Heavenly Bamboo

Also known as: Sacred Bamboo, Southern Heaven Bamboo, Nanten (Jap.)

Botanical Overview

Heavenly Bamboo (Nandina domestica) is a flowering plant in the Berberidaceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. The barberry family (Berberidaceae) includes shrubs and herbs with alternate or basal leaves and yellow wood or roots due to alkaloid content. The flowers have six sepals and six petals arranged in whorls, and the fruits are berries or capsules. Many species produce isoquinoline alkaloids like berberine with antimicrobial activity.

General Description

It is the only member of the monotypic genus Nandina. Despite its name, it is not a true bamboo.

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

Family Context

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

Geographic Distribution

Heavenly Bamboo has been recorded in 10 countries and territories worldwide, including Australia, Switzerland, China, Hong Kong, Italy, and others.

Traditional Uses

Heavenly Bamboo has been traditionally used for digestive health, respiratory conditions, and fever management.

Digestive health.

  • 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.

Respiratory conditions.

  • Bronchitis
  • Cold

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.

Fever management.

  • Fever

Febrifuge preparations are typically administered as hot teas to induce perspiration, which helps the body regulate temperature. The patient is kept warm and encouraged to rest while the herb promotes sweating.

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
  • 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 Poison. 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: Australia, Switzerland, China, Hong Kong, Italy, Japan, South Korea, Macao, New Zealand, United States.

Complete Use Records

CategoryCultural Context
CyanogeneticChina, Elsewhere, US
AntitussiveChina, Elsewhere
PoisonChina, Elsewhere
BreathChina
BronchitisChina
CariesChina
DyspepsiaChina
FeverChina
GastritisChina
HungerChina
LongevityChina
PertussisChina
SenilityChina
VirilityChina
Ache(Bones)China
TendonChina
ColdChina
ComplexionChina
EnteritisChina
LethargyChina
MedicineJapan
TraumaChina
FluChina
Ache(Tooth)China

Complete Chemical Inventory

CompoundFormulaMW
(-)-EPISYRINGARESINOLC₂₂H₂₆O₈418.4 Da
ACETONEC₃H₆O58.08 Da
ALKALOIDS
AMENTOFLAVONEC₃₀H₁₈O₁₀538.5 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
BERBERINEC₂₀H₁₈NO₄+336.4 Da
CALISTEPHIN
DEHYDRONANTENINEC₂₀H₁₉NO₄337.4 Da
DOMESTICINEC₁₉H₁₉NO₄325.4 Da
FATC₁₆H₃₂O₂256.42 Da
FUMARIC-ACIDC₄H₄O₄116.07 Da
HCNCHN27.025 Da
HYDROXYPROLINEC₅H₉NO₃131.13 Da
ISOBOLDINEC₁₉H₂₁NO₄327.4 Da
ISOCORYDINEC₂₀H₂₃NO₄341.4 Da
ISODOMESTICINEC₁₉H₁₉NO₄325.4 Da
JATRORRHIZINEC₂₀H₂₀NO₄+338.4 Da
LIGNANSC₂₂H₂₂O₈414.4 Da
MAGNOFLORINEC₂₀H₂₄NO₄+342.4 Da
MENISPERMINEC₂₁H₂₆NO₄+356.4 Da
N-METHYLISOCORYDINIUM
NANDAZURINEC₁₉H₁₄NO₅+336.3 Da
NANDINENE
NANTENINEC₂₀H₂₁NO₄339.4 Da
O-METHYLDOMESTICINEC₂₀H₂₁NO₄339.4 Da
P-GLUCOSYLOXYMANDELONITRILEC₁₄H₁₇NO₇311.29 Da
P-GLUCOSYLOXYMANDELONITRILE-4'-CAFFEIC-ACID-ESTER
PELARGONIDIN-3-XYLOSYLGLUCOSIDE
PROTEIN

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


References & Further Reading

External Research Links

Data Sources