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Family Araceae
Dieffenbachia
Dieffenbachia picta (Lodd.) Schott.
DUMB CANE

Scientific names Common names
Dieffenbachia picta (Lodd.) Schott. Dieffenbachia (Engl.)
Dieffenbachia maculata (Lodd.) G. Don Dumb cane (Engl.)
Caladium maculatum Lodd.  

Botany
Dieffenbachia picta is a long-lived, evergreen, perennial herb growing to height of 1 to 1.5 meters. Stem is branchless, about 2.5 centimeters thick, cylindrical, tinged with leaf scars, and erect with the base usually reclining. Leaves concentrated towards the apical part of the stem, the stalk elongated, broadly grooved, the lower part forming a sheath around the stem. Leaves are 20 to 40 centimeters long, 10 to 20 centimeters wide, oblong to broadly lanced-shaped, dark to glossy green on both sides, with numerous white or yellowish spots or streaks, the base rounded to acute, the tip narrow. Flower cluster is white, erect, subtended and partly enclosed by a leaflike spathe. Flowers are stalkless, the males crowded on the upper part of the cluster, the females on the lower, the latter enclosed the spathe's tubular base. Fruits are berries, orange when ripe.

Distribution
- The most common cultivated Diffenbachia species of the Philippines.
- Usually grown as a potted plant for its handsome foliage.
- Native to Brazil.

Constituents
- Leaf oil yielded major constituents of pyrimidine-5-carboxylic acid, 4-(1,3-dimethyl-1H-pyrazol-4-yl)-6-methyl-2- thioxo-1,2,3,4-tetrahydro-methyl ester (5.814%), 5-methyl-2-phenylindolizine (2.957%), 1- (3-methylbutyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-Pyrazole (2.764%),
Dichotine, 19-hydroxy-11methoxytriacetate methylpiperazin-1-yl)benzo[1,2,5]diazol-1-oxide methoxycarbonyl-1H-2-benzopyran-3-one ethanediylbis[diphenylphosphine]-p-p']hydro[(1,2,3,4,5-β)-1-methyl-2,4-cyclopentadien-1- yl] Iron (2.067%) and 9,10-dihyro-9,10,11-trimethyl-9,10-methano anthracen-11-ol (1.011%).

Properties
- The common name dumb-cane derives from the acrid and poisonous juice numbs the tongue.

Uses

Folkloric
No reported folkloric medicinal use in the Philippines.

Studies
Toxicity:
Toxicity results from brine shrimp lethality test showed a higher level of toxicity in the leaf than the stem essential oils.
Antimicrobial: Essential oil exhibited appreciable antimicrobial activity against E. coli, S. aureus, B. subtilis, P. aeruginosa, K. pneumonia, S. typhii, Candida albicans, C. krusei, A. niger and Penicillum aotatum.
Antioxidant: Tests using a DPPH assay showed the essential oils with higher activity than a-tocopherol. Results showed Dp with promising antioxidant activity as a free radical scavenger.
Eugenol / Toxicity: When chewed, the juice from the leaves causes a painful edema of the oral mucous membrane, buccal ulcerations and tongue hypertrophy - severe enough to possibly cause glottis obstruction, respiratory compromise and death. Topical application of essential oil extracted from Caryophyllus aromaticus provides about 70% reduction of edema.

Availability
Ornamental cultivation.

March 2012

IMAGE SOURCE: Sparkles leaves at Walmart Kahului, Maui / Forest and Kim Starr - Plants of Hawaii / Creative Commons Attribution 3.0 License / alterVISTA

Additional Sources and Suggested Readings
(1)
Chemical Composition, Toxicity, Antimicrobial and Antioxidant Activities of Leaf and Stem Essential Oils of Dieffenbachia picta (Araceae) / Ganiyat K Oloyede, Patricia Onocha, Sunday Abimbade / European Journal of Scientific Research ISSN 1450-216X Vol.49 No.4 (2011), pp. 567-580
(2)
Studies on Dieffenbachia picta Schott: Toxic effects in guinea pigs / Ângela M. Ladeira, Sylvia O. Andrade, Paulo Sawaya / Toxicology and Applied Pharmacology, Vol 34, No 3, December 1975, Pages 363–373
(3)
Ability of eugenol to reduce tongue edema induced by Dieffenbachia picta Schott in mice
/ Etyene Castro Dip, Nuno Alvarez Pereira, Patricia Dias Fernandes / Toxicon, Volume 43, Issue 6, May 2004, Pages 729–735


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