4.6 Article

Developmentally divergent effects of Rho-kinase inhibition on cocaine- and BDNF-induced behavioral plasticity

Journal

BEHAVIOURAL BRAIN RESEARCH
Volume 243, Issue -, Pages 171-175

Publisher

ELSEVIER
DOI: 10.1016/j.bbr.2013.01.004

Keywords

Orbitofrontal; Fasudil; Learning; ROCK; Dependence; Sensitization

Funding

  1. Children's Healthcare of Atlanta
  2. Emory Egleston Children's Research Center
  3. National Center for Research Resources [P51RR165]
  4. Office of Research Infrastructure Programs/OD [P510D11132]
  5. NINDS [P30NS055077]

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Prefrontal cortical dendritic spine remodeling during adolescence may open a window of vulnerability to pathological stimuli that impact long-term behavioral outcomes, but causal mechanisms remain unclear. We administered the Rho-kinase inhibitor HA-1077 during three adolescent periods in mice to destabilize dendritic spines. In adulthood, cocaine-induced locomotor activity was exaggerated. By contrast, when administered in adulthood, HA-1077 had no psychomotor consequences and normalized food-reinforced instrumental responding after orbitofrontal-selective knockdown of Brain-derived neurotrophic factor, a potential factor in addiction. Thus, early-life Rho-kinase inhibition confers cocaine vulnerability, but may actually protect against pathological reward-seeking - particularly in cases of diminished neurotrophic support - in adulthood. (C) 2013 Elsevier B.V. All rights reserved.

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