Photoperiod cues and the modulatory action of octopamine and 5-hydroxytryptamine on locomotor and pheromone response in male gypsy moths,Lymantria dispar

Experiments were conducted to determine whether the biogenic amines octopamine (OA) and 5-hydroxytryptamine (5-HT) exert modulatory effects on pheromone responsiveness and random locomotor activity in male gypsy moths. When injected into males, OA significantly enhanced sensitivity to pheromone, while 5-HT enhanced general locomotor activity, results that were very similar to those previously shown for the cabbage looper. Maximal effect of the amines, however, was observed when injection occurred just prior to the onset of scotophase, rather than photophase, as we had originally hypothesized for this diurnally active insect. Male gypsy moths also displayed a prominent scotophase response, with sensitivity to pheromone greater in the scotphase compared with photophase, but with the level of random locomotor activity lower in scotophase than in photophase. The upwind flight behavior of males to a pheromone source in a wind tunnel, as well as the time spent at the source, were also significantly different in the two light regimes. Furthermore, when exposed to a 1 h scotophase (instead of the normal 8), or to continuous dark conditions, while males exhibited response to pheromone and locomotor activity during the same scotophase and photophase periods as observed in a 16:8 light : dark cycle, the levels of response, as well as qualitative aspects of the upwind flight behaviors in both periods were a function of the light intensity. Our combined results suggest that male gypsy moths display a bimodal rhythm of locomotor and pheromone response over the diel cycle, with light intensity and scotophase onset providing critical cues for the expression of behaviors, as well as the modulatory action of the amines. © 1992 Wiley-Liss, Inc.     

Physiological Mechanisms of Pheromonostatic Responses: effects of Adrenergic Agonists and Antagonists on Moth (Helicoverpa armigera) Pheromone Biosynthesis

The adrenergic agonists octopamine, tyramine and clonidine inhibited the normal pheromonotropic action due to PBAN (pheromone biosynthesis activating neuropeptide) in incubations of intersegmental tissues that are situated between the 8th and 9th abdominal segments of the moth ovipositor tip. This inhibition was reversed in the presence of the adrenergic antagonists phentolamine, yohimbine and chlorpromazine. Incubations of 8th segments alone, which do not produce pheromone, resulted in elevated levels of intracellular cAMP in the presence of octopamine. The physiological significance of this phenomenon is unclear. However, clonidine (an alpha(2) selective agonist) did not duplicate octopamine stimulation of intracellular cAMP in 8th segment cultures. In intersegmental membrane cultures clonidine successfully duplicated the octopamine inhibition of both pheromone and intracellular cAMP production. The physiological significance of octopaminergic receptors mediating the inhibitory response of intersegments was investigated by experiments in vivo. When PBAN was injected into photophase females the normal pheromonotropic activity due to the injected PBAN dropped after 2h. In the presence of clonidine, normal peak stimulatory levels were never attained and a faster decline was observed. Clonidine also inhibited the pheromonotropic response of 24h-decapitated females to PBAN. Adrenergic antagonists successfully reversed the inhibitory effect of clonidine in decapitated females, but did not reverse the effect of clonidine in photophase females. In addition, when clonidine was injected into female moths during the scotophase normal peak pheromone titers were reduced although no effect on calling behavior was observed. Copyright 1997 Elsevier Science Ltd. All rights reserved     

Diel changes in the presence and physiological actions of octopamine in the female sex-pheromone glands of heliothine moths

Recent evidence suggests that the biogenic monoamine octopamine (OA) may be involved in the regulation of female sex-pheromone production in Lepidoptera. A radioenzymatic assay coupled with high performance liquid chromatography revealed the presence of OA in the innervated sex-pheromone gland of the corn earworm moth Helicoverpa (Heliothis) zea. Significantly more OA was found in glands just before the onset of scotophase (ca 320 fmol/gland), compared to levels at mid-photophase or just after the onset of scotophase (ca 160 fmol/gland).

