Registro:

Referencias:

• Anton, S., Homberg, U., Antennal lobe structure (1999) Insect Olfaction, pp. 98-125. , In Hansson, B.S. (Ed.), Springer, Berlin
• Anton, S., Dufour, M.C., Gadenne, C., Plasticity of olfactory-guided behaviour and its neurobiological basis: lessons from moths and locusts (2007) Entomol. Exp. Appl., 123, pp. 1-11
• Aversa, A., Mazzilli, F., Rossi, T., Delfino, M., Isidori, A.M., Fabbri, A., Effects of sildenafil [Viagra (TM)] administration on seminal parameters and post-ejaculatory refractory time in normal males (2000) Hum. Reprod., 15, pp. 131-134
• Barrozo, R.B., Gadenne, C., Anton, S., Switching from attraction to inhibition: mating-induced reversed role of sex pheromone in an insect (2010) J. Exp. Biol., 213, pp. 2933-2939
• Barrozo, R.B., Jarriault, D., Simeone, X., Gaertner, C., Gadenne, C., Anton, S., Mating-induced transient inhibition of responses to sex pheromone in a male moth is not mediated by octopamine or serotonin (2010) J. Exp. Biol., 213, pp. 1100-1106
• Blejec, A., Statistical method for detection of firing rate changes in spontaneously active neurons (2005) Neurocomputing, 65, pp. 557-563
• Breunig, E., Manzini, I., Piscitelli, F., Gutermann, B., Di Marzo, V., Schild, D., Czesnik, D., The endocannabinoid 2-arachidonoyl-glycerol controls odor sensitivity in larvae of Xenopus laevis (2010) J. Neurosci., 30, pp. 8965-8973
• Chapman, T., The soup in my fly: evolution, form and function of seminal fluid proteins (2008) PLoS Biol., 6, pp. 1379-1382
• Christensen, T.A., Hildebrand, J.G., Male-specific, sex pheromone-selective projection neurons in the antennal lobes of the moth, Manduca sexta (1987) J. Comp. Physiol. A., 160, pp. 553-569
• Christensen, T.A., Hildebrand, J.G., Pheromonal and host-odor processing in the insect antennal lobe: how different? (2002) Curr. Opin. Neurobiol., 12, pp. 393-399
• Crnjar, R., Yin, C.M., Stoffolano, J.G., Barbarossa, I.T., Liscia, A., Angioy, A.M., Influence of age on the electoantennogram response of the female blowfly (Phormia regina) (1990) J. Insect Physiol., 36, pp. 917-921
• Dacks, A., Christensen, T.A., Hildebrand, J.G., Modulation of olfactory information processing in the antennal lobe of Manduca sexta by serotonin (2008) J. Neurophysiol., 99, pp. 2077-2085
• Deisig, N., Giurfa, M., Lachnit, H., Sandoz, J.-C., Neural representation of olfactory mixtures in the honeybee antennal lobe (2006) Eur. J. Neurosci., 24, pp. 1161-1174
• Domingue, M.J., Roelofs, W.L., Linn, C.E., Baker, T.C., Effects of egg-to-adult development time and adult age on olfactory neuron response to semiochemicals in European corn borers (2006) J. Insect Physiol., 52, pp. 975-983
• Gadenne, C., Anton, S., Central processing of sex pheromone stimuli is differentially regulated by juvenile hormone in a male moth (2000) J. Insect Physiol., 46, pp. 1195-1206
• Gadenne, C., Dufour, M.C., Anton, S., Transient post-mating inhibition of behavioural and central nervous responses to sex pheromone in an insect (2001) Proc. R. Soc. Lond. B, 268, pp. 1631-1635
• Galizia, C.G., Vetter, R., Optical methods for analyzing odor-evoked activity in the insect brain (2005) Methods in Insect Sensory Neuroscience, pp. 349-392. , In Christensen, T.A. (Ed.), CRC Press, London
• Galizia, C.G., Nägler, K., Hölldobler, B., Menzel, R., Odour coding is bilaterally symmetrical in the antennal lobes of honeybees (Apis mellifera) (1998) Eur. J. Neurosci., 10, pp. 2964-2974
