Natural insecticides fromHippocratea excelsa andHippocratea celastroides

Hippocratea excelsa andHippocratea celastroides have therapeutic and insecticide applications in Mexican traditional medicine. The toxicity ofH. excelsa root cortex has been previously demonstrated against the stored grain pest Sitophilus zeamais. To identify the active compounds, several extracts (petroleum ether, CH2Cl2, acetone, methanol, and water) and compounds were obtained from the roots, and tested (1% w/w) with a force-feeding assay againstS. zeamais. AllH. excelsa extracts showed high antifeedant activity, and elicited moderate mortality. The triterpenoid pristimerin and a mixture of sesquiterpene evoninoate alkaloids, isolated from the hexane and methanol extracts, respectively, strongly reduced the insect feeding capacity. Other triterpenoids (friedelin, β-sitosterol, canophyllol) isolated from the hexane extract, and the alditol galactitol obtained from the water extract, were innocuous or its activity was not statistically significant. The organic extracts fromH. celastroides only showed moderate antifeedant activity, while the water extract was innocuous. Galactitol was also obtained from this extract.ResumenA las plantas citadas, se les atribuye en México propiedades medicinales e insecticidas. Estudios previos han demostrado que las raíces (corteza) deHippocratea excelsa poseen actividad insecticida contra la plaga de granos almacenadosSithophilus zeamais. Para identificar las substancias activas de las raíces, se obtuvieron diversos extractos (éter de petróleo, CH2Cl2, acetona, metanol y agua) y compuestos; estos fueron ensayados mediante pruebas de alimentatión obligada (1% p/p) conS. zeamais. Todos los extractos deH. excelsa redujeron drásticamente la alimentatión e incrementaron moderadamente la mortalidad. De los extractos de hexano y metanol se aislaron el triterpeno pristimerina y una mezcla de alcaloides sesquiterpénicos, respectivamente; dichas substancias presentaron actividad antialimentaria alta. Otros triterpenoides aislados del extracte hexánico (friedelina, β-sitosterol, canofilol) y el alditol galactitol obtenido del extracto acuoso resultaron inocuos, o Men, su actividad no fue significativa estadísticamente. Los extractos orgánicos deH. celastroides presentaron actividad antialimentaria moderada, en tanto el extracte acuoso resulto inocuo. De dicho extracto también se obtuvo galactitol.

[1]  P. Hersch-Martínez Medicinal plants and regional traders in Mexico: physiographic differences and conservational challenge , 1997, Economic Botany.

[2]  P. Hersch-Martínez Commercialization of wild medicinal plants from Southwest Puebla, Mexico , 1995, Economic Botany.

[3]  M. Jacobson Plants, insects, and man—their interrelationships , 1982, Economic Botany.

[4]  A. Smith The American species of Hippocrateaceae , 1940, Brittonia.

[5]  D. M. Secoy,et al.  Use of plants in control of agricultural and domestic pests , 2008, Economic Botany.

[6]  M. V. Calsteren,et al.  Two novel Diels-Alder adducts from Hippocratea celastroides roots and their insecticidal activity , 2000 .

[7]  M. Villarreal,et al.  Cytotoxic activity of selected plants used as antitumorals in Mexican traditional medicine. , 1998, Journal of ethnopharmacology.

[8]  K. Goodman,et al.  Implications of Helicobacter pylori infection for stomach cancer prevention. , 1997, Cadernos de saude publica.

[9]  U. Karsten,et al.  The compability with enzyme activity of unusual organic osmolytes from mangrove red algae , 1996 .

[10]  R. Mata,et al.  Hippocrateine III, a sesquiterpene alkaloid from Hippocratea excelsa , 1995 .

[11]  R. Pérez,et al.  Anti-inflammatory activity of the bark of Hippocratea excelsa. , 1995, Journal of ethnopharmacology.

[12]  José Núñez,et al.  Plantas medicinales de la Cuenca del Río Balsas Universidad Nacional Autónoma de México , 1995 .

[13]  Jill P. Benner Pesticidal compounds from higher plants , 1993 .

[14]  R. Bye,et al.  Friedelanes and triterpenoid quinone methides from Hippocratea excelsa. , 1991, Planta medica.

[15]  R. Mata,et al.  Chemical studies on Mexican plants used in traditional medicine, XV. Sesquiterpene evoninoate alkaloids from Hippocratea excelsa. , 1990, Journal of natural products.

[16]  L. Calhoun,et al.  Sesquiterpene alkaloids from Tripterygiumwilfordii (Hook): a nuclear magnetic resonance study of 1-desacetylwilfordine, 1-desacetylwilfortrine, and 2-debenzoyl-2-nicotinoylwilforine , 1990 .

[17]  P. Clemens Galactose and cataract. , 1989, Survey of ophthalmology.

[18]  J. Nawrot,et al.  Antifeeding activity of rotenone and some derivatives towards selected insect storage pests , 1989 .

[19]  M. Jacobson,et al.  Botanical pesticides, past, present, and future , 1989 .

[20]  D. Stambolian,et al.  Galactose and cataract. , 1988, Survey of ophthalmology.

[21]  M. Hämäläinen,et al.  Metabolic effects in rats of high oral doses of galactitol, mannitol and xylitol. , 1985, The Journal of nutrition.

[22]  E. Breitmaier,et al.  THE INFLUENCE OF METHYLATION ON (13)C CHEMICAL SHIFTS OF GALACTOSE DERIVATIVES , 1974 .

[23]  E. Breitmaier,et al.  The influence of methylation on 13C chemical shifts of galactose derivatives , 1973 .

[24]  V. Plouvier CHAPTER 11 – Distribution of Aliphatic Polyols and Cyclitols , 1963 .

[25]  J. Steyermark,et al.  Flora of Guatemala. Part I. Cycadaceae to Bromeliaceae. , 1958 .

[26]  M. Beroza Alkaloids from Tripterygium wilfordii Hook. The Structure of Wilforine, Wilfordine, Wilforgine and Wilfortrine , 1953 .

[27]  H. Haller,et al.  Wilfordine, an insecticidal alkaloid from Tripterygium wilfordii Hook. , 1950 .

[28]  M. Schechter,et al.  Identity of the Red Pigment in the Roots of Tripterygium wilfordii and Celastrus scandens , 1942 .