Exogenous OA had several actions on pheromone production. H. zea virgin females normally do not produce pheromone during the photophase, but highly significant levels of pheromone were induced by injection of OA into intact, day-2 photophase females. Importantly, this effect was absent in older females that showed increased levels of flight and oviposition activity. A second action of OA was revealed in isolated abdomen preparations from day-2 H. virescens females. Exogenous OA stimulated highly significant increases in pheromone production if abdomens were treated at the onset of scotophase, but not if they were treated in photophase. This critical period for OA action in these reduced preparations coincided with the time when peak levels of OA were present in the pheromone gland tissue. OA is therefore sufficient to induce pheromone production, but its actions in these short-lived insects depend on factor such as age and photoperiod. Diel fluctuations in OA levels in the pheromone gland, together with the observed phermonotropic actions of this amine, support the hypothesis that OA is involved in the regulation of pheromone production in these insects.     

Diel periodicity and influence of age and mating on female sex pheromone titre in Estigmene acrea (Lep., Arctiidae)

Abstract:  Calling behaviour, diel periodicity, and effect of age and mating on female sex pheromone titre in Estigmene acrea (Drury) were studied under laboratory conditions. Forty-five per cent of females started calling during the first scotophase, but the highest number of calling females was observed during the second, third and fourth scotophases. Calling behaviour occurred from the third hour after dark until just before the end of the scotophase. However, females exhibited a bimodal pattern of calling with the first peak occurring between 4 and 6 h and a second peak at 10 h after the onset of scotophase. The mean onset of calling time differed significantly with age. Older females showed a tendency to call longer, but there was no significant difference. The amount of (Z,Z)-3,6-cis-9, 10-epoxyheneicosadiene in females was quantified from the first scotophase following emergence, until the fifth scotophase. Glands of 0-day-old females presented a higher content of pheromone compared with that found in glands of 1-, 2-, 3- and 4-day-old females. Pheromone titre was determined at 2-h intervals throughout the third scotophase and photophase. (Z,Z)-3,6-cis-9,10-epoxyheneicosadiene was found in the gland during the scotophase as well as the photophase. However, there was no consistent pattern of pheromone production throughout the scotophase or photophase. Mated females of E. acrea produced significantly less pheromone than virgin females.     

Spatial and temporal distribution of pheromone biosynthesis-activating neuropeptide in Helicoverpa (Heliothis) armigera using RIA and in vitro bioassay.

A [3H]-PBAN (pheromone biosynthesis-activating neuropeptide) analog was synthesized, and binding of the radioligand to a specific PBAN-antiserum was achieved. The inhibition of binding of the radioligand by unlabeled PBAN, several PBAN analogs, and other competitors was studied and a specific radio-immunoassay was developed. Using this radioimmunoassay we found PBAN-like immunoreactivity in methanol extracts of hemolymph and neural tissues from females. Higher levels of PBAN-like immunoreactivity in extracts of brain-suboesophageal ganglion complexes, corpora cardiaca, thoracic ganglia, and abdominal ganglia were observed during the 4-5th h scotophase when compared to the PBAN-like immunoactivity levels during the 6-11th h photophase. On the other hand, the concentrations of PBAN-like immunoreactivity, in the terminal abdominal ganglion were higher during the photophase relative to minimal levels observed during the scotophase, indicating an accumulation before the onset of pheromone production. These differences in concentrations of PBAN were also reflected in the stimulation of in vitro pheromone glands, whereby significant stimulations were obtained by scotophase and photophase brain extracts, scotophase thoracic ganglia extracts, and photophase terminal abdominal ganglia extracts. No detectable levels of PBAN were found in hemolymph extracts during the sampling periods.     

