TY - JOUR
T1 - Chronic morphine induces visible changes in the morphology of mesolimbic dopamine neurons
AU - Sklair-Tavron, Liora
AU - Shi, Wei Xing
AU - Lane, Sarah B.
AU - Harris, Herbert W.
AU - Bunney, Benjamin S.
AU - Nestler, Eric J.
PY - 1996/10/1
Y1 - 1996/10/1
N2 - The mesolimbic dopamine system, which arises in the ventral tegmental area (VTA), is an important neural substrate for opiate reinforcement and addiction. Chronic exposure to opiates is known to produce biochemical adaptations in this brain region. We now show that these adaptations are associated with structural changes in VTA dopamine neurons. Individual VTA neurons in paraformaldehyde-fixed brain sections from control or morphine- treated rats were injected with the fluorescent dye Lucifer yellow. The identity of the injected cells as dopaminergic or nondopaminergie was determined by immunnhistochemical labeling of the sections for tyrosine hydroxylase. Chronic morphine treatment resulted in a mean ≃25% reduction in the area and perimeter of VTA dopamine neurons. This reduction in cell size was prevented by concomitant treatment of rats with naltrexone, an opioid receptor antagonist, as well as by intra-VTA infusion of brain-derived neurotrophic factor. In contrast, chronic morphine treatment did not alter the size of nondopaminergic neurons in the VTA, nor did it affect the total number of dopaminergic neurons in this brain region. The results of these studies provide direct evidence for structural alterations in VTA dopamine neurons as a consequence of chronic opiate exposure, which could contribute to changes in mesolimbic dopamine function associated with addiction.
AB - The mesolimbic dopamine system, which arises in the ventral tegmental area (VTA), is an important neural substrate for opiate reinforcement and addiction. Chronic exposure to opiates is known to produce biochemical adaptations in this brain region. We now show that these adaptations are associated with structural changes in VTA dopamine neurons. Individual VTA neurons in paraformaldehyde-fixed brain sections from control or morphine- treated rats were injected with the fluorescent dye Lucifer yellow. The identity of the injected cells as dopaminergic or nondopaminergie was determined by immunnhistochemical labeling of the sections for tyrosine hydroxylase. Chronic morphine treatment resulted in a mean ≃25% reduction in the area and perimeter of VTA dopamine neurons. This reduction in cell size was prevented by concomitant treatment of rats with naltrexone, an opioid receptor antagonist, as well as by intra-VTA infusion of brain-derived neurotrophic factor. In contrast, chronic morphine treatment did not alter the size of nondopaminergic neurons in the VTA, nor did it affect the total number of dopaminergic neurons in this brain region. The results of these studies provide direct evidence for structural alterations in VTA dopamine neurons as a consequence of chronic opiate exposure, which could contribute to changes in mesolimbic dopamine function associated with addiction.
KW - Lucifer yellow
KW - brain-derived neurotrophic factor
KW - mesolimbic dopamine system
KW - opiate addiction
KW - tyrosine hydroxylase
UR - http://www.scopus.com/inward/record.url?scp=0029784475&partnerID=8YFLogxK
U2 - 10.1073/pnas.93.20.11202
DO - 10.1073/pnas.93.20.11202
M3 - Article
C2 - 8855333
AN - SCOPUS:0029784475
SN - 0027-8424
VL - 93
SP - 11202
EP - 11207
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 20
ER -