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      Influence of aging on brain and web characteristics of an orb web spider

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          Abstract

          In animals, it is known that age affects the abilities of the brain. In spiders, we showed that aging affects web characteristics due to behavioral alterations during web building. In this study, we investigated the effects of age on the associations between morphological changes to the spider brain and changes in web characteristics. The orb web spider Zygiella x- notata (Araneae, Araneidae) was used to test these relationships. Experiments were conducted on young (19 ± 2 days after adult molt, N = 13) and old (146 ± 32 days, N = 20) virgin females. The brain volume decreased with age (by 10%). Age also had an impact on the number of anomalies in the capture area generated during web building. The statistical relationships between the volume of the brain and web characteristics showed that there was an effect of age on both. Our results showed that in spiders, aging affects the brain volume and correlates with characteristics (anomalies) of the web. As web building is the result of complex behavioral processes, we suggest that aging affects spider behavior by causing some brain alterations.

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          Functional senescence in Drosophila melanogaster.

          The fruit fly Drosophila melanogaster is one of the principal model organisms used for studying the biology of aging. Flies are well suited for such studies for a number of reasons. Flies develop to adulthood quickly, have a relatively short life span, and are inexpensive to house. Most of the fly genome has been sequenced, powerful genetic tools are available to manipulate it, and most fly genes have obvious homologues in mammals. While the majority of aging studies in flies have focused on regulation of life span, the fly is emerging as a powerful model system for investigating the biology that underlies age-related functional decline. Key to the use of flies in this way is the striking number of parallels between functional senescence in Drosophila and humans. Here, we review age-related functional declines in Drosophila, human correlates of these age-related declines, and common mechanisms that influence longevity and specific aspects of functional senescence in flies.
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            The use of animal models to study the effects of aging on cognition.

            This review addresses the importance of animal models for understanding the effects of normal aging on the brain and cognitive functions. First, studies of laboratory animals can help to distinguish between healthy aging and pathological conditions that may contribute to cognitive decline late in life. Second, research on individual differences in aging, a theme of interest in studies of elderly human beings, can be advanced by the experimental control afforded in the use of animal models. The review offers a neuropsychological framework to compare the effects of aging in human beings, monkeys, and rodents. We consider aging in relation to the role of the medial temporal lobe in memory, the information processing functions of the prefrontal cortex in the strategic use of memory, and the regulation of attention by distributed neural circuitry. We also provide an overview of the neurobiological effects of aging that may account for alterations in psychological functions.
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              Modulation of Drosophila male behavioral choice.

              The reproductive and defensive behaviors that are initiated in response to specific sensory cues can provide insight into how choices are made between different social behaviors. We manipulated both the activity and sex of a subset of neurons and found significant changes in male social behavior. Results from aggression assays indicate that the neuromodulator octopamine (OCT) is necessary for Drosophila males to coordinate sensory cue information presented by a second male and respond with the appropriate behavior: aggression rather than courtship. In competitive male courtship assays, males with no OCT or with low OCT levels do not adapt to changing sensory cues and court both males and females. We identified a small subset of neurons in the suboesophageal ganglion region of the adult male brain that coexpress OCT and male forms of the neural sex determination factor, Fruitless (Fru(M)). A single Fru(M)-positive OCT neuron sends extensive bilateral arborizations to the suboesophageal ganglion, the lateral accessory lobe, and possibly the posterior antennal lobe, suggesting a mechanism for integrating multiple sensory modalities. Furthermore, eliminating the expression of Fru(M) by transformer expression in OCT/tyramine neurons changes the aggression versus courtship response behavior. These results provide insight into how complex social behaviors are coordinated in the nervous system and suggest a role for neuromodulators in the functioning of male-specific circuitry relating to behavioral choice.
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                Author and article information

                Contributors
                alain.pasquet@univ-lorraine.fr
                Journal
                J Ethol
                J Ethol
                Journal of Ethology
                Springer Japan (Tokyo )
                0289-0771
                1439-5444
                23 November 2017
                23 November 2017
                2018
                : 36
                : 1
                : 85-91
                Affiliations
                [1 ]ISNI 0000 0001 2194 6418, GRID grid.29172.3f, Faculté des Sciences et Techniques, , University of Lorraine, UR AFPA, USC INRA n° 340, ; BP 239, Bld des Aiguillettes, 54506 Vandoeuvre-Les-Nancy, France
                [2 ]ISNI 0000 0001 2149 7878, GRID grid.410511.0, University of Paris-Est, Ecole nationale vétérinaire d’Alfort, UMR 7179 CNRS MNHN, ; 94704 Maisons-Alfort, France
                [3 ]ISNI 0000 0001 2112 9282, GRID grid.4444.0, CNRS, National Centre for Scientific Research, ; Paris, France
                Article
                530
                10.1007/s10164-017-0530-z
                6323080
                62c4bc86-fd7f-4071-b455-b9b4aeb5d0aa
                © The Author(s) 2018, corrected publication 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license and indicate if changes were made.

                History
                : 3 February 2017
                : 2 November 2017
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                © Japan Ethological Society and Springer Japan KK, part of Springer Nature 2018

                aging,brain,morphological parameters,web construction,orb web spider

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