Regulation of sex pheromone biosynthesis in the oriental tobacco budworm,Helicoverpa assulta (Lepidoptera: Noctuidae)

The five components, Z9-16:Ald, 16:Ald, Z11-16:Ald, Z9-16:Ac and Z11-16:Ac, of the sex pheromone in Helicoverpa assulta were mostly detected during the scotophase, with their titer peaking at the 4th hour during the scotophase under a 15L/9D regime. They were not detected during the photophase, but were produced during the photophase when decapitated females were injected with extracts of virgin female (FHE), male heads (MHE), homogenates of the brain-suboesophageal ganglion complex (Br-SOG), or synthetic Hez-PBAN. Production of Z9-16:Ald increased during the first 45min after FHE injection and then declined to a very low level after 2h during the photophase. Synthetic Hez-PBAN stimulated the sex pheromone glands for at least 2h and the effect was more or less proportional to the concentration of the peptide. From the present results, we suggest the following: PBAN is released continuously into the haemolymph to stimulate pheromone biosynthesis at least during the first half of the scotophase, PBAN is synthesized and accumulated independent of photoperiod or sex, and the release starts just prior (about 1h) to the beginning of the scotophase.     

Ca2+ stabilizes the membrane potential of moth olfactory receptor neurons at rest and is essential for their fast repolarization

The role of Ca(2+) in insect olfactory transduction was studied in the moth Spodoptera littoralis. Single sensillum recordings were made to investigate in vivo the role of sensillar Ca(2+) on the electrophysiological properties of sex pheromone responsive olfactory receptor neurons (ORNs). Lowering the sensillar Ca(2+) concentration to 2 x 10(-8) M increased ORN spontaneous firing activity and induced long bursts of action potentials (APs) superimposed on spontaneous negative deflections of the transepithelial potential. We inferred that Ca(2+) stabilizes the membrane potential of ORNs, keeping the spontaneous firing activity at a low and regular level. Neither the amplitude and kinetics of the rising phase of sensillar potentials (SPs) recorded in response to pheromone stimuli nor the AP generation during stimulation depended on the extracellular Ca(2+) concentration. Thus, extracellular Ca(2+) is not absolutely necessary for ORN response. Partial inhibition of responses with a calmodulin antagonist, W-7, also indicates that intracellular Ca(2+) contributes to the ORN response and suggests that Ca(2+) release from internal stores is involved. In 2 x 10(-8) M Ca(2+), the repolarization of the SP was delayed when compared with higher Ca(2+) concentrations. Therefore, in contrast to depolarization, ORN repolarization depends on extracellular Ca(2+). Ca(2+)-gated K(+) channels identified from cultured ORNs with whole-cell recordings are good candidates to mediate ORN repolarization.     

Aminergic regulation of pheromone sensillae in the cockroach <Emphasis Type="Italic">Periplaneta americana</Emphasis>

Tremendous adaptability of insects is predominantly provided by fast tuning of physiological functioning of an organism to the permanently changing environmental conditions. One of the mechanisms of plasticity in insects is modulation of performance of their sense organs by neurohormones. Activity of at least three out of four receptor cells located in cockroach pheromonesensitive sensilla is modulated by octopamine. An increase of firing rate of pheromone receptor cells and a decrease of electroantennogram amplitude is accompanied by enhanced behavioral responses of male cockroaches to sex pheromone. The effect of octopamine on reception of a repellent (1,8-cineole, eucalyptol) by an insect is reported for the first time. Simultaneous modulation of responses of receptor cells located in sex specific sensilla to semantically different odorants indicates their cooperation in formation of insect behavior.     

Modulatory effects of octopamine and serotonin on male sensitivity and periodicity of response to sex pheromone in the cabbage looper moth,Trichoplusia ni

The pheromone-mediated flight behavior of male cabbage looper moths in a sustained-flight tunnel and random activity exhibited during scotophase were observed after males were treated with octopamine or serotonin (5 hydroxytryptamine). Octopamine induced a hypersensitivity to the olfactory signal, resulting in a significant lowering of the pheromone dose that elicited peak levels of response. Octopamine, however, did not affect the circadian rhythmicity of response to pheromone. In contrast, serotonin disrupted the circadian rhythmicity of response, resulting in a high percentage of males exhibiting random activity and response to pheromone throughout the entire 8 h scotophase instead of during the normal peak period during the latter part of the scotophase. Serotonin did not effect a decrease in the dose of pheromone eliciting peak response. In addition, at the highest dosages tested octopamine and serotonin induced opposite postures associated with a paralysis that occurred when males attempted to take flight to the pheromone.     

