TY - JOUR
T1 - Transplantation of human retinal pigment epithelial cells in the nucleus accumbens of cocaine self-administering rats provides protection from seeking
AU - Venkiteswaran, Kala
AU - Alexander, Danielle N.
AU - Puhl, Matthew D.
AU - Rao, Anand
AU - Piquet, Amanda L.
AU - Nyland, Jennifer E.
AU - Subramanian, Megha P.
AU - Iyer, Puja
AU - Boisvert, Matthew M.
AU - Handly, Erin
AU - Subramanian, Thyagarajan
AU - Grigson, Patricia Sue
N1 - Funding Information:
This work was supported in part by research grants from the National Institutes of Health National Center for Complementary and Alternative Medicine (NCCAM) R21AT001607 and National Institute of Neurological Disorders and Stroke (NINDS) R01NS42402 , Health Resources and Services Administration grant DIBTH0632 , a grant from the National Institute on Drug Abuse (NIDA) DA009815 , the Pennsylvania Tobacco Settlement Funds Biomedical Research Grant and the American Parkinson’s Disease Association. The Pennsylvania Department of Health specifically disclaims responsibility for any analyses, interpretations, or conclusions. Additional funding was provided by Penn State University Brain Repair Research Fund. We thank NIDA for generously providing the cocaine hydrochloride and Vivek Ananthan and Dr. Chuang Liu for their assistance in the collection of behavioral data.
Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Chronic exposure to drugs and alcohol leads to damage to dopaminergic neurons and their projections in the ‘reward pathway’ that originate in the ventral tegmental area (VTA) and terminate in the nucleus accumbens (NAc). This damage is thought to contribute to the signature symptom of addiction: chronic relapse. In this study we show that bilateral transplants of human retinal pigment epithelial cells (RPECs), a cell mediated dopaminergic and trophic neuromodulator, into the medial shell of the NAc, rescue rats with a history of high rates of cocaine self-administration from drug-seeking when returned, after 2 weeks of abstinence, to the drug-associated chamber under extinction conditions (i.e., with no drug available). Excellent survival was noted for the transplant of RPECs in the shell and/or the core of the NAc bilaterally in all rats that showed behavioral recovery from cocaine seeking. Design based unbiased stereology of tyrosine hydroxylase (TH) positive cell bodies in the VTA showed better preservation (p < 0.035) in transplanted animals compared to control animals. This experiment shows that the RPEC graft provides beneficial effects to prevent drug seeking in drug addiction via its effects directly on the NAc and its neural network with the VTA.
AB - Chronic exposure to drugs and alcohol leads to damage to dopaminergic neurons and their projections in the ‘reward pathway’ that originate in the ventral tegmental area (VTA) and terminate in the nucleus accumbens (NAc). This damage is thought to contribute to the signature symptom of addiction: chronic relapse. In this study we show that bilateral transplants of human retinal pigment epithelial cells (RPECs), a cell mediated dopaminergic and trophic neuromodulator, into the medial shell of the NAc, rescue rats with a history of high rates of cocaine self-administration from drug-seeking when returned, after 2 weeks of abstinence, to the drug-associated chamber under extinction conditions (i.e., with no drug available). Excellent survival was noted for the transplant of RPECs in the shell and/or the core of the NAc bilaterally in all rats that showed behavioral recovery from cocaine seeking. Design based unbiased stereology of tyrosine hydroxylase (TH) positive cell bodies in the VTA showed better preservation (p < 0.035) in transplanted animals compared to control animals. This experiment shows that the RPEC graft provides beneficial effects to prevent drug seeking in drug addiction via its effects directly on the NAc and its neural network with the VTA.
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U2 - 10.1016/j.brainresbull.2015.11.008
DO - 10.1016/j.brainresbull.2015.11.008
M3 - Article
C2 - 26562520
AN - SCOPUS:84947447719
SN - 0361-9230
VL - 123
SP - 53
EP - 60
JO - Journal of Electrophysiological Techniques
JF - Journal of Electrophysiological Techniques
ER -