Jump to content

Ephedra (plant)

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Dcirovic (talk | contribs) at 01:40, 30 May 2016 (clean up, typo(s) fixed: between 1 to → between 1 and using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Ephedra
Ephedra fragilis in Mallorca
Scientific classification
Kingdom:
Division:
Class:
Order:
Ephedrales

Family:
Ephedraceae

Genus:
Ephedra

Map showing the range of Ephedra
Global range of Ephedra
Synonyms[3]

Chaetocladus J.Nelson

Ephedra is a genus of gymnosperm shrubs, the only genus in its family, Ephedraceae, and order, Ephedrales. The various species of Ephedra are widespread in many lands, native to southwestern North America, southern Europe, northern Africa, and southwest and central Asia, northern China, and western South America.[3]

In temperate climates, most Ephedra species grow on shores or in sandy soils with direct sun exposure. Common names in English include joint-pine, jointfir, Mormon-tea or Brigham tea. The Chinese name for Ephedra species is mahuang (simplified Chinese: 麻黄; traditional Chinese: 麻黃; pinyin: máhuáng; Wade–Giles: ma-huang; lit. 'cannabis yellow'). Ephedra is also sometimes called sea grape (from the French raisin de mer), a common name for the flowering plant Coccoloba uvifera.

Ephedra fragilis pollen cones
Ephedra distachya: ripe female cones with seeds
Ephedra ciliata seed

Medical uses

Plant as used in Chinese herbology (crude medicine)

Plants of the genus Ephedra, including E. sinica and others, have traditionally been used by indigenous people for a variety of medicinal purposes, including treatment of asthma, hay fever, and the common cold.[4] The alkaloids ephedrine and pseudoephedrine are active constituents of E. sinica and other members of the genus. These compounds are sympathomimetics with stimulant and decongestant qualities and are chemically substituted amphetamines.

Pollen of Ephedra spp. was found in the Shanidar IV burial site in Iraq, which led to the suggestion that its use as a medicinal plant dates to over 60,000 years ago.[5] Paul B. Pettitt has stated that "[a] recent examination of the microfauna from the strata into which the grave was cut suggests that the pollen was deposited by the burrowing rodent Meriones persicus, which is common in the Shanidar microfauna and whose burrowing activity can be observed today".[6] It has been suggested that Ephedra may be the Soma plant of Indo-Iranian religion.[7]

Adverse Effects

Alkaloids obtained from the species of Ephedra in herbal medicines containing synthetically prepared pseudoephedrine and ephedrine can cause cardiovascular events. These events have been associated with arrhythmias, palpitations, tachycardia and myocardial infarction. Caffeine consumption in combination with ephedrine has been reported to increase the risk of these cardiovascular events.[8]

Species

Accepted species:[3]

Economic botany and alkaloid content

Earliest uses of Ephedra spp. (mahuang) for specific illnesses date back to 5000 BC. Ephedrine and isomers were already isolated in 1881 from Ephedra dystachia and characterized by the Japanese organic chemist Nagai Nagayoshi of the 19th century. His work to access Ephedra drug materials to isolate a pure pharmaceutical substance, and the systematic production of semi-synthetic derivatives thereof is relevant still today as the three species Ephedra sinica, Ephedra vulgaris and to a lesser extent Ephedra equisetina are commercially grown in Mainland China as a source for natural ephedrines and isomers for use in pharmacy. E. sinica and E. vulgaris usually carry six optically active phenylethylamines, mostly ephedrine and pseudoephedrine with minor amounts of norephedrine, norpseudoephedrine as well as the three methylated analogs. Reliable information on the total alkaloid content of the crude drug is difficult to obtain. Based on HPLC analyses in industrial settings, the concentrations of total alkaloids in dried Herba Ephedra ranged between 1 and 4%, and in some cases up to 6%.[9]

For a review of the alkaloid distribution in different species of the genus Ephedra see Jian-fang Cui (1991).[10] Other American and European species of Ephedra, e.g. Ephedra nevadensis (Nevada Mormon tea) have not been systematically assayed; based on unpublished field investigations, they contain very low levels (less than 0.1%) or none at all.[11]

References

  1. ^ "Ephedrales Dumort". EU-NOMEN. Retrieved 20 January 2016.
  2. ^ a b Kramer, K.U.; Green, P.S., eds. (1990). The Families and Genera of Vascular Plants, Vol. 1: Pteridophytes and Gymnosperms. Berlin: Springer-Verlag. pp. 379–381. ISBN 3540517944. {{cite book}}: Unknown parameter |authors= ignored (help)
  3. ^ a b c Kew World Checklist of Selected Plant Families
  4. ^ Abourashed E, El-Alfy A, Khan I, Walker L (2003). "Ephedra in perspective—a current review". Phytother Res. 17 (7): 703–12. doi:10.1002/ptr.1337. PMID 12916063.
  5. ^ Solecki, Ralph S. (1975). "Shanidar IV, a Neanderthal Flower Burial in Northern Iraq". Science. 190 (4217): 880–881. doi:10.1126/science.190.4217.880. JSTOR 1741776.
  6. ^ Paul B. Pettitt (2002). "The Neanderthal dead: exploring mortuary variability in Middle Palaeolithic Eurasia". Before Farming. 1 (4): 1–26.
  7. ^ Rudgley, Richard (1993). The Alchemy of Culture. London: British Museum Press. pp. 44–45. ISBN 0-7141-2711-6.
  8. ^ Skalli, Souad; Zaid, Abdelhamid; Soulaymani, Rachida (December 2007). "Drug Interactions With Herbal Medicines". Ther Drug Monit. 29 (6): 1–8.
  9. ^ Brossi, Arnold (ed) (1989), The Alkaloids: Chemistry and Pharmacology, Vol. 35, ISBN 0-12-469535-3.
  10. ^ Cui, Jian-fang; et al. (1991). "Analysis of alkaloids in Chinese Ephedra species by GC methods". Phytochemical Analysis. 2 (3): 116–119. doi:10.1002/pca.2800020305.
  11. ^ Hegnauer R. (1962) "Chemotaxonomie der Pflanzen. I". Birkhauser Verlag, Basel; Switzerland, pp. 460–462 as cited in Roman MC (2004). "Determination of ephedrine alkaloids in botanicals and dietary supplements by HPLC-UV: collaborative study". J AOAC Int. 87 (1): 1–14. PMID 15084081.