Você está na página 1de 4

Journal of Ethnopharmacology 92 (2004) 163–166

Review
The role of weeds as sources of pharmaceuticals
John R. Stepp
Tropical Conservation and Development Program, Department of Anthropology, University of Florida, Gainesville, FL 32611-7305, USA
Received 5 January 2004; received in revised form 9 March 2004; accepted 10 March 2004

Abstract

Primary tropical forest is generally considered to be the most likely habitat to discover new pharmaceuticals, due to high biodiversity and
endemism. However, many indigenous groups rely on non-forested disturbed environments for medicinal plants. An ethnobotanical approach
to drug discovery suggests that these disturbed environments may also harbor potentially useful medicinal compounds. Despite the neglect by
current researchers to conduct drug discovery in disturbed environments, many source plants for modern pharmaceuticals thrive in disturbed
areas. An analysis of the 101 plant species from which 119 contemporary pharmaceuticals are derived shows that at least 36 of these plants
are considered weeds (χ2 = 343.34, P < 0.0001). These results are an order of magnitude higher than what would be predicted by random
occurrence of weeds in the modern pharmacopeia. Biochemical evidence based on literature is presented to explain this occurrence. This
finding suggests that disturbed habitats may be important areas to search for novel compounds in drug discovery.
© 2004 Elsevier Ireland Ltd. All rights reserved.

Keywords: Weeds; Pharmaceuticals; Drug discovery; Medicinal plants

1. Introduction drugs are currently derived is reported here. While pri-


mary tropical forests likely contain many undiscovered
Natural products can be important sources for new phar- novel compounds that could have medicinal applications,
maceuticals (Abelson, 1990). With regards to plants, primary disturbed habitats may also hold promising leads for drug
tropical forest is often considered to be the most promising discovery. There are also policy implications in these find-
habitat for this search due to high biodiversity and endemism ings related to conservation of medicinal plants utilized in
(Gentry, 1993; Macilwain, 1998). Many researchers have traditional societies. The undervaluing and even destruction
combined this assumption with an ethnobotanical approach of weeds could have an impact on availability of certain
to drug discovery in order to maximize the chance of a medicinal plants. Also, the realization that medicinal plants
successful drug discovery (cf. Prance et al., 1994). How- are readily available in a “living pharmacy” right outside
ever, this focus on tropical forests overlooks the fact that the door and along trailsides rather than deep in the forest
disturbed environments are preferred habitats for medici- could lead governments and NGO’s to encourage and pro-
nal plant procurement by many traditional peoples (Kohn, mote traditional medical practices rather than discourage
1992; Voeks, 1996; Frei et al., 2000). For a more com- them.
plete literature review on this issue see Stepp and Moerman Vascular plants continue to play a role both as sources of
(2001). current drugs and in drug discovery. In 1991, almost half of
Meanwhile, the role of weeds in the present pharma- the best selling pharmaceuticals were either natural prod-
copeia has been overlooked, despite significant evidence that ucts or their derivatives (O’Neill and Lewis, 1993). Over
weeds in particular, are an important source of medicines 25% of prescriptions filled in the United States in 1973
for indigenous peoples and have a highly significant over contained one or more active principles still derived from
representation in indigeous pharmacopoeias in relation to higher plants (Farnsworth and Soejarto, 1985). As sources
other types of plants (Stepp and Moerman, 2001). The sig- of new anti-cancer and anti-infective agents, natural prod-
nificant representation of weeds in the flora from which ucts play an even larger role. From 1989 to 1995, over 60%
of approved drugs and pre-NDA candidates in these disease
areas were from natural products (Cragg et al., 1997). While
E-mail address: stepp@anthro.ufl.edu (J.R. Stepp). natural products drug discovery efforts increasingly focus

0378-8741/$ – see front matter © 2004 Elsevier Ireland Ltd. All rights reserved.
doi:10.1016/j.jep.2004.03.002
164 J.R. Stepp / Journal of Ethnopharmacology 92 (2004) 163–166

