Spiny Restharrow

Also known as: Restharrow, Hauhechel (Ger.)

Botanical Overview

Spiny Restharrow (Ononis spinosa) belongs to the Fabaceae family. Limited but reliable traditional records indicate this plant has recognized medicinal applications in one or more healing traditions. The legume family (Fabaceae) includes trees, shrubs, and herbs that produce pods (legumes) and form nitrogen-fixing root nodules through symbiosis with bacteria. The flowers are typically pea-shaped with five petals. This large family provides food staples, timber, and numerous medicinal species.

General Description

It is found throughout much of Europe including Britain, but rarely as far north as Scotland. It is closely related to Ononis repens ; the two are considered conspecific by the Plants of the World Online database, with O. repens treated as a subspecies of O. spinosa as Ononis spinosa subsp. procurrens. The Botanical Society of Britain and Ireland treats them as separate species.

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

Family Context

The Fabaceae family is large and globally distributed. Notable medicinal members include:

Geographic Distribution

Spiny Restharrow has been recorded in 10 countries and territories worldwide, including Austria, Belgium, Switzerland, Germany, Denmark, and others.

Traditional Uses

Spiny Restharrow has been traditionally used for respiratory conditions, urinary tract health, and pain and inflammation, among other applications.

Respiratory conditions.

  • Expectorant

Respiratory conditions are addressed through steam inhalation of the herb’s vapors or internal use as a warm tea. The hot infusion acts as an expectorant, helping to loosen phlegm and clear congestion. Some traditions combine it with honey for coughs.

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.

  • Gout

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:

  • Flavonoid: antioxidant compounds that protect cells from oxidative damage
  • Phenolic: antioxidant compounds that neutralize free radicals
  • Sterol: cholesterol-like compounds with anti-inflammatory properties
ⓘ 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: Austria, Belgium, Switzerland, Germany, Denmark, Spain, France, United Kingdom, Netherlands, Sweden.

Complete Use Records

CategoryCultural Context
DiureticElsewhere, Spain, Turkey
AperientTurkey
CancerEurope
DepurativeTurkey
GoutEurope
ExpectorantTurkey

Complete Chemical Inventory

CompoundFormulaMW
(-)-MAACKIAIN-3-O-GLUCOSIDEC₂₂H₂₂O₁₀446.4 Da
24-METHYLENE-CYCLOARTANOLC₃₁H₅₂O440.7 Da
5-DEOXYISOFLAVONE
7-DEMETHOXY-7-D-GLUCOSYLOXY-HOMOPTEROCARPIN
ALPHA-ONOCERINC₃₀H₅₀O₂442.7 Da
ALPHA-SPINASTEROLC₂₉H₄₈O412.7 Da
ANETHOLEC₁₀H₁₂O148.20 Da
APIGENINC₁₅H₁₀O₅270.24 Da
BIOCHANINC₁₆H₁₂O₅284.26 Da
BIOCHANIN-AC₁₆H₁₂O₅284.26 Da
BIOCHANIN-A-7-GLUCOSIDE
BIOCHANIN-A-7-GLUCOSIDE-6''-MALONATE
CAMPESTEROLC₂₈H₄₈O400.7 Da
CARVONEC₁₀H₁₄O150.22 Da
CHOLESTEROLC₂₇H₄₆O386.7 Da
CINNAMIC-ACIDC₉H₈O₂148.16 Da
COSMOSIINC₂₁H₂₀O₁₀432.4 Da
CYCLITEC₇H₇Br171.03 Da
CYCLOARTENOLC₃₀H₅₀O426.7 Da
D-INOSITOLC₆H₁₂O₆180.16 Da
D-ODONITOL
D-PINITOLC₇H₁₄O₆194.18 Da
DIHYDROFORMONONETIN-7-O-GLUCOSIDEC₂₂H₂₄O₉432.4 Da
FERULIC-ACIDC₁₀H₁₀O₄194.18 Da
FORMONONETINC₁₆H₁₂O₄268.26 Da
FORMONONETIN-7-O-GLUCOSIDEC₂₂H₂₂O₉430.4 Da
GALLIC-ACIDC₇H₆O₅170.12 Da
GENISTEINC₁₅H₁₀O₅270.24 Da
GENTISIC-ACIDC₇H₆O₄154.12 Da
HOMOPROTOCATECHUIC-ACIDC₈H₈O₄168.15 Da

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


References & Further Reading

External Research Links

Data Sources