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Narcissus and Daffodil

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Pharmacology of <strong>Narcissus</strong> compounds 343<br />

in muscle tone <strong>and</strong> isometric contractions) <strong>and</strong> at an early, rather than late, phase<br />

of treatment (5–15 days of the first course). No improvement was seen where the<br />

muscle showed zero power from the onset or in chronic cases. Very little improvement<br />

was seen in four of the seven cases of pseudo-hypertrophic muscular<br />

dystrophy <strong>and</strong> none in the remaining patients. Some improvement in the two<br />

children with facial paralysis was noted. Galanthamine was described as being well<br />

tolerated; mild reactions included salivation, nausea <strong>and</strong> abdominal pain that<br />

resolved on decreasing the dose.<br />

Improvement in motor function was observed when galanthamine was used as<br />

part of a programme of therapies used to treat polyneuropathy-associated Guillain-<br />

Barre syndrome (Kuyumdzhieva et al., 1996).<br />

Use in poisoning<br />

Reports in animal, <strong>and</strong> later in human, studies, of the reversal of respiratory<br />

depression caused by opiate analgesics are tempered by observations that cholinergic<br />

side effects are likely at the doses required <strong>and</strong> that only temporary reversal<br />

is achieved (Tassonyi et al., 1976). However, galanthamine has been used to<br />

reverse CNS effects in several cases of drug overdose, including scopolamine<br />

(Cozanitis, 1977), M<strong>and</strong>rax (a combination of diphenhydramine, a drug with<br />

marked anticholinergic properties <strong>and</strong> methaqualone, an hypnotic), <strong>and</strong> dextromoramide<br />

(a narcotic analgesic related to methadone, which caused marked<br />

respiratory depression) (Cozanitis <strong>and</strong> Toivakka, 1974).<br />

Analgesia<br />

Poultices of the leaves <strong>and</strong> bulbs of the Amaryllidaceae have been reported in<br />

herbal lore for hundreds of years as being used to treat painful neurological<br />

conditions such as facial neuralgia; this treatment was said to provide analgesic<br />

<strong>and</strong> curative effects (Rainer, 1997).<br />

Despite its apparent ability to reverse the respiratory depression seen with<br />

morphine-like analgesics, galanthamine does not appear to antagonise opiateinduced<br />

analgesia. Indeed, the drug is structurally related to morphine (see<br />

Figure 13.1). Evidence from st<strong>and</strong>ard laboratory tests suggests that the drug may<br />

have mild analgesic properties (Cozanitis et al., 1983). Suggestions that galanthamine<br />

may stimulate opioid receptors directly needs substantiation by direct,<br />

radiolig<strong>and</strong> binding studies.<br />

Migraine<br />

Ikonomoff (1968) was the first to report the use of galanthamine in the management<br />

of migraine patients. Of 140 cases involving galanthamine (in the form of the<br />

commercially available product ‘Nivalin’), 25 (18%) were headache free for 6<br />

years, <strong>and</strong> a further 64 (46%) had shown some improvement. In 42 patients, spontaneous<br />

epistaxis resolved <strong>and</strong> in 56 patients, subcutaneous ecchymosis ceased<br />

when galanthamine was used. Twenty-two of 59 female patients with dysmenorrhoea<br />

accompanying their migraine experienced resolution of period pains.<br />

Neostigmine was found to be superior in a similar range of patients. The author

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