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1.
Toxicol Lett ; 248: 46-51, 2016 Apr 25.
Article in English | MEDLINE | ID: mdl-26952004

ABSTRACT

Dose-response relations can be obtained from systems at any structural level of biological matter, from the molecular to the organismic level. There are two types of approaches for analyzing dose-response curves: a deterministic approach, based on the law of mass action, and a statistical approach, based on the assumed probabilities distribution of phenotypic characters. Models based on the law of mass action have been proposed to analyze dose-response relations across the entire range of biological systems. The purpose of this paper is to discuss the principles that determine the dose-response relations. Dose-response curves of simple systems are the result of chemical interactions between reacting molecules, and therefore are supported by the law of mass action. In consequence, the shape of these curves is perfectly sustained by physicochemical features. However, dose-response curves of bioassays with quantal response are not explained by the simple collision of molecules but by phenotypic variations among individuals and can be interpreted as individual tolerances. The expression of tolerance is the result of many genetic and environmental factors and thus can be considered a random variable. In consequence, the shape of its associated dose-response curve has no physicochemical bearings; instead, they are originated from random biological variations. Due to the randomness of tolerance there is no reason to use deterministic equations for its analysis; on the contrary, statistical models are the appropriate tools for analyzing these dose-response relations.


Subject(s)
Dose-Response Relationship, Drug , Models, Biological , Models, Statistical , Pharmaceutical Preparations/administration & dosage , Pharmacology/statistics & numerical data , Toxicology/statistics & numerical data
2.
J Med Entomol ; 46(3): 511-5, 2009 May.
Article in English | MEDLINE | ID: mdl-19496421

ABSTRACT

The aim of this study was to evaluate the fumigant and repellent activity of five essential oils (from eucalyptus, geranium, lavender, mint, and orange oil) and seven monoterpenes (eucalyptol, geraniol, limonene, linalool, menthone, linalyl acetate, and menthyl acetate) on first-instar nymphs of the bloodsucking bug Rhodnius prolixus Stahl (vector of Chagas disease in several Latin American countries). Fumigant activity was evaluated by exposing the nymphs to the vapors emitted by 100 microl of essential oil or monoterpene in a closed recipient. The knockdown time 50% (KT50) for eucalyptus essential oil was 215.6 min (seven times less toxic than dichlorvos, a volatile organophosphorus insecticide used as a positive control). The remaining essential oils showed a poor fumigant activity: < 50% of nymphs were knocked down after 540 min of exposure. The KT50 values for monoterpenes, expressed in minutes, were as follows: 117.2 (eucalyptol), 408.7 (linalool), 474.0 (menthone), and 484.2 (limonene). Eucalyptol was 3.5 times less toxic than dichlorvos. No affected nymphs were observed after 540 min of exposure to geraniol, linalyl acetate, or menthyl acetate. Repellency was quantified using a video tracking system. Two concentrations of essential oils or monoterpenes were studied (40 and 400 microg/cm2). Only mint and lavender essential oils produced a light repellent effect at 400 microg/cm2. Geraniol and menthyl acetate produced a repellent effect at both tested concentrations and menthone only elicited an effect at 400 microg/cm2. In all cases, the repellent effect was lesser than that produced by the broad-spectrum insect repellent N,N-diethyl-3-methylbenzamide (DEET).


Subject(s)
Fumigation , Insect Control/methods , Insecticides , Monoterpenes , Oils, Volatile , Plant Oils , Rhodnius , Animals , Nymph , Plants/chemistry , Rhodnius/growth & development
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