

Active Compounds

Phytochemical research has identified 30 compounds in this species, including a diverse array of phytochemical classes (see the Complete Chemical Inventory below for the full list).

The identified compounds include the following categories:

  • Coumarin: aromatic compounds with anticoagulant and anti-inflammatory effects
  • Alkaloid: nitrogenous compounds with diverse pharmacological activities
ⓘ Information
Information on this page is compiled from Dr. Duke’s Phytochemical and Ethnobotanical Databases (USDA ARS), a public domain resource. Consult a healthcare professional before using any herbal preparation.
⚠ Caution
Traditional records: This plant has documented uses including Abortifacient. Self-medication with herbs carries risks including allergic reactions, drug interactions, and toxicity. Only use under the supervision of a qualified healthcare professional.

Distribution and Conservation

Reported distribution: Andorra, Switzerland, Germany, Spain, France, Croatia, Italy, Portugal, United States, Unknown.

Complete Use Records

CategoryCultural Context
AbortifacientElsewhere
CancerUS(AZ)
CarminativeFrench
CholagogueItalian
NervineEnglish
StimulantSpanish
SudorificFrench
VermifugeSpanish
Medicine (Veterinary)Elsewhere
DiureticDutch
EmmenagogueElsewhere
FumigantSpain
SpasmPortuguese
StomachicGerman

Complete Chemical Inventory

CompoundFormulaMW
1,8-CINEOLEC₁₀H₁₈O154.25 Da
3-OCTANOLC₈H₁₈O130.23 Da
3-OCTANONEC₈H₁₆O128.21 Da
ALPHA-BISABOLOLC₁₅H₂₆O222.37 Da
ALPHA-CADINOLC₁₅H₂₆O222.37 Da
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
ALPHA-PHELLANDRENEC₁₀H₁₆136.23 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
ALPHA-TERPINYL-ACETATEC₁₂H₂₀O₂196.29 Da
ALPHA-THUJENEC₁₀H₁₆136.23 Da
ALPHA-THUJONEC₁₀H₁₆O152.23 Da
BETA-BISABOLENEC₁₅H₂₄204.35 Da
BETA-PINENEC₁₀H₁₆136.23 Da
BETA-THUJONEC₁₀H₁₆O152.23 Da
BORNEOLC₁₀H₁₈O154.25 Da
BORNYL-ACETATEC₁₂H₂₀O₂196.29 Da
CAMPHENEC₁₀H₁₆136.23 Da
CAMPHORC₁₀H₁₆O152.23 Da
CARVONEC₁₀H₁₄O150.22 Da
CARYOPHYLLENEC₁₅H₂₄204.35 Da
CARYOPHYLLENE-OXIDEC₁₅H₂₄O220.35 Da
CIS-ALPHA-BISABOLENEC₁₅H₂₄204.35 Da
CIS-CARVEOLC₁₀H₁₆O152.23 Da
CIS-LINALOL-EPOXIDE
CIS-OCIMENEC₁₀H₁₆136.23 Da
CITRONELLALC₁₀H₁₈O154.25 Da
CITRONELLOLC₁₀H₂₀O156.26 Da
COUMARINC₉H₆O₂146.14 Da

Data from PubChem (NIH/NLM, public domain).


References & Further Reading

External Research Links

Data Sources