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Family Lythrceae
Kupea
Cuphea hyssopifolia Kunth
FALSE HEATHER

Other scientific names Common names
Cuphea carthaginensis  (Jacq.) Macbr. Kupea (Tag.)
Parsonia hyssopifolia Jean gaiac(French)
  False heather (Engl.)
  Elphin plant (Engl.)
  Radie raide (FG Creole)

Botany
A small and much-branched shrub growing to 1.5 meters. Stems are semi-woody, slender and crooked. Leaves are green, opposite, stalkless and numerous on the branches, narrow-lanceolate, up to 1.5 cm long. Flowers are small, purplish violet to light purple with green calyx.

Distribution
Recently introduced to the Philippines.
Popular as a hedge plant.
Propagated by stem cuttings.

Chemical constituents and properties
• Study isolated two new ellagitannin dimers, cuphiins D1 and D2, with six known compounds including oenothein B and woodfordin C from the aerial part of Cuphea hyssopifolia.
Contains flavone pigments.
.
Uses
Folkloric
No recorded folkloric medicinal use in the Philippines.
In Brazil, used to treat high cholesterol and triglycerides.
In French Guiana, stem and leaf macerated in rum and rubbed onto sprains. Leaf infusion used for colds and chills.

Studies
Cholesterol Lowering : Biochemical analysis of animals treated with aqueous extract showed a significant reduction of plasma cholesterol in rats; no effect was noted on glucose and triglyceride levels.
Cuphilin / Anti-Tumor Activity: (1) Study isolated cuphilin D1 (CD1), a new macrocyclic hydrolyzable tannin, has been shown to exert in vivo and in vitro antitumor activity. Further study showed CD1 induced cytotoxicity to HL-60 cells (human promyelocytic leukemia cells. The CD1-induced apoptosis was attributed to inhibition of Bcl-2 expression in HL-60. (2) Cuphiin D1 (CD1) significantly inhibited the growth of human cervical carcinoma, i.e. HeLa cells, with less cytotoxicity to normal primary-cultured cervical fibroblasts. CD1 also inhibited Bcl-2 expression in HeLa cells and may account for the Cd1-induced apoptosis.
Anti-Tumore / Anti-Cancer: Study isolated four macrocylic tannin dimers: cuphiin D1, cuphiin D2, cenothein B and woodfordin C. All siginificantly inhibited the growth of the human carcinoma cell lines KB, HeLa, DU-145, Hep 3B and the leukemia cell line HL-60. Results suggest the anti-tumor effects of the compounds are not only related to their cytotoxicity on carcinoma cell lines but also on some host-mediated mechanism.

Availability
Wildcrafted.

Last Update June 2010

Additional Sources and Suggested Readings
(1)
Preliminary studies on Campomanesia xanthocarpa (Berg.) and Cuphea carthagenensis (Jacq.) J.F. Macbr. aqueous extract: weight control and biochemical parameters / Journal of Ethnopharmacology Vol 93, Issues 2-3, August 2004, Pages 385-389 / doi:10.1016/j.jep.2004.04.015
(2)
Cuphiin D1, the macrocyclic hydrolyzable tannin induced apoptosis in HL-60 cell line / Cancer Letters Vol 149, Issues 1-2, 28 February 2000, Pages 77-83 / doi:10.1016/S0304-3835(99)00344-4
(3)
Macrocyclic ellagitannin dimers, cuphiins D1 and D2, and accompanying tannins from Cuphea hyssopifolia / Lih-Geeng Chen et al / Phytochemistry / Volume 50, Issue 2, 26 January 1999, Pages 307-312 / doi:10.1016/S0031-9422(98)00512-3
(4)
Medicinal Plants of the Guianas (Guyana, Surinam, French Guiana)

(5)
Antitumor activity of four macrocyclic ellagitannins from Cuphea hyssopifolia / Ching-Chiung Wang et al / Cancer Letters, Volume 140, Issue 1, Pages 195-200 (1 June 1999)
(6)
Cytotoxic effects of cuphiin D1 on the growth of human cervical carcinoma and normal cells / Wang C C, Chen L G and Yang L L / Anticancer Res. 2002 Sep-Oct;22(5):2677-84.

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