大螟成虫性信息素生物合成和释放及求偶和交配行为的昼夜节律

【目的】探索大螟Sesamia inferens性信息素顺11-十六碳烯乙酸酯(Z11-16∶Ac)和顺11-十六碳烯醇(Z11-16∶OH)的合成和释放及求偶和交配行为的昼夜节律,及其与田间性信息素诱捕的关系。【方法】通过溶剂浸提和固相微萃取(solid phase microextraction, SPME)分析大螟雌蛾性信息素Z11-16∶Ac和Z11--16∶OH的滴度,结合行为观测和多地田间实时性信息素诱捕数据,调查大螟性信息素的生物合成、释放及求偶和交配行为的昼夜节律。【结果】大螟雌蛾腺体内性信息素Z11-16∶Ac和Z11-16∶OH含量可检测到的时间始于暗期前1 h,暗期后4 h快速增加,暗期8 h为第1次高峰,但光期1h又一次高峰,光期5 h还可以被显著检测到。分泌至腺体外的性信息素化合物可检测到的时间始于暗期后6 h,高峰期在暗期后10 h,光期后1 h性信息素Z11-16∶Ac滴度达到96.9±20.9 ng/雌。采用溶剂浸提法获得的Z11-16∶Ac和Z11-16∶OH的比例在暗期平均为2.8±1.9,在光期平均为2.5±0.9,统计上二者没有显著差异,而SPME法获得的Z11-16∶Ac和Z11-16∶OH的比例在暗期平均为8.5±1.2,在光期平均为5.7±0.6,统计上二者差异显著。产卵器伸出时间发生在暗期6-8 h,产卵器伸出持续时间平均为80.8±4.4 min。大螟的交配发生在暗期4-10 h,交配持续时间平均为83.4±5.0 min。广东、四川、浙江、江苏四省性诱自动计数的田间每日每小时实时计数数据显示,越冬代诱蛾比较集中,之后的世代则比较分散,田间雄蛾的性诱昼夜节律受地理环境、季节和世代等因子的影响。【结论】本研究发现大螟交配和性信息素释放的昼夜节律在时间上不一致,交配时间在暗期较早时段。雌蛾性信息素有效的释放时间范围比雄蛾对性信息素反应的要小。产卵器伸展与雌蛾性信息素化合物的释放速率加快和扩散 范围有关。     

Environmental regulation of female calling and male pheromone response periodicities in the codling moth (Laspeyresia pomonella)

Codling moth female calling and male pheromone responsiveness under the defined conditions of 23°C and light:dark (LD) 16:8 occurred primarily during scotophase. Under either continuous photophase or scotophase females called with periodicities very similar to their periodicity under the LD cycle, indicating that the rhythmicity is circadian. Male response rhythmicity was maintained under continuous photophase. A decrease in the temperature from 23° to 16°C resulted in a reduction in the proportion calling when the decrease in temperature occurred during scotophase and a shift of maximal calling into photophase when the decrease in temperature occurred 3 hr prior to the initiation of scotophase. Decreases of temperature from 23° to 16°C and of light intensity did not produce similar shifts in the periodicity of male upwind orientation. Of 6 pheromone dosages from 10^?5 to 10² μg, 10^?1 and 10⁰ μg elicited the most male upwind orientation.     

Fatty acid and sex pheromone changes and the role of glandular lipids in the Z-strain of the European corn borer, Ostrinia nubilalis (Hübner)

