Thesis--Uppsala, 1978. / Summary in English. Includes indexes. Bibliography: p. 213-220.

Akademisk avhandling--Historia--Uppsala, 1978. / Bibliogr. p. 213-220. Index.

This PhD. thesis summarizes the effect of adipokinetic hormones (AKHs) on a spectrum of mobilized lipids in model insect species the locust Locusta migratoria and the firebug Pyrrhocoris apterus. The results revealed that mobilization of diacylglycerols and fatty acids from the fat body into the haemolymph is not uniform and suggested there is partial specificity of individual AKHs. This could contribute to the answer of the question why some insect species have more than one AKH. The results of the thesis are supplemented by studies of AKH effect on lipid metabolism in stress conditions elicited by insecticide treatments. Co-application of AKH and insecticide enhanced the effect of insecticide

Dans le but d’étudier le rôle fonctionnel des neuropeptides chez la drosophile, nous avons essayé d’utiliser le récepteur µ aux opioïdes (MOR) afin d’inhiber temporairement la libération de neuropeptides. Cependant, quand nous l’avons exprimé dans les cellules endocrines produisant l’hormone adipokinétique (AKH), le récepteur MOR a présenté une activité constitutive empêchant tout contrôle dans le temps. Nous proposons d’utiliser les récepteurs RASSL (Receptors Activated Solely by Synthetic Ligands) développés chez les vertébrés. Ces récepteurs, activés uniquement par des ligands synthétiques, ont été modifiés afin qu’ils soient dénués d’activité constitutive. Afin de tester rapidement l’efficacité d’un récepteur RASSL inhibiteur chez la drosophile, nous avons cherché une alternative à la mesure des taux de tréhalose et de glycogène (démontrant la libération d’AKH) qui en plus d’être laborieuse produit des résultats variables. L’hormone GPA2/GPB5, récemment découverte, est particulièrement intéressante, en effet, elle semble avoir un rôle antidiurétique. Nous avons généré des lignées transgéniques exprimant la protéine Gal4 dans les cellules GAP2/GPB5 et nous avons montré que l’ablation génétique de ces cellules compromet la survie suggérant qu’elles pourraient représenter un bon système pour tester l’efficacité du RASSL inhibiteur. Ensuite nous nous sommes intéressés au contrôle de la libération du neuropeptide AKH qui a un rôle fonctionnel homologue à celui du glucagon des vertébrés. Malgré quelques résultats encourageants, nous n’avons pas pu confirmer le rôle inhibiteur de l’AstA sur la libération de l’AKH. Enfin nous nous sommes intéressés au réseau qui contrôle le comportement de cour. Nous avons généré des lignées transgéniques exprimant la protéine Gal4 sous la dépendance du promoteur potentiel du récepteur du neuropeptide SIFamide (SIFR) et nous avons démontré que ce neuropeptide contrôle le comportement de cour via son récepteur SIFR en agissant, du moins en partie, sur les neurones fruitless. / In order to study the functional roles of neuropeptides in Drosophila, I attempted to use the µ opioïd receptor (MOR) to temporarily inhibit liberation of neuropeptides. However, when expressed in the AKH (adipokinetic hormone) endocrine cells of Drosophila, MOR turned out to be constitutively active, making it impossible to use it as envisioned. Others have encountered and subsequently solved similar problems for the so-called RASSL (Receptors Activated Solely by Synthetic Ligands) in vertebrates. As the bioassay for testing release of AKH is cumbersome, time-consuming and variable, I searched for an alternative neuroendocrine system to test the efficiency of an inhibitory RASSL in Drosophila. The recently discovered GPA2/GPB5 seemed particularly attractive, as it is likely an antidiuretic hormone. Transgenic flies expressing Gal4 in the GPA2/GPB5 were produced and genetic ablation of these cells severely compromised survival, suggesting that this might indeed be good model system. Attempts so demonstrate a physiological role of allatostatin A in the release of AKH yielded inconclusive results. In order to study the role of the neuropeptide SIFamide, which modulates sexual behavior in Drosophila, I generated transgenic flies expressing Gal4 under dependence of potential promoter of this neuropeptide receptor (SIFR) and showed that SIFamide controls courtship at least in part by acting directly on fruitless neurons.