• Gemeno, C., Haynes, K.F., Chemical and behavioral evidence for a third pheromone component in a North American population of the black cutworm moth, Agrotis ipsilon (1998) J. Chem. Ecol., 24, pp. 999-1011
• Greiner, B., Gadenne, C., Anton, S., Central processing of plant volatiles in Agrotis ipsilon males is age-independent in contrast to sex pheromone processing (2002) Chem. Senses, 27, pp. 45-48
• Hansson, B.S., Olfaction in Lepidoptera (1995) Experientia, 51, pp. 1003-1027
• Heil, J.E., Oland, L.A., Lohr, C., Acetylcholine-mediated axon-glia signaling in the developing insect olfactory system (2007) Eur. J. Neurosci., 26, pp. 1227-1241
• Homberg, U., Müller, U., Neuroactive substances in the antennal lobe (1999) Insect Olfaction, pp. 181-207. , In Hansson, B.S. (Ed.), Springer, Berlin
• Jarriault, D., Gadenne, C., Rospars, J., Anton, S., Quantitative analysis of sex-pheromone coding in the antennal lobe of the moth Agrotis ipsilon: a tool to study network plasticity (2009) J. Exp. Biol., 212, pp. 1191-1201
• Kaissling, K.E., Single unit and electroantennogram recordings in insect olfactory organs (1995) Experimental Cell Biology of Taste and Olfaction: Current Techniques and Protocols, pp. 361-376. , In Spielman, E.I. & Brand, J.G. (Eds), CRC Press, Boca Raton, FL
• Kaissling, K.E., Thorson, J., Insect olfactory sensilla: structural, chemical and electrical aspects of the functional organization (1980) Receptors for Transmitters, Hormones and Pheromones in Insects, pp. 261-282. , In Sattelle, D.B., Hall, L.M. & Hildebrand, J.G. (Eds), Elsevier, Amsterdam
• Kelliher, K.R., Baum, M.J., Effect of sex steroids and coital experience on ferrets' preference for the smell, sight and sound of conspecifics (2002) Physiol. Behav., 76, pp. 1-7
• Kloppenburg, P., Hildebrand, J.G., Neuromodulation by 5-hydroxytryptamine in the antennal lobe of the sphinx moth, Manduca sexta (1995) J. Exp. Biol., 198, pp. 603-611
• Kloppenburg, P., Ferns, D., Mercer, A.R., Serotonin enhances central olfactory neuron responses to female sex pheromone in the male sphinx moth Manduca sexta (1999) J. Neurosci., 19, pp. 8172-8181
• Koontz, M.A., Schneider, D., Sexual dimorphism in neuronal projections from the antennae of silkmoths (Bombyx mori, Antheraea polyphemus) and the gypsy moth (Lymantria dispar) (1987) Cell Tissue Res., 249, pp. 39-50
• Kubli, E., Sex-peptides: seminal peptides of the Drosophila male (2003) Cell. Mol. Life Sci., 60, pp. 1689-1704
• Kumashiro, M., Tsuji, Y., Sakai, M., Auto-spermatophore extrusion in male crickets (2003) J. Exp. Biol., 206, pp. 4507-4519
• Lemmen, J., Evenden, M., Peripheral and behavioral plasticity of pheromone response and its hormonal control in a long-lived moth (2009) J. Exp. Biol., 212, pp. 2000-2006
• Masante-Roca, I., Gadenne, C., Anton, S., Plant odour processing in the antennal lobe of male and female grapevine moths, Lobesia botrana (Lepidoptera: Tortricidae) (2002) J. Insect Physiol., 48, pp. 1111-1121
• Mercer, A.R., Kloppenburg, P., Hildebrand, J.G., Serotonin-induced changes in the excitability of cultured antennal-lobe neurons of the sphinx moth Manduca sexta (1996) J. Comp. Physiol. A., 178, pp. 21-31
• Namiki, S., Iwabuchi, S., Kanzaki, R., Representation of a mixture of pheromone and host plant odor by antennal lobe projection neurons of the silkmoth Bombyx mori (2008) J. Comp. Physiol. A., 194, pp. 501-515
