Arundo donax var. versicolor
Back to List

Arundo donax var. versicolor

Family: POACEAE
Genus: Arundo
Species: donax
Variety: versicolor
Distribution summary: Central & Southern Asia
Habit: Perennial
Hardiness: H5 - Hardy; cold winter
Garden status: Currently grown
Garden location: Europe & Middle East (J)
Reason for growing: Medicinal, prescription only medicine

Additional Notes

Syn. = Arundo donax 'Versicolor'

Prescription only medicine: lignocaine

Sodium ion channel blockade; GABA transaminase inhibitor. Contains gramine, from which lidocaine and other local anaesthetics were synthesised. Also used for controlling cardiac arrhythmias.

Oakeley, Dr. H.F. (2013). Medicines from RCP plants label list 5-2013.docx.

Lignocaine was synthesised from Arundo donax, (and also Hordeum vulgare - a form without chlorophyll), which contains gramine a bitter substance. From this isogramine was made which had weak local anaesthetic properties (the researchers tasted it !). From this lidocaine (aka lignocaine) was synthesised in 1943. Note: Completely synthetic drugs amylocaine (1903) and procaine (1904) antedated these plant-derived local anaesthetics. VERSATIN lidocaine patches for post herpetic neuralgia; LIDOCAINE im/iv Ventricular arrhythmias especially after heart attack; LIDOCAINE and numerous analogues, for local anaesthesia. ** Intravenous lignocaine has been used to abolish phantom limb pain. ** Cocaine was used as a local anaesthetic before the introduction of lignocaine, and had the serious disadvantage of occasionally causing cardiac arrest, as well as the problem of dependency and psychosis.

Oakeley notes: May 2014

Extracted from: Rev. Bras. Anestesiol. vol.52 no.3 Campinas May/June 2002 *** Arundo donax - By products: lidocaine (Löfgren & Lundquist, 1943) and tryptamine (von Euler, 1929). Achiralic lidocaine was synthesized as from the methylation of a grass byproduct which, “for being so bitter, was rejected even by camels” in Asian plateaus, namely isograss (the translator should have written isogramine). Clinically evaluated in the post-war period by Gordh (1947), lidocaine has become the prototype of new non histaminergic oral anesthetics - amino-amide group – with liver metabolism and more prolonged effects 11-13. REFS: Sten L - Xylocaine (lidocaine, lignocaine), its discovery and Gordh’s contribution to its clinical use. Acta Anaesthesiol Scand, 1998;42:(Suppl113):12. REFS: Gordh T - Xylocaine, a new local analgesic. Anaesthesia, 1949;4:4. REFS: Catterall WA, Mackie K - Local Anesthetics, em: Hardman JG, Limbird LE, Gilman AG - Godman & Gilman´s The Pharmacological Basis of Therapeutics, 10th Ed, New York, McGraw-Hill, 2001;367. REFS: Holmdahl MH - Xylocain (lidocaine, lignocaine), its discovery and Gordh's contribution to its clinical use. Acta Anaesthesiol Scand, 1998;113:8-12.

Rev. Bras. Anestesiol. vol.52 no.3 Campinas May/June 2002

Used to make the reed for oboes.

Oakeley notes: May 2014

Image Gallery

Previous Next

We use cookies to give you the best experience and to help improve our website.

By clicking the Accept button, you agree to us doing so. Find out more

Accept