more on micro-organisms and fungi, research continues Table 1


with vascular plants and much of this work is in areas of Weed species as source plants for pharmaceuticals
high biodiversity and endemism such as the humid tropics Weed Not weed Total species
(Rosenthal, 1997). Pharmaceutical source plant 36 65 101
Not pharmaceutical source plant 7964 241935 249899
Total 8000 242000 250000
2. An analysis of weeds in the modern pharmacopeia
χ2 = 343.34, P < 0.0001.
An analysis was undertaken to determine the role that
weedy plant species currently play as source plants for
modern pharmaceuticals. A species was considered to be a be a nuisance species by foresters because of its invasiveness.
weed if it was included in the standard reference for weeds Other woody species on the list are Azadirachta indica Juss.,
worldwide, containing over 8000 species based on a global Erythroxylum coca Lam., Larrea divaricata Cav., and Salix
literature search (Holm et al., 1979). Because it is a global alba L. Despite their habit as trees or shrubs, these species
compendium based on a comprehensive survey of the liter- are considered invasive enough in certain regions to warrant
ature, Holm et al. (1979) do not offer a singular definition their inclusion in the list of world weeds (Holm et al., 1979).
of weeds. However, they do classify each species as to Also, a few of the species on the list are cultivated (Cannabis
whether it is a serious, principal, or common weed; whether sativa L., Gossypium sp., Nicotiana tabacum L., and Thymus
its rank is unknown; and whether a species is present in vulgaris L.).
the flora but unconfirmed that it behaves as a weed. For While both woody species and cultivated species may be
the purpose of this analysis, only weeds that were consid- considered weeds in the broad sense due to their potentially
ered to be serious, principal, or common are included. A invasive nature, they were not considered in this analysis.
good general definition of a weed that corresponds to those With their subtraction, there remains 36 species from which
species included in this analysis is “a plant . . . if, in any pharmaceuticals are derived that are considered weeds. A
specified geographical area, its populations grow entirely Chi-square analysis demonstrates that this is highly signifi-
or predominantly in situations markedly disturbed by man, cant (χ2 = 343.34, P < 0.0001). A list of the weedy species
without, of course, being a deliberately cultivated plant used in the analysis and their derived compounds are pro-
(Baker, 1965).” Weeds are those plants that are successful vided in Tables 1 and 2.
in disturbed environments, short-lived, fast-growing and
oftentimes, herbaceous.
Based on a World Health Organization survey (Farnsworth 3. Biochemical explanations for weeds as medicinals
et al., 1985) and more recent review articles based on
literature searches for drugs of natural plant product ori- There is increasing evidence to support the hypothesis
gin (Farnsworth and Soejarto, 1991; Cragg et al., 1997), that weeds are relatively high in bioactive secondary com-
there are 121 pharmaceutical compounds used as medicine pounds and are thus likely to hold promise for drug dis-
worldwide that are derived from plants. Of these, 101 plant covery. Secondary compounds in weeds are important for a
species are the primary sources for 119 of these compounds. variety of ecological functions. Chief among these are al-
The remaining two compounds (borneol and pinitol) are lelopathy, where secondary compounds inhibit germination
regularly obtained from dozens of different species and and growth of other plants; and, as chemical defense against
were not included in this analysis. Using a conservative es- herbivory (Harborne, 1993). At least 50 species of weeds
timate of 250,000 flowering plants (Heywood, 1993) and an have been shown to interfere with crops through allopathic
estimate that 8000 of these plants are weeds (Holm et al., secondary compounds (Putnam, 1994). However, because
1979), one would expect that 3% of these 101 species would allelopathy usually occurs through the complex chemical
be weeds. However, the actual number is more than an or- matrix of the soil it is difficult to conclusively show a causal
der of magnitude higher. Forty-five of the 101 are noted as relationship (Zimdahl, 1999).
weedy species in Holm et al. (1979), the definitive global Investigations into plant anti-herbivore defense are per-
reference guide for weeds. It should be noted that the overall haps further developed. The two major anti-herbivory
concept of a “weed” contains a variety of features, not all chemical defense strategies for plants are metabolically
present in any one weed. However, if we take the definition inactive immobile (or quantitative, as defined by Feeny,
stated above the vast majority of these 45 species fit this 1976) defenses such as tannins and lignins that reduce
definition. digestibility; and mobile (or qualitative) defenses such as
There are some notable exceptions. For example, Taxus alkaloids, cardiac glycosides or terpenoids (Feeny, 1976;
brevifolia Nutt. is a long-lived understory tree of the Pacific Coley et al., 1985). It is these latter types of compounds that
Northwest. Even so, it shares some traits of a weed, in that it are the basis for plant-derived pharmaceuticals. Ephemeral,
is aggressive and quickly colonizes a disturbed area. Prior to successional or r-selected species (all common charac-
the development of paclitaxel (TaxolTM ) it was considered to teristics of weeds) tend to rely on these sorts of toxic
J.R. Stepp / Journal of Ethnopharmacology 92 (2004) 163–166 165

