Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Clabough, Erin B.D.a; b; * | Aspili, Christiaa | Fussy, William S.c | Ingersoll, James D.c | Kislyakov, Amya | Li, Elizabeth S.a | Su, Meng-Jiuana | Wiles, Dustin B.c | Watson, Thomas E.c | Willy, Aaron J.c | Thomas Vinyard, H.c | Mollica III, Philip J.c | Taylor, James V.c | Smith, Cody W.c | Roark, Dallas A.c | Tabrani, Zachary P.c | Thomas, Harris L.c | Shin, Mimid | Venton, B. Jillb; d | Hayes, Davide; f | Sipe, Conor W.e; g
Affiliations: [a] Department of Psychology, University of Virginia, Charlottesville, VA, USA | [b] Program in Fundamental Neuroscience, University of Virginia, Charlottesville, VA, USA | [c] Department of Biology, Hampden-Sydney College, Hampden-Sydney, VA, USA | [d] Department of Chemistry, University of Virginia, Charlottesville, VA, USA | [e] Department of Biology, Shepherd University, Shepherdstown, WV, USA | [f] Department of Biology, Kansas State University, Manhattan, KS, USA | [g] Department of Biology, University of Virginia, Charlottesville, VA, USA
Correspondence: [*] Correspondence to: Erin B.D. Clabough, PhD, Department of Psychology, PO Box 400400, University of Virginia, Charlottesville, VA 22904, USA. Tel.: +1 434 297 6883; E-mail: ebd2r@virginia.edu.
Abstract: Background:Huntingtin (htt) protein is an essential regulator of nervous system function through its various neuroprotective and pro-survival functions, and loss of wild-type htt function is implicated in the etiology of Huntington’s disease. While its pathological role is typically understood as a toxic gain-of-function, some neuronal phenotypes also result from htt loss. Therefore, it is important to understand possible roles for htt in other physiological circumstances. Objective:To elucidate the role of htt in the context of ethanol exposure, we investigated how loss of htt impacts behavioral and physiological responses to ethanol in Drosophila. Methods:We tested flies lacking htt for ethanol sensitivity and tolerance, preference for ethanol using capillary feeder assays, and recovery of mobility after intoxication. Levels of dopamine neurotransmitter and numbers of dopaminergic cells in brains lacking dhtt were also measured. Results:We found that dhtt-null flies are both less sensitive and more tolerant to ethanol exposure in adulthood. Moreover, flies lacking dhtt are more averse to alcohol than controls, and they recover mobility faster following acute ethanol intoxication. We showed that dhtt mediates these effects at least in part through the dopaminergic system, as dhtt is required to maintain normal levels of dopamine in the brain and normal numbers of dopaminergic cells in the adult protocerebrum. Conclusions:Our results demonstrate that htt regulates the physiological response to ethanol and indicate a novel neuroprotective role for htt in the dopaminergic system, raising the possibility that it may be involved more generally in the response to toxic stimuli.
Keywords: Drosophila , flies, huntingtin, ethanol, alcohol, dopamine, Huntington’s disease, loss-of-function
DOI: 10.3233/JHD-230581
Journal: Journal of Huntington's Disease, vol. 12, no. 3, pp. 241-252, 2023
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl