Abstract
An HPLC method for the quantitative analysis of cardenolides was developed and applied.
The procedure was optimised for analysing small samples (40 mg dw) of plant and tissue
culture material. Isoplexis canariensis plants obtained from seeds accumulated cardenolides to about 20 - 40 μmol g-1 dw as calculated from the levels of cardenolide genins released after acidic hydrolysis
of methanolic extracts. The relative contents of xysmalogenin, digitoxigenin, uzarigenin
and canarigenin were 5 - 15 %, 0 - 5 %, 10 - 15 % and 70 - 90 %, respectively. Shoot
cultures were initiated from seeds, established as permanent cultures and cultivated
on agar-solidified or in liquid medium. Shoot cultures maintained on solid medium
contained an average of about 6 μmol cardenolides g-1 dw. A relatively high proportion of digitoxigenin was found in two-thirds of the
shoot cultures examined. The cardenolide content of amphibian shoot cultures averaged
to about 1 μmol g-1 dw. Plants regenerated from shoot cultures and maintained under hydroponic conditions
accumulated the same amount of cardenolides as plants collected in the field. No cardenolides
could be detected in callus cultures.
Key words
Isoplexis canariensis
- Plantaginaceae - cardenolides - cardiac glycosides - uzarigenin - xysmalogenin -
digitoxigenin - canarigenin - dianhydroperiplogenin - shoot culture - callus culture
- hydroponics
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Prof. Dr. Wolfgang Kreis
Institut für Biologie
Lehrstuhl Pharmazeutische Biologie
Friedrich-Alexander-Universität Erlangen-Nürnberg
Staudtstr. 5
91058 Erlangen
Germany
Phone: +49-9131-852-8241
Fax: +49-9131-852-8243
Email: wkreis@biologie.uni-erlangen.de