Lipids in the sex pheromone gland of females of the Z-strain of Ostrinia nubilalis were analyzed for fatty acyl pheromone analogs (FAPAs) and other potential biosynthetic intermediates. More than 80% of the FAPAs were found in the triacylglycerols (TGs), with smaller amounts found in the phosphatidyl cholines, ethanolamines, and serines. Analysis of the TGs by lipase revealed that the two FAPAs were distributed fairly evenly among all three stereospecific positions. Comparison of changes in titers of key glandular fatty acids with those of pheromone components, with respect to photoperiodic time and age of females, showed that both FAPA and pheromone titers exhibited a cyclical pattern with peaks in the scotophase and valleys in the photophase. However, whereas pheromone titer tended to peak in the first half of the scotophase, FAPA titer peaked at the end of the scotophase. Significantly, the titer of the FAPA of the minor component, (E)-11-tetradecenyl acetate (3% of pheromone), was always much greater than the titer of the FAPA of the major component, (Z)-11-tetradecenyl acetate (97%), of the pheromone. Titer of myristate, an intermediate in pheromone biosynthesis, was also higher during the scotophase than the photophase. However, myristate titer showed a pronounced dip in the middle of the scotophase. These data suggest two roles for glandular lipids in sex pheromone biosynthesis in O. nubilalis. Firstly, they remove excess FAPA of the minor component so the fatty acid reductase system is not presented with a high ratio of this isomer (which would otherwise result from the reductase's own selectivity), which could cause changes in the final pheromone ratio. Secondly, hydrolysis of the large amounts of stored saturated fatty acids from the TGs may provide substrate for pheromone biosynthesis.     

Octopamine enhances moth olfactory responses to pheromones, but not those to general odorants

Effects of octopamine on responses of olfactory receptor neurons of Bombyx mori males and females, specialized to the reception of pheromone components and general odorants, respectively, were compared. Injections of octopamine had no effect on the transepithelial potential of antennal sensilla trichodea in both sexes. In males, octopamine increased significantly the amplitude of receptor potentials and nerve impulse responses elicited by the pheromone components bombykol and bombykal. However, the responses of homologous female general odorant-sensitive neurons to linalool and benzoic acid were not affected. In control experiments, injection of physiological saline did not increase the responses in any neuron type.     

Pheromone, juvenile hormone, and social status in the male lobster cockroach Nauphoeta cinerea

In this study, the major pheromone component, 3‐hydroxy‐2‐butanone (3H‐2B), released by dominants was measured during early scotophase. Both the JH III titer in the hemolymph and the 3H‐2B content of the sternal glands of the dominants and subordinates were then measured during late scotophase and late photophase. These investigations were performed on encounter days 1, 2, 3, 5, 7, 9, 12, and 20. The results showed that, for non‐aggressive posture (AP)‐adopting socially naïve males (SNMs), both the 3H‐2B release and the hemolymph JH III titer were maintained at a low level. Once a fight occurred, 3H‐2B release was raised significantly in the AP‐adopting dominants, but not in non‐AP‐adopting subordinates, and remained raised throughout the entire experimental period. At 30 min after the first encounter, the hemolymph JH III titer was significantly increased in dominants, but not in subordinates. A significantly higher hemolymph JH III titer was observed in dominants during late scotophase on days 3, 5, 12, and 20 and during late photophase on days 3, 5, and 20. After fighting, the sternal gland 3H‐2B content of the dominants or subordinates was significantly lower than in SNMs. In dominants, the sternal gland 3H‐2B content during late scotophase was significantly lower than that during late photophase in the first 9 domination days, while, in the subordinates, the 3H‐2B content during late scotophase was either similar to, or significantly higher than, that in late photophase. In the dominants, 3H‐2B release and JH III titer were positively correlated. In rank switchers, the switched social status was positively correlated with both 3H‐2B release and JH III titer. Comparison of 3H‐2B release and JH III titer in 1‐time, 3‐time, or 5‐time dominants showed that, although winning significantly increased both 3H‐2B release and JH III titer, there is no significant difference in 3H‐2B release between 3‐ and 5‐time winners, while the JH III titer was most significantly increased in the 3‐time winners. The possible relationship between pheromone release, JH III titer, and social status is discussed. Arch. Insect Biochem. Physiol. 2008. © 2008 Wiley‐Liss, Inc.     

