2012, Number 4
<< Back Next >>
Rev Cubana Plant Med 2012; 17 (4)
Acaricide activity of Lauraceae extracts agaisnt domiciliary mites Dermatophagoides farinae and Blomia tropicalis
Cuca-Suárez LE, Mendoza-Meza DL, Álvarez-Caballero JM, Macías-Villamizar VE, Coy-Barrera ED
Language: Spanish
References: 29
Page: 308-319
PDF size: 123.85 Kb.
ABSTRACT
Introduction: Lauraceae plants are considered as important sources of bioactive substances, as those acting as insecticides. As part of our program for bioprospecting studies on Colombian Lauraceae plants, seven medicinal species belonging to this family were studied for their acaricide activity against Dermatophagoides farinae and Blomia tropicalis, considered public health problems at domiciliary level.
Objective: to evaluate acaricide activity of ethanol extracts from Lauraceae plants on domiciliary mites Dermatophagoides farinae and Blomia tropicalis as well as to characterize ethanol-soluble extracts by preliminary phytochemical assay.
Methods: in vitro acaricide activity of extracts from seven plants belonging to the Lauraceae family, harvested in different regions of Colombia, was assessed on individual adults through direct contact test and fumigant action. Each plant extract was tested for chemical characterization by means of coloration and precipitation tests.
Results: in direct contact bioassay, the leaf extract from Persea caerulea eliminated 100 % of Dermatophagoides farinae. In fumigant action bioassay, the leaf extract of Persea caerulea eliminated 100 % Dermatophagoides farinae and 83.37 % of Blomia tropicalis (after 120 minutes exposure at 0.1 mg/mL). The preliminary phytochemical testing identified the possible presence of metabolites according to the Lauraceae chemotaxonomy.
Conclusions: obtained results indicated that Lauraceae plants could be catalogued as a source of potential biocontrol agents against specific domiciliary mites Dermatophagoides farinae and Blomia tropicalis.
REFERENCES
Chanderbali AS, Werff Hvd, Renner SS. Phylogeny and historical biogeography of Lauraceae: evidence from the chloroplast and nuclear genomes. Ann Mo Bot Gard. 2001;88(1):104-34.
Pagotto CLA Da C, Barros JRT, Borin MR de MB, Gottlieb OR. Quantitative chemical biology II. Chemical mapping of Lauraceae. An Acad Bras Ciências. 1998;70(4):1705-9.
Zanin WSM, Lordello ALL. Alcalóides aporfinóides do gênero Ocotea (Lauraceae). Quimica Nova. 2007;30(1):92-8.
Coy ED, Cuca LE, Sefkow M. Macrophyllin-type bicyclo[3.2.1]octanoid neolignans from the leaves of Pleurothyrium cinereum. J Nat Prod. 2009;72(7):1245-8.
Garcez WS, Garcez FR, da Silva LMGE, Hamerski L. Larvicidal activity against Aedes aegypti of some plants native to the West-Central region of Brazil. Bioresource Technology. 2009;100(24):6647-50.
Cabral MMO, Mendonça PM, Gomes CMS, Barbosa Filho JM, Queiroz MMC, Mello RP. Biological activity of neolignans on the post-embryonic development of Chrysomya megacephala. Fitoterapia. 2007;78(1):20-4.
Soon-Il K, N Y-E, Y J-H, K B-S, Young-Joon A. Contact and fumigant toxicity or oriental medicinal plant extracts against Dermanyssus gallinae/Acari: Dermanyssidae. Vet Parasitol. 2007;145:377-82.
Ronchetti R, Villa MP, Matricardi PM, La Grutta S, Barreto M, Pagani J, et al. Association of asthma with extra-respiratory symptoms in schoolchildren: two cross-sectional studies 6 years apart. Pediatr Allergy Immunol. 2002;13(2):113-8.
Gerth van Wijk R. Allergy: a global problem. Quality of life. Allergy. 2002;57(12):1097-110.
Pawankar R, Baena-Cagnani CE, Bousquet J, Canonica GW, Cruz AA, Kaliner MA, et al. State of world allergy report 2008: Allergy and chronic respiratory diseases. WAO J. 2008;(Sup):4-17.
