Shoshana Eitan
Behavioral and Cellular Neuroscience Program
Department of Psychology
Texas A&M University, USA
Assistant Professor
Email: [email protected]
Qualifications
1997 Ph.D., Weizmann Institute of Science, Neurobiology
1992 M.S., Weizmann Institute of Science, Neurobiology
1990 B.A., Open University, Biology
Publications (Selected)
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Madison, C. A., Debler, R. A., Gallegos, P. L., Hillbrick, L., Chapkin,
R. S., Safe, S., & Eitan, S. (2025). 1, 4-dihydroxy-2-naphthoic acid
prevents 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine-induced motor function
deficits. Behavioural Pharmacology, 36(1), 40-46.
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Debler, R. A., Gallegos, P. L., Ojeda, A. C., Perttula, A. M., Lucio, A.,
Chapkin, R. S., ... & Eitan, S. (2024). TCDD (2, 3, 7,
8-tetrachlorodibenzo-p-dioxin) induces depression-like phenotype.
Neurotoxicology, 103, 71-77.
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Hu, H., Yuan, M., Chen, J., Fan, T., Nguyen, N., Madison, C. A., Eitan,
S.,... & Wang, Y. (2024). Pharmacokinetic modeling of solid and hollow
gold-coated superparamagnetic iron oxide nanoparticles for brain-targeted
therapeutics: prediction and experiment. Advanced Composites and
Hybrid Materials, 7(3), 76.
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Debler, R. A., Madison, C. A., Hillbrick, L., Gallegos, P., Safe, S.,
Chapkin, R. S., & Eitan, S. (2023). Selective aryl hydrocarbon receptor
modulators can act as antidepressants in obese female mice. Journal
of affective disorders, 333, 409-419.
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Madison, C. A., Hillbrick, L., Kuempel, J., Albrecht, G. L., Landrock, K.
K., Safe, S., ... & Eitan, S. (2023). Intestinal epithelium aryl
hydrocarbon receptor is involved in stress sensitivity and maintaining
depressive symptoms. Behavioural brain research, 440, 114256.
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Madison, C. A., Debler, R. A., Vardeleon, N. I., Hillbrick, L.,
Jayaraman, A., Safe, S., ... & Eitan, S. (2022). Sex-dependent differences
in the stress mitigating and antidepressant effects of selective aryl
hydrocarbon receptor modulators. Journal of affective disorders, 319, 213-220.
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Madison, C. A., Kuempel, J., Albrecht, G. L., Hillbrick, L., Jayaraman,
A., Safe, S., ... & Eitan, S. (2022). 3, 3′-Diindolylmethane and 1,
4-dihydroxy-2-naphthoic acid prevent chronic mild stress induced
depressive-like behaviors in female mice. Journal of affective
disorders, 309, 201-210.
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Chen, J., Yuan, M., Madison, C. A., Eitan, S., & Wang, Y. (2022).
Blood-brain barrier crossing using magnetic stimulated nanoparticles. Journal
of Controlled Release, 345, 557-571.
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Eitan, S., Madison, C. A., & Kuempel, J. (2021). The self-serving
benefits of being a good host: A role for our micro-inhabitants in shaping
opioids’ function. Neuroscience & Biobehavioral Reviews, 127, 284-295.
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Madison, C. A., Wellman, P. J., & Eitan, S. (2020). Pre-exposure of
adolescent mice to morphine results in stronger sensitization and reinstatement
of conditioned place preference than pre-exposure to hydrocodone. Journal of
Psychopharmacology, 34(7), 771-777.
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Emery, M. A., & Eitan, S. (2020). Drug-specific differences in the
ability of opioids to manage burn pain. Burns, 46(3), 503-513.
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Madison, C. A., & Eitan, S. (2020). Buprenorphine: prospective novel
therapy for depression and PTSD. Psychological medicine, 50(6), 881-893.
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Madison, C. A., Arora, M., Kumar, M. R., & Eitan, S. (2020). Novel
oral nanoparticle formulation of sustained release naloxone with mild
withdrawal symptoms in mice. ACS Chemical Neuroscience, 11(13), 1955-1964.
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Emery, M. A., & Eitan, S. (2019). Members of the same pharmacological
family are not alike: Different opioids, different consequences, hope for the opioid
crisis?. Progress in Neuro-Psychopharmacology and Biological
Psychiatry, 92, 428-449.
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Bates, M. S., Hofford, R. S., Emery, M. A., Wellman, P. J., & Eitan,
S. (2018). The role of the vasopressin system and dopamine D1 receptors in the
effects of social housing condition on morphine reward. Drug and
Alcohol Dependence, 188, 113-118.
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Bates, M. S., Emery, M. A., Wellman, P. J., & Eitan, S. (2017).
Inhibiting social support from massage-like stroking increases morphine
dependence. Behavioural Pharmacology, 28(8), 642-647.
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Emery, M. A., Shawn Bates, M. L., Wellman, P. J., & Eitan, S. (2017).
Hydrocodone is more effective than morphine or oxycodone in suppressing the
development of burn-induced mechanical allodynia. Pain Medicine, 18(11), 2170-2180.
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Emery, M. A., Bates, M. S., Wellman, P. J., & Eitan, S. (2017).
Hydrocodone, but neither morphine nor oxycodone, is effective in suppressing
burn-induced mechanical allodynia in the uninjured foot contralateral to the
burn. Journal of Burn Care & Research, 38(5), 319-326.
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Bates, M. L. S., Emery, M. A., Wellman, P. J., & Eitan, S. (2016).
Social environment alters opioid‐induced hyperalgesia and antinociceptive tolerance in adolescent mice. European
Journal of Pain, 20(6), 998-1009.
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Emery, M. A., Bates, M. S., Wellman, P. J., & Eitan, S. (2016).
Differential effects of oxycodone, hydrocodone, and morphine on activation
levels of signaling molecules. Pain Medicine, 17(5), 908-914.
Profile Details
https://www.researchgate.net/profile/Shoshana-Eitan
https://scholar.google.com/citations?user=GnmdFRkAAAAJ&hl=en
https://artsci.tamu.edu/psychological-brain-sciences/contact/profiles/shoshana-eitan.html
WoS Researcher ID: ESU-5316-2022