Location: Poisonous Plant ResearchTitle: Alkaloid profiles of Mimosa tenuiflora and associated methods of analysis Author
Submitted to: Poisoning by Plants, Mycotoxins, and Related Toxins
Publication Type: Book / Chapter
Publication Acceptance Date: 5/18/2010
Publication Date: 5/1/2011
Citation: Gardner, D.R., Riet-Correa, F., Panter, K.E. 2011. Alkaloid profiles of Mimosa tenuiflora and associated methods of analysis. In: Riet-Correa, F., Pfister, J., Schild, A.L., Wierenga, T., editors. Poisoning by Plants, Mycotoxins, and Related Toxins. Cambridge, MA: CAB International. 103:600-5. Interpretive Summary: Mimosa tenuiflora is a common shrub/tree found in many parts of South America and northward into Mexico. In northeastern Brazil it is often eaten by livestock including goats, sheep, and cattle and is believed to be responsible for induced malformations observed in many animals from that region. In experimental feeding trails in goats M. tenuiflora was found to produce malformations similar to those observed in field cases. The plant is reported to contain certain alkaloid compounds with known psychoactive properties, but generally the alkaloid content of the plant has not been well investigated and especially not in relation to livestock poisonings and thus the teratogenic principles of M. tenuiflora remain unknown. Here we report on the analysis of the alkaloid content from leaves and seeds of M. tenuiflora collected from northeastern Brazil. Alkaloids were isolated by classical acid/base extraction procedures and also using cation exchange solid phase extraction. The crude alkaloid fractions were then analyzed by thin layer chromatography (TLC), gas chromatography-mass spectrometry (GC-MS) and by liquid chromatography-mass spectrometry (LC-MS).
Technical Abstract: The alkaloid contents of the leaves and seeds of M. tenuiflora collected from northeastern Brazil were studied. Alkaloids were isolated by classical acid/base extraction procedures and by cation exchange solid phase extraction. The crude alkaloid fractions were then analysed by thin layer chromatography (TLC), gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS). In the initial analysis by GC-MS, two major alkaloids were detected and were identified as N,N-dimethyltryptamine (DMT) and 2-methylcarboline. A third alkaloid was only detected when extraction by method A was conducted. TLC analysis of the extracts also showed the presence of two major alkaloids. DMT and 2-methylcarboline were detected following GC-MS analysis. LC/UV/MS detected five alkaloids with UV and MS data consistent with tryptamine type alkaloids. These included DMT and 2-methylcarboline, and three unknown alkaloids. At least three possible minor alkaloids were detected, but their UV spectra was not consistent with the tryptamine type alkaloids. The presence of a possible artifact alkaloid was observed by LC-UV-MS analysis when extracts were prepared using extraction method A. Seed and leaf samples collected at different years were extracted and analysed by TLC and LC-MS. Significant differences were observed in the alkaloid profiles between seed and leaves in that the two major spots in the TLC chromatograms were absent in seed samples. The best method of analysis appeared to be solid phase extraction followed by LC/UV/MS.