Mercado D, Puerta L, Caraballo L. Niveles de alérgenos de ácaros en el polvo de habitación en Cartagena, Colombia. Biomédica. 1996;16(4):307-14.
Fernandez-Caldas E. Annual Meeting of the Aragonese Society of Allergology: first main subjct: biodiversity of dust mites in allergologic pathology: mites and their allergens. J Allergy Clin Immunol. 1999;14(6):410-46. .
Sánchez-Borges M, Capriles-Hulett A, Caballero-Fonseca F, Fernández-Caldas E. Mite and cockroach sensitization in allergic patients from Caracas, Venezuela. Ann Allergy Asthma Immunol. 2003;90(6):664-8.
Almarales RL, Castelló MA, Díaz MR, Canosa JS, Gómez IG, León MG, et al. Sensitization to three species of mites in allergic patients from the coastal area of Havana city. Rev Alerg Mex. 2009;56(2):31-5.
Martínez Jiménez N, Aguilar Angeles D, Rojas Ramos E. Sensitization to Blomia tropicalis and Dermatophagoides pteronyssinus, farinae and siboney prevalence in patients with rhinitis, allergic asthma, or both, in a population of a metropolitan area of Mexico City. Rev Alerg Mex. 2010;57(1):3-10.
Furuno T, Terada Y, Yano S, Uehara T. Activities of leaf oils and their components from Lauraecae trees against house dust mites. Mokuzai Gakkaishi. 1994;40(1):78-87.
Siddiqui S, Verma A, Rather AA, Jabeen F, Meghvansi K. Preliminary phytochemical analysis of some important and aromatic plants. Adv Biol Res. 2009;3(5-6):188-95.
Colloff MJ, Spieksma FT. Pictorial keys for the identification of domestic mites. Clin Exp Allergy. 1992;22(9):823-30.
Perrucci S. Acaricidal Activity of Some Essential Oils and Their Constituents against Tyrophagus longior, a mite of stored food. J Food Protect. 1995;58(5):560-3.
Stendel W, Fuchs R. Biological evaluation of flumethrin, a new synthetic pyrethroid for the control of ticks. In: Griffiths DA, Bowman CE, editors. Acarology VI, Vol. 2. England: Chichester; 1984. p. 1252-5.
Kwon JH, Ahn YJ. Acaricidal activity of butylidenephthalide identified in Cnidium officinale rhizome against Dermatophagoides farinae and Dermatophagoides pteronyssinus (Acari: Pyroglyphidae). J Agr Food Chem. 2002;50(16):4479-83.
Abbott WS. A method of computing the effectiveness of an insecticide. 1925. J Am Mosq Control Assoc. 1925;3(2):302-3.
Ding H, Chin YW, Kinghorn AD, D'Ambrosio SM. Chemopreventive characteristics of avocado fruit. Semin Canc Biol. 2007;17(5):386-94.
Fraga BM, Terrero D, Gutiérrez C, González-Coloma A. Minor diterpenes from Persea indica: their antifeedant activity. Phytochemistry. 2001;56(4):315-20.
Rodriguez-Saona C, Millar J, Trumble J. Isolation, identification, and biological activity of isopersin, a new compound from avocado idioblast oil cells J Nat Prod. 1998;61(9):1168-70.
Rodriguez-Saona C, Maynard DF. Novel antifeedant and insecticidal compounds from avocado idioblast cell oil. J Chem Ecol. 2006;24(5):867-89.
Oberlies NH, Rogers LL, Martin JM, McLaughlin JL. Cytotoxic and insecticidal constituents of the unripe fruit of Persea americana. J Nat Prod. 1998;61(6):781-5.
Jones S, Burnett W, Coile N, Mabry T. Sesquiterpene lactones of Vernonia: influence of glaucolide-A on the growth rate and survival of Lepidopterous larvae. Ecologia. 1979;39(1):71-7.
Gottlieb OR. Chemosystematics of the lauraceae. Phytochemistry. 1972;11(5):1537-70.