甜菜夜蛾雌蛾求偶行为及性信息素产生的时间节律(英文)

研究了甜菜夜蛾雌蛾求偶行为和腺体中性信息素滴度时日变化的规律。结果表明 ,雌蛾求偶行为和性信息素滴度均呈明显的昼夜节律 ,且均在暗期的中后期达到高峰。比较而言 ,雌蛾的求偶活动期较短 ,在暗期中期开始 ,暗期结束后很快停止 ;但峰期较长 ,从中后期达到高峰后一直保持到暗期结束。而腺体内 4种性信息素组份从暗期前 0 .5h到下一个光期 4.5h均有产生 ;但峰期很短 ,暗期 6.5h显著增加达到高峰后 ,在 8.5h又迅速回落。日变化研究表明 ,甜菜夜蛾当日龄即可求偶 ,3日龄起进入求偶盛期 ,至 7日龄末有明显减退。 0～ 3日龄雌蛾的平均初始求偶时间逐日显著提前 ,以后则稳定在暗期 5h左右。不同日龄间性信息素滴度的变化较小     

Hormonal regulation of sex pheromone biosynthesis in the turnip moth,Agrotis segetum

Pheromone production in the female turnip moth, Agrotis segetum, is under the control of a brain factor. This factor was demonstrated to be a proteinaceous substance termed pheromone biosynthesis activating neuropeptide-like substance (PBAN-like substance). The sex pheromone of Swedish A. segetum includes (Z)-5-decenyl acetate, (Z)-7-dodecenyl acetate, and (Z)-9-tetradecenyl acetate as major components. Decapitation of a female decreased pheromone production significantly. Pheromone production was restored by injection of homogenates of either male or female brain-suboesophageal ganglion or the corpora cardiaca alone. Pheromonotropic activity was also found in homogenates of the female thoracic ganglion and abdominal ganglion that were obtained during scotophase. Injection of female brain and thoracic ganglion homogenates made from insects during the scotophase induced two and four times as much Z7-12:OAc, respectively, as injection with similar homogenates from photophase. As little as one-eighth female equivalent (FE) brain homogenate was sufficient to increase the amount of Z7-12:OAc. The effect of brain homogenate on pheromone titer reached its maximum after 30 min. The activity of the PBAN-like substance present in female brain extracts was not correlated to the age of the donor. Injection of hemolymph collected during either photophase or scotophase into decapitated females did not increase the pheromone titer. The target site of the PBAN-like substance was not the pheromone gland, and the ventral nerve cord was not involved in the transportation of the PBAN-like substance, which implies a mode of action different from what has been reported in other moths. Brain homogenates obtained during photophase from females of African A. segetum, Spodoptera littoralis, or Ostrinia nubilalis as well as synthetic Bombyx-PBAN also induced pheromone production in decapitated Swedish female A. segetum. © 1995 Wiley-Liss, Inc.     

DIEL RHYTHMS OF CALLING BEHAVIOR AND SEX PHEROMONE PRODUCTION OF BEET ARMYWORM,SPODOPTERA EXIGUA (LEPIDOPTERA:NOCTUIDAE)*

Abstract Beet armyworm (BAW), Spodoptera exigua, is becoming one of more and more serious pests in China in recent years. As a part of research program of sex pheromone and its application of BAW in China, the hourly and daily variation of calling behavior and pheromone production of BAW females were investigated. Both calling behavior and titers of 4 sex pheromone components showed distinct diel rhythms, and the two peak periods were synchronous. In comparison, the calling activity lasted shorter period of time with a longer peak time, whereas the production of the sex pheromone lasted throughout the whole scotophase and part of the photophase with a very short peak time. The calling behavior began at the middle scotophase, reached the maximum at the middle‐later scotophase, and continued the maximal calling activity until the end of the scotophase. When the light was on, the calling percentage reduced sharply, and all females stopped calling 1 hour later. The variation patterns of the 4 pheromone components in the glands of the 3 day old moths were similar from one to another. From 0.5 h before to 4.5 h into scotophase, the titers increased slightly, but at 6.5 h they showed a significant increase up to the peak values of the scotophase. Soon at 8.5 h into the scotophase, they decreased significantly and thereafter gradually to undetectable level at 4.5 h into the next photophase. The daily change experiment showed that BAW females began calling at 0 scotophase, became fully active in calling at 3rd scotophase, and maintained the calling activity to 7th scotophase. There was no significant difference in pheromone titers among different day‐old moths.     