• Ochieng, S.A., Park, K.C., Baker, T.C., Host plant volatiles synergize responses of sex pheromone-specific olfactory receptor neurons in male Helicoverpa zea (2002) J. Comp. Physiol. A., 188, pp. 325-333
• Ogawa, S., Makino, J., Aggressive behavior in inbred strains of mice during pregnancy (1984) Behav. Neural Biol., 40, pp. 195-204
• Olsen, S.R., Wilson, R.I., Lateral presynaptic inhibition mediates gain control in an olfactory circuit (2008) Nature, 452, pp. 956-962
• Party, V., Hanot, C., Said, I., Rochat, D., Renou, M., Plant terpenes affect intensity and temporal parameters of pheromone detection in a moth (2009) Chem. Senses, 34, pp. 763-774
• Perk, C.G., Mercer, A.R., Dopamine modulation of honey bee (Apis mellifera) antennal-lobe neurons (2006) J. Neurophysiol., 95, pp. 1147-1157
• Phillips-Farfán, B.V., Fernández-Guasti, A., Endocrine, neural and pharmacological aspects of sexual satiety in male rats (2009) Neurosci. Biobehav. Rev., 33, pp. 442-455
• Picimbon, J.F., Gadenne, C., Bécard, J.M., Clément, J.L., Sreng, L., Sex pheromone of the French black cutworm moth, Agrotis ipsilon (Lepidoptera: Noctuidae): identification and regulation of a multicomponent blend (1997) J. Chem. Ecol., 23, pp. 211-230
• Rees, C.J.C., Age dependency of response in an insect chemoreceptor sensillum (1970) Nature, 227, pp. 740-742
• Sachs, B.D., Barfield, R.J., Temporal patterning of sexual behavior in the male rat (1970) J. Comp. Physiol. Psychol., 73, pp. 359-364
• Sachse, S., Galizia, C.G., The coding of odour-intensity on the honeybee antennal lobe: local computation optimizes odour representation (2003) Eur. J. Neurosci., 18, pp. 2119-2132
• Sakai, M., Matsumoto, Y., Takemori, N., Taoda, Y., Postcopulatory sexual refractoriness is maintained under the control of the terminal abdominal-ganglion in the male cricket Gryllus bimaculatus Degeer (1995) J. Insect Physiol., 41, pp. 1055-1070
• Sandoz, J.-C., Odour-evoked responses to queen pheromone components and to plant odours using optical imaging in the antennal lobe of the honey bee drone Apis mellifera L (2006) J. Exp. Biol., 209, pp. 3587-3598
• Schneider, D., Insect antennae (1964) Annu. Rev. Entomol., 9, pp. 103-122
• Seabrook, W.D., Hirai, K., Shorey, H.H., Gaston, L.K., Maturation and senescence of an insect chemosensory response (1979) J. Chem. Ecol., 5, pp. 587-594
• Serguera, C., Triaca, V., Kelly-Barrett, J., Banchaabouchi, A., Minichiello, L., Increased dopamine after mating impairs olfaction and prevents odor interference with pregnancy (2008) Nat. Neurosci., 11, pp. 949-956
• Sokal, R.R., Rohlf, F.J., (1995) Biometry, , W.H. Freeman, New York
• Wang, L., Chen, L., Jacob, T., Evidence for peripheral plasticity in human odour response (2004) J. Physiol. (Lond.), 554, pp. 236-244
• Wang, S., Zhang, S., Sato, K., Srinivasan, M.V., Maturation of odor representation in the honeybee antennal lobe (2005) J. Insect Physiol., 51, pp. 1244-1254
• Wynne, J.W., Keaster, A.J., Gerhardt, K.O., Krause, G.F., Plant species identified as food sources for adult black cutworm in Northwestern Missouri (1991) J. Kans. Entomol. Soc., 64, pp. 381-387
• Zhu, Y., Keaster, A.J., Gerhardt, K.O., Field observations on attractiveness of selected blooming plants to noctuid moths and electroantennogram responses of black cutworm (Lepidoptera: Noctuidae) moths to flower volatiles (1993) Environ. Entomol., 22, pp. 162-166

Citas:

---------- APA ----------

---------- CHICAGO ----------

---------- MLA ----------

---------- VANCOUVER ----------