In this thesis, the effect of infection elicited by entomopathogenic nematodes (EPNs) Steinernema carpocapsae on Pyrrhocoris apterus and Drosophila melanogaster models were evaluated, and a role of adipokinetic hormones (AKHs) during the infection was characterized. These were monitored by determination of mortality, and various biochemical and physiological characteristics such as AKH levels both in the central nervous system (CNS) and in hemolymph, AKH gene expression in CNS, level of anti-oxidative stress markers, general metabolism and level of nutrients in normal and genetically modified insects. At P. apterus the mortality tests revealed that application of AKH increases the efficacy of EPN treatment. This result was confirmed using the firebugs with AKH receptor deficiency. Further, the increase of AKH expression and AKH levels in CNS and hemolymph seemed to be coordinated after the nematode treatment. At the D. melanogaster model also, the effect of adenosine into the above-mentioned characteristics was included. For this, mutants in AKH (AHK1), adenosine receptor (AdoR1) genes, and in both these genes together (AHK1 AdoR1 double mutant) were employed. Altogether, the results confirmed the involvement of AKH, and partially also adenosine into the antistress defense reactions elicited by the nematobacterial infection. Finally, the last part of the study was focused on examination of the vitellogenin (Vg) role in the defense reaction in firebug body P. apterus affected by two entomopathogenic organisms, the nematode S. carpocapsae and the fungus Isaria fumosorosea. The results revealed that Vg proteins play an important role in the defense against both types of the infections and are also able to kill entomopathogenic bacteria Xenorhabdus nematophila, that are symbionts of S. carpocapsae and that increase toxicity of this nematode.

The aim of the thesis was evaluation of various metabolic characteristics in the fruit flies Drosophila melanogaster with deficiency of adipokinetic hormone (AKH) production, and with adenosine receptor dysfunction. The experiments were done with a goal to evaluate involment of AKH and adenosine into control of the metabolic pathways. For that measuring of basic nutrients, level of Drome-AKH, mortality and some others characteristics in the fruit flies during starvation were performed. Results revealed the effect of AKH on metabolism of storage nutrients, however, the role of adenosine was unclear.

<p> Obesity is a growing concern as 42.3% of people in the U.S were considered obese in the years 2017- 2018. Little is known about the genetic components that contribute to weight gain. In humans, the hormone glucagon is a major contributor to the body’s energy demand as it helps break down lipids. Therefore, learning more about this pathway could enable a range of therapeutics. In fact, studies have shown that glucagon treatments have helped patients with both weight loss and appetite suppression. In this project, we analyzed candidate genes that modify the glucagon pathway in <em>Drosophila melanogaster.</em> We reduced the expression of the fly version of the glucagon receptor (AKHR) in our model. This induces fat retention in the L3 larvae, which mimics obesity in humans. We then crossed our model to the DGRP and looked for natural variation in fat content using a density assay. The density assay examines the relative fat levels of the larvae by slowly increasing the amount of sucrose in water. This enables us to observe whether we have lean larvae which float later or fat larvae which float early on. We used the variation in floating concentration to identify candidate modifier genes through GWA or genome-wide association study. We crossed our <em>AKHR</em> RNAi model to RNAi for various candidate modifier genes that may enhance or suppress fat retention. We screened these candidates initially with the same density assay used in the original study. This resulted in four candidate genes that significantly impacted the density of the larvae: <em>THADA</em>, <em>AmyD</em>, <em>GluRIIC</em>, and <em>CG9826</em>. We further characterized these candidates using biochemical assays to analyze stored metabolites such as triglycerides, glucose, glycogen, and protein. These have been further analyzed under control, high sugar, and high fat conditions to see if the larvae are resistant to environmental changes. <em>CG9826</em> showed significant increase in stored fats across all environments. <em>THADA</em> RNAi showed an increase in fat in the high fat environment. Overexpression of <em>THADA</em> showed a decrease in fat storage in the high fat environment. Our goal is to advance our understanding of the glucagon signaling pathway, obesity, and lipid metabolism. We are also hopeful to provide candidate genes that can be regarded as future therapeutic targets. </p>

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