Table 2 4. Conclusions
Weeds from which pharmaceuticals have been derived
Plant species Drug Ecological data can provide important clues in the search
Adonis vernalis L. Adoniside
for plants with bioactive compounds. The evidence presented
Agrimonia eupatoria L. Agrimophol here suggests that screening of the 8000 plant species con-
Ammi visnaga (L.) Lamk. Khellin sidered to be weeds may yield more medicinal compounds
Anabasis aphylla L. Anabasine when compared to a random screening of flora.
Andrographis paniculata Nees Andrographolide, Some drug discovery programs are screening or plan to
neoandrographolide
Artemisia annua L. Artemisinin
screen secondary growth species. The prematurely termi-
Atropa belladonna L. Atropine nated Maya International Cooperative Biodiversity Group
Berberis vulgaris L. Berberine (ICBG), for example, concentrated almost exclusively on
Brassica nigra (L.) Koch Allyl isothiocynate secondary growth herbaceous species (Berlin et al., 1999).
Cassia senna L. var. senna Sennosides A & B Other ICBG projects that focus on indigenous pharma-
Cassia spp. Danthron
Catharanthus roseus (L.) G. Don Vinblastine, vincristine
copoeias are also screening plants found in secondary and
Centella asiatica (L.) Asiaticoside disturbed habitats (Lewis et al., 1999; Kingston et al.,
Cissampelos pareira L. Cissampeline 1999).
Colchicum autumnale L. Colchiceine amide, Will new pharmaceuticals be found in weedy floras? The
colchiceine, demecolcine possibility exists that because weeds are so well known, their
Convallaria majalis L. Convallatoxin
Crotalaria spectabilis Roth Monocrotaline
chemistry is also well known and unlikely to yield novel
Cytisus scoparius (L.) Link Sparteine compounds. On the other hand the search for pharmaceuti-
Datura metel L. Scopolamine cals in far off remote jungles may have led to some of the
Digitalis purpurea L. Digitalin, digitoxin, ditalin weedy species being overlooked as a potential source for
Dioscorea spp. Diosgenin novel compounds. Regardless, their current use as sources
Glaucium flavum Crantz Glaucine
Glycyrrhiza glabra L. Glycyrrhizin
of pharmaceuticals has certainly been overlooked and its
Hyoscamus niger L. Hyoscyamine time that the much maligned weeds be given more respect
Lobelia inflata L. Lobeline for their use as phytomedicines.
Mentha spicata L. Menthol
Papaver somniferum L. Codeine, morphine,
papaverine, noscapine
Ricinus communis L. Castor oil
References
Rorippa indica (L.) Hiern Rorifone
Silybum marianum (L.) Gaertn. Silymarin Abe, T., Higashi, M., 1991. Cellulose centered perspective on terrestrial
Sophora pachycarpa Schrenk ex Pachycarpine community structure. Oikos 60, 127–133.
C. A. Meyer Abelson, P.H., 1990. Medicine from plants. Science 247, 513.
Symphytum officinale L. Allantoin Baker, H.G., 1965. Characteristics and modes of origin of weeds. In:
Urginea maritama (L.) Baker Scillaren A Baker, H.G., Stebbins, G.L. (Eds.), The Genetics of Colonizing Species.
Valeriana officinalis L. Valepotriates Academic Press, New York, pp. 147–172.
Veratrum album L. Protoveratines A & B Berlin, B.B., Berlin, E.A., Fernández, J.C., Garcı́a, L., Puett, D., Nash,
Vinca minor L. Vincamine R., González-Espinoza, M., 1999. The Maya ICBG: drug discovery,
medicinal ethnobiology, and alternative forms of economic develop-
ment in the highland Maya region of Chiapas, Mexico. Pharmaceutical
Biology 37, 127–144.
chemical defenses (Rhoades and Cates, 1976; Abe and Coley, P.D., 1988. Effects of plant growth rate and leaf lifetime on the
Higashi, 1991). A positive correlation has been demon- amount and type of plant anti-herbivore defense. Oecologia 74, 531–
strated between long-living plants and a reliance on immo- 536.
bile compounds (Coley et al., 1985). Further support for Coley, P.D., Bryant, J.P., Chapin, F.S., 1985. Resource availability and
plant antiherbivore defense. Science 230, 895–899.
the relationship between lifespan and type of defense is Cragg, G.M., Newman, D.J., Snader, K.M., 1997. Natural products in drug
provided by the fact that alkaloids are twice as likely to discovery and development. Journal of Natural Products 60, 52–60.
appear in annuals than perennials (Levin, 1976). Leaf life Farnsworth, N.R., Akerele, O., Bingel, A.S., Soejarto, D.D., Guo, Z., 1985.
is also an important predictor of defense strategy (Coley, Medicinal plants in therapy. Bulletin of the World Health Organization
1988). Plants with long-lived leaves rely on immobile de- 63, 965–981.
Farnsworth, N.R., Soejarto, D.D., 1985. Potential consequence of plant
fenses while plants with short-lived leaves invest in toxic extinction in United States on the current and future availability of
compounds. Leaves on weeds are generally short-lived. prescription drugs. Economic Botany 39, 231–240.
Also, fast-growing species tend to invest in mobile de- Farnsworth, N.R., Soejarto, D.D., 1991. Global importance of medicinal
fense compounds rather than immobile (Coley et al., 1985). plants. In: Akerele, O., Heywood, V., Synge, H. (Eds.), The Conser-
Weeds are generally fast-growing. Taken as a whole, it is vation of Medicinal Plants. Cambridge University Press, Cambridge,
pp. 25–52.
reasonable to infer from these data that weedy plant species Feeny, P.P., 1976. Plant apparency and chemical defense. In: Wallace,
will usually rely on bioactive defense compounds against J.W., Mansell, R.L. (Eds.), Recent Advances in Phytochemistry, vol.
herbivory. 10. Plenum, New York, pp. 1–40.
166 J.R. Stepp / Journal of Ethnopharmacology 92 (2004) 163–166

