全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Effects of Aging, Potassium Channel, Stimulus Parameters on Visual Habituation in Drosophila melanogaster Using the Light off Jump Response

DOI: 10.4236/ae.2026.143012, PP. 194-215

Keywords: Habituation, Dishabituation, Neural Mechanisms, Spontaneous Recovery

Full-Text   Cite this paper   Add to My Lib

Abstract:

Habituation, one of the simplest forms of learning, is a basic adaptive process that enables organisms to filter repetitive, irrelevant stimuli. This project investigates the effects of stimulus parameters, aging and potassium channels mutations on visual habituation in white-eyed cn bw mutant Drosophila melanogaster using the jump response, a quantifiable escape behavior mediated by the Giant Fiber System (GFS). Using Generalized Linear Mixed Models (GLMM), we quantified habituation as a significant decline in response across 15 dimming pulses. We confirmed habituation through spontaneous recovery and dishabituation tests. The results produced three findings. Habituation was highly dependent on the interstimulus interval (delay), being strongest at 2 s and undetected at 5 s. Older (30-day-old) flies showed a slower habituation process than younger (10-day-old) flies, confirming that age-related decline affects neural plasticity. Since the basic neural mechanisms for learning to ignore stimuli are believed to be similar across species, the modification of this process in our aging flies helps explain why older humans often find it difficult to focus on a busy environment. Finally, flies carrying mutations in voltage-gated potassium channels, eag Sh; cn bw showed an increased in habituation process compared with cn bw alone. The increase may be attributed to faster short-term synaptic depression caused by hyperexcitability in these mutants.

References

[1]  Wilson, D.A. and Linster, C. (2008) Neurobiology of a Simple Memory. Journal of Neurophysiology, 100, 2-7.
https://doi.org/10.1152/jn.90479.2008
[2]  Rankin, C.H., Abrams, T., Barry, R.J., Bhatnagar, S., Clayton, D.F., Colombo, J., et al. (2009) Habituation Revisited: An Updated and Revised Description of the Behavioral Characteristics of Habituation. Neurobiology of Learning and Memory, 92, 135-138.
https://doi.org/10.1016/j.nlm.2008.09.012
[3]  Rankin, C.H., Beck, C.D.O. and Chiba, C.M. (1990) Caenorhabditis elegans: A New Model System for the Study of Learning and Memory. Behavioural Brain Research, 37, 89-92.
https://doi.org/10.1016/0166-4328(90)90074-o
[4]  Thompson, R.F. and Spencer, W.A. (1966) Habituation: A Model Phenomenon for the Study of Neuronal Substrates of Behavior. Psychological Review, 73, 16-43.
https://doi.org/10.1037/h0022681
[5]  Vivanti, G., Hocking, D.R., Fanning, P.A.J., Uljarevic, M., Postorino, V., Mazzone, L., et al. (2018) Attention to Novelty versus Repetition: Contrasting Habituation Profiles in Autism and Williams Syndrome. Developmental Cognitive Neuroscience, 29, 54-60.
https://doi.org/10.1016/j.dcn.2017.01.006
[6]  Freedman, R., Adler, L.E., Gerhardt, G.A., Waldo, M., Baker, N., Rose, G.M., et al. (1987) Neurobiological Studies of Sensory Gating in Schizophrenia. Schizophrenia Bulletin, 13, 669-678.
https://doi.org/10.1093/schbul/13.4.669
[7]  Cavanagh, J.F., Kumar, P., Mueller, A.A., Richardson, S.P. and Mueen, A. (2018) Diminished EEG Habituation to Novel Events Effectively Classifies Parkinson’s Patients. Clinical Neurophysiology, 129, 409-418.
https://doi.org/10.1016/j.clinph.2017.11.023
[8]  Marsland, S. (2009) Using Habituation in Machine Learning. Neurobiology of Learning and Memory, 92, 260-266.
https://doi.org/10.1016/j.nlm.2008.05.014
[9]  Marsland, S., Nehmzow, U. and Shapiro, J. (2000) Novelty Detection on a Mobile Robot Using Habituation.
https://arxiv.org/abs/cs/0006007
[10]  Rosenbaum, R., Rubin, J. and Doiron, B. (2012) Short Term Synaptic Depression Imposes a Frequency Dependent Filter on Synaptic Information Transfer. PLOS Computational Biology, 8, e1002557.
https://doi.org/10.1371/journal.pcbi.1002557
[11]  Groves, P.M. and Thompson, R.F. (1970) Habituation: A Dual-Process Theory. Psychological Review, 77, 419-450.
https://doi.org/10.1037/h0029810
[12]  Boulianne, G. (2001) Neuronal Regulation of Lifespan: Clues from Flies and Worms. Mechanisms of Ageing and Development, 122, 883-894.
https://doi.org/10.1016/s0047-6374(01)00245-7
[13]  Burke, S.N. and Barnes, C.A. (2006) Neural Plasticity in the Ageing Brain. Nature Reviews Neuroscience, 7, 30-40.
https://doi.org/10.1038/nrn1809
[14]  Engel, J.E. and Wu, C. (1996) Altered Habituation of an Identified Escape Circuit in Drosophila Memory Mutants. The Journal of Neuroscience, 16, 3486-3499.
https://doi.org/10.1523/jneurosci.16-10-03486.1996
[15]  Card, G. and Dickinson, M.H. (2008) Visually Mediated Motor Planning in the Escape Response of Drosophila. Current Biology, 18, 1300-1307.
https://doi.org/10.1016/j.cub.2008.07.094
[16]  Tearle, R. (1991) Tissue Specific Effects of Ommochrome Pathway Mutations in Drosophila melanogaster. Genetical Research, 57, 257-266.
https://doi.org/10.1017/s0016672300029402
[17]  Kim, D.M. and Nimigean, C.M. (2016) Voltage-Gated Potassium Channels: A Structural Examination of Selectivity and Gating. Cold Spring Harbor Perspectives in Biology, 8, a029231.
https://doi.org/10.1101/cshperspect.a029231
[18]  Thompson, R.F. (2009) Habituation: A History. Neurobiology of Learning and Memory, 92, 127-134.
https://doi.org/10.1016/j.nlm.2008.07.011
[19]  Singh, S. and Wu, C.F. (1990) Properties of Potassium Currents and Their Role in Membrane Excitability in Drosophila Larval Muscle Fibers. Journal of Experimental Biology, 152, 59-76.
https://doi.org/10.1242/jeb.152.1.59
[20]  Engel, J.E. and Wu, C. (1998) Genetic Dissection of Functional Contributions of Specific Potassium Channel Subunits in Habituation of an Escape Circuit in Drosophila. The Journal of Neuroscience, 18, 2254-2267.
https://doi.org/10.1523/jneurosci.18-06-02254.1998

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133