| Butterbur
Extract (Petasites Hybridus) Effective in Reducing Migraine Attacks
by Jim English
It is estimated that 240 million people worldwide
suffer 1.4 billion migraine attacks each year. Current therapeutic
options are often not effective or are accompanied by troublesome
side effects. New research reveals that an extract of the ancient
medicinal plant, Petasites hybridus (butterbur), can reduce the
frequency, duration and pain of migraine attacks by up to 60% with
a degree of safety and tolerance superior to most pharmaceutical
drugs.
Migraines strike women three times as frequently as men, affecting
5% of men and 17% of women in the United States. (1,2) In direct
medical costs and lost productivity, the annual cost in the United
States is estimated to exceed $17 billion. (3) In spite of these
numbers, according to the International Headache Society many migraines
go unrecognized and undertreated due largely to the fact that there
are no recognized biological markers to confirm the diagnosis. (4,5,6)
While the exact cause of migraine is not fully
understood, migraines can be triggered by internal and external
factors, such as stress, anxiety, food allergies, hormones and environmental
changes, such as light, heat and altitude. When triggered, the nervous
system responds with increased serotonergic activity in the brain,
vasodilation of the extra-cranial blood vessels, and concomitant
vasoconstriction of the intra-cranial blood vessels. (7)
Unlike tension headaches, migraines are a full-blown neurologic
disorder characterized by recurrent attacks of headache that, if
not successfully treated, can last anywhere from 2 to 72 hours.
Migraine pain is usually unilateral, appearing as a throbbing, pounding
pain on only one side of the head. During different phases of a
migraine attack, pain can move from one part of the head to another,
or radiate down into the neck and the shoulders. Skin hypersensitivity,
including scalp irritation and tenderness, also occur frequently
during a migraine attack.
Migraine sufferers often experience nausea and
vomiting accompanied by a pronounced and extreme sensitivity to
light (photophobia), sounds (phonophobia) and odors (osmophobia).
In severe attacks, even normal activities such as standing or walking
can intensify pain to the point where normal function is completely
disrupted.
Approximately 20% of all migraine sufferers experience visual disturbances
that are referred to as the migraine aura. In addition to alterations
in perception of light, sound and smell, aura can include bizarre
visual distortions such as blurry vision, spots, flashing lights,
wavy lines, flashing lights, and/or partial loss of sight. Other
symptoms may include vertigo, tingling or numbness of the face or
extremities, auditory hallucinations, difficulty or confusion when
forming words, and impaired hearing. Some patients even have the
aura without the headaches.
Standard treatments aim to control symptoms by calming sensitive
nerve pathways and reducing the inflammatory response while preventing
future attacks. As with tension headaches, some individuals find
that very mild migraine attacks can be treated with standard analgesics
such as aspirin, acetaminophen, ibuprofen and naproxen. These drugs,
in addition to their potential gastrointestinal side effects, have
been shown to increase risk of rebound (medication-induced) headaches.
(8) Combination medications such as acetaminophen with codeine,
aspirin with codeine and caffeine, and aspirin with butalbital and
caffeine (with or without codeine) are sometimes used. However,
overuse of combination medications is one of the most prominent
causes of rebound headache, which is the leading form of chronic
daily headache. (7)
Sumatriptan, a selective 5-hydroxy-triptamine 1 (5-HT1) receptor
agonist, has been shown more effective than placebo in treating
moderate to severe migraines (50-80% versus 20-40%) when administered
by subcutaneous injection. Reported side effects include tightness
in the chest, chest pain, pain in the throat, tingling in the head
or limbs, nausea, and a high rate (44%) of migraine recurrence within
24 hours. (9,10)
Dihydroergotamine (DHE), a nonselective 5-HT1
receptor agonist, has also been shown effective in relieving headache
when used subcutaneously, intramuscularly or intravenously, but
side effects are similar to those of sumatriptan. (11,12) Ergotamine
has also been used for many years to treat migraine, but meta-analysis
has demonstrated little benefit from oral dosing. (13) Side effects
of ergotamine resemble those of DHE, but nausea is usually more
severe. (14,15,16)
Other migraine medications include:
- Beta-blockers (Propranolol)
- Tricyclic anti-depressants (Amitriptyline)
- MAO inhibitors (Phenelzine)
- Adrenergic blockers (Clonidine)
- Serotonin antagonists (Cyproheptadine)
- Calcium channel antagonists (Verapamil)
- Anticonvulsants (Phenytoin)
- Butorphanol nasal-spray (Stadol)
As with the previous medications, side effects
of these medications are substantial. In the case of beta-blockers,
they are contraindicated for patients with asthma, chronic obstructive
pulmonary disease, insulin-dependent diabetes mellitus, heart failure,
or peripheral vascular disease. Calcium-channel blockers, which
can take several months to become effective, are contraindicated
in pregnancy and in patients with hypotension, congestive heart
failure, arrhythmias or depressive illness. (17,18,19,20)
Petasites hybridus (butterbur) is an herbal plant found throughout
Europe, Asia and North America. For centuries the leaves and rhizomes
of this perennial shrub have been used as an important medicinal
herb. (21,22) Modern researchers have discovered that extracts of
petasites contain active ingredients that prevent migraines and
act as an antispasmodic to support chronic cough or asthma. (23)
The main active ingredients of petasites hybridus are two sesquiterpenes,
petasin and isopetasin. Research has shown that petasin possesses
anti-spasmodic properties that help to reduce spasms in smooth muscle
and vascular walls. Petasin has also been found to be a powerful
anti-inflammatory agent that inhibits synthesis of leukotrienes
that act as potent pro-inflammatory agents in blood vessel walls,
causing bronchoconstriction in asthma. (24)
The second active ingredient, isopetasin, has
also been found to reduce inflammation by modulating prostaglandin
metabolism. Together these ingredients have an antispasmodic effect
on vascular walls, with a marked affinity for cerebral blood vessels.
(25)
Researchers in Germany conducted a randomized, placebo-controlled,
double-blind clinical study using a standardized extract of petasites
(Petadolex®). 60 patients suffering from headaches with and
without aura randomly received either 50 mg of a standardized petasites
extract or placebo, twice daily for 12 weeks. At the conclusion
of the test the researchers found that, compared to placebo, petasites
hybridus significantly reduced the frequency of migraine attacks
and days with migraine per month, as well as the frequency of accompanying
symptoms. Compared to baseline, petasites hybridus reduced the frequency
of attacks by 46% after 4 weeks, 60% after 8 weeks and 50% after
12 weeks of treatment (placebo group: 24%, 17% and 10%, respectively).
(26)
 |
The researchers also found that the extract reduced
the total number of migraine days (Fig. 1). Of particular interest
was the finding that patients who entered the study reporting at
least three migraine attacks per month showed the most pronounced
reduction in events. (Fig. 2) Patients also reported significant
alleviation of intensity of migraine pain, leading researchers to
conclude that petasites extract is most effective in reducing migraine
in patients who suffer the most from frequent severe attacks.
 |
Petadolex® is a special standardized extract of Petasites hybridus
that offers a new option for migraine sufferers. Petadolex is effective
in reducing the number of days with migraines per month, in decreasing
migraine-associated symptoms, and in reducing both the duration
and intensity of migraine pain. Petasites extract has a history
of excellent tolerance, and no adverse side effects have been reported.
It should be noted that it is important to take Petadolex on a daily
basis for maximum effectiveness.
References
1. Stewart WF, Shechter A, Rasmussen BK. Migraine prevalence: a
review of population-based studies. Neurology 1994;44(6 suppl 4):S17-S23.
2. Celentano DD, Stewart WF, Lipton RB, Reed ML. Medication use
and disability among migraineurs: a national probability sample.
Headache 1992;32:237-8.
3. De Lissvoy G, Lazarus SS. The economic cost of migraine: present
state of knowledge. Neurology 1994;44(6 suppl 4):S56-S62.
4. Lipton RB, Stewart WF, Celentano DD, Reed ML. Undiagnosed migraine:
a comparison of symptom-based and physician diagnosis. Arch Intern
Med 1992;152:1273-8.
5. Headache Classification Committee, International Headache Society.
Classification and diagnostic criteria for headache disorders, cranial
neuralgias and facial pain. Cephalalgia 1988;8(suppl 7):1-96.
6. Ad Hoc Committee on Classification of Headache. Classification
of headache. JAMA 1962;179:717-8.
7. Mathew NT. Chronic daily headache: clinical features and natural
history. In: Nappi G, et al, editors. Headache and depression: serotonin
pathways as a common clue. New York: Raven Press; 1991:49-58.
8. Saper JR, Silberstein S, Gordon CD, et al. Handbook of headache
management. Baltimore: Williams and Wilkins; 1993.
9. Subcutaneous Sumatriptan International Study Group. Treatment
of migraine attacks with sumatriptan. N Engl J Med 1991;325:316-21.
10. Winner P, Ricalde O, Le Fortce B, Saper J, Margul B. A double
blind study of subcutaneous dihydroergotamine vs subcutaneous sumatriptan
in the treatment of acute migraine. Arch Neurol 1996;53:180-4.
11. Winner P, Ricalde O, Le Fortce B, Saper J, Margul B. A double
blind study of subcutaneous dihydroergotamine vs subcutaneous sumatriptan
in the treatment of acute migraine. Arch Neurol 1996;53:180-4.
12. Scherl ER, Wilson JF. Comparison of dihydroergotamine with metoclopramide
versus meperidine with promethazine in the treatment of acute migraine.
Headache 1995;35:256-9.
13. (Dahlof C. Placebo-controlled clinical trials with ergotamine
in the acute treatment of migraine. Cephalalgia 1993;13(3):166-71.
14. Hakkarainen H, Allonen H. Ergotamine vs metoclopramide vs their
combination in acute migraine attacks. Headache 1982;22:10-2.
15. Kangasniemi P, Kaaja R. Ketoprofen and ergotamine in acute migraine.
J Intern Med 1992;231:551-4.
16. Kinnunen E, Erkinjuntti T, Farkkila M, et al. Placebo-controlled
double-blind trial of pirprofen and an ergotamine tartrate compound
in migraine attacks. Cephalalgia 1988;8:175-9.
17. Al-Qassab HK, Findley LJ. Comparison of propranolol LA 80 mg
and propranolol LA 160 mg in migraine prophylaxis: a placebo controlled
study. Cephalalgia 1993;13:128-31.
18. Ryan Sr RE, Ryan Jr RE, Sudilovsky A. Nadolol: its use in the
prophylactic treatment of migraine. Headache 1983;23:26-31.
19. Gerber WD, Diener HC, Scholz E, Niederberger U. Responders and
non-responders to metoprolol, propranolol and nifedipine treatment
in migraine prophylaxis: a dose-range study based on time-series
analysis. Cephalalgia 1991;11:37-45.
20. Markley HG. Verapamil and migraine prophylaxis: mechanisms and
efficacy. Am J Med 1991;90(suppl 5A):48S-53S.
21. Eaton J. Butterbur, herbal help for migraine. Nat Pharm 1998;2:1,23-24.
22. Mauskop, A. Petasites hybridus: ancient medicinal plant is effective
prophylactic treatment for migraine. Townsend Lett 2000;202:104-106.)
23. Grieve M. Butterbur. In: Leyel CF, ed. A Modern Herbal, electronic
version. New York, NY: Dover Publications, Inc. 1971.
24. Thomet OA, Wiesmann UN, Schapowal A, Bizer C, Simon H. Role
of petasin in the potential anti-inflammatory activity of a plant
extract of petasites hybridus. Biochem Pharmacol 2001 Apr 15;61(8):1041-1047.
25. Altern Med Rev 2001 Jun;6(3):303-310. 26. Grossmann M, Schmidramsl
H. An extract of Petasites hybridus is effective in the prophylaxis
of migraine. Int J Clin Pharmacol Ther 2000 Sep;38(9):430-435. |