The smelling of Hedione results in sex-differentiated human brain activity.

A large family of vomeronasal receptors recognizes pheromone cues in many animals including most amphibia, reptiles, rhodents, and other mammals. Humans possess five vomeronasal-type 1 receptor genes (VN1R1-VN1R5), which code for proteins that are functional in recombinant expression systems. We used two different recombinant expression systems and identified Hedione as a ligand for the putative human pheromone receptor VN1R1 expressed in the human olfactory mucosa. Following the ligand identification, we employed functional magnetic resonance imaging (fMRI) in healthy volunteers to characterize the in vivo action of the VN1R1 ligand Hedione. In comparison to a common floral odor (phenylethyl alcohol), Hedione exhibited significantly enhanced activation in limbic areas (amygdala, hippocampus) and elicited a sex-differentiated response in a hypothalamic region that is associated with hormonal release. Utilizing a novel combination of methods, our results indicate that the putative human pheromone receptor VN1R1 is involved in extra-olfactory neuronal activations induced by the odorous substance Hedione. The activation of VN1R1 might play a role in gender-specific modulation of hormonal secretion in humans.

Effects of deltamethrin on the specific discrimination of sex pheromones in two sympatric Trichogramma species.

The large amounts of insecticides used for crop protection lead to widespread environmental pollution. Determination of the potential impacts induced by this contamination on key species involved in the equilibrium of ecosystems is therefore a necessity. In this study, we tested the effects of a pyrethroid insecticide, deltamethrin, on the capacity of males from two sympatric Trichogramma species to discriminate the sex pheromones emitted by females of their own species (Trichogramma are parasitoids of Lepidopterous). The impact of an acute exposure as could occur at field edges was evaluated using a dose inducing 20% mortality (LD 20). The impact of a low exposure corresponding to diffuse environmental pollution was evaluated by applying an LD 0.1 (a dose inducing no apparent mortality). For T. semblidis, deltamethrin decreased the specific recognition of sexual pheromones at the higher dose (LD 20) but had no effect on this recognition at the lower dose (LD 0.1). However, deltamethrin decreased the saturation of pheromone receptors at both doses. For T. evanescens, deltamethrin increased the recognition of sexual pheromones at both doses, though not during the same period of observation (at the beginning for the LD 20, at the end for the LD 0.1), but it did not decrease the saturation of the pheromone receptors. These differing results were analyzed considering the behavior of the insects, their level of sensitivity to the insecticide and its mode of action. They provide new insights regarding possible consequences of environmental pollution by insecticides on functional biodiversity.

Dose-to-duration encoding and signaling beyond saturation in intracellular signaling networks.

The cellular response elicited by an environmental cue typically varies with the strength of the stimulus. For example, in the yeast Saccharomyces cerevisiae, the concentration of mating pheromone determines whether cells undergo vegetative growth, chemotropic growth, or mating. This implies that the signaling pathways responsible for detecting the stimulus and initiating a response must transmit quantitative information about the intensity of the signal. Our previous experimental results suggest that yeast encode pheromone concentration as the duration of the transmitted signal. Here we use mathematical modeling to analyze possible biochemical mechanisms for performing this "dose-to-duration" conversion. We demonstrate that modulation of signal duration increases the range of stimulus concentrations for which dose-dependent responses are possible; this increased dynamic range produces the counterintuitive result of "signaling beyond saturation" in which dose-dependent responses are still possible after apparent saturation of the receptors. We propose a mechanism for dose-to-duration encoding in the yeast pheromone pathway that is consistent with current experimental observations. Most previous investigations of information processing by signaling pathways have focused on amplitude encoding without considering temporal aspects of signal transduction. Here we demonstrate that dose-to-duration encoding provides cells with an alternative mechanism for processing and transmitting quantitative information about their surrounding environment. The ability of signaling pathways to convert stimulus strength into signal duration results directly from the nonlinear nature of these systems and emphasizes the importance of considering the dynamic properties of signaling pathways when characterizing their behavior. Understanding how signaling pathways encode and transmit quantitative information about the external environment will not only deepen our understanding of these systems but also provide insight into how to reestablish proper function of pathways that have become dysregulated by disease.

Unusual response characteristics of pheromone-specific olfactory receptor neurons in the Asian corn borer moth, Ostrinia furnacalis.

Male moth pheromone-detecting receptor neurons are known to be highly specific and very sensitive. We investigated physiological and behavioral responses to female sex pheromone components in male Ostrinia furnacalis moths (Lepidoptera: Crambidae). Using recordings from a cut-sensillum technique, trichoid sensilla could be grouped into four physiological types (1-4), according to the response of receptor neurons to the two major pheromone components, (E)-12- and (Z)-12-tetradecenyl acetate (E12- and Z12-14:OAc). These types could subsequently be characterized as four subtypes (A-D) depending on neural responses to pheromone components from various sister species of O. furnacalis, (Z)-9-, (E)-11- and (Z)-11-tetradecenyl acetate. The peripheral pheromone detection system of O. furnacalis is different to that of other moths. A large majority of the neurons investigated responded to both of the two principal pheromone components. Dose-response and cross-adaptation studies showed that olfactory receptor neurons with large amplitude action potentials responded equally well to E12- and Z12-14:OAc in sensillum types 1-3. Field experiments showed that O. furnacalis males are sensitive to ratios of E12- and Z12-14:OAc and that (Z)-9-tetradecenyl acetate acts as a behavioral antagonist. O. furnacalis males thus display an unusual coding system for odors involved in sexual communication, mainly built on less specific neurons, but still have the ability to detect and respond to the correct female blend. We hypothesize that the pheromone detection system of O. furnacalis consists of two parts, where one is devoted to high sensitivity to Delta12 isomers of tetradecenyl acetate, E12- and Z12-14:OAc and the other to highly specific responses to the E12- or Z12-14:OAc. The unusual feature is thus that a large part of the system is devoted to sensitivity and only a minor part to selectivity. This could be explained by the fact that no other moth species are known to use E12- and/or Z12-14:OAc and that no strong selective pressure to increase selectivity between the isomers has been determined.