Ph.D. Weizmann Institute of Science (1997)
Area: Behavioral and Cellular Neuroscience
Member: Institute for Neuroscience
247 Psychology Building
CV | Scholar | ResearchGate
PSYC/NRSC 333: Biology of Psychological Disorders
PSYC/NRSC 335: Physiological Psychology
PSYC/NRSC 635: Physiological Psychology (graduate level)
 Drug abuse during adolescence and adulthood
 Social influences on drug abuse
 Co-morbidity of drug abuse with mood and anxiety disorders
 The effects of age of drug use initiation on long term outcomes
 Emotional maturation and adolescent brain development
 Molecular and cellular mechanisms
Adolescent brain development is a very exciting and growing area of research. Of special interest is the study of the brain mechanisms of emotional perception in adolescents. Adolescents evaluate and prioritize emotional aspects of a task differently than adults. Examples of common factors responsible for many characteristic adolescence behaviors are the high value placed on their peers opinions as compared with adults, a propensity toward risk-taking or sensation-seeking behaviors, impulsivity, restlessness, boredom, dissatisfaction and a lower basal motivation. The ontogenesis of the second wave of brain development and neuronal pruning during adolescence, and more specifically the maturation of the motivational system plays a crucial role in determining emotional well-being of adulthood. Alteration of this process may in fact underlie the manifestation of many psychological diseases and syndromes including schizophrenia, panic attacks, and obsessive-compulsive disorder (OCD). As part of their risk-taking sensation-seeking behavior, adolescents are also more prone to self-administer drugs of abuse. In many cases, first exposure occurs during adolescence and correlates with the increased probability of developing a drug addiction. Using rodent models, the lab is currently exploring the contributions of the opioid system to the function of the emotional system during adolescence and adulthood. We are interested in the roles of specific signaling pathways in different brain areas in the maturation of emotional systems.
- Eitan S., Emery MA, Bates MLS, & Horrax C.T. (In press, 2017). Opioid addiction: Who are your real friends? Review article. Neuroscience and Biobehavioral Reviews. doi:10.1016/j.neubiorev.2017.05.017.
- Bates, MLS, Emery, MA, Wellman, PJ, & Eitan S (2017). Inhibiting social support from massage-like stroking increases morphine dependence. Behavioural Pharmacology 28(8):642-647. doi:10.1097/FBP.0000000000000351.
- Emery MA, Bates, MLS, Wellman PJ, & Eitan S (2017). Hydrocodone is more effective than either morphine or oxycodone in supressing the development of burn-induced mechanical allodynia. Pain Medicine 18(11):2170-2180. doi:10.1093/pm/pnx050
- Emery MA, Bates MLS, Wellman PJ, & 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 and Research 38(5):319-326. doi:10.1097/BCR.0000000000000517
- Emery MA, Bates MLS, Wellman PJ, & Eitan S. (2017). Burn-injury decreases the antinociceptive effects of opioids. Behavioural Pharmacology 28(4):285-293. doi:10.1097/FBP.0000000000000286
- Bates MLS, Emery MA, Wellman PJ, & Eitan S. (2016). Social environment alters opioid‐induced hyperalgesia and antinociceptive tolerance in adolescent mice. European Journal of Pain 20(6):998-1009. doi:10.1002/ejp.825
- Emery MA, Bates MLS, Wellman PJ, & Eitan S. (2016). Differential effects of oxycodone, hydrocodone, and morphine on activation levels of signaling molecules. Pain Medicine 17(5):908-914. doi:10.1111/pme.12918
- Emery MA, Bates MLS, Wellman PJ, & Eitan S. (2015). Differential effects of oxycodone, hydrocodone, and morphine on the responses of D2/D3 dopamine receptors. Behavioural Brain Research 284:37–41. doi:10.1016/j.bbr.2015.01.023.
- Bates MLS, Emery MA, Wellman PJ, & Eitan S. (2014). Social housing conditions influence morphine dependence and the extinction of morphine place preference in adolescent mice. Drug and Alcohol Dependence 142:283–289. doi:10.1016/j.drugalcdep.2014.06.036.
- Cole SL, Hofford RS, Evert DJ, Wellman PJ, Eitan S. (2013). Social influences on morphine conditioned place preference in adolescent mice. Addiction Biology 18(2):274-85.
- Barwatt JW, Hofford RS, Emery MA, Bates ML, Wellman PJ, Eitan S. (2013). Differential effects of methadone and buprenorphine on the response of D2/D3 dopamine receptors in adolescent mice. Drug and Alcohol Dependence 132(3):420-6.
- Hofford RS, Wellman PJ, Eitan S. (2012). Morphine alters the locomotor responses to a D2/D3 dopamine receptor agonist differentially in adolescent and adult mice. Journal of Psychopharmacology 26(10):1355-65.
- Hofford RS, Schul DL, Wellman PJ, Eitan S. (2012). Social influences on morphine sensitization in adolescent rats. Addiction Biology 17(3):547-56.
- Hofford RS, Wellman PJ, Eitan S. (2011). Social influences on plasma testosterone levels in morphine withdrawn adolescent mice and their drug-naïve cage-mates. Psychoneuroendocrinology 36(5):728-36.
- Hodgson SR, Hofford RS, Roberts KW, Wellman PJ, Eitan S. (2010) Socially induced morphine pseudosensitization in adolescent mice. Behavioral Pharmacology 21(2):112-20.
CURRENT GRADUATE STUDENTS
FORMER GRADUATE STUDENTS
(Melvin Lee) Shawn Bates (Postdoctoral Fellow, Bhatnagar Lab, Children’s Hospital of Philadelphia & University of Pennsylvania)
Rebecca S Hofford (Postdoctoral Fellow, Bardo Lab, University of Kentucky)