Celery

Botanical Overview

Celery (Apium graveolens) is a flowering plant in the Apiaceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. The carrot family (Apiaceae) includes herbs with hollow stems, alternate leaves, and distinctive umbrella-shaped flower clusters called umbels. Many species have aromatic roots and seeds used as culinary spices and medicines. The family includes both nutritious vegetables and highly toxic species.

General Description

It was first described by Carl Linnaeus in 1753. The species is widely naturalised outside of its natural range and is used as a vegetable; modern cultivars have been selected for their leaf stalks (celery), a large bulb-like hypocotyl (celeriac), and their leaves (leaf celery).

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

Family Context

The Apiaceae family is widely distributed in temperate regions. Notable medicinal members include:

Geographic Distribution

Celery has been recorded in 10 countries and territories worldwide, including Australia, Belgium, Germany, Denmark, Spain, and others.

Traditional Uses

Celery has been traditionally used for digestive health, urinary tract health, and pain and inflammation, among other applications.

Digestive health.

  • Carminative
  • Stomachic
  • Colic
  • Dyspepsia

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.

Pain and inflammation.

  • Rheumatism
  • Arthritis
  • Anodyne

For pain and inflammation, preparations are applied both topically as compresses and taken internally. A warm poultice draws blood to the area and promotes healing, while internal preparations address systemic inflammation.

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:

  • 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.

Distribution and Conservation

Reported distribution: Australia, Belgium, Germany, Denmark, Spain, France, United Kingdom, Netherlands, Portugal, United States.

Complete Use Records

CategoryCultural Context
CarminativeElsewhere, Haiti, Iraq, Turkey
DiureticDominican Republic, Elsewhere, Iraq, Turkey
RheumatismElsewhere, Haiti, Iraq, Mexico
TumorCuba, Philippines, Spain(Balearic I), US(NM)
NervineElsewhere, Iraq, Turkey
StimulantElsewhere, Haiti, Iraq
TonicChina, Elsewhere, Iraq
AlterativeChina, Iraq
AntisepticIndia, Iraq
ArthritisElsewhere, Iraq
EmmenagogueElsewhere, Turkey
SedativeElsewhere, Iraq
StomachicElsewhere, Turkey
AnasarcaElsewhere
AnodyneElsewhere
AntigalactogogueMexico
ApertifTurkey
BruiseDominican Republic
CalmativeChina
ColicElsewhere
DeobstruentTurkey
DepurativeTurkey
DigestiveChina
DysmenorrheaTurkey
DyspepsiaChina
HoarsenessDominican Republic
PoulticeElsewhere
RefrigerantChina
ResolventTurkey
ScurvyHaiti

Complete Chemical Inventory

CompoundFormulaMW
(+)-LIMONENEC₁₀H₁₆136.23 Da
(+)-SELINENEC₁₅H₂₄204.35 Da
(-)-MARMESINC₁₄H₁₄O₄246.26 Da
(E)-8(9)-P-MENTHEN-1,2-DIOL?
(E)-ALPHA-BERGAMOTENEC₁₅H₂₄204.35 Da
(E)-BETA-OCIMENEC₁₀H₁₆136.23 Da
(Z)-BETA-OCIMENEC₁₀H₁₆136.23 Da
1(7),8(10)-P-MENTHADIEN-2-OL?
1,4-DIMETHYL-7-(1-METHYLETHENYL)-OCTAHYDRO-AZULENE
1-P-MENTHENE-9-ALC₁₀H₁₆O152.23 Da
3,7,11-TRIMETHYL-1,2,6,10-DODECATRIENOL?
3-BUTYLPHTHALIDEC₁₂H₁₄O₂190.24 Da
3-ISOBUTLIDENE-3-(A)-4-DIHYDROPHTHALIDE
3-ISOBUTYLIDENE-3-A,4-DIHYDROPHTHALIDE
3-ISOBUTYLIDENE-PHTHALIDEC₁₂H₁₂O₂188.22 Da
3-ISOVALERIDENE-3A,4-DIHYDROPHTHALIDE
3-ISOVALERIDENE-PHTHALIDE
3-ISOVALIDENE-3A,4-DIHYDROPHTHALIDEC₁₃H₁₆O₂204.26 Da
3-ISOVALIDENE-PHTHALIDE
3-METHYL-4-ETHYL-HEXANE
3-N-BUTYL-4,5-DIHYDROPHTHALIDEC₁₂H₁₆O₂192.25 Da
3-N-BUTYL-PHTHALIDE
3-N-BUTYLHEXAHYDROPHTHALIDE
4-DIHYDROPHTHALIDEC₈H₈O₂136.15 Da
5,6,7-TRIMETHYLPSORALENC₁₄H₁₂O₃228.24 Da
5-ALPHA-ANDROST-16-EN-3-ONEC₁₉H₂₈O272.4 Da
5-METHOXY-8-O-BETA-D-GLUCOSYL-OXYPSORALEN
5-METHOXY-PSORALENC₁₂H₈O₄216.19 Da
6,10,14-TRIMETHYL-2-PENTADECANONEC₁₈H₃₆O268.5 Da
7-[3-(3,4-DIHYDROXY-4-HYDROXYMETHYL-TETRAHYDRO-FURAN-2-YLOXY)-4,5-DIHYDROXY-6-HYDROXYMETHYL-TETRAHYDRO-PYRAN-2-YLOXY]...

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


References & Further Reading

External Research Links

Data Sources