Frei, B., Sticher, O., Heinrich, M., 2000. Zapotec and Mixe use of tropical Macilwain, C., 1998. When rhetoric hits reality in debate on bioprospect-
habitats for securing medicinal plants in Mexico. Economic Botany ing. Nature 392, 535–540.
54, 73–81. Putnam, A.R., 1994. Weed allelopathy. In: Duke, S.O. (Ed.), Weed Phys-
Gentry, A.H., 1993. Tropical forest biodiversity and the potential for iology, vol. I. Reproduction and Ecophysiology. CRC Press, Boca Ra-
new medicinal plants. In: Kinghorn, A.D., Balandrin, M.F. (Eds.), ton, pp. 131–155.
Human Medicinal Agents from Plants. American Chemical Society, O’Neill, M.J., Lewis J.A., 1993. The renaissance of plant research in the
Washington, DC, pp. 13–24. pharmaceutical industry. In: Kinghorn, A.D., Balandrin, M.F. (Eds.),
Harborne, J.B., 1993. Introduction to Ecological Biochemistry, 4th ed. Human Medicinal Agents from Plants. American Chemical Society,
Harcourt Brace & Company, London. Washington, DC, pp. 48–55.
Heywood, V.H., 1993. Flowering Plants of the World. Oxford University Prance, G.T., Chadwick, D.J., Marsh, J. (Eds.), 1994. Ethnobotany and
Press, New York. the Search for New Drugs: Ciba Foundation Symposium 185. John
Holm, L., Pancho, J.V., Herberger, J.P., Plucknett, D.L., 1979. A Geo- Wiley and Sons, New York, 280 pp.
graphical Atlas of World Weeds. John Wiley & Sons, New York. Rhoades, D.F., Cates R.G., 1976. A general theory of plant antiherbivore
Kingston, D., et al., 1999. The Surinamese International Cooperative Bio- chemistry. In: Wallace, J.W., Mansell, R.L. (Eds.), Recent Advances
diversity Group program: lessons from the first five years. Pharmaceu- in Phytochemistry, vol. 10. Plenum, New York, pp. 168–213.
tical Biology 37, 22–34. Rosenthal J., 1997. Integrating drug discovery, biodiversity conservation,
Kohn, E., 1992. Some observations on the use of medicinal plants from and economic development: early lessons from the international coop-
primary and secondary growth by the Runa of Eastern lowland Ecuador. erative biodiversity groups. In: Grifo, F., Rosenthal, J. (Eds.), Biodiver-
Journal of Ethnobiology 12, 141–152. sity and Human Health. Island Press, Washington. DC, pp. 281–301.
Levin, D.A., 1976. Alkaloid-bearing plants: an ecogeographic perspective. Stepp, J.R., Moerman, D.E., 2001. The importance of weeds in ethnophar-
American Naturalist 110, 261–284. macology. Journal of Ethnopharmacology 75, 25–31.
Lewis, W., Lames, G., Vaisberg, A., Corley, D.G., Sarasara, C., 1999. Voeks, R., 1996. Tropical forest healers and habitat preference. Economic
Peruvian medicinal plant sources of new pharmaceuticals (International Botany 50, 381–400.
Cooperative Biodiversity Group—Peru). Pharmaceutical Biology 37, Zimdahl, R.L., 1999. Fundamentals of Weed Science, 2nd ed. Academic
69–83. Press, San Diego.

Você também pode gostar