Sex pheromone biosynthetic pathway in Spodoptera littoralis and its activation by a neurohormone

Deuterium-labeled fatty acids have been used to elucidate the sex pheromone biosynthetic pathway in Spodoptera littoralis. Label from palmitic acid was incorporated during the scotophase into all the pheromone acetates and their corresponding fatty acyl intermediates. (Z,E)-9,11-tetradecadienyl acetate, the major component of the pheromone blend, is synthesized from palmitic acid via tetradecanoic acid, which, by the action of a specific (E)-11 desaturase and subsequently a (Z)-9 desaturase, is converted into (Z,E)-9,11-tetradecadienoate. By further reduction and acetylation, this compound leads to the dienne acetate. Deuterated precursors applied to the pheromone gland during the photophase were also incorporated into the pheromone. The percentage of labeled (Z,E)-9,11-tetradecadienyl acetate relative to natural compound was significantly higher during the light period. Label incorporation from different intermediates into the pheromone was stimulated by injection of brain-subesophageal ganglion extract during the photophase. The influence of the pheromone biosynthesis-activating neuropeptide on the biosynthetic pathway is discussed.     

The circadian rhythm of the sex-pheromone-mediated behavioral response in the turnip moth, Agrotis segetum, is not controlled at the peripheral level

The pheromone-mediated upwind flight of male turnip moths was observed in a flight tunnel at different times of day under conditions of a light-dark (LD) cycle, constant darkness (DD), and a shifted photoperiod. Under both LD and DD conditions, a significantly larger number of males flew to the pheromone during both the scotophase and the subjective scotophase than during the photophase and the subjective photophase for 2 consecutive days. When 1-day-old moths were transferred to a shifted LD cycle with lights turned off 4 h earlier, male behavioral responses to the pheromone advanced in time accordingly by 4 h. This showed that male behavioral responses to the pheromone are under the control of an endogenous oscillator. To further examine the level at which the circadian rhythm of the male behavioral response is regulated, the authors tested the olfactory responses of male antennal receptors to pheromone stimuli by means of electroantennograms (EAG) at different times of day. No significant variation in the sensitivity of the male antennal response to the pheromone was observed in terms of time of day. The results suggest that circadian regulation of the rhythmic behavioral response to pheromones in the male Agrotis occurs at the central nervous system level.     

Octopamine Regulates Antennal Sensory Neurons via Daytime-Dependent Changes in cAMP and IP3 Levels in the Hawkmoth Manduca sexta

The biogenic amine octopamine (OA) mediates reward signals in olfactory learning and memory as well as circadian rhythms of sleep and activity. In the crepuscular hawkmoth Manduca sexta, OA changed pheromone detection thresholds daytime-dependently, suggesting that OA confers circadian control of olfactory transduction. Thus, with enzyme-linked immunosorbent assays we searched hawkmoth antennae for daytime-dependent changes in the concentration of OA and its respective second messengers. Antennal stimulation with OA raised cAMP- and IP₃ levels. Furthermore, antennae expressed daytime-dependent changes in the concentration of OA, with maxima at Zeitgebertime (ZT) 20 when moths were active and also maximal concentrations of cAMP occurred. Maximal IP₃ levels at ZT 18 and 23 correlated with maximal flight activity of male moths, while minimal IP₃ levels at dusk correlated with peaks of feeding activity. Half maximal effective concentration (EC₅₀) for activation of the OA-receptor decreased during the moth’s activity phase suggesting daytime-dependent changes in OA receptor sensitivity. With an antiserum against tyramine, the precursor of OA, two centrifugal neurons were detected projecting out into the sensory cell layer of the antenna, possibly mediating more rapid stimulus-dependent OA actions. Indeed, in fast kinetic assays OA receptor stimulation increased cAMP concentrations within 50 msec. Thus, we hypothesize that fast, stimulus-dependent centrifugal control of OA-release in the antenna occurs. Additional slow systemic OA actions might be based upon circadian release of OA into the hemolymph mediating circadian rhythms of antennal second messenger levels. The resulting rhythms of odor sensitivity are suggested to underlie circadian rhythms in odor-mediated behavior.